Reconfigurable Hanging Drop Microarray Platform for On‐Demand Preparation and Analysis of Spheroid Array

Author:

Kim Hwisoo1ORCID,Kim Bumsoo2,Kim Soo Jee1,Choi Yejin1,Kim Irene Hae‐Rim1,Han Jieun1,Park Young‐Gyun1,Han Yong‐Mahn3,Park Je‐Kyun145ORCID

Affiliation:

1. Department of Bio and Brain Engineering Korea Advanced Institute of Science and Technology (KAIST) 291 Daehak‐ro, Yuseong‐gu Daejeon 34141 Republic of Korea

2. Department of Biological Sciences Korea Advanced Institute of Science and Technology (KAIST) 291 Daehak‐ro, Yuseong‐gu Daejeon 34141 Republic of Korea

3. Graduate School of Medical Science and Engineering Korea Advanced Institute of Science and Technology (KAIST) 291 Daehak‐ro, Yuseong‐gu Daejeon 34141 Republic of Korea

4. KI for Health Science and Technology KAIST Institutes (KI) 291 Daehak‐ro, Yuseong‐gu Daejeon 34141 Republic of Korea

5. KI for NanoCentury KAIST Institutes (KI) 291 Daehak‐ro, Yuseong‐gu Daejeon 34141 Republic of Korea

Abstract

AbstractIn response to the increasing demand for spheroid‐based cancer research, the importance of developing integrated platforms that can simultaneously facilitate high‐throughput spheroid production and multiplexed analysis is emphasized. In addition, the understanding of how the size and cellular composition of tumors directly influence their internal structures and functionalities underlines the critical need to produce spheroids of diverse sizes and compositions on a large scale. To address this rising demand, this work presents a configurable and linkable in vitro three‐dimensional (3D) cell culture kit (CLiCK) for spheroids, termed CLiCK‐Spheroid. This platform consists of three primary components: a hanging drop microarray (HDMA), a concave pillar microarray (CPMA), and gradient blocks. The HDMA alone produces a homogeneous spheroid array, while its combination with the gradient block enables one‐step generation of a size‐gradient spheroid array. Using the size‐gradient spheroid arrays, the occurrence of necrotic cores based on spheroid size is demonstrated. Additionally, spheroids in a single batch can be conveniently compartmentalized and regrouped using a CPMA, enhancing the versatility of spheroid arrays and enabling multiplexed drug treatments. By combining the different assembly methods, this work has achieved high‐throughput production of cell composition‐gradient spheroid arrays, with noticeable variations in morphology and vascularization based on cell compositions.

Funder

National Research Foundation of Korea

Publisher

Wiley

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