Preclinical and clinical In vitro in vivo correlation of an hGH dextran microsphere formulation

被引:43
|
作者
Vlugt-Wensink, K. D. F.
de Vrueh, R.
Gresnigt, M. G.
Hoogerbrugge, C. M.
van Buul-Offers, S. C.
de Leede, L. G. J.
Sterkman, L. G. W.
Crommelin, D. J. A.
Hennink, W. E.
Verrijk, R.
机构
[1] OctoPlus Technol, OctoPlus BV, NL-2333 CL Leiden, Netherlands
[2] Univ Utrecht, Dept Pharmaceut, Utrecht Inst Pharmaceut Sci, NL-3508 TB Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Metab & Endocrine Dis, NL-3508 AB Utrecht, Netherlands
关键词
dex-HEMA microspheres; hGH; dextran; in vitro in vivo correlation;
D O I
10.1007/s11095-007-9433-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. To investigate the in vitro in vivo correlation of a sustained release formulation for human growth hormone (hGH) based on hydroxyethyl methacrylated dextran (dex-HEMA) microspheres in Pit-1 deficient Snell dwarf mice and in healthy human volunteers. Materials and Methods. A hGH-loaded microsphere formulation was developed and tested in Snell dwarf mice (pharmacodynamic study) and in healthy human volunteers (pharmacokinetic study). Results. Single subcutaneous administration of the microspheres in mice resulted in a good correlation between hGH released in vitro and in vivo effects for the hGH-loaded microsphere formulation similar to daily injected hGH indicating a retained bioactivity. Testing the microspheres in healthy volunteers showed an increase (over 7-8 days) in hGH serum concentrations (peak concentrations: 1-2.5 ng/ml). A good in vitro in vivo correlation was obtained between the measured and calculated (from in vitro release data) hGH serum concentrations. Moreover, an increased serum concentration of biomarkers (insulin-like growth factor-I (IGF-I), IGF binding protein-3 (IGFBP-3) was found again indicating that bioactive hGH was released from the microspheres. Conclusions. Good in vitro in vivo correlations were obtained for hGH-loaded dex-HEMA microspheres, which is an important advantage in predicting the effect of the controlled drug delivery product in a clinical situations.
引用
收藏
页码:2239 / 2248
页数:10
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