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Accessing the biocompatibility of layered double hydroxide by intramuscular implantation: histological and microcirculation evaluation
Biocompatibility of layered double hydroxides (LDHs), also known as hydrotalcite-like materials or double metal hydroxides, was investigated by in vivo assays via intramuscular tablets implantation in rat abdominal wall. The tablets were composed by chloride ions intercalated into LDH of magnesium/a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969587/ https://www.ncbi.nlm.nih.gov/pubmed/27480483 http://dx.doi.org/10.1038/srep30547 |
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author | Cunha, Vanessa Roberta Rodrigues de Souza, Rodrigo Barbosa da Fonseca Martins, Ana Maria Cristina Rebello Pinto Koh, Ivan Hong Jun Constantino, Vera Regina Leopoldo |
author_facet | Cunha, Vanessa Roberta Rodrigues de Souza, Rodrigo Barbosa da Fonseca Martins, Ana Maria Cristina Rebello Pinto Koh, Ivan Hong Jun Constantino, Vera Regina Leopoldo |
author_sort | Cunha, Vanessa Roberta Rodrigues |
collection | PubMed |
description | Biocompatibility of layered double hydroxides (LDHs), also known as hydrotalcite-like materials or double metal hydroxides, was investigated by in vivo assays via intramuscular tablets implantation in rat abdominal wall. The tablets were composed by chloride ions intercalated into LDH of magnesium/aluminum (Mg(2)Al-Cl) and zinc/aluminum (Zn(2)Al-Cl). The antigenicity and tissue integration capacity of LDHs were assessed histologically after 7 and 28 days post-implantation. No fibrous capsule nearby the LDH was noticed for both materials as well any sign of inflammatory reactions. Sidestream Dark Field imaging, used to monitor in real time the microcirculation in tissues, revealed overall integrity of the microcirculatory network neighboring the tablets, with no blood flow obstruction, bleeding and/or increasing of leukocyte endothelial adhesion. After 28 days Mg(2)Al-Cl promoted multiple collagen invaginations (mostly collagen type-I) among its fragments while Zn(2)Al-Cl induced predominantly collagen type–III. This work supports previous results in the literature about LDHs compatibility with living matter, endorsing them as functional materials for biomedical applications. |
format | Online Article Text |
id | pubmed-4969587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49695872016-08-10 Accessing the biocompatibility of layered double hydroxide by intramuscular implantation: histological and microcirculation evaluation Cunha, Vanessa Roberta Rodrigues de Souza, Rodrigo Barbosa da Fonseca Martins, Ana Maria Cristina Rebello Pinto Koh, Ivan Hong Jun Constantino, Vera Regina Leopoldo Sci Rep Article Biocompatibility of layered double hydroxides (LDHs), also known as hydrotalcite-like materials or double metal hydroxides, was investigated by in vivo assays via intramuscular tablets implantation in rat abdominal wall. The tablets were composed by chloride ions intercalated into LDH of magnesium/aluminum (Mg(2)Al-Cl) and zinc/aluminum (Zn(2)Al-Cl). The antigenicity and tissue integration capacity of LDHs were assessed histologically after 7 and 28 days post-implantation. No fibrous capsule nearby the LDH was noticed for both materials as well any sign of inflammatory reactions. Sidestream Dark Field imaging, used to monitor in real time the microcirculation in tissues, revealed overall integrity of the microcirculatory network neighboring the tablets, with no blood flow obstruction, bleeding and/or increasing of leukocyte endothelial adhesion. After 28 days Mg(2)Al-Cl promoted multiple collagen invaginations (mostly collagen type-I) among its fragments while Zn(2)Al-Cl induced predominantly collagen type–III. This work supports previous results in the literature about LDHs compatibility with living matter, endorsing them as functional materials for biomedical applications. Nature Publishing Group 2016-08-02 /pmc/articles/PMC4969587/ /pubmed/27480483 http://dx.doi.org/10.1038/srep30547 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Cunha, Vanessa Roberta Rodrigues de Souza, Rodrigo Barbosa da Fonseca Martins, Ana Maria Cristina Rebello Pinto Koh, Ivan Hong Jun Constantino, Vera Regina Leopoldo Accessing the biocompatibility of layered double hydroxide by intramuscular implantation: histological and microcirculation evaluation |
title | Accessing the biocompatibility of layered double hydroxide by intramuscular implantation: histological and microcirculation evaluation |
title_full | Accessing the biocompatibility of layered double hydroxide by intramuscular implantation: histological and microcirculation evaluation |
title_fullStr | Accessing the biocompatibility of layered double hydroxide by intramuscular implantation: histological and microcirculation evaluation |
title_full_unstemmed | Accessing the biocompatibility of layered double hydroxide by intramuscular implantation: histological and microcirculation evaluation |
title_short | Accessing the biocompatibility of layered double hydroxide by intramuscular implantation: histological and microcirculation evaluation |
title_sort | accessing the biocompatibility of layered double hydroxide by intramuscular implantation: histological and microcirculation evaluation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969587/ https://www.ncbi.nlm.nih.gov/pubmed/27480483 http://dx.doi.org/10.1038/srep30547 |
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