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反相高效液相色谱法、紫外比率光谱的导数和小波变换同时测定三元和四元混合物中的氯霉素、地塞米松和萘甲唑啉

Simultaneous determination of chloramphenicol, dexamethasone and naphazoline in ternary and quaternary mixtures by RP-HPLC, derivative and wavelet transforms of UV ratio spectra.

作者信息

Hoang Vu Dang, Hue Nguyen Thu, Tho Nguyen Huu, Nguyen Hue Minh Thi

机构信息

Department of Analytical Chemistry and Toxicology, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hanoi, Viet Nam.

Department of Analytical Chemistry and Toxicology, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hanoi, Viet Nam.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2015 Mar 15;139:20-7. doi: 10.1016/j.saa.2014.11.101. Epub 2014 Dec 12.

Abstract

The application of chemometrics-assisted UV spectrophotometry and RP-HPLC to the simultaneous determination of chloramphenicol, dexamethasone and naphazoline in ternary and quaternary mixtures is presented. The spectrophotometric procedure is based on the first-order derivative and wavelet transforms of ratio spectra using single, double and successive divisors. The ratio spectra were differentiated and smoothed using Savitzky-Golay filter; whereas wavelet transform realized with wavelet functions (i.e. db6, gaus5 and coif3) to obtain highest spectral recoveries. For the RP-HPLC procedure, the separation was achieved on a ZORBAX SB-C18 (150×4.6 mm; 5 μm) column at ambient temperature and the total run time was less than 7 min. A mixture of acetonitrile - 25 mM phosphate buffer pH 3 (27:73, v/v) was used as the mobile phase at a flow rate of 1.0 mL/min and the effluent monitored by measuring absorbance at 220 nm. Calibration graphs were established in the range 20-70 mg/L for chloramphenicol, 6-14 mg/L for dexamethasone and 3-8 mg/L for naphazoline (R(2)>0.990). The RP-HPLC and ratio spectra transformed by a combination of derivative-wavelet algorithms proved to be able to successfully determine all analytes in commercial eye drop formulations without sample matrix interference (mean percent recoveries, 97.4-104.3%).

摘要

介绍了化学计量学辅助紫外分光光度法和反相高效液相色谱法用于同时测定三元和四元混合物中的氯霉素、地塞米松和萘甲唑啉。分光光度法基于使用单除数、双除数和连续除数的比率光谱的一阶导数和小波变换。比率光谱使用Savitzky-Golay滤波器进行微分和平滑;而小波变换通过小波函数(即db6、gaus5和coif3)实现以获得最高的光谱回收率。对于反相高效液相色谱法,在室温下于ZORBAX SB-C18(150×4.6 mm;5μm)柱上实现分离,总运行时间少于7分钟。以乙腈-25 mM pH 3的磷酸盐缓冲液(27:73,v/v)的混合物作为流动相,流速为1.0 mL/min,并通过在220 nm处测量吸光度来监测流出物。建立了氯霉素在20-70 mg/L、地塞米松在6-14 mg/L和萘甲唑啉在3-8 mg/L范围内的校准曲线(R(2)>0.990)。经导数-小波算法组合变换的反相高效液相色谱法和比率光谱被证明能够成功测定市售眼药水制剂中的所有分析物,而无样品基质干扰(平均回收率为97.4-104.3%)。

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