Targeted drug delivery to macrophages

被引:152
作者
Jain, Narendra K. [1 ]
Mishra, Vijay [1 ]
Mehra, Neelesh Kumar [1 ]
机构
[1] Dr HS Gour Cent Univ, Dept Pharmaceut Sci, Pharmaceut Res Lab, Sagar 470003, MP, India
关键词
carbon nanotubes; dendrimers; drug delivery; macrophages targeting; nanocarriers; nanoparticles; IMMUNODEFICIENCY-VIRUS TYPE-1; WALLED CARBON NANOTUBES; RAT ALVEOLAR MACROPHAGES; INHIBITORY FACTOR MIF; INTRACELLULAR DELIVERY; MANNOSE RECEPTOR; AMPHOTERICIN-B; MANNOSYLATED LIPOSOMES; ACTIVATED MACROPHAGES; POLYMERSOME DELIVERY;
D O I
10.1517/17425247.2013.751370
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Targeted drug delivery to the macrophages appears to be an attractive proposition to improve therapeutic efficacy of enclosed drug. Thus, macrophages can be exploited as Trojan horses for targeted drug delivery. Nanocarriers can migrate across the different membrane barriers and release their drug cargo at sites of infection. Areas covered: This review discusses the current status and utilization of various micro-as well as nanocarriers like microspheres/microparticles, liposomes, nanoparticles, dendrimers, niosomes, and carbon nanotubes for targeted delivery of bioactives to the macrophages. Expert opinion: The design of nanocarriers for cell-mediated drug delivery may differ from those used for conventional drug delivery systems. The literature review shows that nanocarriers could supplement sustained drug delivery to the macrophages, extended duration of action, reduced therapeutic dose, improved patient compliance, and reduced adverse effects of highly toxic, potent drugs. There is still a need to identify more specific receptors that are responsible for macrophage targeting. The identification of such receptors may also facilitate drug targeting to further specific parts of the body containing different types of macrophages.
引用
收藏
页码:353 / 367
页数:15
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