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用于鱼腥草精油肺部持续递送的固体脂质纳米粒:制备、表征及体内评价

Solid lipid nanoparticles for sustained pulmonary delivery of Yuxingcao essential oil: Preparation, characterization and in vivo evaluation.

作者信息

Zhao Yun, Chang Yue-Xing, Hu Xiao, Liu Chun-Yu, Quan Li-Hui, Liao Yong-Hong

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, China.

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, China.

出版信息

Int J Pharm. 2017 Jan 10;516(1-2):364-371. doi: 10.1016/j.ijpharm.2016.11.046. Epub 2016 Nov 21.

Abstract

The objective of this study was to prepare solid lipid nanoparticles (SLNs) for sustained pulmonary delivery of Yuxingcao essential oil (YEO). Three YEO loaded SLNs (SLN-200, SLN-400 and SLN-800) with different particle size were prepared and separated following a high-shear homogenization technique using Compritol 888 ATO as lipid and polyvinyl alcohol as an emulsifier. The particle size, zeta potential, drug encapsulation efficiency and drug loading of the SLNs were determined to be between 171 and 812nm, -17.1 and -19.3mV, between 76.6 and 90.2% and between 2.34 and 3.12%, respectively whereas the in vitro release data showed that the SLNs led to sustained drug release up to 48h. In addition, the SLN suspensions after nebulization conferred the fine particle fractions (<5.4μm) of 67.4-75.8%. Following intratracheal administration to rats, YEO loaded SLNs not only prolonged pulmonary retention up to 24h, but also increased AUC values (15.4, 18.2 and 26.3μg/gh for SLN-200, SLN-400 and SLN-800, respectively) by 4.5-7.7 folds compared to the intratracheally dosed YEO solution and by 257-438 folds to the intravenously dosed YEO solution, respectively. The present results were the first to show that YEO loaded SLNs may sustain YEO inhalation delivery and improve local bioavailability, representing a promising inhalable carrier to attain once daily application.

摘要

本研究的目的是制备用于鱼腥草精油(YEO)肺部持续递送的固体脂质纳米粒(SLN)。采用高剪切均质技术,以Compritol 888 ATO为脂质、聚乙烯醇为乳化剂,制备了三种不同粒径的载YEO的SLN(SLN - 200、SLN - 400和SLN - 800)并进行分离。测定的SLN的粒径、ζ电位、药物包封率和载药量分别在171至812nm、-17.1至-19.3mV、76.6至90.2%以及2.34至3.12%之间,而体外释放数据表明SLN可导致药物持续释放长达48小时。此外,雾化后的SLN悬浮液的细颗粒分数(<5.4μm)为67.4 - 75.8%。对大鼠进行气管内给药后,载YEO的SLN不仅将肺部滞留时间延长至24小时,而且与气管内给药的YEO溶液相比,AUC值(SLN - 200、SLN - 400和SLN - 800分别为15.4、18.2和26.3μg/gh)增加了4.5至7.7倍,与静脉给药的YEO溶液相比分别增加了257至438倍。目前的结果首次表明,载YEO的SLN可能维持YEO的吸入递送并提高局部生物利用度,是一种有望实现每日一次应用的可吸入载体。

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