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Presented By:
Mr. Abhay Rajpoot
CHANNELS OF
DRUG
ADMINISTRATI
ON
ENTER
AL
PARENTER
AL
TOPIC
AL
ENTERAL
ORAL
RECTAL
BUCCAL
SUBLINGUAL
ORAL ROUTE
 Oral refers to
Two methods of administration:
Applying topically to the mouth
Swallowing for absorption along the gastrointestinal
(GI) tract into systemic circulation
 po (from the Latin per os) is the abbreviation used
to indicate oral route of medication administration
ORAL
 Advantages
Convenient - can be self- administered, pain free,
easy to take
Absorption - takes place along the whole length of
the GI tract
Cheap - compared to most other parenteral routes
ORAL
 Disadvantages
Sometimes inefficient - only part of the drug may be
absorbed
First-pass effect - drugs absorbed orally are
initially transported to the liver via the portal
vein
irritation to gastric mucosa - nausea and vomiting
ORAL
 Disadvantages cont.
Destruction of drugs by gastric acid and
digestive juices
Effect too slow for emergencies
Unpleasant taste of some drugs
Unable to use in unconscious patient
First-pass Effect
The first-pass effect is the term used for the
hepatic metabolism of a pharmacological
agent when it is absorbed from the gut and
delivered to the liver via the portal circulation.
The greater the first-pass effect, the less the
agent will reach the systemic circulation when
the agent is administered orally
First-pass Effect
Oral Dosage Forms
 Common dose forms for oral administration
Tablets
Capsules
Liquids
Solutions
Suspensions
Syrups
Elixirs
SUBLINGUAL ROUTE
 Sublingual administration is
where the dosage form is
placed under the tongue
apidly absorbed by
sublingual mucosa
SUBLINGUAL ROUTE
ADVANTAGES
 ECONOMICAL
 QUICK TERMINATION
 FIRST-PASSAVOIDED
 DRUG ABSORPTION IS QUICK
DISADVANTAGES
 UNPALATABLE & BITTER DRUGS
 IRRITATION OF ORAL MUCOSA
 LARGE QUANTITIES NOT GIVEN
 FEW DRUGS AREABSORBED
12
BUCCAL ROUTE
 Buccal
administration is
where the dosage
form is placed
between gums and
inner lining of the
cheek (buccal
pouch)
absorbed by
buccal mucosa
BUCCAL ROUTE
ADVANTAGES
– Avoid first pass effect
– Rapid absorption
– Drug stability
DISADVANTAGES
– Inconvenience
– advantages lost if
swallowed
– Small dose limit
RECTAL ROUTE
ADVANTAGES
 LITTLE OR N
 USED IN
VOMITING/
 VED
O FIRST PASS EFFECT
UNCONSCIOUS
CENTRATIONS RAPIDLYACHIE
GESDISADVANTA
 INCONVENIENT
 ABSORPTION IS SLOW AND ERRATIC
 IRRITATION OR INFLAMMATION OF RECTAL
MUCOSA CAN OCCUR
15
 USED IN CHILDREN
HIGHER CON
SYSTEMIC-PARENTERAL
 Parenteral administration is
injection or infusion by means of
a needle or catheter inserted into
the body
 The term parenteral comes from
Greek words
para, meaning outside
enteron, meaning the intestine
 This route of administration
bypasses the alimentary canal
SYSTEMIC-PARENTERAL
17
.
 INJECTABLE
 INHALATION - Absorption through the lungs
 Intradermal (I.D.) (into skin)
 Subcutaneous (S.C.) (into subcutaneous tissue)
 Intramuscular (I.M.) (into skeletal muscle)
 Intravenous (I.V.) (into veins)
 Intra-arterial (I.A.) (into arteries)
 Intrathecal (I.T.) (cerebrospinal fluids )
 Intraperitoneal (I.P.) (peritoneal cavity)
 Intra - articular (Synovial fluids)
INTRAVENOUS
ADVANTAGES
 BIOAVAILABILITY 100%
 DESIRED BLOOD
CONCENTRATIONSACHIEVED
 LARGE QUANTITIES
 VOMITING & DIARRHEA
 EMERGENCY SITUATIONS
 FIRST PASSAVOIDED
 GASTRIC MANUPALATION
AVOIDED
DISADVANTAGES
 IRRITATION & CELLULITIS
 THROMBOPHELEBITIS
 REPEATED INJECTIONS NOT
ALWAYS FEASIBLE
 LESS SAFE
 TECHNICALASSISTANCE
REQUIRED
 DANGER OF INFECTION
 EXPENSIVE
 LESS CONVENIENTAND
PAINFUL
18
INTRAMUSULAR ROUTE
ADVANTAGES
 ABSORPTION
REASONABLY UNIFORM
 RAPID ONSET OF
ACTION
 MILD IRRITANTS CAN BE
GIVEN
 FIRST PASSAVOIDED
 GASTRIC FACTORS CAN
BEAVOIDED
DISADVANTAGES
 ONLY UPTO 10MLDRUG
GIVEN
 LOCAL PAIN ANDABCESS
 EXPENSIVE
 INFECTION
 NERVE DAMAGE
19
SUBCUTANEOUS
 Injected under the skin.
