Platelet-rich plasma (PRP) was obtained by centrifuging fresh human whole blood containing 3.8 wt.% citrate acid at 1500 rpm for 15 min. Then, the SS, Ti–O, P50, P50R5, P50R20, and P50R42 samples were immersed in 0.5 mL PRP individually, and incubated at 37 °C for 45 min. Next, the samples were rinsed with PBS three times to remove the weakly adherent platelets, and the adherent platelets were fixed in 2.5% glutaraldehyde solution for 12 h. After the treatment of dehydrating, dealcoholizing, and critical point drying, the samples were sputter-coated with gold and imaged by scanning electron microscopy (SEM, Quanta200, Philips, Amsterdam, Netherlands).
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.