ABSTRACT
Enoxacin is a second-generation quinolone with increased antibacterial activity both in potency as well as in terms of broad spectrum against a wide range of clinically important pathogens over the first generation quinolones and produces its effect by inhibiting bacterial enzyme DNA gyrase. There are a number of drug interactions reported for enoxacin. On the other hand H[2]-receptor antagonists block gastric acid secretion and some cardiovascular effects of histamine. As the later drug are used for a long-term therapy, they may be coadministered with other drugs. In present study in vitro release of enoxacin in presence of cimetidine, ranitidine and famotidine has been studied on a B.P. 2003 dissolution test and compared with the availability of enoxacin and H[2]-receptor antagonists alone. The interacting drugs were analyzed spectrophotometrically. These studies were carried out in simulated gastric juice, simulating empty stomach, simulated intestinal juice [pH 9] and buffers of pH 7.4 simulating blood pH at 37 degree C. In order to support these interaction studies, the effect of H[2]-receptor antagonists on the antibacterial efficacy [MIC] of enoxacin was also studies by turbidity method and compared with parent drug against Staphylococcus aureus, Staphylococcus pyogens, Staphylococcus pneumonia, Enterococcus, Escherichia coli, Salmonella typhi, Pseudomonas aeruginosa, Klebsiella pneumonia, Proteus mirabilis and Bacillus subtilis. On the basis of these results, it is suggested that enoxacin should be coadministered with care along with H[2]-receptor antagonists especially in case of ranitidine; although chances of adverse reactions are rare but decrease in MIC of enoxacin may result in delayed effect or require prolonged use of the drug