Pang Xiao Bing, Huang Cheng Zhi
Laboratory of Supramolecular Chemistry and Biomedical Analysis, College of Chemistry and Chemical Engineering, Southwest China Normal University, Chongqing 400715, China.
J Pharm Biomed Anal. 2004 Apr 1;35(1):185-91. doi: 10.1016/j.jpba.2003.12.013.
An assay of berberine (BE) was developed with good selectivity and sensitivity based on the total internal reflected resonance light scattering (TIR-RLS) signals from water/1,2-dichloroethane (H(2)O/DCE) interface. Under optimal conditions, amphiphilic complex formed by BE and fluorescein (Flu) was adsorbed to H(2)O/DCE interface, resulting in good separation of BE from the coexisting foreign substances in aqueous phase and significant enrichment of BE at the interface. This enriched species at the interface was found corresponding to enhanced TIR-RLS signals located at 370.0 nm. Proportional relationships were established between the enhanced TIR-RLS intensity and the BE in the range of 3.2 x 10(-9) to 3.2 x 10(-6) mol l(-1) with the limit of detections (3sigma) being 1.3 ng ml(-1). Favorable sensitivity of TIR-RLS technique was demonstrated superior to that of high-performance liquid-chromatography (HPLC) method. The feasibility of the proposed technique was validated by the satisfactory performance of intra-assay and inter-assay BE in tablets.
基于水/1,2-二氯乙烷(H₂O/DCE)界面的全内反射共振光散射(TIR-RLS)信号,开发了一种具有良好选择性和灵敏度的小檗碱(BE)检测方法。在最佳条件下,BE与荧光素(Flu)形成的两亲性复合物吸附在H₂O/DCE界面上,使BE与水相中共存的杂质良好分离,并在界面处显著富集。发现界面处这种富集的物质对应于位于370.0 nm处增强的TIR-RLS信号。在3.2×10⁻⁹至3.2×10⁻⁶ mol l⁻¹范围内,增强的TIR-RLS强度与BE之间建立了比例关系,检测限(3σ)为1.3 ng ml⁻¹。结果表明,TIR-RLS技术具有良好的灵敏度,优于高效液相色谱(HPLC)法。通过片剂中BE的批内和批间检测的良好性能验证了该方法的可行性。