D Dilution of AntibioticsTo prepare the antibiotic solution for the experiments, the antibiotics were reconstituted and diluted to the concentration for decontamination ?100 ug/ml for amikacin (Lisapharma, Erba Italy) and 50 ug/ml for vancomycin (Cheil Jedang, Seoul Korea). A vial of 2-ml of 500-mg amikacin was opened. 0.1 ml of amikacin was removed and injected into 250 ml of M199. A vial of 500-mg of vancomycin hydrochloride powder was reconstituted by dissolving it with 10 ml of water for infusion. After complete dissolution of the powder, 0.25 ml of the reconstituted vancomycin solution was transferred to the other 250 ml of M199. The antibiotic solutions were mixed thoroughly. These procedures were performed aseptically.Incubation Condition of AntibioticsThe test antibiotics were subjected to the following incubation temperatures and duration to examine the optimal decontamination condition for homografts. Experiments were performed to investigate the individual antibiotic potencies of amikacin and vancomycin after 6-hours incubation at 4uC and 37uC. We also investigated the antibiotic potencies after incubation at 4uC forAntibiotic Decontamination of Homografts-Singaporeequal standard deviations (SDs). The results are considered significant if the p-value is less than 0.05.bility results for bacteria isolated in tissue and solution samples during penicillin-streptomycin regimen were also analysed.Vancomycin ?Cylinder Plate AssayThe potency of vancomycin was determined using the cylinder plate diffusion assay. The assay is based on the diffusion of antibiotics solution from the cylindrical disc through a solidified agar layer in a petri dish. The diffusion of antibiotics from a cylindrical disc through a solidified agar medium resulted in the inhibition of CASIN price growth of Bacillus subtilis (ATCC 6633) sporulate. A clear circular zone of microbial inhibition around the disc containing antibiotics solution would form. The diameter of the inhibition zone, which directly correlates to the potency of antibiotics, was subsequently measured. Agar plates were lawned with 105 to 106 cells/ml Bacillus subtilis sporulate suspension for the analysis. The seed layer of inoculum was added on the agar plates. The plates were tilted back and forth to spread the inoculum evenly over the surface. The inoculum was allowed to dry. Six assay wells were created on the inoculated 38916-34-6 surface on each plate, 3 on each half of the plate with a uniform spacing, of radius 2.8 cm per well. 20 ul standard reference was transferred into each of the 3 wells on the left half of the plate. The other 3 wells on the right half of the plate were then filled with 20 ul of the corresponding concentration of test vancomycin. The test vancomycin were incubated at various test conditions, in accordance to “Incubation Condition of Antibiotics”. Five different vancomycin concentrations of 15.6 ug/ml, 12.5 ug/ml, 10 ug/ml, 8 ug/ml and 6.4 ug/ml, of standard reference and test vancomycin, were evaluated. 1379592 The plates were then incubated at 30uC for 18 hours. The diameter of the inhibition zone was measured to the nearest 0.1 mm, using a pair of calipers. A straight-line graph was subsequently plotted based on the mean diameter of inhibition zones obtained from the standard references, with log dose of antibiotics as the x-axis and the diameter of inhibition zone as the y-axis. The log doses of vancomycin after incubation in various test conditions, were interpolated from the diameter re.D Dilution of AntibioticsTo prepare the antibiotic solution for the experiments, the antibiotics were reconstituted and diluted to the concentration for decontamination ?100 ug/ml for amikacin (Lisapharma, Erba Italy) and 50 ug/ml for vancomycin (Cheil Jedang, Seoul Korea). A vial of 2-ml of 500-mg amikacin was opened. 0.1 ml of amikacin was removed and injected into 250 ml of M199. A vial of 500-mg of vancomycin hydrochloride powder was reconstituted by dissolving it with 10 ml of water for infusion. After complete dissolution of the powder, 0.25 ml of the reconstituted vancomycin solution was transferred to the other 250 ml of M199. The antibiotic solutions were mixed thoroughly. These procedures were performed aseptically.Incubation Condition of AntibioticsThe test antibiotics were subjected to the following incubation temperatures and duration to examine the optimal decontamination condition for homografts. Experiments were performed to investigate the individual antibiotic potencies of amikacin and vancomycin after 6-hours incubation at 4uC and 37uC. We also investigated the antibiotic potencies after incubation at 4uC forAntibiotic Decontamination of Homografts-Singaporeequal standard deviations (SDs). The results are considered significant if the p-value is less than 0.05.bility results for bacteria isolated in tissue and solution samples during penicillin-streptomycin regimen were also analysed.Vancomycin ?Cylinder Plate AssayThe potency of vancomycin was determined using the cylinder plate diffusion assay. The assay is based on the diffusion of antibiotics solution from the cylindrical disc through a solidified agar layer in a petri dish. The diffusion of antibiotics from a cylindrical disc through a solidified agar medium resulted in the inhibition of growth of Bacillus subtilis (ATCC 6633) sporulate. A clear circular zone of microbial inhibition around the disc containing antibiotics solution would form. The diameter of the inhibition zone, which directly correlates to the potency of antibiotics, was subsequently measured. Agar plates were lawned with 105 to 106 cells/ml Bacillus subtilis sporulate suspension for the analysis. The seed layer of inoculum was added on the agar plates. The plates were tilted back and forth to spread the inoculum evenly over the surface. The inoculum was allowed to dry. Six assay wells were created on the inoculated surface on each plate, 3 on each half of the plate with a uniform spacing, of radius 2.8 cm per well. 20 ul standard reference was transferred into each of the 3 wells on the left half of the plate. The other 3 wells on the right half of the plate were then filled with 20 ul of the corresponding concentration of test vancomycin. The test vancomycin were incubated at various test conditions, in accordance to “Incubation Condition of Antibiotics”. Five different vancomycin concentrations of 15.6 ug/ml, 12.5 ug/ml, 10 ug/ml, 8 ug/ml and 6.4 ug/ml, of standard reference and test vancomycin, were evaluated. 1379592 The plates were then incubated at 30uC for 18 hours. The diameter of the inhibition zone was measured to the nearest 0.1 mm, using a pair of calipers. A straight-line graph was subsequently plotted based on the mean diameter of inhibition zones obtained from the standard references, with log dose of antibiotics as the x-axis and the diameter of inhibition zone as the y-axis. The log doses of vancomycin after incubation in various test conditions, were interpolated from the diameter re.
