Lecture 11 - Dec 2 Flashcards
-read Rh and Hep B for exam
menti https://www.menti.com/alhcthccnpis
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metabolism in pregnancy
-in general most drugs are cleared by CYP1A2 which is decreased, so drugs are metabolised slower, also decreased blood flow to liver due to uteroplacenatal circulation
-so drugs metabolized by liver are cleared slower in pregnancy
-though some enzymes like CYP3A6 are increased
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placental transfer of drugs
-in general, transfer across placenta follows same kinetics as any other tissue
-can transfer antibodies drugs, hormones, nutrients, oxygen, pathogens/viruses, vitamins, water
-easily transfer: lipid soluble/non-ionized, low molecular weight, low protein binding in the parturients plasma
Drugs can cross placenta by:
-passive diffusion: oxygen, carbon dioxide, fatty acids, steroids, electrodes, fat-soluble vitamins, drugs
-facilitated diffusion: sugars
-solvent drag: electrolytes (bulk flow, paracellular (passing through the intercellular space between cells in the epithelium - passive diffusion process)
-active transport: amino acids, some cations (calcium, iron, iodine, phosphate), water soluble vitamins
-most drugs cross placenta by diffusion
factors affecting placenta transfer
-surface area of the placenta and diffusing distance
-physiochemical properties of drugs - lipid solubility, moceluclar weight (most drugs above 1000Da will not cross placenta), degree of ionization (pH), protein binding
-concentration gradients
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-placenta starts to thin/flatten (but also as it grows throughout pregnancy it has more vessels for diffusion) as baby gets bigger so distance that things need to diffuse across gets smaller
Maternal metabolites can also cross placenta