Idioma: Inglés
Publicado por LAP LAMBERT Academic Publishing, 2020
ISBN 10: 6202528818 ISBN 13: 9786202528818
Librería: Books Puddle, New York, NY, Estados Unidos de America
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Idioma: Inglés
Publicado por LAP LAMBERT Academic Publishing, 2020
ISBN 10: 6202528818 ISBN 13: 9786202528818
Librería: preigu, Osnabrück, Alemania
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Añadir al carritoTaschenbuch. Condición: Neu. The Use of Chemically Modified and Optimized Starches in Drug Delivery | Preparation, Optimization and Evaluation of Epichlorohydrincross-Linked Enset [Ensete Ventricosum (Welw.) Cheesman]) St | Desta Tesfay | Taschenbuch | 52 S. | Englisch | 2020 | LAP LAMBERT Academic Publishing | EAN 9786202528818 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
Idioma: Inglés
Publicado por LAP LAMBERT Academic Publishing, 2020
ISBN 10: 6202528818 ISBN 13: 9786202528818
Librería: Mispah books, Redhill, SURRE, Reino Unido
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Idioma: Inglés
Publicado por LAP LAMBERT Academic Publishing Apr 2020, 2020
ISBN 10: 6202528818 ISBN 13: 9786202528818
Librería: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Alemania
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Añadir al carritoTaschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Ensete ventricosum (Welw.) cheeseman which belongs to the family of Musaceae is one of the main sources of starch in Ethiopia. This study aimed at evaluating epichlorohydrin cross-linked enset starch as a drug release sustaining excipient in microsphere formulations of theophylline. Extracted Enset starch was cross-linked using epichlorohydrin as a cross-linking agent. The effect of cross- linker concentration, cross-linking duration and cross- linking temperature on the degree of cross- linking and release rate of microspheres prepared by emulsion solvent evaporation method was investigated using two-level full factorial design. Accordingly, the concentration of epichlorohydrin and duration of cross-linking were the most significant factors affecting both the degree of cross-linking and drug release rate. Thus, the effects of these two factors were further studied and optimized using the central composite design. As per the numerical method of central composite design, the optimal points were obtained at epichlorohydrin concentration of 13.70% and cross-linking time of 3.82h. Under these optimal conditions, the model predicts the degree of cross-linking of 74.70% and drug release 52 pp. Englisch.
Idioma: Inglés
Publicado por LAP LAMBERT Academic Publishing, 2020
ISBN 10: 6202528818 ISBN 13: 9786202528818
Librería: Majestic Books, Hounslow, Reino Unido
EUR 62,31
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Idioma: Inglés
Publicado por LAP LAMBERT Academic Publishing, 2020
ISBN 10: 6202528818 ISBN 13: 9786202528818
Librería: Biblios, Frankfurt am main, HESSE, Alemania
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Idioma: Inglés
Publicado por LAP LAMBERT Academic Publishing, 2020
ISBN 10: 6202528818 ISBN 13: 9786202528818
Librería: moluna, Greven, Alemania
EUR 34,25
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Añadir al carritoCondición: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Tesfay DestaI am called Desta Tesfay Mezgebo. I am a senior pharmacist and lecturer of pharmaceutics with the experience of working in teaching hospital, participating and coordinating different team works and conferences, teaching, .
Idioma: Inglés
Publicado por LAP LAMBERT Academic Publishing Apr 2020, 2020
ISBN 10: 6202528818 ISBN 13: 9786202528818
Librería: buchversandmimpf2000, Emtmannsberg, BAYE, Alemania
EUR 39,90
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Añadir al carritoTaschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Ensete ventricosum (Welw.) cheeseman which belongs to the family of Musaceae is one of the main sources of starch in Ethiopia. This study aimed at evaluating epichlorohydrin cross-linked enset starch as a drug release sustaining excipient in microsphere formulations of theophylline. Extracted Enset starch was cross-linked using epichlorohydrin as a cross-linking agent. The effect of cross- linker concentration, cross-linking duration and cross- linking temperature on the degree of cross- linking and release rate of microspheres prepared by emulsion solvent evaporation method was investigated using two-level full factorial design. Accordingly, the concentration of epichlorohydrin and duration of cross-linking were the most significant factors affecting both the degree of cross-linking and drug release rate. Thus, the effects of these two factors were further studied and optimized using the central composite design. As per the numerical method of central composite design, the optimal points were obtained at epichlorohydrin concentration of 13.70% and cross-linking time of 3.82h. Under these optimal conditions, the model predicts the degree of cross-linking of 74.70% and drug releaseVDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 52 pp. Englisch.
Idioma: Inglés
Publicado por LAP LAMBERT Academic Publishing, 2020
ISBN 10: 6202528818 ISBN 13: 9786202528818
Librería: AHA-BUCH GmbH, Einbeck, Alemania
EUR 40,89
Cantidad disponible: 1 disponibles
Añadir al carritoTaschenbuch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Ensete ventricosum (Welw.) cheeseman which belongs to the family of Musaceae is one of the main sources of starch in Ethiopia. This study aimed at evaluating epichlorohydrin cross-linked enset starch as a drug release sustaining excipient in microsphere formulations of theophylline. Extracted Enset starch was cross-linked using epichlorohydrin as a cross-linking agent. The effect of cross- linker concentration, cross-linking duration and cross- linking temperature on the degree of cross- linking and release rate of microspheres prepared by emulsion solvent evaporation method was investigated using two-level full factorial design. Accordingly, the concentration of epichlorohydrin and duration of cross-linking were the most significant factors affecting both the degree of cross-linking and drug release rate. Thus, the effects of these two factors were further studied and optimized using the central composite design. As per the numerical method of central composite design, the optimal points were obtained at epichlorohydrin concentration of 13.70% and cross-linking time of 3.82h. Under these optimal conditions, the model predicts the degree of cross-linking of 74.70% and drug release.