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Definition of Pharmacology 
Pharmacology is the study of the interactions that 
occur between our body and chemicals. Knowing 
more about the action and uses of a drug.
Importance of Pharmacology 
to OHT 
• Knowledge of how and when 
the drug is administered 
• Improve patient experience 
• Increase the efficiency of 
dental procedures 
• Provide clear explanation of 
drug to patient (only when 
prescribed) 
• Improve infection control and 
prevent fatality
HOW PHARMACOLOGY IS 
INCORPORATED IN 
DAILY PRACTICES?
WHAT TYPE OF SCENARIOS 
CAN WE FACE? 
Medications/ Ulcer Creams/ Local Anesthesia
Medication/ Ulcer Creams/ Local Anesthesia 
MEDICATIONS
MEDICATIONS 
Medication/ Ulcer Creams/ Local Anesthesia 
In what situations is medication incorporated to 
the job of a OHT? 
Almost everyday! 
When taking medical history 
we need to be aware of 
diseases that the patient 
might have. Especially if poses 
any risks during dental 
procedures.
MEDICATIONS 
Medication/ Ulcer Creams/ Local Anesthesia 
In what situations is medication incorporated to 
the job of a OHT? 
When treating patients who are 
at high risk of infective 
endocarditis, sudden bacteremia 
may be produced by dental 
manipulation within the mouth.
MEDICATIONS 
Medication/ Ulcer Creams/ Local Anesthesia 
Who are at high risk of infective endocarditis? 
Congenital Heart 
Disease 
Rheumatic 
Heart Disease 
Congenital 
Heart Disease
MEDICATIONS 
Medication/ Ulcer Creams/ Local Anesthesia 
So, when treating such patients… 
 To get approval from doctor 
 Example of common medication 
given is antibiotics-amoxillin. 
 Better absorbed, following oral 
administration 
 Amoxicillin is one of the most 
common antibiotics prescribed 
for children
MEDICATIONS 
Medication/ Ulcer Creams/ Local Anesthesia 
In a dental clinic
ULCER CREAMS 
Medication/ Ulcer Creams/ Local Anesthesia 
When a patient walks in to a clinic… 
1.We need to identify the 
cause of the ulcer 
2. Consider treating it 
3. Prescribe ulcer cream
ULCER CREAMS 
Medication/ Medication/ Ulcer Ulcer Creams/ Creams/ Local Local Anesthesia 
Anesthesia 
And now, an advertisement
LOCAL ANESTHESIA 
Medication/ Ulcer Creams/ Local Anesthesia 
When local anesthesia is used? 
Cavity Preparation Extraction of teeth Removal of Gum Polyp
LOCAL ANESTHESIA 
Medication/ Ulcer Creams/ Local Anesthesia 
Medication/ Ulcer Creams/ Local Anesthesia 
A live extraction in class
ACTIVITY 
Purpose/ Route of Entry/ Packaging/ Form of Medicine
USES OF DRUGS
Uses of Drugs 
ANTIBIOTICS 
• Also known as antibacterials 
• Organic substances either produced by micro-organisms or 
synthetically manufactured 
• Drugs used to treat infections caused by bacteria 
• Inhibit growth of bacteria and other micro-organisms 
• Not effective against viruses
Uses of Drugs 
ANTISEPTICS & DISINFECTANT / 
HAEMOSTATICS & STYPTICS 
Antiseptics & Disinfectants 
• Basic tools of cleaning 
and sanitizing 
• Eliminate disease-causing 
organisms 
Haemostatics & Styptics 
• Blood clotting agents 
• Arrest the flow of blood 
(clotting) 
• Promote vasoconstriction
Uses of Drugs 
Pain & Pain Control / Vasoconstriction 
Pain & Pain Control 
• Manage and subdue 
pain faced by patience 
• Provide ease to operator 
to carry out procedure 
Vasoconstriction drugs 
• Blanching of tissues 
• Narrows blood vessels
Internal/ External 
ROUTE OF ADMINISTRATION
Route of Entry 
External Route 
On the skin 
Mucous 
membrane of 
mouth 
Mucous 
membrane of 
rectum 
Internal Route 
Ingestion, Oral 
Route Injection 
Inhalation
Internal/ External 
EXTERNAL ROUTE
External Route 
• Applied on the surface: local 
effects only. 
