Poly(NIPAM-co-MPS)-grafted multimodal porous silica nanoparticles as reverse thermoresponsive drug delivery system

Hybrid drug delivery systems (DDS) have been prepared by grafting poly(NIPAM-co-MPS) chains on multimodal porous silica nanoparticles having an inner mesoporous structure and an outer thin layer of micropores. The hybrid thermoresponsive DDS were fully characterized and loaded with a model drug. The...

Full description

Bibliographic Details
Main Authors: Sushilkumar A. Jadhav, Valentina Brunella, Dominique Scalarone, Gloria Berlier
Format: Article
Language:English
Published: Elsevier 2017-05-01
Series:Asian Journal of Pharmaceutical Sciences
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1818087616302719
id doaj-85f21776ca954ce09a3c7fc4d9f2deb5
record_format Article
spelling doaj-85f21776ca954ce09a3c7fc4d9f2deb52020-11-24T23:22:20ZengElsevierAsian Journal of Pharmaceutical Sciences1818-08762017-05-0112327928410.1016/j.ajps.2017.02.002Poly(NIPAM-co-MPS)-grafted multimodal porous silica nanoparticles as reverse thermoresponsive drug delivery systemSushilkumar A. JadhavValentina BrunellaDominique ScalaroneGloria BerlierHybrid drug delivery systems (DDS) have been prepared by grafting poly(NIPAM-co-MPS) chains on multimodal porous silica nanoparticles having an inner mesoporous structure and an outer thin layer of micropores. The hybrid thermoresponsive DDS were fully characterized and loaded with a model drug. The in vitro drug release tests are carried out at below and above the lower critical solution temperature (LCST) of the copolymer. The results have revealed that due to the presence of small diameter (~1.3 nm) micropores at the periphery of the particles, the collapsed globules of the thermoresponsive copolymer above its LCST hinders the complete release of the drug which resulted in a reverse thermoresponsive drug release profile by the hybrid DDS.http://www.sciencedirect.com/science/article/pii/S1818087616302719Porous silica nanoparticlesThermoresponsive polymerDrug delivery systemIbuprofenDrug loadingDrug release profile
collection DOAJ
language English
format Article
sources DOAJ
author Sushilkumar A. Jadhav
Valentina Brunella
Dominique Scalarone
Gloria Berlier
spellingShingle Sushilkumar A. Jadhav
Valentina Brunella
Dominique Scalarone
Gloria Berlier
Poly(NIPAM-co-MPS)-grafted multimodal porous silica nanoparticles as reverse thermoresponsive drug delivery system
Asian Journal of Pharmaceutical Sciences
Porous silica nanoparticles
Thermoresponsive polymer
Drug delivery system
Ibuprofen
Drug loading
Drug release profile
author_facet Sushilkumar A. Jadhav
Valentina Brunella
Dominique Scalarone
Gloria Berlier
author_sort Sushilkumar A. Jadhav
title Poly(NIPAM-co-MPS)-grafted multimodal porous silica nanoparticles as reverse thermoresponsive drug delivery system
title_short Poly(NIPAM-co-MPS)-grafted multimodal porous silica nanoparticles as reverse thermoresponsive drug delivery system
title_full Poly(NIPAM-co-MPS)-grafted multimodal porous silica nanoparticles as reverse thermoresponsive drug delivery system
title_fullStr Poly(NIPAM-co-MPS)-grafted multimodal porous silica nanoparticles as reverse thermoresponsive drug delivery system
title_full_unstemmed Poly(NIPAM-co-MPS)-grafted multimodal porous silica nanoparticles as reverse thermoresponsive drug delivery system
title_sort poly(nipam-co-mps)-grafted multimodal porous silica nanoparticles as reverse thermoresponsive drug delivery system
publisher Elsevier
series Asian Journal of Pharmaceutical Sciences
issn 1818-0876
publishDate 2017-05-01
description Hybrid drug delivery systems (DDS) have been prepared by grafting poly(NIPAM-co-MPS) chains on multimodal porous silica nanoparticles having an inner mesoporous structure and an outer thin layer of micropores. The hybrid thermoresponsive DDS were fully characterized and loaded with a model drug. The in vitro drug release tests are carried out at below and above the lower critical solution temperature (LCST) of the copolymer. The results have revealed that due to the presence of small diameter (~1.3 nm) micropores at the periphery of the particles, the collapsed globules of the thermoresponsive copolymer above its LCST hinders the complete release of the drug which resulted in a reverse thermoresponsive drug release profile by the hybrid DDS.
topic Porous silica nanoparticles
Thermoresponsive polymer
Drug delivery system
Ibuprofen
Drug loading
Drug release profile
url http://www.sciencedirect.com/science/article/pii/S1818087616302719
work_keys_str_mv AT sushilkumarajadhav polynipamcompsgraftedmultimodalporoussilicananoparticlesasreversethermoresponsivedrugdeliverysystem
AT valentinabrunella polynipamcompsgraftedmultimodalporoussilicananoparticlesasreversethermoresponsivedrugdeliverysystem
AT dominiquescalarone polynipamcompsgraftedmultimodalporoussilicananoparticlesasreversethermoresponsivedrugdeliverysystem
AT gloriaberlier polynipamcompsgraftedmultimodalporoussilicananoparticlesasreversethermoresponsivedrugdeliverysystem
_version_ 1725568506629455872