纳米技术在给药中的应用

I. Uchegbu, A. Schätzlein
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引用次数: 3

摘要

纳米技术涉及在纳米尺度(<1000纳米)上操纵物质;也就是说,小于千分之一毫米的操作,对于药物输送应用,这通常采取创建纳米颗粒(5 ~ 800纳米)的形式,然后用于包装药物分子和基因。通过将具有药理活性的化合物包装在纳米颗粒中,纳米药物就产生了。利用这些纳米药物可以控制药物的生物分布并获得治疗效果。本章概述了用于生产纳米颗粒的各种化学和纳米药物制备策略,并强调了通过这些纳米级安排可以实现的药物递送益处。用于构建这些纳米药物的化合物如下:低分子量自组装两亲体、自组装两亲体聚合物、聚合物-药物偶联物、水不溶性聚合物/交联聚合物、树状大分子和碳纳米管。对这些粒子进行工程改造,可以制造出纳米药物,将药物和基因靶向肿瘤,并改善大脑对肽和其他分子的输送。这些颗粒还能够促进口服药物吸收和药物跨越其他生物屏障(如角膜和皮肤)的运输。目前这些技术中只有少数是商业上可用的,例如脂质体(例如Doxil®),低分子量胶束(例如Fungizone®)和聚合物药物偶联物(Oncaspar®);但在临床前研究和早期临床试验中观察到的治疗益处表明,未来将有更多的这些技术出现在患者领域。关键词:碳纳米管;壳聚糖;树枝状分子;药物输送;基因治疗;脂质体;纳米;纳米颗粒;保利(lactide-co-glycolide)块-(聚氧化乙烯);聚合物药物配合
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nanotechnology in Drug Delivery
Nanotechnology involves manipulating matter at the nanoscale (<1000 nm); that is, manipulations at less than thousandth of a millimeter, and for drug delivery applications this typically takes the form of creating nanoparticles (5 ∼ 800 nm) that are then used to package drug molecules and genes. By packaging pharmacologically active compounds within nanoparticles, nanomedicines are created. It is possible to control drug biodistribution and achieve therapeutic benefit with these nanomedicines. This chapter outlines the various chemistries and nanomedicine preparation strategies that have been used to produce nanoparticles and highlights the drug delivery benefits that are achievable from these nanoscale arrangements. The chemical compounds used to construct these nanomedicines are as follows: low molecular weight self-assembling amphiphiles, self-assembling amphiphilic polymers, polymer–drug conjugates, water insoluble polymers/cross-linked polymers, dendrimers, and carbon nanotubes. Engineering of these particles has produced nanomedicines that target drugs and genes to tumors and improve the brain delivery of peptides and other molecules. These particles are also capable of promoting oral drug absorption and drug transport across other biological barriers such as the cornea and the skin. Only a few of these technologies are commercially available presently, such as liposomes (e.g., Doxil®), low molecular weight micelles (e.g., Fungizone®), and polymer–drug conjugates (Oncaspar®); but the therapeutic benefits being observed in both preclinical studies and early clinical testing suggest that more of these technologies will emerge into the patient arena in the future. Keywords: carbon nanotubes; chitosan; dendrimers; drug delivery; gene therapy; liposomes; nanomedicine; nanoparticles; poly(lactide-co-glycolide)-block-(polyethylene oxide); polymer–drug conjugates
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