• Depending on chemical 
structure and quantity applied 
• Can be absorbed by the skin 
and mucous membrane 
• Greatest Penetration: drugs 
with low molecular weight 
with a high water and lipid 
solubility
External Route 
Point of Entry Examples 
On the skin Creams, Lotions 
On the mucous membrane 
of mouth 
Lozenges, Gargles 
On the mucous membrane 
of rectum 
Suppositories
Internal/ External 
INTERNAL ROUTE
Internal Route 
1) Ingestion or Oral Route 
a. In the mouth, some drugs are readily and rapidly 
absorbed via the mucous membrane in the mouth 
b. In the stomach and small intestine, drugs that are 
swallowed are absorbed through the lining mucosa
Internal Route 
2) Injection 
a) Intradermal – in the layers of the skin 
b) Subcutaneous – into the undersurface of the skin 
c) Intramuscular – into the deep-seated muscles 
d) Intravenous – into the veins 
e) Intraspinal – into the spinal space
Internal Route 
3) Inhalation 
• Drugs in the form of vapor 
may be inhaled into the lungs. 
• Very small molecular 
structure and pass easily 
through the thin epithelium. 
• Absorbed through pulmonary 
endothelium at alveoli to gain 
rapid access to the general 
circulation
PACKAGING
• To carry the product and keep it stable, till it is 
consumed 
• Transparent 
capsules & syrup in 
a transparent glass 
bottle is preferred a 
lot more
• They are not only attractive but are also more 
trustworthy because patients can “see” what they are 
consuming 
• Most manufacturers are no longer hiding the 
medicines behind opaque covers
FORM OF MEDICINE
• Many tablets today are coated after being pressed. 
Some coatings are just to provide colour or a smooth 
finish, or to facilitate printing on the tablet
• Some tablets have coatings which is designed to hold 
the tablet together when it is in the stomach 
• The coating is designed to hold together in acid 
conditions and break down in non-acid conditions and 
therefore release the drug in the intestines 
• Example: Aspirin 
• An enteric coating is 
there usually for a good 
reason and therefore 
such tablets or the 
contents of enteric 
coated capsules should 
never be crushed before 
being taken.
• Hard-shelled capsules, which are normally used for 
dry, powdered ingredients or miniature pellets
• Soft-shelled capsules, primarily used for oils and for 
active ingredients that are dissolved or suspended 
in oil
• Solutions, syrups and mixtures 
• Commonly used in patients that have difficulty 
swallowing medicines like children and the elderly 
• The liquid medicine should be made such that the 
dose needed will be a sensible volume such as 5ml 
(one teaspoon)
ACTIVITY 
Purpose/ Route of Entry/ Packaging/ Form of Medicine 
ENTRY PACKAGING FORM OF 
PURPOSE ROUTE OF 
MEDICINE 
1. Antiseptics 
2. Pain control 
3. Haemostatics 
and Styptics 
4. Antibiotics 
5. Vasoconstriction 
External route 
1. Skin 
2. Oral Mucosa 
3. Membrane of 
rectum 
Internal Route 
1. Ingestion 
2. Injection 
3. Inhalation 
1. Hard shelled 
Capsules 
2. Soft Shell 
Capsules 
3. Liquid 
4. Coated Tablets 
1. Blister 
Pack 
2. Bottle 
3. Tube
ABSORPTION OF DRUG
ALVEOLI 
Absorption
Absorption of Drug 
• Absorption is the process by which a drug 
passes from its site of administration into the 
circulation (bloodstream). 
• The blood receives a drug from the site of 
administration and carries it to all the organs, 
including those on which the drug acts. 
• The speed, ease, and degree of absorption 
are related to the route of administration.
Absorption of Drug 
• The absorption rates of drugs depend on its 
physical and chemical properties, on the site 
of absorption and the solubility of drug. 
Site of Absorption Rate of Absorption 
In mucous membrane Rapid 
In small intestine Depends on health of stomach 
and its activity and 
presence/absence of food 
Subcutaneous and 
Intramuscular injections 
Depends on water solubility of 
drug, dose form and blood 
supply at site. 
Intravenous Injection Immediate 
Inhalation Immediate
DISTRIBUTION OF DRUG
Distribution of Drug 
• After the drug is absorbed, it is then distributed to 
various organs of the body. 
• Influenced by how well each organ is perfused, organ 
size, binding of the drug to various components of 
blood and tissues, and permeability of tissue 
membranes. 
• The more fat-soluble a drug is, the higher its ability to 
pass across the cell membrane is. 
• Protein binding is an important consideration 
influencing drug distribution. 
• Many drugs are bound to blood proteins such as 
serum albumin and are not available as active drugs.
METABOLISM OF DRUG
METABOLISM
METABOLISM
Metabolism of Drug 
• Metabolism occurs via two types of reactions: 
and 
• Goal: Change the active part of medications (a.k.a 
functional group) making them more water-soluble and 
more readily excreted by the kidney. 
