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Quantification of prochlorperazine maleate in human plasma by liquid chromatography–mass spectrometry: Application to a bioequivalence study
A sensitive and specific method using a one-step liquid–liquid extraction with dichloromethane followed by liquid chromatographic–electrospray ionization-mass spectrometric was developed and validated to determine prochlorperazine maleate in human plasma using amitriptyline hydrochloride as an inter...
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Published in: | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2009-10, Vol.877 (27), p.3243-3247 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A sensitive and specific method using a one-step liquid–liquid extraction with dichloromethane followed by liquid chromatographic–electrospray ionization-mass spectrometric was developed and validated to determine prochlorperazine maleate in human plasma using amitriptyline hydrochloride as an internal standard. The samples were separated using a Thermo Hypersil-Hypurity C18 reversed-phase column (150
mm
×
2.1
mm i.d., 5
μm). A mobile phase containing 10
mM ammonium acetate (pH 3.6)–methanol–acetonitrile (27:68:5, v/v/v) was used isocratically eluting at a flow rate of 0.22
ml/min. The average extraction recovery of prochlorperazine and internal standard were 81.8
±
2.2% and 79.5
±
3.7%, respectively. Prochlorperazine maleate and internal standard were measured by electrospray ion source in positive selective ion monitoring mode. The method demonstrated that good linearity ranged from 0.20 to 6.40
ng/ml with
r
2
=
0.9989. The limit of quantification for prochlorperazine maleate in the plasma was 0.20
ng/ml. The established method has been successfully applied to a bioequivalence study of two prochlorperazine maleate formulations in 18 healthy male Chinese volunteers. |
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ISSN: | 1570-0232 1873-376X |
DOI: | 10.1016/j.jchromb.2009.07.038 |