...
首页> 外文期刊>ACS applied materials & interfaces >Fluorescent Detection of Tadalafil Based on Competitive Host-Guest Interaction Using p-Sulfonated Calix[6]arene Functionalized Graphene
【24h】

Fluorescent Detection of Tadalafil Based on Competitive Host-Guest Interaction Using p-Sulfonated Calix[6]arene Functionalized Graphene

机译:基于对位磺化杯[6]芳烃官能化石墨烯的竞争性宾客相互作用荧光检测他达拉非

获取原文
获取原文并翻译 | 示例
           

摘要

A competitive fluorescence method toward tadalafil detection has been developed based on host guest recognition by selecting rhodamine B (RhB) and p-sulfonated calix[6]arene functionalized graphene (CX6-Gra) as the "reporter pair". Upon the presence of tadalafil to the performed CX6-Gra-RhB complex, the RhB molecules are displaced by tadalafil, leading to a "switch-on" fluorescence signal. The observed fluorescence signal can be used for quantitative detection of tadalafil ranging from 1.00 to 50.00 mu M with a detection limit of 0.32 mu M (S/N = 3). The inclusion complex of tadalafil and CX6 was studied by molecular docking and the results indicated that a 1:1 host-guest stoichiometry had the lowest Delta G value of -7.18 kcal/mol. The docking studies demonstrated that the main forces including pi-pi interactions, electrostatic interactions, and hydrophobic interactions should be responsible for the formation of this inclusion compound. The mechanism of the competitive host-guest interaction was clarified. The binding constant (K) of the tadalafil/CX6 complex was more than 5 times greater than that of RhB/CX6.
机译:通过选择若丹明B(RhB)和对磺化杯[6]芳烃功能化石墨烯(CX6-Gra)作为“报告物对”,开发了一种基于宿主客体识别的竞争性tadalafil荧光检测方法。当他达拉非存在于所进行的CX6-Gra-RhB复合物中时,RhB分子被他达拉非置换,导致“开启”荧光信号。所观察到的荧光信号可用于定量检测他达拉非的范围为1.00至50.00μM,检测极限为0.32μM(S / N = 3)。通过分子对接研究了他达拉非和CX6的包合物,结果表明:1:1客体-客体化学计量关系的ΔG值最低,为-7.18 kcal / mol。对接研究表明,包括pi-pi相互作用,静电相互作用和疏水相互作用在内的主要作用力应负责形成这种包合物。阐明了竞争性宾客互动的机制。他达拉非/ CX6复合物的结合常数(K)比RhB / CX6大5倍以上。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号