US20140094432A1

US20140094432A1 - Methods and systems for polymer precipitation and generation of particles

Info

Publication number: US20140094432A1
Application number: US14/042,996
Authority: US
Inventors: J. Michael Ramstack
Original assignee: Cerulean Pharma Inc
Current assignee: Dare Bioscience Inc
Priority date: 2012-10-02
Filing date: 2013-10-01
Publication date: 2014-04-03
Also published as: US20180264136A1; US11464871B2; WO2014055493A1

Abstract

Processes for precipitating polymers from a polymer-containing solution are disclosed.

Description

CLAIMS OF PRIORITY

This application claims priority to U.S. Ser. No. 61/708,797 filed Oct. 2, 2012, the entire contents of which is incorporated herein by reference.

BACKGROUND

Cyclodextrin-containing polymer (CDP) conjugates can be utilized as carriers of therapeutic agents. Typically, such CDP-therapeutic agent conjugates can be prepared by introducing a polymer-containing solution into a non-solvent, such as acetone, to precipitate the polymer conjugate. The precipitation process is relatively slow and generally includes formation of a cloudy solution followed by generation of polymeric strands, which eventually coalesce into a polymeric aggregate. Multiple decantation and rinsing steps are then performed to remove unreacted impurities, e.g., unconjugated polymer, unconjugated therapeutic agent, and solvents. The CDP-therapeutic agent conjugates can then be dispersed in water to spontaneously form particles, e.g., nanoparticles.
The scaling of the above process for generating particles, e.g., nanoparticles on a commercial scale can be difficult. For example, the precipitated CDP-therapeutic agent conjugates have a tendency to wrap around mixing impellors and must be manually stripped off. Additionally, the process for precipitating these polymer conjugates can be difficult to reproduce. Accordingly, there exists a need for improved methods for precipitating CDP-therapeutic agent conjugates from a polymer-containing solution and for generating particles, e.g., nanoparticles.

SUMMARY

The disclosure provides, inter alia, processes for precipitating a cyclodextrin-containing polymer (CDP) inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from a polymer-containing solution.
In some embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is as shown below, which is referred to herein as “CRLX101.”
In the above structure:
m=about 77 or the molecular weight of the PEG moiety is 3.4 kDa, e.g., 3.4 kDa+/−10%;
n=is from about 10 to about 18 (e.g., about 14);
the molecular weight of the polymer backbone (i.e., the polymer minus the camptothecin-glycine (CPT-gly), which results in the cysteine moieties having a free —C(O)OH) is from about 48 to about 85 kDa;
the polydispersity of the polymer backbone is less than about 2.2; and
the loading of the CPT onto the polymer backbone is from about 6 to about 13% by weight, wherein 13% is theoretical maximum, meaning, in some instances, one or more of the cysteine residues has a free —C(O)OH (i.e., it lacks the CPT-gly).
The precipitation process can include providing a vessel containing an agitated cooled non-solvent, e.g., a solvent which does not solubilize the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, introducing a polymer-containing solution into the cooled non-solvent to form a mixture comprising a liquid and the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. The mixture is maintained under conditions to precipitate at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from the mixture, thereby precipitating at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. The mixture can then be filtered to separate the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from the liquid. The precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be stored as a solid, e.g., stored in a non-solvent or under an inert environment, or can be stored as a liquid, e.g., stored in an ambient environment.
The precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be further processed. In some embodiments, the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be incorporated into a particle, e.g., a nanoparticle. The resulting particle can be formulated into a pharmaceutical composition or dosage form, which can be administered to a subject, e.g., a subject in need thereof, for example in the treatment of a disorder, e.g. a proliferative disorder, an inflammatory/autoimmune disorder, cardiovascular disorder, a metabolic disorder, a central nervous system disorder, or neurological deficit disorder.
Accordingly, in a first aspect, the disclosure provides a process for precipitating a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from a polymer-containing solution, the process comprising: providing a vessel containing a volume of a cooled non-solvent; agitating the cooled non-solvent; introducing the polymer-containing solution into the cooled non-solvent to form a mixture comprising a liquid and the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein; and maintaining the mixture under conditions to precipitate at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from the mixture, thereby precipitating at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein.
In some embodiments, the mixture is maintained at a temperature of about −50 to about −100 degrees Celsius.
In some embodiments, the temperature of the mixture is less than −90 degrees Celsius, less than −80 degrees Celsius, less than −70 degrees Celsius, or less than −60 degrees Celsius. In some embodiments, the temperature of the mixture is −78 degrees Celsius.
In some embodiments, at least a portion of the liquid from the vessel can be removed subsequent to precipitation of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, thereby separating the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from the mixture.
In some embodiments, the portion of the liquid containing the cooled non-solvent and the polymer-containing solution can be re-introduced into the vessel, thereby precipitating a second portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein.
In some embodiments, a second volume of cooled non-solvent is added to the vessel subsequent to removal of at least a portion of the liquid from the vessel.
In some embodiments, the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is filtered from the mixture.
In some embodiments, the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, comprises a plurality of particles, e.g., nanoparticles, in the non-solvent.
In some embodiments, the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is filtered cold, e.g., at a temperature of about −50 degrees Celsius to about −100 degrees Celsius.
In some embodiments, the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is filtered at room temperature.
In some embodiments, the filtered precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is stored in the cooled non-solvent, e.g., in a solid form, e.g., flakes or shards.
In some embodiments, the filtered precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is stored under a vacuum environment, e.g., in a solid form, e.g., flakes or chards.
In some embodiments, the filtered precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is stored under an ambient environment, e.g., the filtered precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is stored in a form other than a solid, e.g., a liquid or oil.
In some embodiments, the non-solvent comprises acetone, e.g., a polar aprotic solvent.
In some embodiments, the non-solvent comprises acetone comprising less than 20% by volume of water, less than 15% by volume of water, less than 10% by volume of water, less than 5% by volume of water, less than 2% by volume of water, less than 1% by volume of water, less than 0.5% by volume of water, or less than 0.1% by volume of water.
In some embodiments, the temperature of the non-solvent is from about −50 to about −100 degrees Celsius.
In some embodiments, the temperature of the non-solvent is less than −90 degrees Celsius, less than −80 degrees Celsius, less than −70 degrees Celsius, or less than −60 degrees Celsius. In some embodiments, the temperature of the non-solvent is −78 degrees Celsius.
In some embodiments, the temperature of the non-solvent is −78 degrees Celsius.
In some embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, comprises a plurality of cyclodextrin moieties.
In some embodiments, the polymer-containing solution comprises one or more of a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, an unconjugated topoisomerase inhibitor, e.g., camptothecin or camptothecin derivative, an unconjugated CDP, a conjugation reaction side product, and a process solvent.
In some embodiments, the polymer-containing solution comprises an unconjugated polymer, e.g., a CDP that did not conjugate with an inhibitor, e.g., camptothecin or camptothecin derivative, during the conjugation reaction. In some embodiments, the polymer-containing solution comprises an unconjugated inhibitor, e.g., camptothecin or camptothecin derivative that did not conjugate with the CDP during the conjugation reaction. In some embodiments, the polymer-containing solution comprises one or more of the reagents utilized in the preparation of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. In some embodiments, the polymer-containing solution comprises unreacted reagents such as cyclodextrin (CD), e.g., beta-cyclodextrin, CD-biscysteine. In some embodiments, the unconjugated therapeutic agent is camptothecin (CPT), camptothecin modified with glycine, e.g., CPT-glycine. In some embodiments, the polymer-containing solution comprises CD-biscysteine copolymerized with PEG 3.4 kDa, e.g., 3.4 kDa+/−10%. In some embodiments, the polymer-containing solution comprises one or more of an activated monomer, such as PEG-DiSBA.
In some embodiments, the process solvent comprises acetone, ether, alcohol, tetrahydrofuran, 2-pyrrolidone, N-methyl-2-pyrrolidone, dimethylformamide, dimethylacetamide, methyl acetate, ethyl formate, methyl ethyl ketone, methyl isobutyl ketone, methyl propyl ketone, isopropyl ketone, isopropyl acetate, acetonitrile and dimethyl sulfoxide, or a combination thereof.
In some embodiments, at least one of the cyclodextrin moieties comprises α-cyclodextrin.
In some embodiments, at least one of the cyclodextrin moieties comprises β-cyclodextrin.
In some embodiments, at least one of the cyclodextrin moieties comprises γ-cyclodextrin.
In another aspect, the disclosure provides a system for precipitating a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from a polymer-containing solution, the system comprising:
a vessel for containing a fluid (e.g., a cooled non-solvent or a mixture comprising a liquid and the polymer) the vessel having at least one input port and an output port;
a cooling system in communication with the vessel, e.g., a cooling jacket, configured to cool and maintain the temperature of the fluid, e.g., a cooled non-solvent or a mixture comprising a liquid and the polymer, in the vessel;
wherein said input port is configured to allow introduction of the polymer-containing solution into the vessel to precipitate at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein.
In some embodiments, a pump can be in communication with the vessel and configured to cause a flow of the fluid, e.g., the cooled non-solvent or the mixture comprising the liquid and the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, through the vessel.
In some embodiments, the vessel further comprises an agitator, e.g., magnetic or mechanical agitator.
In some embodiments, the non-solvent is cooled prior to introduction of the polymer-containing solution into the vessel.
In some embodiments, the temperature of the non-solvent is less than −90 degrees Celsius, less than −80 degrees Celsius, less than −70 degrees Celsius, or less than −60 degrees Celsius. In some embodiments, the temperature of the non-solvent is −78 degrees Celsius.
In some embodiments, the output port is configured to allow the removal of the fluid, subsequent to the precipitation of at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein.
In some embodiments, a reservoir can be in fluid communication with the vessel for storing a quantity of the polymer-containing solution.
In some embodiments, a fluid passage can extend between the output port and the input port.
In some embodiments, the pump can be in communication with the fluid passage for establishing a liquid recirculation loop through the vessel.
In some embodiments, a recovery port can be in communication with the fluid passage to drain any of the cooled solvent and the liquid from the recirculation loop.
In some embodiments, a reservoir for storing the non-solvent, the reservoir can be in fluid communication with the vessel.
In some embodiments, the vessel can contain a quantity of the non-solvent.
In another aspect, the disclosure provides a process for generating particles, e.g., nanoparticles, comprising:
providing a vessel containing a cooled non-solvent; agitating the cooled non-solvent; introducing a polymer-containing solution comprising a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, into the cooled non-solvent to form a mixture comprising a liquid and the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein; and maintaining the mixture under conditions to precipitate at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from the mixture, thereby precipitating at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein; and isolating at least a portion of the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein; and suspending the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, in an aqueous solution, thereby generating particles, e.g., nanoparticles.
In some embodiments, the pH of the aqueous solution is from about 2 to about 6, e.g., pH 3.
In some embodiments, the polymer-containing solution comprises one or more of a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, an unconjugated therapeutic agent, an unconjugated polymer, a conjugation reaction side product, and a process solvent.
In some embodiments, the polymer-containing solution comprises an unconjugated polymer, e.g., a CDP that did not conjugate with an inhibitor, e.g., camptothecin or camptothecin derivative, during the conjugation reaction. In some embodiments, the polymer-containing solution comprises an unconjugated camptothecin or camptothecin derivative, e.g., camptothecin or camptothecin derivative that did not conjugate with the CDP during the conjugation reaction. In some embodiments, the polymer-containing solution comprises one or more of the reagents utilized in the preparation of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. In some embodiments, the polymer-containing solution comprises unreacted reagents such as cyclodextrin (CD), e.g., beta-cyclodextrin, CD-biscysteine. In some embodiments, the unconjugated therapeutic agent inhibitor is camptothecin (CPT), or a camptothecin modified with glycine, e.g., CPT-glycine. In some embodiments, the polymer-containing solution comprises CD-biscysteine copolymerized with PEG 3.4 kDa, e.g., 3.4 kDa+/−10%. In some embodiments, the polymer-containing solution comprises one or more of an activated monomer, such as PEG-DiSBA.
In some embodiments, the process can cause a recirculating flow of the cooled non-solvent through the vessel and introducing the polymer-containing solution into the flowing cooled non-solvent.
In some embodiments, at least one of the cyclodextrin moieties comprises α-cyclodextrin.
In some embodiments, at least one of the cyclodextrin moieties comprises β-cyclodextrin.
In some embodiments, at least one of the cyclodextrin moieties comprises γ-cyclodextrin.
In some embodiments, the process solvent comprises acetone, ether, alcohol, tetrahydrofuran, 2-pyrrolidone, N-methyl-2-pyrrolidone, dimethylformamide, dimethylacetamide, methyl acetate, ethyl formate, methyl ethyl ketone, methyl isobutyl ketone, methyl propyl ketone, isopropyl ketone, isopropyl acetate, acetonitrile, and dimethyl sulfoxide, or a combination thereof.
In some embodiments, the non-solvent comprises methanol, ethanol, acetone, n-propanol, isopropanol, n-butanol, ethyl ether, methyl isobutyl ketone or ethyl acetate or a combination thereof.
In some embodiments, the process can comprise filtering the particles, e.g., nanoparticles.
In some embodiments, the filtering step can comprise utilizing tangential flow filtration.
In some embodiments, the process can comprise collecting the particles, e.g., nanoparticles.
In some embodiments, the process can comprise lyophilizing the collected particles, e.g., nanoparticles.
In some embodiments, the particles, e.g., nanoparticles, exhibit an average particle size less than about 1 micron.
In some embodiments, the nanoparticles exhibit an average particle size less than about 500 nm.
In some embodiments, the nanoparticles exhibit an average particle size less than about 200 nm.
In some embodiments, the nanoparticles exhibit an average particle size less than about 100 nm.
In some embodiments, the nanoparticles exhibit an average particle size less than about 50 nm.
In some embodiments, the nanoparticles exhibit an average particle size in a range of about 5 nm to about 200 nm.
In some embodiments, the process can comprise analyzing the particle, e.g., nanoparticle by any of transmission electron microscopy, dynamic light scattering, static light scattering, and size exclusion chromatography.
In a further aspect, the disclosure provides a plurality of particles, e.g., nanoparticles, generated according to the process described herein.
In some embodiments, the plurality of particles includes at least about 100 grams of the particles.
In some embodiments, the plurality of particles includes at least about 200 grams of the particles.
In some embodiments, the nanoparticles exhibit an average particle size less than about 200 nm.
In some embodiments, the nanoparticles exhibit an average particle size less than about 100 nm.
In some embodiments, the nanoparticles exhibit an average particle size less than about 50 nm.
In some embodiments, the nanoparticles exhibit an average particle size in a range of about 5 nm to about 200 nm.
In a further aspect, the disclosure provides a product produced by the process described herein.
In a further aspect, the disclosure provides a preparation comprising the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, precipitated by the process described herein.
In some embodiments, the preparation contains less than about 50, less than about 40, less than about 30, less than about 20, less than about 10, less than about 5, or less than about 1% by weight of a solvent.
In some embodiments, the solvent comprises acetone.
In some embodiments, the solvent comprises acetone comprising less than 20% by volume of water, less than 15% by volume of water, less than 10% by volume of water, less than 5% by volume of water, less than 2% by volume of water, less than 1% by volume of water, less than 0.5% by volume of water, or less than 0.1% by volume of water.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a flow chart depicting various steps of a process for precipitating CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein.

