pharmacokinetics i drug administration and absorption prof. hanan hagar pharmacology department
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Pharmacokinetics I Drug administration and absorption Prof. Hanan Hagar Pharmacology Department. Pharmacokinetics. By the end of this lecture, the student should be able to Discuss the different routes of drug administration - PowerPoint PPT PresentationTRANSCRIPT
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Pharmacokinetics IPharmacokinetics I Drug administration and absorptionDrug administration and absorption
Prof. Hanan HagarProf. Hanan HagarPharmacology DepartmentPharmacology Department
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By the end of this lecture, the student should be able to
Discuss the different routes of drug administration Identify the advantages and disadvantages of various routes
of drug administration Know the various mechanisms of drug absorption List different factors affecting drug absorption
Pharmacokinetics
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Recommended books
Lippincott’s illustrated reviews (Pharmacology) by Howland and Mycek
Basic and Clinical Pharmacology by Katzung
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Pharmacokinetics of drugs
(ADME)
Are studies of ADME of drugs
Absorption Distribution Metabolism Excretion
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Administration
Blood
Absorption
Distribution
Metabolism
Excretion
Different organs &tissues
Drug
Site of action
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Sites of Administration
Absorption & distribution Elimination
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Enteral via gastrointestinal tract (GIT). Oral Sublingual Rectal
Parenteral administration = injections. Topical application Inhalation
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Advantages Disadvantages
- Easy- Self use-Safe- convenient
- cheap
- No need for sterilization
- Slow effect-No complete absorption- Destruction by pH and enzymes- GIT irritation- Food - Drug interactions-Drug-Drug interactions- First pass effect- (low bioavailability).Not suitable for vomiting & unconscious patient emergency & bad taste drugs
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First pass Metabolism
Drugs taken orally are first taken to liver (via portal circulation) where they are metabolized before reaching to rest of body via general circulation.
so the amount reaching blood circulation is less than the amount absorbed
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Where first pass metabolism can happen?LiverGut wallGIT Lumen
What are results of first pass metabolism? Low bioavailability of drugs = low serum level
of active drug that can produce action. Short duration of action of drugs (t ½).
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First pass effect
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Oral Dosage Forms (oral formulations)
Tablets (enteric coated tablets that dissolve only in intestine).
Capsules (hard and soft gelatin capsules).
Syrup Suspension (mixture of insoluble solid in a liquid)
Emulsion (mixture of two immiscible liquids)
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TabletsTablets
Hard- gelatin Hard- gelatin capsulecapsule
SpansuleSpansule
Soft- gelatin Soft- gelatin capsulecapsule
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Advantages Disadvantages
Rapid effect can be used in emergency High bioavailability No first pass effect. No GIT irritation No food drug - interaction
Dosage form: friable tablet
Not for
Irritant drugs
Frequent use
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Advantages Disadvantages Suitable for children Vomiting or unconscious
patients Irritant & Bad taste drugs. less first pass metabolism
than oral (50%)
Dosage form:
suppository or enema
Irritation of rectal mucosa.
Irregular absorption & bioavailability.
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Intradermal (I.D.) (into skin)
Subcutaneous (S.C.) (under skin)
Intramuscular (I.M.) (into muscles)
Intravenous (I.V.) (into veins)
Intra-arterial (I.A.) (into arteries)
Intrathecal (I.T.) (cerebrospinal fluids )
Intraperitoneal (I.P.) (peritoneal cavity)
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Advantages Disadvantages Rapid action (emergency) High bioavailability No food-drug interaction No first pass metabolism No gastric irritation
Suitable for Vomiting &unconscious Irritant & Bad taste drugs.Dosage form: Vial or ampoule or infusion drip
Only for water soluble drugs Infection Sterilization. Pain Needs skill Anaphylaxis Expensive
Not suitable for oily solutions or poorly soluble substance
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Ampoule Vial
Single useSingle use Repeated useRepeated use
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Injection Special Utility Limitations
I.D. minute volume (0.1 ml)
suitable for vaccinations
& sensitivity test
not suitable for large volumes
S.C. 0.1 ml – 1 ml
suitable for poorly soluble suspensions and for slow-release implants
not suitable for large volumes
I.M. Suitable for moderate volumes (3-5 ml), for oily solutions or poorly soluble substances
not suitable for irritant drugs
Abscess- necrosis may happen
I.V. suitable for large volumes and for irritating substances
not suitable for oily solutions or poorly soluble substances
Must inject solutions slowly as a rule
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Drugs are applied to skin, ear, eye, nose, vagina, Usually used to provide local action. No first pass metabolism. Used for lipid soluble drugs Drugs can be applied to
Skin (percutaneous administration) e.g. topical local anesthesia
Eye drops e.g. conjunctivitis Ear drops e.g. otitis externa Intranasal, e.g. decongestant nasal spray
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a medicated adhesive patch applied to skin to provide systemic effect (prolonged drug action)
e.g. the nicotine patches
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Advantages Disadvantages mucous membrane of respiratory system rapid absorption (due to large surface area) provide local action limited systemic effect Low bioavailability less side effects. no first pass effect
Dosage form: aerosol, nebulizer
Not suitable for irritant drugs
Only for some drugs as inhalation anesthetics & bronchodilators
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Nebulizer AtomizerNebulizer Atomizer
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Is the passage of drug from its site of administration to its site of action through cell membranes.
