Study on Pharmacokinetics of Guaifenesin Sustained Release Pellets in Beagle Dogs
XIONG Long-qi,CHEN Qing-hua
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Shanghai Institute of Pharmaceutical Industry,Shanghai 200437,China
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History+
Received
Published
2006-07-19
2007-10-10
Issue Date
2007-10-10
Abstract
OBJECTIVE To study the pharmacokinetics of guaifenesin sustained release pellets in healthy beagle dogs and to evaluate the bioequivalence.METHODS The concentrations of guaifenesin in plasma were determined by RP-HPLC.The pharmacokinetic parameters were calculated and the relative bioequivalence was evaluated.RESULTS The main pharmacokinetic parameters of guaifenesin sustained release pellets were as follows:AUC0-16(20 407.49±2 120.62)μg·h·L-1;tmax(0.92±0.36)h;ρmax(3 699.85±806.39)mg·L-1;Ke(0.20±0.039)h-1;t1/2(Ke)(3.58±0.64)h,respectively.The relative bioavailability of AUC0-16 and AUC0-inf were(99.8±9.8)% and(101.6±10.1)%.CONSLUSION The reference and test formulations are bioequivalent.
XIONG Long-qi;CHEN Qing-hu.
Study on Pharmacokinetics of Guaifenesin Sustained Release Pellets in Beagle Dogs [J]. Chinese Pharmaceutical Journal, 2007, 42(20): 1574-1576
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References
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