Ates Berna, Eroglu Tolga, Sahsuvar Seray, Kirimli Ceyhun Ekrem, Kocaturk Ozgur, Senay Sahin, Gok Ozgul
Department of Biomedical Engineering, Faculty of Engineering and Natural Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul 34752, Turkey.
School of Medicine, Acibadem Mehmet Ali Aydinlar University, Istanbul 34752, Turkey.
ACS Omega. 2024 Sep 30;9(41):42103-42115. doi: 10.1021/acsomega.4c02121. eCollection 2024 Oct 15.
Organ-on-a-chip platform scans offer a controllable environment and a physiological similarity to mimic human pathophysiology. In this study, a single-channel PDMS microchip was fabricated, characterized, and optimized to obtain a heart-on-a-chip platform, which is integrated with a hydrogel scaffold suitable for cardiomyocyte growth inside its channel. Single-channel chips with a size of 20 × 12 mm and a channel height ranging from 60 to 100 μm were produced using photolithography and soft lithography techniques. A gelatin-embedded alginate network-based hydrogel was further augmented with 3% (v/v) collagen type I. Pore sizes were in the range of 74-153 μm for H9C2 implantation and biomimicry. The hydrogels are characterized both on PDMS surfaces and in capillaries. The primary feature distinguishing this study from previous microchip studies is that it mimics the cell microenvironment much better using different hydrogel formulations instead of creating a 2D cell culture by passing fluids, such as fibronectin, for cell adhesion. Instead of using complex microchip designs, the chip system we created intends to provide a physiologically relevant copy by using a 3D cell culture to its advantage and a simple, single-channel architecture. The microchip study was combined with cardiomyocytes to create the heart-on-a-chip system and tested under normoxic and hypoxic conditions to create a myocardial ischemia model inside this channel. As a result, this heart-on-a-chip platform was shown to be utilized for the detection of several small-size biomarkers such as adenosine, ADP, lactic acid, l-isoleucine, l-glutamic acid, and oxidized glutathione via LC-MS/MS from control conditions and a myocardial ischemia model. Cell-embedded and hydrogel matrix-supported versions of this heart-on-a-chip system were successfully prepared and shown to provide powerful outputs with myocardial ischemia markers. In light of this research, these outputs aim to develop simple and biologically effective organ-on-a-chip systems for future research.
器官芯片平台扫描提供了一个可控的环境以及与人类病理生理学相似的生理特性。在本研究中,制造、表征并优化了一个单通道聚二甲基硅氧烷(PDMS)微芯片,以获得一个芯片上的心脏平台,该平台在其通道内集成了适合心肌细胞生长的水凝胶支架。使用光刻和软光刻技术制作了尺寸为20×12毫米且通道高度在60至100微米范围内的单通道芯片。一种基于明胶包埋藻酸盐网络的水凝胶进一步添加了3%(v/v)的I型胶原蛋白。用于H9C2植入和仿生的孔径在74 - 153微米范围内。这些水凝胶在PDMS表面和毛细管中都进行了表征。本研究与先前微芯片研究的主要区别在于,它通过使用不同的水凝胶配方更好地模拟了细胞微环境,而不是通过诸如纤连蛋白等流体来创建二维细胞培养以实现细胞黏附。我们创建的芯片系统没有采用复杂的微芯片设计,而是旨在利用三维细胞培养的优势和简单的单通道架构提供与生理相关的复制品。该微芯片研究与心肌细胞相结合,创建了芯片上的心脏系统,并在常氧和缺氧条件下进行测试,以在该通道内创建心肌缺血模型。结果表明,这个芯片上的心脏平台可用于通过液相色谱 - 串联质谱(LC - MS/MS)从对照条件和心肌缺血模型中检测几种小尺寸生物标志物,如腺苷、二磷酸腺苷(ADP)、乳酸、L - 异亮氨酸、L - 谷氨酸和氧化型谷胱甘肽。成功制备了这种芯片上的心脏系统的细胞嵌入和水凝胶基质支持版本,并显示它们能提供有关心肌缺血标志物的有力输出。鉴于这项研究,这些输出旨在为未来研究开发简单且生物有效的器官芯片系统。