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Scaffold‐Free Bio‐3D Printing Using Spheroids as “Bio‐Inks” for Tissue (Re‐)Construction and Drug Response Tests
In recent years, scaffold‐free bio‐3D printing using cell aggregates (spheroids) as “bio‐inks” has attracted increasing attention as a method for 3D cell construction. Bio‐3D printing uses a technique called the Kenzan method, wherein spheroids are placed one‐by‐one in a microneedle array (the “Kenz...
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Published in: | Advanced healthcare materials 2020-08, Vol.9 (15), p.e1901831-n/a |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | In recent years, scaffold‐free bio‐3D printing using cell aggregates (spheroids) as “bio‐inks” has attracted increasing attention as a method for 3D cell construction. Bio‐3D printing uses a technique called the Kenzan method, wherein spheroids are placed one‐by‐one in a microneedle array (the “Kenzan”) using a bio‐3D printer. The bio‐3D printer is a machine that was developed to perform bio‐3D printing automatically. Recently, it has been reported that cell constructs can be produced by a bio‐3D printer using spheroids composed of many types of cells and that this can contribute to tissue (re‐)construction. This progress report summarizes the production and effectiveness of various cell constructs prepared using bio‐3D printers. It also considers the future issues and prospects of various cell constructs obtained by using this method for further development of scaffold‐free 3D cell constructions.
Scaffold‐free bio‐3D printing using spheroids as “bio‐inks” contributes to tissue (re‐)construction and drug response tests. Spheroids are placed one‐by‐one in a microneedle array (the “Kenzan”) using a bio‐3D printer. The production and effectiveness of various cell constructs prepared using the bio‐3D printer are summarized, and the future issues and prospects for further development of the constructs are considered. |
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ISSN: | 2192-2640 2192-2659 |
DOI: | 10.1002/adhm.201901831 |