کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5136596 1494019 2017 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Short communicationA fabric phase sorptive extraction-High performance liquid chromatography-Photo diode array detection method for the determination of twelve azole antimicrobial drug residues in human plasma and urine
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Short communicationA fabric phase sorptive extraction-High performance liquid chromatography-Photo diode array detection method for the determination of twelve azole antimicrobial drug residues in human plasma and urine
چکیده انگلیسی


- Simultaneous analysis of 12 azole drugs in human plasma and urine reported.
- FPSE-HPLC-PDA method developed for multi-residual analysis from biological samples.
- FPSE-HPLC-PDA method can be used in routine clinical and biomedical applications.
- The new approach is fast, sensitive, simple, robust and green.
- FPSE-HPLC-PDA method substantially simplified the overall analytical work-flow.

This paper reports a novel fabric phase sorptive extraction-high performance liquid chromatography-photodiode array detection (FPSE-HPLC-PDA) method for the simultaneous extraction and analysis of twelve azole antimicrobial drug residues that include ketoconazole, terconazole, voriconazole, bifonazole, clotrimazole, tioconazole, econazole, butoconazole, miconazole, posaconazole, ravuconazole, and itraconazole in human plasma and urine samples. The selected azole antimicrobial drugs were well resolved by using a Luna C18 column (250 mm × 4.6 mm; 5 μm particle size) in gradient elution mode within 36 min. The analytical method was calibrated and validated in the range from 0.1 to 8 μg/mL for all the drug compounds. Blank human plasma and urine were used as the sample matrix for the analysis; while benzyl-4-hydroxybenzoate was used as the internal standard (IS). The limit of quantification of the FPSE-HPLC-PDA method was found as 0.1 μg/mL and the weighted-matrix matched standard calibration curves of the drugs showed a good linearity upto a concentration of 8 μg/mL. The parallelism tests were also performed to evaluate whether overrange sample can be analyzed after dilution, without compromising the analytical performances of the validated method. The intra- and inter-day precision (RSD%) values were found ≤13.1% and ≤13.9%, respectively. The intra- and inter-day trueness (bias%) values were found in the range from −12.1% to 10.5%. The performances of the validated FPSE-HPLC-PDA were further tested on real samples collected from healthy volunteers after a single dose administration of itraconazole and miconazole. To the best of our knowledge, this is the first FPSE extraction procedure applied on plasma and urine samples for the simultaneous determination of twelve azole drugs possessing a wide range of logKow values (extending from 0.4 for fluconazole to 6.70 of butoconazole) and could be adopted as a rapid and robust green analytical tool for clinical and pharmaceutical applications.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography B - Volume 1040, 1 January 2017, Pages 192-198
نویسندگان
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