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Monitoring of trace amounts of some anti-fungal drugs in biological fluids by hollow fiber based liquid phase microextraction followed by high performance liquid chromatography

机译:中空纤维基液相微萃取,然后用高效液相色谱法监测生物液中痕量的某些抗真菌药物

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This paper reports the applicability of hollow fiber based liquid phase microextraction (HF-LPME) for the extraction of three anti-fungal drugs (Ketoconazole (KZ), Clotrimazole (CZ) and Miconazole (MZ)) from biological fluids. The drugs were extracted from 10 mL of the aqueous sample into an organic phase with microliter volume located inside the pores of a polypropylene hollow fiber, and then back extracted into 24 μL of a second aqueous solution (pH 2.5) located inside the lumen of the hollow fiber. The effects of organic solvent, stirring rate, salt concentration, pH of the source and receiving phases and extraction time on the extraction recovery were investigated and optimized. Under optimized conditions preconcentration factors for KZ, CZ and MZ were obtained as 133,127.9 and 71, respectively. The calibration curves were linear (r~2≥0.99) in the concentration range of 5.0-500μg L~(-1) for both KZ and CZ and 8.0-500 μg L~(-1) for MZ. The limits of detections (LODs) for KZ, CZ and MZ were obtained as 0.9 μg L~(-1),1.8 μg L~(-1) and 4.0 μg L~(-1), respectively. The intra-day and inter-day RSD% based on 5 replicates were obtained as ≤6.3% and ≤12.1%, respectively. The method was successfully applied for determining the concentration of the drugs in plasma and urine samples.
机译:本文报道了中空纤维基液相微萃取(HF-LPME)在从生物液体中提取三种抗真菌药物(酮康唑(KZ),克霉唑(CZ)和咪康唑(MZ))的适用性。将药物从10 mL水性样品中提取到微相体积位于聚丙烯中空纤维孔内的有机相中,然后反提取到24μL第二种水溶液中(pH 2.5),该第二种水溶液位于样品管腔内。中空纤维。研究并优化了有机溶剂,搅拌速率,盐浓度,原料和接收相的pH以及萃取时间对萃取回收率的影响。在最佳条件下,KZ,CZ和MZ的预富集系数分别为133、127.9和71。在KZ和CZ浓度范围为5.0-500μgL〜(-1)和MZ浓度范围为8.0-500μgL〜(-1)时,校正曲线为线性(r〜2≥0.99)。对KZ,CZ和MZ的检出限(LOD)分别为0.9μgL〜(-1),1.8μgL〜(-1)和4.0μgL〜(-1)。基于5次重复的日内和日间RSD%分别为≤6.3%和≤12.1%。该方法已成功用于测定血浆和尿液中药物的浓度。

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