TY - JOUR
T1 - 3D Printing of PDMS Improves Its Mechanical and Cell Adhesion Properties
AU - Ozbolat, Veli
AU - Dey, Madhuri
AU - Ayan, Bugra
AU - Povilianskas, Adomas
AU - Demirel, Melik C.
AU - Ozbolat, Ibrahim T.
N1 - Funding Information:
The authors thank Dr. Jian Yang and Ethan Gerhard from Biomedical Engineering Department at Pennsylvania State University for their assistance with mechanical testing experiments. The authors also thank Bruce Perrulli and Julia-Grace Polish from Anton-Paar USA, Inc., for their assistance with the rheology experiments. The authors are grateful to Dr. Dino Ravnic (Department of Surgery at the Pennsylvania State University) for providing the INCREDIBLE 3D bioprinter. The authors also thank Dr. Thomas Neuberger with his assistance with the MRI scan. Veli Ozbolat acknowledges the support from the International Postdoctoral Research Scholarship Program (BIDEP 2219) of the Scientific and Technological Research Council of Turkey (TUBITAK), and Bugra Ayan acknowledges support from the Turkish Ministry of National Education. The authors are also thankful to Materials Research Institute at the Pennsylvania State University in supporting the porosity experiments.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2018/2/12
Y1 - 2018/2/12
N2 - Despite extensive use of polydimethylsiloxane (PDMS) in medical applications, such as lab-on-a-chip or tissue/organ-on-a-chip devices, point-of-care devices, and biological machines, the manufacturing of PDMS devices is limited to soft-lithography and its derivatives, which prohibits the fabrication of geometrically complex shapes. With the recent advances in three-dimensional (3D) printing, use of PDMS for fabrication of such complex shapes has gained considerable interest. This research presents a detailed investigation on printability of PDMS elastomers over three concentrations for mechanical and cell adhesion studies. The results demonstrate that 3D printing of PDMS improved the mechanical properties of fabricated samples up to three fold compared to that of cast ones because of the decreased porosity of bubble entrapment. Most importantly, 3D printing facilitates the adhesion of breast cancer cells, whereas cast samples do not allow cellular adhesion without the use of additional coatings such as extracellular matrix proteins. Cells are able to adhere and grow in the grooves along the printed filaments demonstrating that 3D printed devices can be engineered with superior cell adhesion qualities compared to traditionally manufactured PDMS devices.
AB - Despite extensive use of polydimethylsiloxane (PDMS) in medical applications, such as lab-on-a-chip or tissue/organ-on-a-chip devices, point-of-care devices, and biological machines, the manufacturing of PDMS devices is limited to soft-lithography and its derivatives, which prohibits the fabrication of geometrically complex shapes. With the recent advances in three-dimensional (3D) printing, use of PDMS for fabrication of such complex shapes has gained considerable interest. This research presents a detailed investigation on printability of PDMS elastomers over three concentrations for mechanical and cell adhesion studies. The results demonstrate that 3D printing of PDMS improved the mechanical properties of fabricated samples up to three fold compared to that of cast ones because of the decreased porosity of bubble entrapment. Most importantly, 3D printing facilitates the adhesion of breast cancer cells, whereas cast samples do not allow cellular adhesion without the use of additional coatings such as extracellular matrix proteins. Cells are able to adhere and grow in the grooves along the printed filaments demonstrating that 3D printed devices can be engineered with superior cell adhesion qualities compared to traditionally manufactured PDMS devices.
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U2 - 10.1021/acsbiomaterials.7b00646
DO - 10.1021/acsbiomaterials.7b00646
M3 - Article
AN - SCOPUS:85041919986
SN - 2373-9878
VL - 4
SP - 682
EP - 693
JO - ACS Biomaterials Science and Engineering
JF - ACS Biomaterials Science and Engineering
IS - 2
ER -