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Scaffold-free Bioprinting of Mesenchymal Stem Cells with the Regenova Printer: Optimization of Printing Parameters.
Aguilar, Izath Nizeet; Smith, Lester J; Olivos, David J; Chu, Tien-Min Gabriel; Kacena, Melissa A; Wagner, Diane R.
Afiliação
  • Aguilar IN; Department of Orthopaedic Surgery, Indiana University School of Medicine, Indianapolis, Indiana, USA.
  • Smith LJ; Department of Radiology and Imaging Sciences, Indiana University of School of Medicine, Indianapolis, Indiana, USA.
  • Olivos DJ; Department of Biochemistry and Molecular Biology, Indiana University of School of Medicine, Indianapolis, Indiana, USA.
  • Chu TG; Department of Orthopaedic Surgery, Indiana University School of Medicine, Indianapolis, Indiana, USA.
  • Kacena MA; Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47908, USA.
  • Wagner DR; Department of Biomedical and Applied Sciences, Indiana University School of Dentistry, Indianapolis, Indiana, USA.
Bioprinting ; 152019 Sep.
Article em En | MEDLINE | ID: mdl-31457110
The Kenzan bioprinting method provides a high-resolution biofabrication process by facilitating the fusion of submillimeter cell aggregates (spheroids) into larger tissue constructs on a needle array that is removed upon spheroid fusion. Although the method is relatively straightforward in principle, Kenzan method bioprinting relies on a complex 3D bioprinter (Regenova Bio 3D Printer, Cyfuse, K.K., Japan) implementing an advanced vision system to verify the microscopic spheroids' geometry and high-precision mechatronics to aseptically manipulate the spheroids into position. Due to the complexity of the operation, the need for aseptic conditions, and the size of the spheroids, proficiency with the Regenova Bio 3D Printer and the Kenzan method requires development of best practices and troubleshooting techniques to ensure a robust print and minimize the use of resources. In addition, managing the construct post-bioprinting both in culture and for surgical implantation requires careful consideration and workflow design. Here, we describe methods for generating a competent tissue construct and optimizing the bioprinting process. Optimization resulted in a 4-fold reduction in print times, a 20-fold reduction in the use of bioprinting nozzles, and more robust constructs. The results and procedures described herein will have potential applications for tissue engineering, research, and clinical uses in the future.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Ano de publicação: 2019 Tipo de documento: Article