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Liquid crystal gel hepatic artery embolic agent and preparation method thereof

A gel hepatic artery and embolic agent technology, which is applied in surgical adhesives, medical science, surgery, etc., can solve the problems of poor embolization time stability of lipiodol, phytantriol hemolysis, and poor fluidity of gelatin sponge, etc. The effect of loading dose and encapsulation rate, low equipment cost and raw material cost, and easy raw material

Active Publication Date: 2018-09-07
武汉百纳礼康生物制药有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the above-mentioned embolic materials have certain defects, such as poor fluidity of gelatin sponge, poor dispersion of microspheres, and liquid embolic materials are prone to cause vascular toxicity, etc.
Based on the theoretical basis that amphiphilic liquid crystal materials and water can self-assemble into thermodynamically stable systems with different structures, scientists use the unique structure, bio-affinity and stability characteristics of cubic liquid crystals to prepare solvent-induced liquid crystal solutions by using in-situ gel technology , but most of them use liquid crystal materials such as glycerol monooleate and phytantriol to prepare gels. Although they have good embolism properties and good biocompatibility, a certain concentration of unsaturated monofatty acids Glycerides can cause hemolysis in animals
Han Ke "Research on Hepatic Artery Embolic Agent Based on Phytantriol Cubic Liquid Crystal" - (2010.06) proposed to use phytantriol as liquid crystal material to prepare embolism, although it has good embolism performance, but a certain concentration of phytantriol It is easy to cause hemolysis. CN103120640A patent introduces a preparation method of embolic agent, in which liposomes are wrapped with 131I-iodol and magnetic nanoparticles, and the magnetic nanoparticles are dispersed in the 131I-iodol. There are anti-tumor drugs on the face, but this preparation method is too complicated, and the time stability of lipiodol embolization is poor

Method used

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  • Liquid crystal gel hepatic artery embolic agent and preparation method thereof
  • Liquid crystal gel hepatic artery embolic agent and preparation method thereof
  • Liquid crystal gel hepatic artery embolic agent and preparation method thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0036] Example 1: Preparation of a liquid crystal gel hepatic artery embolization agent, for the method see figure 1 :

[0037] Weigh 0.42g of glyceryl dioleate, 0.52g of soybean phosphatidylcholine, and 0.06g of poloxamer and heat and melt at 70°C to obtain phase A; weigh 0.80g of mitomycin, 0.20g of anhydrous Ethanol, mix evenly on a mixer to dissolve it completely, and obtain the dissolved medicinal solution, which is phase B; at 20-35°C, add phase B in the mass percentage of 14:86, 10:90, and 6:94 respectively In phase A, fully mix to obtain liquid crystal gel hepatic artery embolism precursor preparation a 1 , b 1 、c 1 , protected from light, sealed, and stored in a refrigerator at 4°C.

Embodiment 2

[0039] Weigh 0.51g of glyceryl dioleate, 0.34g of soybean phosphatidylcholine, and 0.15g of poloxamer and heat and melt at 70°C to obtain phase A; weigh 0.92g of mitomycin, 0.08g of anhydrous Ethanol, mix evenly on a mixer to dissolve it completely, and obtain the dissolved medicinal solution, which is phase B; at 20-35°C, add phase B in the mass percentage of 14:86, 10:90, and 6:94 respectively In phase A, fully mix to obtain liquid crystal gel hepatic artery embolism precursor preparation a 2 , b 2 、c 2 , protected from light, sealed, and stored in a refrigerator at 4°C.

Embodiment 3

[0041]Weigh 0.45g of glyceryl dioleate, 0.50g of soybean phosphatidylcholine, and 0.05g of poloxamer and heat and melt at 70°C to obtain phase A; weigh 0.90g of mitomycin, 0.10g of anhydrous Ethanol, mix evenly on a mixer to dissolve it completely, and obtain the dissolved medicinal solution, which is phase B; at 20-35°C, add phase B according to the mass percentage of 14:86, 10:90, and 6:94 respectively In phase A, fully mix to obtain liquid crystal gel hepatic artery embolism precursor preparation a 3 , b 3 、c 3 , protected from light, sealed, and stored in a refrigerator at 4°C.

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Abstract

The invention discloses a liquid crystal gel hepatic artery embolic agent and a preparation method thereof, wherein the liquid crystal gel hepatic artery embolic agent is mainly formed by mixing 85-95wt% of an A phase and 5-15 wt% of a B phase, and the A phase comprises 33-52 wt% of at least one diacylglycerol, 33-52 wt% of at least one phosphatidylcholine and 0-15 wt% of a surfactant; the B phase comprises 8-20 wt% of a solvent and 80-92 wt% of an active ingredient; the active ingredient is an anti-tumor drug; diacylglycerol comprises glycerol dioleate; phosphatidylcholine comprises soybeanphosphatidylcholine; and the solvent is ethanol. With use of the consisting composition of the liquid crystal gel and unique liquid crystal phase structure, the release of a carrier can be effectivelycontrolled, the circulation time in vivo is prolonged, and the bioavailability is improved.

Description

technical field [0001] The invention belongs to the field of pharmaceutical preparations, and in particular relates to a liquid crystal gel hepatic artery embolization agent and a preparation method thereof. Background technique [0002] Liquid crystal is a molecular aggregate with long-range order and short-range disorder. It is the fourth state besides the three states of matter. It is a thermodynamically stable intermediate phase state between solid and liquid. On the one hand, it has a flow like a liquid. On the other hand, it has anisotropy like crystal, which is a kind of substance with special structure. Liquid crystals can be divided into lyotropic liquid crystals and thermotropic liquid crystals. Lyotropic liquid crystals are mainly a system formed by two or more components under certain conditions. This system is mostly composed of amphiphilic molecules and solvents. When amphiphilic molecules and solvents When mixed, the solvent impregnates the solid lattice of a...

Claims

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Application Information

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IPC IPC(8): A61L24/00
CPCA61L24/00A61L24/0015A61L2300/216
Inventor 罗亮黄丽萍张一漪孟凡玲
Owner 武汉百纳礼康生物制药有限公司
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