吸附
吸附剂
血液灌流
肿瘤坏死因子α
朗缪尔吸附模型
败血症
抗体
化学
色谱法
药理学
免疫学
医学
内科学
有机化学
血液透析
作者
Jiewen Chen,Guangshuai Yao,Chundong Huang,Qidong Shen,Jian Miao,Lingyun Jia
出处
期刊:ACS Biomaterials Science & Engineering
[American Chemical Society]
日期:2024-02-16
卷期号:10 (3): 1788-1795
标识
DOI:10.1021/acsbiomaterials.3c01765
摘要
Removing the overexpressed TNF-α by hemoperfusion positively affects clinical treatments for diseases such as autoimmune disease and sepsis. However, clearance ratios of adsorbents targeting TNF-α were limited by the extremely low concentration of TNF-α (mostly <1000 ng/L in sepsis) and hydrophobic interactions. In this work, biparatopic nanobodies (NbC21) with a high affinity of 19.9 pM, which bind to two distinct sites of TNF-α, were constructed as high-affinity ligands for the immunosorbent. The theoretical maximum adsorption capacity estimated from the Langmuir isotherm was up to 18.22 mg/g gel. The prepared immunosorbent (NbC21-sorbent) had an outstanding TNF-α clearance ratio of approximately 96% during the dynamic adsorption test, with a sorbent-to-serum ratio of 1:1000. Additionally, it demonstrated favorable hemocompatibility and a prolonged storage capability. The results indicated that the biparatopic nanobody immunosorbent exhibited significant potential for clinical applications as it met the stringent criteria for both efficacy and safety.
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