Isbn: 9786202667678 - development and evaluation of poorly soluble rilpivirine by snedds: self nanoemulsifying drug delivery system (5 risultati)

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  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing Okt 2020, 2020

    6202667672 / 9786202667678

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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 -In this work a SNEDDS formulation of a poorly water-soluble drug, Rilpivirine was developed by using different polymers. The solubility study was conducted to find out the suitable oil, surfactant and co-surfactant for Rilpivirine and was shown good solubility in oil like Captex 355, surfactant Kolliphor RH 40 and co-surfactant Propylene glycol. The drug content of all the formulations was performed. Maximum drug content was found in the formulation F5. The in vitro dissolution studies were performed for all the fifteen SNEDDS formulations. The release from liquid SNEDDS formulation F5 was faster than SNEDDS formulations F1 toF15 indicating the influence of droplet size on the rate of drug dissolution. On the basis of visual observation test and faster dissolution rate, formulation F5 was finalized as optimized formulation. The present exploratory work successfully illustrates the potential utility of liquid SNEDDS formulation for the delivery of poor water-soluble compound such as Rilpivirine. The results from this study demonstrate the utility of SNEDDS to enhance solubility and dissolution of Rilpivirine which may result in improved therapeutic performance. 100 pp. Englisch.…

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2020

    6202667672 / 9786202667678

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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 - In this work a SNEDDS formulation of a poorly water-soluble drug, Rilpivirine was developed by using different polymers. The solubility study was conducted to find out the suitable oil, surfactant and co-surfactant for Rilpivirine and was shown good solubility in oil like Captex 355, surfactant Kolliphor RH 40 and co-surfactant Propylene glycol. The drug content of all the formulations was performed. Maximum drug content was found in the formulation F5. The in vitro dissolution studies were performed for all the fifteen SNEDDS formulations. The release from liquid SNEDDS formulation F5 was faster than SNEDDS formulations F1 toF15 indicating the influence of droplet size on the rate of drug dissolution. On the basis of visual observation test and faster dissolution rate, formulation F5 was finalized as optimized formulation. The present exploratory work successfully illustrates the potential utility of liquid SNEDDS formulation for the delivery of poor water-soluble compound such as Rilpivirine. The results from this study demonstrate the utility of SNEDDS to enhance solubility and dissolution of Rilpivirine which may result in improved therapeutic performance.…

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2020

    6202667672 / 9786202667678

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    Da: moluna, Greven, Germaniamoluna

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    Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Sandhya PamuDr. Pamu Sandhya, M. Pharm, Ph.D, Head, Department of Pharmaceutics, at Shadan Women s College of Pharmacy, Hyderabad. She has research experience in NDDS by using QbD. She published 62 research papers in reputed Internat.…

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing Okt 2020, 2020

    6202667672 / 9786202667678

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    Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000

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    Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -In this work a SNEDDS formulation of a poorly water-soluble drug, Rilpivirine was developed by using different polymers. The solubility study was conducted to find out the suitable oil, surfactant and co-surfactant for Rilpivirine and was shown good solubility in oil like Captex 355, surfactant Kolliphor RH 40 and co-surfactant Propylene glycol. The drug content of all the formulations was performed. Maximum drug content was found in the formulation F5. The in vitro dissolution studies were performed for all the fifteen SNEDDS formulations. The release from liquid SNEDDS formulation F5 was faster than SNEDDS formulations F1 toF15 indicating the influence of droplet size on the rate of drug dissolution. On the basis of visual observation test and faster dissolution rate, formulation F5 was finalized as optimized formulation. The present exploratory work successfully illustrates the potential utility of liquid SNEDDS formulation for the delivery of poor water-soluble compound such as Rilpivirine. The results from this study demonstrate the utility of SNEDDS to enhance solubility and dissolution of Rilpivirine which may result in improved therapeutic performance.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 100 pp. Englisch.…

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2020

    6202667672 / 9786202667678

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    Da: preigu, Osnabrück, Germaniapreigu

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    Condizione: Nuovo

    EUR 47,20

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    Taschenbuch. Condizione: Neu. Development and Evaluation of Poorly Soluble Rilpivirine by Snedds | Self Nanoemulsifying Drug Delivery System | Pamu Sandhya (u. a.) | Taschenbuch | Englisch | 2020 | LAP LAMBERT Academic Publishing | EAN 9786202667678 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu Print on Demand. …