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Injectable Thermosensitive Nanocomposites Based on Poly(N-vinylcaprolactam) and Silica Particles for Localized Release of Hydrophilic and Hydrophobic Drugs
[Image: see text] The systemic delivery of drugs employed by conventional methods has shown to be less effective than a localized delivery system. Many drugs have the effectiveness reduced by fast clearance, increasing the amount required for an efficient treatment. One way to overcome this drawback...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933531/ https://www.ncbi.nlm.nih.gov/pubmed/36744422 http://dx.doi.org/10.1021/acs.langmuir.2c03160 |
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author | Ribeiro, Lucas S. Sala, Renata L. Robeldo, Thaiane A. Borra, Ricardo C. Camargo, Emerson R. |
author_facet | Ribeiro, Lucas S. Sala, Renata L. Robeldo, Thaiane A. Borra, Ricardo C. Camargo, Emerson R. |
author_sort | Ribeiro, Lucas S. |
collection | PubMed |
description | [Image: see text] The systemic delivery of drugs employed by conventional methods has shown to be less effective than a localized delivery system. Many drugs have the effectiveness reduced by fast clearance, increasing the amount required for an efficient treatment. One way to overcome this drawback is through the use of thermoresponsive polymers that undergo a sol–gel transition at physiological temperature, allowing their injection directly in the desired site. In this work, thermosensitive nanocomposites based on poly(N-vinylcaprolactam) and silica particles with 80 and 330 nm were synthesized to be employed as delivery systems for hydrophobic (naringin) and hydrophilic (doxorubicin hydrochloride) drugs. The insertion of SiO(2) increased the rheological properties of the nanocomposite at 37 °C, which helps to prevent its diffusion away from the site of injection. The synthesized materials were also able to control the drug release for a period of 7 days under physiological conditions. Due to its higher hydrophobicity and better interaction with the PNVCL matrix, naringin presented a more controlled release. The Korsmeyer–Peppas model indicated different release mechanisms for each drug. At last, a preliminary in vitro study of DOX-loaded nanocomposites cultured with L929 and MB49 cells showed negligible toxic effects on healthy cells and better efficient inhibition of carcinoma cells. |
format | Online Article Text |
id | pubmed-9933531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99335312023-02-17 Injectable Thermosensitive Nanocomposites Based on Poly(N-vinylcaprolactam) and Silica Particles for Localized Release of Hydrophilic and Hydrophobic Drugs Ribeiro, Lucas S. Sala, Renata L. Robeldo, Thaiane A. Borra, Ricardo C. Camargo, Emerson R. Langmuir [Image: see text] The systemic delivery of drugs employed by conventional methods has shown to be less effective than a localized delivery system. Many drugs have the effectiveness reduced by fast clearance, increasing the amount required for an efficient treatment. One way to overcome this drawback is through the use of thermoresponsive polymers that undergo a sol–gel transition at physiological temperature, allowing their injection directly in the desired site. In this work, thermosensitive nanocomposites based on poly(N-vinylcaprolactam) and silica particles with 80 and 330 nm were synthesized to be employed as delivery systems for hydrophobic (naringin) and hydrophilic (doxorubicin hydrochloride) drugs. The insertion of SiO(2) increased the rheological properties of the nanocomposite at 37 °C, which helps to prevent its diffusion away from the site of injection. The synthesized materials were also able to control the drug release for a period of 7 days under physiological conditions. Due to its higher hydrophobicity and better interaction with the PNVCL matrix, naringin presented a more controlled release. The Korsmeyer–Peppas model indicated different release mechanisms for each drug. At last, a preliminary in vitro study of DOX-loaded nanocomposites cultured with L929 and MB49 cells showed negligible toxic effects on healthy cells and better efficient inhibition of carcinoma cells. American Chemical Society 2023-02-06 /pmc/articles/PMC9933531/ /pubmed/36744422 http://dx.doi.org/10.1021/acs.langmuir.2c03160 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Ribeiro, Lucas S. Sala, Renata L. Robeldo, Thaiane A. Borra, Ricardo C. Camargo, Emerson R. Injectable Thermosensitive Nanocomposites Based on Poly(N-vinylcaprolactam) and Silica Particles for Localized Release of Hydrophilic and Hydrophobic Drugs |
title | Injectable
Thermosensitive Nanocomposites Based on
Poly(N-vinylcaprolactam) and Silica Particles
for Localized Release of Hydrophilic and Hydrophobic Drugs |
title_full | Injectable
Thermosensitive Nanocomposites Based on
Poly(N-vinylcaprolactam) and Silica Particles
for Localized Release of Hydrophilic and Hydrophobic Drugs |
title_fullStr | Injectable
Thermosensitive Nanocomposites Based on
Poly(N-vinylcaprolactam) and Silica Particles
for Localized Release of Hydrophilic and Hydrophobic Drugs |
title_full_unstemmed | Injectable
Thermosensitive Nanocomposites Based on
Poly(N-vinylcaprolactam) and Silica Particles
for Localized Release of Hydrophilic and Hydrophobic Drugs |
title_short | Injectable
Thermosensitive Nanocomposites Based on
Poly(N-vinylcaprolactam) and Silica Particles
for Localized Release of Hydrophilic and Hydrophobic Drugs |
title_sort | injectable
thermosensitive nanocomposites based on
poly(n-vinylcaprolactam) and silica particles
for localized release of hydrophilic and hydrophobic drugs |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933531/ https://www.ncbi.nlm.nih.gov/pubmed/36744422 http://dx.doi.org/10.1021/acs.langmuir.2c03160 |
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