Enhanced stability and activity of temozolomide in primary glioblastoma multiforme cells with cucurbit[n]uril

被引:73
作者
Appel, Eric A. [1 ]
Rowland, Matthew J. [1 ]
Loh, Xian Jun [1 ]
Heywood, Richard M. [2 ]
Watts, Colin [2 ,3 ]
Scherman, Oren A. [1 ]
机构
[1] Univ Cambridge, Dept Chem, Melville Lab Polymer Synth, Cambridge CB2 1EW, England
[2] Cambridge Ctr Brain Repair, Cambridge CB2 0PY, England
[3] Univ Cambridge, Div Neurosurg, Dept Clin Neurosci, Cambridge CB2 1EW, England
基金
英国工程与自然科学研究理事会;
关键词
AQUEOUS-SOLUTION; RECOGNITION; MECHANISM; PEPTIDES; BINDING;
D O I
10.1039/c2cc35131e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Temozolomide (TMZ) is the primary chemotherapeutic agent for treatment of glioblastoma multiforme (GBM) yet it has a fast rate of degradation under physiological conditions to the 'active' MTIC, which has poor penetration of the blood-brain barrier and cellular absorption. Herein we have demonstrated binding of TMZ within the cavity of nano-container cucurbit[7]uril, resulting in a decreased rate of drug degradation. Prolonging the lifetime of the TMZ under physiological conditions through encapsulation dramatically improved the drug's activity against primary GBM cell lines as more TMZ could be absorbed by the cells before degradation. This work can potentially lead to increases in the drug's propensity for crossing the blood-brain barrier and absorption into the GBM cells, thereby increasing the efficacy of this chemotherapy.
引用
收藏
页码:9843 / 9845
页数:3
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