Chromatographic separation and sensitive determination of teriflunomide, an active metabolite of leflunomide in human plasma by liquid chromatography-tandem mass spectrometry
A sensitive, selective and high throughput liquid chromatography tandem mass spectrometry (LC–ESI-MS/MS) method has been developed for the determination of teriflunomide, an active metabolite of leflunomide in human plasma. Plasma samples were prepared by liquid–liquid extraction of teriflunomide an...
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Published in | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Vol. 878; no. 24; pp. 2217 - 2225 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
15.08.2010
Elsevier |
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Abstract | A sensitive, selective and high throughput liquid chromatography tandem mass spectrometry (LC–ESI-MS/MS) method has been developed for the determination of teriflunomide, an active metabolite of leflunomide in human plasma. Plasma samples were prepared by liquid–liquid extraction of teriflunomide and valsartan as internal standard (IS) in ethyl acetate from 200
μL human plasma. The chromatographic separation was achieved on an Inertsil ODS-3 C18 (50
mm
×
4.6
mm, 3
μm) analytical column using isocratic mobile phase, consisting of 20
mM ammonium acetate–methanol (25:75, v/v), at a flow-rate of 0.8
mL/min. The precursor
→
product ion transition for teriflunomide (
m/
z 269.0
→
82.0) and IS (
m/
z 434.1
→
350.3) were monitored on a triple quadrupole mass spectrometer, operating in the multiple reaction monitoring (MRM) and negative ion mode. The method was validated over a wide dynamic concentration range of 10.1–4001
ng/mL. Matrix effect was assessed by post-column infusion experiment and the mean process efficiency were 91.7% and 88.2% for teriflunomide and IS respectively. The method was rugged and rapid with a total run time of 2.0
min and is applied to a bioequivalence study of 20
mg leflunomide (test and reference) tablet formulation in 12 healthy Indian male subjects under fasting condition. |
---|---|
AbstractList | A sensitive, selective and high throughput liquid chromatography tandem mass spectrometry (LC-ESI-MS/MS) method has been developed for the determination of teriflunomide, an active metabolite of leflunomide in human plasma. Plasma samples were prepared by liquid-liquid extraction of teriflunomide and valsartan as internal standard (IS) in ethyl acetate from 200microL human plasma. The chromatographic separation was achieved on an Inertsil ODS-3 C18 (50mmx4.6mm, 3microm) analytical column using isocratic mobile phase, consisting of 20mM ammonium acetate-methanol (25:75, v/v), at a flow-rate of 0.8mL/min. The precursor-->product ion transition for teriflunomide (m/z 269.0-->82.0) and IS (m/z 434.1-->350.3) were monitored on a triple quadrupole mass spectrometer, operating in the multiple reaction monitoring (MRM) and negative ion mode. The method was validated over a wide dynamic concentration range of 10.1-4001ng/mL. Matrix effect was assessed by post-column infusion experiment and the mean process efficiency were 91.7% and 88.2% for teriflunomide and IS respectively. The method was rugged and rapid with a total run time of 2.0min and is applied to a bioequivalence study of 20mg leflunomide (test and reference) tablet formulation in 12 healthy Indian male subjects under fasting condition.A sensitive, selective and high throughput liquid chromatography tandem mass spectrometry (LC-ESI-MS/MS) method has been developed for the determination of teriflunomide, an active metabolite of leflunomide in human plasma. Plasma samples were prepared by liquid-liquid extraction of teriflunomide and valsartan as internal standard (IS) in ethyl acetate from 200microL human plasma. The chromatographic separation was achieved on an Inertsil ODS-3 C18 (50mmx4.6mm, 3microm) analytical column using isocratic mobile phase, consisting of 20mM ammonium acetate-methanol (25:75, v/v), at a flow-rate of 0.8mL/min. The precursor-->product ion transition for teriflunomide (m/z 269.0-->82.0) and IS (m/z 434.1-->350.3) were monitored on a triple quadrupole mass spectrometer, operating in the multiple reaction monitoring (MRM) and negative ion mode. The method was validated over a wide dynamic concentration range of 10.1-4001ng/mL. Matrix effect was assessed by post-column infusion experiment and the mean process efficiency were 91.7% and 88.2% for teriflunomide and IS respectively. The method was rugged and rapid with a total run time of 2.0min and is applied to a bioequivalence study of 20mg leflunomide (test and reference) tablet formulation in 12 healthy Indian male subjects under fasting condition. A sensitive, selective and high throughput liquid chromatography tandem mass spectrometry (LC-ESI-MS/MS) method has been developed for the determination of teriflunomide, an active metabolite of leflunomide in human plasma. Plasma samples were prepared by liquid-liquid extraction of teriflunomide and valsartan as internal standard (IS) in ethyl acetate from 200 mu L human plasma. The chromatographic separation was achieved on an Inertsil ODS-3 C18 (50 mm x 4.6 mm, 3 mu m) analytical column using isocratic mobile phase, consisting of 20 mM ammonium acetate-methanol (25:75, v/v), at a flow-rate of 0.8 mL/min. The precursor --> product ion transition for teriflunomide (m/z 269.0 --> 82.0) and IS (m/z 434.1 --> 350.3) were monitored on a triple quadrupole mass spectrometer, operating