Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Microencapsulated multivesicular liposome drug carrier and preparation method thereof

A multivesicular liposome and microcapsule technology, applied in microcapsules, capsule delivery, pharmaceutical formulations, etc., can solve the problems of general biocompatibility, differences in physical and chemical properties, cross-contamination of drugs, etc., and achieve smooth surface of microcapsules, Easy to operate and reduce toxic and side effects

Active Publication Date: 2015-05-20
HUAQIAO UNIVERSITY
View PDF2 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At the same time, due to the differences in physical and chemical properties between different drugs, they may face problems such as drug cross-contamination when mixed in drug carriers
[0003] In addition, liposome-based drug carriers usually have good biocompatibility but are not very stable, while polymer-based drug carriers usually have good stability but poor biocompatibility.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0022] The present invention also relates to a preparation method of the above-mentioned microcapsule-embedded polyvesicular liposome drug carrier, the steps of the preparation method are as follows:

[0023] Step 10, using sucrose solution as the inner water phase, glucose and L-lysine solution as the outer water phase, and lipid-dissolved dichloromethane solution as the oil phase, high-speed homogenizing and emulsifying the inner water phase and the oil phase to form an initial phase After milking, add the external water phase, vortex emulsify to form a double emulsion, and then rotate to evaporate the dichloromethane to obtain the multivesicular liposome suspension;

[0024] Step 20, take quantitative multivesicular liposomes and disperse them in the sodium alginate solution, disperse evenly with the aid of ultrasonic waves, and then drop the sodium alginate solution dispersed in multivesicular liposomes into the chlorine Calcium alginate beads embedded with multivesicular ...

Embodiment 1

[0030] Example 1: prepare 7.5% (w / v) sucrose solution as the inner aqueous phase; prepare a solution containing 5% (w / v) glucose and 30mM L-lysine as the outer aqueous phase; prepare a solution containing 16.5mg / mL Soybean lecithin, 8mg / mL cholesterol, 8mg / mL triolein and 1mg / mL oleic acid in dichloromethane are used as the oil phase; mix the same volume of the internal water phase and oil phase, and stir on a high-speed homogenizer for 10min , with a rotating speed of 14,000 rpm, to prepare colostrum; add 9 mL of external aqueous phase solution to the colostrum, emulsify on a vortex suspension apparatus for 10 seconds, and prepare double milk. Subsequently, the double emulsion was transferred to a rotary evaporator, and the organic solvent was removed by rotary evaporation at 35° C. and 10 rpm. After centrifugation at 3500 rpm for 5 minutes, the multivesicular liposome suspension was obtained. The microsphere has a smooth surface, good dispersibility, good sphericity, an aver...

Embodiment 2

[0032] Embodiment 2: This embodiment is basically the same as Embodiment 1, except that the sodium alginate solution in the syringe pump is mixed with 2 mg / mL insulin solution. A microcapsule-embedded multivesicular liposome drug carrier system that distributes different drugs in different spaces is prepared, that is, MET is embedded inside the multivesicular liposome, and insulin is embedded outside the multivesicular liposome and inside the microcapsule. The drug loading capacity of MET and insulin in the multivesicular liposome drug carrier system embedded in microcapsules was 0.39% and 1.91%, respectively, and the encapsulation efficiency was 57.10% and 11.41%, respectively. The cumulative release of MET was 18.97% and 0% of insulin when the system was simulated in vitro for 4 hours; the cumulative release of MET and INS was close to 22% at 8 hours. It shows a sequential release phenomenon within a certain period of time.

[0033]The invention adopts the double emulsifica...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
particle diameteraaaaaaaaaa
particle diameteraaaaaaaaaa
particle sizeaaaaaaaaaa
Login to View More

Abstract

The invention provides a microencapsulated multivesicular liposome drug carrier and a preparation method thereof. The method comprises the following steps: with a sucrose solution as an inner water phase, glucose and an L-lysine solution as outer water phases, and a dichloromethane solution dissolved with lipid as an oil phase, carrying out high-speed homogenate emulsification on the inner water phase and the oil phase to form colostrums; adding the outer water phase, carrying out vortex emulsification to form a compound emulsion, carrying out rotary evaporation to remove dichloromethane, so as to obtain a multivesicular liposome suspension; dispersing the multivesicular liposome into a sodium alginate solution, dispersing uniformly, and then dropping into a calcium chloride solution through a high-pressure microcapsule molding device and an injection pump, so as to prepare calcium alginate gel beads embedded with the multivesicular liposome; and finally forming a film from the gel beads and a cationic polymer solution, so as to form a sample, wherein the drug is carried on at least one part in the multivesicular liposome or out of the multivesicular liposome in the microcapsule. According to the microencapsulated multivesicular liposome drug carrier, space allocation of different drugs is ensured; the long-acting release and absorption of the drug are improved; and toxic and side effects caused by simple use of the drug are reduced.

Description

【Technical field】 [0001] The invention relates to a microcapsule-embedded multivesicle liposome drug carrier and a preparation method thereof. 【Background technique】 [0002] In recent years, microcapsules / spheres and other particulate drug sustained-release systems have developed rapidly and have been widely used clinically. In addition, for many diseases, such as cancer, AIDS, malaria, multiple sclerosis, hypertension, etc., single drug therapy and drug sustained release system often cannot achieve the desired therapeutic effect, and drug combination therapy can pass through the diseased cells. Modulate different signaling pathways to maximize therapeutic effect. Therefore, combined with drug combination therapy and drug carrier system to achieve slow / controlled release of drugs, it can reduce the frequency of drug application and alleviate the suffering of patients. However, at present, drug sustained-release microcapsules / spheres often face problems such as drug burst ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): A61K9/50A61K47/36A61K47/34
Inventor 刘源岗王士斌吴柯静陈莉李腾腾陈爱政吴文果
Owner HUAQIAO UNIVERSITY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products