Open hour: senin - sabtu 09:00:00 - 20:00:00; minggu & tanggal merah tutup
Methods : Platelet-rich fibrin prepared from stored whole-blood samples [3]

Methods : Platelet-rich fibrin prepared from stored whole-blood samples [3]

author: Kazushige Isobe, Masashi Suzuki, Taisuke Watanabe, Yutaka Kitamura, Taiji Suzuki, Hideo Kawabata, Masayuki Nakamura, Toshimitsu | publisher: drg. Andreas Tjandra, Sp. Perio, FISID

PRF extracts prepared as described above were subjected to measurement of PDGF-BB levels using the Human PDGF-BB Quantikine ELISA Kit (R&D Systems, Inc., Minneapolis, MN, USA) as described previously [8].

The PRF clots that were compressed in a stainless-steel compressor were fixed with 2.5% neutralized glutaraldehyde, dehydrated with a series of ethanol solutions and t-butanol, freeze-dried, and then examined under a scanning electron microscope (TM-1000, Hitachi, Tokyo, Japan) with an accelerating voltage of 15 kV, as described elsewhere [7, 14].

The data were expressed as mean ± standard deviation (SD). For multigroup comparisons, statistical analyses were conducted to compare the mean values by one-way analysis of variance (ANOVA) followed by Tukey’s multiple-comparison test (SigmaPlot 12.5; Systat Software, Inc., San Jose, CA, USA). Differences with P values <0.05 were considered significant.

Serial posts:


id post:
New thoughts
Me:
search
glossary
en in