环糊精
超分子化学
纳米技术
基因传递
药物输送
组合化学
化学
共价键
结合
计算生物学
材料科学
遗传增强
基因
生物化学
生物
有机化学
分子
数学分析
数学
作者
Carmen Ortiz Mellet,José M. Garcı́a Fernández,Juan M. Benito
摘要
Cyclodextrin (CD) history has been largely dominated by their unique ability to form inclusion complexes with guests fitting in their hydrophobic cavity. Chemical funcionalization was soon recognized as a powerful mean for improving CD applications in a wide range of fields, including drug delivery, sensing or enzyme mimicking. However, 100 years after their discovery, CDs are still perceived as novel nanoobjects of undeveloped potential. This critical review provides an overview of different strategies to promote interactions between CD conjugates and genetic material by fully exploiting the inside-outside/upper-lower face anisotropy of the CD nanometric platform. Covalent modification, self-assembling and supramolecular ligation can be put forward with the ultimate goal to build artificial viruses for programmed and efficient gene therapy (222 references).
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