Coated hard capsules as the pH-dependent drug transport systems to ileo-colonic compartment
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- biologický transport MeSH
- časové faktory MeSH
- deriváty hypromelózy MeSH
- ileum metabolismus MeSH
- kofein farmakokinetika MeSH
- kolon metabolismus MeSH
- koncentrace vodíkových iontů MeSH
- kyseliny polymethakrylové chemie MeSH
- lékové transportní systémy metody MeSH
- léky s prodlouženým účinkem MeSH
- lidé MeSH
- methylcelulosa analogy a deriváty chemie MeSH
- rozpustnost MeSH
- tobolky chemie MeSH
- želatina chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- deriváty hypromelózy MeSH
- kofein MeSH
- kyseliny polymethakrylové MeSH
- léky s prodlouženým účinkem MeSH
- methylcelulosa MeSH
- methylmethacrylate-methacrylic acid copolymer MeSH Prohlížeč
- tobolky MeSH
- želatina MeSH
PURPOSE: The aim of this study was to investigate the suitability of hard capsules of different composition (gelatin-G, gelatin coated with hydroxypropyl cellulose-G/HPC, and hypromellose-H) for a coating with aqueous dispersion of pH-dependent synthetic polymer Eudragit(®) FS (E(FS)) and to evaluate in vitro the coated capsules as transport systems for ileo-colonic drug delivery. METHODS: Three sets of hard capsules with increasing coating levels (5-30%) were obtained by Wurster technique. The release of model drug (caffeine) from prepared samples was tested using paddle dissolution method with continual pH change (pH 1.2-2 h, 6.8-4 h and 7.5-2 h). RESULTS: During the coating process, no problems occurred and similar suitability of capsules materials for E(FS) application was observed in contrast to some published reports. The application of HPC subcoating onto gelatin capsules surface was shown as the redundant step. The samples G/E(FS)10-15% and H/E(FS)15-20% with 6 h lag time and fast drug release after the pH adjustment to 7.5 corresponded with the requirements for ileic drug delivery. Samples releasing the drug after the pH change to 7.5 in 2-h interval such as G/E(FS) 20%, G/HPC/E(FS) 25% and H/E(FS) 25% are considered as promising transport systems to ileo-colonic area. Samples G/E(FS) 25-30%, G/HPC/E(FS) 30% and H/E(FS) 30% with 7 h lag time could be used for colon delivery. CONCLUSION: The desired intestinal part could be targeted without significant formulation changes only by the selection of capsules shell forming material and suitable E(FS) coating thickness.
Citace poskytuje Crossref.org
Commercially Available Enteric Empty Hard Capsules, Production Technology and Application