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Synthesis and Characterization of a pH- and Temperature-Sensitive Fe(3)O(4)-SiO(2)-Poly(NVCL-co-MAA) Nanocomposite for Controlled Delivery of Doxorubicin Anticancer Drug

This work reports the synthesis, characterization, and in vitro release studies of pH- and temperature-sensitive Fe(3)O(4)-SiO(2)-poly(NVCL-co-MAA) nanocomposite. Fe(3)O(4) nanoparticles were prepared by chemical coprecipitation, coated with SiO(2) by the Stöber method, and functionalized with vinyl...

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Autores principales: Sánchez-Orozco, Jorge Luis, Meléndez-Ortiz, Héctor Iván, Puente-Urbina, Bertha Alicia, Rodríguez-Fernández, Oliverio Santiago, Martínez-Luévanos, Antonia, García-Cerda, Luis Alfonso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963235/
https://www.ncbi.nlm.nih.gov/pubmed/36850252
http://dx.doi.org/10.3390/polym15040968
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author Sánchez-Orozco, Jorge Luis
Meléndez-Ortiz, Héctor Iván
Puente-Urbina, Bertha Alicia
Rodríguez-Fernández, Oliverio Santiago
Martínez-Luévanos, Antonia
García-Cerda, Luis Alfonso
author_facet Sánchez-Orozco, Jorge Luis
Meléndez-Ortiz, Héctor Iván
Puente-Urbina, Bertha Alicia
Rodríguez-Fernández, Oliverio Santiago
Martínez-Luévanos, Antonia
García-Cerda, Luis Alfonso
author_sort Sánchez-Orozco, Jorge Luis
collection PubMed
description This work reports the synthesis, characterization, and in vitro release studies of pH- and temperature-sensitive Fe(3)O(4)-SiO(2)-poly(NVCL-co-MAA) nanocomposite. Fe(3)O(4) nanoparticles were prepared by chemical coprecipitation, coated with SiO(2) by the Stöber method, and functionalized with vinyl groups. The copolymer poly(N-vinylcaprolactam-co-methacrylic acid) (poly(NVCL-co-MAA)) was grafted onto the functionalized Fe(3)O(4)-SiO(2) nanoparticles by free radical polymerization. XRD, FTIR, TGA, VSM, and TEM techniques were performed to characterize the nanocomposite. The release behavior of Doxorubicin (DOX) loaded in the nanocomposite at pH 5.8 and 7.4, and two temperatures, 25 and 37 °C, was studied. According to the release studies, approximately 55% of DOX is released in 72 h at pH 7.4, regardless of temperature. At pH 5.8, 78% of DOX was released in 48 h at 25 °C, and when increasing the temperature to 37 °C, more than 95 % of DOX was released in 24 h. The DOX release data treated with Zero-order, first-order, Higuchi, and Korsmeyer–Peppas models showed that Higuchi’s model best fits the data, indicating that the DOX is released by diffusion. The findings suggest that the synthesized nanocomposite may be useful as a DOX carrier in biomedical applications.
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spelling pubmed-99632352023-02-26 Synthesis and Characterization of a pH- and Temperature-Sensitive Fe(3)O(4)-SiO(2)-Poly(NVCL-co-MAA) Nanocomposite for Controlled Delivery of Doxorubicin Anticancer Drug Sánchez-Orozco, Jorge Luis Meléndez-Ortiz, Héctor Iván Puente-Urbina, Bertha Alicia Rodríguez-Fernández, Oliverio Santiago Martínez-Luévanos, Antonia García-Cerda, Luis Alfonso Polymers (Basel) Article This work reports the synthesis, characterization, and in vitro release studies of pH- and temperature-sensitive Fe(3)O(4)-SiO(2)-poly(NVCL-co-MAA) nanocomposite. Fe(3)O(4) nanoparticles were prepared by chemical coprecipitation, coated with SiO(2) by the Stöber method, and functionalized with vinyl groups. The copolymer poly(N-vinylcaprolactam-co-methacrylic acid) (poly(NVCL-co-MAA)) was grafted onto the functionalized Fe(3)O(4)-SiO(2) nanoparticles by free radical polymerization. XRD, FTIR, TGA, VSM, and TEM techniques were performed to characterize the nanocomposite. The release behavior of Doxorubicin (DOX) loaded in the nanocomposite at pH 5.8 and 7.4, and two temperatures, 25 and 37 °C, was studied. According to the release studies, approximately 55% of DOX is released in 72 h at pH 7.4, regardless of temperature. At pH 5.8, 78% of DOX was released in 48 h at 25 °C, and when increasing the temperature to 37 °C, more than 95 % of DOX was released in 24 h. The DOX release data treated with Zero-order, first-order, Higuchi, and Korsmeyer–Peppas models showed that Higuchi’s model best fits the data, indicating that the DOX is released by diffusion. The findings suggest that the synthesized nanocomposite may be useful as a DOX carrier in biomedical applications. MDPI 2023-02-15 /pmc/articles/PMC9963235/ /pubmed/36850252 http://dx.doi.org/10.3390/polym15040968 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sánchez-Orozco, Jorge Luis
Meléndez-Ortiz, Héctor Iván
Puente-Urbina, Bertha Alicia
Rodríguez-Fernández, Oliverio Santiago
Martínez-Luévanos, Antonia
García-Cerda, Luis Alfonso
Synthesis and Characterization of a pH- and Temperature-Sensitive Fe(3)O(4)-SiO(2)-Poly(NVCL-co-MAA) Nanocomposite for Controlled Delivery of Doxorubicin Anticancer Drug
title Synthesis and Characterization of a pH- and Temperature-Sensitive Fe(3)O(4)-SiO(2)-Poly(NVCL-co-MAA) Nanocomposite for Controlled Delivery of Doxorubicin Anticancer Drug
title_full Synthesis and Characterization of a pH- and Temperature-Sensitive Fe(3)O(4)-SiO(2)-Poly(NVCL-co-MAA) Nanocomposite for Controlled Delivery of Doxorubicin Anticancer Drug
title_fullStr Synthesis and Characterization of a pH- and Temperature-Sensitive Fe(3)O(4)-SiO(2)-Poly(NVCL-co-MAA) Nanocomposite for Controlled Delivery of Doxorubicin Anticancer Drug
title_full_unstemmed Synthesis and Characterization of a pH- and Temperature-Sensitive Fe(3)O(4)-SiO(2)-Poly(NVCL-co-MAA) Nanocomposite for Controlled Delivery of Doxorubicin Anticancer Drug
title_short Synthesis and Characterization of a pH- and Temperature-Sensitive Fe(3)O(4)-SiO(2)-Poly(NVCL-co-MAA) Nanocomposite for Controlled Delivery of Doxorubicin Anticancer Drug
title_sort synthesis and characterization of a ph- and temperature-sensitive fe(3)o(4)-sio(2)-poly(nvcl-co-maa) nanocomposite for controlled delivery of doxorubicin anticancer drug
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963235/
https://www.ncbi.nlm.nih.gov/pubmed/36850252
http://dx.doi.org/10.3390/polym15040968
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