2012
DOI: 10.1016/j.jchromb.2012.06.037
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Simultaneous determination of blonanserin and its metabolite in human plasma and urine by liquid chromatography–tandem mass spectrometry: Application to a pharmacokinetic study

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Cited by 19 publications
(16 citation statements)
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“…The intra‐day and inter‐day precision and relative errors were less than 8.03% and 6.55% for the three QC levels in plasma. The current LC‐MS/MS method was validated, proved to be simple, sensitive, and accurate, and has been successfully applied to investigate the PKs of blonanserin in human subjects (Ogawa et al ., ; Wen et al ., ).…”
Section: Participants and Methodsmentioning
confidence: 97%
“…The intra‐day and inter‐day precision and relative errors were less than 8.03% and 6.55% for the three QC levels in plasma. The current LC‐MS/MS method was validated, proved to be simple, sensitive, and accurate, and has been successfully applied to investigate the PKs of blonanserin in human subjects (Ogawa et al ., ; Wen et al ., ).…”
Section: Participants and Methodsmentioning
confidence: 97%
“…To date procedures for determination of blonanserin [11][12][13][14][15] along with is degradant product [16][17][18][19] and in biometrics [20][21][22][23] using HPLC had been reported. In addition to this GC method for residual solvent 24,25 determination in blonanserin and blonanserin determination in human plasma 26 In addition to this Kalariya et al stated that blonanserin is thermally stable.…”
Section: Fig 1: Chemical Structure Of Blonanserinmentioning
confidence: 99%
“…Observed values were calculated based on each accompanying calibration curve. Accuracy is represented as deviation, which is defined as the mean observed QC concentration minus the nominal concentration divided by the nominal concentration and multiplied by 100 [15]. The mean, as well as the SD, were evaluated following recommendations published by the FDA.…”
Section: Precision and Accuracymentioning
confidence: 99%