FIRST-PASS METABOLISM,BIOAVAILABILITY - Pharmawiki.in · Estimation of Reduced Bioavailability Due...
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FIRST-PASS METABOLISM,BIOAVAILABILITY
BY P.RENUKA
M.PHARMACY(1ST Semester)
DEPARTMENT OF INDUSTRIAL PHARMACY
UNIVERSITY COLLEGE OF PHARMACEUTICAL SCIENCES
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CONTENTS1. INTRODUCTION
2. PHARMACOKINETICS
3. BIOAVAILABILITY
4. FIRST PASS METABOLISM
5. PRIMARY SYSTEMS EFFECT PRESYSTEMIC METABOLISM
6. HEPATIC ENZYMES
7. DRUG INTERACTIONS INVOLVING DRUG METABOLISM
8. EVIDENCES OF FIRST PASS EFFECT
9. LIVER EXTRACTION RATIO
10. RELATIONSHIP BETWEEN ABSOLUTE BIOAVAILABILITY ANDLIVER EXTRACTION
11. ESTIMATION OF REDUCEDS BIOAVAILABILITY DUE TO LIVERMETABOLISM & VARIABLE BLOOD FLOW
12. HEPATIC EXTRACTION RATIOS
13. RELATIONSHIP BETWEEN BLOOD FLOW, INTRINSIC CLEARANCEAND HEPATIC CLEARANCE
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14. EFECT OF CHANGING INTRINSIC CLEARANCE & BLOODFLOW ON HEPATIC EXTRACTION AND ELIMINATION HALF-LIFE AFTER IV & ORAL DOSING
15. EFFECT OF CHANGING BLOOD FLOW ON DRUGS WITHHIGH OR LOW EXTRACTION RATIO
16. PREVENTION OF FIRST PASS METABOLISM
17. CONCLUSIONS
18. REFERENCES
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PHARMACOKINETICS
It is concerned with the ADME
of drugs as elicited by the
plasma drug concentration-time
profile and its relationship with
the dose, dosage form and
frequency and route of
administration.
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Bioavailability is a measurement of rate and extent
of a therapeutically active drug that reaches the
systemic circulation and is available at the site of
action. It is denoted by letter ‘F’
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The absolute availability of drug is the systemicavailability of a drug after extra vascularadministration (e.g., oral, rectal, transdermal,subcutaneous) compared to IV dosing.
The absolute availability of a drug is generallymeasured by comparing the respective AUCsafter extra vascular and IV administration.
ABSOLUTE BIOAVAILABILITY
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0
10
20
30
40
50
60
70
0 2 4 6 8 10
Plas
ma
conc
entr
atio
n
Time (hours)
Bioavailability (AUC)o(AUC)iv
=
i.v. route
oral route
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FIRST PASS METABOLISM/ FIRSTPASS EFFECTS/
PRESYSTEMIC METABOLISM
It is the phenomenon of drugmetabolism. Where theconcentration of a drug is greatlyreduced before it reaches thesystemic circulation
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Dose
Destroyedin gut
Notabsorbed
Destroyedby gut wall
Destroyedby liver
tosystemiccirculation
BIOAVAILABILITY
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Uptake of orally administered drug proceeds afterthe stomach passage via the small intestine.In the gut and liver, a series of metabolictransformation occurs.
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Primary systems which effect
presystemic metabolism
1. Luminal enzymes
2. Gut wall enzymes/ mucosalenzymes
3. Bacterial enzymes
4. Hepatic enzymes.
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HEPATIC ENZYMES INVOLVED IN DRUG METABOLISM
MIXED FUNCTION OXIDASES(MFO’s)/ MONOOXYGENASES
Requires both molecular oxygenand the reducing agent NADPH
Electron transfer chain consisting 3components
1. Heme protein ‘cytochrome p-450’
2. Flavoprotein cytochrome p-450reductase
3. Heat stable lipid componentphosphatidylcholine
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Cytochrome P450
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DRUG INTERACTIONS INVOLVING DRUG METABOLISM
The enzymes involved in the metabolism of drugs may be altered by dietand the co-administration of other drugs and chemicals.
Enzyme induction is a drug- or chemical-stimulated increase in enzyme activity,usually due to an increase in the amount of enzyme present.
Enzyme inhibition may be due to substrate competition or due to direct inhibitionof drug-metabolizing enzymes, particularly one of several of the cytochrome P-450enzymes.
Diet also affects drug-metabolizing enzymes. For example, plasma theophyllineconcentrations and theophylline clearance in patients ona high-protein diet are lower than in subjects whose diets are highin carbohydrates.