FIG. 2 is a schematic diagram of a system for precipitating CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, and generating particles, e.g., nanoparticles.

FIG. 3 depicts a beaker containing precipitated CRLX101 in cooled acetone.

FIG. 4 depicts CRLX101 as an oil at room temperature.

FIG. 5 depicts a free flowing suspension of CRLX101 in acetone at room temperature.

DETAILED DESCRIPTION

Described herein are methods of precipitating CDP-inhibitor conjugates, e.g., CDP-camptothecin conjugates, e.g., CRLX101, or CDP-inhibitor conjugates described herein, from a polymer-containing solution. The CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be precipitated from a polymer-containing solution by contacting the solution with a cooled non-solvent, e.g., cooled acetone, to provide a mixture comprising a liquid and the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. The mixture is maintained under conditions to precipitate at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from the mixture, thereby precipitating at least a portion of the polymer. The precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be filtered to separate the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from the mixture.
The CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be precipitated from a polymer-containing solution using a precipitation system as described herein. For example, the precipitation system can comprise a vessel for housing a cooled non-solvent, the vessel having at least one input port and an output port; a cooling system in communication with the vessel for cooling and maintaining the temperature of the cooled non-solvent; and a pump in communication with the vessel and configured to cause a flow of the cooled non-solvent through the vessel; wherein said input port is configured to allow introduction of the polymer-containing solution into the cooled non-solvent, thereby precipitating at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. The purity of the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be determined using standard analytical methods. Methods for evaluating preparations of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, are also described herein.
The CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, and related preparations, which are precipitated by the methods described herein, can be further processed. For example, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, described herein can be incorporated into a particle (e.g., a nanoparticle). The resulting particle can be formulated into a pharmaceutical composition or dosage form, which can be administered to a subject (e.g., a subject in need thereof), for example in the treatment of a disorder as described herein.
In preferred embodiments, the inhibitor in the CDP-inhibitor conjugate, particle or composition is camptothecin or a camptothecin derivative. The term “camptothecin derivative”, as used herein, includes camptothecin analogues and metabolites of camptothecin. For example, camptothecin derivatives can have the following structure:
wherein
R¹is H, OH, optionally substituted alkyl (e.g., optionally substituted with NR^a ₂or OR_a, or SiR^a ₃), or SiR^a ₃; or R¹and R²may be taken together to form an optionally substituted 5- to 8-membered ring (e.g., optionally substituted with NR^a ₂or OR^a);
R²is H, OH, NH₂, halo, nitro, optionally substituted alkyl (e.g., optionally substituted with NR^a ₂or OR^a, NR^a ₂, OC(═O)NR^a ₂, or OC(═O)OR^a);
R³is H, OH, NH₂, halo, nitro, NR^a ₂, OC(═O)NR^a ₂, or OC(═O)OR^a
R⁴is H, OH, NH₂, halo, CN, or NR^a ₂; or R³and R⁴taken together with the atoms to which they are attached form a 5- or 6-membered ring (e.g. forming a ring including —OCH₂O— or —OCH₂CH₂O—);
each R^ais independently H or alkyl; or two R^as, taken together with the atom to which they are attached, form a 4- to 8-membered ring (e.g., optionally containing an O or NR^b)
R_bis H or optionally substituted alkyl (e.g., optionally substituted with OR^cor NR^c ₂);
R^cis H or alkyl; or, two R^cs, taken together with the atom to which they are attached, form a 4- to 8-membered ring; and
n=0 or 1.
In some embodiments, the camptothecin or camptothecin derivative is the compound as provided below.
In one embodiment, R¹, R², R³and R⁴of the camptothecin derivative are each H, and n is 0.
In one embodiment, R¹, R², R³and R⁴of the camptothecin derivative are each H, and n is 1.
In one embodiment, R¹of the camptothecin derivative is H, R²is —CH₂N(CH₃)₂, R³is —OH, R⁴is H; and n is 0.
In one embodiment, the camptothecin derivative is SN-38, or derivative thereof, having the following structure:
In one embodiment, R¹of the camptothecin derivative is —CH₂CH₃, R²is H, R³is:

R⁴is H, and n is 0.

In one embodiment, R¹of the camptothecin derivative is —CH₂CH₃, R²is H, R³is —OH, R⁴is H, and n is 0.
In one embodiment, R¹of the camptothecin derivative is tert-butyldimethylsilyl, R²is H, R³is —OH and R⁴is H, and n is 0.
In one embodiment, R¹of the camptothecin derivative is tert-butyldimethylsilyl, R²is hydrogen, R³is —OH and R⁴is hydrogen, and n is 1.
In one embodiment, R¹of the camptothecin derivative is tert-butyldimethylsilyl, R², R³and R⁴are each H, and n is 0.
In one embodiment, R¹of the camptothecin derivative is tert-butyldimethylsilyl, R², R³and R⁴are each H, and n is 1.
In one embodiment, R¹of the camptothecin derivative is —CH₂CH₂Si(CH₃)₃and R², R³and R⁴are each H.
In one embodiment, R¹and R²of the camptothecin derivative are taken together with the carbons to which they are attached to form an optionally substituted ring. In one embodiment, R¹and R²of the camptothecin derivative are taken together with the carbons to which they are attached to form a substituted 6-membered ring. In one embodiment, the camptothecin derivative has the following formula:
In one embodiment, R³is methyl and R⁴is fluoro.
In one embodiment, R³and R⁴are taken together with the carbons to which they are attached to form an optionally substituted ring. In one embodiment, R³and R⁴are taken together with the carbons to which they are attached to form a 6-membered heterocyclic ring. In one embodiment, the camptothecin derivative has the following formula:
In one embodiment, R¹is:
and R²is hydrogen.
In one embodiment, the camptothecin derivative has the following formula:
In one embodiment, R¹is:
and R²is hydrogen.
In one embodiment, R¹is:
R²is H, R³is methyl, R⁴is chloro; and n is 1.
In one embodiment, R¹is —CH═NOC(CH₃)₃, R², R³and R⁴are each H, and n is 0.
In one embodiment, R¹is —CH₂CH₂NHCH(CH₃)₂, R², R³and R⁴are each H; and n is 0.
In one embodiment, R¹and R²are H, R³and R⁴are fluoro, and n is 1.
In one embodiment, each of R¹, R³, and R⁴is H, R²is NH₂, and n is 0.
In one embodiment, each of R¹, R³, and R⁴is H, R²is NO₂, and n is 0.

