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Microphysiometry

Microphysiometry is the in vitro measurement of the functions and activities of life or of living matter (as organs, tissues, or cells) and of the physical and chemical phenomena involved on a very small (micrometer) scale.[1][2] The term microphysiometry emerged in the scientific literature at the end of the 1980s.[3][4]

The primary parameters assessed in microphysiometry comprise pH and the concentration of dissolved oxygen, glucose, and lactic acid, with an emphasis on the first two. Measuring these parameters experimentally in combination with a fluidic system for cell culture maintenance and a defined application of drugs or toxins provides the quantitative output parameters extracellular acidification rates (EAR), oxygen consumption rates (OUR), and rates of glucose consumption or lactate release to characterize the metabolic situation.

Due to the label-free nature of sensor-based measurements, dynamic monitoring of cells or tissues for several days or even longer is feasible.[5] On an extended timescale, a dynamic analysis of a cell's metabolic response to an experimental treatment can distinguish acute effects (e.g., one hour after a treatment), early effects (e.g., at 24 hours), and delayed, chronic responses (e.g., at 96 hours). As stated by Alajoki et al., "The concept is that it is possible to detect receptor activation and other physiological changes in living cells by monitoring the activity of energy metabolism".[6]

See also edit

References edit

  1. ^ McConnel HM, Owicki JC, Parce JW, Miller DL, Baxter GT, Wada HG, Pitchford S (1992). "The Cytosensor Microphysiometer: Biological Applications of Silicon Technology", Science, 257, 1906-1912
  2. ^ Brischwein, M.; Wiest, J. (2018). "Microphysiometry". Bioanalytical Reviews. Springer. doi:10.1007/11663_2018_2.
  3. ^ Hafeman DG, Parce JW, McConnell H (1988). "Light-addressable potentiometric sensor for biochemical systems", Science 240, 1182–1185
  4. ^ Owicki JC, Parce JW (1990). "Bioassays with a microphysiometer". Nature 344, 271–272
  5. ^ Wiest, J. (2022). "Systems engineering of microphysiometry". Organs-on-a-Chip. Elsevier B.V. doi:10.1016/j.ooc.2022.100016.
  6. ^ Alajoki ML, Bayter GT, Bemiss WR, Blau D, Bousse LJ, Chan SDH, Dawes TD, Hahnenberger KM, Hamilton JM, Lam P, McReynolds RJ, Modlin DN, Owicki C, Parce JW, Redington D, Stevenson K, Wada HG, Williams J (1997). "High-performance microphysiometry in drug discovery", Devlin JP (ed) High Throughput Screening: The Discovery of Bioactive Substances. Marcel Dekker, New York, 427–442.

microphysiometry, vitro, measurement, functions, activities, life, living, matter, organs, tissues, cells, physical, chemical, phenomena, involved, very, small, micrometer, scale, term, microphysiometry, emerged, scientific, literature, 1980s, primary, paramet. Microphysiometry is the in vitro measurement of the functions and activities of life or of living matter as organs tissues or cells and of the physical and chemical phenomena involved on a very small micrometer scale 1 2 The term microphysiometry emerged in the scientific literature at the end of the 1980s 3 4 The primary parameters assessed in microphysiometry comprise pH and the concentration of dissolved oxygen glucose and lactic acid with an emphasis on the first two Measuring these parameters experimentally in combination with a fluidic system for cell culture maintenance and a defined application of drugs or toxins provides the quantitative output parameters extracellular acidification rates EAR oxygen consumption rates OUR and rates of glucose consumption or lactate release to characterize the metabolic situation Due to the label free nature of sensor based measurements dynamic monitoring of cells or tissues for several days or even longer is feasible 5 On an extended timescale a dynamic analysis of a cell s metabolic response to an experimental treatment can distinguish acute effects e g one hour after a treatment early effects e g at 24 hours and delayed chronic responses e g at 96 hours As stated by Alajoki et al The concept is that it is possible to detect receptor activation and other physiological changes in living cells by monitoring the activity of energy metabolism 6 See also editOrgan on a chipReferences edit McConnel HM Owicki JC Parce JW Miller DL Baxter GT Wada HG Pitchford S 1992 The Cytosensor Microphysiometer Biological Applications of Silicon Technology Science 257 1906 1912 Brischwein M Wiest J 2018 Microphysiometry Bioanalytical Reviews Springer doi 10 1007 11663 2018 2 Hafeman DG Parce JW McConnell H 1988 Light addressable potentiometric sensor for biochemical systems Science 240 1182 1185 Owicki JC Parce JW 1990 Bioassays with a microphysiometer Nature 344 271 272 Wiest J 2022 Systems engineering of microphysiometry Organs on a Chip Elsevier B V doi 10 1016 j ooc 2022 100016 Alajoki ML Bayter GT Bemiss WR Blau D Bousse LJ Chan SDH Dawes TD Hahnenberger KM Hamilton JM Lam P McReynolds RJ Modlin DN Owicki C Parce JW Redington D Stevenson K Wada HG Williams J 1997 High performance microphysiometry in drug discovery Devlin JP ed High Throughput Screening The Discovery of Bioactive Substances Marcel Dekker New York 427 442 Retrieved from https en wikipedia org w index php title Microphysiometry amp oldid 1189480541, wikipedia, wiki, book, books, library,

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