The formulation with deduction of acid secretion Famotidine is histamine H2 receptor antagonist. It has bioavailability of 40 to 45% and it has shorter plasma half life of 2.5 to 3.5 hrs.… mais…
The formulation with deduction of acid secretion Famotidine is histamine H2 receptor antagonist. It has bioavailability of 40 to 45% and it has shorter plasma half life of 2.5 to 3.5 hrs. The effective treatment of erosive esophagitis and Zolinger-Elisons syndrome requires administration of 20 mg of Famotidine 4 times a day. A conventional dose of 20 mg can inhibit gastric acid secretion up to 5 hours but not up to 10 hours. An alternative dose of 40 mg leads to plasma fluctuations thus a sustained release dosage form of famotidine is desirable. Direct access to the systemic circulation bypasses drugs from the hepatic first pass metabolism leading to high bioavailability. Moreover, the buccal route is easily accessible, has a good patient compliance and can be used in patients who can t swallow. Bilayer buccal tablet was prepared by using mucoadhesive polymer combination of Sodium CMC and Carbopol934P, by direct compression with backing layer of Ethyl cellulose. The optimized formulation F1 had given release of 102.57% in 8hrs and it had optimum swelling, mucoadhesive property and permeation from buccal mucosa. It also had desired drug release kinetics and found to be stable for the period of 1 month. Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine: Famotidine is histamine H2 receptor antagonist. It has bioavailability of 40 to 45% and it has shorter plasma half life of 2.5 to 3.5 hrs. The effective treatment of erosive esophagitis and Zolinger-Elisons syndrome requires administration of 20 mg of Famotidine 4 times a day. A conventional dose of 20 mg can inhibit gastric acid secretion up to 5 hours but not up to 10 hours. An alternative dose of 40 mg leads to plasma fluctuations thus a sustained release dosage form of famotidine is desirable. Direct access to the systemic circulation bypasses drugs from the hepatic first pass metabolism leading to high bioavailability. Moreover, the buccal route is easily accessible, has a good patient compliance and can be used in patients who can t swallow. Bilayer buccal tablet was prepared by using mucoadhesive polymer combination of Sodium CMC and Carbopol934P, by direct compression with backing layer of Ethyl cellulose. The optimized formulation F1 had given release of 102.57% in 8hrs and it had optimum swelling, mucoadhesive property and permeation from buccal mucosa. It also had desired drug release kinetics and found to be stable for the period of 1 month., LAP Lambert Academic Publishing<
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Famotidine is histamine H2 receptor antagonist. It has bioavailability of 40 to 45% and it has shorter plasma half life of 2.5 to 3.5 hrs. The effective treatment of erosive esophagitis a… mais…
Famotidine is histamine H2 receptor antagonist. It has bioavailability of 40 to 45% and it has shorter plasma half life of 2.5 to 3.5 hrs. The effective treatment of erosive esophagitis and Zolinger-Elisons syndrome requires administration of 20 mg of Famotidine 4 times a day. A conventional dose of 20 mg can inhibit gastric acid secretion up to 5 hours but not up to 10 hours. An alternative dose of 40 mg leads to plasma fluctuations; thus a sustained release dosage form of famotidine is desirable. Direct access to the systemic circulation bypasses drugs from the hepatic first pass metabolism leading to high bioavailability. Moreover, the buccal route is easily accessible, has a good patient compliance and can be used in patients who can t swallow. Bilayer buccal tablet was prepared by using mucoadhesive polymer combination of Sodium CMC and Carbopol934P, by direct compression with backing layer of Ethyl cellulose. The optimized formulation F1 had given release of 102.57% in 8hrs and it had optimum swelling, mucoadhesive property and permeation from buccal mucosa. It also had desired drug release kinetics and found to be stable for the period of 1 month. Bücher / Naturwissenschaften, Medizin, Informatik & Technik / Medizin / Pharmazie<
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Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel: Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine als Buch von Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel - encadernado, livro de bolso
Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine:The formulation with deduction of acid secretion Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel Formulation and In … mais…
Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine:The formulation with deduction of acid secretion Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine:The formulation with deduction of acid secretion Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel Bücher > Wissenschaft > Medizin, LAP Lambert Academic Publishing<
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Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel: Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine als Buch von Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel - encadernado, livro de bolso
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Lieferung innerhalb 1-4 Werktagen. Versandkostenfrei, wenn Buch oder Hörbuch enthalten ist, sonst 2,95 EUR. Ab 19,90 EUR versandkostenfrei. (Deutschland) Bücher > Wissenschaft > Medizin, LAP Lambert Academic Publishing<
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The formulation with deduction of acid secretion Famotidine is histamine H2 receptor antagonist. It has bioavailability of 40 to 45% and it has shorter plasma half life of 2.5 to 3.5 hrs.… mais…
