Pharmacokinetics Flashcards
(35 cards)
1
Q
1 X t1/2 =
A
50%
2
Q
3.3 X t1/2 =
A
90%
3
Q
4 to 5 X t1/2 =
A
95%
4
Q
Basic WA drugs
A
- Asprin
- Penicllin
- Cephalosporin
- Diuretics
5
Q
Basic WB drugs
A
- Morphine
- Local Anesthetics
- Amphetamines
- PCP
6
Q
Bioavailability (f) =
A
AUC[Oral] / AUG[IV]
7
Q
Blood volume VD
A
5L
8
Q
CYP450 - 1A2 Inhibitors
A
- Quinolones
- Macrolides
9
Q
CYP450 - 1A2 Substrate
A
- Theophylline
- Acetaminophen
10
Q
CYP450 - 2C9 Substrate
A
- Phenytoin
- Warfarin
11
Q
CYP450 - 2D6 inhibitors
A
- Haloperidol
- Quinidine
12
Q
CYP450 - 2D6 Substrate
A
CVS and CNS drugs
13
Q
CYP450 General inducers
CRAP GPS
A
- Carbamazapine
- Rifampin
- Alcohol (Chronic)
- Phenytoin
- Griseofluvin
- Phenobarbs
- Sulphonylureas
14
Q
CYP450 General Inhibitors
SICKFACES.COM Group
A
- Sodium Valproate
- Isoniazid
- Cimetidine
- Ketoconazole
- Flucoconazole
- Alcohol (bindge)
- Chloremphemicol
- Erythromycin
- Sulfonamide
- Ciprofloxacin
- Omeprazole
- Metronidazole
- Grape fruit
15
Q
Drugs that undergo first-pass metabolism
A
- Lidocaine
- Nitroglycerin
16
Q
Drugs with Zero-order elimination
A
- Ethanol
- Phenytoin
- Salicylate
17
Q
ECF volume VD
A
- 12-14L
- 16%
- Mannitol
18
Q
Extraction rate =
A
Cliver / Q
Q: Hepatic blood flow
19
Q
First Order of Elimination
A
- Constant FRACTION of the drug is eliminated per unit time
- t1/2 is CONSTANT
- Follows and exponential decay versus time
- Rate if elimination is Directly Proportional to plasma level
20
Q
Infusion rate (k0) =
A
Cl X Css
21
Q
Loading Dose (LD) =
A
(VD X [Plasma]) / f
22
Q
Maintenance dose (MD) =
A
(Cl X Css X Γ) / f
23
Q
pH-pKa = -2 WB
A
1% nonionized
24
Q
pH-pKa= -2 for WA
A
99% nonionized
25
Phase 1 Biotransformation
* Oxidation, reduction, or hydrolysis
* Involves Cytochrome P40 found in **Smooth Endoplastic Reticulum**
26
Phase 2 Biotransformation
Conjugation (attaching something to drug) with endogenous compounds via the activity of transferases
* Glucuronidation
* Acetylation
* Glutathione Conjugation
27
Plasma volume VD
* 3L
* 4%
* Heparin
28
Systemic Bioavailability (F) =
f X (1-ER)
29
t1/2 =
.7 X (VD/Cl)
30
TBW volume VD
* 40-42L
* Ethanol
31
Tissue Conc. VD
* Over 49L
* Chloroquine
32
Urine acidifier
1. NH4Cl
2. Vit C
3. Cranberry Juice
33
Urine Alkalinizer
1. NaHCO3
2. Acetazolamide
34
Volume of Distribution (VD) =
Dose / C0
C0: [Plasma] at zero time
35
Zero Order Elimination rate
* A Constant **AMOUNT** of drug is eleminated per unit time
* Rate is **INDEPENDENT** of plasma concentration
* Have **NO FIXED t1/2**