4.5 Review

Targeting Anticancer Drugs to Tumor Vasculature Using Cationic Liposomes

期刊

PHARMACEUTICAL RESEARCH
卷 27, 期 7, 页码 1171-1183

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11095-010-0110-1

关键词

angiogenesis; anti-angiogenic therapy; anticancer drugs; dosing schedule; dual targeting; PEG-coated cationic liposome; vascular targeting

资金

  1. Ministry of Education, Culture, Sports and Technology, Japan [20015033]
  2. Grants-in-Aid for Scientific Research [20015033] Funding Source: KAKEN

向作者/读者索取更多资源

Liposomal drug delivery systems improve the therapeutic index of chemotherapeutic agents, and the use of cationic liposomes to deliver anticancer drugs to solid tumors has recently been recognized as a promising therapeutic strategy to improve the effectiveness of conventional chemotherapeutics. This review summarizes the selective targeting of cationic liposomes to tumor vasculature, the merits of incorporating the polymer polyethylene-glycol (PEG), and the impact of the molar percent of the cationic lipid included in cationic liposomes on liposomal targeting efficacy. In addition, the discussion herein includes the therapeutic benefit of a dual targeting approach, using PEG-coated cationic liposomes in vascular targeting (of tumor endothelial cells), and tumor targeting (of tumor cells) of anticancer drugs. Cationic liposomes have shown considerable promise in preclinical xenograft models and are poised for clinical development.

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