Sites of Administration
Sites of action
Cell membrane
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1. Simple diffusion = passive diffusion.
2. Active transport.
3. Facilitated diffusion.
4. Pinocytosis (Endocytosis).
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water soluble drug (ionized or polar) is readily absorbed via diffusion through aqueous channels or pores in cell membrane.
Lipid soluble drug (nonionized or non polar) is readily absorbed via diffusion through lipid cell membrane itself.
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Characters common. Occurs along concentration gradient. Requires no energy No carrier is needed Non selective Not saturable Depends on lipid solubility. Depends on pka of drug - pH of medium.
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Drugs exist in two forms ionized (water soluble) nonionized forms (lipid soluble) in equilibrium. Drug ionized form + nonionized
form Only nonionized form (lipid soluble) is absorbable. The ratio between nonionized form / ionized form is determined by pH of the medium and pKa of the drug.
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pKa of the drug (Dissociation or ionization constant):
is defined as pH at which half of the substance is ionized & half is unionized.
The lower the pKa value of the acidic drug the stronger the acid e.g aspirin (Pka= 3.0 ).
The higher the pKa value of a basic drug, the stronger the base e.g propranolol ( pKa= 9.4)
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pH of the medium Affects degree of ionization of drugs.Weak acids best absorbed in stomach. weak acid drug will exist mainly in its unionized form
(lipid soluble form) in an acidic medium and can be more readily absorbed from the stomach into the systemic circulation.
Weak bases best absorbed in intestine. Basic drugs are more ionized and less absorbable in
acidic medium. On the contrary, basic drugs are more lipid soluble (nonionized) and more absorbable in an alkaline medium.
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Which one of the following drugs will be best absorbed in stomach (pH=3)?
Aspirin pka=3.0
warfarin pka=5.0
Arrange the following drugs in ascending order from least to greatest in rate of absorption in small intestine (pH=7.8)?
Propranolol pka= 9.4
Aspirin pka=3.0
warfarin pka=5.0
Answer: Aspirin (the least aborption), warfarin, propranolol (the greatest absorption).
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Relatively unusual. Occurs against concentration gradient. Requires carrier and energy. Specific Saturable. Iron absorption. Uptake of levodopa by brain.
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Occurs along concentration gradient. Requires carriers Selective. Saturable. No energy is required.
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Passive transport Active transport
along concentration gradient
(From high to low)
against concentration gradient
(From low to high)
No carriers Needs carriers
Not saturable saturable
Not selective Selective
No energy energy is required
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Active transport Carrier-mediated facilitated diffusion
Against concentration gradient
(From low to high)
along concentration gradient
(From high to low)
Needs carriers Needs carriers
saturable saturable
Selective Selective
Energy is required No energy is required
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Endocytosis: uptake of membrane-bound particles. Exocytosis: expulsion of membrane-bound particles.
Phagocytosis occurs for high molecular weightDrugs or highly lipid insoluble drugs.
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OUTINOUT IN
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Factors modifying drug absorptionGENERAL FACTORS Lipid solubility Degree of ionization Drug solubility (aqueous sol better than oily, susp, sol) Dosage forms (depending on particle size and
disintegration) Concentration of drugs Circulation at site of absorption Area of absorbing surface Route of administration.
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Summary Different routes of administration are available. Parenteral administration is the suitable route to
provide rapid effect. IV is used in emergency and provide high
availability. Oral administration is best avoided during
emergency or when severe first pass metabolism may occur.
Drugs may cross any cell membrane by simple diffusion, active transport, facilitated diffusion, and pinocytosis.
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Questions?