首页|期刊导航|分析化学|基于环糊精的主客体竞争作用的比率型电化学传感器用于色氨酸对映体检测

基于环糊精的主客体竞争作用的比率型电化学传感器用于色氨酸对映体检测OA

A Ratiometric Electrochemical Sensor Based on Host-Guest Competitive Interactions of Cyclodextrin for Enantiomer Detection of Tryptophan

中文摘要英文摘要

基于β-环糊精(β-Cyclodextrin,β-CD)的手性识别能力与还原氧化石墨烯(Reduced graphene oxide,rGO)的优良导电性,以亚甲基蓝(Methylene blue,MB)作为内参比探针,构建了基于竞争性主客体相互作用的比率型电化学传感平台,用于色氨酸对映体(L/D-Trp)的检测.通过水热还原法制备 rGO,进一步与β-CD复合得到 β-CD-rGO复合物,将此复合物修饰玻碳电极(GCE),构建了手性传感界面.通过浸泡使MB进入 β-CD的疏水空腔形成主客体包合物.当试样中存在L/D-Trp时,L/D-Trp与MB竞争结合 β-CD空腔,其中L-Trp与β-CD的结合能力更强,导致L/D-Trp和MB的氧化峰电流发生显著变化.通过目标物与参比物质的峰电流的比值(ITrp/IMB)可实现对L/D-Trp的区分,且该比值与样品中L/D-Trp的浓度呈相关性.在优化条件下,此传感平台检测L-Trp的线性范围为1.8×10-5~2.0×10-2 mol/L,检出限(LOD,3σ/k)为4.4×10-7 mol/L;检测D-Trp的线性范围为2.0×10-5~1.0×10-2 mol/L,LOD为6.8×10-7 mol/L.通过密度泛函理论计算和接触角测量,探究了此传感平台的手性识别机理.将本方法应用于实际苏打水样品中L-Trp的分析,加标回收率为100.2%~104.7%,表明本方法具有良好的实际应用潜力.

Based on the chiral recognition ability of β-cyclodextrin(β-CD)and the excellent conductivity of reduced graphene oxide(rGO),and with methylene blue(MB)as an internal reference probe,a ratiometric electrochemical sensing platform based on competitive host-guest interactions for detection of tryptophan enantiomers(L/D-Trp)was constructed.rGO was prepared by hydrothermal reduction and then combined with β-CD to obtain aβ-CD-rGO composite,which was used to modify the electrode surface to construct a chiral sensing interface.By soaking,MB entered the hydrophobic cavity of β-CD to form a host-guest inclusion complex.When L/D-Trp was present in the sample,L/D-Trp competed with MB to bind toβ-CD cavity.L-Trp exhibited a stronger binding ability,leading to significant changes in the oxidation peak currents of L/D-Trp and MB.The ratio of the peak currents of the target and reference substances(ITrp/IMB)could be used to identify L/D-Trp,and this ratio was correlated with the concentration of L/D-Trp in the sample.The research results showed that under optimized conditions,the linear range for detecting L-Trp by this sensor was 1.8×10-5~2.0×10-2 mol/L,with a detection limit(LOD,3σ/k)of 4.4×10-7 mol/L;the linear range for detecting D-Trp was 2.0×10-5~1.0×10-2 mol/L,with a LOD of 6.8×10-7 mol/L.The chiral recognition mechanism of this sensing platform was investigated through density functional theory(DFT)calculations and contact angle measurements.In addition,this method was applied to analysis of L-Trp in actual soda water samples,and the obtained recoveries ranged from 100.2%to 104.7%,verifying that the method had good application potential.

吴俊隆;庞元昊;汪思健;高明远;叶清菁;张云;袁亚利

桂林理工大学化学与生物工程学院,桂林 541004桂林理工大学化学与生物工程学院,桂林 541004桂林理工大学化学与生物工程学院,桂林 541004桂林理工大学化学与生物工程学院,桂林 541004桂林理工大学化学与生物工程学院,桂林 541004桂林理工大学化学与生物工程学院,桂林 541004桂林理工大学化学与生物工程学院,桂林 541004||广西茶树种质创新与资源利用重点实验室,桂林 541004

比率型电化学传感器色氨酸对映体主客体相互作用环糊精

Ratiometric electrochemical sensorTryptophan enantiomersHost-guest interactionCyclodextrin

《分析化学》 2026 (8)

1336-1345,10

广西自然科学基金项目(No.2025GXNSFAA069229)和广西科技创新平台项目(No.GuikeLT2600640006)资助. Supported by the Guangxi Natural Science Foundation(No.2025GXNSFAA069229)and the Guangxi Science and Technology Innovation Platform Project(No.GuikeLT2600640006).

10.19756/j.issn.0253-3820.261210

评论