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对由固体分散体辅料(Soluplus®)稳定的纳米混悬剂进行研究以提高生物利用度。

Investigation of a nanosuspension stabilized by Soluplus® to improve bioavailability.

作者信息

Yang Hua, Teng Fei, Wang Puxiu, Tian Bin, Lin Xia, Hu Xi, Zhang Ling, Zhang Keru, Zhang Yu, Tang Xing

机构信息

Department of Pharmaceutics, Shenyang Pharmaceutical University, Wen Hua Road No. 103, Shenyang 110016, China.

School of Pharmacy, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Int J Pharm. 2014 Dec 30;477(1-2):88-95. doi: 10.1016/j.ijpharm.2014.10.025. Epub 2014 Oct 14.

Abstract

The purpose of this work was to explore the feasibility of using Soluplus(®) in preparing a fenofibrate (FBT) nanosuspension adopting wet media milling technology. HPMC and Soluplus(®) were used as stabilizers to prepare FBT/HPMC nanosuspension (F1) and FBT/Soluplus(®) nanosuspension (F2), respectively. The nanosuspensions were subjected to evaluations involving particle size, dissolution, preliminary stability and pharmacokinetic behavior. A marked reduction in particle size was achieved by nanosuspensions (from 17.55 μm to 642 nm (F1) and 344 nm (F2)). The nanosuspensions displayed almost complete dissolution while percentages of 30% and 13% were obtained by physical mixtures and coarse FBT separately. Soluplus(®) could stabilize the nanosuspension more effectively due to a weaker Ostwald ripening effect resulting from a slower diffusion of micelles formed by Soluplus(®) entrapping dissolved FBT than FBT exposed to pure water directly. In the in vivo evaluation, larger AUC0-72h and Cmax, and shorter Tmax were obtained by the nanosuspensions. Significant differences were observed between the physical mixtures. The phenomenon of double peaks was present in this study. The major factor may be the multiple absorption sites of FBT. The current work indicated that Soluplus(®) is well suited for preparation of a nanosuspension with good stability and improved dissolution and bioavailability.

摘要

本研究旨在探讨采用湿介质研磨技术,使用固体分散体辅料(Soluplus(®))制备非诺贝特(FBT)纳米混悬液的可行性。分别使用羟丙基甲基纤维素(HPMC)和固体分散体辅料(Soluplus(®))作为稳定剂,制备FBT/HPMC纳米混悬液(F1)和FBT/固体分散体辅料(Soluplus(®))纳米混悬液(F2)。对纳米混悬液进行了粒径、溶出度、初步稳定性和药代动力学行为等评价。纳米混悬液使粒径显著减小(从17.55μm降至642nm(F1)和344nm(F2))。纳米混悬液几乎完全溶解,而物理混合物和粗品FBT的溶出百分比分别为30%和13%。固体分散体辅料(Soluplus(®))能更有效地稳定纳米混悬液,因为由固体分散体辅料(Soluplus(®))包裹溶解的FBT形成的胶束扩散较慢,奥斯特瓦尔德熟化效应较弱,比直接暴露于纯水中的FBT更稳定。在体内评价中,纳米混悬液的AUC0-72h和Cmax更大,Tmax更短。物理混合物之间观察到显著差异。本研究中出现了双峰现象。主要因素可能是FBT的多个吸收位点。目前的研究表明,固体分散体辅料(Soluplus(®))非常适合制备具有良好稳定性、改善溶出度和生物利用度的纳米混悬液。

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