Notes in Pharmacokinetics

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Published 08/30/2023 Three phases of drug development
Published 08/30/2023 The purpose of clinical trials are to show {{c1::safety}}, {{c2::efficacy}}, {{c3::approval,}} and {{c4::long-term use}} of investigational new drugs.…
Published 08/30/2023 Purpose of Phase I Clinical Trial 
Published 08/30/2023 Purpose of Phase II Clinical Trial 
Published 08/30/2023 Purpose of Phase III Clinical Trial 
Published 08/30/2023 Purpose of Phase IV Clinical Trial 
Published 08/30/2023 Pharmacokinetics
Published 08/30/2023 Pharmacodynamics
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Published 08/30/2023 Pharmacokinetics is divided into {{c1::absorption}}, {{c1::distribution,}} {{c1::metabolism}}, {{c1::excretion}}. {{c1::ADME}}
Published 08/30/2023 General MOA for an administered drug
Published 08/30/2023 Therapeutic Index (definition) 
Published 08/30/2023 Therapeutic Index (formula)
Published 08/30/2023 High ratio of TD50 / ED50 -> {{c1::increased safety}}
Published 08/30/2023 Drug-drug interactions in pharmacokinetics affects {{c1::ADME}} of each drug.
Published 08/30/2023 Drug-drug interactions in pharmacodynamics can have {{c1::synergistic/antagonistic effects}} on intented function. 
Published 08/30/2023 enteral administration
Published 08/30/2023 peroral administration
Published 08/30/2023 buccal administration 
Published 08/30/2023 rectal administration
Published 08/30/2023 parenteral administration
Published 08/30/2023 intravenous administration
Published 08/30/2023 SC/IM Administration
Published 08/30/2023 topical administration
Published 08/30/2023 Route of administration depends on medication {{c2::stability}} and {{c1::structure}}
Published 08/30/2023 first-pass metabolism
Published 08/30/2023 bioavailability of a drug administed IV
Published 08/30/2023 bioavailability
Published 08/30/2023 dosing regimen 
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Published 08/30/2023 single dosing
Published 08/30/2023 continuous infusion
Published 08/30/2023 steady state concentration (Css)
Published 08/30/2023 Drugs reach steady-state concentration in {{c1::4-5 half-lives}} (time). 
Published 08/30/2023 intermittent dosing
Published 08/30/2023 Maintenance Dosing Rate (mg/h) (formula)
Published 08/30/2023 Maintenance Dose (mg) (formula)
Published 08/30/2023 Meds with {{c1::small Vd}} remain in {{c2::plasma }}
Published 08/30/2023 Meds with {{c1::large Vd}} are {{c2:: distributed extensively }}
Published 08/30/2023 Loading Dose (mg) (formula) 
Published 08/30/2023 Maintenance dose and loading dose depend on {{c1::clearance}}, {{c1::bioavailability}}, and {{c1::volume of distribution}}
Published 08/30/2023 Which aspects of prescription writing are affected by pharmacokinetic parameters?
Published 08/30/2023 What three major pharmacodynamic parameters affect dosing?
Published 08/30/2023 How does efficacy affect dosing?
Published 08/30/2023 How does potency affect dosing?
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Published 08/30/2023 Phase 1 reactions are carried out by {{c1::CYPs (cytochrome proteins)}}
Published 08/30/2023 Metabolic reaction turns active meds into {{c2::inactive metabolites}} for {{c1::excretion}}
Published 08/30/2023 Phase 1 reactions
Published 08/30/2023 Phase 2 reactions
Published 08/30/2023 Phase 1 and Phase II reactions modify metabolites to {{c2::inactivate and excrete}} them by increasing {{c1::polarity}} and {{c1::solubility.}}&n…
Published 08/30/2023 Oral prodrug
Published 08/30/2023 Absorption (definition)
Published 08/30/2023 Endocytosis
Published 08/30/2023 Most drugs are either {{c1::weak acids}} or {{c1::weak bases}}, and are {{c2::uncharged, lipid-soluble, and non-polar}}
Published 08/30/2023 Weakly acidic medication is best absorbed in {{c1::a low pH environment. }}
Published 08/30/2023 Weakly basic medication is best absorbed in {{c1::a high pH environment. }}
Published 08/30/2023 Drugs absorbed in the {{c3::small intestine}} are transported to the {{c2::liver}} via {{c1::the portal vein}}
Published 08/30/2023 Bioavailabiliy (formula, in terms of AUC)
Published 08/30/2023 Three main factors affecting the distribution of medication
Published 08/30/2023 Volume of Distribution (Vd) (definition)
Published 08/30/2023 A low Vd means {{c1::more of the drug}} remains in {{c2::the plasma}}
Published 08/30/2023 A high Vd means {{c1::more of the drug}} remains in {{c2:: extracellular fluid and interstitial spaces}}
Published 08/30/2023 Weak acidic medications are trapped in {{c1::alkaline (high pH)}} urine
Published 08/30/2023 Weak basic medications are trapped in {{c1::acidc (low pH)}} urine
Published 08/30/2023 Enterohepatic circulation (mechanism of elimination)
Published 08/30/2023 Two surfaces of the nephron tubule are the {{c1::apical}} and {{c1::basolateral}} surface. 
Published 08/30/2023 The apical surface faces the {{c1::tubular lumen}}
Published 08/30/2023 The basolateral surface faces the {{c1:: peritubular capillaries}}
Published 08/30/2023 In the Proximal convoluted tubule, the concetration of drugs is {{c1::higher}} in the {{c2::peritublar capillaries}} than the {{c2::tubular lumen}}.&n…
Published 08/30/2023 In the DCT, the concetration of drugs is {{c1::higher}} in the {{c2::tubular lumen}} than the {{c2:: peritubular capillaries}}. 
Published 08/30/2023 Clearance of a medication (definition)
Published 08/30/2023 First order-kinetics
Published 08/30/2023 Zero-order kinetics
Published 08/30/2023 Steady-state concentration, Css (formula)
Published 08/30/2023 Clearance (formula)
Published 08/30/2023 Loading dose beneficial for {{c1::life-threatening situations}} and {{c1::toxic meds }}
Published 08/30/2023 In the proximal convoluted tubule, the concetration of drugs is {{c1::higher}} in the {{c2::peritublar capillaries}} than the {{c2::tubular lumen}}.
Published 08/30/2023 In the proximal convoluted tubule, the concetration of drugs is {{c1::higher}} in the {{c2::peritublar capillaries}} than the {{c2::tubular lumen}}.&n…
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