Definitions

The term “precipitate,” as used herein, refers to the separation of a solid substance, e.g., a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from a mixture, e.g., a solution, dispersion, or a mixed solution/dispersion, of that solid substance and a liquid. The term “precipitation” refers to the act of precipitating.
The term “separate” or “separating,” as used herein, is defined as increasing the amount of a first component, e.g., a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, relative to the amounts of at least one, and in embodiments, more than one, other component, e.g., a contaminant, in a mixture, e.g., a mixture comprising one or more of a non-solvent, a polymer-containing solution, a process solvent. In some embodiments, the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is separated from the liquid component of a mixture, e.g., a mixture comprising a non-solvent, a process solvent, unreacted starting materials, e.g., from the conjugation reaction of a polymer, e.g., a CDP, with a therapeutic agent, e.g., a camptothecin or camptothecin conjugate, such as CRLX101. After separation of the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, the amount of the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is substantially increased relative to the amount of at least one, and in embodiments, more than one, of the other components of the mixture. In some embodiments, the separated precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, contains less than 20, 10, 5, 1, 0.5%, or 0.1%, by dry weight, of a component of the mixture, e.g., contaminant, e.g., non-solvent, process solvent, polymer-containing solution, an unreacted starting material, and other conjugation reaction side products. In some embodiments, the separated precipitated polymer conjugate is substantially free, by dry weight analysis, of a component of the mixture, e.g., contaminant, e.g., non-solvent, process solvent, polymer-containing solution, an unreacted starting material, and other conjugation reaction side products.
The term “polymer-containing solution,” as used herein, refers to a solution in which a polymer is disposed, e.g., in the form of a polymer solution, dispersion, or mixed solution/dispersion. In some embodiments, the polymer-containing solution comprises a reaction mixture, e.g., from a conjugation reaction between a polymer, e.g., a polymer comprising cyclodextrin, e.g., beta-cyclodextrin, and an inhibitor, e.g., a camptothecin or camptothecin derivative, such as CRLX101, or a CDP-inhibitor conjugate described herein.
In some embodiments, the polymer-containing solution comprises the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. In some embodiments, the polymer-containing solution comprises an unconjugated polymer, e.g., a CDP that did not conjugate with an inhibitor, e.g., camptothecin or camptothecin derivative, during the conjugation reaction. In some embodiments, the unconjugated polymer, e.g., CDP, can be a polymer that comprises a reactive group, which can include a hydroxyl moiety, a thiol moiety, an amine moiety, a carboxylic acid moiety, or an activated ester moiety.
In some embodiments, the polymer-containing solution comprises a process solvent, e.g., a solvent present in the reaction mixture, e.g., conjugation reaction mixture. The term “process solvent” as used herein refers to a solvent that acts to keep the reactants of a reaction mixture, e.g., conjugation reaction, soluble. In some embodiments, the polymer is typically sufficiently soluble in the solvent such that a concentration of at least about 0.1 percent by weight, and preferably at least about 0.2 percent by weight, of the polymer, e.g., CDP, can be dissolved in the solvent at room temperature.
The term “about” or “approximately,” as used herein refers to within an acceptable error range for the particular value as determined by one of ordinary skill in the art, which will depend in part on how the value is measured or determined, e.g., the limitations of the measurement system, or the degree of precision required for a particular purpose. For example, “about” can mean within 1 or more than 1 standard deviations, as per the practice in the art. Alternatively, “about” can mean a range of up to 20%, up to 10%, up to 5%, and up to 1% of a given value. Where particular values are described in the application and claims, unless otherwise stated, the term “about” meaning within an acceptable error range for the particular value should be assumed.
The term “non-solvent” as used herein refers to a liquid, or a mixture of liquids, which is incapable of dissolving any appreciable concentration (e.g., a concentration less than about 5%, less than about 2%, less than about 1%, less than about 0.5%, less than about 0.2%, less than about 0.1% at room temperature) of a polymer of interest, e.g., the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. In some embodiments, the non-solvent can be cooled so as to lower the concentration of the dissolution of the polymer of interest, e.g., the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, in the non-solvent. For example, the non-solvent can be cooled to a temperature of about 0° C. to about −100° C., e.g., about −10° C. to about −90° C., about −20° C. to about −80° C. In some embodiments, the non-solvent can be cooled to a temperature of −78° C.
The term “ambient conditions,” as used herein, refers to surrounding conditions at about one atmosphere of pressure, 50% relative humidity and about 25° C., unless specified as otherwise.
The term “attach,” or “attached,” as used herein, with respect to the relationship of a first moiety to a second moiety, e.g., the attachment of an agent to a polymer, refers to the formation of a covalent bond between a first moiety and a second moiety. In the same context, the noun “attachment” refers to a covalent bond between the first and second moiety. For example, a therapeutic agent, e.g., topoisomerase inhibitor, e.g., camptothecin or camptothecin derivative, can be covalently bonded to the polymer, e.g., cyclodextrin, e.g., beta-cyclodextrin polymer (CDP). The attachment can be a direct attachment, e.g., through a direct bond of the first moiety to the second moiety, or can be through a linker (e.g., through a covalently linked chain of one or more atoms disposed between the first and second moiety). For example, where an attachment is through a linker, a first moiety (e.g., a therapeutic agent, such as camptothecin or camptothecin derivative) is covalently bonded to a linker, which in turn is covalently bonded to a second moiety.
The term “biodegradable” includes polymers, compositions and formulations, such as those described herein, that are intended to degrade during use. Biodegradable polymers typically differ from non-biodegradable polymers in that the former may be degraded during use. In certain embodiments, such use involves in vivo use, such as in vivo therapy, and in other certain embodiments, such use involves in vitro use. In general, degradation attributable to biodegradability involves the degradation of a biodegradable polymer into its component subunits, or digestion, e.g., by a biochemical process, of the polymer into smaller, non-polymeric subunits. In certain embodiments, two different types of biodegradation may generally be identified. For example, one type of biodegradation may involve cleavage of bonds (whether covalent or otherwise) in the polymer backbone. In such biodegradation, monomers and oligomers typically result, and even more typically, such biodegradation occurs by cleavage of a bond connecting one or more of subunits of a polymer. In contrast, another type of biodegradation may involve cleavage of a bond (whether covalent or otherwise) internal to a side chain or that connects a side chain to the polymer backbone. In certain embodiments, one or the other or both general types of biodegradation can occur during use of a polymer.
The term “biodegradation,” as used herein, encompasses both general types of biodegradation described above. The degradation rate of a biodegradable polymer often depends in part on a variety of factors, including the chemical identity of the linkage responsible for any degradation, the molecular weight, crystallinity, biostability, and degree of cross-linking of such polymer, the physical characteristics (e.g., shape and size) of a polymer, assembly of polymers or particle, and the mode and location of administration. For example, a greater molecular weight, a higher degree of crystallinity, and/or a greater biostability, usually lead to slower biodegradation.
The phrase “cleavable under physiological conditions” refers to a bond having a half life of less than about 50 or 100 hours, when subjected to physiological conditions. For example, enzymatic degradation can occur over a period of less than about five years, one year, six months, three months, one month, fifteen days, five days, three days, or one day upon exposure to physiological conditions (e.g., an aqueous solution having a pH from about 4 to about 8, and a temperature from about 25° C. to about 37° C.
The term “contaminant,” as used herein, is a compound other than the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. A contaminant can be an unconjugated component or starting material in the mixture, e.g., conjugation reaction mixture. A contaminant can be a product of the conjugation reaction other than the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, such as an unconjugated therapeutic agent, e.g., unconjugated inhibitor, e.g., camptothecin or camptothecin derivative, unconjugated polymer, e.g., unconjugated CDP, process solvent, or conjugation reaction side products.
In some embodiments, the contaminant can be an unconjugated inhibitor. In some embodiments, the contaminant can be a glycine-derivatized camptothecin (CPT-glycine) that failed to conjugate with the polymer, e.g., CDP.
In some embodiments, the contaminant can be an unconjugated polymer, e.g., CDP. In some embodiments, the unconjugated polymer, e.g., CDP, can include a hydroxyl, a thiol moiety, an amine moiety, or a carboxylic acid moiety. In some embodiments, the unconjugated polymer can have a molecular weight of about 5 kDa to about 200 kDa.
In some embodiments, the contaminant can be any of the reagents used in the conjugation reaction between an inhibitor, e.g., camptothecin, and a polymer, e.g., a CDP. For example, the contaminant can be a carbodiimide, e.g., N,N′-dicyclohexylcarbodiimide (DCC), N,N′-Diisopropylcarbodiimide (DIC), and (1-Ethyl-3-(3-dimethyllaminopropyl)carbodiimide (EDC). Other contaminants include, but are not limited to, hydroxysuccinimide (NHS), diethylamine, and triethylamine.
In some embodiments, the contaminant is a process solvent such as water, dimethylsulfoxide (DMSO), N,N-dimethylformamide (DMF), or acetonitrile.
An “effective amount” or “an amount effective” refers to an amount of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, particle, or composition which is effective, upon single or multiple dose administrations to a subject, in treating a cell, or curing, alleviating, relieving or improving a symptom of a disorder. An effective amount of the composition may vary according to factors such as the disease state, age, sex, and weight of the individual, and the ability of the compound to elicit a desired response in the individual. An effective amount is also one in which any toxic or detrimental effects of the composition are outweighed by the therapeutically beneficial effects.
“Pharmaceutically acceptable carrier or adjuvant,” as used herein, refers to a carrier or adjuvant that may be administered to a patient, together with a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, described herein, and which does not destroy the pharmacological activity thereof and is nontoxic when administered in doses sufficient to deliver a therapeutic amount of the particle. Some examples of materials which can serve as pharmaceutically acceptable carriers include: (1) sugars, such as lactose, glucose, mannitol and sucrose; (2) starches, such as corn starch and potato starch; (3) cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; (4) powdered tragacanth; (5) malt; (6) gelatin; (7) talc; (8) excipients, such as cocoa butter and suppository waxes; (9) oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; (10) glycols, such as propylene glycol; (11) polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; (12) esters, such as ethyl oleate and ethyl laurate; (13) agar; (14) buffering agents, such as magnesium hydroxide and aluminum hydroxide; (15) alginic acid; (16) pyrogen-free water; (17) isotonic saline; (18) Ringer's solution; (19) ethyl alcohol; (20) phosphate buffer solutions; and (21) other non-toxic compatible substances employed in pharmaceutical compositions.
The term “polymer,” as used herein, is given its ordinary meaning as used in the art, i.e., a molecular structure featuring one or more repeat units (monomers), connected by covalent bonds. The repeat units may all be identical, or in some cases, there may be more than one type of repeat unit present within the polymer. In some cases, the polymer is biologically derived, i.e., a biopolymer. Non-limiting examples of biopolymers include peptides or proteins (i.e., polymers of various amino acids), or nucleic acids such as DNA or RNA. In some instances, a polymer may be comprised of subunits, e.g., a subunit described herein, wherein a subunit comprises polymers, e.g., PEG, but the subunit may be repeated within a conjugate. In some embodiments, a conjugate may comprise only one subunit described herein; however conjugates may comprise more than one identical subunit.