The formulation with deduction of acid secretion Famotidine is histamine H2 receptor antagonist. It has bioavailability of 40 to 45% and it has shorter plasma half life of 2.5 to 3.5 hrs. The effective treatment of erosive esophagitis and Zolinger-Elisons syndrome requires administration of 20 mg of Famotidine 4 times a day. A conventional dose of 20 mg can inhibit gastric acid secretion up to 5 hours but not up to 10 hours. An alternative dose of 40 mg leads to plasma fluctuations thus a sustained release dosage form of famotidine is desirable. Direct access to the systemic circulation bypasses drugs from the hepatic first pass metabolism leading to high bioavailability. Moreover, the buccal route is easily accessible, has a good patient compliance and can be used in patients who can t swallow. Bilayer buccal tablet was prepared by using mucoadhesive polymer combination of Sodium CMC and Carbopol934P, by direct compression with backing layer of Ethyl cellulose. The optimized formulation F1 had given release of 102.57% in 8hrs and it had optimum swelling, mucoadhesive property and permeation from buccal mucosa. It also had desired drug release kinetics and found to be stable for the period of 1 month. Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine: Famotidine is histamine H2 receptor antagonist. It has bioavailability of 40 to 45% and it has shorter plasma half life of 2.5 to 3.5 hrs. The effective treatment of erosive esophagitis and Zolinger-Elisons syndrome requires administration of 20 mg of Famotidine 4 times a day. A conventional dose of 20 mg can inhibit gastric acid secretion up to 5 hours but not up to 10 hours. An alternative dose of 40 mg leads to plasma fluctuations thus a sustained release dosage form of famotidine is desirable. Direct access to the systemic circulation bypasses drugs from the hepatic first pass metabolism leading to high bioavailability. Moreover, the buccal route is easily accessible, has a good patient compliance and can be used in patients who can t swallow. Bilayer buccal tablet was prepared by using mucoadhesive polymer combination of Sodium CMC and Carbopol934P, by direct compression with backing layer of Ethyl cellulose. The optimized formulation F1 had given release of 102.57% in 8hrs and it had optimum swelling, mucoadhesive property and permeation from buccal mucosa. It also had desired drug release kinetics and found to be stable for the period of 1 month., LAP Lambert Academic Publishing<
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Famotidine is histamine H2 receptor antagonist. It has bioavailability of 40 to 45% and it has shorter plasma half life of 2.5 to 3.5 hrs. The effective treatment of erosive esophagitis a… mais…
Famotidine is histamine H2 receptor antagonist. It has bioavailability of 40 to 45% and it has shorter plasma half life of 2.5 to 3.5 hrs. The effective treatment of erosive esophagitis and Zolinger-Elisons syndrome requires administration of 20 mg of Famotidine 4 times a day. A conventional dose of 20 mg can inhibit gastric acid secretion up to 5 hours but not up to 10 hours. An alternative dose of 40 mg leads to plasma fluctuations; thus a sustained release dosage form of famotidine is desirable. Direct access to the systemic circulation bypasses drugs from the hepatic first pass metabolism leading to high bioavailability. Moreover, the buccal route is easily accessible, has a good patient compliance and can be used in patients who can t swallow. Bilayer buccal tablet was prepared by using mucoadhesive polymer combination of Sodium CMC and Carbopol934P, by direct compression with backing layer of Ethyl cellulose. The optimized formulation F1 had given release of 102.57% in 8hrs and it had optimum swelling, mucoadhesive property and permeation from buccal mucosa. It also had desired drug release kinetics and found to be stable for the period of 1 month. Bücher / Naturwissenschaften, Medizin, Informatik & Technik / Medizin / Pharmazie<
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Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel: Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine als Buch von Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel - encadernado, livro de bolso
Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine:The formulation with deduction of acid secretion Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel Formulation and In … mais…
Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine:The formulation with deduction of acid secretion Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine:The formulation with deduction of acid secretion Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel Bücher > Wissenschaft > Medizin, LAP Lambert Academic Publishing<
Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel: Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine als Buch von Jalpeshkumar Bhavsar, Mukesh Patel, Natvarlal Patel - encadernado, livro de bolso
Lieferung innerhalb 1-4 Werktagen. Versandkostenfrei, wenn Buch oder Hörbuch enthalten ist, sonst 2,95 EUR. Ab 19,90 EUR versandkostenfrei. (Deutschland) Bücher > Wissenschaft > Mediz… mais…
Lieferung innerhalb 1-4 Werktagen. Versandkostenfrei, wenn Buch oder Hörbuch enthalten ist, sonst 2,95 EUR. Ab 19,90 EUR versandkostenfrei. (Deutschland) Bücher > Wissenschaft > Medizin, LAP Lambert Academic Publishing<
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Dados detalhados do livro - Formulation and In Vitro Evaluation of Buccal Tablet of Famotidine
EAN (ISBN-13): 9783659137501 ISBN (ISBN-10): 3659137502 Livro de capa dura Livro de bolso Ano de publicação: 2012 Editor/Editora: LAP Lambert Academic Publishing
Livro na base de dados desde 2009-02-18T13:22:14+00:00 (Lisbon) Página de detalhes modificada pela última vez em 2018-03-16T06:34:25+00:00 (Lisbon) Número ISBN/EAN: 3659137502
Número ISBN - Ortografia alternativa: 3-659-13750-2, 978-3-659-13750-1 Ortografia alternativa e termos de pesquisa relacionados: Título do livro: tablet, vitro
