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Thus, these salts may be readily prepared by treating the tetracycline compound of the invention with an aqueous solution of the desired pharmaceutically acceptable cation and evaporating the resulting solution to dryness, preferably under reduced pressure?
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These include acid, prevacid prescription lysozyme, lactoferrin, defensins, BPI, azurocidin, serine proteinases, elastase, cathepsin G, and proteinase 3?

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