1. The Effect Of Food On The Pharmacokinetic Properties And Bioequivalence Of Two Formulations Of Levocetirizine Dihydrochloride In Healthy Chinese Volunteers
- Author
-
Jin-Hua Guo, Bi-Juan Lin, Wancai Que, Bing-Lin Huang, Yu Cheng, Maobai Liu, Xin-Feng Chen, Hongqiang Qiu, and Lin-Ping Fang
- Subjects
Adult ,Male ,0301 basic medicine ,Histamine H1 Antagonists, Non-Sedating ,Adolescent ,healthy Chinese volunteers ,Administration, Oral ,Biological Availability ,Pharmaceutical Science ,Pilot Projects ,Bioequivalence ,Pharmacology ,Levocetirizine ,Single oral dose ,Food-Drug Interactions ,Young Adult ,03 medical and health sciences ,0302 clinical medicine ,Pharmacokinetics ,Tandem Mass Spectrometry ,Drug Discovery ,food effect ,medicine ,Drugs, Generic ,Humans ,Levocetirizine Dihydrochloride ,Chromatography, High Pressure Liquid ,Original Research ,bioequivalence ,Drug Design, Development and Therapy ,Cross-Over Studies ,business.industry ,levocetirizine ,Cetirizine ,Confidence interval ,Bioavailability ,030104 developmental biology ,Therapeutic Equivalency ,Area Under Curve ,030220 oncology & carcinogenesis ,Female ,Erratum ,Geometric mean ,business ,pharmacokinetics ,medicine.drug - Abstract
Purpose The aim of this study is to assess the bioequivalence of a new generic formulation and the branded formulation of levocetirizine dihydrochloride in healthy Chinese volunteers under fasting and fed conditions, and food-intake effect on the pharmacokinetic properties is also evaluated. Patients and methods Volunteers were randomly allocated into two groups to receive a single oral dose of generic formulation and branded formulation under fasting or fed conditions, respectively. Blood samples were collected at designated time points. Plasma concentrations of levocetirizine were determined by UFLC-MS/MS. Safety evaluations were carried out through the study. The main pharmacokinetic parameters of the two formulations of levocetirizine were calculated using non-compartmental analysis incorporated in WinNonlin® 7.0 software. Results Forty-nine volunteers were enrolled; 46 completed the studies. Under fasting and fed conditions, the 90% confidence intervals for the geometric mean of generic/branded ratios were in the range of 94.75–107.24% and 99.98–114.69% for the maximum observed concentration, and 97.13–102.50% and 98.36–103.98% for the area under the concentration–time curve. As a result of food intake before administration, the reduced rate and extent of absorption of levocetirizine were observed. Both formulations were generally well tolerated, with no serious adverse reactions reported. Conclusion The two formulations demonstrated essentially identical pharmacokinetic profiles and were all well within the FDA/CFDA bioequivalence standards. Meanwhile, food intake can delay the absorption rate and reduced the bioavailability of levocetirizine in healthy Chinese volunteers., Video abstract Point your SmartPhone at the code above. If you have a QR code reader the video abstract will appear. Or use: https://youtu.be/-Xhw5uFbQfw
- Published
- 2019
- Full Text
- View/download PDF