Active Targeting Strategies for Anticancer Drug Nanocarriers

被引:74
作者
Basile, Livia [1 ,2 ]
Pignatello, Rosario [1 ]
Passirani, Catherine [3 ]
机构
[1] Univ Catania, Dept Drug Sci, I-95125 Catania, Italy
[2] ETNALEAD Srl, I-95123 Catania, Italy
[3] Univ Angers, INSERM, U1066, F-49933 Angers 9, France
关键词
Cancer; drug targeting; controlled drug delivery; liposomes; solid lipid nanoparticles; SLN; nanoparticles; micelles; lipid nanocapsules (LNC); STERICALLY STABILIZED LIPOSOMES; IN-VIVO FATE; ANTITUMOR EFFICACY; FOLATE RECEPTOR; CYANOACRYLATE) NANOPARTICLES; CHITOSAN NANOPARTICLES; THERAPEUTIC-EFFICACY; POLYMERIC MICELLES; PEG NANOPARTICLES; CIRCULATION TIME;
D O I
10.2174/156720112800389089
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Chemotherapy at present remains the main form of treatment for cancer, though there is no clinically available antineoplastic drug that acts selectively on the tumor mass. For this reason, the scientific research is focused towards the development of novel cancer therapies and drug delivery strategies, like drug targeting, that would enhance the therapeutic efficacy of drugs while reducing their side toxicity. This review describes tree types of nanoparticles used in active targeting for cancer treatment: liposomes, lipid and polymer nanoparticles, and micelles. The opportunities and challenges achieved by the proposed strategies of active targeting have been highlighted, as well as the necessity to conciliate the targeting efficiency of drug nanocarriers with their longevity in the bloodstream.
引用
收藏
页码:255 / 268
页数:14
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