Ching Lau Chi, Reardon Philip James Thomas, Campbell Knowles Jonathan, Tang Junwang
Department of Chemical Engineering, University College London, Torrington Place, London WC1E 7JE, United Kingdom.
Division of Biomaterials and Tissue Engineering, University College London Eastman Dental Institute, 256 Gray's Inn Road, London WC1X 8LD, United Kingdom.
ACS Biomater Sci Eng. 2015 Oct 12;1(10):947-954. doi: 10.1021/acsbiomaterials.5b00179. Epub 2015 Sep 1.
Calcium phosphates (CaP) are important biomaterials used in tissue engineering and drug delivery, due to their biocompatibility, low toxicity, and osteoconductivity. However, controlling the phase of CaP, especially tricalcium phosphate (TCP), is very challenging under mild conditions, particularly when using one preparation protocol for all CaP phases. It is also crucial to produce these biomaterials economically and reproducibly. Herein, three of the most commonly employed CaP, including beta-tricalcium phosphate (β-TCP), dicalcium phosphate anhydrous (DCPA), and hydroxyapatite (HA) were, for the first time, successfully synthesized by altering the reaction solvent, using calcium acetate monohydrate as a precursor and a rapid microwave-assisted synthetic method. A variety of CaP particle morphologies were obtained, including elliptical and plate-shaped with different porosities. Compared with conventional heating, CaP biomaterials synthesized using microwave heating showed greater reproducibility, higher yields, and shorter reaction time. By varying the reaction solvents, morphologies and phases of CaP were controlled, leading to an enhanced protein bovine serum albumin (BSA) loading, with a higher BSA absorption observed according to the trend DCPA> β-TCP > HA. Furthermore, the phase, specific surface area, and pore size were shown to play decisive roles in protein desorption with a higher release amount observed according to the trend DCPA > β-TCP > HA. Finally, it is found that larger pores are also beneficial to BSA adsorption.
磷酸钙(CaP)由于其生物相容性、低毒性和骨传导性,是组织工程和药物递送中使用的重要生物材料。然而,在温和条件下控制CaP的相,尤其是磷酸三钙(TCP),极具挑战性,特别是当对所有CaP相使用一种制备方案时。经济且可重复地生产这些生物材料也至关重要。在此,首次通过改变反应溶剂,使用一水合醋酸钙作为前体并采用快速微波辅助合成方法,成功合成了三种最常用的CaP,包括β-磷酸三钙(β-TCP)、无水磷酸二钙(DCPA)和羟基磷灰石(HA)。获得了多种CaP颗粒形态,包括具有不同孔隙率的椭圆形和板状。与传统加热相比,使用微波加热合成的CaP生物材料具有更高的可重复性、更高的产率和更短的反应时间。通过改变反应溶剂,可以控制CaP的形态和相,从而提高蛋白质牛血清白蛋白(BSA)的负载量,根据DCPA>β-TCP>HA的趋势观察到更高的BSA吸收。此外,相、比表面积和孔径在蛋白质解吸中起决定性作用,根据DCPA>β-TCP>HA的趋势观察到更高的释放量。最后,发现较大的孔隙也有利于BSA吸附。