| Literature DB >> 30613436 |
Na Zhao1, Martin C Woodle2, A James Mixson1.
Abstract
Doxorubicin is a widely used chemotherapy agent. Despite its utility, several adverse side effects, especially its irreversible cardiotoxicity and reversible nephrotoxicity, have prompted the development of liposomal carriers, many of which are FDA approved. Antitumor efficacies of approved liposome-Dox preparations can equal or exceed that of conventional doxorubicin. Because these liposomes carriers accumulate in solid tumor tissues via an enhanced permeation and retention (EPR) effect, these carriers have an improved safety profile. Nevertheless, a significant problem with the current drug delivery preparations of doxorubicin is a lack of efficacy toward tumors that exhibit multidrug resistance. In this review, we consider the development of drug delivery systems for doxorubicin, which improve the therapeutic window (efficacy and safety) and which address limitations of the current FDA-approved doxorubicin formulations.Entities:
Keywords: Doxorubicin; intratumoral; multidrug resistance; nanoparticle; systemic
Year: 2018 PMID: 30613436 PMCID: PMC6319900 DOI: 10.4172/2157-7439.1000519
Source DB: PubMed Journal: J Nanomed Nanotechnol