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ERHS 601 Exam 1 Questions & Answers 2024/2025 £7.69   Add to cart

Exam (elaborations)

ERHS 601 Exam 1 Questions & Answers 2024/2025

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  • Module
  • ERHS 601
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  • ERHS 601

ERHS 601 Exam 1 Questions & Answers 2024/2025 Metabolism involves breaking bonds - ANSWERSStructure (size, shape, electronegativity, electron density) determine where bonds break Chemical properties that determine function - ANSWERS-Physical state -Solubility -Reactivity -Interaction wit...

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  • November 20, 2024
  • 17
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • ERHS 601
  • ERHS 601
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ERHS 601 Exam 1 Questions & Answers
2024/2025

Metabolism involves breaking bonds - ANSWERSStructure (size, shape, electronegativity, electron
density) determine where bonds break



Chemical properties that determine function - ANSWERS-Physical state

-Solubility

-Reactivity

-Interaction with biological molecules

-Atomic size

-Affinity for electrons



ADME - ANSWERSAbsorption - Uptake

Distribution - Chemical Fate

Metabolism - Biotransformation

Excretion



-Chemical properties determine absorption, distribution, excretion

-Biotransformation alters chemical structure

-Chemical structure dictates properties



Organs most affected by toxins - ANSWERSTarget organs (use a lot of ATP/oxygen)

-Lungs

-Heart

-Kidneys

-Brain

-Liver

,Peripheral nerves



Toxicokinetics - ANSWERSQuantitative description of the concentration of a xenobiotic in body

-How concentration changes with time

-Has effects on duration of action

-Influenced by ADME



Toxicodynamics - ANSWERSQuantitative description of the effects of a xenobiotic

-Tissue, cellular, molecular



Measurable components of ADME - ANSWERSAbsorption - can measure administered drug and
concentration in blood



Distribution - difficult to measure (requires tissue samples that can be difficult to obtain)



Metabolism - can measure blood, but not target tissue



Excretion - can measure excreted concentration of drug



Elimination kinetics - ANSWERSRate(el) = k(el) x concentration in blood

-First order



First order elimination - ANSWERSC(t) = C(o) x e^(-kt)



t(1/2) = 0.693/k



Half Life - ANSWERS-Varies based on chemical properties

-Synthetic drugs like Asprin are designed to have a short enough half-life to allow for re-dosing

, -Bioaccumulation is usually due to increased half life

-Half life of metals in bone is extremely high (can only be removed from blood using chelation)



One-compartment model - ANSWERSAbsorption and Elimination

-Difficult to measure due to complexity/barriers

-Oral/dermal absorption increases C(a)

-Uptake from air will not alter C(a)



dC/dt = k(a)C(a) - k(el)C(1)

= rate in - rate out



Dosing/Exposure - ANSWERSSingle dose: Almost never happens



Intermittent exposure: Chance for bioaccumulation based on t1/2

-Possible to increase elimination from body, but easier to decrease exposure

-Extremely lipophilic compounds can actually be released by fat loss



Repeated dosing: Want short t1/2 to prevent accumulation to toxic levels



Continuous exposure: Doesn't happen except sometimes in air

-Concentration depends on elimination



Two-compartment model - ANSWERSC = A(e)^(-at) + B(e)^(-bt)



a (alpha) - distribution phase

b (beta) - elimination phase



Three-compartment model - ANSWERSC = A(e)^(-at) + B(e)^(-bt) + C(e)^(-yt)

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