Department of Chemistry, Manipal Institute of Technology, Manipal University, Manipal 576104. India.
Department of Chemistry, Manipal Institute of Technology, Manipal-576104. India.
Mini Rev Med Chem. 2017;17(15):1457-1487. doi: 10.2174/1389557517666170228105731.
BACKGROUND: Cancer is one of the most awful lethal diseases all over the world and the success of its current chemotherapeutic treatment strategies is limited due to several associated drawbacks. The exploration of cancer cell physiology and its microenvironment has exposed the potential of various classes of nanocarriers to deliver anticancer chemotherapeutic agents at the tumor target site. These nanocarriers must evade the immune surveillance system and achieve target selectivity. Besides, they must gain access into the interior of cancerous cells, evade endosomal entrapment and discharge the drugs in a sustained manner. Chitosan, the second naturally abundant polysaccharide is a biocompatible, biodegradable and mucoadhesive cationic polymer which has been exploited extensively in the last few years in the effective delivery of anticancer chemotherapeutics to the target tumor cells. Therapeutic agent-loaded surface modified chitosan nanoparticles are established to be more stable, permeable and bioactive. CONCLUSION: This review will provide an up-to-date evidence-based background on recent pharmaceutical advancements in the transformation of chitosan nanoparticles for smart anticancer therapeutic drug delivery. HIGHLIGHTS: • Efforts to improve cancer chemotherapy by exploiting the intrinsic differences between normal and neoplastic cells to achieve maximum effective drug delivery to target cancer cells through bioengineered chitosan nano delivery vectors are discussed. • The easy manipulation of surface characteristics of chitosan based nanoparticles by various functionalization methods to achieve targeted drug delivery proves its potential to be an essential tool for the advancement of anticancer drug-delivery vectors.
背景:癌症是全球最可怕的致命疾病之一,由于存在多种相关缺陷,其当前化疗治疗策略的成功率有限。对癌细胞生理学及其微环境的探索揭示了各种纳米载体类药物将抗癌化疗药物递送到肿瘤靶位的潜力。这些纳米载体必须逃避免疫监视系统并实现靶向选择性。此外,它们必须进入癌细胞内部,逃避内体捕获并以持续的方式释放药物。壳聚糖是第二种丰富的天然多糖,是一种生物相容、可生物降解和粘多糖阳离子聚合物,近年来在将抗癌化疗药物有效递送到靶肿瘤细胞方面得到了广泛的开发。载药表面修饰壳聚糖纳米粒更稳定、更渗透、更具生物活性。
结论:本综述将提供最新的循证背景信息,介绍壳聚糖纳米粒在智能抗癌治疗药物输送方面的最新药物制剂进展。
重点:通过生物工程壳聚糖纳米递药载体,利用正常细胞和肿瘤细胞之间的固有差异来提高癌症化疗效果,实现最大程度地将有效药物递送到靶癌细胞,讨论了这方面的进展。通过各种功能化方法轻松操纵壳聚糖基纳米粒的表面特性,以实现靶向药物传递,证明了其作为抗癌药物递药载体发展的重要工具的潜力。
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