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葡聚糖接枝聚丙烯酰胺/氧化锌纳米体系的血液相容性:溶血还是红细胞皱缩?

Hemocompatibility of dextran-graft-polyacrylamide/zinc oxide nanosystems: hemolysis or eryptosis?

机构信息

Research Institute of Experimental and Clinical Medicine, Kharkiv National Medical University, 4 Nauky ave., 61022 Kharkiv, Ukraine.

Department of Cryobiochemistry, Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, 23 Pereyaslavskaya st., 61015 Kharkiv, Ukraine.

出版信息

Nanotechnology. 2023 Oct 30;35(3). doi: 10.1088/1361-6528/ad02a3.

Abstract

. In this study, blood compatibility of ZnO nanoparticles-polymer nanocomplex (D-PAA/ZnONPs(SO42-)) synthesizedinto dextran-graft-polyacrylamide (D-PAA) using zinc sulphate as a precursor was tested using hemolysis, osmotic fragility and eryptosis assays.. Dose-dependent ability to induce eryptosis was assessed following 24 h incubation at concentrations of 0-800 mg lanalyzing hallmarks of eryptosis (cell shrinkage and phosphatidylserine externalization), as well as reactive oxygen species generation. Hemolysis was detected spectrophotometrically based on hemoglobin release following exposure to the D-PAA/ZnONPs(SO42-) nanocomplex. Osmotic fragility test (OFT) involved detection of hemolysis of red blood cells exposed to 0.2% saline solution following incubation with the D-PAA/ZnONPs(SO42-) nanocomplex. Additional incubation of the nanocomplex in the presence or absence of either ascorbic acid or EGTA was used to reveal the implication of oxidative stress- or Ca-mediated mechanisms in D-PAA/ZnONPs(SO42-) nanocomplex-induced erythrotoxicity.. Hemocompatibility assessment of the D-PAA/ZnONPs(SO42-) nanocomplex revealed that it induced hemolysis and reduced resistance of erythrocytes to osmotic stress at concentrations of above 400 and 200 mg l, respectively. Oxidative stress- or Ca-mediated mechanisms were not involved in D-PAA/ZnONPs(SO42-) nanocomplex-induced hemolysis. Strikingly, the D-PAA/ZnONPs(SO42-) nanocomplex did not promote cell membrane scrambling, cell shrinkage and oxidative stress in red blood cells following the direct exposure for 24 h. Thus, the D-PAA/ZnONPs(SO42-) nanocomplex did not induce eryptosis. Eryptosis is generally considered to occur earlier than hemolysis in response to stress in order to prevent hemolytic cell death. Counterintuitively, our data suggest that hemolysis can be triggered by nanomaterials prior to eryptosis indicating that eryptosis and hemolysis assays should be used in combination for testing blood compatibility of nanomaterials.. The D-PAA/ZnONPs(SO42-) nanocomplex has a good hemocompatibility profile at low concentrations. Hemocompatibility testing in nanotoxicology should include both eryptosis and hemolysis assays.

摘要

. 在这项研究中,使用硫酸锌作为前体,将氧化锌纳米粒子-聚合物纳米复合物(D-PAA/ZnONPs(SO42-))合成到葡聚糖接枝聚丙烯酰胺(D-PAA)中,测试了其血液相容性。通过孵育 24 小时,在 0-800mg l 的浓度下,评估了剂量依赖性诱导细胞凋亡的能力,分析细胞凋亡的特征(细胞收缩和磷脂酰丝氨酸外翻)以及活性氧的产生。通过暴露于 D-PAA/ZnONPs(SO42-)纳米复合物后血红蛋白的释放,用分光光度法检测溶血。渗透脆性试验(OFT)涉及在孵育 D-PAA/ZnONPs(SO42-)纳米复合物后,检测暴露于 0.2%生理盐水的红细胞溶血。在存在或不存在抗坏血酸或 EGTA 的情况下进一步孵育纳米复合物,以揭示氧化应激或 Ca 介导机制在 D-PAA/ZnONPs(SO42-)纳米复合物诱导的红细胞毒性中的作用。. D-PAA/ZnONPs(SO42-)纳米复合物的血液相容性评估表明,它在浓度高于 400 和 200mg l 时分别诱导溶血和降低红细胞对渗透胁迫的抵抗力。氧化应激或 Ca 介导机制不参与 D-PAA/ZnONPs(SO42-)纳米复合物诱导的溶血。引人注目的是,D-PAA/ZnONPs(SO42-)纳米复合物在直接暴露 24 小时后,不会促进红细胞细胞膜混乱、细胞收缩和氧化应激。因此,D-PAA/ZnONPs(SO42-)纳米复合物不会诱导细胞凋亡。细胞凋亡通常被认为是在对胁迫作出反应时比溶血更早发生,以防止溶血细胞死亡。与直觉相反,我们的数据表明,纳米材料可以在细胞凋亡之前引发溶血,这表明在测试纳米材料的血液相容性时,应该将细胞凋亡和溶血试验结合使用。. D-PAA/ZnONPs(SO42-)纳米复合物在低浓度下具有良好的血液相容性。纳米毒理学中的血液相容性测试应包括细胞凋亡和溶血试验。

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