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p.282-287

Quiz yourself by thinking what should be in each of the black spaces below before clicking on it to display the answer.
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Question
Answer
Vd   Conc in the body/plasma drug concentration  
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CL   Rate of Elimination/Plasma drug conc.  
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T1/2   .7 x Vd/CL  
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Loading Dose   Conc (target) x Vd/Bioavailabitily  
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Maintenance Dose   C (target) x CL/Bioavailability  
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Zero order Kinetics   Rate of elimination is constant (linear reduction in drug concentration over time)  
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First Order Kinetics   Rate of Elimination is proportional to the drug Conc. (constant Fraction) so that the elimination varies exponentially with time  
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what is more predictable first or zero order kinetics   Zero (there is nothing to thing about )  
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what is a Phase I metabolism   HOR, Hydrolysis, Oxidation, Reduction (yields slightly polar water soluble often still active metabolite)  
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What is a Phast II metabolism   GAS (Glucuronidation, acetylation, and sulfation) yields very polar inactive metabolites  
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how long does it take to get to the IND level of drug dev   4 years (requires dev. of a lead compound and animal testing)  
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what are the phases after IND status has been granted   Phase 1(safe?) 2 (does it work?) 3 (Double blind study)  
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How long does it take to get to the NDA   New drug application can typically be filed 8-9 years after the intiation  
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what is phase 4 of drug development   post marketing surveillance  
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what is the order of drug dev.   lead compound, animals, IND, Safe?, Work on patients?, Double blind study?, NDA, Phase 4 surveillance  
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what effect does a competitive antagonist have on the curve   it shifts it to the right (can still overcome)  
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what effect does a non-competitive antagonist have on the curve   shifts the curve downward, you can't overcome the effect  
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what is Kd   refers to the number of receptors involved  
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what is Ed   Effective Dose (refers to the effect the drug is having)  
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how does a partial agonist compare to a full with respect to potency and efficacy   a partial will always have lower efficacy but may be more or less potent  
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Any thing that ends in -cillin Mech   blocks cell wall synthesis by inhibiting cross linking  
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Imipenem Mech   blocks cell wall synthesis by inhibiting cross linking  
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Aztreonam Mech   blocks cell wall synthesis by inhibiting cross linking  
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Cephalosporin   blocks cell wall synthesis by inhibiting cross linking  
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Vancomycin mech   blocks peptidoglycan synthesis  
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Cycloserine Mech   blocks peptidoglycan synthesis  
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bacitracin Mech   blocks peptidoglycan synthesis  
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Chloramphenicol mech   50S block  
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allmost all Mycins (not vanco or aminoglycosides) mech   50S block  
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Aminoglycosides (Amikamycin, Gobramycin, Tobramycin) Mech   30S block  
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Sulfonamides and Trimethoprim Mech   Block Nucleotide synthesis  
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Created by: FIRST AID
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