1996
DOI: 10.1016/s0065-7743(08)60472-8
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Chapter 33. Plasma Protein Binding of Drugs

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Cited by 265 publications
(129 citation statements)
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“…Under these experimental conditions, K 2 = 2/3, N= 1.336, φ=0.118 (Olson and Christ, 1996), and J were given using the equation:…”
Section: Resultsmentioning
confidence: 99%
“…Under these experimental conditions, K 2 = 2/3, N= 1.336, φ=0.118 (Olson and Christ, 1996), and J were given using the equation:…”
Section: Resultsmentioning
confidence: 99%
“…As is well known, serum albumins are the most abundant proteins in circulatory system, playing the most important physiological role in transportation of numerous exogenous and endogenous ligands, such as drugs in the bloodstream to their target organs. 15 So, it is very meaningful to explore the action mode between K 4 Sm 0.4 La 0.6 (L 4 )Cl 3 ·5H 2 O and bovine serum albumin (BSA), which can provides a theoretical basis for their potential medicinal value.…”
Section: -13mentioning
confidence: 99%
“…2,3,4 In addition, the role of plasma protein binding has been recognized as an important factor in drug disposition and efficacy. 5 In this context, drug binding to TP is a key process, which is involved in phenomena such as modulation of drugs solubility in plasma, toxicity, in vivo half-life, etc. 6 Concerning serum albumins, they are major carriers of small organic molecules, which bind primarily to two high-affinity sites (called site I or warfarin binding site and site II or indole-benzodiazepine binding site), with typical association constants in the range of 10 4 -10 6 M -1 .…”
Section: Introductionmentioning
confidence: 99%