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The effects of chrysene and the ozonated byproducts on in vitro gap junctional intercellular communication (GJIC) were evaluated using the scrape loading/dye transfer (SL/DT) technique. A 1 mM solution of chrysene was ozonated at dosages of 1.75, 3, 4.25, and 5 mol O3/mol chrysene (Chr). The early ozonation mixture, 1.75 mol O3/mol Chr, exhibited greater inhibition to GJIC than chrysene and irreversible damage to cells leading to cell death. To determine the compounds potentially responsible for the increase in toxicity, the byproducts formed upon treatment with 1.44 mol O3/mol Chr were separated into 14 fractions using RP-HPLC. The major compounds identified in the fractions were 2-(2'-formyl) phenyl-1-naphthaldehyde, 2-(2'formyl) phenyl-1-naphthoic acid, and 2-2-carboxyphenyl-1-naphthoic acid. 2-(2'-Formyl) phenyl-1-naphthaldehyde was determined to be the compound causing GJIC inhibition in sample fractions and byproduct mixtures.

Potassium permanganate (KMnO 4) has been used widely as an oxidant for remediation of contaminated soil and water systems. The present study evaluates the release of this oxidant from Polycaprolactone (PCL) polymer as part of a patented controlled release process (CRP) to be applied for targeted removal of contaminants from water. KMnO 4 was encapsulated into PCL at a 1:5 oxidant to polymer ratio and placed in batch reactor systems with reagent water to be evaluated over a 96 hour period. SEM images showed that over time, the number of cavities and their sizes increased on the waxy surface of the PCL polymer. The experimental data from the release of KMnO 4 from PCL was found to fit non-Fickian diffusion model after dissolution (R 2 = 0.93) similar to other systems that describe the dispersal of other oxidants from wax matrices. In addition, the model parameters for data of this present study were also found to be comparable to previous release studies with the same oxidant encapsulated in different wax matrices at similar ratios. Overall, the similarity of release data between the diversity of polymers shows that the controlled release biodegradable polymer utilizing PCL provides effective release of the KMnO 4 with the added benefit biodegradable nature of PCL.

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