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用于雾化的pH依赖性纳米球的研制——体外扩散、空气动力学及细胞毒性研究

Development of pH-Dependent Nanospheres for Nebulisation- In vitro Diffusion, Aerodynamic and Cytotoxicity Studies.

作者信息

Ige Pradum P, Pardeshi Sagar R, Sonawane Raju O

机构信息

Department of Pharmaceutics, R C Patel Institute of Pharmaceutical Education and Research, Shirpur, Dhule, Maharashtra, India.

出版信息

Drug Res (Stuttg). 2018 Dec;68(12):680-686. doi: 10.1055/a-0595-7678. Epub 2018 Apr 17.

DOI:10.1055/a-0595-7678
PMID:29665591
Abstract

The aim of this work was to evaluate the in vitro performance of nebulized nanosuspension formulation when nebulized using ultrasonic nebulizer. The present investigation deals with successful formulation of Beclomethasone dipropionate loaded HPMCP nanospheres prepared by solvent evaporation technique using PEG 400 as a stabilizer. Beclomethasone dipropionate is a water insoluble drug molecule was encapsulated in HPMCP nanospheres to have pH dependent solubility at basic pH for targeted drug delivery in lung and studied for in vitro cytotoxicity and immediate release capability. The synthesized nanospheres were characterized through drug excipient compatibility, surface topography; mean particle size , zeta potential, PDI, entrapment efficiency and drug loading, in vitro diffusion, aerodynamic, in vitro cytotoxicity and stability studies. The mean particle size and PDI of the optimized batch (F1) had 197.6±0.40 nm and 0.324 ±0.35, respectively. The % entrapment efficiency and % drug loading was found to be 86.56±1.32 and 8.30±0.27, respectively. The optimized batch F1 showed % cumulative drug release 94.77±0.24 at 1 h. The formulation showed cell viability up to 91.28%. It can be concluded that, Beclomethasone dipropionate loaded HPMCP nanospheres was found to be safe, stable with significant increase in solubility and bypass the liver.

摘要

本研究的目的是评估使用超声雾化器雾化时雾化纳米混悬液制剂的体外性能。本研究涉及通过溶剂蒸发技术,以聚乙二醇400(PEG 400)作为稳定剂,成功制备载有二丙酸倍氯米松的羟丙甲纤维素邻苯二甲酸酯(HPMCP)纳米球。二丙酸倍氯米松是一种水不溶性药物分子,被包裹在HPMCP纳米球中,使其在碱性pH值下具有pH依赖性溶解度,以实现肺部的靶向给药,并对其进行体外细胞毒性和速释能力研究。通过药物辅料相容性、表面形貌、平均粒径、zeta电位、多分散指数(PDI)、包封率和载药量、体外扩散、空气动力学、体外细胞毒性和稳定性研究对合成的纳米球进行表征。优化批次(F1)的平均粒径和PDI分别为197.6±0.40 nm和0.324±0.35。包封率和载药量分别为86.56±1.32和8.30±0.27。优化批次F1在1小时时的累积药物释放率为94.77±0.24。该制剂的细胞活力高达91.28%。可以得出结论,载有二丙酸倍氯米松的HPMCP纳米球被发现是安全、稳定的,溶解度显著增加,并且能够绕过肝脏。

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