Abstract

Scaffolds synthesized from synthetic polymers, though mechanically robust, are hydrophobic in nature, lack sufficient cell attracting cues and are not amenable to monitoring. These drawbacks, however, can be overcome by fabricating a new generation of biocompatible scaffolds with quantum nanoparticle additives and surface functionalization. The objective of the present work was to investigate the enhancement of cellular adhesion, growth, proliferation, differentiation and migration on polymer-based scaffolds. To achieve this, carbon dots (CDs) were melt blended with poly(L-Lactide) acid or PLA, followed by rapid prototyping to generate photoluminescent scaffolds with the advantages of hydrophilicity and built-in monitoring opportunity via two-photon microscopy. Apart from these, cell proliferation and migration aspects in the biological environment are found to be enhanced by oxygen plasma treatment which enables polymer superhydrophilicity. Carbon dots introduces nanoscale roughness, and plasma incorporates hydrophilic oxygen and hydroxyl groups on the scaffolds. After a 7 min plasma treatment, PLA-CD surfaces were found to gain superhydrophilicity (contact angle of 0˚) and cell proliferation increased by 70% relative to the untreated scaffold. Quantitative analysis and bioimaging showed significant increases in ECM mineralization. Thus, the plasma treated PLA-CD composite supports the potential for producing high-performance, monitorable scaffolds for tissue engineering.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.