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一种集成式、模块化的分隔式微流控系统,带有可调静电纺多孔膜,用于类器官芯片上的上皮化器官。

An Integrated and Modular Compartmentalized Microfluidic System with Tunable Electrospun Porous Membranes for Epithelialized Organs-on-a-Chip.

机构信息

Strathclyde Institute of Pharmacy and Biomedical Sciences, Strathclyde University, Glasgow G4 0RE, U.K.

Alfaisal University, Riyadh 11533, Kingdome Saudi Arabia.

出版信息

ACS Appl Mater Interfaces. 2024 Aug 7;16(31):40767-40786. doi: 10.1021/acsami.4c08864. Epub 2024 Jul 24.

Abstract

A modular and 3D compartmentalized microfluidic system with electrospun porous membranes (PMs) for epithelialized organ-on-a-chip systems is presented. Our novel approach involves direct deposition of polymer nanofibers onto a patterned poly(methyl methacrylate) (PMMA) substrate using electrospinning, resulting in an integrated PM within the microfluidic chip. The in situ deposition of the PM eliminates the need for additional assembly processes. To demonstrate the high throughput membrane integration capability of our approach, we successfully deposited nanofibers onto various chip designs with complex microfluidic planar structures and expanded dimensions. We characterized and tested the fully PMMA chip by growing an epithelial monolayer using the Caco-2 cell line to study drug permeability. A comprehensive analysis of the bulk and surface properties of the membrane's fibers made of PMMA and polystyrene (PS) was conducted to determine the polymer with the best performance for cell culture and drug transport applications. The PMMA-based membrane, with a PMMA/PVP ratio of 5:1, allowed for the fabrication of a uniform membrane structure along the aligned nanofibers. By modulating the fiber diameter and total thickness of the membrane, we could adjust the membrane's porosity for specific cell culture applications. The PMMA-PVP nanofibers exhibited a low polydispersity index value, indicating monodispersed nanofibers and a more homogeneous and uniform fiber network. Both types of membranes demonstrated excellent mechanical integrity under medium perfusion flow rates. However, the PMMA-PVP composition offered a tailored porous structure with modulable porosity based on the fiber diameter and thickness. Our developed platform enables dynamic in vitro modeling of the epithelial barrier and has applications in drug transport and in vitro microphysiological systems.

摘要

本文提出了一种模块化的、具有 3D 隔室的微流控系统,该系统带有用于上皮细胞类器官芯片系统的静电纺丝多孔膜(PM)。我们的新方法涉及使用静电纺丝将聚合物纳米纤维直接沉积到图案化的聚甲基丙烯酸甲酯(PMMA)基底上,从而在微流控芯片内形成集成的 PM。PM 的原位沉积消除了对额外组装工艺的需求。为了展示我们方法的高通量膜集成能力,我们成功地将纳米纤维沉积到具有复杂微流平面结构和扩展尺寸的各种芯片设计上。我们通过使用 Caco-2 细胞系在完全的 PMMA 芯片上生长上皮单层来研究药物通透性,对其进行了表征和测试。我们对由 PMMA 和聚苯乙烯(PS)制成的纤维的整体和表面性质进行了全面分析,以确定用于细胞培养和药物输送应用的最佳性能的聚合物。PMMA 基膜,其 PMMA/PVP 比为 5:1,允许沿着取向的纳米纤维制造均匀的膜结构。通过调节纤维直径和膜的总厚度,我们可以针对特定的细胞培养应用调整膜的孔隙率。PMMA-PVP 纳米纤维表现出低的多分散指数值,表明单分散纳米纤维和更均匀和一致的纤维网络。两种类型的膜在中等灌注流速下都表现出优异的机械完整性。然而,PMMA-PVP 组成提供了一种基于纤维直径和厚度的可调节孔隙率的定制多孔结构。我们开发的平台能够对上皮屏障进行动态体外建模,并在药物输送和体外微生理系统中有应用。

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