 Absorption is slow, so action is prolonged.
IMPLANT :a tablet or porous capsule is inserted into
the loose tissues by incision of the skin, which is
then stiched up.
example : certain hormonal drugs
INTRA-ARTERIAL
 Rarely used
 Anticancer drugs are given for localized effects
 Drugs used for diagnosis of peripheral vascular
diseases
INTRA-ARTICULAR
 Injections of antibiotics
and corticosteroids are
administered in
inflammed joined
cavities by experts.
example: hydrocortisone
in rheumatoid arthritis
INTRADERMAL
 Drug is given within skin
layers (dermis)
 Painful
 Mainly used for testing sensitivity
to drugs.
e.g. penicillin, ATS (anti tetanus
serum)
INOCULATION :administration of
vaccine (like small pox vaccine )
Topical Routes of Administration
 Topical administration is the application of a drug
directly to the surface of the skin
 Includes administration of drugs to any mucous
membrane
– vagina
– urethra
– colon
eye
nose
ears
lungs
Topical Dosage Forms
Dose forms for topical administration include:
 Skin:
Creams
Ointments
Lotions
Gels
Transdermal
patches
Disks
• Eye or ear:
– Solutions
– Suspensions
– Ointments
• Nose and lungs:
– Sprays and
powders
Advantages and Disadvantages of the
Topical Route
 Local therapeutic effects
 Not well absorbed into the deeper layers of the
skin or mucous membrane
lower risk of side effects
 Transdermal route offers steady level of drug in
the system
sprays for inhalation through the nose
may be for local or systemic effects
Transdermal
absorption of drug through skin (systemic action)
i. stable blood levels
ii. no first pass metabolism
iii. drug must be potent or patch
becomes too large
 Intravenous
 Intraosseous
 Endotracheal
 Inhalation
 Sublingual
 Intramuscular
 Subcutaneous
 Rectal
 Ingestion
 Transdermal
(topical)
30-60 seconds
30-60 seconds
2-3 minutes
2-3 minutes
3-5 minutes
10-20 minutes
15-30 minutes
5-30 minutes
30-90 minutes
variable (minutes to hours)
Route for administration
-Time until effect-
SELECTION OF ROUTE
The ROA is determined by :
 The physical characteristics of the drug
 The speed which the drug is absorbed and/
or released
 The need to bypass hepatic metabolism
 To achieve high conc. At particular sites
 Accuracy of dosage
 Condition of the patient
Route of Drug Administration

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Route of Drug Administration

  • 4. ORAL ROUTE  Oral refers to Two methods of administration: Applying topically to the mouth Swallowing for absorption along the gastrointestinal (GI) tract into systemic circulation  po (from the Latin per os) is the abbreviation used to indicate oral route of medication administration
  • 5. ORAL  Advantages Convenient - can be self- administered, pain free, easy to take Absorption - takes place along the whole length of the GI tract Cheap - compared to most other parenteral routes
  • 6. ORAL  Disadvantages Sometimes inefficient - only part of the drug may be absorbed First-pass effect - drugs absorbed orally are initially transported to the liver via the portal vein irritation to gastric mucosa - nausea and vomiting
  • 7. ORAL  Disadvantages cont. Destruction of drugs by gastric acid and digestive juices Effect too slow for emergencies Unpleasant taste of some drugs Unable to use in unconscious patient
  • 8. First-pass Effect The first-pass effect is the term used for the hepatic metabolism of a pharmacological agent when it is absorbed from the gut and delivered to the liver via the portal circulation. The greater the first-pass effect, the less the agent will reach the systemic circulation when the agent is administered orally
  • 10. Oral Dosage Forms  Common dose forms for oral administration Tablets Capsules Liquids Solutions Suspensions Syrups Elixirs
  • 11. SUBLINGUAL ROUTE  Sublingual administration is where the dosage form is placed under the tongue apidly absorbed by sublingual mucosa
  • 12. SUBLINGUAL ROUTE ADVANTAGES  ECONOMICAL  QUICK TERMINATION  FIRST-PASSAVOIDED  DRUG ABSORPTION IS QUICK DISADVANTAGES  UNPALATABLE & BITTER DRUGS  IRRITATION OF ORAL MUCOSA  LARGE QUANTITIES NOT GIVEN  FEW DRUGS AREABSORBED 12
  • 13. BUCCAL ROUTE  Buccal administration is where the dosage form is placed between gums and inner lining of the cheek (buccal pouch) absorbed by buccal mucosa
