| Literature DB >> 24275447 |
Mengmeng Niu1, Ya'nan Tan1, Peipei Guan1, Lars Hovgaard2, Yi Lu1, Jianping Qi1, Ruyue Lian1, Xiaoyang Li1, Wei Wu3.
Abstract
Liposomes containing bile salts (BS-liposomes) significantly enhanced the oral bioavailability of insulin (rhINS). However, the underlying absorption mechanisms have not been well understood yet. In this study, the transiting fate of the liposomes was first investigated using fluorescent imaging tools to confirm the effect of enhanced gastrointestinal stability. In order to obtain evidence of enhanced transcellular permeation, the interaction between BS-liposomes and the biomembrane was investigated in Caco-2 cell lines. BS-liposomes were found to be more stable in the gastrointestinal tract by showing prolonged residence time in comparison with conventional liposomes. BS-liposomes were significantly more effective for cellular uptake and transport of rhINS; and this effect was found to be size- and concentration-dependent. A good linear correlation was observed between the concentration of the liposomes and uptake/transport of rhINS. Confocal laser scanning microscopy visualization further validated the transcellular transit of BS-liposomes. The BS-liposomes showed little effect on cytotoxicity and did not induce apoptosis within 24h investigation. It was concluded that BS-liposomes showed improved in vivo residence time and enhanced permeation across the biomemebranes. Mechanisms of trans-enterocytic internalization could be proposed as an interpretation for enhanced absorption of insulin-loaded liposomes.Entities:
Keywords: Bile salt; Cellular uptake; Cytotoxicity; Insulin; Liposomes; Transport
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Year: 2013 PMID: 24275447 DOI: 10.1016/j.ijpharm.2013.11.028
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875