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Pharm Exam 1
| Term | Definition |
|---|---|
| Loading dose | higher amount of drug given, plateau reached faster, quickly produces therapeutic response |
| Maintenance dose | Keeps plasma-drug concentration in therapeutic range |
| Pharmacokinetics | Study of drug movement throughout the body |
| Greatest barrier for many drugs is... | Crossing many membranes |
| 4 categories of pharmacokinetic processes | Absorption, Distribution, Metabolism, Excretion ADME (Think ADME on snap) |
| Active transport | Usually large, ionized, or water soluble molecules |
| Passive transport | Usually small, nonionized, or lipid soluble molecules |
| Absorption | Movement from site of administration, across body membranes, to circulating fluids |
| TWhat category of the pharmacokinetic process is the primary factor determining length of time for drug to produce effect? | Absorption |
| Distribution | Transport of drugs throughout the body Simplest factor is amount of bloodflow to body tissues |
| Drug-protein complex | Drugs bind reversibly to plasma proteins and never reach the target cell |
| Blood brain and fetal placenta barriers | Amniotic barriers that prevent many chemicals from entering the brain or fetus |
| Biotransformation | Metabolism of medication |
| Conjugates | Side chains that make drugs more water soluble and easily excreted by the kidneys |
| Hepatic microsomal enzyme system | Inactivates drug, accelerates drug excretion |
| Prodrugs | No pharmacologic activity unless first metabolized to active form by body |