CN117531020A - Drug carrier targeting CD74+ pro-inflammatory macrophages and preparation method and application thereof - Google Patents
Drug carrier targeting CD74+ pro-inflammatory macrophages and preparation method and application thereof Download PDFInfo
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- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
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- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
- A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
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Abstract
The invention discloses a preparation method of a drug carrier targeting CD74+ pro-inflammatory macrophages, which comprises the steps of firstly synthesizing MIF polypeptide (MIF) specifically combined with CD74 Peptide ) And coupling the MIF polypeptide to PLGA-PEG5K-Mal, thereby constructing a polypeptide having the ability to pass MIF Peptide Drug carrier targeting cd74+ pro-inflammatory Macrophages (MIF) Peptide‑ PLGA)。MIF Peptide PLGA may be further loaded with anti-inflammatory drugs. The invention is helpful for pushingThe preparation of the related targeted anti-inflammatory medicament improves the curative effect of the related medicament for osteoarthritis and provides clues for the research and development of new medicaments.
Description
Technical Field
The invention relates to the biomedical field, in particular to a drug carrier targeting CD74+ pro-inflammatory macrophages, a preparation method and application thereof.
Background
Knee osteoarthritis (Knee Osteoarthritis, hereinafter referred to as OA) is one of the major orthopedic diseases causing dysfunction of lower limbs, severely affecting the quality of life of patients and exacerbating the economic burden of the home and society. However, there is currently no effective drug against OA, and only surgical treatment is accepted when the disease progresses to an advanced stage.
Macrophages are closely related to the progression of Osteoarthritis (OA). The tissue injury in knee joint caused by trauma and other factors can generate aseptic inflammatory exudation, generate inflammatory factors, stimulate local infiltration, proliferation and activation of mononuclear macrophages, and the activated macrophages are pro-inflammatory macrophages, can secrete a large amount of soluble pro-inflammatory factors, act on synovial cells, immune cells and the like, further aggravate inflammatory reaction in joint, recruit more macrophages, and form malignant circulation.
The increased macrophages and pro-inflammatory cytokines can be detected in the early synovial tissues of OA to generate a chronic inflammatory microenvironment, stimulate synovial cells or chondrocytes to generate MMPs or ADMTS4/5 and the like, cause cartilage injury and exacerbate the progress of OA. The pro-inflammatory macrophage plays an important role in synovial tissue inflammation and OA progression, and timely and effectively relieves the inflammatory state of the macrophage, and is an effective way for relieving synovial tissue inflammation and delaying OA progression.
Early research results show that in the development process of OA, pro-inflammatory macrophages in synovium are greatly increased and highly express CD74, and CD74 is a specific binding receptor of macrophage migration inhibitory factor (Macrophage migration inhibitory factor, MIF), so that the invention can achieve the effect of targeting CD74+ pro-inflammatory macrophages and further achieving the effect of anti-inflammatory by constructing an MIF polypeptide structure capable of specifically binding with CD74 and coupling the polypeptide structure to a PLGA-PEG5K-Mal bracket and loading an anti-inflammatory drug, thereby being used for preparing targeted anti-inflammatory drugs and relieving inflammatory reaction in knee joints and OA development.
Disclosure of Invention
The invention aims to provide a drug carrier targeting CD74+ pro-inflammatory macrophages, a preparation method and application thereof, so as to solve the problem that early and medium stage knee osteoarthritis lacks specific anti-inflammatory drugs in the prior art, and simultaneously provide a novel therapeutic target point of knee joint synovial tissue inflammation.
The aim of the invention is achieved by the following technical scheme:
in one aspect, the invention provides a method for preparing a drug carrier targeting CD74+ pro-inflammatory macrophages, wherein the drug carrier comprises a CD 74-targeting MIF polypeptide structure (MIF) Peptide ),MIF Peptide The amino acid sequence N '-C' of (2) is leucine-cysteine-glycine-leucine-serine-aspartic acid-arginine-cysteine, and FITC is coupled at the N end for tracing.
Further, first combineCD74 targeting MIF polypeptide Structure MIF Peptide MIF is then subjected to Peptide Coupling to PLGA-PEG5K-Mal to obtain drug carrier MIF targeting CD74+ pro-inflammatory macrophage Peptide -PLGA。
The invention also provides application of the drug carrier targeting CD74+ pro-inflammatory macrophages, which is obtained by the preparation method, in preparation of drugs or drug compositions for treating knee osteoarthritis.