• Changing the molecular structure of drugs= water 
solubility= fat solubility= faster excretion of drug in the 
urine.
Metabolism of Drug: Phase I 
• Phase I: reactions involve oxidation, hydrolysis, 
and reduction. 
• Oxidation and reduction processes make a 
molecule's charge more positive or negative than 
the original drug. 
• Regardless of the positivity or negativity, a 
charged molecule = dissolvable in water 
• Take place primarily in the liver by enzymes 
• Oxidative metabolism may result in formation of 
an active metabolite or inactive compound.
Metabolism of Drug: Phase II 
• Phase II: reactions involve conjugation to form 
glucuronides, acetates, or sulfates, by adding 
glucose, acetate, or sulfate molecules, respectively. 
• These reactions generally inactivate the 
pharmacologic activity of the drug and may make it 
more prone to elimination by the kidney.
EXCRETION OF DRUG
EXCRETION
Excretion of Drug 
• Excretion of a drug = duration of action= 
toxicity. 
• Drugs may be eliminated as a parent drug 
(unchanged) or as metabolites (changed form). 
• PharmacoDYNAMICS: what the drug does to the 
body; this term refers to the action of the drug at 
the tissue-,cellular-, and molecular level. 
– Specific and different for each drug
PharmacoKINETICS: what the human body does to the drug 
Excretion occurs primarily through the urine. 
Fecal excretion is seen with drugs that are not absorbed 
from the intestines or have been secreted in the bile. 
sweat
KIDNEY 
• Most important organ for elimination of drugs 
and its metabolites 
• Eliminated in the urine 
① Passive glomerular filtration (most drugs) 
② Active tubular secretion (e.g. penicillin) 
③ Passive tubular secretion (e.g. salicylates) 
• In the case of renal damage: 
 excretion of drugs;  toxicity
BILE 
• Usually involve orally ingested unabsorbed 
drugs or metabolites excreted in the bile, that 
are not reabsorbed from the small intestine 
• Eliminated through feces 
• Examples of drugs 
– Phenytoin 
– Phenolphthalein
INTESTINES 
• Oral and enteral medications (like purgatives) are 
absorbed in small intestine 
• Excreted in large intestine 
• Eliminated through stools 
• Example: 
– senna 
– cascara
LUNGS 
• Drugs like volatile general anaesthetics, ethyl alcohol are 
excreted through lungs 
• Most drugs excreted here are not metabolized first 
• Example: 
– Ketamine 
– propofol
SALIVA 
• Drugs like iodides and 
metallic salts are excreted 
through saliva. 
• Such as lead is eliminated 
through saliva and its 
deposition produces black 
lining of teeth.
SWEAT 
• Heavy metals like arsenic 
and mercury are excreted 
through skin.
BREAST MILK 
• Breast milk is more acidic than 
plasma 
• May produce drug toxicity in the 
nursing infant 
• Pulmonary excretion (e.g. 
breathing) is important as it 
pertains to the elimination of 
anesthetic gases and vapors, as 
well as alcohol. 
• Example: pethidine
Video
FACTORS TO CONSIDER WHEN 
PRESCRIBING DRUGS
FACTORS TO CONSIDER WHEN PRESCRIBING DRUGS 
Dosage of 
drugs 
Presence of 
other drugs 
Time of 
administration 
Patient 
compliance 
Weight of 
patient 
Age 
Sex 
Severity of 
the disease
Dosage of drugs 
• Weight of patient 
Dose = Adult Dose x Weight (kg) 
• Age 
Age x Adult dose 
70 
Age + 12 
• Sex 
Females are given 7/8 male dose. 
• Neonates-new born(calibrated 
dose) 
• Infants-1-6 years(1/4 adults dose) 
• Children- 6-12 years(1/2 adult 
dose)
Presence of other drugs 
• Some drugs cancel each other’s effects 
• Combined effect would be harmful to the 
patient 
• Hence, consideration must be taken if patient 
is on other drugs
Time of administration 
• Time relationship to meals could influence the 
actual effective therapeutic dose 
• Absorption occurs more rapidly if stomach 
and upper portion of body are free from food 
• Drug action may depreciate when medication 
given after a meal 
• Irritant forms of medication are better 
tolerated if food already present in gut.
