Bergaglio Talia, Bhattacharya Shayon, Thompson Damien, Nirmalraj Peter Niraj
Transport at Nanoscale Interfaces Laboratory, Swiss Federal Laboratories for Materials Science and Technology, Dübendorf CH-8600, Switzerland.
Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern CH-3012, Switzerland.
ACS Nanosci Au. 2023 Apr 5;3(3):241-255. doi: 10.1021/acsnanoscienceau.3c00004. eCollection 2023 Jun 21.
Understanding the dose-dependent effect of over-the-counter drugs on red blood cells (RBCs) is crucial for hematology and digital pathology. Yet, it is challenging to continuously record the real-time, drug-induced shape changes of RBCs in a label-free manner. Here, we demonstrate digital holotomography (DHTM)-enabled real-time, label-free concentration-dependent and time-dependent monitoring of ibuprofen on RBCs from a healthy donor. The RBCs are segmented based on three-dimensional (3D) and four-dimensional (4D) refractive index tomograms, and their morphological and chemical parameters are retrieved with their shapes classified using machine learning. We directly observed the formation and motion of spicules on the RBC membrane when aqueous solutions of ibuprofen were drop-cast on wet blood, creating rough-membraned echinocyte forms. At low concentrations of 0.25-0.50 mM, the ibuprofen-induced morphological change was transient, but at high concentrations (1-3 mM) the spiculated RBC remained over a period of up to 1.5 h. Molecular simulations confirmed that aggregates of ibuprofen molecules at high concentrations significantly disrupted the RBC membrane structural integrity and lipid order but produced negligible effect at low ibuprofen concentrations. Control experiments on the effect of urea, hydrogen peroxide, and aqueous solutions on RBCs showed zero spicule formation. Our work clarifies the dose-dependent chemical effects on RBCs using label-free microscopes that can be deployed for the rapid detection of overdosage of over-the-counter and prescribed drugs.
了解非处方药对红细胞(RBC)的剂量依赖性效应对于血液学和数字病理学至关重要。然而,以无标记方式连续记录药物诱导的红细胞实时形状变化具有挑战性。在这里,我们展示了基于数字全息断层扫描(DHTM)的对健康供体红细胞上布洛芬的实时、无标记浓度依赖性和时间依赖性监测。基于三维(3D)和四维(4D)折射率断层图对红细胞进行分割,并通过机器学习对其形状进行分类来检索其形态和化学参数。当将布洛芬水溶液滴加到湿血上时,我们直接观察到红细胞膜上刺突的形成和运动,形成了膜粗糙的棘红细胞形态。在0.25 - 0.50 mM的低浓度下,布洛芬诱导的形态变化是短暂的,但在高浓度(1 - 3 mM)下,有刺突的红细胞可持续长达1.5小时。分子模拟证实,高浓度的布洛芬分子聚集体显著破坏了红细胞膜的结构完整性和脂质有序性,但在低布洛芬浓度下产生的影响可忽略不计。关于尿素、过氧化氢和水溶液对红细胞影响的对照实验显示没有刺突形成。我们的工作使用无标记显微镜阐明了对红细胞的剂量依赖性化学效应,该显微镜可用于快速检测非处方药和处方药的过量使用情况。