http://dx.doi.org/10.4314/tjpr.v11i2.13
Abstract
Purpose:
The purpose of the present study was to investigate
interaction between ketotifen fumarate and anhydrous
theophylline in aqueous media of various pH.
Methods:
By
using Job’s continuous-variation analysis and Ardon’s
spectrophotomeric methods, the values of stability
constants of theophylline with ketotifen were
determined at a fixed temperature (37 0C) at
each of the medium pH. In vitro study of protein (bovine
albumin, fraction v) binding was carried out by
equilibrium dialysis method at pH 7.4 to ascertain the
influence of ketotifen on the protein binding of
theophylline.
Results:
Stability constant, ranging between 5.07 and 6.35, were
derived from Ardon’s plot, indicating that complexes
formed, as a result of interaction between the drugs,
were comparatively stable. However, following
theophylline interaction with ketotifen, stability
constant was < 1 at gastric pH (0.4 and 2.0) and 4.12 at
intestinal pH. (6.0)The highest degree of protein
binding by ketotifen was 98 % and the lowest 90 %. For
theophylline, the highest and lowest degrees of protein
binding were 90 and 85 %, respectively.
Conclusion: Concurrent administration of
ketotifen and theophylline would result in the formation
of a stable complex and this is likely to reduce the
therapeutic activities of both drugs. With regard to
protein binding, the concentration of theophylline
increased with decrease in ketotifen concentration.
Keywords: Stability constant, Job’s method, Ardon’s
method, Ketotifen fumarate, Complex formation, Protein
binding, Theophylline