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Chapter 4

Pharmacokinetics: Drug Distribution and Protein Binding

医薬品流通:概要
医薬品流通:概要
Distribution refers to the two-way movement of a drug between different compartments within the body. It is a passive process driven by the concentration ...
薬物分布に影響を与える要因:組織透過性
薬物分布に影響を与える要因:組織透過性
Drug distribution across biological membranes to target tissues relies on the drug's physicochemical properties, such as molecular size, ionization ...
薬物分布に影響を与える要因:生理学的障壁
薬物分布に影響を与える要因:生理学的障壁
Drug distribution is governed by several physiological barriers. The simple capillary endothelial barrier limits the passage of drugs larger than 600 ...
薬物分布に影響を与える要因:臓器灌流率
薬物分布に影響を与える要因:臓器灌流率
Drug distribution can be perfusion rate-limited, particularly when the drug is highly lipophilic, and the membrane to cross is highly permeable. The ...
薬物流通に影響を与える要因:その他の要因
薬物流通に影響を与える要因:その他の要因
Drug distribution can be affected by various factors. It can vary with age due to differences in body composition. For instance, older adults have less ...
配布量
配布量
The apparent volume of distribution or Vd is a key pharmacokinetic parameter signifying the hypothetical body fluid volume into which a drug disperses. It ...
タンパク質-薬物結合:メカニズムと速度論
タンパク質-薬物結合:メカニズムと速度論
Protein-drug binding is the interaction between drugs and proteins in the body. It can be either intracellular binding, which involves drug interactions ...
血液成分への薬物結合
血液成分への薬物結合
When drugs enter the systemic circulation, they interact with blood components like human serum albumin or HSA, α1-acid glycoprotein or AAG, ...
組織-薬物結合:薬物の局在とその意義
組織-薬物結合:薬物の局在とその意義
Body tissues comprise 40-90% of body weight depending on body composition. They can serve as drug storage sites, competing with plasma binding sites. ...
タンパク質-薬物結合:測定法
タンパク質-薬物結合:測定法
Protein-drug binding is determined through indirect and direct methods. Indirect methods involve isolating the bound drug from its free form in biological ...
タンパク質-薬物結合に影響を与える因子:薬物関連因子
タンパク質-薬物結合に影響を与える因子:薬物関連因子
Protein-drug binding can be affected by various drug-related factors. The degree of protein binding is closely related to a drug's lipophilicity, with ...
タンパク質-薬物結合に影響を与える要因:タンパク質関連因子
タンパク質-薬物結合に影響を与える要因:タンパク質関連因子
Drug binding to proteins depends on various factors, including physicochemical properties, protein concentration, disease states, and the number of ...
タンパク質-薬物結合に影響を与える因子:薬物相互作用
タンパク質-薬物結合に影響を与える因子:薬物相互作用
Drug displacement interactions arise when drugs compete for the same binding site, leading to displacement. The extent of displacement depends on the ...
タンパク質-薬物結合に影響を与える要因:患者関連因子
タンパク質-薬物結合に影響を与える要因:患者関連因子
Protein-drug binding varies with many patient-related factors. Age impacts binding due to varying protein content in different age groups. Neonates ...
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