Development and Characterization of Sodium Alginate-Hydroxypropyl Methylcellulose-Polyester Multilayered Hydrogel Membranes for Drug Delivery through Skin.

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Title: Development and Characterization of Sodium Alginate-Hydroxypropyl Methylcellulose-Polyester Multilayered Hydrogel Membranes for Drug Delivery through Skin.
Authors: Kulkarni, Raghavendra V.1, Wagh, Yogesh J.1, Setty, C. Mallikarjun2, Sa, Biswanath3
Source: Polymer-Plastics Technology & Engineering. Mar2011, Vol. 50 Issue 5, p490-497. 8p. 1 Black and White Photograph, 1 Diagram, 2 Charts, 7 Graphs.
Subjects: Sodium alginate, Cellulose, Polyesters, Artificial membranes, Drug delivery systems, Skin, Diethylamine, Anti-inflammatory agents, Permeability
Abstract: The multi-layered hydrogel membranes of sodium alginate-hydroxypropyl methylcellulose-polyester were developed for controlled delivery of anti-inflammatory drug, diclofenac diethylamine through intact skin. The XRD studies indicated the amorphous dispersion of drug in the membranes. DSC analysis suggested that as cross-linking increases, the stiffer membranes were formed. The prepared membranes were permeable to water vapors depending upon the cross-link density. The in vitro drug diffusion through excised rat abdominal skin depends on the cross-link density and polymer concentration. The primary skin irritation study indicated that the prepared membranes were less irritant and safe for drug delivery across the skin. [ABSTRACT FROM AUTHOR]
Copyright of Polymer-Plastics Technology & Engineering is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Development and Characterization of Sodium Alginate-Hydroxypropyl Methylcellulose-Polyester Multilayered Hydrogel Membranes for Drug Delivery through Skin.
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  Data: <searchLink fieldCode="AR" term="%22Kulkarni%2C+Raghavendra+V%2E%22">Kulkarni, Raghavendra V.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Wagh%2C+Yogesh+J%2E%22">Wagh, Yogesh J.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Setty%2C+C%2E+Mallikarjun%22">Setty, C. Mallikarjun</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Sa%2C+Biswanath%22">Sa, Biswanath</searchLink><relatesTo>3</relatesTo>
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  Data: <searchLink fieldCode="JN" term="%22Polymer-Plastics+Technology+%26+Engineering%22">Polymer-Plastics Technology & Engineering</searchLink>. Mar2011, Vol. 50 Issue 5, p490-497. 8p. 1 Black and White Photograph, 1 Diagram, 2 Charts, 7 Graphs.
– Name: Subject
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  Data: <searchLink fieldCode="DE" term="%22Sodium+alginate%22">Sodium alginate</searchLink><br /><searchLink fieldCode="DE" term="%22Cellulose%22">Cellulose</searchLink><br /><searchLink fieldCode="DE" term="%22Polyesters%22">Polyesters</searchLink><br /><searchLink fieldCode="DE" term="%22Artificial+membranes%22">Artificial membranes</searchLink><br /><searchLink fieldCode="DE" term="%22Drug+delivery+systems%22">Drug delivery systems</searchLink><br /><searchLink fieldCode="DE" term="%22Skin%22">Skin</searchLink><br /><searchLink fieldCode="DE" term="%22Diethylamine%22">Diethylamine</searchLink><br /><searchLink fieldCode="DE" term="%22Anti-inflammatory+agents%22">Anti-inflammatory agents</searchLink><br /><searchLink fieldCode="DE" term="%22Permeability%22">Permeability</searchLink>
– Name: Abstract
  Label: Abstract
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  Data: The multi-layered hydrogel membranes of sodium alginate-hydroxypropyl methylcellulose-polyester were developed for controlled delivery of anti-inflammatory drug, diclofenac diethylamine through intact skin. The XRD studies indicated the amorphous dispersion of drug in the membranes. DSC analysis suggested that as cross-linking increases, the stiffer membranes were formed. The prepared membranes were permeable to water vapors depending upon the cross-link density. The in vitro drug diffusion through excised rat abdominal skin depends on the cross-link density and polymer concentration. The primary skin irritation study indicated that the prepared membranes were less irritant and safe for drug delivery across the skin. [ABSTRACT FROM AUTHOR]
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  Data: <i>Copyright of Polymer-Plastics Technology & Engineering is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1080/03602559.2010.543244
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      – Code: eng
        Text: English
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      Pagination:
        PageCount: 8
        StartPage: 490
    Subjects:
      – SubjectFull: Sodium alginate
        Type: general
      – SubjectFull: Cellulose
        Type: general
      – SubjectFull: Polyesters
        Type: general
      – SubjectFull: Artificial membranes
        Type: general
      – SubjectFull: Drug delivery systems
        Type: general
      – SubjectFull: Skin
        Type: general
      – SubjectFull: Diethylamine
        Type: general
      – SubjectFull: Anti-inflammatory agents
        Type: general
      – SubjectFull: Permeability
        Type: general
    Titles:
      – TitleFull: Development and Characterization of Sodium Alginate-Hydroxypropyl Methylcellulose-Polyester Multilayered Hydrogel Membranes for Drug Delivery through Skin.
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            NameFull: Kulkarni, Raghavendra V.
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            NameFull: Wagh, Yogesh J.
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            NameFull: Setty, C. Mallikarjun
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            NameFull: Sa, Biswanath
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              Text: Mar2011
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              Y: 2011
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