in the multiple reaction monitoring (MRM) and negative ion mode. The method was validated over a wide dynamic concentration range of 10.1-4001 ng/mL. Matrix effect was assessed by post-column infusion experiment and the mean process efficiency were 91.7% and 88.2% for teriflunomide and IS respectively. The method was rugged and rapid with a total run time of 2.0 min and is applied to a bioequivalence study of 20 mg leflunomide (test and reference) tablet formulation in 12 healthy Indian male subjects under fasting condition. A sensitive, selective and high throughput liquid chromatography tandem mass spectrometry (LC-ESI-MS/MS) method has been developed for the determination of teriflunomide, an active metabolite of leflunomide in human plasma. Plasma samples were prepared by liquid-liquid extraction of teriflunomide and valsartan as internal standard (IS) in ethyl acetate from 200microL human plasma. The chromatographic separation was achieved on an Inertsil ODS-3 C18 (50mmx4.6mm, 3microm) analytical column using isocratic mobile phase, consisting of 20mM ammonium acetate-methanol (25:75, v/v), at a flow-rate of 0.8mL/min. The precursor-->product ion transition for teriflunomide (m/z 269.0-->82.0) and IS (m/z 434.1-->350.3) were monitored on a triple quadrupole mass spectrometer, operating in the multiple reaction monitoring (MRM) and negative ion mode. The method was validated over a wide dynamic concentration range of 10.1-4001ng/mL. Matrix effect was assessed by post-column infusion experiment and the mean process efficiency were 91.7% and 88.2% for teriflunomide and IS respectively. The method was rugged and rapid with a total run time of 2.0min and is applied to a bioequivalence study of 20mg leflunomide (test and reference) tablet formulation in 12 healthy Indian male subjects under fasting condition. A sensitive, selective and high throughput liquid chromatography tandem mass spectrometry (LC–ESI-MS/MS) method has been developed for the determination of teriflunomide, an active metabolite of leflunomide in human plasma. Plasma samples were prepared by liquid–liquid extraction of teriflunomide and valsartan as internal standard (IS) in ethyl acetate from 200 μL human plasma. The chromatographic separation was achieved on an Inertsil ODS-3 C18 (50 mm × 4.6 mm, 3 μm) analytical column using isocratic mobile phase, consisting of 20 mM ammonium acetate–methanol (25:75, v/v), at a flow-rate of 0.8 mL/min. The precursor → product ion transition for teriflunomide ( m/ z 269.0 → 82.0) and IS ( m/ z 434.1 → 350.3) were monitored on a triple quadrupole mass spectrometer, operating in the multiple reaction monitoring (MRM) and negative ion mode. The method was validated over a wide dynamic concentration range of 10.1–4001 ng/mL. Matrix effect was assessed by post-column infusion experiment and the mean process efficiency were 91.7% and 88.2% for teriflunomide and IS respectively. The method was rugged and rapid with a total run time of 2.0 min and is applied to a bioequivalence study of 20 mg leflunomide (test and reference) tablet formulation in 12 healthy Indian male subjects under fasting condition. |
Author | Parekh, Jignesh M. Sanyal, Mallika Yadav, Manish Vaghela, Rajendrasinh N. Sutariya, Dipen K. Shrivastav, Pranav S. |
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Keywords | Teriflunomide Bioequivalence study Human plasma LC–ESI-MS/MS Human Prostaglandin-endoperoxide synthase Biological fluid Isoxazole derivatives Bioequivalence Enzyme Metabolite Enzyme inhibitor HPLC chromatography Determination Leflunomide Electrospray Blood plasma Non steroidal antiinflammatory agent LC―ESI-MS/MS Oxidoreductases Antirheumatic agent Immunosuppressive agent Pharmacokinetics Quantitative analysis |
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Snippet | A sensitive, selective and high throughput liquid chromatography tandem mass spectrometry (LC–ESI-MS/MS) method has been developed for the determination of... A sensitive, selective and high throughput liquid chromatography tandem mass spectrometry (LC-ESI-MS/MS) method has been developed for the determination of... |
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SubjectTerms | Acetates Adult Analysis Analytical, structural and metabolic biochemistry Bioequivalence study Biological and medical sciences Chromatography Chromatography, Liquid - methods Computational efficiency Computing time Crotonates - blood Crotonates - chemistry Crotonates - metabolism Crotonates - pharmacokinetics Drug Stability Fundamental and applied biological sciences. Psychology General pharmacology High-Throughput Screening Assays - methods Human Human plasma Humans Isoxazoles - administration & dosage Isoxazoles - chemistry Isoxazoles - metabolism Isoxazoles - pharmacokinetics LC-ESI-MS LC–ESI-MS/MS Least-Squares Analysis Liquid chromatography Male Mass spectrometry Medical sciences Metabolites Middle Aged Pharmacology. Drug treatments Reproducibility of Results Run time (computers) Sensitivity and Specificity Separation Spectrometry, Mass, Electrospray Ionization - methods Tandem Mass Spectrometry - methods Teriflunomide Therapeutic Equivalency Toluidines - blood Toluidines - chemistry Toluidines - metabolism Toluidines - pharmacokinetics |
Title | Chromatographic separation and sensitive determination of teriflunomide, an active metabolite of leflunomide in human plasma by liquid chromatography-tandem mass spectrometry |
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