The authors investigated the poly-L-lysine-coated alginate beads as an anti
biotic delivery system for the treatment of various surgical infections. Th
e sodium alginate was mixed with vancomycin, coated with poly-L-lysine, and
lyophilized to form five types of the biodegradable antibiotic beads. Type
I, 2.5% alginate, nonpoly-L-lysine coated and nonlyophilized; Type II, 2.5
% alginate, poly-L-lysine coated but nonlyophilized; Type III, 2.5% algina
te, poly-L-lysine coated and lyophilized; Type IV, 5% alginate, poly-L-lysi
ne coated and lyophilized; and Type V, 7.5% alginate, poly-L-lysine coated
and lyophilized, Cytotoxicity of the alginate beads to fibroblasts and HeLa
cells was evaluated by the MTT [3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-
2H tetrazolium bromide] colorimetric assay. A study of in vitro elution of
vancomycin of the alginate antibiotic beads was performed. The results sug
gested that the alginate antibiotic beads present no obvious toxic risk to
their use as a drug delivery system. The concentration of vancomycin in the
se five types of beads was well above the breakpoint sensitivity concentrat
ion (the antibiotic concentration at the transition point between bacterial
killing and resistance to the antibiotic) for 9,11,12, 14, and 17 days res
pectively. The release was most marked during the first 3 days. The duratio
n of antibiotic release was prolonged by using techniques of poly-L-lysine
coating, lyophilization, and by increasing the content of alginate. This st
udy offers a biodegradable delivery system of antibiotics to treat various
surgical infections.