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ROUTES OF DRUG 
ADMINISTRATION 
Dr. Chandane R. D. 
Asst Professor 
Dept of Pharmacology 
Govt Medical College, Akola
SYSTEMIC 
CLASSIFICATION 
Enteral Parenteral 
Oral Inhalational 
Sublingual Injections 
Rectal Transdermal 
LOCAL 
Skin topical 
Intranasal 
Ocular drops 
Mucosal-throat, 
vagina, mouth, ear 
Inhalational 
Transdermal 
Intravenous 
Intramuscular 
Subcutaneous 
Intra-arterial 
Intra-articular 
Intrathecal 
Intradermal
Enteral; oral, sub-lingual (buccal), 
rectal. Note soluble, enteric coated 
or slow release formulations 
Parenteral; iv, im, sc, id, it, etc. 
Different rates of absorption, 
different plasma peaks. Note iv 
infusors 
Skin; for local or systemic effect - 
note patches 
Lungs; inhalation; local or 
systemic effect? 
Vaginal; (usually local) 
Eye; (usually local)
FACTORS GOVERNING CHOICE 
OF ROUTE 
• Physical & chemical properties of drug-solid/ 
liquid/gas; solubility, stability, PH, irritancy 
• Site of desired action- localized and approachable or 
generalized and non approachable 
• Rate & extent of absorption from various routes 
• Effect of digestive juices & first pass effect 
• Rapidity of the desired response- emergency/routine 
• Accuracy of dosage 
• Condition of the patient- unconscious, vomiting
ORAL ROUTE 
The most common route of drug administration. 
Drug is given through oral cavity. 
ADVANTAGES 
Safe 
Convenient- self- administered, 
pain free, noninvasive 
and easy to take 
Economical- compared to other parentral routes 
Usually good absorption- takes place along the 
whole length of the GI tract 
No need for sterilization
ORAL ROUTE 
DISADVANTAGES 
1. Slow absorption slow action - can not used in 
emergency 
2. Irritable and unpalatable drugs- nausea and 
vomiting 
3. Cannot be used Unco-operative, vomiting and 
unconscious patients 
4. Some drugs destroyed 
5. Sometimes inefficient drug absorbed, some 
drugs are not absorbed like streptomycin 
6. First-pass effect- Due to Biotransformation 
7. Food–Drug interactions and Drug-Drug interactions
Dosage forms 
Capsules, powders 
Tablets, spansules 
Syrup, emulsion 
Suspension, elixirs 
Tablets 
Hard- gelatin capsule 
Spansule 
Syrup 
Soft- gelatin capsule
SUBLINGUAL/BUCCAL ROUTE 
Tab or pellet containing the drug is placed under tongue or 
crushed in mouth and spread over the buccal mucosa. Ex- GTN, 
buprenorphine, desaminooxytocin 
ADVANTAGES 
•Drug absorption is quick 
•Quick termination 
•First-pass avoided 
•Can be self administered 
•Economical 
DISADVANTAGES 
•Unpalatable & bitter 
drugs 
•Irritation of oral mucosa 
•Large quantities not 
given 
•Few drugs are absorbed
RECTAL ROUTE 
- Drugs that are administered rectally as a suppository. 
- In this form, a drug is mixed with a waxy substance that 
dissolves or liquefies after it is inserted into the rectum. 
- ex- Diazepam, indomethacin, paraldehyde, ergotamine 
ADVANTAGES 
Used in children 
Little or no first pass effect 
(ext haemorrhoidal vein) 
Used in vomiting or 
unconscious 
Higher concentrations rapidly 
achieved 
DISADVANTAGES 
Inconvenient 
Absorption is slow and 
erratic 
Irritation or inflammation of 
rectal mucosa can occur
PARENTERAL ROUTES 
Direct delivery of drug in to systemic circulation 
without intestinal mucosa 
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)
A) Intradermal – inj 
into skin 
B) Subcutaneous - 
Absorption of drugs 
from the subcutaneous 
tissues 
C) Intramuscular (IM) 
drug injected into 
skeletal muscle 
D) Intravascular (IV)- 
placing a drug directly 
into the blood stream
First pass Metabolism 
Metabolism of drug in the gut wall or portal 
circulation before reaching systemic circulation 
so the amount reaching system circulation is less 
than the amount absorbed 
Where ? 
Liver 
Gut wall 
Gut Lumen 
Result ? 
Low bioavailability. 
Short duration of action (t ½).
First-pass 
metabolism can occur 
with orally 
administered drugs.
Advantages Disadvantages 
– Infection 
– Sterilization. 
–Invasive 
assistance require 
– Pain 
– Needs skill 
– Anaphylaxis 
– Expensive. 