  • 14. BUCCAL ROUTE ADVANTAGES – Avoid first pass effect – Rapid absorption – Drug stability DISADVANTAGES – Inconvenience – advantages lost if swallowed – Small dose limit
  • 15. RECTAL ROUTE ADVANTAGES  LITTLE OR N  USED IN VOMITING/  VED O FIRST PASS EFFECT UNCONSCIOUS CENTRATIONS RAPIDLYACHIE GESDISADVANTA  INCONVENIENT  ABSORPTION IS SLOW AND ERRATIC  IRRITATION OR INFLAMMATION OF RECTAL MUCOSA CAN OCCUR 15  USED IN CHILDREN HIGHER CON
  • 16. SYSTEMIC-PARENTERAL  Parenteral administration is injection or infusion by means of a needle or catheter inserted into the body  The term parenteral comes from Greek words para, meaning outside enteron, meaning the intestine  This route of administration bypasses the alimentary canal
  • 17. SYSTEMIC-PARENTERAL 17 .  INJECTABLE  INHALATION - Absorption through the lungs  Intradermal (I.D.) (into skin)  Subcutaneous (S.C.) (into subcutaneous tissue)  Intramuscular (I.M.) (into skeletal muscle)  Intravenous (I.V.) (into veins)  Intra-arterial (I.A.) (into arteries)  Intrathecal (I.T.) (cerebrospinal fluids )  Intraperitoneal (I.P.) (peritoneal cavity)  Intra - articular (Synovial fluids)
  • 18. INTRAVENOUS ADVANTAGES  BIOAVAILABILITY 100%  DESIRED BLOOD CONCENTRATIONSACHIEVED  LARGE QUANTITIES  VOMITING & DIARRHEA  EMERGENCY SITUATIONS  FIRST PASSAVOIDED  GASTRIC MANUPALATION AVOIDED DISADVANTAGES  IRRITATION & CELLULITIS  THROMBOPHELEBITIS  REPEATED INJECTIONS NOT ALWAYS FEASIBLE  LESS SAFE  TECHNICALASSISTANCE REQUIRED  DANGER OF INFECTION  EXPENSIVE  LESS CONVENIENTAND PAINFUL 18
  • 19. INTRAMUSULAR ROUTE ADVANTAGES  ABSORPTION REASONABLY UNIFORM  RAPID ONSET OF ACTION  MILD IRRITANTS CAN BE GIVEN  FIRST PASSAVOIDED  GASTRIC FACTORS CAN BEAVOIDED DISADVANTAGES  ONLY UPTO 10MLDRUG GIVEN  LOCAL PAIN ANDABCESS  EXPENSIVE  INFECTION  NERVE DAMAGE 19
  • 20. SUBCUTANEOUS  Injected under the skin.  Absorption is slow, so action is prolonged. IMPLANT :a tablet or porous capsule is inserted into the loose tissues by incision of the skin, which is then stiched up. example : certain hormonal drugs
  • 21. INTRA-ARTERIAL  Rarely used  Anticancer drugs are given for localized effects  Drugs used for diagnosis of peripheral vascular diseases
  • 22. INTRA-ARTICULAR  Injections of antibiotics and corticosteroids are administered in inflammed joined cavities by experts. example: hydrocortisone in rheumatoid arthritis
  • 23. INTRADERMAL  Drug is given within skin layers (dermis)  Painful  Mainly used for testing sensitivity to drugs. e.g. penicillin, ATS (anti tetanus serum) INOCULATION :administration of vaccine (like small pox vaccine )
  • 24. Topical Routes of Administration  Topical administration is the application of a drug directly to the surface of the skin  Includes administration of drugs to any mucous membrane – vagina – urethra – colon eye nose ears lungs
  • 25. Topical Dosage Forms Dose forms for topical administration include:  Skin: Creams Ointments Lotions Gels Transdermal patches Disks • Eye or ear: – Solutions – Suspensions – Ointments • Nose and lungs: – Sprays and powders
  • 26. Advantages and Disadvantages of the Topical Route  Local therapeutic effects  Not well absorbed into the deeper layers of the skin or mucous membrane lower risk of side effects  Transdermal route offers steady level of drug in the system sprays for inhalation through the nose may be for local or systemic effects
  • 27. Transdermal absorption of drug through skin (systemic action) i. stable blood levels ii. no first pass metabolism iii. drug must be potent or patch becomes too large
  • 28.  Intravenous  Intraosseous  Endotracheal  Inhalation  Sublingual  Intramuscular  Subcutaneous  Rectal  Ingestion  Transdermal (topical) 30-60 seconds 30-60 seconds 2-3 minutes 2-3 minutes 3-5 minutes 10-20 minutes 15-30 minutes 5-30 minutes 30-90 minutes variable (minutes to hours) Route for administration -Time until effect-
  • 29. SELECTION OF ROUTE The ROA is determined by :  The physical characteristics of the drug  The speed which the drug is absorbed and/ or released  The need to bypass hepatic metabolism  To achieve high conc. At particular sites  Accuracy of dosage  Condition of the patient