Researchers, including those from the University of Tokyo, pioneered a new method for encapsulating cells within small, soft capsules. This is useful for various kinds of research where the properties of a cell, including its behaviors and interactions, need to be isolated and measured. Previous methods required more specialized equipment, time and expertise. The new method needs only basic lab equipment and can open up access to advanced 3D cell culture research to a broad range of researchers.
Cells are typically studied outside the body under controlled laboratory conditions. However, conventional flat cell culture methods do not fully reproduce the complex three-dimensional environments that cells experience in living tissues. Tiny hydrogel capsules offer one way to culture cells in a confined three-dimensional space, allowing researchers to study how cells grow, organize and interact under more tissue like conditions. Current methods to do this come with a high cost and set of requirements that put such research out of reach to many.
“Using conventional methods, creating these cell-containing capsules requires what is known as a microfluidic device to encapsulate cells one by one. The use of microfluidic devices requires expensive and complex specialized equipment, which can limit accessibility and scalability,” said Professor Sadao Ota of the Research Center for Advanced Science and Technology at the University of Tokyo. “So we invented a different approach. Instead of encapsulating cells individually during droplet generation, we first prepared uniform gelatin beads as templates in advance. Cells were then introduced into these templates during what we call the emulsion-templated gel-embedding (ETE) process, followed by formation of the surrounding hydrogel shell to yield cell-containing capsules.”
ETE needs only simple laboratory tools, such as a vortex mixer and temperature controls, which are common in many labs. Using ETE, the team demonstrated scalable production of more than 100,000 cell-containing capsules in a single workflow. Cells grown inside the capsules remained viable and proliferated comparably to those produced using conventional microfluidic approaches. The team’s method worked with suspension cells, which grow while floating freely in culture, and the researchers also explored its applicability to adherent cell types, which normally grow while attached to other cells or supporting materials. Tests showed that different cell types can exist within capsules in predictable ways, potentially enabling future studies looking into dynamic interactions such as those seen between tumors and immune cells.
“One of the biggest challenges was achieving two goals at the same time: producing capsules with uniform size, while also ensuring the cells remained healthy,” said Ota. “Simpler methods often yield more variation in capsule size or can even damage cells during the process. By using prefabricated gelatin beads as templates, we were able to control capsule size while maintaining cell viability.”
The capsules are customizable, and researchers can alter their size and properties depending on their usage. This flexibility could make the technique useful in areas including drug screening, regenerative medicine, and basic cell biology research. Although the technology is currently aimed at research use, medical applications may be possible too. Hydrogel capsules could potentially help protect transplanted cells from immune-system attack, though this possibility was not tested in the study and requires further investigation.
“At this stage, the technology is primarily intended for research applications, such as drug screening and cell biology studies. We did not test primary or patient-derived cells in this study, so their compatibility remains to be determined. Further optimization of the system may be needed to better support the growth of adherent cells and other cell types,” said Ota. “We hope this method will allow more laboratories to perform advanced cell culture experiments without requiring specialized engineering expertise. By making the materials and protocols more accessible, we aim to support broader adoption and collaborative development of this technology.”
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Journal: Natsuko Otaki, Yuki Goda, Pooja Shukla, Hiromi Kirisako, Yuko Yamagata, Megumi Matsuo, Kazuki Hattori, Eiryo Kawakami, Sadao Ota, “Emulsion-Templated Gel Embedding: A Microfluidics Free Method for Scalable Cell Encapsulation in Hydrogel Microcapsules”, ACS Biomaterials Science & Engineering, 10.1021/acsbiomaterials.5c02129
Competing interests: N.O., Y.G., E.K., S.O., K.H., and H.K. are listed as inventors on a patent application related to this work (PCT/JP2025/043191), filed by Chiba University and The University of Tokyo. The other authors declare no competing interests.
Funding:
Japan Science and Technology Agency (JST): JPMJPR24N3, JPMJMS2025, JPMJCR23B6, JPMJGX23B1
Japan Agency for Medical Research and Development (AMED): JP21gm1210003, JP223fa627003, JP23tk0124003, JP22gm6710008, JP256f0137008
Japan Society for the Promotion of Science (JSPS): JPJSCCA20200006, JP22K12797, JP25K18827, 25H01359
Cell Science Research Foundation
Institute for Fermentation
Takeda Science Foundation
Nakatani Foundation
Mochida Memorial Foundation for Medical and Pharmaceutical Research
Useful links:
Research Center for Advanced Science and Technology - https://www.rcast.u-tokyo.ac.jp/en/
Ota lab - https://www.sadaotalab.net/
Research Contact:
Professor Sadao Ota
Networked Biophotonics and Microfluidics (Ota Lab), RCAST at University of Tokyo, 3-8-1 Komaba Meguro-ku Tokyo 153-8902 JAPAN
sadaota@g.ecc.u-tokyo.ac.jp
Press contact:
Mr. Rohan Mehra
Strategic Communications Group, The University of Tokyo,
7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan
press-releases.adm@gs.mail.u-tokyo.ac.jp
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ACS Biomaterials Science & Engineering
10.1021/acsbiomaterials.5c02129
Experimental study
Cells
Emulsion-Templated Gel Embedding: A Microfluidics Free Method for Scalable Cell Encapsulation in Hydrogel Microcapsules
21-May-2026
N.O., Y.G., E.K., S.O., K.H., and H.K. are listed as inventors on a patent application related to this work (PCT/JP2025/043191), filed by Chiba University and The University of Tokyo. The other authors declare no competing interests.