Contribution of diafiltration and adsorption to vancomycin clearance in a continuous hemodiafiltration circuit model in vitro
Contribution of diafiltration and adsorption to vancomycin clearance in a continuous hemodiafiltration circuit model in vitro
复制标题
体外连续血液透析滤过回路模型中透析滤过和吸附对万古霉素清除率的贡献
DOI:
10.1111/aor.14178
复制
发表时间:
2022
影响因子:
2.4
通讯作者:
Ishii Itsuko
中科院分区:
文献类型:
--
作者:
Uchida Masashi;Sawada Mifuyu;Yamazaki Shingo;Suzuki Tatsuya;Suzuki Takaaki;Ishii Itsuko
BackgroundVancomycin (VCM) is eliminated mainly by diafiltration under continuous hemodiafiltration (CHDF), but the contribution of adsorption to CHDF clearance (CLCHDF) of VCM using a polyacrylonitrile and sodium methallyl sulfonate copolymer membrane coated with polyethylenimine (AN69ST) or a polymethylmethacrylate (PMMA) membrane is unknown. This study sought to investigate the contribution of diafiltration and adsorption to the CLCHDFof VCM using AN69ST and PMMA membranes in vitro.MethodsAn in vitro CHDF circuit model was developed. The initial concentration of VCM was 50 μg/mL and human serum albumin (HSA) was prepared at a concentration of 0, 2.5, or 5.0 g/dL. The effluent flow rate (Qe) was set at 800, 1500, or 3000 mL/h. The CLCHDF, diafiltration rate, and adsorption rate of VCM were calculated.ResultsTotal CLCHDFof VCM using the AN69ST membrane increased and decreased with increasing Qe and HSA concentration, respectively. Diafiltration and adsorption rates were 82.1 ± 9.8% and 12.1 ± 6.1% under all conditions, respectively. Total CLCHDFusing the PMMA membrane increased with increasing Qe. Diafiltration and adsorption rates were 89.2 ± 20.4% and 4.6 ± 17.0% under all conditions, respectively. The observed CLCHDFvalues significantly correlated with the predicted CLCHDF, calculated according to a previous study as the product of Qe and the plasma unbound fraction.ConclusionsDiafiltration predominantly contributed to CLCHDFof VCM using AN69ST and PMMA membranes. When diafiltration rather than adsorption mainly contributes to the CLCHDFof VCM, the CLCHDFcould be predicted from the Qe and HSA concentration, at least in vitro.