TY - JOUR
T1 - Spatiotemporal quantification of acoustic cell patterning using Voronoï tessellation
AU - Armstrong, James P.K.
AU - Maynard, Stephanie A.
AU - Pence, Isaac J.
AU - Franklin, Amanda C.
AU - Drinkwater, Bruce W.
AU - Stevens, Molly M.
N1 - Funding Information:
J. P. K. A. was funded by Arthritis Research U.K. Foundation (21138) and the Medical Research Council (MR/S00551X/1). S. A. M. was supported by a Ph.D. studentship within Biomedicine and Bioengineering in Osteoarthritis, Imperial College London. I. J. P. was supported by the Whitaker International Program, Institute of International Education, U.S.A. A. C. F. acknowledges PhD funding through an Engineering and Physical Sciences Research Council (EPSRC) DRP studentship. B. W. D. acknowledges support from the Royal Society and the Wolfson Foundation (WM160081). M. M. S. acknowledges support from the grants from the UK Regenerative Medicine Platform “Acellular Approaches for Therapeutic Delivery” (MR/K026682/1) and “Acellular/Smart Materials – 3D Architecture” (MR/R015651/1), the European Research Council (ERC) Seventh Framework Programme Consolidator grant “Naturale CG” (616417), the Rosetrees Trust and the Wellcome Trust Senior Investigator Award (098411/Z/12/Z). The authors acknowledge the use of the Facility for Imaging and Light Microscopy (FILM) at Imperial College London and assistance provided by the Department of Physics Mechanical Instrumentation Workshop at Imperial College London, as well as Håkon Høgset for assistance with rheological testing. Research raw data is available on request from https://rdm-enquiries@imperial.ac.uk.
Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2019/2/21
Y1 - 2019/2/21
N2 - Acoustic patterning using ultrasound standing waves has recently emerged as a potent biotechnology enabling the remote generation of ordered cell systems. This capability has opened up exciting opportunities, for example, in guiding the development of organoid cultures or the organization of complex tissues. The success of these studies is often contingent on the formation of tightly-packed and uniform cell arrays; however, a number of factors can act to disrupt or prevent acoustic patterning. Yet, to the best of our knowledge, there has been no comprehensive assessment of the quality of acoustically-patterned cell populations. In this report we use a mathematical approach, known as Voronoï tessellation, to generate a series of metrics that can be used to measure the effect of cell concentration, pressure amplitude, ultrasound frequency and biomaterial viscosity upon the quality of acoustically-patterned cell systems. Moreover, we extend this approach towards the characterization of spatiotemporal processes, namely, the acoustic patterning of cell suspensions and the migration of patterned, adherent cell clusters. This strategy is simple, unbiased and highly informative, and we anticipate that the methods described here will provide a systematic framework for all stages of acoustic patterning, including the robust quality control of devices, statistical comparison of patterning conditions, the quantitative exploration of parameter limits and the ability to track patterned tissue formation over time.
AB - Acoustic patterning using ultrasound standing waves has recently emerged as a potent biotechnology enabling the remote generation of ordered cell systems. This capability has opened up exciting opportunities, for example, in guiding the development of organoid cultures or the organization of complex tissues. The success of these studies is often contingent on the formation of tightly-packed and uniform cell arrays; however, a number of factors can act to disrupt or prevent acoustic patterning. Yet, to the best of our knowledge, there has been no comprehensive assessment of the quality of acoustically-patterned cell populations. In this report we use a mathematical approach, known as Voronoï tessellation, to generate a series of metrics that can be used to measure the effect of cell concentration, pressure amplitude, ultrasound frequency and biomaterial viscosity upon the quality of acoustically-patterned cell systems. Moreover, we extend this approach towards the characterization of spatiotemporal processes, namely, the acoustic patterning of cell suspensions and the migration of patterned, adherent cell clusters. This strategy is simple, unbiased and highly informative, and we anticipate that the methods described here will provide a systematic framework for all stages of acoustic patterning, including the robust quality control of devices, statistical comparison of patterning conditions, the quantitative exploration of parameter limits and the ability to track patterned tissue formation over time.
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U2 - 10.1039/c8lc01108g
DO - 10.1039/c8lc01108g
M3 - Article
C2 - 30667009
AN - SCOPUS:85061363468
SN - 1473-0197
VL - 19
SP - 562
EP - 573
JO - Lab on a Chip - Miniaturisation for Chemistry and Biology
JF - Lab on a Chip - Miniaturisation for Chemistry and Biology
IS - 4
ER -