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Preparation of calcium-phosphate microspheres by salt-assisted ultrasonic spray-pyrolysis technique and their drug release behavior using anti-angiogenic agent, TNP-470

机译:盐辅助超声喷雾热解法制备磷酸钙微球及其抗血管生成剂TNP-470的释药行为

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摘要

Synthetic clcium phosphate based materials, such as hydroxyapatite (Ca_(10)(PO_4)_6(OH)_2; HAp) and tricalcium phosphate (Ca_3(PO_4)_2; TCP), are compounds with high potential for clinical applications to orthopedic and dental region. In previous study, we have reported that the hollow and porous apatite microsphere could be prepared by salt-assisted ultrasonic spray-pyrolysis (SAUSP) technique using sodium chloride (NaCl). In this case, these microspheres have some problems of (ⅰ) decrease of dissolubility of microspheres and (ⅱ) cytotoxicity arising from chloride ions elution. To overcome these disadvantages, we prepared novel microspheres by SAUSP technique using potassium nitrate (KNO_3) instead of NaCl. The resulting microsphere was washed with pure water to remove the KNO_3 phase. The particle shapes of the powders were observed by scanning electron microscopy (SEM); the diameters of the microspheres were of 0.5 - 3.0 μm, and the fine pores with the sizes of ~50 nm were present on the surface of the microspheres. The TNP-470 agent as a model of drug were loaded on these microspheres with nano-pores in the surface. In the KNO_3 concentration of 1.00 moldm~(-3), 70 % of the total TNP-470 from the microspheres was rapidly released within 1 h. The remaining 30 % was slowly released up to 24 h following immersion, and total amount of TNP-470 released from the microspheres was 42 μg-mg~(-1).
机译:合成的基于磷酸钙的材料,例如羟基磷灰石(Ca_(10)(PO_4)_6(OH)_2; HAp)和磷酸三钙(Ca_3(PO_4)_2; TCP),对于在整形外科和牙科领域的临床应用具有很高的潜力区域。在以前的研究中,我们已经报道了可以通过盐辅助超声喷雾热解(SAUSP)技术使用氯化钠(NaCl)来制备空心和多孔的磷灰石微球。在这种情况下,这些微球具有一些问题(ⅰ)降低了微球的溶解性和(ⅱ)由于氯离子洗脱而产生的细胞毒性。为了克服这些缺点,我们通过SAUSP技术使用硝酸钾(KNO_3)代替NaCl制备了新型微球。用纯水洗涤所得的微球以除去KNO_3相。通过扫描电子显微镜(SEM)观察粉末的颗粒形状。微球的直径为0.5-3.0μm,并且在微球表面上存在〜50nm尺寸的细孔。将TNP-470药剂作为药物模型加载到这些微球上,这些微球的表面具有纳米孔。在1.00molm〜(-3)的KNO_3浓度下,微球中TNP-470总量的70%在1小时内迅速释放。剩余的30%在浸入后缓慢释放直至24 h,从微球中释放的TNP-470总量为42μg-mg〜(-1)。

著录项

  • 来源
    《Bioceramics 23》|2011年|p.672-677|共6页
  • 会议地点 Istanbul(TR);Istanbul(TR)
  • 作者单位

    Department of Applied Chemistry, School of Science and Technology, Meiji University, 1-1-1 Higashimita, Tama-ku, Kawasaki, Kanagawa, 214-8571, Japan;

    Department of Obstetrics and Gynecology, School of Medicine, Fukuoka University, 8-19-1 Nanakuma, Jyounan-ku, Fukuoka, Fukuoka, 814-0180, Japan,International University of Health and Welfare, 3-6-45 Momochihama, Sawara-ku, Fukuoka, Fukuoka, 814-0001, Japan;

    Department of Applied Chemistry, School of Science and Technology, Meiji University, 1-1-1 Higashimita, Tama-ku, Kawasaki, Kanagawa, 214-8571, Japan;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物材料学;
  • 关键词

    ultrasonic spray-pyrolysis technique; calcium phosphate; microsphere; anti-angiogenic agent; drug release;

    机译:超声喷雾热解技术;磷酸钙;微球抗血管生成剂药物释放;

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