三氧化二砷
化学
体内
环糊精
纳米纤维
毒性
静电纺丝
砷
质子核磁共振
药理学
立体化学
生物物理学
核化学
纳米技术
生物化学
有机化学
材料科学
医学
生物技术
生物
聚合物
作者
Jee Young Chung,Hyun Lin Lee,Qurrat Ul Ain,Yoon Sung Song,Yong-Hee Kim
标识
DOI:10.1016/j.jconrel.2015.05.077
摘要
In this paper, we examined arsthinol–cyclodextrin complexes, which display an anticancer activity. The association constants were 17,502 ± 522 M−1 for hydroxypropyl-β-cyclodextrin and 12,038 ± 10,168 M−1 for randomized methylated β-cyclodextrin. 1H NMR experiments in solution also confirmed the formation of these complexes and demonstrated an insertion of the arsthinol (STB) with its dithiarsolane extremity into the wide rim of the hydroxypropyl-β-cyclodextrin cavity. Complexed arsthinol was more effective than arsenic trioxide (As2O3) and melarsoprol on the U87 MG cell line. Importantly, in the in vivo study, we observed significant antitumor activity against heterotopic xenografts after i.p. administration and did not see any signs of toxicity. This remains to be verified using an orthotopic model.
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