Patient compliance 
• Patient does not take medication due to: 
o Lack of faith in medication 
o Poor understanding of illness 
• Patient takes medication incorrectly 
• Patient stops taking medication midway
FACTORS THAT MODIFY 
DRUG EFFECTS
FACTORS THAT MODIFY DRUG EFFECTS 
Patient compliance 
Other drugs 
Age & Weight 
Rate of elimination 
Physiological factors 
Tolerence and cross-tolerence 
Sex 
Pathologic factors 
Route of administration 
Time of administration 
Psychological factors 
Genetic variation
10 
8 
6 
4 
2 
0 
Blood Concentration VS Time Curve 
of Repeated Dosing 
8 16 24 32 
1st Dose 
2nd Dose 
3rd Dose 
No Effect 
Toxic Level 
Blood Concentration 
Time 
Distribution 
+ 
Metabolism 
HALF –LIFE/ 
THERAPEUTIC 
LEVEL
CONCLUSION! 
1. Pharmacology and it’s 
use 
2. Route of administration 
3. Packaging 
4. Form of drugs 
5. Absorption, Distribution, 
Metabolism, Excretion of 
Drugs
THANK YOU FOR LISTENING 
NYP DENTAL HYGIENE AND THERAPY 2012

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Fundamentals of LA Administration

  • 1.
  • 2. Definition of Pharmacology Pharmacology is the study of the interactions that occur between our body and chemicals. Knowing more about the action and uses of a drug.
  • 3. Importance of Pharmacology to OHT • Knowledge of how and when the drug is administered • Improve patient experience • Increase the efficiency of dental procedures • Provide clear explanation of drug to patient (only when prescribed) • Improve infection control and prevent fatality
  • 4. HOW PHARMACOLOGY IS INCORPORATED IN DAILY PRACTICES?
  • 5. WHAT TYPE OF SCENARIOS CAN WE FACE? Medications/ Ulcer Creams/ Local Anesthesia
  • 6. Medication/ Ulcer Creams/ Local Anesthesia MEDICATIONS
  • 7. MEDICATIONS Medication/ Ulcer Creams/ Local Anesthesia In what situations is medication incorporated to the job of a OHT? Almost everyday! When taking medical history we need to be aware of diseases that the patient might have. Especially if poses any risks during dental procedures.
  • 8. MEDICATIONS Medication/ Ulcer Creams/ Local Anesthesia In what situations is medication incorporated to the job of a OHT? When treating patients who are at high risk of infective endocarditis, sudden bacteremia may be produced by dental manipulation within the mouth.
  • 9. MEDICATIONS Medication/ Ulcer Creams/ Local Anesthesia Who are at high risk of infective endocarditis? Congenital Heart Disease Rheumatic Heart Disease Congenital Heart Disease
  • 10. MEDICATIONS Medication/ Ulcer Creams/ Local Anesthesia So, when treating such patients…  To get approval from doctor  Example of common medication given is antibiotics-amoxillin.  Better absorbed, following oral administration  Amoxicillin is one of the most common antibiotics prescribed for children
  • 11. MEDICATIONS Medication/ Ulcer Creams/ Local Anesthesia In a dental clinic
  • 12. ULCER CREAMS Medication/ Ulcer Creams/ Local Anesthesia When a patient walks in to a clinic… 1.We need to identify the cause of the ulcer 2. Consider treating it 3. Prescribe ulcer cream
  • 13. ULCER CREAMS Medication/ Medication/ Ulcer Ulcer Creams/ Creams/ Local Local Anesthesia Anesthesia And now, an advertisement
  • 14. LOCAL ANESTHESIA Medication/ Ulcer Creams/ Local Anesthesia When local anesthesia is used? Cavity Preparation Extraction of teeth Removal of Gum Polyp
  • 15. LOCAL ANESTHESIA Medication/ Ulcer Creams/ Local Anesthesia Medication/ Ulcer Creams/ Local Anesthesia A live extraction in class
  • 16. ACTIVITY Purpose/ Route of Entry/ Packaging/ Form of Medicine
  • 18. Uses of Drugs ANTIBIOTICS • Also known as antibacterials • Organic substances either produced by micro-organisms or synthetically manufactured • Drugs used to treat infections caused by bacteria • Inhibit growth of bacteria and other micro-organisms • Not effective against viruses
  • 19. Uses of Drugs ANTISEPTICS & DISINFECTANT / HAEMOSTATICS & STYPTICS Antiseptics & Disinfectants • Basic tools of cleaning and sanitizing • Eliminate disease-causing organisms Haemostatics & Styptics • Blood clotting agents • Arrest the flow of blood (clotting) • Promote vasoconstriction
  • 20. Uses of Drugs Pain & Pain Control / Vasoconstriction Pain & Pain Control • Manage and subdue pain faced by patience • Provide ease to operator to carry out procedure Vasoconstriction drugs • Blanching of tissues • Narrows blood vessels
  • 21. Internal/ External ROUTE OF ADMINISTRATION
  • 22. Route of Entry External Route On the skin Mucous membrane of mouth Mucous membrane of rectum Internal Route Ingestion, Oral Route Injection Inhalation
