2005Zhongguo yaofangRequires access

Study on Pharmacokinetics of the Sustained-release Tablets and Common Tablets of Melatonin in Beagle Dogs in Vivo

Yu Lei, Yuanda Zhou

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Abstract

OBJECTIVE:To compare pharmacokinetic parameters of the common tablets and sustained-release melatonin tablets in beagle dogs in vivo.METHODS:The blood concentration of melatonin of6Beagle dogs was determined by HPLC and the pharmacokinetic parameters were calculated with3p97software after administered random crossover with single dose of sustained-release melatonin tablets6mg or the common tablets3mg.RESULTS:The concentration-time curves of both the common tablets and sustained-release melatonin tablets were in conformity with two-compartment model,C max of common tablets and sustained-release tablets were(11.27±3.77)ng/ml and(8.31±5.11)ng/ml respectively,t max of which were(0.50±0.18)h and(1.00±0.37)h respectively,t 1/2ke of which were(1.21±0.52)h and(3.27±0.89)h,AUC 0~t of which were(25.23±7.71)(ng·h)/ml and(38.03±16.45)(ng·h)/ml respectively.CONCLUSION:Compared with the common tablets,the sustained-release tablets showed slower absorption,longer peak time,lower peak concentration,slower elimination and longer duration.

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OBJECTIVE:To compare pharmacokinetic parameters of the common tablets and sustained-release melatonin tablets in beagle dogs in vivo.METHODS:The blood concentration of melatonin of6Beagle dogs was determined by HPLC and the pharmacokinetic parameters were calculated with3p97software after administered random crossover with single dose of sustained-release melatonin tablets6mg or the common tablets3mg.RESULTS:The concentration-time curves of both the common tablets and sustained-release melatonin tablets were in conformity with two-compartment model,C max of common tablets and sustained-release tablets were(11.27±3.77)ng/ml and(8.31±5.11)ng/ml respectively,t max of which were(0.50±0.18)h and(1.00±0.37)h respectively,t 1/2ke of which were(1.21±0.52)h and(3.27±0.89)h,AUC 0~t of which were(25.23±7.71)(ng·h)/ml and(38.03±16.45)(ng·h)/ml respectively.CONCLUSION:Compared with the common tablets,the sustained-release tablets showed slower absorption,longer peak time,lower peak concentration,slower elimination and longer duration.

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Available abstract

OBJECTIVE:To compare pharmacokinetic parameters of the common tablets and sustained-release melatonin tablets in beagle dogs in vivo.METHODS:The blood concentration of melatonin of6Beagle dogs was determined by HPLC and the pharmacokinetic parameters were calculated with3p97software after administered random crossover with single dose of sustained-release melatonin tablets6mg or the common tablets3mg.RESULTS:The concentration-time curves of both the common tablets and sustained-release melatonin tablets were in conformity with two-compartment model,C max of common tablets and sustained-release tablets were(11.27±3.77)ng/ml and(8.31±5.11)ng/ml respectively,t max of which were(0.50±0.18)h and(1.00±0.37)h respectively,t 1/2ke of which were(1.21±0.52)h and(3.27±0.89)h,AUC 0~t of which were(25.23±7.71)(ng·h)/ml and(38.03±16.45)(ng·h)/ml respectively.CONCLUSION:Compared with the common tablets,the sustained-release tablets showed slower absorption,longer peak time,lower peak concentration,slower elimination and longer duration.

Key concepts: Beagle, Pharmacokinetics, Melatonin, Pharmacology, Chemistry, Absorption (acoustics), In vivo, High-performance liquid chromatography

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Study on Pharmacokinetics of the Sustained-release Tablets and Common Tablets of Melatonin in Beagle Dogs in Vivo — Research Paper | ScholarLens