Cargando…

Dual drug-loaded nanoparticles on self-integrated scaffold for controlled delivery

Antioxidant (quercetin) and hypoglycemic (voglibose) drug-loaded poly-D,L-lactideco-glycolide nanoparticles were successfully synthesized using the solvent evaporation method. The dual drug-loaded nanoparticles were incorporated into a scaffold film using a solvent casting method, creating a control...

Descripción completa

Detalles Bibliográficos
Autores principales: Bennet, Devasier, Marimuthu, Mohana, Kim, Sanghyo, An, Jeongho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414208/
https://www.ncbi.nlm.nih.gov/pubmed/22888222
http://dx.doi.org/10.2147/IJN.S32800
_version_ 1782240174277656576
author Bennet, Devasier
Marimuthu, Mohana
Kim, Sanghyo
An, Jeongho
author_facet Bennet, Devasier
Marimuthu, Mohana
Kim, Sanghyo
An, Jeongho
author_sort Bennet, Devasier
collection PubMed
description Antioxidant (quercetin) and hypoglycemic (voglibose) drug-loaded poly-D,L-lactideco-glycolide nanoparticles were successfully synthesized using the solvent evaporation method. The dual drug-loaded nanoparticles were incorporated into a scaffold film using a solvent casting method, creating a controlled transdermal drug-delivery system. Key features of the film formulation were achieved utilizing several ratios of excipients, including polyvinyl alcohol, polyethylene glycol, hyaluronic acid, xylitol, and alginate. The scaffold film showed superior encapsulation capability and swelling properties, with various potential applications, eg, the treatment of diabetes-associated complications. Structural and light scattering characterization confirmed a spherical shape and a mean particle size distribution of 41.3 nm for nanoparticles in the scaffold film. Spectroscopy revealed a stable polymer structure before and after encapsulation. The thermoresponsive swelling properties of the film were evaluated according to temperature and pH. Scaffold films incorporating dual drug-loaded nanoparticles showed remarkably high thermoresponsivity, cell compatibility, and ex vivo drug-release behavior. In addition, the hybrid film formulation showed enhanced cell adhesion and proliferation. These dual drug-loaded nanoparticles incorporated into a scaffold film may be promising for development into a transdermal drug-delivery system.
format Online
Article
Text
id pubmed-3414208
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-34142082012-08-10 Dual drug-loaded nanoparticles on self-integrated scaffold for controlled delivery Bennet, Devasier Marimuthu, Mohana Kim, Sanghyo An, Jeongho Int J Nanomedicine Original Research Antioxidant (quercetin) and hypoglycemic (voglibose) drug-loaded poly-D,L-lactideco-glycolide nanoparticles were successfully synthesized using the solvent evaporation method. The dual drug-loaded nanoparticles were incorporated into a scaffold film using a solvent casting method, creating a controlled transdermal drug-delivery system. Key features of the film formulation were achieved utilizing several ratios of excipients, including polyvinyl alcohol, polyethylene glycol, hyaluronic acid, xylitol, and alginate. The scaffold film showed superior encapsulation capability and swelling properties, with various potential applications, eg, the treatment of diabetes-associated complications. Structural and light scattering characterization confirmed a spherical shape and a mean particle size distribution of 41.3 nm for nanoparticles in the scaffold film. Spectroscopy revealed a stable polymer structure before and after encapsulation. The thermoresponsive swelling properties of the film were evaluated according to temperature and pH. Scaffold films incorporating dual drug-loaded nanoparticles showed remarkably high thermoresponsivity, cell compatibility, and ex vivo drug-release behavior. In addition, the hybrid film formulation showed enhanced cell adhesion and proliferation. These dual drug-loaded nanoparticles incorporated into a scaffold film may be promising for development into a transdermal drug-delivery system. Dove Medical Press 2012 2012-07-16 /pmc/articles/PMC3414208/ /pubmed/22888222 http://dx.doi.org/10.2147/IJN.S32800 Text en © 2012 Bennet et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Bennet, Devasier
Marimuthu, Mohana
Kim, Sanghyo
An, Jeongho
Dual drug-loaded nanoparticles on self-integrated scaffold for controlled delivery
title Dual drug-loaded nanoparticles on self-integrated scaffold for controlled delivery
title_full Dual drug-loaded nanoparticles on self-integrated scaffold for controlled delivery
title_fullStr Dual drug-loaded nanoparticles on self-integrated scaffold for controlled delivery
title_full_unstemmed Dual drug-loaded nanoparticles on self-integrated scaffold for controlled delivery
title_short Dual drug-loaded nanoparticles on self-integrated scaffold for controlled delivery
title_sort dual drug-loaded nanoparticles on self-integrated scaffold for controlled delivery
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414208/
https://www.ncbi.nlm.nih.gov/pubmed/22888222
http://dx.doi.org/10.2147/IJN.S32800
work_keys_str_mv AT bennetdevasier dualdrugloadednanoparticlesonselfintegratedscaffoldforcontrolleddelivery
AT marimuthumohana dualdrugloadednanoparticlesonselfintegratedscaffoldforcontrolleddelivery
AT kimsanghyo dualdrugloadednanoparticlesonselfintegratedscaffoldforcontrolleddelivery
AT anjeongho dualdrugloadednanoparticlesonselfintegratedscaffoldforcontrolleddelivery