  • 24. External Route • Applied on the surface: local effects only. • Depending on chemical structure and quantity applied • Can be absorbed by the skin and mucous membrane • Greatest Penetration: drugs with low molecular weight with a high water and lipid solubility
  • 25. External Route Point of Entry Examples On the skin Creams, Lotions On the mucous membrane of mouth Lozenges, Gargles On the mucous membrane of rectum Suppositories
  • 27. Internal Route 1) Ingestion or Oral Route a. In the mouth, some drugs are readily and rapidly absorbed via the mucous membrane in the mouth b. In the stomach and small intestine, drugs that are swallowed are absorbed through the lining mucosa
  • 28. Internal Route 2) Injection a) Intradermal – in the layers of the skin b) Subcutaneous – into the undersurface of the skin c) Intramuscular – into the deep-seated muscles d) Intravenous – into the veins e) Intraspinal – into the spinal space
  • 29. Internal Route 3) Inhalation • Drugs in the form of vapor may be inhaled into the lungs. • Very small molecular structure and pass easily through the thin epithelium. • Absorbed through pulmonary endothelium at alveoli to gain rapid access to the general circulation
  • 31. • To carry the product and keep it stable, till it is consumed • Transparent capsules & syrup in a transparent glass bottle is preferred a lot more
  • 32. • They are not only attractive but are also more trustworthy because patients can “see” what they are consuming • Most manufacturers are no longer hiding the medicines behind opaque covers
  • 34. • Many tablets today are coated after being pressed. Some coatings are just to provide colour or a smooth finish, or to facilitate printing on the tablet
  • 35. • Some tablets have coatings which is designed to hold the tablet together when it is in the stomach • The coating is designed to hold together in acid conditions and break down in non-acid conditions and therefore release the drug in the intestines • Example: Aspirin • An enteric coating is there usually for a good reason and therefore such tablets or the contents of enteric coated capsules should never be crushed before being taken.
  • 36.
  • 37. • Hard-shelled capsules, which are normally used for dry, powdered ingredients or miniature pellets
  • 38. • Soft-shelled capsules, primarily used for oils and for active ingredients that are dissolved or suspended in oil
  • 39. • Solutions, syrups and mixtures • Commonly used in patients that have difficulty swallowing medicines like children and the elderly • The liquid medicine should be made such that the dose needed will be a sensible volume such as 5ml (one teaspoon)
  • 40. ACTIVITY Purpose/ Route of Entry/ Packaging/ Form of Medicine ENTRY PACKAGING FORM OF PURPOSE ROUTE OF MEDICINE 1. Antiseptics 2. Pain control 3. Haemostatics and Styptics 4. Antibiotics 5. Vasoconstriction External route 1. Skin 2. Oral Mucosa 3. Membrane of rectum Internal Route 1. Ingestion 2. Injection 3. Inhalation 1. Hard shelled Capsules 2. Soft Shell Capsules 3. Liquid 4. Coated Tablets 1. Blister Pack 2. Bottle 3. Tube
  • 42.
  • 43.
  • 44.
  • 45.
  • 47. Absorption of Drug • Absorption is the process by which a drug passes from its site of administration into the circulation (bloodstream). • The blood receives a drug from the site of administration and carries it to all the organs, including those on which the drug acts. • The speed, ease, and degree of absorption are related to the route of administration.
  • 48. Absorption of Drug • The absorption rates of drugs depend on its physical and chemical properties, on the site of absorption and the solubility of drug. Site of Absorption Rate of Absorption In mucous membrane Rapid In small intestine Depends on health of stomach and its activity and presence/absence of food Subcutaneous and Intramuscular injections Depends on water solubility of drug, dose form and blood supply at site. Intravenous Injection Immediate Inhalation Immediate
  • 50.
  • 51. Distribution of Drug • After the drug is absorbed, it is then distributed to various organs of the body. • Influenced by how well each organ is perfused, organ size, binding of the drug to various components of blood and tissues, and permeability of tissue membranes. • The more fat-soluble a drug is, the higher its ability to pass across the cell membrane is. • Protein binding is an important consideration influencing drug distribution. • Many drugs are bound to blood proteins such as serum albumin and are not available as active drugs.
