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Development of a stem cell spheroid‐laden patch with high retention at skin wound site.

Authors :
Jeong, Gun‐Jae
Im, Gwang‐Bum
Lee, Tae‐Jin
Kim, Sung‐Won
Jeon, Hye Ran
Lee, Dong‐Hyun
Baik, Sangyul
Pang, Changhyun
Kim, Tae‐Hyung
Kim, Dong‐Ik
Jang, Young Charles
Bhang, Suk Ho
Source :
Bioengineering & Translational Medicine. May2022, Vol. 7 Issue 2, p1-10. 10p.
Publication Year :
2022

Abstract

Mesenchymal stem cells such as human adipose tissue‐derived stem cells (hADSCs) have been used as a representative therapeutic agent for tissue regeneration because of their high proliferation and paracrine factor‐secreting abilities. However, certain points regarding conventional ADSC delivery systems, such as low cell density, secreted cytokine levels, and cell viability, still need to be addressed for treating severe wounds. In this study, we developed a three‐dimensional (3D) cavity‐structured stem cell‐laden system for overdense delivery of cells into severe wound sites. Our system includes a hydrophobic surface and cavities that can enhance the efficiency of cell delivery to the wound site. In particular, the cavities in the system facilitate hADSC spheroid formation, increasing therapeutic growth factor expression compared with 2D cultured cells. Our hADSC spheroid‐loaded patch exhibited remarkably improved cell localization at the wound site and dramatic therapeutic efficacy compared to the conventional cell injection method. Taken together, the hADSC spheroid delivery system focused on cell delivery, and stem cell homing effect at the wound site showed a significantly enhanced wound healing effect. By overcoming the limitations of conventional cell delivery methods, our overdense cell delivery system can contribute to biomedical and clinical applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23806761
Volume :
7
Issue :
2
Database :
Academic Search Index
Journal :
Bioengineering & Translational Medicine
Publication Type :
Academic Journal
Accession number :
156939568
Full Text :
https://doi.org/10.1002/btm2.10279