We describe the use of large unilamellar liposomes of a defined size a
nd containing cholesterol as vehicles in commercial dyeing of untreate
d wool with a milling acid dye. To this end, we have investigated lipo
somes prepared with egg phosphatidylcholine (PC) and cholesterol (CH)
at different lipid compositions (from 10:0 to 8:2 molar ratios) contai
ning the commercial acid dye Polar blue G, CI acid blue 90. We assesse
d the physical stability of these systems by measuring the mean vesicl
e size of the suspensions during dyeing. We also investigated kinetic
aspects involving dye adsorption and bonding to untreated wool samples
at different PC:CH lipid compositions. Increasing amounts of CH in bi
layers enhance both the physical stability of complete liposomes and t
he inhibition of dye exhaustion on untreated wool. Using only the dye
trapped in bilayers, dyeing kinetics follows a different tendency, rea
ching the maximum initial inhibition and final exhaustion for the PC:C
H 8.5:1.5 molar ratio. Bonding of dye to wool fibers also improves, re
aching the optimum value for the PC: CH molar ratio 8.5:1.5 in all cas
es. The smoothness of dyed wool samples is also enhanced, the best res
ults being reached with the highest proportion of CH.