  • 55. Metabolism of Drug • Metabolism occurs via two types of reactions: and • Goal: Change the active part of medications (a.k.a functional group) making them more water-soluble and more readily excreted by the kidney. • Changing the molecular structure of drugs= water solubility= fat solubility= faster excretion of drug in the urine.
  • 56. Metabolism of Drug: Phase I • Phase I: reactions involve oxidation, hydrolysis, and reduction. • Oxidation and reduction processes make a molecule's charge more positive or negative than the original drug. • Regardless of the positivity or negativity, a charged molecule = dissolvable in water • Take place primarily in the liver by enzymes • Oxidative metabolism may result in formation of an active metabolite or inactive compound.
  • 57. Metabolism of Drug: Phase II • Phase II: reactions involve conjugation to form glucuronides, acetates, or sulfates, by adding glucose, acetate, or sulfate molecules, respectively. • These reactions generally inactivate the pharmacologic activity of the drug and may make it more prone to elimination by the kidney.
  • 60. Excretion of Drug • Excretion of a drug = duration of action= toxicity. • Drugs may be eliminated as a parent drug (unchanged) or as metabolites (changed form). • PharmacoDYNAMICS: what the drug does to the body; this term refers to the action of the drug at the tissue-,cellular-, and molecular level. – Specific and different for each drug
  • 61. PharmacoKINETICS: what the human body does to the drug Excretion occurs primarily through the urine. Fecal excretion is seen with drugs that are not absorbed from the intestines or have been secreted in the bile. sweat
  • 62. KIDNEY • Most important organ for elimination of drugs and its metabolites • Eliminated in the urine ① Passive glomerular filtration (most drugs) ② Active tubular secretion (e.g. penicillin) ③ Passive tubular secretion (e.g. salicylates) • In the case of renal damage:  excretion of drugs;  toxicity
  • 63. BILE • Usually involve orally ingested unabsorbed drugs or metabolites excreted in the bile, that are not reabsorbed from the small intestine • Eliminated through feces • Examples of drugs – Phenytoin – Phenolphthalein
  • 64. INTESTINES • Oral and enteral medications (like purgatives) are absorbed in small intestine • Excreted in large intestine • Eliminated through stools • Example: – senna – cascara
  • 65. LUNGS • Drugs like volatile general anaesthetics, ethyl alcohol are excreted through lungs • Most drugs excreted here are not metabolized first • Example: – Ketamine – propofol
  • 66. SALIVA • Drugs like iodides and metallic salts are excreted through saliva. • Such as lead is eliminated through saliva and its deposition produces black lining of teeth.
  • 67. SWEAT • Heavy metals like arsenic and mercury are excreted through skin.
  • 68. BREAST MILK • Breast milk is more acidic than plasma • May produce drug toxicity in the nursing infant • Pulmonary excretion (e.g. breathing) is important as it pertains to the elimination of anesthetic gases and vapors, as well as alcohol. • Example: pethidine
  • 69. Video
  • 70. FACTORS TO CONSIDER WHEN PRESCRIBING DRUGS
  • 71. FACTORS TO CONSIDER WHEN PRESCRIBING DRUGS Dosage of drugs Presence of other drugs Time of administration Patient compliance Weight of patient Age Sex Severity of the disease
  • 72. Dosage of drugs • Weight of patient Dose = Adult Dose x Weight (kg) • Age Age x Adult dose 70 Age + 12 • Sex Females are given 7/8 male dose. • Neonates-new born(calibrated dose) • Infants-1-6 years(1/4 adults dose) • Children- 6-12 years(1/2 adult dose)
  • 73. Presence of other drugs • Some drugs cancel each other’s effects • Combined effect would be harmful to the patient • Hence, consideration must be taken if patient is on other drugs
  • 74. Time of administration • Time relationship to meals could influence the actual effective therapeutic dose • Absorption occurs more rapidly if stomach and upper portion of body are free from food • Drug action may depreciate when medication given after a meal • Irritant forms of medication are better tolerated if food already present in gut.
