• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

头孢羟氨苄及其他一些头孢菌素的蛋白结合研究(作者译)

[Studied on protein binding of cefadroxil and some other cephalosporins (author's transl)].

作者信息

Nakanomyo H, Imai K, Hiraoka M, Hasegawa Y

出版信息

Jpn J Antibiot. 1980 Aug;33(8):773-7.

PMID:7206223
Abstract
  1. Human serum protein binding of cefadroxil and some other cephalosporins were determined by centrifugal ultrafiltration (U.F.) method and equilibrium dialysis (E.D.) method. The binding rates of cefadroxil were 28.1% by U.F. method and 3.8% (beta 1*), 11.6% (beta 2*) by E.D. method. 2. Protein binding of cefadroxil with sera of various animal species were also determined by E.D. method. The binding rates were low as well as that with human serum. 3. With two popular calculation formula for E.D. method, binding rate was considered on the alteration of the ratio of V2/V1.
摘要
  1. 采用离心超滤(U.F.)法和平衡透析(E.D.)法测定了头孢羟氨苄与人血清蛋白的结合率以及其他一些头孢菌素与人血清蛋白的结合率。通过超滤法测得头孢羟氨苄的结合率为28.1%,通过平衡透析法测得其结合率为3.8%(β1*)、11.6%(β2*)。2. 还采用平衡透析法测定了头孢羟氨苄与不同动物物种血清的蛋白结合率。其结合率与在人血清中的结合率一样低。3. 对于平衡透析法的两个常用计算公式,结合率是根据V2/V1比值的变化来考虑的。

相似文献

1
[Studied on protein binding of cefadroxil and some other cephalosporins (author's transl)].头孢羟氨苄及其他一些头孢菌素的蛋白结合研究(作者译)
Jpn J Antibiot. 1980 Aug;33(8):773-7.
2
[General pharmacology of cefadroxil (author's transl)].
Jpn J Antibiot. 1979 Dec;32(12):1356-71.
3
[Comparative pharmacokinetics of oral cephalosporins: cephalexin, cefaclor and cefadroxil (author's transl)].
Arzneimittelforschung. 1980;30(3):505-9.
4
[Pharmacokinetics of cefadroxil in rats: comparison of fasting and non-fasting (author's transl)].头孢羟氨苄在大鼠体内的药代动力学:禁食与非禁食状态的比较(作者译)
Jpn J Antibiot. 1980 Aug;33(8):778-81.
5
[Microbiological assay method of cefadroxil in biological specimens (author's transl)].生物样本中头孢羟氨苄的微生物测定方法(作者译)
Jpn J Antibiot. 1980 Aug;33(8):767-72.
6
[Cefadroxil].头孢羟氨苄
Jpn J Antibiot. 1982 Dec;35(12):2736-47.
7
[Pharmacokinetics of cefadroxil, a new oral cephalosporin (author's transl)].新型口服头孢菌素头孢羟氨苄的药代动力学(作者译)
Arzneimittelforschung. 1980;30(3):502-4.
8
[Studies on the toxicity of cefadroxil (S-578). VII. Teratogenic study in rabbits (author's transl)].头孢羟氨苄(S-578)的毒性研究。VII. 家兔致畸研究(作者译)
Jpn J Antibiot. 1980 Apr;33(4):497-502.
9
[Laboratory and clinical studies on cefadroxil in the field of pediatrics (author's transl)].
Jpn J Antibiot. 1981 Jan;34(1):77-94.
10
Disposition of cefadroxil administered orally to rabbits with experimentally induced renal impairment.对实验性诱导肾功能损害的家兔口服头孢羟氨苄后的处置情况。
Arzneimittelforschung. 1981;31(9):1459-61.

引用本文的文献

1
Therapeutic efficacy of cefadroxil and cephalexin for pneumonia in a rat test model.头孢羟氨苄和头孢氨苄在大鼠肺炎试验模型中的治疗效果。
Antimicrob Agents Chemother. 1986 Jul;30(1):105-9. doi: 10.1128/AAC.30.1.105.