CN108159428A - A kind of Thermosensitive Material Used for Controlled Releasing of Medicine and preparation method thereof - Google Patents

A kind of Thermosensitive Material Used for Controlled Releasing of Medicine and preparation method thereof Download PDF

Info

Publication number
CN108159428A
CN108159428A CN201810033600.6A CN201810033600A CN108159428A CN 108159428 A CN108159428 A CN 108159428A CN 201810033600 A CN201810033600 A CN 201810033600A CN 108159428 A CN108159428 A CN 108159428A
Authority
CN
China
Prior art keywords
parts
material used
medicine
thermosensitive material
low
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
CN201810033600.6A
Other languages
Chinese (zh)
Inventor
王金英
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Foshan Ruisheng Technology Co Ltd
Original Assignee
Foshan Ruisheng Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Foshan Ruisheng Technology Co Ltd filed Critical Foshan Ruisheng Technology Co Ltd
Priority to CN201810033600.6A priority Critical patent/CN108159428A/en
Publication of CN108159428A publication Critical patent/CN108159428A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02Inorganic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/20Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing sulfur, e.g. dimethyl sulfoxide [DMSO], docusate, sodium lauryl sulfate or aminosulfonic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/34Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/38Cellulose; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/42Proteins; Polypeptides; Degradation products thereof; Derivatives thereof, e.g. albumin, gelatin or zein
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/44Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Inorganic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicinal Preparation (AREA)

Abstract

The present invention provides a kind of Thermosensitive Material Used for Controlled Releasing of Medicine and preparation method thereof.Preparation method is as follows:(1)Low-molecular weight chitoglycan, polyanion cellulose, silk peptide, polycaprolactone, bovine serum albumin, glycolic, aloe polysaccharide and deionized water are mixed, obtain component A;(2)By garlic oil, N, the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N' and polyethylene glycol are mixed, and obtain component B;(3)Component A and B are mixed, ultrasonic shear;(4)Add in sodium tripolyphosphate and glutaraldehyde, heating stirring;(5)Water phase is obtained after standing separation, adjusts pH value to 8, low-speed centrifugal removes larger particle;(6)Suspension pH value is adjusted to neutrality, centrifugation discards solvent, is drying to obtain.The Thermosensitive Material Used for Controlled Releasing of Medicine of the present invention has higher water absorption rate, and hydrophily is good, and envelop rate is high, while has good sustained drug release effect, the most suitable for 1/drug for 24 hours.