As used herein the term “low aqueous solubility” refers to water insoluble compounds having poor solubility in water, that is <5 mg/ml at physiological pH (6.5-7.4). Preferably, their water solubility is <1 mg/ml, more preferably <0.1 mg/ml. It is desirable that the drug is stable in water as a dispersion; otherwise a lyophilized or spray-dried solid form may be desirable.
A “hydroxy protecting group” as used herein, is well known in the art and includes those described in detail in Protecting Groups in Organic Synthesis, T. W. Greene and P. G. M. Wuts, 3^rdedition, John Wiley & Sons, 1999, the entirety of which is incorporated herein by reference. Suitable hydroxy protecting groups include, for example, acyl (e.g., acetyl), triethylsilyl (TES), t-butyldimethylsilyl (TBDMS), 2,2,2-trichloroethoxycarbonyl (Troc), and carbobenzyloxy (Cbz).
“Inert atmosphere” or “inert environment,” as used herein, refers to an atmosphere composed primarily of an inert gas, which does not chemically react with the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, particles, compositions or mixtures described herein. Examples of inert gases are nitrogen (N₂), helium, and argon.
“Linker,” as used herein, is a moiety having at least two functional groups. One functional group is capable of reacting with a functional group on a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, and a second functional group is capable of reacting with a functional group on agent described herein. In some embodiments, the linker has just two functional groups. A linker may have more than two functional groups (e.g., 3, 4, 5, 6, 7, 8, 9, 10 or more functional groups), which may be used, e.g., to link multiple agents to a polymer. Depending on the context, linker can refer to a linker moiety before attachment to either of a first or second moiety (e.g., agent or polymer), after attachment to one moiety but before attachment to a second moiety, or the residue of the linker present after attachment to both the first and second moiety.
The term “lyoprotectant,” as used herein refers to a substance present in a lyophilized preparation. Typically it is present prior to the lyophilization process and persists in the resulting lyophilized preparation. It can be used to protect nanoparticles, liposomes, and/or micelles during lyophilization, for example to reduce or prevent aggregation, particle collapse and/or other types of damage. In an embodiment the lyoprotectant is a cryoprotectant. In an embodiment the lyoprotectant is a carbohydrate.
As used herein, the term “prevent” or “preventing” as used in the context of the administration of an agent to a subject, refers to subjecting the subject to a regimen, e.g., the administration of a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, such that the onset of at least one symptom of the disorder is delayed as compared to what would be seen in the absence of the regimen.
As used herein, the term “subject” is intended to include human and non-human animals. Exemplary human subjects include a human patient having a disorder, e.g., a disorder described herein, or a normal subject. The term “non-human animals” includes all vertebrates, e.g., non-mammals (such as chickens, amphibians, reptiles) and mammals, such as non-human primates, domesticated and/or agriculturally useful animals, e.g., sheep, dog, cat, cow, pig, etc.
The term “nanoparticle” is used herein to refer to a material structure whose size in any dimension (e.g., x, y, and z Cartesian dimensions) is less than about 1 micrometer (micron), e.g., less than about 500 nm or less than about 200 nm or less than about 100 nm, and greater than about 5 nm. A nanoparticle can have a variety of geometrical shapes, e.g., spherical, ellipsoidal, etc. The term “nanoparticles” is used as the plural of the term “nanoparticle.”
The term “average particle size,” as used herein with respect to polymeric particles, is a length dimension which is designated herein as Z average or Z_ave, and as used herein refers to the intensity weighted mean hydrodynamic size of an ensemble collection of particles measured by dynamic light scattering (DLS). The Z average is derived from a Cumulants analysis of a measured autocorrelation curve, wherein a single particle size is assumed and a single exponential fit is applied to the autocorrelation function. The autocorrelation function (G(τ)) is defined as follows:
$\begin{matrix} G (τ) = 〈 I (t) \cdot I (t + τ) 〉 = A [1 + B \exp (- 2 Γ τ)] wherein, & Eq . (3) \\ Γ = {Dq}^{2} & Eq . (4) \\ q = \frac{4 π \tilde{n}}{λ_{0}} \sin (\frac{θ}{2}) & Eq . (5) \\ D = \frac{kT}{6 π μ R_{H}}, & Eq . (6) \end{matrix}$
wherein,
I represents the light scattering intensity,
t represents an initial time,
τ represents the delay time,
A represents an amplitude (or intercept) of the autocorrelation function,
B represents the baseline,
D represents the diffusion coefficient,
q represents the scattering vector,
k represents the Boltzmann constant,
λ₀represents the vacuum wavelength of a laser source employed for the light scattering measurements,
ñ represents the index of refraction of the medium,
θ represents the scattering angle,
T represents the absolute temperature (Kelvin),
μ represents the viscosity of the medium, and
R_Hrepresents the hydrodynamic radius.
In the Cumulants analysis, the exponential fitting expression of Eq. (3) is expanded as indicated below as expression y(τ) in Eq. (7) to account for polydispersity, which is defined in more detail below, or peak broadening,
$\begin{matrix} \begin{matrix} y (τ) = \frac{1}{2} \ln [G (τ) - A] \\ = \frac{1}{2} \ln [AB \exp (- 2 Γ τ + μ_{2} τ^{2})] \\ ≅ \frac{1}{2} \ln [AB] - 〈 Γ 〉 τ + \frac{μ_{2}}{2} τ^{2} \\ = a_{0} - a_{1} τ + a_{2} τ^{2} \end{matrix} & Eq . (7) \end{matrix}$
wherein μ₂is a fitting parameter and the other parameters are defined above.
The dynamic light scattering data can be fit to the above expression (Eq. (7)) to obtain values of the parameters a₀, a₁, and a₂. The first Cumulant moment (a₁) can be utilized to obtain Z_aveas follows:
$\begin{matrix} Z_{ave} = \frac{1}{a_{1}} {\frac{kT}{3 π μ} [\frac{4 π \tilde{n}}{λ_{0}} \sin (\frac{θ}{2})]}^{2} & Eq . (8) \end{matrix}$
wherein the parameters are defined above.
The first Cumulant moment (a₁) and the second Cumulant moment (a₂) can be used to calculate another parameter known as polydispersity index (PdI), which is discussed in more detail below, as follows:
$\begin{matrix} Pdl = \frac{2 a_{2}}{a_{1}^{2}} & Eq . (9) \end{matrix}$
The term “polydispersity index” is used herein as a measure of the size distribution of an ensemble of particles, e.g., nanoparticles. The polydispersity index is calculated as indicated in the above Eq. (9) based on dynamic light scattering measurements.
The term “acyl” refers to an alkylcarbonyl, cycloalkylcarbonyl, arylcarbonyl, heterocyclylcarbonyl, or heteroarylcarbonyl substituent, any of which may be further substituted (e.g., by one or more substituents). Exemplary acyl groups include acetyl (CH₃C(O)—), benzoyl (C₆H₅C(O)—), and acetylamino acids (e.g., acetylglycine, CH₃C(O)NHCH₂C(O)—).
The term “alkyl” refers to the radical of saturated aliphatic groups, including straight-chain alkyl groups, branched-chain alkyl groups, cycloalkyl (alicyclic) groups, alkyl-substituted cycloalkyl groups, and cycloalkyl-substituted alkyl groups. In preferred embodiments, a straight chain or branched chain alkyl has 30 or fewer carbon atoms in its backbone (e.g., C₁-C₃₀for straight chains, C₃-C₃₀for branched chains), and more preferably 20 or fewer, and most preferably 10 or fewer. Likewise, preferred cycloalkyls have from 3-10 carbon atoms in their ring structure, and more preferably have 5, 6 or 7 carbons in the ring structure. The term “alkylenyl” refers to a divalent alkyl, e.g., —CH₂—, —CH₂CH₂—, and —CH₂CH₂CH₂—.
The term “alkenyl” refers to an aliphatic group containing at least one double bond.
The terms “alkoxyl” or “alkoxy” refers to an alkyl group, as defined below, having an oxygen radical attached thereto. Representative alkoxyl groups include methoxy, ethoxy, propyloxy, tert-butoxy and the like. An “ether” is two hydrocarbons covalently linked by an oxygen.
The term “alkynyl” refers to an aliphatic group containing at least one triple bond.
The term “aralkyl” or “arylalkyl” refers to an alkyl group substituted with an aryl group (e.g., a phenyl or naphthyl).
The term “aryl” includes 5-14 membered single-ring or bicyclic aromatic groups, for example, benzene, naphthalene, and the like. The aromatic ring can be substituted at one or more ring positions with such substituents as described above, for example, halogen, azide, alkyl, aralkyl, alkenyl, alkynyl, cycloalkyl, polycyclyl, hydroxyl, alkoxyl, amino, nitro, sulfhydryl, imino, amido, phosphate, phosphonate, phosphinate, carbonyl, carboxyl, silyl, ether, alkylthio, sulfonyl, sulfonamido, ketone, aldehyde, ester, heterocyclyl, aromatic or heteroaromatic moieties, —CF₃, —CN, or the like. The term “aryl” also includes polycyclic ring systems having two or more cyclic rings in which two or more carbons are common to two adjoining rings (the rings are “fused rings”) wherein at least one of the rings is aromatic, e.g., the other cyclic rings can be cycloalkyls, cycloalkenyls, cycloalkynyls, aryls and/or heterocyclyls. Each ring can contain, e.g., 5-7 members. The term “arylene” refers to a divalent aryl, as defined herein.
The term “carboxy” refers to a —C(O)OH or salt thereof.
The term “hydroxy” and “hydroxyl” are used interchangeably and refer to —OH. The term “substituents” refers to a group “substituted” on an alkyl, cycloalkyl, alkenyl, alkynyl, heterocyclyl, heterocycloalkenyl, cycloalkenyl, aryl, or heteroaryl group at any atom of that group. Any atom can be substituted. Suitable substituents include, without limitation, alkyl (e.g., C1, C2, C3, C4, C5, C6, C7, C8, C9, C10, C11, C12 straight or branched chain alkyl), cycloalkyl, haloalkyl (e.g., perfluoroalkyl such as CF₃), aryl, heteroaryl, aralkyl, heteroaralkyl, heterocyclyl, alkenyl, alkynyl, cycloalkenyl, heterocycloalkenyl, alkoxy, haloalkoxy (e.g., perfluoroalkoxy such as OCF₃), halo, hydroxy, carboxy, carboxylate, cyano, nitro, amino, alkyl amino, SO₃H, sulfate, phosphate, methylenedioxy (—O—CH₂—O— wherein oxygens are attached to vicinal atoms), ethylenedioxy, oxo, thioxo (e.g., C═S), imino (alkyl, aryl, aralkyl), S(O)_nalkyl (where n is 0-2), S(O)_naryl (where n is 0-2), S(O)_nheteroaryl (where n is 0-2), S(O)_nheterocyclyl (where n is 0-2), amine (mono-, di-, alkyl, cycloalkyl, aralkyl, heteroaralkyl, aryl, heteroaryl, and combinations thereof), ester (alkyl, aralkyl, heteroaralkyl, aryl, heteroaryl), amide (mono-, di-, alkyl, aralkyl, heteroaralkyl, aryl, heteroaryl, and combinations thereof), sulfonamide (mono-, di-, alkyl, aralkyl, heteroaralkyl, and combinations thereof). In one aspect, the substituents on a group are independently any one single, or any subset of the aforementioned substituents. In another aspect, a substituent may itself be substituted with any one of the above substituents.
The terms “halo” and “halogen” means halogen and includes chloro, fluoro, bromo, and iodo.
The terms “hetaralkyl”, “heteroaralkyl” or “heteroarylalkyl” refers to an alkyl group substituted with a heteroaryl group.
The term “heteroaryl” refers to an aromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of N, O, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2, 3, or 4 atoms of each ring may be substituted by a substituent. Examples of heteroaryl groups include pyridyl, furyl or furanyl, imidazolyl, benzimidazolyl, pyrimidinyl, thiophenyl or thienyl, quinolinyl, indolyl, thiazolyl, and the like. The term “heteroarylene” refers to a divalent heteroaryl, as defined herein.
“Heterocycloalkyl” refers to a stable 3- to 18-membered non-aromatic ring radical that comprises two to twelve carbon atoms and from one to six heteroatoms selected from nitrogen, oxygen and sulfur. Whenever it appears herein, a numerical range such as “3 to 18” refers to each integer in the given range; e.g., “3 to 18 ring atoms” means that the heterocycloalkyl group may consist of 3 ring atoms, 4 ring atoms, etc., up to and including 18 ring atoms. In some embodiments, it is a C₅-C₁₀heterocycloalkyl. In some embodiments, it is a C₄-C₁₀heterocycloalkyl. In some embodiments, it is a C₃-C₁₀heterocycloalkyl. Unless stated otherwise specifically in the specification, the heterocycloalkyl radical is a monocyclic, bicyclic, tricyclic or tetracyclic ring system, which may include fused or bridged ring systems. The heteroatoms in the heterocycloalkyl radical may be optionally oxidized. One or more nitrogen atoms, if present, are optionally quaternized. The heterocycloalkyl radical is partially or fully saturated. The heterocycloalkyl may be attached to the rest of the molecule through any atom of the ring(s). Examples of such heterocycloalkyl radicals include, but are not limited to, dioxolanyl, thienyl[1,3]dithianyl, decahydroisoquinolyl, imidazolinyl, imidazolidinyl, isothiazolidinyl, isoxazolidinyl, morpholinyl, octahydroindolyl, octahydroisoindolyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, oxazolidinyl, piperidinyl, piperazinyl, 4-piperidonyl, pyrrolidinyl, pyrazolidinyl, quinuclidinyl, thiazolidinyl, tetrahydrofuryl, trithianyl, tetrahydropyranyl, thiomorpholinyl, thiamorpholinyl, 1-oxo-thiomorpholinyl, and 1,1-dioxo-thiomorpholinyl.
“Heterocycloalkyl” also includes bicyclic ring systems wherein one non-aromatic ring, usually with 3 to 7 ring atoms, contains at least 2 carbon atoms in addition to 1-3 heteroatoms independently selected from oxygen, sulfur, and nitrogen, as well as combinations comprising at least one of the foregoing heteroatoms; and the other ring, usually with 3 to 7 ring atoms, optionally contains 1-3 heteroatoms independently selected from oxygen, sulfur, and nitrogen and is not aromatic.
“Nitro” refers to the —NO₂radical.