Further, in the drug carrier MIF targeting CD74+ pro-inflammatory macrophages Peptide -PLGA loaded with an anti-inflammatory drug, such as Luteolin.
The invention has the outstanding effects that:
the present invention first synthesizes MIF polypeptide (MIF) specifically binding to CD74 Peptide ) And coupling the MIF polypeptide to PLGA-PEG5K-Mal, thereby constructing a polypeptide having the ability to pass MIF Peptide Drug carrier targeting cd74+ pro-inflammatory Macrophages (MIF) Peptide -PLGA)。MIF Peptide PLGA may be further loaded with anti-inflammatory drugs. The invention is helpful for promoting the preparation of related targeted anti-inflammatory drugs, improving the curative effect of related drugs for osteoarthritis and providing clues for the research and development of new drugs.
The following describes the specific embodiments of the present invention in further detail with reference to examples, so that the technical solution of the present invention is easier to understand and grasp.
Drawings
FIG. 1A is a graph showing immunofluorescence staining results of normal and osteoarthritis synovial tissue of a mouse according to example 1 of the present invention;
FIG. 1B is a graph showing the results of cell flow analysis of normal and osteoarthritis synovial tissue of a mouse according to example 1 of the present invention;
FIG. 1C is a graph showing immunofluorescence staining of synovial tissue of patients with clinically normal and synovitis according to example 1 of the present invention;
FIG. 2A is a graph showing the results of flow analysis of Raw 264.7 cells treated with LPS in example 2 of the present invention;
FIG. 2B is a statistical analysis of FIG. 2A;
FIG. 2C is a co-staining of synovial tissue inflammatory macrophage markers CD86 and CD74 in normal and OA patients according to example 2 of the invention;
FIG. 3 is a CD74 targeting MIF of example 3 of the present invention Peptide Schematic representation of amino acid sequence;
FIG. 4 is a pharmaceutical carrier MIF targeting CD74+ pro-inflammatory macrophages in example 4 of the present invention Peptide -schematic structural diagram of PLGA-PEG-MAL;
FIG. 5 is a graph showing immunofluorescence staining results of example 5 of the present invention;
FIG. 6 shows an anti-inflammatory drug MIF targeting CD74+ pro-inflammatory macrophages according to example 6 of the present invention Peptide -schematic structural diagram of PLGA-Luteolin;
FIG. 7A is safranin O/fast green staining of cartilage tissue in example 7 of the present invention;
FIG. 7B is a graph of HE staining of knee joint in example 7 of the invention, assessing synovial inflammation levels;
fig. 7C is a graph of Mankin score for osteoarthritis severity in example 7 of the invention, the higher the score, the more severe the cartilage damage;
FIG. 7D is a Synovitis score showing the severity of Synovitis in example 7, showing that the higher the score, the more severe the synovial tissue inflammation;
Detailed Description
In order to make the objects, technical solutions and effects of the present invention more clear and clear, the present invention will be described in further detail with reference to examples. It should be understood that the specific embodiments described herein are for purposes of illustration only and are not intended to limit the scope of the invention.
The reagents used in the context of the present invention are all commercially available. PLGA-PEG5K-Mal of the present invention was purchased from Ruixibio and Luteolin was purchased from MedChemexpress. The experimental methods used in the present invention, such as molecular cloning, cell experiments, animal experiments, etc., are all conventional methods and techniques in the art. For animal experiments, the related procedures and methods meet the medical ethical requirements. The experimental methods used in the present invention are all conventional methods and techniques in the art.
Example 1: increased expression of CD74+ macrophages in synovial tissue of osteoarthritis
Immunofluorescent staining of normal synovial tissue (Sham group) and osteoarthritis synovial tissue (OA group) was performed in mice, and the result is shown in fig. 1A, in which F4/80+cd74+ macrophages were significantly increased compared to Sham group. Normal synovial tissue (Sham group) and osteoarthritis synovial tissue (OA group) were extracted from mice, and the number of F4/80+cd74+ macrophages was analyzed by flow cytometry, resulting in a 3.32-fold increase in F4/80+cd74+ macrophages in OA group compared to Sham group, as shown in fig. 1B. Immunofluorescent staining of clinically normal synovial tissue (Control group) and synovial tissue of synovial patients (OA group) resulted in a significant increase in F4/80+cd74+ macrophages in OA group compared to Control group, as shown in fig. 1C.
