Self-referencing luminescent optrodes for non-invasive, real time measurement of extracellular flux

Autonomous technologies are needed which are capable of sensing real time changes in biophysical transport across cell membranes/organelles. These technologies must not only be highly sensitive/selective, but must also be minimally invasive/intrusive, causing no significant physical/chemical effects on cell behavior. Challenges with mainstream technologies (e.g., assays, fluorescent dyes, microsensors) include signal noise/drift, low temporal resolution, requirement of large sample sizes, cytoxicity, organelle sequestration, and intracellular buffering. Recent advancements in fiber optics have greatly enhanced the performance of microsensors (e.g., increased sensitivity/selectivity, response time), but used in concentration mode near cells/tissues these sensors suffer from poor signal to noise ratio. Work over the last few decades has advanced microsensor utility through sensing modalities that extend and enhance the data recorded by sensors. This technique, known as self-referencing, converts static micro/nanosensors with otherwise low signal-to-noise ratios into dynamic flux sensors capable of filtering out signals not associated with active transport by acquisition and amplification of differential signals. Here, we demonstrate the use of a self-referencing referencing frequency domain fiber optic microsensor containing a quenched dye (platinum tetrakis-pentafluorophenyl porphyrin) for quantifying cell/tissue flux in biomedical, agricultural, and environmental applications.

[1]  D Marshall Porterfield,et al.  Non-invasive quantification of endogenous root auxin transport using an integrated flux microsensor technique. , 2010, The Plant journal : for cell and molecular biology.

[2]  R Margreiter,et al.  Mitochondrial respiration in the low oxygen environment of the cell. Effect of ADP on oxygen kinetics. , 1998, Biochimica et biophysica acta.

[3]  Stefano Mancuso,et al.  Noninvasive and continuous recordings of auxin fluxes in intact root apex with a carbon nanotube-modified and self-referencing microelectrode. , 2005, Analytical biochemistry.

[4]  B. Corkey,et al.  Oxygen Consumption Oscillates in Single Clonal Pancreatic-Cells ( HIT ) , 2000 .

[5]  B. Jørgensen,et al.  Spectral light measurements in microbenthic phototrophic communities with a fiber‐optic microprobe coupled to a sensitive diode array detector , 1992 .

[6]  L. Jaffe,et al.  Detection of extracellular calcium gradients with a calcium-specific vibrating electrode , 1990, The Journal of cell biology.

[7]  A. Murphy,et al.  Flavonoids and auxin transport: modulators or regulators? , 2007, Trends in plant science.

[8]  Rongsheng Chen,et al.  Plastic fibre optic oxygen sensors based on polymer matrix doped with Pt (II) complexes , 2009, International Conference on Optical Fibre Sensors.

[9]  John Alderman,et al.  A low-volume platform for cell-respirometric screening based on quenched-luminescence oxygen sensing. , 2004, Biosensors & bioelectronics.

[10]  Célia Baroux,et al.  Cellular efflux of auxin catalyzed by the Arabidopsis MDR/PGP transporter AtPGP1. , 2005, The Plant journal : for cell and molecular biology.

[11]  O. Wolfbeis Fiber-optic chemical sensors and biosensors. , 2002, Analytical chemistry.

[12]  P. Verslues,et al.  Root growth and oxygen relations at low water potentials. Impact Of oxygen availability in polyethylene glycol solutions , 1998, Plant physiology.

[13]  Eric S. McLamore,et al.  Self-referencing optrodes for measuring spatially resolved, real-time metabolic oxygen flux in plant systems , 2010, Planta.

[14]  K. Lewis Persister cells, dormancy and infectious disease , 2007, Nature Reviews Microbiology.

[15]  P. Smith,et al.  Oxygen consumption oscillates in single clonal pancreatic beta-cells (HIT). , 2000, Diabetes.

[16]  Ichiro Okura,et al.  Photostable Optical Oxygen Sensing Material: Platinum Tetrakis(pentafluorophenyl)porphyrin Immobilized in Polystyrene , 1997 .

[17]  M. Hodson,et al.  Antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis: a European consensus. , 2000, The European respiratory journal.

[18]  D. Buckley,et al.  A cell viability assay based on monitoring respiration by optical oxygen sensing. , 2000, Analytical biochemistry.

[19]  Bindley Bioscience Self-referencing optrode technology for non-invasive real-time measurement of biophysical flux and physiological sensing† , 2009 .

[20]  Ingo Klimant,et al.  Optical sensors for application in intelligent food-packaging technology , 2003, SPIE OPTO-Ireland.

[21]  D Marshall Porterfield,et al.  Measuring metabolism and biophysical flux in the tissue, cellular and sub-cellular domains: recent developments in self-referencing amperometry for physiological sensing. , 2007, Biosensors & bioelectronics.

[22]  V. Chodavarapu,et al.  Enhancement of luminescent quenching based oxygen sensing by gold nanoparticles: comparison between luminophore:matrix:nanoparticle thin films on glass and gold coated substrates , 2010 .

[23]  Mahvash Zuberi,et al.  Large naturally-produced electric currents and voltage traverse damaged mammalian spinal cord , 2008, Journal of biological engineering.

[24]  E. McLamore,et al.  Membrane-aerated biofilm proton and oxygen flux during chemical toxin exposure. , 2010, Environmental science & technology.

[25]  Joost T. van Dongen,et al.  Regulation of respiration when the oxygen availability changes. , 2009, Physiologia plantarum.

[26]  R. Shi,et al.  The critical role of voltage-dependent calcium channel in axonal repair following mechanical trauma , 2007, Neuroscience.

[27]  D M Porterfield,et al.  Oxygen-depleted zones inside reproductive structures of Brassicaceae: implications for oxygen control of seed development. , 1999, Canadian journal of botany. Journal canadien de botanique.