使用3d打印模具快速制作肺芯片模型

Jesus Shrestha , Maliheh Ghadiri , Melane Shanmugavel , Sajad Razavi Bazaz , Steven Vasilescu , Lin Ding , Majid Ebrahimi Warkiani
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引用次数: 51

摘要

器官芯片是一种在体外复制关键器官特异性微结构和病理生理的微流控细胞培养模型。目前制造这些设备的方法依赖于软光刻,这通常是繁琐的,费力的,并且需要熟练的用户以及洁净室设施。最近,使用3d打印技术快速制造聚二甲基硅氧烷(PDMS)铸造模具的趋势正在上升。然而,大多数3d打印材料不适合PDMS铸造。为了解决这个问题,我们改进了现有的技术,并引入了一种改进的方案,用于3d打印模具的表面处理,使其成为重复长期PDMS铸造的理想选择。利用这一方案,我们制作了一个简单的开孔肺片模型来模拟动态条件下气液界面气道的体内环境。为了验证开发的芯片的功能,Calu-3 细胞在芯片中培养并保持在气液界面。模型显示,培养的细胞复制了三维培养特异性形态,保持了良好的屏障完整性,分泌粘液,表达细胞表面功能性p -糖蛋白;所有这些都表明一个有希望的体外模型用于渗透性试验,毒理学试验和肺给药研究。为了验证该肺芯片体外模型的适用性,我们检测了香烟烟雾提取物(CSE)对体外培养Calu-3 细胞白细胞介素-6 (IL-6)和白细胞介素-8 (IL-8)释放的影响。与CSE和布地奈德(一种抗炎药)处理的细胞相比,CSE处理的细胞在24 h内分泌的IL-6和IL-8显著增加。此外,我们的研究结果表明,CSE降低了E-cadherin作为粘附连接蛋白的表达。总之,所提出的方案展示了一种简单且低成本的制造技术,它将允许生物学家以最低的技术技能快速为不同/多功能器官芯片模型制作模具原型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rapidly prototyped lung-on-a-chip model using 3D-printed molds

Organ-on-a-chip is a microfluidic cell culture model that replicates key organ-specific microarchitecture and pathophysiology in vitro. The current methods to fabricate these devices rely on softlithography, which is usually tedious, laborious, and requires adroit users as well as cleanroom facilities. Recently, the use of 3D-printing technologies for the rapid fabrication of molds for polydimethylsiloxane (PDMS) casting is on the rise. However, most of the 3D-printed materials are unsuitable for PDMS casting. To address this issue, we have improved the existing techniques and introduced a modified protocol for the surface treatment of 3D-printed molds, making them ideal for repeated long-term PDMS casting. Using this protocol, we have fabricated a simple open well lung-on-a-chip model to simulate the in vivo environment of airway at air-liquid interface under dynamic condition. To validate the functionality of the developed chip, Calu-3 cells were cultured in the chip and maintained at an air-liquid interface. The model demonstrated that the cultured cells replicated the 3D culture-specific-morphology, maintained excellent barrier integrity, secreted mucus, and expressed cell surface functional P-glycoprotein; all indicative of a promising in vitro model for permeability assays, toxicological tests, and pulmonary drug delivery studies. To validate the suitability of this lung-on-a-chip in vitro model, the effects of cigarette smoke extract (CSE) on Interleukin-6 (IL-6) and Interleukin-8 (IL-8) release from cultured Calu-3 cells were examined. CSE treated cells showed significantly higher secretion of IL-6 and IL-8 over 24 h compared to the cells treated with both CSE and Budesonide, an anti-inflammatory drug. Moreover, our results illustrated that CSE reduced the expression of E-cadherin as an adherent junctional protein. In conclusion, the proposed protocol demonstrated an easy and low-cost fabrication technique which will allow a biologist with minimal technical skills to rapidly prototype molds for different/versatile organ-on-a-chip models.

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来源期刊
Organs-on-a-chip
Organs-on-a-chip Analytical Chemistry, Biochemistry, Genetics and Molecular Biology (General), Cell Biology, Pharmacology, Toxicology and Pharmaceutics (General)
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