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1 DEHY3007 Pharmacology DEHY3007 Pharmacology 2007 2007- 2008 2008 Antibiotics Antibiotics Tue Oct 2 2.00 – 3.00 4116 Tue Oct 9 2.00 – 3.00 4116 2 Before we start Before we start… Watch out for the term ‘antibiotics’. We usually mean ‘..........................’ or ...................................’ (as in your text). But it really means a chemical produced by one organism that’s harmful to another. Some anticancer agents are ‘antibiotics’.

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DEHY3007 PharmacologyDEHY3007 Pharmacology20072007--20082008

AntibioticsAntibiotics

Tue Oct 2 2.00 – 3.00 4116

Tue Oct 9 2.00 – 3.00 4116

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Before we startBefore we start……

Watch out for the term ‘antibiotics’.

We usually mean ‘..........................’ or ‘...................................’ (as in your text).

But it really means a chemical produced by one organism that’s harmful to another.

Some anticancer agents are ‘antibiotics’.

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Before we startBefore we start……

There are many antibiotics.

We’ll focus on those that are used in dental practice.

I’ll only examine what we cover in class (on the completed handouts).

Help ease the pain - give me feedback!

[email protected]

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Streptococcal tonsillitis caused by a group A β-haemolytic streptococcus. Courtesy of Prof C. Gemmell.

(Bagg, Jeremy. Essentials of Microbiology for Dental Students, 2nd Edition. Oxford University Press)

Bacterial infections in the oral cavity

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HAVELES: APPLIED PHARMACOLOGY FOR THE

DENTAL HYGIENIST, 5TH EDITION

The types of bacteria in dental infections

The details on this slide

will not be in the exam

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Antibiotic use in dentistry

1. Treatment of ........... dental infections.

First-line antibiotics are penicillin V,

amoxicillin.

2. ..................... in patients who are .................................

- AIDS etc

- chemotherapy for cancer

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(Antibiotic use in dentistry)

3. .................... in patients at risk of ................

.....................

Dental procedures may introduce bacteria into the bloodstream.

These bacteria may lodge in susceptible areas:

- ......................... plaques

- artificial surfaces e.g. ...........

They are known to cause bacterial endocarditis.

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Relative Bacteremia Incidence with Dental

Treatment Procedures

Dental Treatment Bacteremias

Tooth extraction: 40% to 89%Periodontal surgery: 36% to 88%Simple prophylaxis: 0% to 40%Buccal anesthetic injection: 16%

Intraligamentary injection: 97%Rubber dam/matrix/wedge: 9% to 32%

Endodontic treatment: 0% to 15%

(Yagiela, John A.. Pharmacology and Therapeutics

for Dentistry, 5th Edition. C.V. Mosby).For information only

– not on the exam

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Antimicrobials that are commonly used in dentistry

• Penicillin V is the most frequently prescribed antibiotic for oral infections.

• Amoxicillin use is also common. It has better pharmacokinetics and a wider spectrum.

• Erythromycin is used against acute orofacial infections, particularly in patients who cannot tolerate penicillin-like drugs.

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Antimicrobials that are less commonly used in dentistry

• Tetracyclines are not widely used but can be

used for infections resistant to other drugs and have specific uses such as in the management of localized juvenile periodontitis (LJP).

• Many other drugs are only used for orofacial infections if they are indicated for use by sensitivity testing of the microorganism, e.g. aminoglycosides, fluoroquinolones.

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Penicillin V

Amoxicillin

Penicillins

Cephalosporins

....................

antibiotics

Vancomycin

Bacitracin

Attack the

...............

...............

Penicillin-like antibiotics

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The ‘attack strategy’ for penicillins etc

Bacteria have a ......... cell wall.

They need this to survive and grow.

It’s made up of a fibrous ..............

The scaffold is assembled using ................

So… if we can block those enzymes, the

cell wall will not be made properly and the

bacteria will not survive!!!!!!

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Structure of the Bacterial Cell Wall

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Terminology

• Peptidoglycan – the fibrous ............. in the wall that we are trying to destroy.

• Penicillin-binding protein (PBP) – the ............. that helps to make the scaffold.

• Membranes – .......... membranes that are very difficult for drugs to get through.

• Beta lactamase – another kind of ..............., that causes resistance (see later).