  • 75. Patient compliance • Patient does not take medication due to: o Lack of faith in medication o Poor understanding of illness • Patient takes medication incorrectly • Patient stops taking medication midway
  • 76. FACTORS THAT MODIFY DRUG EFFECTS
  • 77. FACTORS THAT MODIFY DRUG EFFECTS Patient compliance Other drugs Age & Weight Rate of elimination Physiological factors Tolerence and cross-tolerence Sex Pathologic factors Route of administration Time of administration Psychological factors Genetic variation
  • 78. 10 8 6 4 2 0 Blood Concentration VS Time Curve of Repeated Dosing 8 16 24 32 1st Dose 2nd Dose 3rd Dose No Effect Toxic Level Blood Concentration Time Distribution + Metabolism HALF –LIFE/ THERAPEUTIC LEVEL
  • 79. CONCLUSION! 1. Pharmacology and it’s use 2. Route of administration 3. Packaging 4. Form of drugs 5. Absorption, Distribution, Metabolism, Excretion of Drugs
  • 80. THANK YOU FOR LISTENING NYP DENTAL HYGIENE AND THERAPY 2012

Editor's Notes

  1. The study of drugs used in the dental field would give us the knowledge of how and when the drug is administered To improve the patient experience when visiting the OHT Increase the efficiency of dental procedures Provide clear explanation of the drug to the patients, which may be prescribed by the dentist Improve infection control and prevent fatality The implications of the drugs we prescribe to them.
  2. Extraction Ulcer Creams Antibiotics Prescription Other dental procedures
  3. High risk of infective endocartitis. Sudden bacteraemia may be produced by dental manipulation within the mouth Other examples:- Congenital heart disease Rheumatic heart disease history of Infective Endocartitis.
  4. High risk of infective endocartitis. Sudden bacteraemia may be produced by dental manipulation within the mouth Other examples:- Congenital heart disease Rheumatic heart disease history of Infective Endocartitis.
  5. High risk of infective endocartitis. Sudden bacteraemia may be produced by dental manipulation within the mouth Other examples:- Congenital heart disease Rheumatic heart disease history of Infective Endocartitis.
  6. High risk of infective endocartitis. Sudden bacteraemia may be produced by dental manipulation within the mouth Other examples:- Congenital heart disease Rheumatic heart disease history of Infective Endocartitis.
  7. For patients who are at high risk of experiencing infective endocartitis. Sudden bacteraemia may be produced by dental manipulation within the mouth or by any trauma in the soft tissues, especially during prophylaxis. Examples: Congenital heart disease, Rheumatic heart disease, history of Infective Endocartitis. OHT: Hello, Nisa, are you fine today? Nisa: Okay ah. OHT: Open your mouth, I will check your teeth okay? (checks teeth) Haiyo, how come so dirty. You never brush teeth is it? You see got a lot of dirty things inside your mouth. Nisa: Hmmm OHT: Aiya nevermind la. I will clean your teeth. Open your mouth. (Checks board) You have heart problem ah? But your parents know that you’re going for cleaning today right? Nisa: Uh, yah. (In the middle of treatment) Cough, cough. Drama, drama, die. OHT: Nisa? Nisa? NISA? OH NO! Parent: Nisa, I’m hear to pick you up! Nisa? NISA?! IS SHE DEAD?! OHT: *mumbles* Parent: My child! (cry, sob, sob, wail) I’m going to sue you
  8. Ulcer Creams P: Doc, I have these multiple ulcers and they are extremely painful. They come and go every 3 months. Is there any way I can heal them instantly? D: Most mouth ulcers do not require specific treatment. They will usually heal naturally without the need of treatment. But if you’re at home and you really cannot hold the pain, we can provide you with……….*commercial transition* “USE BONJELA, BECAUSE SOME SAY IT TASTES BETTER THAN NUTELLA-insert catchphrase*
  9. High risk of infective endocartitis. Sudden bacteraemia may be produced by dental manipulation within the mouth Other examples:- Congenital heart disease Rheumatic heart disease history of Infective Endocartitis.
  10. Local Anaesthesia D: Oh no! Look’s like you have an extremely decayed tooth! I may have to extract it today…. P: Ah?! Means I will bogay ah? D: Sit quiet it will only be for a short while. *not injecting before procedure* P: *fidgets like crazy* AHHHHHHHHHHHHHHHHHH OW!!!!!!!!
  11. Drugs applied on the surface are for local effects only. Depending on chemical structure and quantity applied Can be absorbed by the skin and mucous membrane It is a passive diffusion process, depending on the integrity of the epidermal barrier Drugs with low molecular weight with a high water and lipid solubility show the greatest penetration.
  12. 1) Ingestion or Oral Route In the mouth, some drugs are readily and rapidly absorbed via the mucous membrane in the mouth In the stomach and small intestine, drugs that are swallowed are absorbed through the lining mucosa
  13. Injection/Parenteral route-Routes of administration other than oral (enteral) route are termed as parenteral. Intradermal- within the skin (e.g BCG vaccine) Subcutaneous- under the skin: rate is even and slow Intramuscular- drug is injected deep into muscle tissue Intravenous- directly into veins: quick and immediate 
Adv: Absorption is rapid and quick. Accurate dose of the drug can be given. Disadv: Pain may be produced by injection. It is an expensive route. Self medication and withdrawal of drug is not possible.

