Polylactic acid microsphere and preparation method and application thereof

A technology of polylactic acid microspheres and polylactic acid, which is applied in the fields of polymer materials and biomedical engineering, can solve the problems of human body or environmental hazards, without mentioning the removal of organic solvents, and achieve good fluidity, sieving and grading and labeling particles The effect of accurate diameter and strong shearing force

Active Publication Date: 2019-01-25
张海军
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

When the level of organic solvent contained in the microspheres (generally 0.17%-0.6%) is higher than the safe value (the residual amount of dichloromethane in the Chinese Pharmacopoeia is ≤0.06%, and the residual amount of acetone is ≤0.5%), it will be harmful to the human body. Or the environment is harmful, but none of the above methods mentions the removal of residual organic solvents

Method used

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  • Polylactic acid microsphere and preparation method and application thereof
  • Polylactic acid microsphere and preparation method and application thereof
  • Polylactic acid microsphere and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] (1) Weigh 60g of PDLGA with a viscosity of 50ml / g, add it to 100ml of dichloromethane, and make a polylactic acid solution with a concentration of 60g / ml;

[0044] (2) Add 6 g of sodium carboxymethyl starch to the above polylactic acid solution, and at a speed of 300 rpm, use mechanical stirring to uniformly disperse the sodium carboxymethyl starch in the polylactic acid solution in solid form to obtain a polylactic acid suspension;

[0045] (3) Under stirring at 200rpm, add 5ml of mineral oil to the polylactic acid suspension obtained in step (2) to obtain a layered mixed solution;

[0046] (4) Under stirring at 200 rpm, add 1000 ml of mineral oil to the mixed solution obtained in step (3), after stirring overnight, collect the solid by filtration, wash, and freeze-dry to obtain microspheres.

[0047] Determination of microsphere properties

[0048] a. Morphological observation

[0049] Soak the microspheres in saline, observe and take pictures under an ordinary opti...

Embodiment 2

[0059] (1) Weigh 20g of PDLGA with a viscosity of 40ml / g, add it to 100ml of dichloromethane, and make a polylactic acid solution with a concentration of 20g / ml;

[0060] (2) Add 6 g of sodium carboxymethyl starch to the above polylactic acid solution, and at a speed of 300 rpm, use mechanical stirring to uniformly disperse the sodium carboxymethyl starch in the polylactic acid solution in solid form to obtain a polylactic acid suspension;

[0061] (3) Under stirring at 200rpm, add 5ml of mineral oil to the polylactic acid suspension obtained in step (2) to obtain a layered mixed solution;

[0062] (4) Under stirring at 200 rpm, add 1000 ml of mineral oil to the mixed solution obtained in step (3), after stirring overnight, collect the solid by filtration, wash, and freeze-dry to obtain microspheres.

[0063] Determination of microsphere properties

[0064] According to the same measuring method as in Example 1, it is observed that the microspheres of this embodiment are regu...

Embodiment 3

[0066] (1) Weigh 30g of PDLGA with a viscosity of 40ml / g, add it to 100ml of dichloromethane, and make a polylactic acid solution with a concentration of 30g / ml;

[0067] (2) Add 6 g of sodium carboxymethyl starch to the above polylactic acid solution, and at a speed of 300 rpm, use mechanical stirring to uniformly disperse the sodium carboxymethyl starch in the polylactic acid solution in solid form to obtain a polylactic acid suspension;

[0068] (3) Under stirring at a rotating speed of 180rpm, add 5ml of mineral oil to the polylactic acid suspension obtained in step (2) to obtain a layered mixed solution;

[0069] (4) Under stirring at a rotating speed of 180rpm, add 1000ml of mineral oil to the mixed solution obtained in step (3), after stirring overnight, collect the solid by filtration, wash, and freeze-dry to obtain microspheres.

[0070] Determination of microsphere properties

[0071] According to the same measuring method as in Example 1, it is observed that the mi...

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Abstract

The invention discloses a polylactic acid microsphere and a preparation method and application thereof. The grain size of the microsphere is between 100 mu m and 1000 mu m, preferably between 100 mu mand 300 mu m, between 300 mu m and 500 mu m, between 500 mu m and 700 mu m or between 700 mu m and 1000 mu m, the microsphere is a regular sphere, and the surface and interior of the microsphere areprovided with holes. Because the polylactic acid microsphere is a regular sphere, by adjusting the variety and molecular weight of polylactic acid, the degradation time of the microsphere can be controlled, which is favorable for the determination of the degradation time of the microsphere in the body and the recanalization time of blood vessels in clinical application. The preparation method disclosed by the invention can cut out drops with small grain size under low flow velocity, moreover, the stability of oil-phase fluid is good, the drops do not have tails after coagulant is added, the sphericity of the solidified microsphere is good, and the effect is best. Moreover, by forming the holes in the surface and interior of the microsphere, solvent can be conveniently volatilized, so thatthe amount of remaining solvent is small, meeting the standard of the pharmacopoeia.

Description

technical field [0001] The invention relates to the technical fields of polymer materials and biomedical engineering, in particular to a polylactic acid microsphere and its preparation method and application. Background technique [0002] Embolization therapy is a major means of intervention in the field of oncology. Tumor embolization therapy is aimed at blocking tumor nutrient vessels or controlling bleeding disorders. In the past two decades, due to the emergence of microcatheters and the development of new embolic agents, the clinical application of tumor embolization has shown a clear upward trend. Most notably, the use of selective embolization is critical for tumor therapy based on individual pathology, anatomy, and hemodynamic studies. At present, particle embolization agents are the main dosage forms for the treatment of liver tumors, especially arterial embolization (TAE) or chemoembolization (TACE) for the treatment of hepatocellular carcinoma (HCC). [0003] T...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08L67/04B01J13/06A61L24/00A61L24/04A61K9/16A61K47/34A61P35/00A61P7/04
CPCA61K9/1641A61L24/001A61L24/0042A61L24/046A61L2400/04A61P7/04A61P35/00B01J13/06C08L67/04
Inventor 张海军鲁手涛刘黎明曹文瑞周超尹玉霞段翠海侯文博刘光李茂全
Owner 张海军
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