Technical Bulletin No. CD 0330
Abstract
A study was conducted to compare blood and lung levels
of Aureomycin (chlortetracycline) and sulfamethazine from
Aureo S 700 or oxytetracycline in cattle fed these antimicrobials.
Sixteen calves, averaging 400 lb body weight, were randomly
allotted to two groups of four steers and four heifers
each. Animals in Group A were fed Aureo S 700 at the
levels of 350 mg Aureomycin and 350 mg sulfamethazine
per head daily for 5 consecutive days, and those in Group
B received oxytetracycline at 2 grams per head daily for 5
consecutive days.
Medication was included in a small amount of feed. The
rest of the feed was withheld until all medicated feed was
consumed.
Blood samples for Aureomycin, sulfamethazine, or oxytetracycline
analysis were obtained from each animal prior to
administration of medication on day 1 and on day 4 at 0,
2, 4, 6, 8, 12, 16, 20, and 24 hours after the medication
was fed. The last blood sample was taken from all
animals on day 5 of medication at 12 hours after treatment
was started on that day. Then lung tissue was
collected for Aureomycin, sulfamethazine, or oxytetracycline
analysis.
Summary
The mean peak blood level of total medication from Aureo
S 700 fed at the recommended levels of 350 mg of
Aureomycin and 350 mg of sulfamethazine per head
daily was 8 times greater than that from oxytetracycline
fed at 2 g/head/day (Figure 1).
Although the Aureomycin feeding level (350 mg/head/day)
was 5.7 times lower than the oxytetracycline feeding level
(2 g/head/day), the Aureomycin and oxytetracycline mean
lung tissue levels were similar (Figure 2). In addition, the
mean peak lung tissue level of total medication from
Aureo S 700 (350 mg/350 mg) was 3 times higher than
that from oxytetracycline (2 g) (Figure 3).
Experimental Results -
Blood Levels
Mean maximum Aureomycin blood levels in cattle fed
Aureo S 700 were 0.017 and 0.013 ppm and occurred
between 12 and 16 hours after treatment was initiated on
day 4. Mean highest sulfamethazine blood levels were
0.50 and 0.51 ppm at 4 and 6 hours on that day,
respectively, after treatment was started.
Mean peak blood levels of 0.017 ppm Aureomycin plus
0.51 ppm sulfamethazine produced a mean peak total
medication blood level of 0.527 ppm (Figure 1). This was
considerably higher than the mean peak oxytetracycline
blood levels, which were 0.066 and 0.057 ppm at 12 and
16 hours on day four after treatment was initiated,
respectively.
Lung Tissue Levels
Medication levels in lung tissue of cattle were (Figure 2):
- Aureo S 700:
- Aureomycin (350 mg/head/day): average
0.150 ppm; range 0.089 to 0.172 ppm
- Sulfamethazine (350 mg/head/day): average 0.33
ppm; range 0.18 to 0.51 ppm.
- Oxytetracycline (2 g/head/day): average 0.16 ppm;
range non-detectable to 0.54 ppm.
The variation for oxytetracycline was 6.5 times greater
than for Aureomycin. This demonstrates the increased
confidence that Aureo S 700 will more likely achieve an
effective level of tetracycline antimicrobial (Aureomycin) at
the infection site than oxytetracycline.
Conclusions
This study demonstrates the greater affinity of Aureomycin
and sulfamethazine for lung tissue compared to oxytetracycline,
which is important in the control of respiratory disease.
The mean peak lung tissue level of Aureomycin from
Aureo S 700 was almost equal to that of oxytetracycline
(0.15 vs 0.16 ppm), even though the feeding level of oxytetracycline
was 5.7 times higher than the feeding level of
Aureomycin (2 g vs 350 mg/head/day) (Figure 3). Also,
adding 0.33 ppm, the mean peak lung tissue level of sulfamethazine
from Aureo S 700, to that of Aureomycin
(0.15 ppm) resulted in a mean peak lung tissue level of
0.48 ppm of total medication. This was 3 times higher
than the tissue level of oxytetracycline (0.16 ppm) even
though the feeding level of oxytetracycline (2 g/head/day)
was 2.9 times higher than the feeding level of total medication
from Aureo S 700 (700 mg/head/day).
Aureo S 700® is a registered trademark of Alpharma Inc.
Aureomycin® is a registered trademark of Alpharma Inc.
Data in Alpharma research file.
Copyright © 2002 Alpharma Inc.
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