Description

A kind of Thermosensitive Material Used for Controlled Releasing of Medicine and preparation method thereof
Technical field
The present invention relates to biomedical materials fields, and in particular to a kind of Thermosensitive Material Used for Controlled Releasing of Medicine and preparation method thereof.
Background technology
It is administered by traditional approach, most drugs ingredient discharges quickly, causes the rapid raising of internal levels of drugs, reaches It is reduced rapidly after to peak value.And for drug, effect is closely related with the concentration of drug in blood serum, and violent fluctuation is past Unacceptable side effect is generated in peak value toward causing, insufficient control then is caused since the concentration of drug in blood serum is too low Therapeutic effect.In order to maintain internal necessary drug concentration, regular medicine taking or injection for several times on the one can only be used, even if with medicament It is arranged on amount and administration time interval, internal blood concentration is still within fluctuation status.And controlled release drug delivery system It comes across in the 1970s, being one kind in drug delivery system, it can be such that drug is discharged with a kind of scheduled rate, make Drug concentration in blood or tissue is maintained in a long time in the range of effective therapeutic index, extends drug in medicine-feeding part Residence time, improve bioavilability, achieve the effect that slow-release controlled-release.Relative to traditional administering mode, drug control is released Place system have can adjust drug releasing rate, reduce administration number of times, generate appropriateness reaction, improve curative effect of medication, reduce medicine Object toxic side effect, the pain for mitigating patient's medication, it is important so as to increase the safety of drug therapy, high efficiency and reliability etc. Meaning.
Invention content
Technical problems to be solved:The object of the present invention is to provide a kind of Thermosensitive Material Used for Controlled Releasing of Medicine, have higher water absorption rate, Hydrophily is good, and envelop rate is high, while has good sustained drug release effect, the most suitable for 1/drug for 24 hours.
Technical solution:A kind of Thermosensitive Material Used for Controlled Releasing of Medicine is prepared by following component with parts by weight:0.5-1.5 parts of silk peptide, 1-2 parts of polycaprolactone, 1-3 parts of bovine serum albumin, 1-2 parts of glycolic, 2-4 parts of garlic oil, 0.5-1 parts of sodium tripolyphosphate, aloe 1-2 parts of polysaccharide, 3-6 parts of low-molecular weight chitoglycan, 2-3 parts of polyanion cellulose, bis- two ethanesulfonic acids of oleoyl ethylenediamine of N, N'- 1-3 parts of sodium, 5-7 parts of polyethylene glycol, 2-4 parts of glutaraldehyde, 50-70 parts of deionized water.
It is further preferred that a kind of Thermosensitive Material Used for Controlled Releasing of Medicine, is prepared by following component with parts by weight:1 part of silk peptide, 1.5 parts of polycaprolactone, 2 parts of bovine serum albumin, 1.5 parts of glycolic, 3 parts of garlic oil, 0.8 part of sodium tripolyphosphate, aloe polysaccharide 1.5 Part, 4.5 parts of low-molecular weight chitoglycan, 2.5 parts of polyanion cellulose, 2 parts of the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N, N'-, 6 parts of polyethylene glycol, 3 parts of glutaraldehyde, 60 parts of deionized water.
Further, the weight average molecular weight of the low-molecular weight chitoglycan is 4.8 × 104, deacetylation 92%.
The preparation method of said medicine slow-release material includes the following steps:
(1) by low-molecular weight chitoglycan, polyanion cellulose, silk peptide, polycaprolactone, bovine serum albumin, glycolic, aloe 20-30min is mixed in polysaccharide and deionized water, obtains component A;
(2) 10-20min is mixed in garlic oil, N, the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N'- and polyethylene glycol, obtains group Divide B;
(3) component A and B are mixed, ultrasonic shear 5-10min;
(4) sodium tripolyphosphate and glutaraldehyde are added in, is heated to 40-50 DEG C of stirring 5-6h;
(5) water phase is obtained after standing separation, adjusts pH value to 8, low-speed centrifugal removes larger particle;
(6) suspension pH value is adjusted to neutrality, is centrifuged 3-5min under rotating speed 2500-3000r/min, is discarded solvent, drying is .
Further, 45 DEG C are heated in the step (4), mixing time 5.5h.
Further, rotating speed is 2800r/min, centrifugation time 4min in the step (6).
