以菲罗啉为连接体合成叶酸加成β-环糊精用于癌症靶向给药

Nadim S. Russel, Punam K. Paul, M. R. Karim, B. Song
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引用次数: 1

摘要

本文合成了以β-环糊精为药物载体,叶酸为靶向配体的癌症靶向给药系统。叶酸被选为癌症靶向配体,因为叶酸受体在多种肿瘤类型中高度表达。β-环糊精和叶酸通过连接体[1,10-菲罗啉或5-(羟甲基)糠醛连接。β-环糊精和叶酸分别通过席夫碱和酯的形式连接到连接体上。我们的目标合成产物通过核磁共振、质谱和红外光谱得到了证实。我们预计,我们的合成产品可以赋予癌症细胞特异性药物递送以及所需的性质,如纳米颗粒的形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of Folate-Appended β-Cyclodextrin Using Phenanthroline as Linker for Cancer Targeting Drug Delivery
Here we have synthesized cancer targeting drug delivery system that contains β-cyclodextrin as a drug carrier and folic acid as a targeting ligand. Folic acid was selected as a cancer targeting ligand because folic acid receptors are highly expressed in a variety of tumor types. β-cyclodextrin and folic acid were connected through a linker [1,10-phenanthroline or 5-(hydroxymethyl) furfural]. β-cyclodextrin and folic acid were attached to the linker by formation of Schiffbase and ester, respectively. Our targeted synthetic products were confirmed by NMR, Mass and IR spectroscopy. We anticipate that our synthetic products can confer cancer cell-specific drug delivery as well as desired properties such as nanoparticle formation.
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