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2018 | OriginalPaper | Chapter

21. High Speed Imaging Techniques to Study Effects of Pressure Waves from Detonating Explosive Charges on Biological Materials

Authors : Thuvan Piehler, Nicole Zander, Rohan Banton, Richard Benjamin, Ray Sparks, Kimberly Byrnes, Josh Duckworth, Ben A. Bahr

Published in: Dynamic Behavior of Materials, Volume 1

Publisher: Springer International Publishing

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Abstract

Threshold shock-impulse levels required to induce cellular injury and cumulative effects upon single and/or multiple exposures are not well-characterized. There are very few in vitro experimental model with blast pressure waves generated by using explosives in the laboratory for investigating the effects of primary blast induced traumatic brain injury. Hence, it is critical to develop a reliable experimental research tool in the laboratory to study how functional and structural alteration or damage at the cellular and tissue levels following explosive blast impacts for future improvement of detection and subsequent treatment and protection. US Army Research Laboratory (ARL) developed the unique in vitro indoor experimental platform that uses military explosive charges to accurately represent battle-field blast exposure and to probe the effects of primary explosive blast on dissociated neurons and tissue slices. We believe this is one of the controlled experimental methods to analyze, characterize primary explosive blast induced cellular injury, and understand threshold injury phenomenon.

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Literature
1.
go back to reference Zander, N.E., Piehler, T., Boggs, M.E., Banton, R., Benjamin, R.: In vitro studies of primary explosive blast loading on neurons. J. Neurosci. Res. 93, 1353–1363 (2015)CrossRef Zander, N.E., Piehler, T., Boggs, M.E., Banton, R., Benjamin, R.: In vitro studies of primary explosive blast loading on neurons. J. Neurosci. Res. 93, 1353–1363 (2015)CrossRef
2.
go back to reference Zander, N.E., Piehler, T., Banton, R., Boggs, M.: The effect of explosive blast loading on human neuroblastoma cells. Anal. Biochem. 504, 4–6 (2016)CrossRef Zander, N.E., Piehler, T., Banton, R., Boggs, M.: The effect of explosive blast loading on human neuroblastoma cells. Anal. Biochem. 504, 4–6 (2016)CrossRef
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go back to reference Wisniewski, M.L., Hwang, J., Bahr, B.A.: Submicromolar Aβ42 reduces hippocampal glutamate receptors and presynaptic markers in an aggregation-dependent manner. Biochim. Biophys. Acta. 1812, 1664–1674 (2011)CrossRef Wisniewski, M.L., Hwang, J., Bahr, B.A.: Submicromolar Aβ42 reduces hippocampal glutamate receptors and presynaptic markers in an aggregation-dependent manner. Biochim. Biophys. Acta. 1812, 1664–1674 (2011)CrossRef
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go back to reference Smith, M., Piehler, T., Benjamin, R., Farizatto, K.L., Pait, M.C., Almeida, M.F., Ghukasyan, V.V., Bahr, B.A.: Blast waves from detonated RDX explosive reduce GluR1 and synaptophysin levels in hippocampal slice cultures. Exp. Neurol. 286, 107–115 (2016)CrossRef Smith, M., Piehler, T., Benjamin, R., Farizatto, K.L., Pait, M.C., Almeida, M.F., Ghukasyan, V.V., Bahr, B.A.: Blast waves from detonated RDX explosive reduce GluR1 and synaptophysin levels in hippocampal slice cultures. Exp. Neurol. 286, 107–115 (2016)CrossRef
Metadata
Title
High Speed Imaging Techniques to Study Effects of Pressure Waves from Detonating Explosive Charges on Biological Materials
Authors
Thuvan Piehler
Nicole Zander
Rohan Banton
Richard Benjamin
Ray Sparks
Kimberly Byrnes
Josh Duckworth
Ben A. Bahr
Copyright Year
2018
DOI
https://doi.org/10.1007/978-3-319-62956-8_21

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