首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >IL-6 adsorption dynamics in hemoadsorption beads studied using confocal laser scanning microscopy.
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IL-6 adsorption dynamics in hemoadsorption beads studied using confocal laser scanning microscopy.

机译:使用共聚焦激光扫描显微镜研究了血液吸附珠中的IL-6吸附动力学。

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Sepsis is characterized by a systemic inflammatory response caused by infection, and can result in organ failure and death. Removal of inflammatory mediators such as cytokines from the circulating blood is a promising treatment for severe sepsis. We are developing an extracorporeal hemoadsorption device to remove cytokines from the blood using biocompatible, polymer sorbent beads. In this study, we used confocal laser scanning microscopy (CLSM) to directly examine adsorption dynamics of a cytokine (IL-6) within hemoadsorption beads. Fluorescently labeled IL-6 was incubated with sorbent particles, and CLSM was used to quantify spatial adsorption profiles of IL-6 within the sorbent matrix. IL-6 adsorption was limited to the outer 15 microm of the sorbent particle over a relevant clinical time period, and intraparticle adsorption dynamics was modeled using classical adsorption/diffusion mechanisms. A single model parameter, alpha = q(max) K/D, was estimated by fitting CLSM intensity profiles to our mathematical model, where q(max) and K are Langmuir adsorption isotherm parameters, and D is the effective diffusion coefficient of IL-6 within the sorbent matrix. Given the large diameter of our sorbent beads (450 microm), less than 20% of available sorbent surface area participates in cytokine adsorption. Development of smaller beads may accelerate cytokine adsorption by maximizing available surface area per bead mass.
机译:败血症的特征在于感染引起的全身性炎症反应,并可能导致器官衰竭和死亡。从循环血液中去除炎性介质,例如细胞因子,对于严重的败血症是一种有前途的治疗方法。我们正在开发一种使用生物相容性聚合物吸附剂珠粒的体外血液吸附装置,以去除血液中的细胞因子。在这项研究中,我们使用共聚焦激光扫描显微镜(CLSM)直接检查了血液吸附珠中细胞因子(IL-6)的吸附动力学。将荧光标记的IL-6与吸附剂颗粒一起孵育,然后使用CLSM量化吸附剂基质中IL-6的空间吸附曲线。在相关的临床时间内,IL-6的吸附仅限于吸附剂颗粒的外部15微米,并且使用经典的吸附/扩散机制对颗粒内部的吸附动力学进行了建模。通过将CLSM强度曲线拟合到我们的数学模型中,可以估算出一个模型参数α= q(max)K / D,其中q(max)和K是Langmuir吸附等温线参数,D是IL-的有效扩散系数6在吸附剂基质内。考虑到我们的吸附剂珠的直径较大(450微米),不到20%的可用吸附剂表面积参与细胞因子的吸附。通过使每个珠子质量的可用表面积最大化,较小的珠子的发育可以加速细胞因子的吸附。

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