• high bioavailability 
• Rapid action (emergency) 
• No first pass metabolism 
Suitable for 
–Vomiting &unconsciousness 
– Irritant & Bad taste drugs. 
– No gastric irritation 
– No food-drug interaction 
Dosage form: 
Vial or ampoule
Ampoule iv infusion Vial
INTRAVENOUS ROUTE 
ADVANTAGES 
IV is the most common parenteral route. For drugs that are not 
absorbed orally. 
Avoids first-pass metabolism by the liver. 
Intravenous delivery permits a rapid effect and a maximal degree 
of control over the circulating levels of the drug. Titration of dose 
with response. 
large quantities can be given, fairly pain free 
(100% bioavailability) Absorption phase is bypassed 
DISADVANTAGES 
However, unlike drugs in the GI tract, those that are injected 
cannot be recalled by strategies such as emesis or by binding to 
activated charcoal. 
IV injection may also induce hemolysis or cause other adverse 
reactions by the too-rapid delivery of high concentrations of drug 
to the plasma and tissues also vital organs like heart, brain etc. 
Thrombophlebitis of vein and necrosis of adjoining tissue if 
extravasation occurs
INTRAMUSULAR ROUTE 
Large skeletal muscle- Deltoid, triceps, gluteus 
maximus, rectus femoris 
ADVANTAGES 
Absorption reasonably 
uniform 
Rapid onset of action 
Mild irritants can be 
given 
First pass avoided 
Gastric factors can be 
avoided 
DISADVANTAGES 
Only upto 10ml drug 
given 
Local pain and abcess 
Expensive 
Infection 
Nerve damage 
Local hematoma can 
occur in anticoagulant 
treated pt.
SUBCUTANEOUS ROUTE 
Drug is deposited in loose subcutaneous tissue – rich nerve 
supply- irritant drugs cannot be inj. Less vascular- slow 
absorption than im route 
Avoid in shock pt – vasoconstriction 
Only Small volume can be injected 
Subcutaneous injection minimizes the risks associated with 
intravascular injection 
Depot preparation can be injected- Dermojet, Pellet 
implantation, Sialistic and biodegradable implants 
Intradermal Route 
Inj into skin raising bleb – BCG Vaccine, Sensitivity test 
Intrathecal/intraventricular 
It is sometimes necessary to introduce drugs directly into 
the cerebrospinal fluid. For example, amphotericin B is used 
in treating Cryptococcal meningitis
Transdermal 
This route of administration achieves systemic effects by application of 
drugs to the skin, usually via a transdermal medicated adhesive patch. 
The rate of absorption can vary markedly, depending on the physical 
characteristics of the drug (lipid soluble) and skin at the site of 
application. 
Slow effect (prolonged drug action) 
This route is most often used for the sustained delivery of drugs, such 
as the antianginal drug nitroglycerin, the antiemetic scopolamine. 
the nicotine patches 
 Site – Upper arm, chest, 
abdomen, mastoid region 
First pass effect avoided 
Absorption- increase by oily 
base, occlusive dressing, 
rubbing preparation
Transdermal therapeutic system 
Drug in solution or bound to a polymer is held in reservoir between 
occlusive backing film and rate controlling microporemembrane 
under surface of which is smeared with an adhesive impregnated 
with priming dose of drug. Adhesive layer protected with film which 
is peeled off just before application 
To provide smooth plasma conc without fluctuations 
More convinient pt compliance is better
 Produce local effect to 
 Skin (percutaneous) e.g. allergy testing, 
topical local anesthesia 
 Mucous membrane of respiratory tract 
(Inhalation) e.g. asthma 
 Eye drops e.g. conjunctivitis 
 Ear drops e.g. otitis externa 
 Intranasal, e.g. decongestant nasal spray
Advantages Disadvantages 
Only few 
drugs can be 
used 
• Mucous membrane of 
respiratory system 
• Rapid absorption 
(large surface area) 
•Provide local action 
• Minor systemic effect 
• Low bioavailability 
• Less side effects. 
• No first pass effect 
Dosage form: aerosol, nebulizer
Nebulizer Atomizer
Inhalation 
Inhalation provides the rapid delivery of a drug across the large 
surface area of the mucous membranes of the respiratory tract and 
pulmonary epithelium, producing an effect almost as rapidly as with IV 
injection. 
This route of administration is used for drugs that are gases (for 
example, some anesthetics) or those that can be dispersed in an aerosol. 
This route is particularly effective and convenient for patients with 
respiratory complaints (such as asthma, or chronic obstructive 
pulmonary disease) because the drug is delivered directly to the site of 
action and systemic side effects are minimized. 
Examples of drugs administered via this route include albuterol, and 
corticosteroids, such as fluticasone.
Intranasal 
This route involves administration of drugs directly into the 
nose. Agents include nasal decongestants such as the anti-inflammatory 
corticosteroid. 
