| Literature DB >> 35093460 |
Zonghua Tian1, Yue Zhao1, Yaping Mai2, Fangxia Qiao1, Jueshuo Guo1, Luning Dong1, Yang Niu3, Guojing Gou4, Jianhong Yang5.
Abstract
Using nanocrystals (NCs) technology may be a promising drug delivery strategy for oral administration of multicomponent anticancer drugs. However, the intestinal epithelium and the mucus layer on the intestine extremely limited drug transport and absorption by orally. In this study, we selected multicomponent inartificial compound Bufadienolides (BU) with broad spectrum antitumor activity as the model drug to prepare BU NCs with different stabilizers by wet grinding, and explored the efficiency of penetrating through the mucus layer and transporting intestinal epithelial cells in vitro and ex vivo. Results revealed that BU NCs can dramatically improve dissolution behavior synergistically and the efficiency of mucus permeation. Besides, we found that BU NCs with different stabilizers enhanced cellular uptake, which was mainly attributed to increasing or changing the endocytosis pathway and plasma membrane/Endoplasmic reticulum (ER) pathway involved in the transmembrane transport of NCs. Furthermore, BU NCs could definitely improve intestinal absorption efficiency and change the absorption site of BU ex vivo. This multi-angle exploration will provide reference for the development of BU oral delivery formulations.Entities:
Keywords: Bufadienolides; Intestinal absorption; Multicomponent; Nanocrystals; Transcytosis
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Year: 2022 PMID: 35093460 DOI: 10.1016/j.ijpharm.2022.121522
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875