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Routes of Drug Administration www.freelivedoctor.com
Drug Absorption ,[object Object],[object Object],www.freelivedoctor.com
Drug Absorption ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
Drug Absorption ,[object Object],[object Object],[object Object],www.freelivedoctor.com
Drug Absorption ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
www.freelivedoctor.com
Ion Trapping cont: Body fluids where a pH difference from blood pH will favor trapping or reabsorption: stomach contents  small intestine  breast milk  aqueous humor (eye)  vaginal secretions  prostatic secretions  www.freelivedoctor.com
Ion Trapping: ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
Lipid-Water Partition Coefficient ,[object Object],www.freelivedoctor.com
Lipid-Water Partition Coefficient ,[object Object],[object Object],[object Object],www.freelivedoctor.com
Routes of Drug Administration ,[object Object],www.freelivedoctor.com Important Info
[object Object],[object Object],[object Object],www.freelivedoctor.com
Enteral Routes ,[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
Sublingual/Buccal ,[object Object],[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
Sublingual/Buccal ,[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
Oral ,[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
Oral ,[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
Oral ,[object Object],[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
First-pass Effect ,[object Object],www.freelivedoctor.com
First-pass Effect cont. Magnitude of first pass hepatic effect:   Extraction ratio (ER) ER = CL liver / Q ; where Q is hepatic blood flow (usually about 90 L per hour. Systemic drug bioavailability (F) may be determined from the extent of absorption (f) and the extraction ratio (ER): F = f x (1 -ER)  www.freelivedoctor.com
First-pass Effect www.freelivedoctor.com
Rectal 1. unconscious patients and children  2. if patient is nauseous or vomiting  3. easy to terminate exposure  4. absorption may be variable  5. good for drugs affecting the bowel such  as laxatives 6. irritating drugs contraindicated www.freelivedoctor.com
Parenteral Routes ,[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
www.freelivedoctor.com
www.freelivedoctor.com
Intravascular Absorption phase is bypassed (100% bioavailability) 1.precise, accurate and almost immediate onset of  action,  2. large quantities can be given, fairly pain free 3. greater risk of adverse effects a. high concentration attained rapidly  b. risk of embolism c. OOPS factor or !@#$% www.freelivedoctor.com
Intramuscular 1. very rapid absorption of drugs in aqueous solution  2.repository and slow release preparations 3.pain at injection sites for certain drugs www.freelivedoctor.com
Subcutaneous 1. slow and constant absorption  2. absorption is limited by blood flow,   affected if circulatory problems exist  3. concurrent administration of  vasoconstrictor will slow absorption www.freelivedoctor.com
Inhalation 1.gaseous and volatile agents and aerosols  2.rapid onset of action due to rapid access to circulation a.large surface area  b.thin membranes separates alveoli from  circulation  c.high blood flow Particles larger than 20 micron and the particles impact in the mouth and throat. Smaller than 0.5 micron and they aren't retained.   www.freelivedoctor.com
Inhalation cont. ,[object Object],[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
Topical ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],www.freelivedoctor.com
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Route for administration  -Time until effect- www.freelivedoctor.com
Time-release preparations ,[object Object],[object Object],[object Object],www.freelivedoctor.com
Time-release preparations ,[object Object],www.freelivedoctor.com
The ROA is determined by the physical characteristics of the drug, the speed which the drug is absorbed  and/ or released, as well as the need to bypass hepatic metabolism and achieve high conc. at particular sites www.freelivedoctor.com Important Info
No  single  method of drug administration is ideal for all drugs in all circumstances   Very Important Info! www.freelivedoctor.com

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Routes of drug administration

  • 1. Routes of Drug Administration www.freelivedoctor.com
  • 2.
  • 3.
  • 4.
  • 5.
  • 7. Ion Trapping cont: Body fluids where a pH difference from blood pH will favor trapping or reabsorption: stomach contents small intestine breast milk aqueous humor (eye) vaginal secretions prostatic secretions www.freelivedoctor.com
  • 8.
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.
  • 18.
  • 19.
  • 20. First-pass Effect cont. Magnitude of first pass hepatic effect: Extraction ratio (ER) ER = CL liver / Q ; where Q is hepatic blood flow (usually about 90 L per hour. Systemic drug bioavailability (F) may be determined from the extent of absorption (f) and the extraction ratio (ER): F = f x (1 -ER) www.freelivedoctor.com
  • 22. Rectal 1. unconscious patients and children 2. if patient is nauseous or vomiting 3. easy to terminate exposure 4. absorption may be variable 5. good for drugs affecting the bowel such as laxatives 6. irritating drugs contraindicated www.freelivedoctor.com
  • 23.
  • 26. Intravascular Absorption phase is bypassed (100% bioavailability) 1.precise, accurate and almost immediate onset of action, 2. large quantities can be given, fairly pain free 3. greater risk of adverse effects a. high concentration attained rapidly b. risk of embolism c. OOPS factor or !@#$% www.freelivedoctor.com
  • 27. Intramuscular 1. very rapid absorption of drugs in aqueous solution 2.repository and slow release preparations 3.pain at injection sites for certain drugs www.freelivedoctor.com
  • 28. Subcutaneous 1. slow and constant absorption 2. absorption is limited by blood flow, affected if circulatory problems exist 3. concurrent administration of vasoconstrictor will slow absorption www.freelivedoctor.com
  • 29. Inhalation 1.gaseous and volatile agents and aerosols 2.rapid onset of action due to rapid access to circulation a.large surface area b.thin membranes separates alveoli from circulation c.high blood flow Particles larger than 20 micron and the particles impact in the mouth and throat. Smaller than 0.5 micron and they aren't retained. www.freelivedoctor.com
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.
  • 35. The ROA is determined by the physical characteristics of the drug, the speed which the drug is absorbed and/ or released, as well as the need to bypass hepatic metabolism and achieve high conc. at particular sites www.freelivedoctor.com Important Info
  • 36. No single method of drug administration is ideal for all drugs in all circumstances Very Important Info! www.freelivedoctor.com