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HOLLOW HYDROXYAPATITE MICROSPHERES FOR CONTROLLED DELIVERY OF PROTEINS

机译:空心羟基磷灰石微球,可控制地输送蛋白质

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Hollow hydroxyapatite (HA) microspheres were prepared by reacting solid microspheres of a lithium-calcium-borate glass (106-150 microns) for 2 days in K_2HPO_4 solution (0.02 M; 37°C), and evaluated as a controlled delivery device for a model protein, bovine serum albumin (BSA). The as-prepared HA microspheres had a hollow core with a diameter equal to 0.6 the external diameter, a surface area of ∨100 m~2/g, and a mesoporous shell wall (pore size of = 13 nm). After loading the hollow HA microspheres with a solution of BSA, release of the BSA into a medium of phosphate-buffered saline (PBS) was measured as a function of time using a micro bicinchoninic acid (BCA) protein assay reagent. BSA release initially increased linearly with time, but almost ceased after 24-48 hours. Modification of the BSA release kinetics was achieved by altering the microstructure of the shell wall of the as-prepared HA microspheres using a controlled heat treatment (5 h at 600°C-900°C). Sustained release of BSA was achieved over than 7-14 days from HA microspheres heated for 5 h at 600°C. The potential application of these hollow HA microspheres as a device for controlled local delivery of protein growth factors and drugs is discussed.
机译:空心羟基磷灰石(HA)微球是通过使硼酸锂钙玻璃的固体微球(106-150微米)在K_2HPO_4溶液(0.02 M; 37°C)中反应2天而制备的,并被评估为可控释药装置模型蛋白,牛血清白蛋白(BSA)。所制备的HA微球具有中空的核,其直径等于外径的0.6,表面积为约100m 2 / g,并且具有中孔壳壁(孔径为= 13nm)。在用BSA溶液填充空心HA微球后,使用微双金鸡宁酸(BCA)蛋白测定试剂测量BSA在磷酸盐缓冲盐水(PBS)介质中的释放随时间的变化。 BSA释放最初随时间线性增加,但在24-48小时后几乎停止。通过使用受控的热处理(在600°C-900°C下5h)改变所制备的HA微球壳壁的微观结构,可以实现BSA释放动力学的改变。通过在600°C下加热5小时的HA微球,可以在7-14天以上的时间内实现BSA的持续释放。讨论了这些空心HA微球作为控制蛋白质生长因子和药物局部递送的装置的潜在应用。

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