Advantageous effect:The Thermosensitive Material Used for Controlled Releasing of Medicine of the present invention has higher water absorption rate, reaches as high as 44.4%, and hydrophily is good, packet Envelope rate is high, reaches as high as 94.1%, and drug release rate is only in minimum only 26.2%, the 8h of drug release rate in 2h Drug release rate is 79.6% in 57.4%, 16h, and interior drug release is basically completed for 24 hours, has good sustained drug release effect, It is suitable for 1/drug for 24 hours the most.
Specific embodiment
Embodiment 1
A kind of Thermosensitive Material Used for Controlled Releasing of Medicine is prepared by following component with parts by weight:0.5 part of silk peptide, 1 part of polycaprolactone, ox blood 1 part of albumin, 1 part of glycolic, 2 parts of garlic oil, 0.5 part of sodium tripolyphosphate, 1 part of aloe polysaccharide, 3 parts of low-molecular weight chitoglycan, 2 parts of polyanion cellulose, 1 part of the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N, N'-, 5 parts of polyethylene glycol, 2 parts of glutaraldehyde, go from Sub- 50 parts of water.
The preparation method of said medicine slow-release material is:
(1) by low-molecular weight chitoglycan, polyanion cellulose, silk peptide, polycaprolactone, bovine serum albumin, glycolic, aloe 20min is mixed in polysaccharide and deionized water, obtains component A;
(2) 10min is mixed in garlic oil, N, the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N'- and polyethylene glycol, obtains component B;
(3) component A and B are mixed, ultrasonic shear 5min;
(4) sodium tripolyphosphate and glutaraldehyde are added in, is heated to 40 DEG C of stirring 5h;
(5) water phase is obtained after standing separation, adjusts pH value to 8, low-speed centrifugal removes larger particle;
(6) suspension pH value is adjusted to neutrality, is centrifuged 3min under rotating speed 2500r/min, is discarded solvent, is drying to obtain.
Embodiment 2
A kind of Thermosensitive Material Used for Controlled Releasing of Medicine is prepared by following component with parts by weight:0.8 part of silk peptide, 1.5 parts of polycaprolactone, ox 1.5 parts of haemocyanin, 1.5 parts of glycolic, 2.5 parts of garlic oil, 0.7 part of sodium tripolyphosphate, 1.5 parts of aloe polysaccharide, low molecular weight 4 parts of chitosan, 2.5 parts of polyanion cellulose, 2 parts of the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N, N'-, 6 parts of polyethylene glycol, penta 2.5 parts of dialdehyde, 55 parts of deionized water.
The preparation method of said medicine slow-release material is:
(1) by low-molecular weight chitoglycan, polyanion cellulose, silk peptide, polycaprolactone, bovine serum albumin, glycolic, aloe 25min is mixed in polysaccharide and deionized water, obtains component A;
(2) 15min is mixed in garlic oil, N, the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N'- and polyethylene glycol, obtains component B;
(3) component A and B are mixed, ultrasonic shear 7min;
(4) sodium tripolyphosphate and glutaraldehyde are added in, is heated to 45 DEG C of stirring 5.5h;
(5) water phase is obtained after standing separation, adjusts pH value to 8, low-speed centrifugal removes larger particle;
(6) suspension pH value is adjusted to neutrality, is centrifuged 4min under rotating speed 2700r/min, is discarded solvent, is drying to obtain.
Embodiment 3
A kind of Thermosensitive Material Used for Controlled Releasing of Medicine is prepared by following component with parts by weight:1 part of silk peptide, 1.5 parts of polycaprolactone, ox blood 2 parts of albumin, 1.5 parts of glycolic, 3 parts of garlic oil, 0.8 part of sodium tripolyphosphate, 1.5 parts of aloe polysaccharide, low-molecular weight chitoglycan 4.5 parts, 2.5 parts of polyanion cellulose, 2 parts of the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N, N'-, 6 parts of polyethylene glycol, glutaraldehyde 3 parts, 60 parts of deionized water.
The preparation method of said medicine slow-release material is:
(1) by low-molecular weight chitoglycan, polyanion cellulose, silk peptide, polycaprolactone, bovine serum albumin, glycolic, aloe 25min is mixed in polysaccharide and deionized water, obtains component A;
(2) 15min is mixed in garlic oil, N, the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N'- and polyethylene glycol, obtains component B;
(3) component A and B are mixed, ultrasonic shear 8min;
(4) sodium tripolyphosphate and glutaraldehyde are added in, is heated to 45 DEG C of stirring 5.5h;
(5) water phase is obtained after standing separation, adjusts pH value to 8, low-speed centrifugal removes larger particle;
(6) suspension pH value is adjusted to neutrality, is centrifuged 4min under rotating speed 2800r/min, is discarded solvent, is drying to obtain.
Embodiment 4
