Toxicity of hemimethyl-substituted cucurbit[7]uril

被引:11
作者
Yang, Xue [1 ]
Zhao, Wenxuan [1 ,2 ]
Wang, Ziyi [1 ,3 ]
Huang, Ying [2 ]
Lee, Simon M. Y. [1 ]
Tao, Zhu [2 ]
Wang, Ruibing [1 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Taipa, Macau Sar, Peoples R China
[2] Guizhou Univ, Key Lab Macrocycl & Supramol Chem Guizhou Prov, Guiyang 550025, Guizhou, Peoples R China
[3] China Pharmaceut Univ, Pharmaceut Undergrad Res Program, Nanjing, Jiangsu, Peoples R China
关键词
Hemimethyl-substituted cucurbit[7]uril; Macrocyclic molecule; Zebrafish; Toxicity; DRUG-DELIVERY; IN-VIVO; ZEBRAFISH MODELS; AQUEOUS-SOLUTION; ANTICANCER DRUG; ENCAPSULATION; CYCLODEXTRINS; BINDING; CARDIOTOXICITY; SOLUBILIZATION;
D O I
10.1016/j.fct.2017.01.003
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Hemimethyl-substituted cucurbit[7]uril (HMeCB[7]), a derivative of cucurbit[7]uril (CB[7]) with nearly identical host guest complexation properties to that of the parent, has significant potential in biomedical sciences due to its superior solubility in water. Its toxicity profile has been investigated in this work, including its developmental and organ-specific toxicities, with both in vivo zebrafish models and a relevant in vitro cellular model. These results demonstrated that HMeCB[7] has negligible developmental toxicity at concentrations up to 3.2 mM and very moderate cardiotoxicity and hepatotoxicity at concentrations of >= 0.8 mM, and is thus generally less toxic than the parent CB[7]. Our results suggest that HMeCB[7] may be a promising candidate of excipient in medicinal and pharmaceutical research fields. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:510 / 518
页数:9
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