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An oral multiparticulate, modified‐release, hydrocortisone replacement therapy that provides physiological cortisol exposure
Author(s) -
Whitaker Martin J.,
Debono Miguel,
Huatan Hiep,
Merke Deborah P.,
Arlt Wiebke,
Ross Richard J.
Publication year - 2014
Publication title -
clinical endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 147
eISSN - 1365-2265
pISSN - 0300-0664
DOI - 10.1111/cen.12316
Subject(s) - hydrocortisone , bioavailability , cmax , endocrinology , medicine , dexamethasone , absorption (acoustics) , pharmacology , pharmacokinetics , glucocorticoid , chemistry , physics , acoustics
Summary Objective It is not possible with current hydrocortisone replacement to mimic the diurnal cortisol profile in patients with adrenal insufficiency. Previous attempts with modified‐release technology were unsuccessful. Our objective was to develop hydrocortisone formulations that recreate the diurnal cortisol profile using multiparticulate technology. Design and Measurements Screening by in vitro dissolution profiles, pharmacokinetic (PK) testing in dexamethasone‐suppressed dogs and humans, and comparison with a reference population. Setting Field laboratories and clinical research facility. Results Formulations were generated using an enteric (delayed release) design configuration with an extended (sustained release) dissolution profile. In vitro dissolution confirmed delayed and sustained hydrocortisone release. However, in dogs and humans, sustained release resulted in reduced bioavailability. A formulation, DIURF ‐006, was developed that maintained delayed release but omitted the sustained‐release functionality. PK characterization of DIURF ‐006 showed that, despite absence of a sustained‐release component, absorption was sufficiently sustained to deliver extended hydrocortisone absorption. In dexamethasone‐suppressed volunteers ( n  = 16) receiving a twice‐daily ‘toothbrush’ regimen (20 mg at 23:00 h and 10 mg at 07:00 h), DIURF ‐006 gave a similar cortisol profile to physiological cortisol levels: DIURF ‐006 vs physiological, Geomean AUC 5610 vs 4706 h * nmol/l, Geomean C max 665 vs 594 nmol/l and Median T max 8·5 h vs clock time 08:12 h for peak cortisol. The relative bioavailability of DIURF ‐006 vs hydrocortisone was 89%, and cortisol levels increased linearly with doses between 5 and 30 mg. Conclusion A multiparticulate oral hydrocortisone formulation with only an enteric coat provides delayed and sustained absorption and when given in a ‘toothbrush’ regimen provides physiological cortisol exposure.

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