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首页> 外文期刊>International journal of organic chemistry >Synthesis of Folate-Appended &i&β&/i&-Cyclodextrin Using Phenanthroline as Linker for Cancer Targeting Drug Delivery
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Synthesis of Folate-Appended &i&β&/i&-Cyclodextrin Using Phenanthroline as Linker for Cancer Targeting Drug Delivery

机译:使用菲咯啉作为用于靶向癌症的药物递送的接头,合成叶酸附加的i /β-i/环糊精

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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.
机译:在这里,我们已经合成了包含i-β-环糊精作为药物载体和叶酸作为靶向配体的癌症靶向药物递送系统。由于叶酸受体在多种肿瘤类型中高度表达,因此选择叶酸作为癌症靶向配体。 β-环糊精和叶酸通过接头[1,10-菲咯啉或5-(羟甲基)糠醛]连接。 β-环糊精和叶酸分别通过形成席夫碱和酯而连接到接头上。我们的目标合成产品已通过NMR,质谱和IR光谱确认。我们预计,我们的合成产品可以赋予癌细胞特异性药物递送以及所需的特性,例如纳米颗粒形成。

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