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Advances in delivery systems for doxorubicin.
Zhao, Na; Woodle, Martin C; Mixson, A James.
Affiliation
  • Zhao N; Department of Pathology, University Maryland School of Medicine, 10 S. Pine St., University of Maryland School of Medicine, Baltimore, Maryland 21201, United States.
  • Woodle MC; Aparna Biosciences Corp, 9119 Gaither Rd., Gaithersburg, MD 20877, United States.
  • Mixson AJ; Department of Pathology, University Maryland School of Medicine, 10 S. Pine St., University of Maryland School of Medicine, Baltimore, Maryland 21201, United States.
Article in En | MEDLINE | ID: mdl-30613436
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Nanomed Nanotechnol Year: 2018 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Nanomed Nanotechnol Year: 2018 Document type: Article Affiliation country: Country of publication: