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可生物降解聚合物微球上羟基磷灰石涂层的生长。

Growth of hydroxyapatite coatings on biodegradable polymer microspheres.

机构信息

Departments of Biomedical Engineering, Pharmacology, and Materials Science and Engineering, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

ACS Appl Mater Interfaces. 2009 Jul;1(7):1504-11. doi: 10.1021/am9001716.

Abstract

Mineral-coated microspheres were prepared via a bioinspired, heterogeneous nucleation process at physiological temperature. Poly(d,l-lactide-co-glycolide) (PLG) microspheres were fabricated via a water-in-oil-in-water emulsion method and were mineral-coated via incubation in a modified simulated body fluid (mSBF). X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy with associated energy-dispersive X-ray spectroscopy confirmed the presence of a continuous mineral coating on the microspheres. The mineral grown on the PLG microsphere surface has characteristics analogous to those of bone mineral (termed "bonelike" mineral), with a carbonate-containing hydroxyapatite phase and a porous structure of platelike crystals at the nanometer scale. The assembly of mineral-coated microspheres into aggregates was observed when microsphere concentrations above 0.50 mg/mL were incubated in mSBF for 7 days, and the size of the aggregates was dependent on the microsphere concentration in solution. In vitro mineral dissolution studies performed in Tris-buffered saline confirmed that the mineral formed was resorbable. A surfactant additive (Tween 20) was incorporated into mSBF to gain insight into the mineral growth process, and Tween 20 not only prevented aggregation but also significantly inhibited mineral formation and influenced the characteristics of the mineral formed on the surface of PLG microspheres. Taken together, these findings indicate that mineral-coated PLG microspheres or mineral-coated microsphere aggregates can be synthesized in a controllable manner using a bioinspired process. These materials may be useful in a range of applications, including controlled drug delivery and biomolecule purification.

摘要

采用生理温度下的仿生非均相成核工艺制备了矿化微球。通过油包水包水乳液法制备了聚(DL-丙交酯-共-乙交酯)(PLG)微球,并通过在改良的模拟体液(mSBF)中孵育进行矿化涂层。X 射线衍射、傅里叶变换红外光谱和带有能量色散 X 射线光谱的扫描电子显微镜证实了微球表面存在连续的矿化涂层。在 PLG 微球表面生长的矿物质具有类似于骨矿物质的特性(称为“类骨”矿物质),具有含碳酸盐的羟基磷灰石相和纳米尺度的板状晶体的多孔结构。当微球浓度高于 0.50mg/mL 时,在 mSBF 中孵育 7 天,观察到矿化微球聚集成团,聚集体的大小取决于溶液中微球的浓度。在 Tris 缓冲盐水(Tris-buffered saline)中进行的体外矿物溶解研究证实,形成的矿物是可吸收的。在 mSBF 中加入表面活性剂添加剂(吐温 20)以深入了解矿物生长过程,吐温 20 不仅防止了聚集,而且还显著抑制了矿物的形成,并影响了 PLG 微球表面形成的矿物的特性。总之,这些发现表明可以通过仿生工艺以可控的方式合成矿化 PLG 微球或矿化微球聚集体。这些材料可能在一系列应用中有用,包括控制药物释放和生物分子纯化。

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