Abstract

The concentration‐dependent effects of sodium dodecyl sulfate (SDS) on the in vitro permeability of the buccal mucosa were assessed using caffeine (CAF) and estradiol (E2) as model hydrophilic and lipophilic markers, respectively. The permeability of CAF and E2 through porcine buccal mucosa was determined in modified Ussing chambers, with and without exposure to different concentrations of SDS (0.01, 0.05, 0.1, and 1% w/v in physiological buffer). Permeability experiments were complemented with light microscopic evaluation of untreated and SDS‐treated tissues. Additionally, the critical micellar concentration of SDS in the physiological buffer and the effect of SDS pretreatment on drug solubility were determined. Pretreatment of buccal mucosa with SDS 0.01% had no effect on CAF or E2 permeability. SDS 0.05, 0.1, and 1% significantly enhanced CAF flux by a factor of 1.57, 1.63, and 1.81, respectively, and caused significant removal of superficial cells, as observed with light microscopy. Interestingly, pretreatment with SDS 0.05% did not affect E2 flux, whereas SDS at ≥0.1% significantly reduced E2 permeability, possibly as a result of micellar solubilization. These results demonstrate that the effect of SDS on buccal permeability depends on both the concentration of SDS used and the physicochemical properties of the permeant. © 2004 Wiley‐Liss, Inc. and the American Pharmacists Association J Pharm Sci 93:431–440, 2004

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call