Construction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection

Zhenhua Chen,* Mengen Zhao,* Jie Zhang, Kang Zhou, Xiuli Ren, Xifan Mei Jinzhou Medical University, Jinzhou, 121001, People’s Republic of China *These authors contributed equally to this work Introduction: Treatment of infection within bone is difficult, and conventional surgical treatm...

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Autores principales: Chen Z, Zhao M, Zhang J, Zhou K, Ren X, Mei X
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Publicado: Dove Medical Press 2018
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spelling oai:doaj.org-article:b6647f11c4414bd483736b37c62a0b362021-12-02T00:19:16ZConstruction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection1178-2013https://doaj.org/article/b6647f11c4414bd483736b37c62a0b362018-06-01T00:00:00Zhttps://www.dovepress.com/construction-of-injectable-ph-sensitive-antibacterial-mineralized-amin-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Zhenhua Chen,* Mengen Zhao,* Jie Zhang, Kang Zhou, Xiuli Ren, Xifan Mei Jinzhou Medical University, Jinzhou, 121001, People’s Republic of China *These authors contributed equally to this work 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 CaCO3 microspheres (MSs). The morphologies of the obtained MSs were investigated by scanning electron microscopy and transmission electron microscopy. The composition of CaCO3 MSs was identified by using Fourier transform infrared spectroscopy. The as-prepared CaCO3 MSs were examined with power X-ray diffraction analysis to obtain the crystallographic structure of the MSs. Results: The as prepared Lys encapsulated CaCO3 MSs (Lys@CaCO3 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@CaCO3 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@CaCO3 MSs can effectively kill Staphylococcus aureus and promote proliferation and differentiation of osteoblasts under stimulation of H2O2 at pH = 5.5. Keywords: osteomyelitis, oxidative stress, L-Lysine, micro-medicine, delivery vehicleChen ZZhao MZhang JZhou KRen XMei XDove Medical PressarticleOsteomyelitisoxidative stressL-Lysinemicro-medicinedelivery vehicleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 13, Pp 3493-3506 (2018)
institution DOAJ
collection DOAJ
language EN
topic Osteomyelitis
oxidative stress
L-Lysine
micro-medicine
delivery vehicle
Medicine (General)
R5-920
spellingShingle Osteomyelitis
oxidative stress
L-Lysine
micro-medicine
delivery vehicle
Medicine (General)
R5-920
Chen Z
Zhao M
Zhang J
Zhou K
Ren X
Mei X
Construction of injectable, pH sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection
description Zhenhua Chen,* Mengen Zhao,* Jie Zhang, Kang Zhou, Xiuli Ren, Xifan Mei Jinzhou Medical University, Jinzhou, 121001, People’s Republic of China *These authors contributed equally to this work 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 CaCO3 microspheres (MSs). The morphologies of the obtained MSs were investigated by scanning electron microscopy and transmission electron microscopy. The composition of CaCO3 MSs was identified by using Fourier transform infrared spectroscopy. The as-prepared CaCO3 MSs were examined with power X-ray diffraction analysis to obtain the crystallographic structure of the MSs. Results: The as prepared Lys encapsulated CaCO3 MSs (Lys@CaCO3 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@CaCO3 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@CaCO3 MSs can effectively kill Staphylococcus aureus and promote proliferation and differentiation of osteoblasts under stimulation of H2O2 at pH = 5.5. Keywords: osteomyelitis, oxidative stress, L-Lysine, micro-medicine, delivery vehicle
format article
author Chen Z
Zhao M
Zhang J
Zhou K
Ren X
Mei X
author_facet Chen Z
Zhao M
Zhang J
Zhou K
Ren X
Mei X
author_sort Chen Z
title 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_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_sort construction of injectable, ph sensitive, antibacterial, mineralized amino acid yolk-shell microspheres for potential minimally invasive treatment of bone infection
publisher Dove Medical Press
publishDate 2018
url https://doaj.org/article/b6647f11c4414bd483736b37c62a0b36
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