A procedure is described for the rapid micro-determination of bronoPol
, based on the measurement of inhibition of a thiol protease, papain.
The inhibition follows a linear relationship with concentration in the
range 0.8-4.0 mug ml-1. The method utilizes the property of bronopol
that is primarily responsible for its antimicrobial activity (ability
to form disulfide bonds) and hence is also indicative of its antimicro
bial potency. The method showed sensitivity towards the degradation of
bronopol and can, therefore, be used in stability analysis. Results f
or the determination of bronopol in the presence of various pharmaceut
ical ingredients and also in the presence of much higher amounts of so
me antibiotics and anti-histamine and anti-inflammatory drugs confirme
d the validity of the method in the determination of bronopol in compl
ex pharmaceuticals.