Hydrogen Peroxide Microsensors

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Prices valid in USA, Canada, and PR only.
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Prices valid in USA, Canada, and PR only.

The hydrogen peroxide sensors developed by WPI are designed to compliment existing high sensitivity fluorescent approaches with direct quantitative measurement in biological samples in the low nM range.

Prices valid in USA, Canada, and PR only.

Direct quantitative measurements of hydrogen peroxide in biological samples

  • Incorporated reference electrode
  • Non-breakable integrated hydrogen peroxide sensor with tip dimension of 100 µm
  • For use with Apollo1000, Apollo4000, TBR4100 and TBR1025
  • Requires cable 91580 (sold separate)
  • Package of 3

Options

Order codeTip LengthFiber DiameterShapePackage Quantity
ISO-HPO-1001-5 mm100 µmStraightpkg. of 3
ISO-HPO-100-LXX 1-10 mm100 µmL Shape, Customize lengthpkg. of 2

- Sensor available in 1 mm length increments (for example, 1 mm, 2mm, 3mm...)
- Sensor sensitivity varies with length and diameter.

See the latest Biosensor Data Sheet.

Benefits

  • Response Time: < 5 s (90%)
  • Detection Limit: 1 nM - 1 mM
  • Drift: < 1.0 pA/min. (< 2 pA/min. for the L-Shaped)
  • Sensitivity: 1 pA/nM 

Applications

  • Tissue/Microvessels detection of HPO
  • L-Shaped for tissue bath studies
  • Hypodermic for easy insertion into tissue

Despite the recognized importance of this oxidant in biology, real-time measurements at low concentration have been difficult. The hydrogen peroxide sensors developed by WPI are designed to compliment existing high sensitivity fluorescent approaches with direct quantitative measurement in biological samples in the low nM range.

The ISO-HPO-2 is a 2.0 mm stainless steel sensor, with replaceable membrane sleeves (600012) and an internal refillable electrolyte (100042). It is designed for use in cell cultures and similar applications.

The ISO-HPO-100 is a 100 µm tip diameter hydrogen peroxide micro sensor designed for use in tissues and similar applications. The design is based on a platinum wire sensing electrode coated with a proprietary membrane to enhanceH2Odetection.

These sensors incorporate WPI’s proprietary combination electrode technology whereby the hydrogen peroxide sensing element and separate reference electrode are encased within a single Faraday-shielded probe design. This design has been shown to enhance performance during measurements and minimizes overall sensor size.

Our hydrogen peroxide (H2O2) sensors work with the TBR4100 and TBR1025 free radical analyzers.

Hydrogen peroxide in biological systems

Hydrogen Peroxide is produced in biological systems by controlled pathways at low concentrations that impact on cell signaling. At higher concentrations inflammatory cells produce local intense amounts of this oxidant to kill pathogens. In the progress of human disease, uncontrolled formation of hydrogen peroxide from the mitochondrial respiratory chain and enzymes, such as xanthine oxidase, can occur (Prof. Victor Darley-Usmar, Univ. of Alabama, personal communication). 

Hydrogen peroxide sensor in a hypodermic sheath

The ISO-HPO-100H is enclosed in a hypodermic needle. The image below shows the needle tip and enclosed sensor as viewed through a microscope.

Needle tip 

L-shaped hydrogen peroxide sensor

The ISO-HPO-100-L is a unique L-shaped nitric oxide sensor designed specifically for use in tissue bath studies and similar applications (e.g., see WPI's MYOBATH). The shape of the sensor has been engineered to facilitate placement of the electrode within the lumen of the tissue vessel under study.

L-shaped ISO-HPO-100L

 

More Information
SKU VAR-2962

 

ISO-HPO-100

ISO-HPO-100 H

APPLICATIONTissue/MicrovesselsHypodermic Sheath
SENSOR DIAMETER100 µm100 µm
RESPONSE TIME< 5 SEC (90%)< 5 SEC (90%)
DETECTION LIMIT1 nM to 1 mM< 10 nM to 1 mM
DRIFT< 2.0 pA/min< 2.0 pA/min
SENSITIVITY1 pA/nM1 pA/nM
PHYSIOLOGICAL INTERFERENCEContact WPIContact WPI

Xie, L., Feng, H., Li, S., Meng, G., Liu, S., Tang, X., … Ji, Y. (2016). SIRT3 Mediates the Antioxidant Effect of Hydrogen Sulfide in Endothelial Cells. Antioxidants & Redox Signaling, 24(6), 329–343. http://doi.org/10.1089/ars.2015.6331 

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