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环丙沙星和诺氟沙星的荧光标记及其在地表水残留分析中的应用。

Fluorescent labelling of ciprofloxacin and norfloxacin and its application for residues analysis in surface water.

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayuddhaya Rd., Rajathevee, Bangkok 10400, Thailand.

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayuddhaya Rd., Rajathevee, Bangkok 10400, Thailand.

出版信息

Talanta. 2016 Oct 1;159:74-79. doi: 10.1016/j.talanta.2016.05.080. Epub 2016 Jun 4.

DOI:10.1016/j.talanta.2016.05.080
PMID:27474281
Abstract

Sensitivity enhancement for residue analysis of ciprofloxacin and norfloxacin in surface water was performed by liquid chromatography with fluorescent detection (LC-FD). Labelling of both drugs were studied with fluorescent probes (e.g. Nile blue perchlorate (NBP) and 4- (N,N-Dimethylaminosulfonyl)-7-(N-chloroformylmethyl-N-methylamino)-2,1,3-benzoxadiazole (DBD-COCl). Factors affecting the derivatization (e.g. stoichiometric ratios, reaction time and base catalysts) were optimized. The derivatization was achieved in 15min using a stoichiometric ratio between the substrate and DBD-COCl of 1:3, whereas NBP gave unsatisfactory results. Separation of the derivatives by LC was achieved (resolution (RS) > 1.8) on a C8 column using a mobile phase consisting of 50mM formic acid and acetonitrile (ACN) (68:32% v/v) in 20min. The method was linear (r(2) > 0.99) in a range of 200-2,000µg/L, precise (%RSD < 9.17) and accurate (%recovery of 102.5-122.2%) for the determination of the derivatives. The uses of fluoroquinolone molecularly imprinted polymer in conjunction with hydrophilic-lipophilic balance sorbents demonstrated an efficient procedure for sample pre-concentration and clean-up for water sample resulting in the improved percent recovery. Applications of the proposed method was shown in surface water samples in Thailand.

摘要

采用荧光检测的液相色谱法(LC-FD)对环丙沙星和诺氟沙星在地表水中的残留分析进行了灵敏度增强。用荧光探针(如尼罗蓝过氯酸(NBP)和 4-(N,N-二甲基氨基磺酰基)-7-(N-氯甲酰基-N-甲基氨基)-2,1,3-苯并恶二唑(DBD-COCl))对两种药物进行了标记研究。优化了影响衍生化的因素(例如化学计量比、反应时间和碱催化剂)。使用底物与 DBD-COCl 的化学计量比为 1:3 可在 15min 内完成衍生化,而 NBP 的结果则不理想。通过在 C8 柱上使用包含 50mM 甲酸和乙腈(ACN)(68:32%v/v)的流动相可实现衍生物的 LC 分离(分辨率(RS)>1.8),在 20min 内即可完成分离。该方法在 200-2000µg/L 范围内呈线性(r(2) > 0.99),精密度(%RSD<9.17)和准确度(%回收率为 102.5-122.2%)均良好,可用于测定衍生物。氟喹诺酮分子印迹聚合物与亲水-疏水平衡吸附剂结合使用,为水样的预浓缩和净化提供了一种有效的方法,从而提高了回收率。该方法已应用于泰国地表水样品中。

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