Bioprinting Toward Organ Fabrication: Challenges and Future Trends
By Ibrahim T. Ozbolat, Yin Yu. IEEE Transactions on Biomedical Engineering, 2013
583 citations recorded by the source corpus.
Subfields: Automotive Engineering, Biomedical Engineering, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/976b8e5d453c212ea2704df77ec2226b8a17a484
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Automotive Engineering
In Biomedical Engineering
In Molecular Biology
- Madhuri Dey
- Monika Hospodiuk
- Deok‐Ho Kim
- Y. Liu
- Ibrahim T. Ozbolat
- K. Leong
- Keekyoung Kim
- Christian J Mandrycky
Citations in the corpus
- 3D Bioprinting for Engineering Complex Tissues (2015, background): “For clinical applications, cells for bioprinting would ideally be isolated from the patients themselves to avoid negative immune responses (Ozbolat and Yu 2013).”
- 3D printing of smart materials: A review on recent progresses in 4D printing (2015, background): “Moreover, the current tissue engineering technology has a few major limitations such as non-automated manipulation, small manufacturing scale, inability to produce complex 3D organs and non-ordered and weak tissue microstructure (Ozbolat and Yu 2013, Chua and Yeong 2015).”
- A comprehensive review on droplet-based bioprinting: Past, present and future. (2016, background): “Different bioprinting modalities, including DBB, are envisioned to fabricate functional replacement human organs in the future [10,138]; however, several challenges have yet to be overcome to make it a reality.”
- 3D bioprinting for biomedical devices and tissue engineering: A review of recent trends and advances (2018, background): “The main reason for that is the inherent inability of printing head to provide a continuous flow which limits its application in bioprinting [8].”
- Current advances and future perspectives in extrusion-based bioprinting. (2016, background): “In addition, parenchymal cells in highly metabolic organs do not secrete many ECM components, and the resulting cell aggregates are very weak in mechanical and structural integrity [174].”