Methods of Precipitating Polymer Conjugates

Methods for precipitating CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from a polymer-containing solution are described herein. Methods described herein comprise providing a vessel housing a volume of a cooled non-solvent; agitating the cooled non-solvent; introducing the polymer-containing solution into the cooled non-solvent to form a mixture comprising a liquid and CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein; and maintaining the mixture under conditions to precipitate at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from the mixture, thereby precipitating at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein.
With reference to the flow chart of FIG. 1, in one embodiment, a vessel is provided that houses a volume of a cooled non-solvent (Step 1). A polymer-containing solution is introduced into the vessel to form a mixture comprising a liquid and a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein; and maintaining the mixture under conditions to precipitate at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from the mixture, thereby precipitating at least a portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein (Step 2). In some embodiments, the polymer-containing solution comprises one or more of a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, an unconjugated inhibitor, e.g., an unconjugated camptothecin or camptothecin derivative, an unconjugated polymer, e.g., unconjugated CDP, a conjugation reaction side product, and a process solvent.
In some embodiments, the non-solvent comprises any of a solvent or a mixture of two or more solvents. The solvents can be either organic or inorganic solvents. By way of example, the non-solvent can include any of acetone, methanol, ethanol, n-propanol, isopropanol, n-butanol, and ethyl ether, methyl isobutyl ketone (MIBK), ethyl acetate (ETAC), water, among others.
In some embodiments, the non-solvent comprises acetone. In some embodiments, the acetone comprises less than 20% by volume of water, less than 15% by volume of water, less than 10% by volume of water, less than 5% by volume of water, less than 2% by volume of water, less than 1% by volume of water, less than 0.5% by volume of water, or less than 0.1% by volume of water.
In some embodiments, the vessel can be a 5 mL, 10 mL, 50 mL, 100 mL, 250 mL, 500 mL, 1 liter, or 2 liter glass beaker. In some embodiments, the vessel can be a 5 liter, 10 liter, 25 liter, 50 liter reactor used in a scale up process. The vessel housing the non-solvent can be cooled and maintained at a constant temperature throughout the precipitation process. In some embodiments, the non-solvent is cooled before the polymer-containing solution is introduced into the vessel. For example, the vessel housing the non-solvent can be cooled and maintained at a temperature of about 0° C. to about −100° C., e.g., about −10° C. to about −90° C., about −20° C. to about −80° C. In some embodiments, the vessel is cooled and maintained at a temperature of −78° C.
In some embodiments, the process further includes extracting at least a portion of the liquid comprising the polymer-containing solution and the non-solvent from the vessel and recirculating the liquid through the vessel to induce further precipitation of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein (Step 3).
In some embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is immiscible, or at least exhibits low miscibility in the non-solvent. For example, in some embodiments, the miscibility of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, in the non-solvent is less than about 0.5% at −78° C. (e.g., at 25° C.). In some embodiments, the process solvent is miscible, or at least partially miscible, with the non-solvent.
Without wishing to be bound by theory, as the polymer-containing solution flows into the vessel and comes into contact with the cooled non-solvent, the polymer-containing solution can diffuse into the non-solvent due to its miscibility with the non-solvent. The CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is not miscible, or exhibits low miscibility, with the non-solvent, and hence precipitates out of solution. Such precipitation of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, in the cooled non-solvent continues as fresh polymer-containing solution is introduced into the vessel. As noted above, optionally, in some embodiments, a portion of the liquid in the vessel can be extracted and recirculated back to the vessel for precipitating at least a second portion of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, which is contained in the extracted liquid, in the cooled non-solvent.
Referring again to the flow chart of FIG. 1, in some embodiments, after the introduction of the polymer-containing solution into the vessel is terminated; a second volume of cooled non-solvent is added to the vessel (Step 4).
Referring again to the flow chart of FIG. 1, in some embodiments, the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be optionally collected, e.g., via filtration (Step 5). Alternatively, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be separated from the liquid via centrifugation.
In some embodiments, the collected CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be optionally dried, e.g., by utilizing a vacuum or a flow of a gas such as dry nitrogen or argon, to remove at least a portion of residual liquid present in the particles (Step 6). Otherwise, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be filtered using the cooled non-solvent and then stored in the non-solvent, either at room temperature or at a lower temperature, e.g., less than about 0° C., less than about −10° C., less than about −20° C., less than about −30° C., less than about −40° C., less than about −50° C., less than about −60° C., less than about −70° C., less than about −80° C.
In some embodiments, the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be dried using a vacuum or inert gas such as nitrogen or argon, and then stored dry under vacuum or an inert atmosphere in a solid form, e.g., as flakes or shards. Alternatively, the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be filtered and washed with cooled non-solvent and stored using the non-solvent, in a solid form, e.g., as flakes or shards, either at room temperature or at a lower temperature. The CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be stored at a lower temperature, e.g., less than about 0° C., less than about −10° C., less than about −20° C., less than about −30° C., less than about −40° C., less than about −50° C., less than about −60° C., less than about −70° C., less than about −80° C., refrigerated or frozen, for later use (Step 7). In some embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be subsequently exposed to a liquid, a polar protic solvent, such as water, to form particles, e.g., nanoparticles.
In a further embodiment, a lyoprotectant can be optionally added to the particles, e.g., nanoparticles, to protect the particles, e.g., nanoparticles, from damage and/or to retard permanent aggregation of the particles, e.g., nanoparticles, when subsequently subjected to lyophilization. The lyoprotectant can also facilitate the resuspension of the particles, e.g., nanoparticles. Some examples of suitable lyoprotectants include, without limitation, conventional lyoprotectants, e.g., mannitol, lactose, trehalose, sucrose, or a derivatized cyclic oligosaccharide, e.g., a derivatized cyclodextrin, e.g., 2 hydroxy propyl-β cyclodextrin, e.g., partially etherified cyclodextrins (e.g., partially etherified (3 cyclodextrins) disclosed in U.S. Pat. No. 6,407,079, the contents of which are incorporated herein by this reference.
In some embodiments, the particles, e.g., nanoparticles, and the lyoprotectant can then be optionally stored in one or more suitable vessels, e.g., vials, and lyophilized in a manner known in the art. The vials can then be sealed to protect the particles, e.g., nanoparticles, from contamination. For example, the lyophilization can be achieved by initially freezing the particles, e.g., nanoparticles, followed by a primary drying phase in which the ambient pressure to which the concentrated suspension is subjected is lowered (e.g., to a few millibars) while supplying enough heat to cause sublimation of bulk frozen liquid, mostly frozen water in many implementations at this stage. In a secondary drying phase, bound liquid (e.g., water molecules bound to product or lyoprotectant), if any, can be removed by raising the temperature above that in the primary. In some embodiments, upon completion of the freeze-drying process, an inert gas, such as nitrogen, can be introduced into the vessel containing the lyophilized particles, e.g., nanoparticles, prior to sealing the vessel.
In some embodiments, the particles, e.g., nanoparticles, prepared according to the methods described herein can exhibit an average particle size equal to or less than about 1 micron. For example, the polymeric nanoparticle can exhibit an average particle size equal or less than about 500 nm. For example, the polymeric nanoparticles can exhibit an average particle size in a range of about 5 nm to about 500 nm, or in a range of about 10 nm to about 500 nm, or in a range of about 20 nm to about 500 nm, or in a range of about 30 nm to about 500 nm, or in a range of about 40 nm to about 500 nm, or in a range of about 50 nm to about 500 nm.
In some embodiments, the particles, e.g., nanoparticles, prepared according to the methods described herein can exhibit an average particle size equal to or less than about 400 nm. For example, the polymeric nanoparticles can exhibit an average particle size in a range of about 5 nm to about 400 nm, or in a range of about 10 nm to about 400 nm, or in a range of about 20 nm to about 400 nm, or in a range of about 30 nm to about 400 nm, or in a range of about 40 nm to about 400 nm, in a range of about 50 nm to about 400 nm.
In some embodiments, the particles, e.g., nanoparticles, prepared according to the methods described herein can exhibit an average particle size equal to or less than about 300 nm. For example, the polymeric nanoparticles can exhibit an average particle size in range of about 5 nm to about 300 nm, or in a range of about 10 nm to about 300 nm, or in a range of about 20 nm to about 300 nm, or in a range of about 30 nm to about 300 nm, or in a range of about 40 nm to about 300 nm, or in a range of about 50 nm to about 300 nm.
In some embodiments, the particles, e.g., nanoparticles, prepared according to the methods described herein can exhibit an average particle size equal to or less than about 200 nm. For example, the particles, e.g., nanoparticles, can exhibit an average particle size in a range of about 5 nm to about 200 nm, or in a range of about 10 nm to about 200 nm, or in a range of 20 nm to about 200 nm, or in a range of about 30 nm to about 200 nm, or in a range of about 40 nm to about 200 nm, or in a range of about 50 nm to about 200 nm.
In some embodiments, the particles, e.g., nanoparticles, prepared according to the methods described herein can exhibit an average particle size equal to or less than about 100 nm. For example, the nanoparticles can exhibit an average particle size in a range of about of 5 nm to about 100 nm, or in a range of about 10 nm to about 100 nm, or in a range of about 20 nm to about 100 nm, or in a range of about 30 nm to about 100 nm, or in a range of about 40 nm to about 100 nm, or in a range of about 50 nm to about 100 nm.

