Abstract
The permeability of polymers, electrosynthesized at neutral pH on Pt–Ir cylinders from each of the three isomers of phenylenediamine ( oPD, mPD and pPD), to H 2O 2 (signal transduction molecule in many oxidase-based biosensors) and ascorbic acid (AA, archetypal interference species in biological applications of biosensors) was measured, and used to determine the permselectivity of the three polymers. P mPD was the coating with the greatest permselectivity for H 2O 2 over AA, for low concentrations of AA. For AA levels greater than 200 μM, however, poly- ortho-phenylenediamine (P oPD) was superior. Furthermore, stability studies indicated that the permselectivity of P mPD degraded rapidly, even after 1 day, supporting the choice of P oPD as the permselective membrane for biosensor implantation where AA levels are high, such as in brain monitoring. A variety of techniques were used to gain further insight into the PPD layers, specifically electrochemical quartz crystal microbalance, mass spectrometry and scanning electron microscopy. Together these studies indicate that P mPD forms the thickest layer (∼15 nm) and is the least soluble of the polymers, that the P oPD layer is ∼4 nm thick and may consist mostly of tetramers, while P pPD is the thinnest (∼3 nm) and appears to consist of trimers.
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