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Core–Shell Nanoparticles as an Efficient, Sustained, and Triggered Drug-Delivery System
[Image: see text] One of the challenges in designing a successful drug-delivery vehicle is the control over drug release. Toward this, a number of multifunctional nanoparticles with multiple triggers and complex chemistries have been developed. To achieve an efficient and maximum therapeutic effect,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044672/ https://www.ncbi.nlm.nih.gov/pubmed/30023520 http://dx.doi.org/10.1021/acsomega.7b01016 |
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author | Deshpande, Sonal Sharma, Sapna Koul, Veena Singh, Neetu |
author_facet | Deshpande, Sonal Sharma, Sapna Koul, Veena Singh, Neetu |
author_sort | Deshpande, Sonal |
collection | PubMed |
description | [Image: see text] One of the challenges in designing a successful drug-delivery vehicle is the control over drug release. Toward this, a number of multifunctional nanoparticles with multiple triggers and complex chemistries have been developed. To achieve an efficient and maximum therapeutic effect, a trigger dependent drug-delivery system with sustained release is desirable. In this paper, we report the use of a combination of thermoresponsive gold core and polymeric shell nanoparticles that can provide a sustained, triggered release of doxorubicin, making the system more efficient compared to individual nanoparticles. The selection of the system was dependent on the best trigger applicable in biological systems and a component responsive to that trigger. Because of the best tissue penetration depth observed for radiofrequency (rf), we chose rf as a trigger. Whereas the gold nanoparticles (AuNPs) provided hyperthermia trigger on exposure to rf fields, the thermoresponsiveness was endowed by poly(N-isopropylacrylamide) (pNIPAm)-based polymer shells. AuNPs with three different compositions of shells, only pNIPAm and p(NIPAm-co-NIPMAm) with the ratio of NIPAm/N-(isopropylmethacrylamide) (NIPMAm) 1:1 (pNIPMAm(50)) and 1:3 (pNIPMAm(75)), were synthesized. We observed that the polymer coating on the AuNPs did not affect the heating efficiency of AuNPs by rf and exhibited a temperature-dependent release of the chemotherapeutic drug, doxorubicin. The nanoparticles were biocompatible, stable in biologically relevant media, and were able to show a burst as well as a sustained release, which was rf-dependent. Interestingly, we observed that when HeLa cells were treated with doxorubicin-loaded gold core–polymeric shell NPs and exposed to rf for varying times, the mixture of the two polymeric shell nanoparticles induced more cell death as compared to the cells treated with single nanoparticles, suggesting that such multi-nanoparticle systems can be more efficacious delivery systems instead of a single multicomponent system. |
format | Online Article Text |
id | pubmed-6044672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60446722018-07-16 Core–Shell Nanoparticles as an Efficient, Sustained, and Triggered Drug-Delivery System Deshpande, Sonal Sharma, Sapna Koul, Veena Singh, Neetu ACS Omega [Image: see text] One of the challenges in designing a successful drug-delivery vehicle is the control over drug release. Toward this, a number of multifunctional nanoparticles with multiple triggers and complex chemistries have been developed. To achieve an efficient and maximum therapeutic effect, a trigger dependent drug-delivery system with sustained release is desirable. In this paper, we report the use of a combination of thermoresponsive gold core and polymeric shell nanoparticles that can provide a sustained, triggered release of doxorubicin, making the system more efficient compared to individual nanoparticles. The selection of the system was dependent on the best trigger applicable in biological systems and a component responsive to that trigger. Because of the best tissue penetration depth observed for radiofrequency (rf), we chose rf as a trigger. Whereas the gold nanoparticles (AuNPs) provided hyperthermia trigger on exposure to rf fields, the thermoresponsiveness was endowed by poly(N-isopropylacrylamide) (pNIPAm)-based polymer shells. AuNPs with three different compositions of shells, only pNIPAm and p(NIPAm-co-NIPMAm) with the ratio of NIPAm/N-(isopropylmethacrylamide) (NIPMAm) 1:1 (pNIPMAm(50)) and 1:3 (pNIPMAm(75)), were synthesized. We observed that the polymer coating on the AuNPs did not affect the heating efficiency of AuNPs by rf and exhibited a temperature-dependent release of the chemotherapeutic drug, doxorubicin. The nanoparticles were biocompatible, stable in biologically relevant media, and were able to show a burst as well as a sustained release, which was rf-dependent. Interestingly, we observed that when HeLa cells were treated with doxorubicin-loaded gold core–polymeric shell NPs and exposed to rf for varying times, the mixture of the two polymeric shell nanoparticles induced more cell death as compared to the cells treated with single nanoparticles, suggesting that such multi-nanoparticle systems can be more efficacious delivery systems instead of a single multicomponent system. American Chemical Society 2017-10-06 /pmc/articles/PMC6044672/ /pubmed/30023520 http://dx.doi.org/10.1021/acsomega.7b01016 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Deshpande, Sonal Sharma, Sapna Koul, Veena Singh, Neetu Core–Shell Nanoparticles as an Efficient, Sustained, and Triggered Drug-Delivery System |
title | Core–Shell Nanoparticles as an Efficient, Sustained,
and Triggered Drug-Delivery
System |
title_full | Core–Shell Nanoparticles as an Efficient, Sustained,
and Triggered Drug-Delivery
System |
title_fullStr | Core–Shell Nanoparticles as an Efficient, Sustained,
and Triggered Drug-Delivery
System |
title_full_unstemmed | Core–Shell Nanoparticles as an Efficient, Sustained,
and Triggered Drug-Delivery
System |
title_short | Core–Shell Nanoparticles as an Efficient, Sustained,
and Triggered Drug-Delivery
System |
title_sort | core–shell nanoparticles as an efficient, sustained,
and triggered drug-delivery
system |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044672/ https://www.ncbi.nlm.nih.gov/pubmed/30023520 http://dx.doi.org/10.1021/acsomega.7b01016 |
work_keys_str_mv | AT deshpandesonal coreshellnanoparticlesasanefficientsustainedandtriggereddrugdeliverysystem AT sharmasapna coreshellnanoparticlesasanefficientsustainedandtriggereddrugdeliverysystem AT koulveena coreshellnanoparticlesasanefficientsustainedandtriggereddrugdeliverysystem AT singhneetu coreshellnanoparticlesasanefficientsustainedandtriggereddrugdeliverysystem |