利用基于水凝胶的液滴微流控技术生产均匀大小的癌症球体:综述。

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Sungjin Kim, Po Yi Lam, Arul Jayaraman, Arum Han
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引用次数: 0

摘要

三维(3D)细胞培养模型作为比传统的二维(2D)细胞培养模型更优越的体外平台,已被广泛用于各种机理研究和药物开发研究。尤其是在癌症生物学领域,球形或有机体等三维癌症模型已被广泛用于了解癌症的发展机制。最近,许多复杂的三维模型(如芯片上器官模型)作为先进的体外模型出现,可以更准确地模拟体内组织功能。尽管取得了这些进步,球体仍被认为是一种功能强大的三维癌症模型,因为其结构相对简单,与现有的实验室仪器兼容,而且其通量比复杂的体外模型高出几个数量级,这对药物开发来说是极其重要的方面。然而,创建定义明确的球状体仍然具有挑战性,无论是在生成的吞吐量方面,还是在大小和形状的可重复性方面,都会使药物测试应用面临挑战。过去几十年来,利用水凝胶的液滴微流体技术因其潜力而备受瞩目。重要的是,核壳结构凝胶液滴可以避免球体与球体之间的粘连,这种粘连会导致检测结果的巨大差异,同时,通过保护核心类器官区域不受外界环境影响,而外部多孔凝胶层仍可进行营养交换,从而实现球体的长期培养,提高均匀性。因此,基于核壳凝胶液滴的球形体形成可以提高药物筛选试验的预测性和可重复性。本综述论文将重点介绍基于液滴微流控技术的癌症球形体生产技术,该技术使用了各种凝胶材料和结构。此外,我们还将讨论有可能推动球形体生产的新兴技术、此类技术的前景以及仍然存在的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Uniform sized cancer spheroids production using hydrogel-based droplet microfluidics: a review

Uniform sized cancer spheroids production using hydrogel-based droplet microfluidics: a review

Three-dimensional (3D) cell culture models have been extensively utilized in various mechanistic studies as well as for drug development studies as superior in vitro platforms than conventional two-dimensional (2D) cell culture models. This is especially the case in cancer biology, where 3D cancer models, such as spheroids or organoids, have been utilized extensively to understand the mechanisms of cancer development. Recently, many sophisticated 3D models such as organ-on-a-chip models are emerging as advanced in vitro models that can more accurately mimic the in vivo tissue functions. Despite such advancements, spheroids are still considered as a powerful 3D cancer model due to the relatively simple structure and compatibility with existing laboratory instruments, and also can provide orders of magnitude higher throughput than complex in vitro models, an extremely important aspects for drug development. However, creating well-defined spheroids remain challenging, both in terms of throughputs in generation as well as reproducibility in size and shape that can make it challenging for drug testing applications. In the past decades, droplet microfluidics utilizing hydrogels have been highlighted due to their potentials. Importantly, core-shell structured gel droplets can avoid spheroid-to-spheroid adhesion that can cause large variations in assays while also enabling long-term cultivation of spheroids with higher uniformity by protecting the core organoid area from external environment while the outer porous gel layer still allows nutrient exchange. Hence, core-shell gel droplet-based spheroid formation can improve the predictivity and reproducibility of drug screening assays. This review paper will focus on droplet microfluidics-based technologies for cancer spheroid production using various gel materials and structures. In addition, we will discuss emerging technologies that have the potential to advance the production of spheroids, prospects of such technologies, and remaining challenges.

Graphical abstract

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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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