Systems for Precipitating a Polymer

The methods described herein for precipitating a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, from a polymer-containing solution and/or generating particles, e.g., nanoparticles, can be performed using a system as described in FIG. 2. For example, FIG. 2 schematically depicts a system 10, which includes a vessel 12 for housing a cooled non-solvent. The vessel 12 includes an input port 16 for receiving a fluid and an output port 18 through which a fluid contained in the vessel can exit the vessel. The input and output ports 16 and 18 are in fluid communication via a loop fluid passage 20. In some embodiments, a recirculation pump (e.g., peristaltic or gear pump) 22 facilitates the flow of a fluid from the output port 18 of the vessel 12 to its input port 16. Further, a valve 24 disposed in the fluid loop 20 allows recovery of a product and/or waste from the vessel 12. The vessel 12 also includes a cooling jacket 13 in communication with the vessel 12 to cool the non-solvent, and also maintain the cooled temperature of the mixture in the vessel. The vessel 12 can optionally include a magnetic agitator 15 for mixing the contents of the vessel 12. In some embodiments, the vessel 12 can optionally include a mechanical agitator (not shown), such as an overhead stirrer, for mixing the contents of the vessel 12.
The system 10 further includes a reservoir 26 for storing a polymer-containing solution. The reservoir 26 includes an output port 28 that is in fluid communication with the input port 16 of the vessel 12 to allow the flow of the polymer-containing solution into the vessel 12. In some embodiments, the polymer-containing solution comprises an unconjugated polymer, e.g., an unconjugated CDP, e.g., a CDP that did not conjugate with an inhibitor, e.g., a camptothecin or camptothecin derivative, during the conjugation reaction. In some embodiments, the unconjugated polymer, e.g., the unconjugated CDP, can have a molecular weight of about 5 kDa to about 200 kDa. In some embodiments, the polymer-containing solution comprises an unconjugated inhibitor, e.g., an unconjugated camptothecin or camptothecin derivative, which did not conjugate with the polymer during the conjugation reaction. In some embodiments, the inhibitor, e.g., a camptothecin or camptothecin derivative, can be camptothecin modified with glycine, e.g., CPT-glycine. In some embodiments, the polymer-containing solution comprises one or more of the reagents utilized in the preparation of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. In some embodiments, the polymer-containing solution comprises unreacted polymer, e.g., unreacted CDP, e.g., CD-biscysteine. In some embodiments, the polymer-containing solution comprises CD-biscysteine copolymerized with PEG 3.4 kDa, e.g., PEG 3.4 kDa+/−10%. In some embodiments, the polymer-containing solution comprises one or more of an activated monomer, such as PEG-DiSBA. In some embodiments, the polymer-containing solution comprises a process solvent such as, one or more of acetone, ether, alcohol, tetrahydrofuran, 2-pyrrolidone, N-methyl-2-pyrrolidone, dimethylformamide, dimethylacetamide, methyl acetate, ethyl formate, methyl ethyl ketone, methyl isobutyl ketone, methyl propyl ketone, isopropyl ketone, isopropyl acetate, acetonitrile and dimethyl sulfoxide.
The exemplary system 10 further includes an additional reservoir 30. The reservoir 30 stores non-solvent. The reservoir 30 is in fluid communication with the input port 16 of the vessel 12 via its respective output port (shown here as output port 36) and a fluid passage 42. It should be understood that the number of reservoirs is not restricted to those disclosed herein and can be more than that illustrated. For example, in some embodiments, more than one reservoir may be employed, for storing two or more different non-solvents, e.g., reservoir 32.
In this exemplary implementation, the system 10 can further include a tangential flow filtration module 52 (e.g., a TFF module) that can be placed in fluid communication with vessel 12 for optional use, e.g., in concentrating a collection of particles (e.g., nanoparticles) generated in the vessel 12.
In some embodiments, in use, the vessel 12 is initially filled, or at least partially filled, with a quantity of a non-solvent, e.g., the non-solvent stored in the reservoir 30, by establishing a flow of the non-solvent from the non-solvent reservoir to the vessel 12. The cooling jacket is then activated to cool the non-solvent to the desired temperature, e.g., −50 to −100 degrees Celsius, e.g., −78 degrees Celsius. The cooled non-solvent can be agitated using the magnetic agitator 15. The pump 22 is then activated to establish a recirculating flow of the cooled non-solvent through the vessel 12 through a recirculation loop 20. Once the recirculating flow of the non-solvent is established, the polymer-containing solution stored in the reservoir 26 is injected into the vessel 12 to come into contact with the flowing cooled non-solvent. In some embodiments, a metering valve (not shown) at the output of the reservoir 26 is employed to control the rate of the flow of the polymer-containing solution into the flowing non-solvent.
As discussed above, the introduction of the polymer-containing solution into the recirculating non-solvent results in the precipitation of the inhibitor, e.g., a camptothecin or camptothecin derivative, e.g., CRLX101, in the cooled non-solvent housed in the vessel 12.
After a desired amount of the polymer-containing solution has been transferred to the vessel 12—typically after the exhaustion of the polymer-containing solution that is stored in the reservoir 26—the fluid connection between the reservoir 26 and the vessel 12 can be terminated and the liquid contained in the reaction vessel and recirculating loop 20 (which can contain a mixture of the non-solvent and the solution in which the inhibitor, e.g., a camptothecin or camptothecin derivative, e.g., CRLX101, was initially disposed) is drained via the valve 24.
Subsequently, the vessel 12 can be at least partially filled with the non-solvent stored in the reservoir 30 (non-solvent (1)) and the pump 22 can be activated to recirculate the resultant mixture comprising a liquid and the topoisomerase inhibitor, e.g., a camptothecin or camptothecin derivative, e.g., CRLX101, through the reaction vessel 12. The recirculating mixture can remove certain impurities that can be solubilized by the mixture. The recirculation of the mixture can continue for a desired time period after which the recirculation can be stopped, and the liquid in the reaction vessel and the recirculating loop can be drained, e.g., via the valve 24.
In some embodiments, after rinsing the precipitated inhibitor, e.g., a camptothecin or camptothecin derivative, e.g., CRLX101, with the cooled non-solvent the vessel 12 can be swept with dry nitrogen, or other suitable gas, to dry the precipitated inhibitor, e.g., a camptothecin or camptothecin derivative, e.g., CRLX101, and remove solvent residuals. The precipitated inhibitor, e.g., a camptothecin or camptothecin derivative, e.g., CRLX101, can be stored for later use, or alternatively it can be exposed to a solvent, such as water, supplied by reservoir 34, to generate particles, e.g., nanoparticles, in a suspension. The suspension of the particles, e.g., nanoparticles, in water can be optionally subjected to a filtration step for purification and concentration. The concentrated suspension of the particles, e.g., nanoparticles, can be optionally lyophilized and stored for later use.
For example, the aqueous suspension of the particles, e.g., nanoparticles, can be drained from the reaction vessel and routed through a second recirculating loop 44 using a plurality of control valves 46, 48, 50. In particular, the control valve 46 can be closed and the control valves 48 and 50 can be opened to route the aqueous suspension of the particles, e.g., nanoparticles, through the second recirculating loop 44 and through a tangential flow filter 52, where the suspension of particles, e.g., nanoparticles, is subjected to tangential flow filtration (TFF). For example, a recirculating flow of the particle suspension can be established between the vessel 12 and the TFF module 52, e.g., by shutting off valve 46, opening valves 48 and 50 and activating the pump 22. During diafiltration, a flow of a make-up fluid, e.g., water, stored in a reservoir 33 can be established from the reservoir 33 to the filtration module 52. The particle suspension enters the filtration module 52 via an input port 54. The retentate generated through the filtration process exits the TFF module via an output port 56 and is returned via a return fluid passage 58 to the reservoir 12. The filtrate is drained from the filtration module 52 via another output port 60 and associated valve 62. The filtration process continues for a desired time period, e.g., until a desired concentration of the particles, e.g., nanoparticles, in the vessel 12, is achieved. In some embodiments, the concentrated particles, e.g., nanoparticles, can then be collected and lyophilized for storage.

Methods of Analyzing the Precipitated Polymer Conjugates

The precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, prepared by the methods described herein can be analyzed for yield and purity using any of the following analytical methods that are known to those skilled in the art.

Spectrometric Analytical Methods

In some embodiments, precipitation methods described herein include the use of spectrometric analysis, to analyze the purity of the separated precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein. Example spectrometric instruments that can be used to analyze the purity of the precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, include, but are not limited to, ultraviolet (UV) spectrometry, infrared spectrometry, proton nuclear magnetic resonance spectrometry (¹H-NMR), carbon-13 nuclear magnetic resonance spectrometry (¹³C-NMR), correlation nuclear magnetic resonance spectrometry (2-D NMR), ultraviolet-visible spectrometry (UV-Vis), and mass spectrometry (MS). In some embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be detected using a wavelength of 434 nm, e.g., the emission wavelength of camptothecin.
In some embodiments, the desired precipitated CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be recovered at a purity greater than about 60%, greater than about 70%, greater than about 75%, greater than about 80%, greater than about 85%, greater than about 90%, greater than about 95%, greater than about 98%, or greater than about 99.0%.
In some embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, can be evaluated using dynamic light scattering (DLS), sometimes referred to as Photon Correlation Spectroscopy (PCS) or Quasi-Elastic Light Scattering (QELS) to determine the size of the particles, e.g., nanoparticles.

CDP-Topoisomerase Inhibitor Conjugates, Particles, and Compositions

Cyclodextrin-containing polymer (CDP) inhibitor conjugates, such as CDP-camptothecin conjugate, e.g., CRLX101, wherein one or more camptothecin, or camptothecin derivative, moieties are covalently attached to the CDP (e.g., either directly or through a linker) are described herein. Exemplary cyclodextrin-containing polymers that may be modified as described herein are taught in U.S. Pat. Nos. 7,270,808, 6,509,323, 7,091,192, 6,884,789, U.S. Publication Nos. 20040087024, 20040109888 and 20070025952.
In some embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is as shown below:
In the above structure:
m=about 77 or the molecular weight of the PEG moiety is 3.4 kDa, e.g., 3.4 kDa+/−10%;
n=is from about 10 to about 18 (e.g., about 14);
the molecular weight of the polymer backbone (i.e., the polymer minus the camptothecin-glycine (CPT-gly), which results in the cysteine moieties having a free —C(O)OH) is from about 48 to about 85 kDa;
the polydispersity of the polymer backbone is less than about 2.2; and
the loading of the CPT onto the polymer backbone is from about 6 to about 13% by weight, wherein 13% is theoretical maximum, meaning, in some instances, one or more of the cysteine residues has a free —C(O)OH (i.e., it lacks the CPT-gly).
In some embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is a polymer having the following formula:
wherein
L, independently for each occurrence, is a linker (e.g, —NH—CH₂—CO—), a bond, or —OH;
D, independently for each occurrence, is camptothecin (“CPT”) or a camptothecin derivative or absent, and
the group
has a Mw of 3.4 kDa+/−10%, e.g. 3.4 kDa, or less (m can be, e.g., 77+/−8, e.g., about 77; and
n is at least 4, e.g., 10-18, e.g., about 14,
provided that at least one D is CPT or a camptothecin derivative.
In some embodiments, the loading of inhibitor moieties on the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, is from about 1 to about 50% (e.g., from about 1 to about 25%, from about 5 to about 20% or from about 5 to about 15%, e.g., from about 6 to about 13% of the weight of the conjugate).
In some embodiments, the loading of inhibitor moieties on the CDP is from about 6% to about 13% by weight of the conjugate.
In embodiments, the molecular weight of the CDP backbone, without attached inhibitor moieties or linker moieties, is from about, 38-95 or 48-85 kDa.
In an embodiment m=77+/−8; n=about 14; and sufficient D is camptothecin such that camptothecin accounts for 6-13% by weight of the conjugate.
In an embodiment m=77+/−8; n=about 14; and sufficient D is a camptothecin derivative such that camptothecin derivative accounts for 6-13% by weight of the conjugate.
In an embodiment one or more of the cysteine residues has a free —C(O)OH (i.e., it lacks camptothecin or a camptothecin derivative).
In some embodiments, the CDP-inhibitor conjugate, has the following formula:
wherein
D=independently for each occurrence, is —OH or
“camptothecin-glycine” (CPT-glycine); and
the group
has a Mw of 3.4 kDa+/−10%, e.g., 3.4 kDa, or less (m can be, e.g., 77+/−8, e.g., about 77; and
n is 10-18, e.g., about 14,
provided that at least 1 D moiety is
In an embodiment sufficient D moieties are
such that 6-13% by weight of the conjugate is camptothecin.
In embodiments, the molecular weight of the CDP backbone, without attached inhibitor moieties or linker moieties, is from about, 38-95 or 48-85 kDa.
In embodiments one or more of the cysteine residues has a free —C(O)OH (i.e., it lacks the CPT-glycine).
In an embodiment m=77+/−8; n=about 14; and sufficient D is camptothecin such that camptothecin accounts for 6-13% by weight of the conjugate.
In an embodiment one or more of the cysteine residues has a free —C(O)OH (i.e., it lacks the CPT-glycine).

Preparations of the CDP-Inhibitor Conjugates

In embodiments the polydispersity of the polymer backbone in a preparation of polymer backbone or CDP-camptothecin conjugates is less than about 2.2.
In embodiments the average value for n in a preparation of the camptothecin-inhibitor conjugate is about 14.
In embodiments, at least 5, 10, 20, 30, 40, 50, 60, 70, 80, 90, or 95% (e.g., by weight or number) of the CDP-camptothecin conjugate molecules in a preparation will have a value for n recited herein, e.g., 10-18.
In embodiments, at least 5, 10, 20, 30, 40, 50, 60, 70, 80, 90, or 95% (e.g., by weight or number) of the CDP backbone, without attached inhibitor moieties or linker moieties, in a preparation will have a molecular weight recited herein, e.g., 48-65 kDa. Molecular weight can be determined by gel permeation chromatography (“GPC”), e.g., mixed bed columns, CH₂Cl₂solvent, light scattering detector, and off-line dn/dc. Other methods are known in the art.
In some embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, particle or composition as described herein have polydispersities less than about 3, or even less than about 2.
In some embodiments, the polydispersity of the PEG is less than about 1.1.

