Ml. Shively et Dc. Thompson, ORAL BIOAVAILABILITY OF VANCOMYCIN SOLID-STATE EMULSIONS, International journal of pharmaceutics, 117(1), 1995, pp. 119-122
Vancomycin was incorporated within water-in-oil-in-water (w/o/w) emuls
ions prepared from solid-state emulsions. Vancomycin, which is not nor
mally orally absorbed, was significantly absorbed, i.e., 30% +/- 0.56
(SE) after 36 h in rats (N = 3). The vancomycin concentration-time pro
file indicated that sustained release of vancomycin was very reproduci
ble. Vancomycin was detected in serum by fluorescence polarization imm
unoassay (TDx, Abbott).