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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2003, Vol. 8 ›› Issue (4): 451-453.

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Determination of flunarizine hydrochloride in humanPlasma by HPLC method and study on its bioequivalence

ZHANG Hui-Jie, ZHANG Hong, XIONG Yu-Qing   

  1. Institute of ClinicalPharmacology,Jiangxi Medical College,Nanchang 330006,J iangxi,China
  • Received:2003-01-22 Revised:2003-03-17 Online:2003-08-26 Published:2020-11-19

Abstract: AIM: To establish a simple HPLC method for determining flunarizine hydrochloride in humanPlasma and to study bioequivalence between twoPreparations.METHODS: The drug and internal standard(diazepam)were extracted from thePlasma with n-hexane.The HPLC method wasPerformed with a diamonsil C18 column,and the mobilePhase was 0.06 mol·L-1sodium acetate(pH =3.76)-acetonitrile(45∶55).The flow rate was 1.0 ml·min-1and the wavelength was 254 nm.The data obtained were fitted with 3p97Program on computer to evaluate the bioequivalence.RESULTS: The calibration curve waslinear in the range of 2.5 -160μg·L-1(r =0.9989).The minimum detection concentration was 2.5μg·L-1.The values of AUC,Cmax,Tmax,and t1/2βof twoPreparations had no significant difference(P>0.05).The relative bioavailability was(98.41±11.23)%(n =20).CONCLUSION: This HPLC method is simple,and twoPreparations of flunarizine hydrochloride are bioequivalent.

Key words: pharmacology, flunarizine hydrochloride, HPLC, pharmacokinetics, bioavailibility, bioequivalent

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