PVA-coated 3D-printed molds for rapid prototyping of PDMS microdevices for stem cell culture

IF 4.4 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Yuma Abe, Daiki Fukai, Taro Toyoda, Naoto Fukumoto, Kyohei Terao
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引用次数: 0

Abstract

Three-dimensional (3D) printing technology is increasingly being utilized as a rapid prototyping method for manufacturing molds for polydimethylsiloxane (PDMS)-based microdevices. Residual photoinitiators and other leachable components derived from photocurable resins often inhibit PDMS curing, while the surface roughness introduced by layer-by-layer printing is known to degrade device performance in cell culture applications. In this study, we propose a surface modification strategy using dip coating with water-soluble and biocompatible poly(vinyl alcohol) (PVA) to improve the compatibility of 3D-printed molds with PDMS replication. Systematic characterization revealed that PVA concentration governs film viscosity and thickness, with the 3–18% (w/w) range yielding uniform and reproducible coatings. PVA-coated molds effectively suppressed PDMS curing inhibition and reduced surface roughness by up to 80%, enabling high-fidelity replication of microstructures. Furthermore, PDMS microwell arrays fabricated from PVA-coated molds supported efficient and uniform embryoid body (EB) formation from human induced pluripotent stem (iPS) cells, with an increased frequency of single EB per well compared to uncoated molds. These findings demonstrate that PVA coating provides a facile, biocompatible, and shape-preserving post-treatment to overcome key limitations of 3D-printed molds. The proposed method offers a robust and accessible pathway for the rapid prototyping of PDMS-based microdevices for stem cell culture and broader biomedical applications.

pva涂层3d打印模具,用于干细胞培养PDMS微设备的快速原型设计。
三维(3D)打印技术越来越多地被用于制造基于聚二甲基硅氧烷(PDMS)的微器件的模具的快速原型方法。残留的光引发剂和其他来自光固化树脂的可浸出成分通常会抑制PDMS的固化,而由逐层印刷引入的表面粗糙度已知会降低细胞培养应用中的设备性能。在这项研究中,我们提出了一种使用水溶性和生物相容性聚乙烯醇(PVA)浸渍涂层的表面改性策略,以提高3d打印模具与PDMS复制的兼容性。系统表征表明,PVA浓度决定了膜的粘度和厚度,在3-18% (w/w)的范围内,可以获得均匀且可复制的涂层。pva涂层模具有效地抑制了PDMS的固化抑制,并将表面粗糙度降低了80%,从而实现了高保真的微观结构复制。此外,pva涂层模具制备的PDMS微孔阵列支持人类诱导多能干细胞(iPS)高效、均匀的胚状体(EB)形成,与未涂层模具相比,每孔单个EB的频率增加。这些发现表明,PVA涂层提供了一种简便、生物相容性和保持形状的后处理,以克服3d打印模具的关键限制。所提出的方法为干细胞培养和更广泛的生物医学应用的基于pdm的微设备的快速原型设计提供了一个强大的和可访问的途径。
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来源期刊
Biomedical Microdevices
Biomedical Microdevices 工程技术-工程:生物医学
CiteScore
6.90
自引率
3.60%
发文量
32
审稿时长
6 months
期刊介绍: Biomedical Microdevices: BioMEMS and Biomedical Nanotechnology is an interdisciplinary periodical devoted to all aspects of research in the medical diagnostic and therapeutic applications of Micro-Electro-Mechanical Systems (BioMEMS) and nanotechnology for medicine and biology. General subjects of interest include the design, characterization, testing, modeling and clinical validation of microfabricated systems, and their integration on-chip and in larger functional units. The specific interests of the Journal include systems for neural stimulation and recording, bioseparation technologies such as nanofilters and electrophoretic equipment, miniaturized analytic and DNA identification systems, biosensors, and micro/nanotechnologies for cell and tissue research, tissue engineering, cell transplantation, and the controlled release of drugs and biological molecules. Contributions reporting on fundamental and applied investigations of the material science, biochemistry, and physics of biomedical microdevices and nanotechnology are encouraged. A non-exhaustive list of fields of interest includes: nanoparticle synthesis, characterization, and validation of therapeutic or imaging efficacy in animal models; biocompatibility; biochemical modification of microfabricated devices, with reference to non-specific protein adsorption, and the active immobilization and patterning of proteins on micro/nanofabricated surfaces; the dynamics of fluids in micro-and-nano-fabricated channels; the electromechanical and structural response of micro/nanofabricated systems; the interactions of microdevices with cells and tissues, including biocompatibility and biodegradation studies; variations in the characteristics of the systems as a function of the micro/nanofabrication parameters.
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