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  • A rapid method for determination of 22 selected drugs in human urine by UHPLC/MS/MS for clinical application.

A rapid method for determination of 22 selected drugs in human urine by UHPLC/MS/MS for clinical application.

Journal of AOAC International (2015-01-30)
Sylwia Magiera, Irena Baranowska
ABSTRACT

A rapid and sensitive ultra-HPLC/MSIMS (UHPLC/MSIMS) assay method for the simultaneous determination in human urine of 22 drugs belonging to different pharmaceutical groups was developed. The drugs were extracted from urine samples and then separated on a Zorbax Rapid Resolution High Definition SB-C18 column. The mobile phase consisted of methanol and water containing formic acid with gradient elution. The chromatographic separation time was 7 min. The MSIMS detector, equipped with an electrospray ionization source, was set up in both positive and negative modes. The lower LOQs for the drugs in this method were between 0.05 and 0.60 ng/mL. Calibration curves in human urine were generated in the range of 0.05-600 ng/mL. Method validation parameters such as intraday and interday precision, accuracy, extraction recovery, stability, selectivity, dilution integrity, and carryover effect for all the compounds were within the acceptable ranges. This simple and fast method was applied successfully to study the pharmacokinetics of four selected drugs in human urine collected from patients. This UHPLC/MS/MS method offers an attractive way forward for the development of a routine rapid analysis for selected substances, particularly given the growing amount of new information about drug properties.

MATERIALS
Product Number
Brand
Product Description

Supelco
Carbamazepine, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Ibuprofen, Pharmaceutical Secondary Standard; Certified Reference Material
Sildenafil citrate, European Pharmacopoeia (EP) Reference Standard
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Methanol, Pharmaceutical Secondary Standard; Certified Reference Material
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Diclofenac sodium salt, Pharmaceutical Secondary Standard; Certified Reference Material
Ibuprofen, European Pharmacopoeia (EP) Reference Standard
Ibuprofen for peak identification, European Pharmacopoeia (EP) Reference Standard
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Propranolol hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Ibuprofen, meets USP testing specifications
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Methanol, anhydrous, 99.8%
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Salicylic acid, ACS reagent, ≥99.0%
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Salicylic acid, ≥99%, FG
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Acetonitrile solution, contains 0.1 % (v/v) trifluoroacetic acid, suitable for HPLC
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N-Acetyl-D-penicillamine, for HPLC derivatization, ≥99.0% (T)
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Methanol, analytical standard
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Salicylic acid, Pharmaceutical Secondary Standard; Certified Reference Material
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Methanol, NMR reference standard
Diclofenac for system suitability, European Pharmacopoeia (EP) Reference Standard
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Methanol, Absolute - Acetone free
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Methanol, HPLC Plus, ≥99.9%
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Methanol, suitable for HPLC, gradient grade, ≥99.9%
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Methanol, BioReagent, ≥99.93%
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Methanol, ACS spectrophotometric grade, ≥99.9%
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Methanol, ACS reagent, ≥99.8%
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Residual Solvent - Acetonitrile(solution in DMSO), Pharmaceutical Secondary Standard; Certified Reference Material
USP
Ibuprofen, United States Pharmacopeia (USP) Reference Standard
USP
Salicylic acid, United States Pharmacopeia (USP) Reference Standard
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Salicylic acid, ReagentPlus®, ≥99%
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Methanol, suitable for HPLC, ≥99.9%
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Naproxen, meets USP testing specifications