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Development of calcium phosphate/calcium sulfate biphasic biomedical material with hyaluronic acid containing collagenase and simvastatin for vital pulp therapy

机译:含有溶态溶酶和辛伐他汀的透明质酸磷酸钙/硫酸钙双相生物医学材料进行重要纸浆疗法

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摘要

Objective. In vital pulp therapy (VPT), a barrier is created with appropriate capping to protect the remaining pulp and thus maintain pulp vitality. Here, we evaluated the feasibility of a biphasic calcium phosphate cement (CPC)-calcium sulfate hemihydrate (CSH) biomaterial containing simvastatin (Sim) and collagenase (Col) for VPT.Methods. Combinations of varying CPC and CSH concentrations were analyzed for their handling properties and setting times, with their structures observed through scanning electron microscopy-energy dispersive X-ray spectrometry (SEM-EDS). Drug release patterns of simvastatin and collagenase combined with CPC-CSH (CPC-CSH-Sim-Col) were also analyzed, followed by biocompatibility and bioactivity tests on human dental pulp stem cells (hDPSCs) and in vivo animal study in canine models; the in vivo results were obtained through microcomputed tomography and histological analysis.Results. The results revealed that 70 wt% CPC (CPC7) with 30 wt% CSH (CSH3) exhibited optimal setting time and porous structure for clinical use. The cell viability and cytotoxicity analysis demonstrated that CPC7-CSH3 with or without simvastatin or collagenase did not injure hDPSCs. In vivo, the CPC7-CSH3-Sim-Col induced dentin bridge formation.Significance. CPC7-CSH3-Sim-Col in this study has great potential as a VPT biomaterial to enhance the dentin bridge formation. (C) 2020 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
机译:客观的。在重要的纸浆疗法(VPT)中,用适当的封盖产生屏障以保护剩余的纸浆,从而保持纸浆活力。在此,我们评估了磷酸钙水泥(CPC)的双相磷酸钙水泥(CPC)的可行性 - 硫酸钙半水合物(CSH)生物材料含有辛伐他汀(SIM)和胶原酶(COL)的vPT.methods。分析改变CPC和CSH浓度的组合,用于处理性能和设定时间,其结构通过扫描电子显微镜 - 能量分散X射线光谱法(SEMEDS)观察。还分析了辛伐他汀和胶原酶的药物释放模式,以及CPC-CSH(CPC-CSH-SIM-COL),然后对人牙牙髓干细胞(HDPSC)的生物相容性和生物活性试验以及犬类模型的体内动物研究;通过微型断层扫描和组织学分析获得体内结果。结果。结果表明,具有30wt%CSH(CSH3)的70wt%CPC(CPC7)表现出用于临床用途的最佳设定时间和多孔结构。细胞活力和细胞毒性分析表明,具有或没有辛伐他汀或胶原酶的CPC7-CSH3没有损伤HDPSC。在体内,CPC7-CSH3-SIM-COL诱导牙本质桥形成。重要性。本研究中的CPC7-CSH3-SIM-COL具有巨大的潜力作为VPT生物材料,以增强牙本质桥梁形成。 (c)2020牙科材料学院。由elsevier Inc.出版的所有权利保留。

著录项

  • 来源
    《Dental materials》 |2020年第6期|755-764|共10页
  • 作者单位

    Natl Taiwan Univ Sch Dent Grad Inst Clin Dent Taipei Taiwan|Natl Taiwan Univ Hosp Dept Dent Taipei Taiwan|Cardinal Tien Hosp Dept Dent Yonghe Branch New Taipei Taiwan;

    Natl Taiwan Univ Sch Dent Grad Inst Clin Dent Taipei Taiwan;

    Natl Taiwan Univ Sch Dent Grad Inst Clin Dent Taipei Taiwan;

    Natl Taiwan Univ Sch Dent Grad Inst Oral Biol Taipei Taiwan;

    Natl Taiwan Univ Sch Dent Grad Inst Clin Dent Taipei Taiwan|Natl Taiwan Univ Hosp Dept Dent Taipei Taiwan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Calcium phosphate; Calcium sulfate hemihydrate; Vital pulp therapy; Simvastatin; Collagenase I;

    机译:磷酸钙;硫酸钙半水合物;重要的纸浆疗法;辛伐他汀;胶原酶I;

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