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Circular dichroism spectra have been measured for oxytetracycline free base dissolved in an ethanol/water solvent system over a wide range of composition. The spectra demonstrate a solvent-dependent equilibrium between the zwitterionic form and the nonionized form. The zwitterion clearly predominates in water-rich solutions, whereas the nonionized form becomes the species of preference when the ethanol content exceeds ca. 85% (v/v). This dependence upon the thermodynamic environment supports the concept that the nonionized form of the free base is the important lipid-soluble tetracycline species and suggests, in the context of the known three-dimensional structure of biologically active and nonactive tetacycline derivatives, that the conformational-structural adaptability of tetracycline free bases is a significant factor in their broad spectrum antibacterial action.
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Hughes et al. (1979) studied this question.
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