Polymers 2012, 4(3), 1535-1553; doi:10.3390/polym4031535
Article

Physical Properties of Polypeptide Electrospun Nanofiber Cell Culture Scaffolds on a Wettable Substrate

1,2,* email, 1email and 1email
Received: 20 April 2012; in revised form: 9 August 2012 / Accepted: 23 August 2012 / Published: 31 August 2012
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Physical properties of poly(L-ornithine) (PLO), a polycation, poly(L-glutamic acid4-co-L-tyrosine) (PLEY), a polyanion, and electrospun fibers made of these polymers have been determined and compared. The polymers adopted random coil-like conformations in aqueous feedstocks at neutral pH and in dehydrated cast films and fibers on glass, and the fibers comprised numerous counterions, according to spectral analysis. Adsorption of model proteins and serum proteins onto hydrated and crosslinked fibers depended on the electrical charge of the proteins and the fibers. The surface charge density of the fibers will be comparable to, but less than, the charge density on the outer leaflet of the plasma membrane of usual eukaryotic cells. The present analysis thus advances understanding of cell behavior on electrospun fiber scaffolds, a topic of considerable current interest.
Keywords: cell; electrospinning; fiber; physics; polypeptide; scaffold
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MDPI and ACS Style

Haynie, D.T.; Khadka, D.B.; Cross, M.C. Physical Properties of Polypeptide Electrospun Nanofiber Cell Culture Scaffolds on a Wettable Substrate. Polymers 2012, 4, 1535-1553.

AMA Style

Haynie DT, Khadka DB, Cross MC. Physical Properties of Polypeptide Electrospun Nanofiber Cell Culture Scaffolds on a Wettable Substrate. Polymers. 2012; 4(3):1535-1553.

Chicago/Turabian Style

Haynie, Donald T.; Khadka, Dhan B.; Cross, Michael C. 2012. "Physical Properties of Polypeptide Electrospun Nanofiber Cell Culture Scaffolds on a Wettable Substrate." Polymers 4, no. 3: 1535-1553.

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