Determination of amantadine and rimantadine using a sensitive fluorescent probe

被引:23
|
作者
Wang, Guang-Quan [1 ,2 ]
Qin, Yan-Fang [1 ]
Du, Li-Ming [1 ]
Li, Jun-Fei [1 ]
Jing, Xu [1 ]
Chang, Yin-Xia [1 ]
Wu, Hao [1 ]
机构
[1] Shanxi Normal Univ, Analyt & Testing Ctr, Linfen 041004, Shanxi, Peoples R China
[2] Inner Mongolia Univ, Transportat Inst, Hohhot 010070, Inner Mongolia, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
Amantadine hydrochloride; Rimantadine hydrochloride; Coptisine; Cucurbit[7]uril; Supramolecular interaction; Fluorescent probe; CAPILLARY-ZONE-ELECTROPHORESIS; POTENTIOMETRIC DETERMINATION; CUCURBITURIL HOMOLOGS; HYDROCHLORIDE; COMPLEXES; DERIVATIVES; COMPONENTS; TABLETS;
D O I
10.1016/j.saa.2012.08.016
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Amantadine hydrochloride (AMA) and rimantadine hydrochloride (RIM) are non-fluorescent in aqueous solutions. This property makes their determination through direct fluorescent method difficult. The competing reactions and the supramolecular interaction mechanisms between the two drugs and coptisine (COP) as they fight for occupancy of the cucurbit[7]uril (CB[7]) cavity, were studied using spectrofluorimetry, H-1 NMR, and molecular modeling calculations. Based on the significant quenching of the supramolecular complex fluorescence intensity, a fluorescent probe method of high sensitivity and selectivity was developed to determine AMA or RIM in their pharmaceutical dosage forms and in urine samples with good precision and accuracy. The linear range of the method was from 0.0040 to 1.0 mu g mL(-1) with a detection limit ranging from 0.0012 to 0.0013 mu g mL(-1). This shows that the proposed method has promising potential for therapeutic monitoring and pharmacokinetics and for clinical application. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:275 / 281
页数:7
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