A kind of Thermosensitive Material Used for Controlled Releasing of Medicine is prepared by following component with parts by weight:1.5 parts of silk peptide, 2 parts of polycaprolactone, ox blood 3 parts of albumin, 4 parts of garlic oil, 1 part of sodium tripolyphosphate, 2 parts of aloe polysaccharide, 6 parts of low-molecular weight chitoglycan, gathers 2 parts of glycolic 3 parts of anionic cellulose, 3 parts of the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N, N'-, 7 parts of polyethylene glycol, 4 parts of glutaraldehyde, deionization 70 parts of water.
The preparation method of said medicine slow-release material is:
(1) by low-molecular weight chitoglycan, polyanion cellulose, silk peptide, polycaprolactone, bovine serum albumin, glycolic, aloe 30min is mixed in polysaccharide and deionized water, obtains component A;
(2) 20min is mixed in garlic oil, N, the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N'- and polyethylene glycol, obtains component B;
(3) component A and B are mixed, ultrasonic shear 10min;
(4) sodium tripolyphosphate and glutaraldehyde are added in, is heated to 50 DEG C of stirring 6h;
(5) water phase is obtained after standing separation, adjusts pH value to 8, low-speed centrifugal removes larger particle;
(6) suspension pH value is adjusted to neutrality, is centrifuged 5min under rotating speed 3000r/min, is discarded solvent, is drying to obtain.
Comparative example 1
Difference lies in do not contain silk peptide and bovine serum albumin with embodiment 1 for the present embodiment.Specifically:
A kind of Thermosensitive Material Used for Controlled Releasing of Medicine is prepared by following component with parts by weight:1 part of polycaprolactone, 1 part of glycolic, garlic oil 2 Part, 0.5 part of sodium tripolyphosphate, 1 part of aloe polysaccharide, 3 parts of low-molecular weight chitoglycan, 2 parts of polyanion cellulose, the bis- oil of N, N'- 1 part of Ethylene Diamine diethyl sodium sulfonate, 5 parts of polyethylene glycol, 2 parts of glutaraldehyde, 50 parts of deionized water.
The preparation method of said medicine slow-release material is:
(1) low-molecular weight chitoglycan, polyanion cellulose, polycaprolactone, glycolic, aloe polysaccharide and deionized water are mixed 20min is stirred, obtains component A;
(2) 10min is mixed in garlic oil, N, the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N'- and polyethylene glycol, obtains component B;
(3) component A and B are mixed, ultrasonic shear 5min;
(4) sodium tripolyphosphate and glutaraldehyde are added in, is heated to 40 DEG C of stirring 5h;
(5) water phase is obtained after standing separation, adjusts pH value to 8, low-speed centrifugal removes larger particle;
(6) suspension pH value is adjusted to neutrality, is centrifuged 3min under rotating speed 2500r/min, is discarded solvent, is drying to obtain.
Comparative example 2
Difference lies in do not contain polycaprolactone and glycolic with embodiment 1 for the present embodiment.Specifically:
A kind of Thermosensitive Material Used for Controlled Releasing of Medicine is prepared by following component with parts by weight:It is 0.5 part of silk peptide, 1 part of bovine serum albumin, big 2 parts of garlic oil, 0.5 part of sodium tripolyphosphate, 1 part of aloe polysaccharide, 3 parts of low-molecular weight chitoglycan, 2 parts of polyanion cellulose, N, N'- Double 1 part of oleoyl ethylenediamine diethyl sodium sulfonates, 5 parts of polyethylene glycol, 2 parts of glutaraldehyde, 50 parts of deionized water.
The preparation method of said medicine slow-release material is:
(1) low-molecular weight chitoglycan, polyanion cellulose, silk peptide, bovine serum albumin, aloe polysaccharide and deionized water are mixed Stirring 20min is closed, obtains component A;
(2) 10min is mixed in garlic oil, N, the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N'- and polyethylene glycol, obtains component B;
(3) component A and B are mixed, ultrasonic shear 5min;
(4) sodium tripolyphosphate and glutaraldehyde are added in, is heated to 40 DEG C of stirring 5h;
(5) water phase is obtained after standing separation, adjusts pH value to 8, low-speed centrifugal removes larger particle;
(6) suspension pH value is adjusted to neutrality, is centrifuged 3min under rotating speed 2500r/min, is discarded solvent, is drying to obtain.
The partial properties index of the Thermosensitive Material Used for Controlled Releasing of Medicine of the present invention see the table below, it will be seen that material of the present invention is with higher Water absorption rate, reach as high as 44.4%, hydrophily is good, and envelop rate is high, reaches as high as 94.1%, drug release rate is minimum in 2h In only 26.2%, 8h drug release rate be only in 57.4%, 16h drug release rate be 79.6%, interior drug release is basic for 24 hours It completes, there is good sustained drug release effect, the most suitable for 1/drug for 24 hours.
The partial properties index of 1 Thermosensitive Material Used for Controlled Releasing of Medicine of table

