首页> 外文期刊>Journal of nanoscience and nanotechnology >Fabrication of a Novel Beta Tricalcium Phosphate/Sodium Alginate/Poly(D,L-lactic acid) Composite Microsphere and Its Drug Releasing Property
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Fabrication of a Novel Beta Tricalcium Phosphate/Sodium Alginate/Poly(D,L-lactic acid) Composite Microsphere and Its Drug Releasing Property

机译:制备新型β三钙磷酸钙/藻酸钠/聚(D,L-乳酸)复合微球及其药物释放性能

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摘要

Bone repair microspheres have been widely studied due to their convenience during clinical operations. In this study, beta tricalcium phosphate/sodium alginate/poly(D, L-lactic acid) (beta-TCP/SA/PDLLA) composite microspheres were successfully prepared using the liquid droplet method. Then, beta-TCP/SA/PDLLA composite microspheres were soaked in simulated body fluids (SBF) for 7 days, and tested in an X-ray diffractometer (XRD). The results indicated that sodium alginate (SA) and poly(D, L-lactic acid) (PDLLA) are not limiting factors for the transformation of beta-TCP to HA. Since sodium ions and bicarbonate ions were abundant, the final products were not pure HA but (Na, CO3)-substituted HA. When soaked in SBF, the structure of beta-TCP/SA/PDLLA composite microspheres remained stable for at least 14 days suggesting that their anti-washout ability was suitable. Furthermore, the absence of calcination during the preparation of beta-TCP/SA/PDLLA composite microspheres enabled the easy incorporation of vancomycin into the microspheres in situ at a final embedding ratio of 26.18%. Furthermore, the beta-TCP/SA/PDLLA composite microspheres possessed excellent sustained drug release capability, and the release of vancomycin (92.8 wt.%) lasted for almost 168 h. Our results suggest that the beta-TCP/SA/PDLLA composite microspheres could be used as a promising graft material particularly for bone repair.
机译:由于它们在临床操作期间,骨修复微球已被广泛研究。在本研究中,使用液滴法成功制备了β-磷酸钙/藻酸钠/聚(D,L-乳酸)(β-TCP / SA / PDLLA)复合微球。然后,将Beta-TCP / SA / PDLLA复合微球浸泡在模拟体液(SBF)中7天,并在X射线衍射仪(XRD)中进行测试。结果表明,海藻酸钠(SA)和聚(D,L-乳酸)(PDLLA)不是限制β-TCP转化为HA的因素。由于钠离子和碳酸氢盐离子丰富,因此最终产物不是纯HA但(Na,CO 3) - 取代的HA。当浸泡在SBF中时,β-TCP / SA / PDLLA复合微球的结构保持稳定,至少14天表明它们的防冲洗能力是合适的。此外,在制备β-TCP / SA / PDLLA复合微球期间没有煅烧,使Vancomycin能够以26.18%的最终嵌入比以原位原位掺入微球中。此外,β-TCP / SA / PDLLA复合微球具有优异的持续药物释放能力,持续近168小时的万古霉素(92.8重量%)的释放。我们的结果表明,β-TCP / SA / PDLLA复合微球可用作尤其是用于骨骼修复的有前途的接枝材料。

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