Liposomal Nanostructures for Drug Delivery in Gastrointestinal Cancers

被引:28
作者
Das, Manisit [1 ]
Huang, Leaf [1 ]
机构
[1] Univ N Carolina, Div Pharmacoengn & Mol Pharmaceut, Eshelman Sch Pharm, 301 Pharm Lane,1315 Kerr Hall,CB 7571, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
TUMOR-ASSOCIATED FIBROBLASTS; LIPID-BASED PRODRUG; PANCREATIC-CANCER; PEGYLATED LIPOSOMES; COLON-CARCINOMA; SOLID TUMORS; PHASE-I; HEPATOCELLULAR-CARCINOMA; ENHANCED PERMEABILITY; THERAPEUTIC ACTIVITY;
D O I
10.1124/jpet.118.254797
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gastrointestinal (GI) cancers like liver, pancreatic, colorectal, and gastric cancer remain some of the most difficult and aggressive cancers. Nanoparticles like liposomes had been approved in the clinic for cancer therapy dating as far back as 1995. Over the years, liposomal formulations have come a long way, facing several roadblocks and failures, and advancing by optimizing formulations and incorporating novel design approaches to navigate therapeutic delivery challenges. The first liposomal formulation for a GI cancer drug was approved recently in 2015, setting the stage for further clinical developments of liposome-based delivery systems for therapies against GI malignancies. This article reviews the design considerations and strategies that can be used to deliver drugs to GI tumors, the wide range of therapeutic agents that have been explored in preclinical as well as clinical studies, and the current therapies that are being investigated in the clinic against GI malignancies.
引用
收藏
页码:647 / 656
页数:10
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