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一种荧光 Zn(II)-配位聚合物:通过减少炎症细胞因子释放来选择性检测呋喃妥因和预防超细晶粒钛植入物引发的种植体周炎症

A Fluorescent Zn(II)-Coordination Polymer: Selective Detection of Nitrofurantoin and Prevention of Peri-Implantitis after Ultrafine-Grained Titanium Implant by Reducing Inflammatory Cytokines Release.

机构信息

Jiamusi University, Jiamusi, Heilongjiang, China.

出版信息

J Fluoresc. 2020 Sep;30(5):1035-1042. doi: 10.1007/s10895-020-02575-2. Epub 2020 Jun 30.

DOI:10.1007/s10895-020-02575-2
PMID:32607733
Abstract

In the current research, a novel coordination polymer (CP) containing Zn(II) ions as nodes with the chemical formula of [Zn(IPT)] (1) has been produced via reaction of Zn(NO)·6HO with 5-(3-(1H-imidazol-1-yl)phenyl)-1H-tetrazolate (HIPT), a heterotopic imidazole-tetrazole-bifunctional ligand. The as-prepared complex 1 has been charactered via single crystal X-ray diffraction, elemental analysis, powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA) and fourier transform infrared spectroscopy (FT-IR). Because of its outstanding luminescent performances and stability, the synthesized complex 1 is a kind of excellent material of luminescent sensor of nitrofurantoin (NFT) in the water. The value of K for the complex 1 to NFT is about 1.4 × 10 M. For the treatment of the peri-implantitis with complex 1, the ELISA test was carried out to determine the levels of the inflammatory cytokines released into the gingival crevicular fluid. The results showed that the levels of the inflammatory cytokines could be significantly reduced by complex 1 treatment. In addition to this, the real time RT-PCR was also conducted, and the data suggested the signaling pathway of TLR-4-NF-κB activation was inhibited by complex 1.

摘要

在当前的研究中,通过将 Zn(NO)·6HO 与 5-(3-(1H-咪唑-1-基)苯基)-1H-四唑(HIPT)反应,合成了一种含有 Zn(II)离子作为节点的新型配位聚合物(CP),其化学式为[Zn(IPT)](1)。所制备的配合物 1 通过单晶 X 射线衍射、元素分析、粉末 X 射线衍射(PXRD)、热重分析(TGA)和傅里叶变换红外光谱(FT-IR)进行了表征。由于其出色的发光性能和稳定性,合成的配合物 1 是水中硝基呋喃妥因(NFT)的发光传感器的一种优秀材料。配合物 1 对 NFT 的 K 值约为 1.4×10^M。为了用配合物 1 治疗种植体周围炎,通过 ELISA 试验测定了释放到龈沟液中的炎症细胞因子的水平。结果表明,配合物 1 处理可显著降低炎症细胞因子的水平。除此之外,还进行了实时 RT-PCR,数据表明 TLR-4-NF-κB 激活的信号通路被配合物 1 抑制。

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