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A review on proniosomal drug delivery system for targeted drug action

Proniosomes are dry formulation of water soluble carrier particles that are coated with surfactant. They are rehydrated to form niosomal dispersion immediately before use on agitation in hot aqueous media within minutes. Proniosomes are physically stable during the storage and transport. Drug encaps...

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Detalles Bibliográficos
Autores principales: Radha, G. V., Rani, T. Sudha, Sarvani, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979263/
https://www.ncbi.nlm.nih.gov/pubmed/24808669
http://dx.doi.org/10.4103/0976-0105.113609
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author Radha, G. V.
Rani, T. Sudha
Sarvani, B.
author_facet Radha, G. V.
Rani, T. Sudha
Sarvani, B.
author_sort Radha, G. V.
collection PubMed
description Proniosomes are dry formulation of water soluble carrier particles that are coated with surfactant. They are rehydrated to form niosomal dispersion immediately before use on agitation in hot aqueous media within minutes. Proniosomes are physically stable during the storage and transport. Drug encapsulated in the vesicular structure of proniosomes prolong the existence of drug in the systematic circulation and enhances the penetration into target tissue and reduce toxicity. From a technical point of view, niosomes are promising drug carriers as they possess greater chemical stability and lack of many disadvantages associated with liposomes, such as high- cost and variable purity problems of phospholipids. The present review emphasizes on overall methods of preparation characterization and applicability of proniosomes in targeted drug action.
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spelling pubmed-39792632014-05-07 A review on proniosomal drug delivery system for targeted drug action Radha, G. V. Rani, T. Sudha Sarvani, B. J Basic Clin Pharm Review Article Proniosomes are dry formulation of water soluble carrier particles that are coated with surfactant. They are rehydrated to form niosomal dispersion immediately before use on agitation in hot aqueous media within minutes. Proniosomes are physically stable during the storage and transport. Drug encapsulated in the vesicular structure of proniosomes prolong the existence of drug in the systematic circulation and enhances the penetration into target tissue and reduce toxicity. From a technical point of view, niosomes are promising drug carriers as they possess greater chemical stability and lack of many disadvantages associated with liposomes, such as high- cost and variable purity problems of phospholipids. The present review emphasizes on overall methods of preparation characterization and applicability of proniosomes in targeted drug action. Medknow Publications & Media Pvt Ltd 2013-03 /pmc/articles/PMC3979263/ /pubmed/24808669 http://dx.doi.org/10.4103/0976-0105.113609 Text en Copyright: © Journal of Basic and Clinical Pharmacy http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Radha, G. V.
Rani, T. Sudha
Sarvani, B.
A review on proniosomal drug delivery system for targeted drug action
title A review on proniosomal drug delivery system for targeted drug action
title_full A review on proniosomal drug delivery system for targeted drug action
title_fullStr A review on proniosomal drug delivery system for targeted drug action
title_full_unstemmed A review on proniosomal drug delivery system for targeted drug action
title_short A review on proniosomal drug delivery system for targeted drug action
title_sort review on proniosomal drug delivery system for targeted drug action
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979263/
https://www.ncbi.nlm.nih.gov/pubmed/24808669
http://dx.doi.org/10.4103/0976-0105.113609
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