K. Fujimoto et al., SUBCUTANEOUS TISSUE DISTRIBUTION OF VANCOMYCIN FROM A FIBRIN GLUE DACRON GRAFT CARRIER/, Journal of biomedical materials research, 36(4), 1997, pp. 564-567
We investigated the tissue distribution of vancomycin (VCM) incorporat
ed in fibrin glue (FG) in a rat model. One VCM-loaded FG Dacron graft
(VCM-FG, VCM 0.6 mg/graft) was implanted in the subcutaneous tissue of
the anterior abdominal wall of each rat. VCM was injected intravenous
ly at an equal dose (0.6 mg/rat) after implantation of one control gra
ft (without VCM-FG). After the implantation and the iv injection of an
equal dose of VCM (0.6 mg/rat), the tissue distribution of VCM for up
to 24 h was determined through analysis of the implanted VCM-FG graft
s, which releasd VCM over a 24 h period. The area under the VCM concen
tration-time curve (AUG) of the tissue was 89.58 mu g.h/g after the im
plantation of the VCM-FG graft, and 7.40 mu g.h/g after the iv injecti
on of VCM, respectively. The targeting index of the tissue, defined as
the ratio of AUC after the implantation of the VCM-FG graft to that a
fter VCM iv injection, was 12.11. None of the six VCM-FG Dacron grafts
after implantation became infected following inoculation with S. aure
us ATCC 25923 (0.1 mt 10(8) CFU/mL). These results suggest that this V
CM-FG Dacron graft delivery may be useful in preventing local infectio
n by enhancing the delivery of VCM to the local areas of the implanted
site in rats. (C) 1997 John Wiley & Sons, Inc.