Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry and Materials Science, Northwest University, 229 North Taibai Road, Xi'an, 710069 Shaanxi Province, China.
Spectrochim Acta A Mol Biomol Spectrosc. 2012 Oct;96:1-9. doi: 10.1016/j.saa.2012.04.097. Epub 2012 May 7.
The interaction of sulfobutylether-β-cyclodextrin (SBE-β-CD) with risperidone (RISP) was first described with luminol-SBE-β-CD chemiluminescence (CL) system by flow injection analysis (FIA). In luminol-SBE-β-CD CL system, the 1:1 SBE-β-CD···luminol() complexation could enhance CL intensity of luminol and produce the effect of complexation enhancement of CL (CEC). It was found that RISP could quench the CL intensity of SBE-β-CD···luminol() and caused the effect of complexation enhancement of quenching (CEQ), the formation constant K(R-CD) 3.4×10(4) L mol(-1) and the stoichiometric ratio 1:1 of RISP···SBE-β-CD complex were obtained by the proposed CL model. Association degree α 0.036 of RISP···SBE-β-CD complex was also given by CL method. Based on the linear relationship to the decrement of luminol-SBE-β-CD-RISP CL intensity and the logarithm of RISP concentration, RISP also can be quantified in the linear range of 3.0-500.0 nmol L(-1) with a detection limit of 1.0 nmol L(-1) (3σ). The proposed method was successfully applied to monitoring excreted RISP in human urine. It was found that RISP reached its maximum after oral administration for 1.5 h with the total excretion of 14.26% within 8.5 h; the elimination rate constant k and half-life time t(1/2) were 0.474 and 1.5 h, respectively.
首先通过流动注射分析(FIA)描述了磺丁基醚-β-环糊精(SBE-β-CD)与利培酮(RISP)的相互作用。在鲁米诺-SBE-β-CD CL 体系中,1:1 的 SBE-β-CD···鲁米诺复合物可以增强鲁米诺的 CL 强度,并产生 CL 增强的复合物效应(CEC)。结果发现,RISP 可以猝灭 SBE-β-CD···鲁米诺(*)的 CL 强度,并引起 CL 增强猝灭效应(CEQ),通过所提出的 CL 模型得到了 RISP···SBE-β-CD 复合物的形成常数 K(R-CD)3.4×10(4) L mol(-1)和化学计量比 1:1。CL 法还给出了 RISP···SBE-β-CD 复合物的缔合度α0.036。基于与鲁米诺-SBE-β-CD-RISP CL 强度的递减和 RISP 浓度的对数的线性关系,也可以在 3.0-500.0 nmol L(-1)的线性范围内定量 RISP,检测限为 1.0 nmol L(-1)(3σ)。该方法成功应用于监测人尿中排泄的 RISP。结果发现,口服后 1.5 h 达到最大值,8.5 h 内总排泄量为 14.26%;消除速率常数 k 和半衰期 t(1/2)分别为 0.474 和 1.5 h。