College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu, 610065, China.
Department of Nephrology, West China Hospital, Sichuan University, Chengdu, 610041, China.
Biomacromolecules. 2022 Sep 12;23(9):3728-3742. doi: 10.1021/acs.biomac.2c00583. Epub 2022 Aug 4.
Hemoperfusion is an important method to remove endotoxins and save the lives of patients with sepsis. However, the current adsorbents for hemoperfusion have disadvantages of insufficient endotoxin adsorption capacity, poor blood compatibility, and so on. Herein, we proposed a novel emulsion templating (ET) method to prepare ultraporous and double-network carboxylated chitosan (CCS)-poly(diallyl dimethylammonium chloride) (PDDA) hydrogel spheres (ET-CCSPD), bearing both negative and positive charges. CCS was introduced to balance the strong positive charges of PDDA to improve hemocompatibility, and emulsion templates endowed the adsorbent with an ultraporous structure for enhanced adsorption efficacy. The ET-CCSPDs neither damaged blood cells nor activated complement responses. In addition, the activated partial thromboplastin time (APTT) was prolonged to 8.5 times, which was beneficial for reducing the injection of anticoagulant in patients. The ET-CCSPDs had excellent scavenging performance against bacteria and endotoxin, with removal ratios of 96.7% for and 99.8% for , respectively, and the static removal ratio of endotoxin in plasma was as high as 99.1% ( = 5.50 EU/mL, critical illness level). An adsorption cartridge filled with the ET-CCSPDs could remove 84.7% of endotoxin within 1 h ( = 100 EU/mL in PBS). Interestingly, the ET-CCSPDs had a good inhibitory effect on the cytokines produced by endotoxin-mediated septic blood. By developing the ET method to prepare ultraporous and double-network adsorbents, the problems of low adsorption efficiency and poor blood compatibility of traditional endotoxin adsorbents have been solved, thus opening a new route to fabricate absorbents for blood purification.
血液灌流是清除内毒素、拯救脓毒症患者生命的重要方法。然而,目前用于血液灌流的吸附剂存在内毒素吸附容量不足、血液相容性差等缺点。在此,我们提出了一种新颖的乳液模板法(ET)来制备具有超多孔和双网络结构的羧基化壳聚糖(CCS)-聚二烯丙基二甲基氯化铵(PDDA)水凝胶球(ET-CCSPD),同时带有负电荷和正电荷。CCS 的引入平衡了 PDDA 的强正电荷,提高了血液相容性,乳液模板则赋予了吸附剂超多孔结构,增强了吸附效果。ET-CCSPD 既不损伤血细胞,也不激活补体反应。此外,激活部分凝血活酶时间(APTT)延长至 8.5 倍,有利于减少患者抗凝剂的注射量。ET-CCSPD 对细菌和内毒素具有优异的清除性能,对 的去除率分别为 96.7%和 99.8%,对血浆内毒素的静态去除率高达 99.1%( = 5.50 EU/mL,危急值)。装满 ET-CCSPD 的吸附柱在 1 h 内可去除 84.7%的内毒素( = 100 EU/mL 的 PBS 中)。有趣的是,ET-CCSPD 对内毒素介导的脓毒症血液中产生的细胞因子具有良好的抑制作用。通过开发 ET 法制备超多孔和双网络吸附剂,解决了传统内毒素吸附剂吸附效率低和血液相容性差的问题,为血液净化用吸附剂的制备开辟了新途径。