Self-emulsifying drug-delivery systems modulate P-glycoprotein activity: role of excipients and formulation aspects

被引:12
作者
AboulFotouh, Khaled [1 ]
Allam, Ayat A. [1 ]
El-Badry, Mahmoud [1 ]
El-Sayed, Ahmed M. [1 ]
机构
[1] Assiut Univ, Fac Pharm, Dept Pharmaceut, Assiut 71526, Egypt
关键词
cancer; effective concentration range; multidrug resistance (MDR); IMPROVED ORAL BIOAVAILABILITY; VITAMIN-E TPGS; IN-VITRO; MULTIDRUG-RESISTANCE; INTESTINAL-ABSORPTION; PHARMACEUTICAL EXCIPIENTS; CACO-2; CELLS; NANOEMULSIFYING FORMULATION; FUNCTIONAL EXCIPIENT; IMPROVED DISSOLUTION;
D O I
10.2217/nnm-2017-0354
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Self-emulsifying drug-delivery systems (SEDDS) have been widely employed to ameliorate the oral bioavailability of P-glycoprotein (P-gp) substrate drugs and to overcome multidrug resistance in cancer cells. However, the role of formulation aspects in the reduced P-gp activity is not fully understood. In this review, we first explore the role of various SEDDS excipients in the reduced P-gp activity with the main emphasis on the effective excipient concentration range for excipient-mediated modulation of P-gp activity and then we discuss the synergistic effect of various formulation aspects on the excipient-mediated modulation of P-gp activity. This review provides an approach to develop a rationally designed SEDDS to overcome P-gp-mediated drug efflux.
引用
收藏
页码:1813 / 1834
页数:22
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