Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.biomaterials.2013.12.033
Title: The reduction of anti-cancer drug antagonism by the spatial protection of drugs with PLA-TPGS nanoparticles
Authors: Tan, G.-R.
Feng, S.-S. 
Leong, D.T. 
Keywords: Anti-cancer drug
Biodegradable polymer
Cancer nanotechnology
Combination therapy
Drug antagonism
Nanomedicine
Issue Date: Mar-2014
Source: Tan, G.-R., Feng, S.-S., Leong, D.T. (2014-03). The reduction of anti-cancer drug antagonism by the spatial protection of drugs with PLA-TPGS nanoparticles. Biomaterials 35 (9) : 3044-3051. ScholarBank@NUS Repository. https://doi.org/10.1016/j.biomaterials.2013.12.033
Abstract: Docetaxel (DCL) and tamoxifen (TAM) individually are potent drugs in the fight against breast cancer. However when used in combination, they become antagonistic because of differential metabolism of both drugs. We reasoned that by spatially protecting them from metabolizing enzymes with poly (lactide). d-α-tocopheryl polyethylene glycol succinate (PLA-TPGS) nanoparticles (NPs), we might reduce this drug antagonism. We now report that the drug antagonism between DCL and TAM in MCF7 cell line, was significantly reduced when co-delivered in PLA-TPGS NPs. In addition, this effect of NPs attenuated at high drug concentrations. To investigate the role of NPs in the reduction of drug antagonism, we quantified cellular uptake of the fluorescent model drug coumarin 6 (C6) encapsulated in a rigorous permutation of drugs-nanoparticles ratios. NPs carrying C6 exhibited enhanced cellular uptake over their free C6 counterparts at correspondingly low drug concentrations. This led us to conclude that the reduction of drug antagonism by NPs is correlated to cellular uptake and being in NPs therefore protects both drugs until they are released intracellular for therapeutic anti-cancer effect. © 2013 Elsevier Ltd.
Source Title: Biomaterials
URI: http://scholarbank.nus.edu.sg/handle/10635/90353
ISSN: 01429612
DOI: 10.1016/j.biomaterials.2013.12.033
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