Peterson L R, Gerding D N
J Infect Dis. 1978 Apr;137(4):452-7. doi: 10.1093/infdis/137.4.452.
The kinetic interaction of cephalothin and cefamandole with human serum protein and of cephalothin with canine serum protein was studied with use of a rate-of-dialysis method. Binding of antibiotic to serum proteins was complete in less than 1 min and was immediately reversible. Human serum bound 76.9% of cephalothin and 73.7% of cefamandole at 10 microgram/ml, and canine serum bound 41.3% of cephalothin at 10 microgram/ml when this technique was used. Quantitative binding determined by ultracentrifugation was 78.5% for cephalothin and 80.1% for cefamandole in human serum and 45.6% for cephalothin and 32.5% for cefazolin in canine serum. There was no delayed binding of these antibiotics to either human or canine serum. In addition, a large number of antibiotic-binding sites appeared to be present on both human and canine serum protein when the antibiotic concentration was increased to 10(5) microgram/ml.
采用透析速率法研究了头孢噻吩和头孢孟多与人血清蛋白以及头孢噻吩与犬血清蛋白的动力学相互作用。抗生素与血清蛋白的结合在不到1分钟内完成,且立即可逆。当采用该技术时,人血清在10微克/毫升时结合76.9%的头孢噻吩和73.7%的头孢孟多,犬血清在10微克/毫升时结合41.3%的头孢噻吩。通过超速离心法测定的人血清中头孢噻吩的定量结合率为78.5%,头孢孟多为80.1%;犬血清中头孢噻吩为45.6%,头孢唑林为32.5%。这些抗生素与人或犬血清均无延迟结合。此外,当抗生素浓度增加到10⁵微克/毫升时,人及犬血清蛋白上似乎都存在大量抗生素结合位点。