Claims (6)

1. a kind of Thermosensitive Material Used for Controlled Releasing of Medicine, it is characterised in that:It is prepared by following component with parts by weight:0.5-1.5 parts of silk peptide, 1-2 parts of polycaprolactone, 1-3 parts of bovine serum albumin, 1-2 parts of glycolic, 2-4 parts of garlic oil, 0.5-1 parts of sodium tripolyphosphate, aloe 1-2 parts of polysaccharide, 3-6 parts of low-molecular weight chitoglycan, 2-3 parts of polyanion cellulose, bis- two ethanesulfonic acids of oleoyl ethylenediamine of N, N'- 1-3 parts of sodium, 5-7 parts of polyethylene glycol, 2-4 parts of glutaraldehyde, 50-70 parts of deionized water.
2. a kind of Thermosensitive Material Used for Controlled Releasing of Medicine according to claim 1, it is characterised in that:By following component with parts by weight prepare and Into:1 part of silk peptide, 1.5 parts of polycaprolactone, 2 parts of bovine serum albumin, 1.5 parts of glycolic, 3 parts of garlic oil, sodium tripolyphosphate 0.8 Part, 1.5 parts of aloe polysaccharide, 4.5 parts of low-molecular weight chitoglycan, 2.5 parts of polyanion cellulose, the bis- oleoyl ethylenediamines of N, N'- 2 parts of diethyl sodium sulfonate, 6 parts of polyethylene glycol, 3 parts of glutaraldehyde, 60 parts of deionized water.
3. a kind of Thermosensitive Material Used for Controlled Releasing of Medicine according to claim 1, it is characterised in that:The weight of the low-molecular weight chitoglycan is equal Molecular weight is 4.8 × 104, deacetylation 92%.
4. a kind of preparation method of Thermosensitive Material Used for Controlled Releasing of Medicine of claim 1 to 2 any one of them, it is characterised in that:Including following Step:
(1)By low-molecular weight chitoglycan, polyanion cellulose, silk peptide, polycaprolactone, bovine serum albumin, glycolic, reed 20-30min is mixed in luxuriant growth polysaccharide and deionized water, obtains component A;
(2)By garlic oil, N, 10-20min is mixed in the bis- oleoyl ethylenediamine diethyl sodium sulfonates of N'- and polyethylene glycol, obtains group Divide B;
(3)Component A and B are mixed, ultrasonic shear 5-10min;
(4)Sodium tripolyphosphate and glutaraldehyde are added in, is heated to 40-50 DEG C of stirring 5-6h;
(5)Water phase is obtained after standing separation, adjusts pH value to 8, low-speed centrifugal removes larger particle;
(6)Suspension pH value is adjusted to neutrality, 3-5min is centrifuged under rotating speed 2500-3000r/min, discards solvent, drying is .
5. a kind of preparation method of Thermosensitive Material Used for Controlled Releasing of Medicine according to claim 4, it is characterised in that:The step(4)In 45 DEG C are heated to, mixing time 5.5h.
6. a kind of preparation method of Thermosensitive Material Used for Controlled Releasing of Medicine according to claim 4, it is characterised in that:The step(6)In Rotating speed is 2800r/min, centrifugation time 4min.
CN201810033600.6A 2018-01-11 2018-01-11 A kind of Thermosensitive Material Used for Controlled Releasing of Medicine and preparation method thereof Withdrawn CN108159428A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810033600.6A CN108159428A (en) 2018-01-11 2018-01-11 A kind of Thermosensitive Material Used for Controlled Releasing of Medicine and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810033600.6A CN108159428A (en) 2018-01-11 2018-01-11 A kind of Thermosensitive Material Used for Controlled Releasing of Medicine and preparation method thereof

