Bhatt، نويسنده , , Jignesh and Subbaiah، نويسنده , , Gunta and Kambli، نويسنده , , Sandeep R Shah، نويسنده , , Bhavin N. Patel، نويسنده , , Mehul and Saxena، نويسنده , , Ashish and Baliga، نويسنده , , Ashok and Nigam، نويسنده , , Samita and Parekh، نويسنده , , Hetal and Yadav، نويسنده , , Gunvat، نويسنده ,
A high throughput and sensitive liquid chromatography–tandem mass spectrometry (LC–MS/MS) method has been developed and validated for the estimation of bisoprolol in human plasma using multiplexing technique (two HPLC units connected to one MS). Bisoprolol was extracted from human plasma using solid-phase extraction technique using metoprolol as internal standard. A Betabasic 8 column provided chromatographic separation of analytes followed by detection with mass spectrometry. The mass transition ion-pair was followed as m/z 326.2 → 116.1 for bisoprolol and m/z 268.2 → 191.0 for metoprolol. The method involves a simple multiplexing, rapid solid-phase extraction, simple isocratic chromatography conditions and mass spectrometric detection which enable detection at sub-nanogram levels. The proposed method has been validated for a linear range of 0.5–70.0 ng/mL with correlation coefficient ≥0.9991. The precision and accuracy were within 10% for intra-HPLC runs and inter-HPLC runs. The overall recoveries for bisoprolol and metoprolol were 93.89% and 77.65%, respectively. Total MS run time was 0.90 min only. The developed method was applied for the determination of pharmacokinetic parameters of bisoprolol following a single oral administration of a 10 mg bisoprolol tablet in 18 healthy male volunteers.
Bisoprolol , LC–MS/MS , ?-Blockers , Human plasma , MULTIPLEXING