pharmacokinetics I- drug administration, absortion, and distribution Flashcards

(66 cards)

1
Q

two primary routes of administration

A

alimentary canal to enteral administration
non-alimentary routes to paraenteral administration

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2
Q

enteral routes

A

oral and rectal

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3
Q

What is the most common method of enteral medications

A

oral

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4
Q

oral advantages

A

easy , safe, convenient

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5
Q

oral disadvantages

A

limited absorption of some drugs
change of first pass inactivation in liver

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6
Q

most oral medication is absorbed from

A

the small intestine

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7
Q

define first pass effect

A

drugs is transported into the liver via the portal vine where a large amount of the drug may be metabolized and destroyed prior to reaching the target tissue

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8
Q

sublingual drugs

A

are placed under the tongue

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9
Q

buccal drug

A

the drug is placed between the check and the gums

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10
Q

do the sublingual or buccal go thru first pass effect?

A

none

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11
Q

rectal drugs

A

via the rectum

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12
Q

rectal advantages

A

local effect on rectal tissues

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13
Q

rectal disadvantages

A

poor or incomplete absorption

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14
Q

parental routes

A

inhalation
injection
topical
trasndermal

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15
Q

parenteral

A

drug administration that does not us the Gi tract
delivers more directly to the target site
more predictable drug quantity

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16
Q

parenteral inhalation advantages

A

rapid onset
direct application fro respiratory disorders
large surface area for absorption

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17
Q

inhalation disadvantages

A

chance of tissue irriatation

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18
Q

parenteral injections advantages

A

provided more direct administration to target tissues
fast

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19
Q

injection disadvantages

A

chance of infraction is sterility is not maintained

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20
Q

intro arterial injection

A

directly into an artery

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21
Q

subcutaneous injection

A

injecting medications directly beneath the skin for locate response

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22
Q

the SC route can also be used when a drug needs

A

it be slowly dispersed from the injection site and absorbed into the bloodstream for several weeks or months

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23
Q

intramuscular injection

A

easily accessible
steady, prolonged release
repaid effect

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24
Q

iontophoresis and photophoresis

A

use the transdermal route

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25
iontophoresis
electric current driver th ionized for of medication thru the skin
26
phonophoresis
uses ultrasound waves to enhance transmission of medication thru the dermis
27
define bioavailability
the extent to which the drug reaches the systemic circulation
28
bioavailability depends on
the route of administration and the drugs ability to cross membrane barriers
29
the cell membrane is so posed primarily of
lipids and proteins
30
membrane lipids are..
phospholipids which are composed of polar, hydrophilic head and a lipid , hydrophobic tail
31
membrane proteins exist where
in the outer or inner portion of the methane
32
lipid soluble compounds..
are able to pass directly thru the membrane by dissolving in the lipid bilayer
33
the ability of a substance to pass thru a specific pore depends on
the size, shape and electrical charge of molecule
34
passive diffusion
does no use energy charged particles , chemical, and pressure difference on the 2 sides of the membrane
35
the rate of passive diffusion depends on
the magnitude of the gradient, size of substance, distance and temp
36
the second essential factor for passive diffusion to occur is that
the membrane must be permeable to the diffusion substances
37
many drug are ..
lipid soluble
38
drugs will diffuse more easily thru the lipid belayer if they are
non-ionized ionization decreases their lipid solubility
39
ph 1-3
acidic
40
ph 5-7
neutral
41
ph 7-8
base
42
When a weak acid drug is in an acidic environment it tends to be
in its neutral, no ionized form
43
when a weak base is ionized in the acidic environment once it reaches the duodenum
is become nonionized and lipid soluble allowing it to be absorbed from the proximal small intestine
44
diffusion trapping
wants the drug to be ionized in the urine or the body can get rid of the drug, by if it becomes nonionized while in the nephron it may be reabsorebed
45
if the urine is basic
weka acids drugs are trapped in the nephron and get ride of fast
46
if the urine is acidic
weak bases are excreted better
47
diffusion between cell junctions
primary way that a drug may diffuse across the barrier by first into and then out of the other side
48
define osmosis
refers to win the diffusing substance is water
49
when osmosis happens ..
the water moves from an area where it si highly concentrated to an area of low concentration
50
active transport
use membrane proteins to transport substances across the cell membrane
51
does active transport need energy?
yes
52
characteristics of active transport
carrier specificity expenditure of energy (ATP hydrolysis) can transport substances against a concentration gradient
53
define facilitated diffusion
has features of both active transport and passive diffusion assist in protein carrier but no net energy
54
best example of facilitated diffusion
glucose into the skeletal muscle cells
55
endocytosis
transport substances across their membranes
56
exocytosis
substances synthesized within the cell can be encapsulated in vesicles and put out of the cell
57
factors affection distribution
tissue permeability blood flow binding to plasma proteins binding to sub cellular components
58
volume of distribution
if the number is high than the volume in ur blood is high and not in the tissue
59
drugs storage sites
adipose bone muscle organs
60
primary organs for drug storage
liver and kidneys
61
what is the primary site for drug storage
adipose tissue bc a lot of lipids and many drugs are lipid soluable
62
adverse consequences of drug storage
high concentration of drugs within the tissue can cause local damage to liver and kidneys
63
drug storage occurs when a reservoir
soaks up the drug and prevents in from reaching the target site
64
nanotechnology
involves the use of very small particles with physical properties that help drug absorption within the body
65
is volume distribution is less than the total body fluid content then..
the drug is retainined in the blood stream due to factors such as plasma protein binding
66
if volume distribution is high than the total body fluid then..
it indicated that the drug is being concentrated in the tissues