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Dual-Targeting and Stimuli-Triggered Liposomal Drug Delivery in Cancer Treatment.
AlSawaftah, Nour; Pitt, William G; Husseini, Ghaleb A.
Afiliação
  • AlSawaftah N; Department of Chemical Engineering, American University of Sharjah, Sharjah, UAE.
  • Pitt WG; Chemical Engineering Department, Brigham Young University, Provo, Utah 84602, United States.
  • Husseini GA; Department of Chemical Engineering, American University of Sharjah, Sharjah, UAE.
ACS Pharmacol Transl Sci ; 4(3): 1028-1049, 2021 Jun 11.
Article em En | MEDLINE | ID: mdl-34151199
ABSTRACT
The delivery of chemotherapeutics to solid tumors using smart drug delivery systems (SDDSs) takes advantage of the unique physiology of tumors (i.e., disordered structure, leaky vasculature, abnormal extracellular matrix (ECM), and limited lymphatic drainage) to deliver anticancer drugs with reduced systemic side effects. Liposomes are the most promising of such SDDSs and have been well investigated for cancer therapy. To improve the specificity, bioavailability, and anticancer efficacy of liposomes at the diseased sites, other strategies such as targeting ligands and stimulus-sensitive liposomes have been developed. This review highlights relevant surface functionalization techniques and stimuli-mediated drug release for enhanced delivery of anticancer agents at tumor sites, with a special focus on dual functionalization and design of multistimuli responsive liposomes.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article