Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2014 May 8;5(2):43-57.
doi: 10.3390/jfb5020043.

HaCaT Keratinocytes Response on Antimicrobial Atelocollagen Substrates: Extent of Cytotoxicity, Cell Viability and Proliferation

Affiliations

HaCaT Keratinocytes Response on Antimicrobial Atelocollagen Substrates: Extent of Cytotoxicity, Cell Viability and Proliferation

Jorge López-García et al. J Funct Biomater. .

Abstract

The effective and widely tested biocides: Benzalkonium chloride, bronopol, chitosan, chlorhexidine and irgasan were added in different concentrations to atelocollagen matrices. In order to assess how these antibacterial agents influence keratinocytes cell growth, cell viability and proliferation were determined by using MTT assay. Acquired data indicated a low toxicity by employing any of these chemical substances. Furthermore, cell viability and proliferation were comparatively similar to the samples where there were no biocides. It means that regardless of the agent, collagen-cell-attachment properties are not drastically affected by the incorporation of those biocides into the substrate. Therefore, these findings suggest that these atelocollagen substrates enhanced by the addition of one or more of these agents may render effectiveness against bacterial stains and biofilm formation, being the samples referred to herein as "antimicrobial substrates" a promising view in the design of novel antimicrobial biomaterials potentially suitable for tissue engineering applications.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Chemical structure of employed antibacterial agents.
Figure 2
Figure 2
Chitosan chemical structure.
Figure 3
Figure 3
Effect of various concentrations of target compounds on HaCaT cell viability. Cell line seeded on atelocollagen matrix with concentration of agent (A) 2.0% (w/w); (B) 1.0% (w/w); (C) 0.5% (w/w); (D) 0.2% (w/w); (E) 0.1% (w/w); (F) 0.02% (w/w) determined by MTT assay (the error bars depict standard deviations and dashed lines define cytotoxicity ranges: non-cytotoxicity > 80%; weak > 60%; moderate > 40%; strong < 40%). *p < 0.05 and **p < 0.01, compared with pristine atelocollagen film.
Figure 4
Figure 4
Concentration-viability curve of studied agents on HaCaT keratinocyte cell line.
Figure 5
Figure 5
Comparison of HaCaT cell growth upon atelocollagen films with and without bactericides determined by measuring absorbance of Formazan product by MTT assay at 570 nm (the error bars signify standard deviation). * p < 0.05 and ** p < 0.01, compared with free of biocide film.
Figure 6
Figure 6
Photomicrographs of Human skin HaCaT keratinocytes in culture upon two atelocollagen films compared with control: (A) Atelocollagen without biocides; (B) An endowed film with cell viability above 80% (non-cytotoxic).

Similar articles

Cited by

References

    1. Parenteau-Bareil R., Gauvin R., Berthod F. Collagen-based biomaterials for tissue enginnering applications. Materials. 2010;3:1863–1887. doi: 10.3390/ma3031863. - DOI
    1. López-García J., Humpolíček P., Lehocký M., Junkar I., Mozetič M. Different source atelocollagen thin films: Preparation, process optimisation and its influence on the interaction with eukaryotic cells. Mater. Tehnol. 2013;47:473–479. doi: 10.1016/j.matdes.2012.12.069. - DOI
    1. Bernal A., Balková R., Kuřítka I., Sáha P. Preparation and characterisation of a new double-sided bio-artificial material prepared by casting of poly(vinyl alcohol) on collagen. Polym. Bull. 2012;70:431–453.
    1. Tanaka Y., Yamaoka H., Nishizawa S., Nagata S., Ogasawara T., Asawa Y., Fujihara Y., Takato T., Hoshi K. The optimization of porous polymeric scaffolds for chondrocyte/atelocollagen based tissue-engineered cartilage. Biomaterials. 2010;31:4506–4516. doi: 10.1016/j.biomaterials.2010.02.028. - DOI - PubMed
    1. Banerjee I., Mishra D., Das T., Maiti S., Maiti T.K. Caprine (Goat) collagen: A potential biomaterial for skin tissue engineering. J. Biomater. Sci. Polym. Ed. 2012;23:355–373. doi: 10.1163/092050610X551943. - DOI - PubMed