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用于测定复杂废水中药物混合物的经验证的单变量和多变量分光光度法。

Validated univariate and multivariate spectrophotometric methods for the determination of pharmaceuticals mixture in complex wastewater.

作者信息

Riad Safaa M, Salem Hesham, Elbalkiny Heba T, Khattab Fatma I

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr-El Aini Street, 11562 Cairo, Egypt.

Analytical Chemistry Department, Faculty of Pharmacy, Deraya University, Menia, Egypt.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2015 Apr 5;140:451-61. doi: 10.1016/j.saa.2014.12.104. Epub 2015 Jan 8.

Abstract

Five, accurate, precise, and sensitive univariate and multivariate spectrophotometric methods were developed for the simultaneous determination of a ternary mixture containing Trimethoprim (TMP), Sulphamethoxazole (SMZ) and Oxytetracycline (OTC) in waste water samples collected from different cites either production wastewater or livestock wastewater after their solid phase extraction using OASIS HLB cartridges. In univariate methods OTC was determined at its λmax 355.7 nm (0D), while (TMP) and (SMZ) were determined by three different univariate methods. Method (A) is based on successive spectrophotometric resolution technique (SSRT). The technique starts with the ratio subtraction method followed by ratio difference method for determination of TMP and SMZ. Method (B) is successive derivative ratio technique (SDR). Method (C) is mean centering of the ratio spectra (MCR). The developed multivariate methods are principle component regression (PCR) and partial least squares (PLS). The specificity of the developed methods is investigated by analyzing laboratory prepared mixtures containing different ratios of the three drugs. The obtained results are statistically compared with those obtained by the official methods, showing no significant difference with respect to accuracy and precision at p=0.05.

摘要

开发了五种准确、精密且灵敏的单变量和多变量分光光度法,用于同时测定从不同城市采集的废水样品(生产废水或牲畜废水)中的三元混合物,这些样品经OASIS HLB柱进行固相萃取后,含有甲氧苄啶(TMP)、磺胺甲恶唑(SMZ)和土霉素(OTC)。在单变量方法中,OTC在其最大吸收波长355.7 nm(0D)处测定,而(TMP)和(SMZ)通过三种不同的单变量方法测定。方法(A)基于连续分光光度分辨率技术(SSRT)。该技术首先采用比率减法,然后采用比率差值法来测定TMP和SMZ。方法(B)是连续导数比率技术(SDR)。方法(C)是比率光谱的均值中心化(MCR)。所开发的多变量方法是主成分回归(PCR)和偏最小二乘法(PLS)。通过分析含有三种药物不同比例的实验室制备混合物,研究了所开发方法的特异性。将所得结果与官方方法所得结果进行统计学比较,在p = 0.05时,在准确性和精密度方面无显著差异。

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