About: 藥物動力學   Sponge Permalink

An Entity of Type : owl:Thing, within Data Space : 134.155.108.49:8890 associated with source dataset(s)

基本概念: 1. * 隔室模型:单隔室模型、二隔室模型、多隔室模型。 2. * 消除速度常数:K = Kb + Ke + Kbi + Klu + ... 3. * 生物半衰期:即体内药量或血药浓度下降一半所需要的时间。 4. * 清除率:Cl = (-dX-dt)/C = KV 。 血液: * 血蛋白:小童及長者的血蛋白生產能力較低 年齡: 有效劑量、有毒劑量:抗生素、腦癇藥物

AttributesValues
rdfs:label
  • 藥物動力學
rdfs:comment
  • 基本概念: 1. * 隔室模型:单隔室模型、二隔室模型、多隔室模型。 2. * 消除速度常数:K = Kb + Ke + Kbi + Klu + ... 3. * 生物半衰期:即体内药量或血药浓度下降一半所需要的时间。 4. * 清除率:Cl = (-dX-dt)/C = KV 。 血液: * 血蛋白:小童及長者的血蛋白生產能力較低 年齡: 有效劑量、有毒劑量:抗生素、腦癇藥物
dcterms:subject
dbkwik:babyish/pro...iPageUsesTemplate
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  • 40.0
quoted
  • 1(xsd:integer)
Source
  • Leslie Z. Benet, Pharmacokinetics: Basic Principles and Its Use as a Tool in Drug Metabolism, p.199 in: Drug Metabolism and Drug Toxicity, JR Mitchell and MG Horning , Raven Press, New York .
Quote
  • Pharmacokinetics may be simply defined as what the body does to the drug, as opposed to pharmacodynamics which may be defined as what the drug does to the body.
abstract
  • 基本概念: 1. * 隔室模型:单隔室模型、二隔室模型、多隔室模型。 2. * 消除速度常数:K = Kb + Ke + Kbi + Klu + ... 3. * 生物半衰期:即体内药量或血药浓度下降一半所需要的时间。 4. * 清除率:Cl = (-dX-dt)/C = KV 。 血液: * 血蛋白:小童及長者的血蛋白生產能力較低 年齡: 有效劑量、有毒劑量:抗生素、腦癇藥物
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