  14. 3) Inhalation Drugs in the form of vapour may be inhaled into the lungs. Such drugs have very small molecular structure and pass easily through the thin epithelium. They are absorbed through the pulmonary endothelium at the alveoli to gain rapid access to the general circulation
  15. Point 3: A vasoconstrictor like adrenalin will reduce blood supply, therefore slows down absorption.
  16. After the drug is absorbed, it is then distributed to various organs of the body. Distribution is influenced by how well each organ is perfused (supplied by blood), organ size, binding of the drug to various components of blood and tissues, and permeability of tissue membranes. The more fat-soluble a drug is, the higher its ability to pass across the cell membrane is. The blood-brain-barrier restricts passage of drugs from the blood into the central nervous system and cerebrospinal fluid. Protein binding (attachment of the drug to blood proteins) is an important consideration influencing drug distribution. Many drugs are bound to blood proteins such as serum albumin (the main blood protein) and are not available as active drugs.
  17. Metabolism aka breakdown
  18. Metabolism occurs via two types of reactions: Phase I and Phase II. The goal of metabolism is to change the active part of medications (also referred to as the functional group), making them more water-soluble and more readily excreted by the kidney. (ie. the body is trying to get rid of the "foreign" drug) Changing the molecular structure of drugs increases their water solubility and decreases their fat solubility, which speeds up the excretion of the drug in the urine.
  19. Phase I: reactions involve oxidation, hydrolysis, and reduction. Oxidation and reduction processes make a molecule's charge more positive or negative than the original drug. Regardless of the positivity or negativity, a charged molecule is dissolvable in water. (blood serum is primarily water) These reactions take place primarily in the liver by enzymes. Oxidative metabolism may result in formation of an active metabolite or inactive compound (unchanged).
  20. Phase II: reactions involve conjugation (which means adding another compound) to form glucuronides, acetates, or sulfates, by adding glucose, acetate, or sulfate molecules, respectively. These reactions generally inactivate the pharmacologic activity of the drug and may make it more prone to elimination by the kidney.
  21. Excretion aka elimanation
  22. Excretion of a drug decreases its duration of action. This in turn decreases the toxicity. Drugs may be eliminated as a parent drug (unchanged) or as metabolites (changed form). What the drug does to the body is called pharmacoDYNAMICS; this term refers to the action of the drug at the tissue-,cellular-, and molecular level. Pharmacodynamic processes are specific to and different for each drug.
  23. What the human body does to the drug (pharmacoKINETICS). Excretion occurs primarily through the urine. Fecal excretion is seen with drugs that are not absorbed from the intestines or have been secreted in the bile (which is discharged into the intestines). After being metabolized completely, partially (or sometimes not at all), the drug I excreted from the body. The various routes through which drugs can be eliminated are:
  24. Drugs may be eliminated through the kidney by:- Passive glomerular filtration- most of the drugs are eliminated by this mechanism Active tubular secretion e.g. penicillin - used to treat infections caused by bacteria eg, ear infections Passive tubular diffusion: from areas of high drug concentration to areas of lower concentration e.g. salicylates -reduce fever, pain and inflammation such as in arthritis- inflammed joints. and mepacrine-treat malaria. In case of renal damage, excretion of drugs is decreased and so the toxicity is increased in the body. There are three processes by which drugs are eliminated through the urine: by pressure filtration of the drug through the kidney component called the Glomerulus, through active tubular secretion (like the shuttle system), and by passive diffusion.
  25. Drugs like diphenylhydantoin-prevent and control seizures and phenolphthalein-laxative are excreted into small intestine through bile. These drugs may be re-absorbed . Carried to the liver and again excreted into small intestine through bile. This process called as ‘enterohepatc circulation’ prolongs the duration of action of such drugs.
  26. Purgative- highly laxative properties Senna, cascara- treat constipation
  27. Drugs like volatile general anaesthetics-Inducing anesthesia (lack of sensation or feeling) before surgery or certain procedures, alcohol-reduces nerves signals and paraldehyde-treat certain convulsive disorders, calm or relax patients who are nervous or tense and to produce sleep are excreted through lungs. Drugs may also be excreted in the expired air through the lungs, in the perspiration, or in breast milk.
  28. Iodide- induce thyroid hormones
  29. Arsenic-Treating a certain type of cancer, blocking the growth of cancer cells Mercury-THIMEROSAL-presevative in vaccines
  30. Breast milk is more acidic than plasma and hence basic drugs like pethidine-Pain relief during childbirth. Pain relief before, during and after an operation are eliminated through it.