Publications (1)

Publication Number Publication Date
CN108159428A true CN108159428A (en) 2018-06-15

Family

ID=62514283

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810033600.6A Withdrawn CN108159428A (en) 2018-01-11 2018-01-11 A kind of Thermosensitive Material Used for Controlled Releasing of Medicine and preparation method thereof

Country Status (1)

Country Link
CN (1) CN108159428A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111374987A (en) * 2020-02-29 2020-07-07 湖北工业大学 Method for improving foaming property and foam stability of serum albumin by using chitosan oligosaccharide

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111374987A (en) * 2020-02-29 2020-07-07 湖北工业大学 Method for improving foaming property and foam stability of serum albumin by using chitosan oligosaccharide
CN111374987B (en) * 2020-02-29 2021-08-24 湖北工业大学 Method for improving foaming property and foam stability of serum albumin by using chitosan oligosaccharide

Similar Documents

Publication Publication Date Title
US20030175354A1 (en) Antiemetic, anti-motion sustained release drug delivery system
US20100136140A1 (en) A use of hypertonic solution composition in manufacturing medicaments for promoting wound healing
DE69824164T2 (en) DRUG PREPARATIONS FOR THE TREATMENT OF SEXUAL MALFUNCTIONS
CN102560887A (en) Silk fibroin nano-fiber film loaded with vitamins A and E and preparation method thereof
KR20160110956A (en) Composition comprising xylitol and cholecalciferol for topical treatment of skin and mucous membranes
JPH01287041A (en) Sustained release preparation
CN108159428A (en) A kind of Thermosensitive Material Used for Controlled Releasing of Medicine and preparation method thereof
CN108324612A (en) A kind of Baby Care cream and preparation method thereof
CN107320716A (en) Basic fibroblast growth factor vesica and preparation method thereof
CN106390179A (en) Polyurethane sponge dressing with anti-adhesion and hemostasis functions and preparation method thereof
CN102988301A (en) Preparation method of long-acting sustained-release microspheres containing bevacizumab
CN106350560A (en) Preparation method of fish protein peptide, prepared fish protein peptide and application
US2530480A (en) Therapeutic preparations for intramuscular and subcutaneous injection and methods of making the same
CN114558046B (en) Ophthalmic preparation for improving stability and preparation method thereof
CN113116856B (en) Eucalyptus and pinene enteric-coated microspheres and preparation method thereof
CN115212290A (en) Atomized inhalation type atomized liquid for preventing and treating virus infection and production method thereof
CN107789320B (en) Fulvestrant sustained-release injection and preparation process thereof
CN113493936B (en) Anti-erythra regenerated cellulose fiber containing pearl traditional Chinese medicine and preparation method thereof
CN1193761C (en) Controllable release system of glucocorticoid and its preparation and use
CN112546101A (en) Traditional Chinese medicine compound for relieving eczema, sustained-release agent, preparation method and application
CN106109400A (en) A kind of oral drugs hydrogel slow-released carrier and preparation method and applications
CN107320730A (en) A kind of nano-medicament carrier material and preparation method thereof
CN1148957A (en) Aqueously soluble powder preparation of taxinol and its preparing method
CN114522194A (en) Temperature-sensitive gel containing periplaneta americana extract as well as preparation method and application of temperature-sensitive gel
CN110893232A (en) Cefoperazone sodium and sulbactam sodium powder injection for injection and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WW01 Invention patent application withdrawn after publication
WW01 Invention patent application withdrawn after publication

Application publication date: 20180615