Example 2: CD74+ macrophages are pro-inflammatory macrophages
After 24h stimulation of the mouse Raw 264.7 macrophage cell line with LPS (50 ng/ml), the results of the cell flow assay are shown in FIGS. 2A and 2B, with a significant increase in F4/80+CD74+ macrophages. Immunofluorescent staining showed that CD74 expression was significantly increased in OA groups compared to Control groups, and that cd74+ cells also expressed the inflammatory macrophage marker CD86 specifically and highly (fig. 2C), so this group of macrophages were referred to as cd74+ pro-inflammatory macrophages, closely related to inflammatory response in the synovial tissue of osteoarthritis, and could be potential therapeutic targets for OA.
Example 3: synthesis of CD74 targeting MIF polypeptide Structure
MIF polypeptide (MIF) was synthesized by the usual Fmoc solid phase synthesis method Peptide ). Comprises 1) selection of resin and fixation of amino acid; 2) Protecting and removing amino, carboxyl and side chains; 3) Peptide formation reaction; 4) Cleavage and purification of the synthetic peptide chain. Firstly selecting carboxyl resin (such as Wang resin) as carrier for solid phase synthesis of polypeptide, connecting hydroxyl group of hydroxy terminal amino acid of peptide chain to be synthesized with Wang resin by covalent bond, then using amino acid combined on Wang resin as amino component, utilizing alkaline solvent piperidine to remove Fmoc protective column and protective group of monomer amino group so as to facilitate subsequent peptide chain synthesis, removing amino protective group and making them react with excessive activated carboxyl component, and making carboxyl group of amino acid and free ammoniaReacting and crosslinking the groups to form peptide bonds; repeating the operation, lengthening the peptide chain, and reaching the length of the peptide chain to be synthesized. Finally, the polypeptide is eluted from the column, the protecting group of the polypeptide is eluted and deprotected by a deprotecting agent TFA, and finally, a peptide segment with an amino acid sequence (N '-C') of leucine-cysteine-glycine-leucine-serine-aspartic acid-arginine-cysteine (figure 3) is synthesized, and FITC is added at the N end of the peptide segment for tracing.
Example 4: construction of a drug Carrier MIF targeting CD74+ proinflammatory macrophages Peptide -PLGA
To mix MIF Peptide Coupling to PLGA-PEG-Mal polymer A maleimide-thiol chemical reaction was chosen to covalently attach the thiol group (SH) present in the C-terminal cysteine of the MIF peptide to the Mal molecule of the PLGA-PEG-Mal polymer. This cysteine is not part of the original MIF peptide amino acid sequence, and is inserted on one side during commercial peptide synthesis. The specific synthesis steps are as follows: to ensure the presence of free SH groups, TCEP was added to MIF before addition of PLGA-PEG-MAL nanoparticles Peptide (molar ratio: 1:1), PLGA-PEG-MAL nanoparticles were added after incubation for 1 hour at room temperature. In order to form covalent bonds between the ends of PLGA-PEG-Mal and the C-terminal sulfhydryl bond of MIF polypeptide, MIFPeptide/TCEP solution and PLGA-PEG-Mal solution (molar ratio: 1.5:1) were mixed together, dissolved in an appropriate amount of neutral PBS solution, stirred overnight in the absence of light and stored at 4 ℃. At the same time, MIF will not be added Peptide As a control. To remove non-conjugated peptides, the polymer was precipitated with cold diethyl ether, centrifuged at 3200g for 5 min, the supernatant collected and sonicated once (3 min) between each polymer precipitation. In addition, the polymer was washed three times with ultrapure water to finally obtain a drug carrier MIF targeting CD74+ pro-inflammatory macrophages Peptide PLGA-PEG-MAL (abbreviated MIF Peptide -PLGA) finally, MIF Peptide The PLGA polymer was freeze-dried and stored at-20 ℃.
(FIG. 4).