Properties of the CDP-Inhibitor Conjugates

In some embodiments, administration of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, to a subject results in release of the inhibitor, e.g., camptothecin or camptothecin derivative, over a period of at least 6 hours. In some embodiments, administration of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, to a subject results in release of the inhibitor, e.g., camptothecin or camptothecin derivative, over a period of 2 hours, 3 hours, 5 hours, 6 hours, 8 hours, 10 hours, 15 hours, 20 hours, 1 day, 2 days, 3 days, 4 days, 7 days, 10 days, 14 days, 17 days, 20 days, 24 days, 27 days up to a month. In some embodiments, upon administration of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, to a subject, the rate of the inhibitor, e.g., camptothecin or camptothecin derivative, release is dependent primarily upon the rate of hydrolysis as opposed to enzymatic cleavage.

Exemplary CDP-Inhibitor Conjugates, Particles and Compositions

In embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, are in the form of a particle, e.g., a nanoparticle, comprising one or more molecules of a CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein.
The nanoparticle ranges in size from 10 to 300 nm in diameter, e.g., 20 to 280, 30 to 250, 40 to 200, 20 to 150, 30 to 100, 20 to 80, 30 to 70, 40 to 60 or 40 to 50 nm diameter. In one embodiment, the particle is 50 to 60 nm, 20 to 60 nm, 30 to 60 nm, 35 to 55 nm, 35 to 50 nm or 35 to 45 nm in diameter.
In one embodiment, the surface charge of the molecule is neutral, or slightly negative. In some embodiments, the zeta potential of the particle surface is from about −80 mV to about 50 mV, about −20 mV to about 20 mV, about −20 mV to about −10 mV, or about −10 mV to about 0.
Cyclodextrin polymer (CDP) inhibitor conjugates, such as CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, particles and compositions of the disclosure may be useful to improve solubility and/or stability of the inhibitor, e.g., camptothecin or camptothecin derivative, reduce drug-drug interactions, reduce interactions with blood elements including plasma proteins, reduce or eliminate immunogenicity, protect the inhibitor, e.g., camptothecin or camptothecin derivative, from metabolism, modulate drug-release kinetics, improve circulation time, improve inhibitor half-life (e.g., in the serum, or in selected tissues, such as tumors), attenuate toxicity, improve efficacy, normalize inhibitor metabolism across subjects of different species, ethnicities, and/or races, and/or provide for targeted delivery into specific cells or tissues.
In other embodiments, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, particle or composition may be a flexible or flowable material. When the CDP used is itself flowable, the CDP composition of the disclosure, even when viscous, need not include a biocompatible solvent to be flowable, although trace or residual amounts of biocompatible solvents may still be present.

Physical Structures of the CDP-Topoisomerase Inhibitor Conjugates, Particles and Compositions

The CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, particles and compositions may be formed in a variety of shapes. For example, in certain embodiments, CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, may be presented in the form of microparticles or nanoparticles. Microspheres typically comprise a biodegradable polymer matrix incorporating a drug. Microspheres can be formed by a wide variety of techniques known to those of skill in the art. Examples of microsphere forming techniques include, but are not limited to, (a) phase separation by emulsification and subsequent organic solvent evaporation (including complex emulsion methods such as oil in water emulsions, water in oil emulsions and water-oil-water emulsions); (b) coacervation-phase separation; (c) melt dispersion; (d) interfacial deposition; (e) in situ polymerization; (f) spray drying and spray congealing; (g) air suspension coating; and (h) pan and spray coating. These methods, as well as properties and characteristics of microspheres are disclosed in, for example, U.S. Pat. No. 4,438,253; U.S. Pat. No. 4,652,441; U.S. Pat. No. 5,100,669; U.S. Pat. No. 5,330,768; U.S. Pat. No. 4,526,938; U.S. Pat. No. 5,889,110; U.S. Pat. No. 6,034,175; and European Patent 0258780, the entire disclosures of which are incorporated by reference herein in their entireties.
To prepare microspheres, several methods can be employed depending upon the desired application of the delivery vehicles. Suitable methods include, but are not limited to, spray drying, freeze drying, air drying, vacuum drying, fluidized-bed drying, milling, co-precipitation and critical fluid extraction. In the case of spray drying, freeze drying, air drying, vacuum drying, fluidized-bed drying and critical fluid extraction; the components (stabilizing polyol, bioactive material, buffers, etc.) are first dissolved or suspended in aqueous conditions. In the case of milling, the components are mixed in the dried form and milled by any method known in the art. In the case of co-precipitation, the components are mixed in organic conditions and processed as described below. Spray drying can be used to load the stabilizing polyol with the bioactive material. The components are mixed under aqueous conditions and dried using precision nozzles to produce extremely uniform droplets in a drying chamber. Suitable spray drying machines include, but are not limited to, Buchi, NIRO, APV and Lab-plant spray driers used according to the manufacturer's instructions.
The shape of microparticles and nanoparticles may be determined by scanning electron microscopy. Spherically shaped nanoparticles are used in certain embodiments, for circulation through the bloodstream. If desired, the particles may be fabricated using known techniques into other shapes that are more useful for a specific application.
In addition to intracellular delivery of an inhibitor, e.g., camptothecin or camptothecin derivative, it also possible that particles of the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, such as microparticles or nanoparticles, may undergo endocytosis, thereby obtaining access to the cell. The frequency of such an endocytosis process will likely depend on the size of any particle.
In one embodiment, the surface charge of the molecule is neutral, or slightly negative. In some embodiments, the zeta potential of the particle surface is from about −80 mV to about 50 mV.

CDPs, Methods of Making Same, and Methods of Conjugating CDPs to Inhibitors

Generally, the CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, particles and compositions described herein can be prepared in one of two ways: monomers bearing inhibitors, e.g., camptothecin or camptothecin derivatives, targeting ligands, and/or cyclodextrin moieties. Exemplary methods of making CDPs and CDP-inhibitor conjugate, e.g., CDP-camptothecin conjugate, e.g., CRLX101, or a CDP-inhibitor conjugate described herein, particles and compositions are described, for example, in U.S. Pat. No. 7,270,808, the contents of which is incorporated herein by reference in its entirety.

EXAMPLES

Example 1

Synthesis of 6^A,6^D-Bis-(2-amino-2-carboxylethylthio)-6^A′6^D-dideoxy-β-cyclodextrin, 4 (CD-BisCys)

167 mL of 0.1 M sodium carbonate buffer were degassed for 45 minutes in a 500 mL 2-neck round bottom flask equipped with a magnetic stir bar, a condenser and septum. To this solution were added 1.96 g (16.2 mmol) of L-cysteine and 10.0 g (73.8 mmol) of diiodo, deoxy-β-cyclodextrin 2. The resulting suspension was heated at a reflux temperature for 4.5 h until the solution turned clear (colorless). The solution was then cooled to room temperature and acidified to pH 3 using 1N HCl. The product was precipitated by slow addition of acetone (3 times weight ratio of the solution). This afforded 9.0 g crude material containing CD-biscysteine (90.0%), unreacted cyclodextrin, CD-mono-cysteine and cysteine. The resulting solid was subjected to anionic exchange column chromatography (SuperQ650M, Tosoh Bioscience) using a gradient elution of 0-0.4M ammonium bicarbonate. All fractions were analyzed by HPLC. The desired fractions were combined and the solvent was reduced to 100 mL under vacuum. The final product was either precipitated by adding acetone or by adding methanol (3 times weight ratio of the solution). 4 was obtained in 60-90% yield. ¹H NMR (D₂O) δ 5.08 (m, 7H, CD-2-CH), 3.79-3.94 (m, 30H, CD-3,4-CH, CD-CH₂, Cys-CH), 3.49-3.62 (m, 14H, CD-5, 6-CH), 2.92-3.30(m, 4H, Cys-CH₂). ¹³C NMR (D₂O) δ 172.3, 101.9, 83.9, 81.6, 81.5, 73.3, 72.2, 72.0, 60.7, 54.0, 34.0, 30.6. ESI/MS (m/z): 1342 [M]⁺, 1364 [M+Na]⁺. Purity of 4 was confirmed by HPLC.

Example 2

Synthesis of Gly-CPT (Structure 11) (Greenwald et al., Bioorg. Med. Chem., 1998, 6, 551-562)

t-Boc-glycine (0.9 g, 4.7 mmol) was dissolved in 350 mL of anhydrous methylene chloride at room temperature, and to this solution were added DIPC (0.75 mL, 4.7 mmol), DMAP (382 mg, 3.13 mmol) and camptothecin (0.55 g, 1.57 mmol) at 0° C. The reaction mixture was allowed to warm to room temperature and left for 16 h. The solution was washed with 0.1 N HCl, dried and evaporated under reduced pressure to yield a white solid, which was recrystallized from methanol to give camptothecin-20-ester of t-Boc-glycine: ¹H NMR(DMSO-d₆) 7.5-8.8 (m), 7.3 (s),5.5 (s), 5.3 (s), 4 (m), 2.1 (m), 1.6 (s), 1.3 (d), 0.9 (t). Camptothecin-20-ester of t-Boc-glycine (0.595 g, 1.06 mmol) was dissolved in a mixture of methylene chloride (7.5 mL) and TFA (7.5 mL) and stirred at room temperature for 1 h. Solvent was removed and the residue was recrystallized from methylene chloride and ether to give 0.45 g of 11. ¹H NMR (DMSO-d₆) δ7.7-8.5 (m); 7.2 (s), 5.6 (s), 5.4 (s), 4.4 (m), 2.2 (m), 1.6 (d), 1.0 (t), ¹³C NMR (DMSO-d₆) δ168.6, 166.6, 156.5, 152.2, 147.9, 146.2, 144.3, 131.9, 130.6, 129.7, 128.8, 128.6, 128.0, 127.8, 119.0, 95.0, 77.6, 66.6, 50.5, 47.9, 30.2, 15.9, 7.9. ESI/MS (m/z) expected 405; Found 406 (M+H).

Example 3

Synthesis and Characterization of CD-BisCys-Peg3400 Copolymers 36 and their CPT Conjugates 37

A. Synthesis and Characterization of CD-BisCys-Peg3400 Copolymers 36

Synthesis of Poly(CDDCys-PA-PEG), 36a 4 (after precipitation with acetone, 63 mg, 0.047 mmol) and PEG-DiSPA (MW 3400, 160 mg, 0.047 mmol) were dried under vacuum for 8 hours. Anhydrous DMSO (1.26 mL) was added to the mixture under argon. After 10 minutes of stirring, anhydrous diisopropylethylamine (DIEA, 19 μL, 2.3 eq.) was added under argon. The reaction mixture was stirred under argon for 120 h. The polymer containing solution was dialyzed using a 10,000 MWCO membrane (Spectra/Por 7) against water for 48 h and lyophilized to yield 196 mg 36a. M_w=57400 Da, M_n=41700 Da, M_w/M_n=1.38. ¹H NMR (D₂O) δ 5.08 (m, CD-2-H), 4.27 (m, Cys-CH), 2.72-3.76 (m, CD-3,4,5,6-CH, CD-CH₂, PEG-CH₂), 2.44 (m, Cys-CH₂).
Synthesis of other poly(CDDCys-PA-PEG) (36b-f), Poly(CDDCys-BA-PEG) (36g) Poly(CDDCys-CB-PEG) (36h-i) were achieved under polymerization condition similar to that of 36a. Details for the polymerization conditions, monomer selection, polymer molecular weight, polydispersity and yields are listed in Table 1. 36g: ¹H NMR (D₂O) δ 5.10 (m, CD-2-H), 4.25-4.37 (m, Cys-CH), 2.72-3.86 (m, CD-3,4,5,6-CH, CD-CH₂, PEG-CH₂), 2.21 (m, Cys-CH₂). 36h-i: ¹H NMR (D₂O) δ 5.05 (m, CD-2-H), 4.56 (m, Cys-CH), 2.70-3.93 (m, CD-3,4,5,6-CH, CD-CH₂, PEG-CH₂), 2.38 (m, —OCH₂CH₂CH₂C(O)—NH-), 2.34 (m, Cys-CH₂), 1.90 (m, —OCH₂CH₂CH₂C(O)—NH—).
Addition of a non-nucleophilic organic base (such as DIEA) was essential for this polymerization as no viscosity changes of the polymerization solutions were observed after 48 hours if no base was added. When 2.3 eq. of DIEA were added, the viscosity of the polymerization solution increased dramatically after 4-6 hours of reaction. DIEA deprotonates the amino groups of 4 to render them more nucleophilic for coupling with PEG-DiSPA. There were essentially no differences in the polymerizations if other bases, such as TEA or DMAP, were used (36b-c, Table 1). Polymerization using 4 recovered by the two different precipitation methods (acetone and methanol) produced polymers with different MWs. 4 that was purified by the methanol-precipitation method (contains no free cysteine) gave higher MW polymer (36d-e) as compared to the less pure 4 that was obtained from the acetone-precipitation method (36a). Polymerization of 4 with PEG-DiSPA typically produced polymer yields greater than 90%.
4 was polymerized with other activated monomers such as PEG-DiSBA, PEG-DiBTC, and PEG-DiNPC. Reaction of 4 with PEG-DiSBA gave polymer 36g with similar linkages as 36a-f (amide bond, but one more —CH₂group than 36a-f at the linker) with M_wover 100,000 Da, while reaction of 4 with PEG-DiBTC and PEG-DiNPC generated polymers 36h and 36i, respectively, with connecting carbamate moiety and M_w's over 50,000 Da (Table 1).

