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  2. Dose–response relationship - Wikipedia

    en.wikipedia.org/wiki/Doseresponse_relationship

    The dose–response relationship, or exposure–response relationship, describes the magnitude of the response of an organism, as a function of exposure (or doses) to a stimulus or stressor (usually a chemical) after a certain exposure time. [1] Dose–response relationships can be described by dose–response curves. This is explained further ...

  3. Threshold dose - Wikipedia

    en.wikipedia.org/wiki/Threshold_dose

    Threshold dose is a dose of drug barely adequate to produce a biological effect in an animal. In dose-response assessment, the term ‘threshold dose’ is refined into several terminologies, such as NOEL, NOAEL, and LOAEL. They define the limits of doses resulting in biological responses or toxic effects. [3]

  4. Toxicology - Wikipedia

    en.wikipedia.org/wiki/Toxicology

    The relationship between dose and its effects on the exposed organism is of high significance in toxicology. Factors that influence chemical toxicity include the dosage, duration of exposure (whether it is acute or chronic), route of exposure, species, age, sex, and environment.

  5. EC50 - Wikipedia

    en.wikipedia.org/wiki/EC50

    The EC 50 of a quantal dose response curve represents the concentration of a compound where 50% of the population exhibit a response, [5] after a specified exposure duration. For clarification, a graded dose response curve shows the graded effect of the drug (y axis) over the dose of the drug (x axis) in one or an average of subjects.

  6. Hormesis - Wikipedia

    en.wikipedia.org/wiki/Hormesis

    In toxicology, hormesis is a dose-response phenomenon to xenobiotics or other stressors. In physiology and nutrition, hormesis has regions extending from low-dose deficiencies to homeostasis, and potential toxicity at high levels. [6]

  7. No-observed-adverse-effect level - Wikipedia

    en.wikipedia.org/wiki/No-observed-adverse-effect...

    In toxicology it is specifically the highest tested dose or concentration of a substance (i.e. a drug or chemical) or agent (e.g. radiation), at which no such adverse effect is found in exposed test organisms where higher doses or concentrations resulted in an adverse effect. [3] [4] [5]

  8. Haber's rule - Wikipedia

    en.wikipedia.org/wiki/Haber's_rule

    For instance, if we assign dose concentration the symbol C, and time the classic t, then for any two dose schema, if C 1 t 1 =C 2 t 2, then under Haber's rule the two dose schema are equivalent. Haber's rule is an approximation, useful with certain inhaled poisons under certain conditions, and Haber himself acknowledged that it was not always ...

  9. PK/PD model - Wikipedia

    en.wikipedia.org/wiki/PK/PD_model

    PK/PD relationships can be described by simple equations such as linear model, Emax model or sigmoid Emax model. [5] However, if a delay is observed between the drug administration and the drug effect, a temporal dissociation needs to be taken into account and more complex models exist: [ 6 ] [ 7 ]