Combined site-specific release retardant mini-matrix tablets (C-SSRRMT) for extended oral delivery of dexketoprofen trometamol: in vitro evaluation and single versus multiple doses pharmacokinetic study in human volunteers
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Date
2019
Authors
Journal Title
Journal ISSN
Volume Title
Type
Article
Publisher
Taylor and Francis Ltd.
Series Info
Drug Development and Industrial Pharmacy
45
45
Scientific Journal Rankings
Abstract
Development of extended release oral formulations of dexketoprofen trometamol (DT), a rapidly eliminated drug with high solubility, poses a great challenge especially when a portion of the dose is to be absorbed from the colon. In this study, site-specific release-retardant mini-matrix tablets (SSRRMTs) were developed and functionally coated with pH-responsive materials to achieve a site-specific delivery of DT at the duodenojejunal (DSRRMT) and ileocecal (ISRRMT) regions. Stomach-specific coated mini-tablets (SSCMTs) were manufactured for immediate release of about 16% of the daily dose of DT in the stomach. The SSCMT, DSRRMT, and ISRRMT were combined into a solid dosage form (C-SSRRMT tablets or capsules) to achieve the required linear release profile for once daily administration of DT. The SSRRMT and C-SSRRMT formulations were evaluated for the physical properties, in vitro-disintegration and in vitro dissolution and proved to be consistent with the pharmacopeial specifications. The in vitro release profiles of both C-SSRRMT tablets and capsules showed a constant release rate of about 6 mg/h and were similar to that of the theoretical target linear release profile. The pharmacokinetic study using human volunteers showed the bioequivalence of a single oral dose of C-SSRRMT capsules compared to three-successive oral doses of the immediate release market tablets with less ups and downs in the drug levels. The C-SSRRMT capsules formulation, may therefore, constitute an advance in the extended oral delivery of DT without the lack of efficacy and the adverse events frequently encountered in multiple daily dosing of the immediate release tablets. � 2019, � 2019 Informa UK Limited, trading as Taylor & Francis Group.
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Keywords
جامعة أكتوبر للعلوم الحديثة والآداب, MSA University, University for Modern Sciences and Arts, October University for Modern Sciences and Arts, Dexketoprofen, extended release, oral, pH-responsive coating, release retardant mini-matrix tablets, dexketoprofen, eudragit, placebo, adult, Article, AUC (0-24 h), bioequivalence, cecum, controlled study, crossover procedure, dosage schedule comparison, drug bioavailability, drug coating, drug half life, drug solubility, duodenum, human, human experiment, ileum, in vitro study, in vivo study, jejunum, male, maximum concentration, microcapsule, normal human, pharmacokinetic parameters, plasma concentration-time curve, randomized controlled trial, single drug dose, stomach, tablet compression, tablet formulation, tablet friability, tablet hardness, time to maximum plasma concentration