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Drug- Grapefruit Juice Interaction
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Drug
Drug
CYP3A4Drug
Drug
100%
70%
30%
Drug
Villus
Nucleus
Enterocytes
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Nucleus
Drug
Drug
Drug
100%
70%
30%
CYP3A4FC
Drug
Enterocytes
Villus
FC
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Time
Dru
g B
lood
Con
cent
rati
on (
AU
C)
Drug Taken with GJ
Drug Taken without GJ
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P. B. Watkins 2003
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CYP3A4
100%
80%
20%
Small Intestine
Drug
Drug
10%
Liver
Drug
10%
Drug
Target
over 90% of saquinavir is metabolized by thecytochrome P450 isozyme CYP3A4 {01} .Saquinavir is thought to undergo extensivefirst-pass metabolism and is rapidlymetabolized to a variety of inactive mono-and di-hydroxylated compounds
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HEPATIC ELIMINATION OF DRUGS
HEPATIC CLEARANCE
It is the measure of drug elimination by the liver..
may be defined as volume of blood that perfuses
the liver and is cleared of drug per unit of time
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EVIDENCES OF FIRSTPASS EFFECTS
For drugs that undergo first-pass effects AUC∞ 0, oral is smaller thanAUC∞ 0, IV and F < 1. Drugs such as propranolol, morphine, andnitroglycerin have F values less than 1 because these drugsundergo significant first-pass effects.
Eq. 1
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LIVER EXTRACTION RATIOThe liver extraction ratio (ER) provides a direct measurement of drug
removal from the liver after oral administration of a drug.
where Ca is the drug concentration in the blood entering the liver and
Cv is the drug concentration leaving the liver.
Eq. 2
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Relationship between AbsoluteBioavailability and Liver Extraction
where F is the fraction of bioavailable drug, ER is the drug fraction extractedby the liver, and F″ is the fraction of drug removed by nonhepatic process.
If F″ is assumed to be negligible
After substitution of Equation 1 in 4
Eq. 3
Eq. 4
Eq. 5
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Estimation of Reduced Bioavailability Due toLiver Metabolism and Variable Blood Flow
where Cl h is the hepatic clearance of the drug andQ is the effective hepatic blood flow.F' is the bioavailability factor obtained from estimates of liver
blood flow and hepatic clearance, ER.
usual effective hepatic blood flow is 1.5 L/min, but it may varyfrom 1 to 2 L/min depending on diet, food intake, physical activity or drug intake
For the drug propoxyphene hydrochloride, F' has been calculated fromhepatic clearance (990 ml/min) and an assumed liver blood flow of 1.53 L/min:
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HEPATIC EXTRACTION RATIOS
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Relationship between Blood Flow, Intrinsic Clearance,and Hepatic Clearance
The ER may vary from 0 to 1.0. An ER of 0.25 means that 25% of the drugwas removed by the liver.
If both the ER for the liver and the blood flow to the liver are known, then hepatic clearance may be calculated by the following expression:
For some drugs (such as isoproterenol, lidocaine, and nitroglycerin),the extraction ratio is high (greater than 0.7),
For drugs with very high extraction ratios,the rate of drug metabolism is sensitive to changes in hepatic blood flow. Thus, anincrease in blood flow to the liver will increase the rate of drug removal by the organ
Eq. 7
Eq. 8
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INTRIINSIC CLEARANCE
Intrinsic clearance (Cl int) is used to describe the total ability of the
liver to metabolize a drug in the absence of flow limitations, reflecting
the inherent activities of the mixed-function oxidases and all other enzymes
Eq. 9
Hepatic clearance changes with blood flow and the intrinsic clearance
of the drug, as described in Equation 9
For drugs with low extraction ratios (eg, theophylline, phenylbutazone
and procainamide), the hepatic clearance is less affected
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The relationship between liver blood flow and total hepaticclearance for drugs with varying extraction rates (ER).
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Effect of Changing Intrinsic Clearanceafter IV and Oral Dosing
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Effect of Changing Blood Flow on Drugs withHigh or Low Extraction Ratio
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PREVENTION OF FIRSTPASS METABOLISM
1. Route of drug administered may be changed
Various transmucosal non invasive routes of drugadministration to bypass presystemic elimination in
GIT / LiverLike ocular delivery
nasal delivery
pulmonary delivery
buccal/ sublingual delivery
rectal delivery
vaginal delivery
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2, alternative routes of administration likesuppository, intravenous, intramuscular,inhalation aerosol avoid the first passeffect because they allow drugs to beallowed directly into systemic circulation
3. Another way to overcome the first pass
effect is to either enlarge the dose or
change the drug product to a more rapidly
absorbable dosage form
4. Prodrugs
e.g. sulfasalazine
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CONCLUSIONSDrugs given parenterally, transdermally or by inhalation
may distribute within the body prior to metabolism by the
liver.
But the drugs that are highly metabolized by the liver or by
the intestinal mucosal cells demonstrate poor systemic
availability when given orally.
In drug design drug candidates may have good drug
likeness but fail on first pass metabolism, because it is
biochemically selective.
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REFERENCES
1. APPLIED BIOPHARMACEUTICS AND PHARMACOKINETICS:
FIFTH EDITION; BY LEON SHARGEL, SUSANNA WU.PANG,
ANDREW B.C YU
2. BIOPHARMACEUTICS AND CLINICAL PHARMACOKINETICS;
FOURTH EDITION; BY MILO GIBALDI.
3. BIOPHARMACEUTICS AND PHARMACOKINETICS BY D.M
BRAHMANKAR, SUNIL B. JAIASWAL.
WEBSITESWWW.GOOGLE.COM
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Thank you