Jose Moran-Mirabal

Prof. Dr. Jose Moran-Mirabal

Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, ON L8S 4M1, Canada
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orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 September 2007 in Nature Materials
Verified
Journal Article
Closed access
JSJason Slinker
Jason Slinker
JDJohn A. DeFranco
John A. DeFranco
MJMichael J. Jaquith
Michael J. Jaquith
WSWilliam R. Silveira
William R. Silveira
YZYu-Wu Zhong
Yu-Wu Zhong
GMGeorge Malliaras
George Malliaras

25 February 2007 in Nature Nanotechnology
Verified
Journal Article
Closed access
PDF file
XZXinjian Zhou
Xinjian Zhou
JMJose Moran-Mirabal
Jose Moran-Mirabal
HCHarold G. Craighead
Harold G. Craighead
PMPaul L. McEuen
Paul L. McEuen

23 January 2007 in Nano Letters
Verified
Journal Article
Closed access
JMJose Moran-Mirabal
Jose Moran-Mirabal
JSJason Slinker
Jason Slinker
JDJohn A. DeFranco
John A. DeFranco
SVScott S. Verbridge
Scott S. Verbridge
RIRob Ilic
Rob Ilic
HCH. G. Craighead
H. G. Craighead

16 August 2013 in Biomacromolecules
Verified
Journal Article
Closed access
TATiffany Abitbol
Tiffany Abitbol
APAnthony Palermo
Anthony Palermo
JMJose Moran-Mirabal
Jose Moran-Mirabal
ECEmily D. Cranston
Emily D. Cranston

16 March 2018 in Chemistry of Materials
Verified
Journal Article
Closed access
AFAyodele Fatona
Ayodele Fatona
RBRichard M. Berry
Richard M. Berry
Michael BrookMichael Brook
Michael Brook
JMJose Moran-Mirabal
Jose Moran-Mirabal

24 November 2021 in Frontiers in Bioengineering and Biotechnology
Verified
Journal Article
Open access
MCMabel Barreiro Carpio
Mabel Barreiro Carpio
MDMohammadhossein Dabaghi
Mohammadhossein Dabaghi
JUJulia Ungureanu
Julia Ungureanu
MKMartin R. Kolb
Martin R. Kolb
JHJeremy A. Hirota
Jeremy A. Hirota
JMJose Moran-Mirabal
Jose Moran-Mirabal
Human lungs are organs with an intricate hierarchical structure and complex composition; lungs also present heterogeneous mechanical properties that impose dynamic stress on different tissue components during the process of breathing. These physiological characteristics combined create a system that is challenging to model in vitro. Many efforts have been dedicated to develop reliable models that afford a better understanding of the structure of the lung and to study cell dynamics, disease evolution, and drug pharmacodynamics and pharmacokinetics in the lung. This review presents methodologies used to develop lung tissue models, highlighting their advantages and current limitations, focusing on 3D bioprinting as a promising set of technologies that can address current challenges. 3D bioprinting can be used to create 3D structures that are key to bridging the gap between current cell culture methods and living tissues. Thus, 3D bioprinting can produce lung tissue biomimetics that can be used to develop in vitro models and could eventually produce functional tissue for transplantation. Yet, printing functional synthetic tissues that recreate lung structure and function is still beyond the current capabilities of 3D bioprinting technology. Here, the current state of 3D bioprinting is described with a focus on key strategies that can be used to exploit the potential that this technology has to offer. Despite today’s limitations, results show that 3D bioprinting has unexplored potential that may be accessible by optimizing bioink composition and looking at the printing process through a holistic and creative lens.