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. 2011 Feb;4(2):40–47.

Table 1.

Key pharmacologic characteristics

TETRACYCLINE DOXYCYCLINE MINOCYCLINE
GI absorption 77–88% 73–95% 95–100%
Solubility High High High
Permeability Low High High
Volume of distribution 108L 50–80L 80–115L
Protein binding 55–64% 82–93% 76%
Lipophilicity Low Intermediate High
Molecular weight 444 462 457
Dietary factors affecting absorption Food, iron, calcium, magnesium, aluminum Food (less affected than tetracycline), iron, calcium, magnesium, aluminum Food (less affected than tetracycline or doxycycline), iron, calcium, magnesium
Availability in ER formulation No No Yes
GI

gastrointestinal

ER

extended release