The effect of surface charge on oral absorption o polymeric nanoparticles

被引:100
作者
Du, Xiao-Jiao [1 ,2 ,3 ]
Wang, Ji-Long [4 ]
Iqbal, Shoaib [4 ]
Li, Hong-Jun [1 ,2 ,3 ]
Cao, Zhi-Ting [4 ]
Wang, Yu-Cai [4 ]
Du, Jin-Zhi [1 ,2 ,3 ]
Wang, Jun [1 ,2 ,3 ,5 ]
机构
[1] South China Univ Technol, Inst Life Sci, Guangzhou 510006, Guangdong, Peoples R China
[2] South China Univ Technol, Sch Med, Guangzhou 510006, Guangdong, Peoples R China
[3] Natl Engn Res Ctr Tissue Restorat & Reconstruct, Guangzhou 510006, Guangdong, Peoples R China
[4] Univ Sci & Technol China, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
[5] South China Univ Technol, Res Inst Food Nutr & Human Hlth, Guangzhou 510641, Guangdong, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
LIPID-BASED FORMULATIONS; DRUG-DELIVERY; GASTROINTESTINAL MUCUS; IN-VIVO; SIZE; CHALLENGES; CHEMISTRY; TRANSPORT; IMPROVES; DENSITY;
D O I
10.1039/c7bm01096f
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Surface charge plays an important role in determining the interactions of nanoparticles with biological components. Substantial studies have demonstrated that surface charge affects the fate of nanoparticles after intravenous administration; however, few studies have investigated the effect of surface charge on the bioavailability and absorption of nanoparticles after oral administration. In this study, polymeric nanoparticles with a similar particle size and surface polyethylene glycol (PEG) density, but with varying surface charges (positive, negative and neutral), were developed to study the effect of surface charge on the oral absorption of polymeric nanoparticles. The nanoparticles were constructed from polyethylene glycol-block-polylactic acid (PEG-PLA) with the incorporation of lipid components with different charges. Our results suggested that the positive surface charge facilitated the cellular uptake and transport of nanoparticles through both Caco-2 cells in vitro and small intestinal epithelial cells in vivo. The positively charged nanoparticles showed a favorable distribution in the small intestine, and significantly improved the oral bioavailability. This study presents valuable information towards the design of nanoparticles for improved oral drug delivery.
引用
收藏
页码:642 / 650
页数:9
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