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S McMorris

Publications and source records attributed to S McMorris.

7 recordsLinked to original sources

Topical antimicrobial toxicity.

Three topical antibiotics and four antiseptics (1% povidone-iodine, 0.25% acetic acid, 3% hydrogen peroxide, and 0.5% sodium hypochlorite) were directly applied to cultured human fibroblasts to quantitatively assess their cytotoxicity. The four antiseptics were found to be cytotoxic; all of the cytotoxic agents except hydrogen peroxide were subsequently found to adversely affect wound healing in an animal model. Comparison of bactericidal and cytotoxic effects of serial dilutions of these four topical agents indicated the cellular toxicity of hydrogen peroxide and acetic acid exceeded their bactericidal potency. Bactericidal noncytotoxic dilutions of povidone-iodine and sodium hypochlorite were identified. These experiments provide evidence that 1% povidone-iodine, 3% hydrogen peroxide, 0.5% sodium hypochlorite, and 0.25% acetic acid are unsuitable for use in wound care. This sequence of experiments could be used to identify bactericidal, noncytotoxic agents prior to their clinical use.

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Cellular and bacterial toxicities of topical antimicrobials.

Cellular and bacterial toxicities of four commonly used topical antimicrobials (1% povidone-iodine, 3% hydrogen peroxide, 0.25% acetic acid, and 0.5% sodium hypochlorite) were assayed in vitro using cultures of human fibroblasts and Staphylococcus aureus. All agents tested at full strength killed 100 percent of exposed fibroblasts. Fibroblast toxicity exceeded bacterial toxicity with serial dilutions of hydrogen peroxide and acetic acid. Dilutions of povidone-iodine (1:1000) and sodium hypochlorite (1:100) were identified where no fibroblast toxicity occurred while full bactericidal activity persisted.

Acetates↗

Neutrophil migration under agarose in healthy and cytomegalovirus-infected mice.

A technique of measuring directed and random migration of mouse neutrophils was developed to study these neutrophil functions in a standardized small animal population into which specific variables could be introduced. Values in healthy animals were highly reproducible; variations in random and directed migration did not exceed 9%. Mouse neutrophils had significant impairment of directed and random migration at 3, 5, and 8 days after infection with cytomegalovirus. Technical reproducibility and the ability to reflect a disease process make this model a promising one for the laboratory study of neutrophil migration.

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