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Beschreibung
Oral drug delivery systems continue to be the most popular route of administration due to its versatility, ease of administration and patient compliance. A number of oral controlled release systems have been developed to improve the delivery of drugs to the systemic circulation. Rapid gastro intestinal transit will prevent complete drug release leading to diminished activity. Gastro retentive drug deliveries are designed to prolong and delay the gastric emptying time (GET). GET, the most important asset which helps the dosage form to reside in the stomach for longer time than convectional dosage form. Retention of oral dosage form in the upper gastrointestinal tract (GIT) causes prolonged contact time of drug with GI mucosa, leading to higher bioavailability. Drugs which are having shorter half lives, the drugs which are eliminated quickly, and the drugs which are incompletely absorbed from the small intestine are the suitable drug candidates for formulating them into gastro retentive systems.
Oral drug delivery systems continue to be the most popular route of administration due to its versatility, ease of administration and patient compliance. A number of oral controlled release systems have been developed to improve the delivery of drugs to the systemic circulation. Rapid gastro intestinal transit will prevent complete drug release leading to diminished activity. Gastro retentive drug deliveries are designed to prolong and delay the gastric emptying time (GET). GET, the most important asset which helps the dosage form to reside in the stomach for longer time than convectional dosage form. Retention of oral dosage form in the upper gastrointestinal tract (GIT) causes prolonged contact time of drug with GI mucosa, leading to higher bioavailability. Drugs which are having shorter half lives, the drugs which are eliminated quickly, and the drugs which are incompletely absorbed from the small intestine are the suitable drug candidates for formulating them into gastro retentive systems.
Über den Autor
K.V. Ratnamala concluiu a licenciatura em Farmácia, o mestrado em Farmácia e o doutoramento na Faculdade de Ciências Farmacêuticas da Universidade de Andhra, Visakhapatnam. Trabalha atualmente como professor assistente na Faculdade de Farmácia I. RBVRR, Hyderabad, desde há 7 anos. O seu domínio de interesse inclui a administração de medicamentos por flutuação gástrica. Orientou cerca de 11 estudantes de Farmácia.
Details
Erscheinungsjahr: 2017
Fachbereich: Toxikologie
Genre: Mathematik, Medizin, Naturwissenschaften, Technik
Rubrik: Wissenschaften
Medium: Taschenbuch
ISBN-13: 9783330084919
ISBN-10: 333008491X
Sprache: Englisch
Einband: Kartoniert / Broschiert
Autor: Venkata Ratnamala, Kolapalli
Anisha, Yelisetti
Hersteller: LAP LAMBERT Academic Publishing
Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, D-49078 Osnabrück, mail@preigu.de
Maße: 220 x 150 x 7 mm
Von/Mit: Kolapalli Venkata Ratnamala (u. a.)
Erscheinungsdatum: 13.12.2017
Gewicht: 0,179 kg
Artikel-ID: 120549656

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