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YUN Yunlei, GAO Shouhong, Fan Chenghui, MIAO Haijun. Pharmacokinetics of mitiglinide calcium tablets in human healthy volunteers[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(1): 45-48. doi: 10.3969/j.issn.1006-0111.2014.01.011
Citation: YUN Yunlei, GAO Shouhong, Fan Chenghui, MIAO Haijun. Pharmacokinetics of mitiglinide calcium tablets in human healthy volunteers[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(1): 45-48. doi: 10.3969/j.issn.1006-0111.2014.01.011

Pharmacokinetics of mitiglinide calcium tablets in human healthy volunteers

doi: 10.3969/j.issn.1006-0111.2014.01.011
  • Received Date: 2013-01-31
  • Rev Recd Date: 2013-10-15
  • Objective To establish a sensitive and specific LC-MS/MS method for the determination of mitiglinide calcium in human plasma, and investigate the pharmacokinetics of mitiglinide calcium tablets in healthy volunteers. Methods 30 healthy volunteers were randomly divided into three groups with 5 men and 5 women in each group. The volunteers in three groups were administrated with single dose of mitiglinide calcium tablets 5, 10, 20 mg, respectively. The pharmacokinetic parameters were calculated by non-compartment model. Results The main pharmacokinetics parameters of mitiglinide in volunteers who were administrated with a single dose of 5, 10, 20 mg were as follows:Cmax(799.5±189.8), (1 689.8±348.4)and(3 032.9±755.6)ng/ml; tmax(0.38±0.16), (0.43±0.16)and(0.54±0.26)h; AUC0-10(1 051.3±276.4), (2 324.5±481.8)and(5 028.8±1 283.6)ng·h/ml; AUC0-∞(1 059.4±278.2), (2 342.8±488.6)and(5 073.9±1 315.9)ng·h/ml; t1/2(1.80±0.42), (1.68±0.37)and(1.56±0.19)h, respectively. Conclusion The present method was accurate, sensitive and reproducible for the determination of mitiglinide levels in human plasma, which was suitable for pharmacokinetic study on mitiglinide tables in human.
  • [1] Kumashiro N,Yoshihara T,Kanazawa Y,et al.Long-term effect of combination therapy with mitiglinide and once daily insulin glargine in patients who were successfully switched from intensive insulin therapy in short-termstudy[J].Endocr J,2007,54(1):163-166.
    [2] Sunaga Y,Gonoi T,Shibasaki T,et al.The efects ofmitiglinide (KAD-1229)a new antidiabetic drug,on ATP-sensitive-K channels and insulin secretion:comparison with the sulfonylureas and nateglinide[J].Eur J Pharmacol,2001,431(1):119.
    [3] Lushan Y,Su Z.Determination of mitiglinide in rat plasma by high performance liquid chromatography with UV detection[J]. Chromatogr B Anal Technol Biomed Life Sci,2006,834(1-2):204-207.
    [4] Jin HW,Yu QX.SPE and LC-ESI-MS for quantitative analysis of mitiglinide in human plasma in a bioequivalence study[J].Chromatographia,2009,70(11-12):1715-1719.
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    [6] Cai S, Huo TG, Feng WY, et al. Quantitative determination of mitiglinide in human plasma by ultra-performance liquid chromatography/electrosprayionization tandem mass spectrometry[J]. J Chromatogr B, 2008,868,83-87.
    [7] Zhang Y, Ding L, Tian Y, et al. Liquid chromatography-electrospray ionization tandem mass spectrometry for the quantification of mitiglinide in human plasma:validation and its application to pharmacokinetic studies[J]. Biomed Chromatogr,2008,22(8):873-878.
    [8] 赵秀丽,王淑民,武 峰,等.米格列奈钙片在健康人体内的药代动力学[J].中国临床药理学杂志,2010,9(26):53-55.
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Pharmacokinetics of mitiglinide calcium tablets in human healthy volunteers

doi: 10.3969/j.issn.1006-0111.2014.01.011

Abstract: Objective To establish a sensitive and specific LC-MS/MS method for the determination of mitiglinide calcium in human plasma, and investigate the pharmacokinetics of mitiglinide calcium tablets in healthy volunteers. Methods 30 healthy volunteers were randomly divided into three groups with 5 men and 5 women in each group. The volunteers in three groups were administrated with single dose of mitiglinide calcium tablets 5, 10, 20 mg, respectively. The pharmacokinetic parameters were calculated by non-compartment model. Results The main pharmacokinetics parameters of mitiglinide in volunteers who were administrated with a single dose of 5, 10, 20 mg were as follows:Cmax(799.5±189.8), (1 689.8±348.4)and(3 032.9±755.6)ng/ml; tmax(0.38±0.16), (0.43±0.16)and(0.54±0.26)h; AUC0-10(1 051.3±276.4), (2 324.5±481.8)and(5 028.8±1 283.6)ng·h/ml; AUC0-∞(1 059.4±278.2), (2 342.8±488.6)and(5 073.9±1 315.9)ng·h/ml; t1/2(1.80±0.42), (1.68±0.37)and(1.56±0.19)h, respectively. Conclusion The present method was accurate, sensitive and reproducible for the determination of mitiglinide levels in human plasma, which was suitable for pharmacokinetic study on mitiglinide tables in human.

YUN Yunlei, GAO Shouhong, Fan Chenghui, MIAO Haijun. Pharmacokinetics of mitiglinide calcium tablets in human healthy volunteers[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(1): 45-48. doi: 10.3969/j.issn.1006-0111.2014.01.011
Citation: YUN Yunlei, GAO Shouhong, Fan Chenghui, MIAO Haijun. Pharmacokinetics of mitiglinide calcium tablets in human healthy volunteers[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(1): 45-48. doi: 10.3969/j.issn.1006-0111.2014.01.011
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