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使用超临界二氧化碳生成脂质体的新方法 第一部分:过程机制

Novel method of niosome generation using supercritical carbon dioxide part I: process mechanics.

作者信息

Wagner Michael E, Rizvi Syed S H

机构信息

a Department of Food Science , Cornell University , Ithaca , NY , USA.

出版信息

J Liposome Res. 2015;25(4):334-46. doi: 10.3109/08982104.2015.1039032. Epub 2015 May 6.

DOI:10.3109/08982104.2015.1039032
PMID:25945392
Abstract

A novel method for the production of non-ionic surfactant vesicles (niosomes) using an rapid expansion of supercritical solution (RESS)-based process coupled with a gas ejector is presented along with an investigation of parameters affecting niosome morphology, size and encapsulation efficiency of a 0.2 M D-glucose solution in Tris buffer at physiological pH. The solubility of the non-ionic surfactant polyoxyethylene(4) sorbitan monostearate in SC-CO2 was determined at three pressures (10, 15 and 20 MPa) and three temperatures (40, 50 and 60 °C). Mole fraction of Tween61 in the vapor phase increased with pressure at 40 °C, but did not change with pressure at 50 or 60 °C. Solubility data were correlated using the Peng-Robinson equation of state (PREOS) with the Panagiotopoulos and Reid mixing rule. Vesicles were either multilamellar or unilamellar, depending on the degree of precipitation of the lipid formulation at the point of aqueous cargo introduction. Vesicle particle size distributions were bimodal, with the 80-99% of the liposomal volume contributed niosomes ranging in size from 3 to 7 μm and the remaining niosomes ranging from 239 to 969 nm, depending on the system configuration. Encapsulation efficiency as high as 28% using the gas ejector to introduce the glucose cargo solution was achieved. Vesicle particle size and encapsulation efficiency were shown to be dependent on cargo droplet formation.

摘要

本文介绍了一种基于超临界溶液快速膨胀(RESS)过程并结合气体喷射器来制备非离子表面活性剂囊泡(脂质体)的新方法,同时研究了在生理pH值下影响脂质体形态、大小以及Tris缓冲液中0.2M D -葡萄糖溶液包封效率的参数。测定了非离子表面活性剂聚氧乙烯(4)山梨醇单硬脂酸酯在三种压力(10、15和20MPa)和三种温度(40、50和60℃)下在SC - CO₂中的溶解度。在40℃时,气相中吐温61的摩尔分数随压力增加,但在50或60℃时不随压力变化。使用带有帕纳吉奥多普洛斯和里德混合规则的彭 - 罗宾逊状态方程(PREOS)对溶解度数据进行了关联。根据脂质制剂在引入水性载药点的沉淀程度,囊泡可以是多层的或单层的。囊泡粒径分布是双峰的,根据系统配置,80 - 99%的脂质体体积由大小在3至7μm之间的脂质体贡献,其余脂质体大小在239至969nm之间。使用气体喷射器引入葡萄糖载药溶液时,包封效率高达28%。结果表明,囊泡粒径和包封效率取决于载药液滴的形成。

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