Karabaliev Miroslav, Paarvanova Boyana, Savova Gergana, Tacheva Bilyana, Georgieva Radostina
Department of Physics and Biophysics, Faculty of Medicine, Trakia University, 11 Armeiska, 6000 Stara Zagora, Bulgaria.
Institute of Transfusion Medicine, Charité-Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany.
Cells. 2025 Mar 21;14(7):469. doi: 10.3390/cells14070469.
Erythrocytes, the most abundant blood cells, are a prevalent cell model for the analysis of the membrane-damaging effects of different molecules, including drugs. In response to stimuli, erythrocytes can change their morphology, e.g., shape or volume, which in turns influences their main function to transport oxygen. Membrane active molecules can induce hemolysis, i.e., release of hemoglobin into the blood plasma. Free hemoglobin in the blood circulation is toxic causing serious health problems including vasoconstriction, high blood pressure and kidney damage. Therefore, early recognition of the risk of massive hemolysis is highly important. Here, we investigated surfactant induced hemolysis applying UV-vis spectrophotometry. Saponin, sodium dodecyl sulfate and Triton X-100, detergents known to provoke hemolysis at different concentrations and by different mechanisms, were applied to initiate the process. Whole absorption spectra of erythrocyte suspensions in the range 300-750 nm were recorded every 15 s for following the process in real-time. The hemolysis process, with respect to morphological changes in the erythrocytes and their influence on the oxygenation state of hemoglobin, was characterized by the absorbance at 700 nm, the height relative to the background and the wavelength of the Soret peak. The results suggest that these UV-vis spectrophotometry parameters provide reliable information in real-time; not only about the process of hemolysis itself, but also about pre-hemolytic changes in the erythrocytes, even at sub-hemolytic surfactant concentrations.
红细胞是最丰富的血细胞,是分析包括药物在内的不同分子对膜损伤作用的常用细胞模型。响应刺激时,红细胞可改变其形态,如形状或体积,这进而会影响其运输氧气的主要功能。膜活性分子可诱导溶血,即血红蛋白释放到血浆中。血液循环中的游离血红蛋白具有毒性,会导致严重的健康问题,包括血管收缩、高血压和肾损伤。因此,早期识别大规模溶血的风险非常重要。在此,我们应用紫外可见分光光度法研究了表面活性剂诱导的溶血。使用已知能在不同浓度下通过不同机制引发溶血的皂苷、十二烷基硫酸钠和 Triton X-100 去污剂来启动该过程。每 15 秒记录一次红细胞悬液在 300 - 750 nm 范围内的全吸收光谱,以实时跟踪该过程。溶血过程,就红细胞的形态变化及其对血红蛋白氧合状态的影响而言,通过 700 nm 处的吸光度、相对于背景的高度以及 Soret 峰的波长来表征。结果表明,这些紫外可见分光光度法参数可实时提供可靠信息;不仅关于溶血过程本身,还关于红细胞的溶血前变化,即使在亚溶血表面活性剂浓度下也是如此。