Amperometry

Amperometry in chemistry is detection of ions in a solution based on electric current or changes in electric current.

Amperometry is used in electrophysiology to study vesicle release events using a carbon fiber electrode. Unlike patch clamp techniques, the electrode used for amperometry is not inserted into or attached to the cell, but brought in close proximity of the cell. The measurements from the electrode originate from an oxidizing reaction of a vesicle cargo released into the medium. Another technique used to measure vesicle release is capacitive measurements.

History

Electrochemical or amperometric detection as it was first used in ion chromatography was single-potential or DC amperometry, useful for certain electrochemically active ions such as cyanide, sulfite, and iodide. The development of pulsed amperometric detection (PAD) for analytes that fouled electrode surfaces when detected eventually helped create a new category of ion chromatography for the determination of carbohydrates. Another advancement, known as integrated amperometry, has increased the sensitivity for other electrochemically active species, such as amines and many compounds that contain reduced sulfur groups, that are sometimes weakly detected by PAD.[1]

It was established that neurotransmitters could be electrochemically detected by placing a carbon electrode into tissue and recording the current from oxidizing neurotransmitters.[2] One of the first measurements was made using an implanted carbon fiber electrode in the neostriatum of rats.[3] Further work was done in chromaffin cells to investigate catecholamine release from large dense core vesicles.[4][5]

Detection methods

Single-Potential Amperometry

Any analyte that can be oxidized or reduced is a candidate for amperometric detection. The simplest form of amperometric detection is single-potential, or direct current (DC), amperometry. A voltage (potential) is applied between two electrodes positioned in the column effluent. The measured current changes as an electroactive analyte is oxidized at the anode or reduced at the cathode. Single-potential amperometry has been used to detect weak acid anions, such as cyanide and sulfide, which are problematic by conductometric methods. Another, possibly more important advantage of amperometry over other detection methods for these and other ions, such as iodide, sulfite, and hydrazine, is specificity. The applied potential can be adjusted to maximize the response for the analyte of interest while minimizing the response for interfering analytes[6]

Pulsed Amperometry (pulsed amperometric detection, PAD)

An extension of single-potential amperometry is pulsed amperometry, most commonly used for analytes that tend to foul electrodes. Analytes that foul electrodes reduce the signal with each analysis and necessitate cleaning of the electrode. In pulsed amperometric detection (PAD), a working potential is applied for a short time (usually a few hundred milliseconds), followed by higher or lower potentials that are used for cleaning the electrode. The current is measured only while the working potential is applied, then sequential current measurements are processed by the detector to produce a smooth output. PAD is most often used for detection of carbohydrates after an anion exchange separation, but further development of related techniques show promise for amines, reduced sulfur species, and other electroactive compounds.

Principle

In order to record vesicle fusion, a carbon fiber electrode is brought close to the cell. The electrode is held at a positive potential, and when the cargo from a fused vesicle is near the electrode, oxidation of the cargo transfers electrons to the electrode. This causes a spike, the size of which can be used to estimate the number of vesicles, and the frequency gives information about the release probability.[7]

References

  1. ↑ D. C. Johnson and W.R. LaCourse, Analytical Chemistry, 62 (1990), 589A-97A
  2. ↑ Kissinger PT, Hart JB, Adams RN (May 1973). "Voltammetry in brain tissue--a new neurophysiological measurement". Brain Research. 55 (1): 209–13. doi:10.1016/0006-8993(73)90503-9. PMID 4145914.
  3. ↑ Gonon F, Cespuglio R, Ponchon JL, et al. (April 1978). "In vivo continuous electrochemical determination of dopamine release in rat neostriatum". Comptes Rendus Hebdomadaires Des Séances De l'Académie Des Sciences. Série D: Sciences Naturelles (in French). 286 (16): 1203–6. PMID 96981.
  4. ↑ Leszczyszyn DJ, Jankowski JA, Viveros OH, Diliberto EJ, Near JA, Wightman RM (September 1990). "Nicotinic receptor-mediated catecholamine secretion from individual chromaffin cells. Chemical evidence for exocytosis". The Journal of Biological Chemistry. 265 (25): 14736–7. PMID 2394692.
  5. ↑ Wightman RM, Jankowski JA, Kennedy RT, et al. (December 1991). "Temporally resolved catecholamine spikes correspond to single vesicle release from individual chromaffin cells". Proceedings of the National Academy of Sciences of the United States of America. 88 (23): 10754–8. doi:10.1073/pnas.88.23.10754. PMC 53009Freely accessible. PMID 1961743.
  6. ↑ Settle, F. (Ed.). (1997). Handbook of Instrumental Techniques for Analytical Chemistry (1 ed.). Prentice Hall.
  7. ↑ Mosharov EV, Sulzer D (September 2005). "Analysis of exocytotic events recorded by amperometry". Nature Methods. 2 (9): 651–8. doi:10.1038/nmeth782. PMID 16118635.
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