Development of In Vitro-In Vivo Correlation for Extended-Release Niacin After Administration of Hypromellose-Based Matrix Formulations to Healthy Volunteers

被引:11
作者
Kesisoglou, Filippos [1 ]
Rossenu, Stefaan [2 ]
Farrell, Colm [3 ]
Van Den Heuvel, Michiel [2 ]
Prohn, Marita [2 ]
Fitzpatrick, Shaun [4 ]
De Kam, Pieter-Jan [5 ]
Vargo, Ryan [6 ]
机构
[1] Merck & Co Inc, Biopharmaceut Pharmaceut Sci & Clin Supply, West Point, PA 19486 USA
[2] Merck Sharp & Dohme Ltd, PPDM, Oss, Netherlands
[3] ICON Dev Solut, Marlow, Bucks, England
[4] Merck Sharp & Dohme Ltd, Formulat Sci, Pharmaceut Sci & Clin Supply, Hoddesdon, Herts, England
[5] MSD Int GmbH, Discovery Med, Singapore, Singapore
[6] Merck & Co Inc, PPDM, West Point, PA 19486 USA
关键词
in vitro; in vivo correlations (IVIVC); controlled release; pharmacokinetics; dissolution; mathematical model; DOSAGE FORMS; IVIVC; PHARMACOKINETICS; DISPOSITION; INVITRO;
D O I
10.1002/jps.24179
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Development of in vitro-in vivo correlations (IVIVCs) for extended-release (ER) products is commonly pursued during pharmaceutical development to increase product understanding, set release specifications, and support biowaivers. This manuscript details the development of Level C and Level A IVIVCs for ER formulations of niacin, a highly variable and extensively metabolized compound. Three ER formulations were screened in a cross-over study against immediate-release niacin. A Multiple Level C IVIVC was established for both niacin and its primary metabolite nicotinuric acid (NUA) as well as total niacin metabolites urinary excretion. For NUA, but not for niacin, Level A IVIVC models with acceptable prediction errors were achievable via a modified IVIVC rather than a traditional deconvolution/convolution approach. Hence, this is in contradiction with current regulatory guidelines that suggest that when a Multiple Level C IVIVC is established, Level A models should also be readily achievable. We demonstrate that for a highly variable, highly metabolized compound such as niacin, development of a Level A IVIVC model fully validated according to agency guidelines may be challenging. However, Multiple Level C models are achievable and could be used to guide release specifications and formulation/manufacturing changes. (c) 2014 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 103:3713-3723, 2014
引用
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页码:3713 / 3723
页数:11
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