Example 5: MIF (MIF) Peptide PLGA targeting CD74+ macrophages in mouse synovial inflammatory tissue
By using the inner sideBuilding an OA model through meniscus instability operation, and performing MIF (metal-inert-gas) through joint cavity injection technology Peptide PLGA (FITC mark) is delivered into the joint cavity of the mouse to act on the local tissue of the knee joint, the knee joint specimen of the mouse and the mouse is collected after 24 hours and cut into slices, immunofluorescence staining shows the result, as shown in figure 5, MIF Peptide The presence of significant co-localization of PLGA (FITC) with CD74 suggests MIF Peptide PLGA can target cd74+ macrophages.
Example 6: construction of targeting anti-inflammatory drug MIF targeting CD74+ pro-inflammatory macrophages Peptide -PLGA-Luteolin
Polymer nanoparticles were prepared using PLGA and PLGA-PEG-MAL blends. PLGA and PLGA-PEG-MAL polymers (w/w=4:1) were dissolved in a solution of ethyl acetate and methylene chloride (v/v=3/7), luteolin was dissolved in methylene chloride, and MIF Peptide The PLGA solution was thoroughly mixed and sonicated in an ice-water bath (power: 180W,3s on, 1s off, 5 minutes). Next, the resulting emulsion was dropped into a 3% polyvinyl alcohol (PVA) solution under ultrasonic treatment. Finally, volatilizing and drying the organic solvent by using a rotary evaporator to obtain MIF Peptide PLGA-Luteolin (its structure is shown in FIG. 6).
Example 7: MIF (MIF) Peptide PLGA-Luteolin delays the progression of osteoarthritis in mice
Immediately after construction of the mouse OA model by DMM surgery, joint cavity injection with PBS, luteolin and MIF was started Peptide- PLGA-Luteolin (30. Mu.M) was injected every 3 weeks for a total of 12 weeks. Safranin O/fast green staining showed that PBS group showed significant cartilage destruction, loss of cartilage surface and intermediate layers, hypertrophic chondrocyte increase, safranin O staining was attenuated, and osteoarthritis Score (Mankin Score) reached 8.6 as shown in fig. 7A; the Luteolin group alone also exhibited significant cartilage damage, structural loss, reduced staining, and an osteoarthritis score of 7.6; whereas MIF Peptide The cartilage structure of the PLGA-Luteolin group was essentially complete, only superficial fibrosis occurred, safranin O staining was good, osteoarthritis score was reduced to 2.4 (fig. 7C); and compared to PBS group and simple Luteolin group, MIF Peptide PLGA-Luteolin groupIs significantly reduced (FIGS. 7B and D), indicating MIF compared to Luteolin alone Peptide PLGA-Luteolin is more effective in delaying the progression of osteoarthritis in mice.
The foregoing is only a preferred embodiment of the present invention, but the scope of the present invention is not limited thereto, and any person skilled in the art, who is within the scope of the present invention, should make equivalent substitutions or modifications according to the technical scheme of the present invention and the inventive concept thereof, and should be covered by the scope of the present invention.
Claims (4)
1. A method for preparing a drug carrier targeting cd74+ pro-inflammatory macrophages, comprising the steps of:
step 1, synthesizing MIF polypeptide: synthesis of CD74 targeting MIF polypeptide Structure MIF Peptide ;
Step 2, coupling MIF polypeptide: MIF (metal inert gas) Peptide Coupling to PLGA-PEG5K-Mal to obtain drug carrier MIF targeting CD74+ pro-inflammatory macrophage Peptide -PLGA。
The MIF Peptide The amino acid sequence N '-C' of (2) is leucine-cysteine-glycine-leucine-serine-aspartic acid-arginine-cysteine, and FITC is coupled at the N end for tracing.
2. A pharmaceutical carrier targeting cd74+ pro-inflammatory macrophages obtained by the method of manufacture according to claim 1.
3. Use of a drug carrier targeting cd74+ pro-inflammatory macrophages obtained according to the method of preparation of claim 1 for the preparation of a medicament or pharmaceutical composition for the treatment of knee osteoarthritis.
4. A use according to claim 3, characterized in that: pharmaceutical carrier MIF targeting CD74+ pro-inflammatory macrophages Peptide -loading anti-inflammatory drug on PLGA.
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