Literature DB >> 22847941

Study on in vitro release and cell response to alendronate sodium-loaded ultrahigh molecular weight polyethylene loaded with alendronate sodium wear particles to treat the particles-induced osteolysis.

Shuxin Qu1, Yinlong Bai, Xiaomin Liu, Rong Fu, Ke Duan, Jie Weng.   

Abstract

The aim of this study is to investigate in vitro release and cell response to wear particles of ultrahigh molecular weight polyethylene loaded with alendronate sodium (UHMWPE-ALN), a potent bone resorption inhibitor. Wear particles of UHMWPE-ALN with different ALN contents (0.5 wt % or 1.0 wt %) and size ranges (<45 μm or 45-75 μm) were cocultured with macrophages (RAW264.7) and osteoblasts (MC3T3-E1), respectively. The in vitro ALN release was divided into three stages: an initial burst release, subsequent rapid release, and final slow release. The particle size and ALN content of UHMWPE-ALN wear particles affected the in vitro release mainly during initial burst and rapid release. Compared with the control cells, UHMWPE-ALN wear particles stimulated a significant elevation of tumor necrosis factor-alpha (TNF-α) release from macrophages but had no obvious effect on interleukin-6 release. However, this stimulation of TNF-α release could be reduced by ALN released from UHMWPE-ALN wear particles. The wear particle size had stronger effect of on the macrophages compared with the ALN concentration. After coculture with UHMWPE-ALN wear particles, osteoblast proliferation and alkaline phosphatase activities increased moderately with the increase in particle sizes and ALN concentrations. These results suggest that incorporation of ALN in UHMWPE-ALN may be an effective approach to prevent or reduce particles-induced osteolysis.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22847941     DOI: 10.1002/jbm.a.34327

Source DB:  PubMed          Journal:  J Biomed Mater Res A        ISSN: 1549-3296            Impact factor:   4.396


  11 in total

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3.  Study on critical-sized ultra-high molecular weight polyethylene wear particles loaded with alendronate sodium: in vitro release and cell response.

Authors:  Yumei Liu; Feng Shi; Kemeng Gong; Yang Liu; Wei Zhi; Jie Weng; Shuxin Qu
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5.  NOX4 blockade suppresses titanium nanoparticle-induced bone destruction via activation of the Nrf2 signaling pathway.

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7.  Alendronate Release from UHMWPE-Based Biomaterials in Relation to Particle Size of the GUR Powder for Manufacturing.

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9.  Harmine Alleviates Titanium Particle-Induced Inflammatory Bone Destruction by Immunomodulatory Effect on the Macrophage Polarization and Subsequent Osteogenic Differentiation.

Authors:  Liangliang Wang; Qing Wang; Wei Wang; Gaoran Ge; Nanwei Xu; Dong Zheng; Shijie Jiang; Gongyin Zhao; Yaozeng Xu; Yuji Wang; Ruixia Zhu; Dechun Geng
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10.  Magnoflorine Suppresses MAPK and NF-κB Signaling to Prevent Inflammatory Osteolysis Induced by Titanium Particles In Vivo and Osteoclastogenesis via RANKL In Vitro.

Authors:  Zhenyu Sun; Junkai Zeng; Wenjuan Wang; Xinlin Jia; Qiang Wu; Degang Yu; Yuanqing Mao
Journal:  Front Pharmacol       Date:  2020-04-02       Impact factor: 5.810

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