Novel formulation approaches for optimising delivery of anticancer drugs based on P-glycoprotein modulation

被引：147

作者：

Bansal, Tripta ^{[1
]}

Akhtar, Naseem ^{[1
]}

Jaggi, Manu ^{[2
]}

Khar, Roop K. ^{[1
]}

Talegaonkar, Sushama ^{[1
]}

机构：

[1] Dept Pharmaceut, New Delhi, India

[2] Dabur Res Fdn, Dept Preclin Res, Ghaziabad, UP, India

来源：

DRUG DISCOVERY TODAY | 2009年 / 14卷 / 21-22期

关键词：

VITAMIN-E-TPGS; ENHANCED ORAL BIOAVAILABILITY; PLURONIC BLOCK-COPOLYMERS; IN-VITRO; MULTIDRUG-RESISTANCE; PHARMACEUTICAL EXCIPIENTS; NONIONIC SURFACTANTS; EFFLUX TRANSPORTERS; CACO-2; CELLS; PACLITAXEL;

D O I：

10.1016/j.drudis.2009.07.010

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

Considerable research efforts have been directed towards understanding the enigma of P-glycoprotein (P-gp) in drug development and delivery. P-gp is a multi-specific drug efflux transporter that plays a significant role in governing the bioavailability of various anti-cancer drugs. Modulation of this efflux transporter by various traditional 'chemosensitisers' forms a distinctive approach in improving pharmacokinetics and conquering drug resistance. However, such inhibitors show limitations associated with their safety and unwanted pharmacokinetic drug interaction restraining their clinical applicability. To address these concerns, several research groups have used pharmaceutical excipients (functional excipients or additives) to inhibit P-gp and enhance drug permeability. This article focuses on such excipients, various co-development strategies for the formulation of cytotoxic drugs with this multi-drug resistance (MDR) reversing additives.

引用

页码：1067 / 1074

页数：8

共 66 条

[1] Block copolymer-based formulation of doxorubicin. From cell screen to clinical trials [J].