International journal of pharmaceutics · 2008
In vitro and in vivo characteristics of prochlorperazine oral disintegrating film.
Сравнительное исследованиеСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Nishimura Misao, Matsuura Katsuhiko, Tsukioka Tadao, Yamashita Hirotaka, Inagaki Naoki, Sugiyama Tadashi, Itoh Yoshinori
Аннотация
Oral disintegrating film containing prochlorperazine, a dopamine D(2) receptor antagonist with anti-emetic property, was newly developed using microcrystalline cellulose, polyethlene glycol and hydroxypropylmethyl cellulose as the base materials. The uniformity of dosage units of the preparation was acceptable according to the criteria of JP15 or USP27. The film showed an excellent stability at least for 8 weeks when stored at 40 degrees C and 75% in humidity. The dissolution test revealed a rapid disintegration property, in which most of prochlorperazine dissolved within 2 min after insertion into the medium. Subsequently, rats were used to compare pharmacokinetic properties of the film preparation applied topically into the oral cavity with those of oral administration of prochlorperazine solution. None of the parameters, including T(max), C(max), area under curves, clearance and steady-state distribution volume was significantly different between oral disintegrating film and oral solution. These findings suggest that the present prochlorperazine-containing oral film is potentially useful to control emesis induced by anti-cancer agents or opioid analgesics in patients who limit the oral intake.
Предметные рубрики MeSH
Administration, BuccalAnimalsAntiemeticsArea Under CurveBiological AvailabilityCelluloseChemistry, PharmaceuticalChromatography, High Pressure LiquidDosage FormsDrug CompoundingDrug Delivery SystemsDrug StabilityExcipientsHypromellose DerivativesMaleMass SpectrometryMethylcellulosePolyethylene GlycolsProchlorperazineRatsRats, Sprague-DawleySolubilityTime Factors