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Construction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection
INTRODUCTION: Treatment of infection within bone is difficult, and conventional surgical treatment brings intense pain to the patients physically and mentally. There is an urgent need to develop injectable nano- and/or micro-medicine for minimally invasive treatment of osteomyelitis. METHODS: In thi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014387/ https://www.ncbi.nlm.nih.gov/pubmed/29950831 http://dx.doi.org/10.2147/IJN.S157463 |
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author | Chen, Zhenhua Zhao, Mengen Zhang, Jie Zhou, Kang Ren, Xiuli Mei, Xifan |
author_facet | Chen, Zhenhua Zhao, Mengen Zhang, Jie Zhou, Kang Ren, Xiuli Mei, Xifan |
author_sort | Chen, Zhenhua |
collection | PubMed |
description | INTRODUCTION: Treatment of infection within bone is difficult, and conventional surgical treatment brings intense pain to the patients physically and mentally. There is an urgent need to develop injectable nano- and/or micro-medicine for minimally invasive treatment of osteomyelitis. METHODS: In this paper, amino acid (L-lysine [Lys]) was mineralized into yolk-shell structured CaCO(3) microspheres (MSs). The morphologies of the obtained MSs were investigated by scanning electron microscopy and transmission electron microscopy. The composition of CaCO(3) MSs was identified by using Fourier transform infrared spectroscopy. The as-prepared CaCO(3) MSs were examined with power X-ray diffraction analysis to obtain the crystallographic structure of the MSs. RESULTS: The as prepared Lys encapsulated CaCO(3) MSs (Lys@CaCO(3) MSs) were used as micro-drug to improve acidic environment of osteomyelitis caused by bacterial infection and promote osteoblast proliferation under oxidative stress. These pH responsive Lys@CaCO(3) MSs have a drug loading efficiency of 89.8 wt % and drug loading content (DLC) of 22.3 wt %. CONCLUSION: Our results demonstrated that Lys@CaCO(3) MSs can effectively kill Staphylococcus aureus and promote proliferation and differentiation of osteoblasts under stimulation of H(2)O(2) at pH = 5.5. |
format | Online Article Text |
id | pubmed-6014387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60143872018-06-27 Construction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection Chen, Zhenhua Zhao, Mengen Zhang, Jie Zhou, Kang Ren, Xiuli Mei, Xifan Int J Nanomedicine Original Research INTRODUCTION: Treatment of infection within bone is difficult, and conventional surgical treatment brings intense pain to the patients physically and mentally. There is an urgent need to develop injectable nano- and/or micro-medicine for minimally invasive treatment of osteomyelitis. METHODS: In this paper, amino acid (L-lysine [Lys]) was mineralized into yolk-shell structured CaCO(3) microspheres (MSs). The morphologies of the obtained MSs were investigated by scanning electron microscopy and transmission electron microscopy. The composition of CaCO(3) MSs was identified by using Fourier transform infrared spectroscopy. The as-prepared CaCO(3) MSs were examined with power X-ray diffraction analysis to obtain the crystallographic structure of the MSs. RESULTS: The as prepared Lys encapsulated CaCO(3) MSs (Lys@CaCO(3) MSs) were used as micro-drug to improve acidic environment of osteomyelitis caused by bacterial infection and promote osteoblast proliferation under oxidative stress. These pH responsive Lys@CaCO(3) MSs have a drug loading efficiency of 89.8 wt % and drug loading content (DLC) of 22.3 wt %. CONCLUSION: Our results demonstrated that Lys@CaCO(3) MSs can effectively kill Staphylococcus aureus and promote proliferation and differentiation of osteoblasts under stimulation of H(2)O(2) at pH = 5.5. Dove Medical Press 2018-06-18 /pmc/articles/PMC6014387/ /pubmed/29950831 http://dx.doi.org/10.2147/IJN.S157463 Text en © 2018 Chen et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Chen, Zhenhua Zhao, Mengen Zhang, Jie Zhou, Kang Ren, Xiuli Mei, Xifan Construction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection |
title | Construction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection |
title_full | Construction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection |
title_fullStr | Construction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection |
title_full_unstemmed | Construction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection |
title_short | Construction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection |
title_sort | construction of injectable, ph sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014387/ https://www.ncbi.nlm.nih.gov/pubmed/29950831 http://dx.doi.org/10.2147/IJN.S157463 |
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