K. Tsuchida, Y. Takemoto, K. Sugimura, R. Yoshimura, K. Yamamoto, T. Nakatani
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引用次数: 22
摘要
我们之前报道了用于β -微球蛋白(BMG)吸附柱的Lixelle不仅可以吸附BMG,还可以吸附炎症细胞因子。我们对Lixelle在内毒素血症患者中的应用产生了兴趣,并研究了Lixelle在体外利用脂多糖(LPS)(大肠杆菌B8)、内毒素(ET)污染的水中吸附微生物成分的能力。各水溶液初始浓度为LPS (ET 29,135 EU/L),污染水(ET 3,523 EU/L)全血溶液为LPS (ET 1,197.6 EU/L)。每2.5 ml的原液和调整后的稀释溶液含有0.5 ml的Lixelle微珠。37℃振荡2小时后,采用内毒素特异性鲎试剂溶栓法测定溶液中的ET。结果显示,尽管脂多糖和污染水在水溶液中孵育和全血中的ET浓度很高,但含有Lixelle珠的样品中ET浓度明显降低。因此,Lixelle微球不仅可以吸附BMG,还可以吸附微生物成分,如LPS和ET。这些发现与Lixelle吸附ET的能力一起显示了应用于内毒素血症治疗的可能性。
Adsorption of endotoxin by beta2-microglobulin adsorbent column (Lixelle): the new approach for endotoxinemia.
We previously reported that Lixelle, which was used for beta2-microglobulin (BMG) adsorption columns, could adsorb not only BMG but also inflammatory cytokines. We became interested in the application of Lixelle for patients with endotoxinemia and researched its ability to adsorb microorganism components in vitro using lipopolysaccharide (LPS) (Escherichia coli B8), endotoxin (ET) contaminated water. The initial concentrations of each water solution were LPS (ET 29,135 EU/L) and contaminated water (ET 3,523 EU/L) whole blood solution was LPS (ET 1,197.6 EU/L). Each 2.5 ml of the stock solution and adjusted diluted solutions contained 0.5 ml of Lixelle beads. After shaking at 37 degrees C for 2 h, ET in the solutions was determined using the endotoxin specific-limulus amebocyte lysate method. The results revealed that even though ET concentrations in LPS and contaminated water incubated in water solution and in whole blood were high, the samples containing Lixelle beads showed significant decreases. Thus, Lixelle beads can adsorb not only BMG but also microorganism components such as LPS and ET. These findings together with the ability of Lixelle to adsorb ET show the possibility of the application for treatment of endotoxinemia.