提高脂质体声敏感性以控制药物递送的策略

An Nguyen, P. Lewin, S. Wrenn
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引用次数: 2

摘要

聚乙二醇(PEG)移植和回声脂质体已被研究,以实现控制药物输送超声作为外部触发。本研究旨在系统地探讨PEG嫁接、回声性和脂质相对声敏感性的单独和联合影响。脂质体暴露于20 kHz超声下,监测钙黄蛋白的释放以量化声敏感性。与先前的结果一致,PEG嫁接和回声增强观察到声敏感性增加;此外,两个脂质体相的回声增强都比PEG接枝强。无回声脂质体钙黄蛋白的释放曲线似乎可以用两个叠加的一级过程来描述,而有回声脂质体钙黄蛋白的释放曲线则可以用单个一级过程来描述。这些结果表明,声敏感性强烈依赖于脂质体的化学性质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Strategies for increasing acoustic susceptibility of liposomes for controlled drug delivery
Polyethylene glycol (PEG) grafted and echogenic liposomes have been investigated to achieve controlled drug delivery with ultrasound as an external trigger. This study was devised to systematically explore the individual and combined effects of PEG grafting, echogenicity, and lipid phase on acoustic susceptibility. Liposome formulations were exposed to 20 kHz ultrasound and the release of calcein was monitored to quantify acoustic susceptibility. Consistent with previous results, PEG grafting and echogenicity were observed to increase acoustic susceptibility; additionally, the enhancement from echogenicity was greater than PEG grafting for both liposome phases. The release profile of calcein from non-echogenic liposomes appeared to be described by a model with two superimposed first order processes whereas that of the echogenic liposomes was better described with a single first order process. These results indicate that acoustic susceptibility is strongly dependent on liposome chemistry and better underst...
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