Recent advance in the mechanism study of polymeric inhibitors of P-glycoprotein.
- Author:
Lei-ming HUANG
1
;
Jin-hua ZHAO
;
Guo-cheng WANG
;
Jian-ping ZHOU
Author Information
1. Department of Pharmaceutics, China Pharmaceutical University, Nanjing 210009, China.
- Publication Type:Journal Article
- MeSH:
ATP-Binding Cassette, Sub-Family B, Member 1;
antagonists & inhibitors;
chemistry;
genetics;
metabolism;
Adenosine Triphosphatases;
metabolism;
Adenosine Triphosphate;
metabolism;
Animals;
Biological Availability;
Excipients;
pharmacology;
Gene Expression;
Humans;
Membrane Fluidity;
drug effects;
Polymers;
pharmacology;
Structure-Activity Relationship
- From:
Acta Pharmaceutica Sinica
2010;45(10):1224-1231
- CountryChina
- Language:Chinese
-
Abstract:
P-glycoprotein (P-gp) is an ATP-dependent multidrug efflux pump that acts as a major obstacle for oral drug delivery and cancer therapy. Recent reports have provided evidence that excipients often used in pharmaceutical formulations, such as Pluronic and TPGS, also have inhibitory effects on P-glycoprotein. Because inhibition of efflux transporters by polymeric inhibitors may dramatically increase the bioavailability of P-gp substrates with negligible side effects, identification of the mechanism and their structure activity relationship is therefore of significant importance for pharmaceutical development. Other than competitive inhibition for traditional inhibitors, polymeric inhibitors may modify P-gp function through alterations on membrane fluidity, inhibition of P-gp ATPase, depletion of intracellular ATP and down-regulating of P-gp expression. In the present review, the inhibition mechanism of potential polymeric inhibitors and their structure activity relationship will be discussed along with a brief introduction to the established methodologies.