TABLE 1

Polymerization of 4 with Difunctionalized PEG

			Polymer-
	PEG		ization	M_w	M_n	M_w/	Yield
CDP	Comonomer	Base	time (h)	(kDa)	(kDa)	M_n	(%)

36a^a	PEG-DiSPA	DIEA	120	57.4	41.7	1.38	90
36b^a	PEG-DiSPA	DMAP	120	54.2	38.1	1.42	91
36c^a	PEG-DiSPA	TEA	120	57.4	42.6	1.35	91
36d^b	PEG-DiSPA	DIEA	120	93.6	58.0	1.48	96
36e^b	PEG-DiSPA	DIEA	144	97.3	58.0	1.67	94
36f^b	PEG-DiSPA	DIEA		2	35.3	25.6	1.38	95
36g	PEG-DiSBA	DIEA	120	114.7	77.9	1.47	96
36h	PEG-DiBTC	DIEA	120	67.6	39.4	1.47	95
36i	PEG-DiNPC	DIEA	120	86.5	57.2	1.51	96

^a4 was washed with acetone before polymerization.
^b4 was washed with methanol before polymerization.

Polymers 36a-i are highly soluble in aqueous solution. They can be easily dissolved in water or phosphate buffered saline (PBS) solution at concentrations of at least 200 mg/mL. Solubility of these polymers in aqueous solution at concentrations higher than 200 mg/mL was not attempted due to the high viscosity. These polymers were also soluble in DMF, DMSO and methanol, slightly soluble in CH₃CN and CHCl₃, but insoluble in THF and ethyl ether.
Molecular Weight Control of CD Polymers 4 (after precipitation with methanol) (56.2 mg, 0.0419 mmol) and PEG-DiSPA (147 mg, 0.0419 mmol) were dried under vacuum for 4-8 hours. To the mixture was added dry DMSO (1.1 mL) under argon. After 10 minutes stirring, DIEA (16 μL, 2.2 eq) was added under argon. A portion of polymerization solution (150 μL) was removed and precipitated with ether at selected times (2 h, 18 h, 43 h, 70 h, 168 h and 288 h). MWs of the precipitated polymers were determined as described above.

B. Synthesis of Poly(CDDCys-PA-PEG)-CPTConjugates (HGGG6, LGGG10, HG6, HGGG10).

Synthesis of Poly(CDDCys-PA-PEG)-GlyGlyGly-CPT (HGGG6): 36e (1.37 g, 0.30 mmol of repeat unit) was dissolved in dry DMSO (136 mL). The mixture was stirred for 10 minutes. 12 (419 mg, 0.712 mmol, 2.36 eq), DIEA (0.092 mL, 0.712 mmol, 2.36 eq), EDC (172 mg, 0.903 mmol, 3 eq), and NHS (76 mg, 0.662 mmol, 2.2 eq) were added to the polymer solution and stirred for ca. 15 hours. The polymer was precipitated with ethyl ether (1 L). The ether was poured out and the precipitate was washed with CH₃CN (3×100 mL). The precipitate was dissolved in water 600 mL. Some insoluble solid was filtered through 0.2 μm filters. The solution was dialyzed using 25,000 MWCO membrane (Spectra/Por 7) for 10 h at 10-15° C. in DI water. Dialysis water was changed every 60 minutes. The polymer-drug conjugate solution was sterilized by passing it through 0.2 μM filters. The solution was lyophilized to yield a yellow solid HGGG6 (1.42 g, 85% yield).
Synthesis of Poly(CDDCys-PA-PEG)-GlyGlyGly-CPT (LGGG10): Conjugation of 12 to 36f was performed in a manner similar to that used to produce HGGG6 except that this conjugate was dialyzed with 10,000 MWCO membrane (Spectra/Por 7) instead of with 25,000 MWCO membrane. The yield of LGGG10 was 83%.
Synthesis of Poly(CDDCys-PA-PEG)-Gly-CPT (HG6): Conjugation of 11 to 36e was performed in a manner similar to that used to produce HGGG6. The yield of HG6 was 83%.
Synthesis of Poly(CDDCys-PA-PEG)-GlyGlyGly-CPT (HGGG10): 36e (1.5 g, 0.33 mmol of repeat unit) was dissolved in dry DMSO (150 mL). The mixture was stirred for 10 minutes. 12 (941 mg, 1.49 mmol, 4.5 eq), DIEA (0.258 mL, 1.49 mmol, 4.5 eq), EDC (283 mg, 1.49 mmol, 4.5 eq), and NHS (113 mg, 0.99 mmol, 3 eq) was added to the polymer solution and stirred for ca. 24 hours. Another portion of EDC (142 mg, 0.75 mmol, 2.3 eq) and NHS (56 mg, 0.5 mmol, 1.5 eq) were added to the conjugation solution. The polymer was stirred for an additional 22 hours. The workup procedure was the same as that for the synthesis of HGGG6. The yield of HGGG10 was 77%.

Example 4

Chilled Precipitation of Poly(CDDCys-PA-PEG)-Gly-CPT (HG6)

A 600 mL beaker of 300 mL of acetone with magnetic stir bar was pre-chilled to −78° C. in a dry ice/acetone bath. A solution of polymer conjugate HG6 (2 grams), obtained without further preparation from Example 3, was added dropwise over a 4 minute period into the beaker with chilled acetone with stirring and maintained in the dry ice/acetone bath. Individual free flowing polymer particles (resembling chards or flakes) were formed (FIG. 3) and remained in suspension under stirring conditions. After 25 minutes, the chilled acetone was decanted and replaced with fresh pre-chilled acetone (300 mL at −78° C.) and stirred for an additional 30 minutes to afford a suspension of polymer particles in chilled acetone.
From the polymer particles/chilled acetone suspension further steps were conducted. First, a portion of polymer particles (still in acetone) was removed from the suspension and allowed to dry at room temperature. The polymer particles eventually melted into yellow oil (FIG. 4). A second portion of polymer particles (still in acetone) was removed from the suspension and frozen in liquid nitrogen (N₂) and lyophilized for 24 hours. Polymer particles maintained their shape immediately after lyophilization, but did not re-disperse in water even after 24 hours and sonication. With addition of acetone, however, re-dispersion was successful. A sample of lyophilized polymer particles was exposed to the ambient environment, and eventually melted into yellow oil. A third portion of polymer particles (still in acetone) was removed from the suspension and was warmed to room temperature for 72 hours and remained a stable free flowing suspension (FIG. 5).
The above described results indicate that HCG at cold temperatures may be precipitated as particles (resembling chards or flakes). The stability of the particles was maintained if the particles remained in an acetone (or possibly a vacuum environment). On exposure to ambient environment, the particles melted into an oil.
The polymer particles will be characterized using dynamic light scattering to determine the size distribution profile of these particles.

Other Embodiments

It is to be understood that while the disclosure has been described in conjunction with the detailed description thereof, the foregoing description is intended to illustrate and not limit the scope of the disclosure, which is defined by the scope of the appended claims. Other aspects, advantages, and modifications are within the scope of the following claims.

Claims

What is claimed is:

1. A process for precipitating a cyclodextrin-containing polymer (CDP) -camptothecin conjugate, from a polymer-containing solution, the process comprising: providing a vessel containing a volume of a cooled non-solvent; agitating the cooled non-solvent; introducing the polymer-containing solution into the cooled non-solvent to form a mixture comprising a liquid and the CDP-camptothecin conjugate; and maintaining the mixture under conditions to precipitate at least a portion of the CDP-camptothecin conjugate, from the mixture, thereby precipitating at least a portion of the CDP-camptothecin conjugate.

2. The process of claim 1, wherein the CDP-camptothecin conjugate is CRLX101.

3. The process of claim 1, wherein the mixture is maintained at a temperature of about −50 to about −100 degrees Celsius.

4. The process of claim 1, further comprising removing at least a portion of the liquid from the vessel subsequent to precipitation of the CDP-camptothecin conjugate, thereby separating the precipitated CDP-camptothecin conjugate, from the mixture.

5. The process of claim 1, wherein the precipitated CDP-camptothecin conjugate is filtered at a temperature of about −50 degrees Celsius to about −100 degrees Celsius.

6. The process of claim 5, wherein the filtered precipitated CDP-camptothecin conjugate is stored in the cooled non-solvent.

7. The process of claim 1, wherein the cooled non-solvent comprises acetone.

8. The process of claim 1, wherein the temperature of the cooled non-solvent is from about −50 to about −100 degrees Celsius.

9. The process of claim 8, wherein the temperature of the cooled non-solvent is about −78 degrees Celsius.

10. A process for generating particles, comprising:

providing a vessel containing a cooled non-solvent; agitating the cooled non-solvent; introducing a polymer-containing solution comprising a CDP-camptothecin conjugate into the cooled non-solvent to form a mixture comprising a liquid and the CDP-camptothecin conjugate; and maintaining the mixture under conditions to precipitate at least a portion of the CDP-camptothecin conjugate from the mixture, thereby precipitating at least a portion of the CDP-camptothecin conjugate; and isolating at least a portion of the precipitated CDP-camptothecin conjugate; and suspending the precipitated CDP-camptothecin conjugate in an aqueous solution, thereby generating particles.

11. The process of claim 10, wherein the CDP-camptothecin conjugate is CRLX101.

12. The process of claim 10, wherein the pH of the aqueous solution is from about 2 to about 6.

13. The process of claim 10, wherein the cooled non-solvent comprises methanol, ethanol, acetone, n-propanol, isopropanol, n-butanol, ethyl ether, methyl isobutyl ketone or ethyl acetate or a combination thereof.

14. The process claim 10, further comprising filtering the particles.

15. The process of claim 14, further comprising collecting the particles.

16. The process of claim 15, further comprising lyophilizing the collected particles.

17. A plurality of particles generated according to the process of claim 10.

18. The plurality of particles of claim 17, wherein the particles are nanoparticles.

19. A preparation comprising the CDP-camptothecin conjugate precipitated by the process of claim 1.

20. The preparation of claim 19, wherein the CDP-camptothecin conjugate is CRLX101.

21. A system for precipitating a CDP-camptothecin conjugate from a polymer-containing solution, the system comprising:

a vessel for containing a fluid, the vessel having at least one input port and an output port;

a cooling system in communication with the vessel configured to cool and maintain the temperature of the fluid in the vessel;

wherein said input port is configured to allow introduction of the polymer-containing solution into the vessel to precipitate at least a portion of the CDP-camptothecin conjugate.