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Lecture 2
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How does water have Hydrogen Bonding?
Partial positive charge on H and partial negative charge on O causes electrostatic attraction between 2 water molecules
Hydrogen donor + hydrogen acceptor = Hydrogen bonding
Solubility of polar and charged molecules in water
Good solvent for polar and charged substances (Amino acids, peptides, carbohydrates)
Poor solvent for nonpolar substances (nonpolar gases)
Noncovalent interaction - Ionic interactions
Electrostatic interaction between PERMANENTLY charged species or between ion and permanent dipole
Noncovalent interaction - Van der Waals interactions
Weak individually and easily broken (reversible)
Universal (Occurs between ANY 2 atoms near each other)
Attractive (dispersion) and repulsive (steric) components
Helps binding + stability
Noncovalent interaction - Hydrophobic Effect
Ordering of water molecules around nonpolar substances & clustering of hydrophobic molecules
NOT due to any attractive force between 2 nonpolar molecules
Osmosis
Water tends to move from low concentration to high concentration of solutes (Osmotic pressure)
Isotonic Osmosis
Solution has the SAME concentration as cell —> No water movement
Hypertonic Osmosis
Solution has HIGHER concentration of solute than cell —> Cell LOSES water and shrinks
Hypotonic Osmosis
Solution has LOWER concentration than cell —> Cell GAINS water and swells
Mannitol
Osmotic diuretic; Used when body fluid pressure is too HIGH; Attracts water + salt in kidneys to excrete through urine; SEVERE DEHYDRATION is a side effect
Explain pH
Always adds up to 14; 0 is most acidic; 14 is most basic; 7 is neutral; pOH has the opposite scale (0 most basic, 14 most acidic)
Define Ka
The extent of dissociation is determined by the acid dissociation constant: Ka
Define Henderson Hasselbalch Equation
Relationship between pH and Ka
pH = Ka + log [A-]/[HA]
pH’s affect on biological systems
Enzymes exhibit pH optima; Cells and organisms maintain specific & constant pH ~7; pKa of drug determines absorption and distribution
Drug ionization & absorption and absorbing organs
Drugs have a pKa that determines how well the body can absorb them
pKa affects absorption, distribution, metabolism, and excretion (ADME)
Solubility depends on pH of target tissue or organ
Ionized drugs are more soluble and are excreted (More hydrophillic)
Non-ionized drugs are absorbed via cell membrane (More hydrophobic)
Dissociation of Aspirin (pH and organ)
Dissociate 50:50 at pH 3.5; Absorbed in STOMACH (Acid pH and ionization)
Dissociation of Amphetamine (pH and organ)
Dissociate 50:50 at pH 9.8; Absorbed in the INTESTINES (Alkaline pH and less ionization at higher pH)