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薛勤
Dr. Qin Xue
Pharmacology
pharmacodynamics pharmacokinetics
absorption
dualism
distribution
therapeutic effect
metabolism
adverse reaction excretion
Summary-phamacokinetics
Absorption: is the movement of a drug
from its site of administration into blood
circulation.
Distribution: is the process of a drug from
blood circulation to tissue, to the interstitial
and intracellular fluids.
Metabolism: biotransformation
Excretion }
Elimination: drug is removed from the body
Summary-phamacokinetics
t1/2 Elimination rate
First order 0.693/Ke proportional to
kinetics constant concentration
Graded response
All or none response
Summary-phamacodynamics
Parameters
Threshold dose
Emax
EC50/ED50
Kd
LD50/TD50
TI=LD50/ED50 >3 Safty
CSF=LD1/ED99 >1
Summary-phamacodynamics
Definition
Potency: Relative amount of drug
needed to produce a given response,
affinity, Kd, High
High affinity / low Kd less amount of
drug needed high potency
Affinity=1/Kd
Summary-phamacodynamics
Definition
Efficacy: the ability of a drug to
produce the maximum response
Intrinsic activity: ɑ
Summary-phamacodynamics
Classification of receptor
① Ligand-gated ion channel receptors (N
receptor)
② G-protein coupled receptors (βreceptor)
③ Kinase-linked receptor (growth hormone
receptor, interferon)
④ Intracellular receptors (Glucocorticoid
receptor)
Summary-phamacodynamics
Drug and receptor
Full agonist
Partial agonist
Inverse agonist
Antagonist
① Competitive antagonist
② Non-competitive antagonist