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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

Sigma-Aldrich
Methanol, ACS reagent, ≥99.8%
Sigma-Aldrich
Methanol, ACS reagent, ≥99.8%
Sigma-Aldrich
Methanol, purification grade, 99.8%
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Methanol, suitable for HPLC, ≥99.9%
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Methanol, HPLC Plus, ≥99.9%
Supelco
Methanol, Pharmaceutical Secondary Standard; Certified Reference Material
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Acenocoumarol, ≥98% (HPLC)
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Salicylic acid, ≥99%, FG
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Methanol, anhydrous, 99.8%
Supelco
Methanol, analytical standard
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Ser-Phe-Leu-Leu-Arg-Asn-Pro-Asn-Asp-Lys-Tyr-Glu-Pro-Phe, ≥97% (HPLC)
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Methanol, BioReagent, ≥99.93%
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Methanol, ACS reagent, ≥99.8%
Sigma-Aldrich
Methanol, suitable for HPLC, gradient grade, ≥99.9%
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Methanol, ACS spectrophotometric grade, ≥99.9%
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Methanol, Laboratory Reagent, ≥99.6%
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Methanol, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥99.8% (GC)
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Methanol, puriss., meets analytical specification of Ph Eur, ≥99.7% (GC)
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Captopril for system suitability, European Pharmacopoeia (EP) Reference Standard
Terbinafine for system suitability, European Pharmacopoeia (EP) Reference Standard
Diclofenac for system suitability, European Pharmacopoeia (EP) Reference Standard
Supelco
Diclofenac sodium salt, analytical standard
Nifedipine, European Pharmacopoeia (EP) Reference Standard
USP
Ibuprofen, United States Pharmacopeia (USP) Reference Standard
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Salicylic acid, ReagentPlus®, ≥99%
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Ibuprofen, ≥98% (GC)
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N-Acetyl-D-penicillamine, for HPLC derivatization, ≥99.0% (T)
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Salicylic acid, BioXtra, ≥99.0%