Single- and multiple-dose pharmacokinetics of pioglitazone in adolescents with type 2 diabetes

被引:38
作者
Christensen, ML
Meibohm, B
Capparelli, EV
Velasquez-Mieyer, P
Burghen, GA
Tamborlane, WV
机构
[1] Univ Tennessee, Pediat Pharmacol Res Units, Memphis, TN 38103 USA
[2] St Jude Childrens Res Hosp, Lebonheur Childrens Med Ctr, Memphis, TN 38101 USA
[3] Univ Calif San Diego, San Diego, CA 92103 USA
[4] Yale Univ, New Haven, CT USA
关键词
pioglitazone; pharmacokinetics; type; 2; diabetes; adolescents;
D O I
10.1177/0091270005279578
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study assessed the single- and multiple-dose pharmacokinetics of 3 doses (15 mg, 30 mg, and 45 mg) Of pioglitazone in 36 adolescents with type 2 diabetes. Blood samples were obtained over a 48-hour interval after the first dose (day 1) and over a 72-hour interval after the last dose (day 15) of pioglitazone and were assayed for pioglitazone and active metabolites (M-III and M-IV). Pioglitazone systemic exposure increased dose dependently but was less than dose proportional during multiple dosing. The median peak pioglitozone concentration occurred at 2 hours. The mean half-life was 8 to 9 hours for pioglitazone and 24 to 32 hours for M-III and M-IV with similar values at each dose level. During multiple dosing, accumulation for pioglitazone was negligible, but it reached 2.5- to 3.0-fold for M-III and M-IV The sustained total serum concentration of active compounds during multiple dosing provides the basis for once-daily dose administration of pioglitazone in adolescents.
引用
收藏
页码:1137 / 1144
页数:8
相关论文
共 22 条
[1]  
Belcher G, 2000, EXP CLIN ENDOCR DIAB, V108, pS267
[2]   Troglitazone action is independent of adipose tissue [J].
Burant, CF ;
Sreenan, S ;
Hirano, KI ;
Tai, TAC ;
Lohmiller, J ;
Lukens, J ;
Davidson, NO ;
Ross, S ;
Graves, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (11) :2900-2908
[3]   Pathogenesis of type 2 diabetes mellitus [J].
Dostou, J ;
Gerich, J .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2001, 109 :S149-S156
[4]   Clinical pharmacokinetics of pioglitazone [J].
Eckland, DA ;
Danhof, M .
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2000, 108 :S234-S242
[5]   The organization, promoter analysis, and expression of the human PPAR gamma gene [J].
Fajas, L ;
Auboeuf, D ;
Raspe, E ;
Schoonjans, K ;
Lefebvre, AM ;
Saladin, R ;
Najib, J ;
Laville, M ;
Fruchart, JC ;
Deeb, S ;
VidalPuig, A ;
Flier, J ;
Briggs, MR ;
Staels, B ;
Vidal, H ;
Auwerx, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (30) :18779-18789
[6]  
FLEMMER M, 2001, CURR OPIN INVESTIG D, V11, P1564
[7]   Troglitazone monotherapy improves glycemic control in patients with type 2 diabetes mellitus: A randomized, controlled study [J].
Fonseca, VA ;
Valiquett, TR ;
Huang, SM ;
Ghazzi, MN ;
Whitcomb, RW .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (09) :3169-3176
[8]  
Gesundheit B, 2004, PEDIATRICS, V114, P259, DOI 10.1542/peds.114.2.e259
[9]   Effects of oral hypoglycemic agents and diet on protein metabolism in type 2 diabetes [J].
Gougeon, R ;
Jones, PJH ;
Styhler, K ;
Marliss, EB ;
Morais, JA .
DIABETES CARE, 2000, 23 (01) :1-8
[10]  
Hanefeld M, 2001, INT J CLIN PRACT, P19