Cole M, Kenig M D, Hewitt V A
Antimicrob Agents Chemother. 1973 Apr;3(4):463-8. doi: 10.1128/AAC.3.4.463.
Penicillins can be metabolized to penicilloic acids in man, the extent being dependent on the penicillin structure. In the phenoxy penicillin series, phenoxymethyl penicillin was found to be particularly unstable, but the higher homologues were more stable. In the isoxazolyl series, oxacillin was unstable, and progressive insertion of halogen in the phenyl ring increased stability. Ampicillin and amoxycillin showed some instability, ampicillin possibly being the more stable. After intramuscular administration, carbenicillin was very stable in the body, ampicillin was fairly stable, and benzyl penicillin was unstable. It is important to take into account the penicilloic acid content of urine when estimating total absorption of a penicillin. Increased stability in the body as well as slower renal clearance can lead to high concentrations in the serum. Penicilloic acids seemed to be more slowly cleared from the body than penicillins. The liver is probably the site of inactivation.
青霉素在人体内可代谢为青霉素酸,其程度取决于青霉素的结构。在苯氧青霉素系列中,苯氧甲基青霉素被发现特别不稳定,但较高的同系物更稳定。在异恶唑基系列中,苯唑西林不稳定,苯环上逐渐引入卤素可增加稳定性。氨苄西林和阿莫西林表现出一定的不稳定,氨苄西林可能更稳定。肌内注射后,羧苄西林在体内非常稳定,氨苄西林相当稳定,而苄青霉素不稳定。在估计青霉素的总吸收量时,考虑尿液中青霉素酸的含量很重要。体内稳定性增加以及肾脏清除较慢可导致血清中浓度升高。青霉素酸似乎比青霉素从体内清除得更慢。肝脏可能是失活的部位。