Isbn: 9783848498642 - drug delivery strategy: co-precipitation method of solid dispersion: a formulation strategy for poorly soluble drugs (6 risultati)

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  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2012

    3848498642 / 9783848498642

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    Da: preigu, Osnabrück, Germaniapreigu

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    Taschenbuch. Condizione: Neu. Drug Delivery Strategy: Co-precipitation Method Of Solid Dispersion | A Formulation Strategy for Poorly Soluble Drugs | Mohammad Fahim Kadir (u. a.) | Taschenbuch | 192 S. | Englisch | 2012 | LAP LAMBERT Academic Publishing | EAN 9783848498642 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2012

    3848498642 / 9783848498642

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    Da: Mispah books, Redhill, SURRE, Regno UnitoMispah books

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    Paperback. Condizione: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing Apr 2012, 2012

    3848498642 / 9783848498642

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    Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.

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    Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Solid dispersion technology has proved to be a powerful technique in the field of drug delivery of poorly water soluble drugs by enhancing the dissolution rate and bioavailability of that drug. Here we used four drugs namely Spironolactone, Etoricoxib, Ibuprofen and Carvedilol. Solid dispersions were prepared by solvent co-precipitation method, where acetone was used as solvent and pet-ether was used as anti solvent. Different water soluble polymer (HPMC 6cps, Kollicoat IR, Kollidon VA 64 and HPC), and as an excipient poloxamer were used to prepare solid dispersion. Paddle type dissolution apparatus was used to study in-vitro dissolution rate, where paddle speed was 75 rpm. at 37°C. The dissolution samples were then analyzed spectrophotometrically by UV-VIS spectrophotometer. At first we tried to identify the effect of poloxamer 407, then with poloxamer others polymer were applied to find out their effect on drugs. Through the entire study, we searched for the suitable polymer and excipient with their proportion in a formulation which would show the best beneficial effect on drugs dissolution rate. 192 pp. Englisch.

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2012

    3848498642 / 9783848498642

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    Da: moluna, Greven, Germaniamoluna

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    Kartoniert / Broschiert. Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Kadir Mohammad FahimMohammad Fahim Kadir obtained Master of Pharmacy Degree in Pharmaceutical Technology from the University of Dhaka, Bangladesh. Muhammad Shahdaat Bin Sayeed Bin Sayeed obtained Bachelor Pharmacy (Hons.)from the Fac.

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2012

    3848498642 / 9783848498642

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    Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH

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    Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Solid dispersion technology has proved to be a powerful technique in the field of drug delivery of poorly water soluble drugs by enhancing the dissolution rate and bioavailability of that drug. Here we used four drugs namely Spironolactone, Etoricoxib, Ibuprofen and Carvedilol. Solid dispersions were prepared by solvent co-precipitation method, where acetone was used as solvent and pet-ether was used as anti solvent. Different water soluble polymer (HPMC 6cps, Kollicoat IR, Kollidon VA 64 and HPC), and as an excipient poloxamer were used to prepare solid dispersion. Paddle type dissolution apparatus was used to study in-vitro dissolution rate, where paddle speed was 75 rpm. at 37°C. The dissolution samples were then analyzed spectrophotometrically by UV-VIS spectrophotometer. At first we tried to identify the effect of poloxamer 407, then with poloxamer others polymer were applied to find out their effect on drugs. Through the entire study, we searched for the suitable polymer and excipient with their proportion in a formulation which would show the best beneficial effect on drugs dissolution rate.

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing Apr 2012, 2012

    3848498642 / 9783848498642

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    Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000

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    Condizione: Nuovo

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    Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Solid dispersion technology has proved to be a powerful technique in the field of drug delivery of poorly water soluble drugs by enhancing the dissolution rate and bioavailability of that drug. Here we used four drugs namely Spironolactone, Etoricoxib, Ibuprofen and Carvedilol. Solid dispersions were prepared by solvent co-precipitation method, where acetone was used as solvent and pet-ether was used as anti solvent. Different water soluble polymer (HPMC 6cps, Kollicoat IR, Kollidon VA 64 and HPC), and as an excipient poloxamer were used to prepare solid dispersion. Paddle type dissolution apparatus was used to study in-vitro dissolution rate, where paddle speed was 75 rpm. at 37°C. The dissolution samples were then analyzed spectrophotometrically by UV-VIS spectrophotometer. At first we tried to identify the effect of poloxamer 407, then with poloxamer others polymer were applied to find out their effect on drugs. Through the entire study, we searched for the suitable polymer and excipient with their proportion in a formulation which would show the best beneficial effect on drugs¿ dissolution rate.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 192 pp. Englisch.