Desmopressin is administered intranasally in the treatment 
of diabetes insipidus; salmon calcitonin, a peptide hormone 
used in the treatment of osteoporosis, is also available as a 
nasal spray. 
The abused drug, cocaine, is generally taken by intranasal 
sniffing. 
Eye drops
SKIN - Topical 
Dermal - Oil or ointment for local action 
Antiseptic cream and lotion 
Sunscreen lotion and powders
No single method of drug 
administration is ideal for all 
drugs in all circumstances

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Routes of Administration Pharmacology

  • 1. ROUTES OF DRUG ADMINISTRATION Dr. Chandane R. D. Asst Professor Dept of Pharmacology Govt Medical College, Akola
  • 2. SYSTEMIC CLASSIFICATION Enteral Parenteral Oral Inhalational Sublingual Injections Rectal Transdermal LOCAL Skin topical Intranasal Ocular drops Mucosal-throat, vagina, mouth, ear Inhalational Transdermal Intravenous Intramuscular Subcutaneous Intra-arterial Intra-articular Intrathecal Intradermal
  • 3. Enteral; oral, sub-lingual (buccal), rectal. Note soluble, enteric coated or slow release formulations Parenteral; iv, im, sc, id, it, etc. Different rates of absorption, different plasma peaks. Note iv infusors Skin; for local or systemic effect - note patches Lungs; inhalation; local or systemic effect? Vaginal; (usually local) Eye; (usually local)
  • 4. FACTORS GOVERNING CHOICE OF ROUTE • Physical & chemical properties of drug-solid/ liquid/gas; solubility, stability, PH, irritancy • Site of desired action- localized and approachable or generalized and non approachable • Rate & extent of absorption from various routes • Effect of digestive juices & first pass effect • Rapidity of the desired response- emergency/routine • Accuracy of dosage • Condition of the patient- unconscious, vomiting
  • 5. ORAL ROUTE The most common route of drug administration. Drug is given through oral cavity. ADVANTAGES Safe Convenient- self- administered, pain free, noninvasive and easy to take Economical- compared to other parentral routes Usually good absorption- takes place along the whole length of the GI tract No need for sterilization
  • 6. ORAL ROUTE DISADVANTAGES 1. Slow absorption slow action - can not used in emergency 2. Irritable and unpalatable drugs- nausea and vomiting 3. Cannot be used Unco-operative, vomiting and unconscious patients 4. Some drugs destroyed 5. Sometimes inefficient drug absorbed, some drugs are not absorbed like streptomycin 6. First-pass effect- Due to Biotransformation 7. Food–Drug interactions and Drug-Drug interactions
  • 7. Dosage forms Capsules, powders Tablets, spansules Syrup, emulsion Suspension, elixirs Tablets Hard- gelatin capsule Spansule Syrup Soft- gelatin capsule
  • 8. SUBLINGUAL/BUCCAL ROUTE Tab or pellet containing the drug is placed under tongue or crushed in mouth and spread over the buccal mucosa. Ex- GTN, buprenorphine, desaminooxytocin ADVANTAGES •Drug absorption is quick •Quick termination •First-pass avoided •Can be self administered •Economical DISADVANTAGES •Unpalatable & bitter drugs •Irritation of oral mucosa •Large quantities not given •Few drugs are absorbed
  • 9. RECTAL ROUTE - Drugs that are administered rectally as a suppository. - In this form, a drug is mixed with a waxy substance that dissolves or liquefies after it is inserted into the rectum. - ex- Diazepam, indomethacin, paraldehyde, ergotamine ADVANTAGES Used in children Little or no first pass effect (ext haemorrhoidal vein) Used in vomiting or unconscious Higher concentrations rapidly achieved DISADVANTAGES Inconvenient Absorption is slow and erratic Irritation or inflammation of rectal mucosa can occur
  • 10. PARENTERAL ROUTES Direct delivery of drug in to systemic circulation without intestinal mucosa 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)
  • 11. A) Intradermal – inj into skin B) Subcutaneous - Absorption of drugs from the subcutaneous tissues C) Intramuscular (IM) drug injected into skeletal muscle D) Intravascular (IV)- placing a drug directly into the blood stream
  • 12. First pass Metabolism Metabolism of drug in the gut wall or portal circulation before reaching systemic circulation so the amount reaching system circulation is less than the amount absorbed Where ? Liver Gut wall Gut Lumen Result ? Low bioavailability. Short duration of action (t ½).
  • 13. First-pass metabolism can occur with orally administered drugs.
