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Hybrid Nanostructures Containing Sulfadiazine Modified Chitosan as Antimicrobial Drug Carriers

Chitosan (CH) nanofibrous structures containing sulfadiazine (SDZ) or sulfadiazine modified chitosan (SCH) in the form of functional nanoparticles attached to nanofibers (hybrid nanostructures) were obtained by mono-axial and coaxial electrospinning. The mono-axial design consisted of a SDZ/CH mixtu...

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Autores principales: Munteanu, Bogdanel Silvestru, Dumitriu, Raluca Petronela, Profire, Lenuta, Sacarescu, Liviu, Hitruc, Gabriela Elena, Stoleru, Elena, Dobromir, Marius, Matricala, Ana Lavinia, Vasile, Cornelia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245742/
https://www.ncbi.nlm.nih.gov/pubmed/28335334
http://dx.doi.org/10.3390/nano6110207
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author Munteanu, Bogdanel Silvestru
Dumitriu, Raluca Petronela
Profire, Lenuta
Sacarescu, Liviu
Hitruc, Gabriela Elena
Stoleru, Elena
Dobromir, Marius
Matricala, Ana Lavinia
Vasile, Cornelia
author_facet Munteanu, Bogdanel Silvestru
Dumitriu, Raluca Petronela
Profire, Lenuta
Sacarescu, Liviu
Hitruc, Gabriela Elena
Stoleru, Elena
Dobromir, Marius
Matricala, Ana Lavinia
Vasile, Cornelia
author_sort Munteanu, Bogdanel Silvestru
collection PubMed
description Chitosan (CH) nanofibrous structures containing sulfadiazine (SDZ) or sulfadiazine modified chitosan (SCH) in the form of functional nanoparticles attached to nanofibers (hybrid nanostructures) were obtained by mono-axial and coaxial electrospinning. The mono-axial design consisted of a SDZ/CH mixture solution fed through a single nozzle while the coaxial design consisted of SCH and CH solutions separately supplied to the inner and outer nozzle (or in reverse order). The CH ability to form nanofibers assured the formation of a nanofiber mesh, while SDZ and SCH, both in form of suspensions in the electrospun solution, assured the formation of active nanoparticles which remained attached to the CH nanofiber mesh after the electrospinning process. The obtained nanostructures were morphologically characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM). The SDZ release profiles and kinetics were analyzed. The SDZ or SCH nanoparticles loosely attached at the surface of the nanofibers, provide a burst release in the first 20 min, which is important to stop the possible initial infection in a wound, while the SDZ and SCH from the nanoparticles which are better confined (or even encapsulated) into the CH nanofibers would be slowly released with the erosion/disruption of the CH nanofiber mesh.
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spelling pubmed-52457422017-03-21 Hybrid Nanostructures Containing Sulfadiazine Modified Chitosan as Antimicrobial Drug Carriers Munteanu, Bogdanel Silvestru Dumitriu, Raluca Petronela Profire, Lenuta Sacarescu, Liviu Hitruc, Gabriela Elena Stoleru, Elena Dobromir, Marius Matricala, Ana Lavinia Vasile, Cornelia Nanomaterials (Basel) Article Chitosan (CH) nanofibrous structures containing sulfadiazine (SDZ) or sulfadiazine modified chitosan (SCH) in the form of functional nanoparticles attached to nanofibers (hybrid nanostructures) were obtained by mono-axial and coaxial electrospinning. The mono-axial design consisted of a SDZ/CH mixture solution fed through a single nozzle while the coaxial design consisted of SCH and CH solutions separately supplied to the inner and outer nozzle (or in reverse order). The CH ability to form nanofibers assured the formation of a nanofiber mesh, while SDZ and SCH, both in form of suspensions in the electrospun solution, assured the formation of active nanoparticles which remained attached to the CH nanofiber mesh after the electrospinning process. The obtained nanostructures were morphologically characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM). The SDZ release profiles and kinetics were analyzed. The SDZ or SCH nanoparticles loosely attached at the surface of the nanofibers, provide a burst release in the first 20 min, which is important to stop the possible initial infection in a wound, while the SDZ and SCH from the nanoparticles which are better confined (or even encapsulated) into the CH nanofibers would be slowly released with the erosion/disruption of the CH nanofiber mesh. MDPI 2016-11-10 /pmc/articles/PMC5245742/ /pubmed/28335334 http://dx.doi.org/10.3390/nano6110207 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Munteanu, Bogdanel Silvestru
Dumitriu, Raluca Petronela
Profire, Lenuta
Sacarescu, Liviu
Hitruc, Gabriela Elena
Stoleru, Elena
Dobromir, Marius
Matricala, Ana Lavinia
Vasile, Cornelia
Hybrid Nanostructures Containing Sulfadiazine Modified Chitosan as Antimicrobial Drug Carriers
title Hybrid Nanostructures Containing Sulfadiazine Modified Chitosan as Antimicrobial Drug Carriers
title_full Hybrid Nanostructures Containing Sulfadiazine Modified Chitosan as Antimicrobial Drug Carriers
title_fullStr Hybrid Nanostructures Containing Sulfadiazine Modified Chitosan as Antimicrobial Drug Carriers
title_full_unstemmed Hybrid Nanostructures Containing Sulfadiazine Modified Chitosan as Antimicrobial Drug Carriers
title_short Hybrid Nanostructures Containing Sulfadiazine Modified Chitosan as Antimicrobial Drug Carriers
title_sort hybrid nanostructures containing sulfadiazine modified chitosan as antimicrobial drug carriers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245742/
https://www.ncbi.nlm.nih.gov/pubmed/28335334
http://dx.doi.org/10.3390/nano6110207
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