  • 14. Advantages Disadvantages – Infection – Sterilization. –Invasive assistance require – Pain – Needs skill – Anaphylaxis – Expensive. • high bioavailability • Rapid action (emergency) • No first pass metabolism Suitable for –Vomiting &unconsciousness – Irritant & Bad taste drugs. – No gastric irritation – No food-drug interaction Dosage form: Vial or ampoule
  • 16. INTRAVENOUS ROUTE ADVANTAGES IV is the most common parenteral route. For drugs that are not absorbed orally. Avoids first-pass metabolism by the liver. Intravenous delivery permits a rapid effect and a maximal degree of control over the circulating levels of the drug. Titration of dose with response. large quantities can be given, fairly pain free (100% bioavailability) Absorption phase is bypassed DISADVANTAGES However, unlike drugs in the GI tract, those that are injected cannot be recalled by strategies such as emesis or by binding to activated charcoal. IV injection may also induce hemolysis or cause other adverse reactions by the too-rapid delivery of high concentrations of drug to the plasma and tissues also vital organs like heart, brain etc. Thrombophlebitis of vein and necrosis of adjoining tissue if extravasation occurs
  • 17. INTRAMUSULAR ROUTE Large skeletal muscle- Deltoid, triceps, gluteus maximus, rectus femoris ADVANTAGES Absorption reasonably uniform Rapid onset of action Mild irritants can be given First pass avoided Gastric factors can be avoided DISADVANTAGES Only upto 10ml drug given Local pain and abcess Expensive Infection Nerve damage Local hematoma can occur in anticoagulant treated pt.
  • 18. SUBCUTANEOUS ROUTE Drug is deposited in loose subcutaneous tissue – rich nerve supply- irritant drugs cannot be inj. Less vascular- slow absorption than im route Avoid in shock pt – vasoconstriction Only Small volume can be injected Subcutaneous injection minimizes the risks associated with intravascular injection Depot preparation can be injected- Dermojet, Pellet implantation, Sialistic and biodegradable implants Intradermal Route Inj into skin raising bleb – BCG Vaccine, Sensitivity test Intrathecal/intraventricular It is sometimes necessary to introduce drugs directly into the cerebrospinal fluid. For example, amphotericin B is used in treating Cryptococcal meningitis
  • 19. Transdermal This route of administration achieves systemic effects by application of drugs to the skin, usually via a transdermal medicated adhesive patch. The rate of absorption can vary markedly, depending on the physical characteristics of the drug (lipid soluble) and skin at the site of application. Slow effect (prolonged drug action) This route is most often used for the sustained delivery of drugs, such as the antianginal drug nitroglycerin, the antiemetic scopolamine. the nicotine patches  Site – Upper arm, chest, abdomen, mastoid region First pass effect avoided Absorption- increase by oily base, occlusive dressing, rubbing preparation
  • 20. Transdermal therapeutic system Drug in solution or bound to a polymer is held in reservoir between occlusive backing film and rate controlling microporemembrane under surface of which is smeared with an adhesive impregnated with priming dose of drug. Adhesive layer protected with film which is peeled off just before application To provide smooth plasma conc without fluctuations More convinient pt compliance is better
  • 21.  Produce local effect to  Skin (percutaneous) e.g. allergy testing, topical local anesthesia  Mucous membrane of respiratory tract (Inhalation) e.g. asthma  Eye drops e.g. conjunctivitis  Ear drops e.g. otitis externa  Intranasal, e.g. decongestant nasal spray
  • 22. Advantages Disadvantages Only few drugs can be used • Mucous membrane of respiratory system • Rapid absorption (large surface area) •Provide local action • Minor systemic effect • Low bioavailability • Less side effects. • No first pass effect Dosage form: aerosol, nebulizer
  • 24. Inhalation Inhalation provides the rapid delivery of a drug across the large surface area of the mucous membranes of the respiratory tract and pulmonary epithelium, producing an effect almost as rapidly as with IV injection. This route of administration is used for drugs that are gases (for example, some anesthetics) or those that can be dispersed in an aerosol. This route is particularly effective and convenient for patients with respiratory complaints (such as asthma, or chronic obstructive pulmonary disease) because the drug is delivered directly to the site of action and systemic side effects are minimized. Examples of drugs administered via this route include albuterol, and corticosteroids, such as fluticasone.
  • 25. Intranasal This route involves administration of drugs directly into the nose. Agents include nasal decongestants such as the anti-inflammatory corticosteroid. Desmopressin is administered intranasally in the treatment of diabetes insipidus; salmon calcitonin, a peptide hormone used in the treatment of osteoporosis, is also available as a nasal spray. The abused drug, cocaine, is generally taken by intranasal sniffing. Eye drops
  • 26. SKIN - Topical Dermal - Oil or ointment for local action Antiseptic cream and lotion Sunscreen lotion and powders
  • 27. No single method of drug administration is ideal for all drugs in all circumstances