• Porins – protein .......... that pierce the membrane.

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What a penicillin does

1. Crosses the cell wall into the bacterium

2. Binds to the penicillin-binding protein

3. Stops the PBP enzyme working

4. The peptidoglycan is not made

5. The cell loses its rigidity

6. The fluid inside exerts outward pressure

7. The bacterium bursts (‘..........’)

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But there are potential problems

1. Getting across the outer lipid membrane

in Gram negative bacteria.

This is why many antibiotics work well against Gram ............. bacteria but not Gram ............... bacteria.

If a Gram negative bacterium has ..........., it may be easier for the drug to get through the outer membrane.

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But there are potential problems

2. Interference by beta lactamases

These enzymes break down many of the common penicillin-like drugs.

The susceptible drugs have a beta lactam group in their structure.

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If this happens:

1.The drug will not work

2.The bacterium is resistant to the drug

Beta lactam ring

.............................

The effect of bacterial beta lactamases

General structure of

beta lactam drug

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What can we do about the beta lactamases?

1. Use a beta-lactamase-............... antibiotic.

e.g. Nafcillin

(Sometimes called ‘penicillinase-resistant)

2. Combine with a beta lactamase ...............

e.g. Clavulanate(Clavulin®: amoxicillin + clavulanate)

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There are different penicillins

..............................e.g. Penicillin V

Penicillinase-resistante.g. Nafcillin

.................................e.g. Amoxicillin

Which differ in their- sensitivity to beta lactamases- ..............................- ................................

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No need to remember the other details here

Pharmacokinetics of common penicillins

e.g. Penicillin G ..................... in acid(which is why we prefer penicillin V).

Amoxicillin has a longer ................

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Spectrum of action of common penicillins

Narrow spectrume.g. Penicillin VMainly active against gram-positive bacteria

(Staphylococci, Streptococci)

Extended-spectrume.g. AmoxicillinActive against gram-positive bacteria but also

some gram-negative bacteria (e.g. E Coli).

.......................

- Wider spectrum

- Better absorbed

- Longer half-life

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Cephalosporins

1st generation e.g. Cefazolin

2nd generation e.g. Cefuroxime

3rd generation e.g. Ceftriaxone

4th generation e.g. Cefepime

You don’t need to remember These 4 drug names

(Generally ..............................................)

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(Cephalosporins)

1st generation

2nd generation

3rd generation

4th generation

Better activity Better ability

against gram- to cross into

negative bacteria tissue spaces

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The drugs that attack the bacterial cell wall

Vancomycin

Works at an earlier stage than the PBPs.Needed when many ........................................

Bacitracin

Works at an earlier stage than the PBPs.Found in ............ (surface-applied) preparations.

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Where else can we attack the bacterium?

© Page, 2002

… by interfering with the ability of the

bacterium to make the ............. it needs.

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A simplified view of protein synthesis

DNA mRNA proteins

What happens here

Can be blocked by

� Erythromycin and other macrolides

� Tetracyclines such as ... tetracycline

� Aminoglycosides such as gentamicin

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Erythromycin and the macrolide antibiotics

Erythromycin

- Somewhat ............... in acid conditions

- Food reduces ..................

Clarithromycin

- Chemically modified from erythromycin

- Improved ......................

- Improved ..........................

Azithromycin

- Further modified

- Excellent tissue penetration

- Longer ...............(about 3 d)

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Erythromycin

- used against acute orofacial infections

- particularly in ............................... infections

- works well against gram-positive organisms

- generally poor against gram-negatives

Clarithromycin

- most active against gram-positive anaerobes

Azithromycin

- has the best activity against gram-negative anaerobes

- also acts against oral spirochetes

- less likely to become involved in ..............................

Therapeutic uses of the macrolides in dentistry

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Also act on bacterial ribosomes to block protein synthesis.

Not widely used in dentistry but have some interesting

properties:

� Interact with ............................ (like calcium)

� Should not be taken alongside ......... or ..................

� Become stored in ........... and ..........................

� Should not be used in:

- second half of pregnancy

- young children

� Concentrate in ............................................

Tetracyclines

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e.g. Gentamicin

Only used for orofacial infections if they are indicated for use by sensitivity testing of the microorganism.

A few relevant points:

� used mostly against gram-negative enteric bacteria.

� oral doses are very poorly absorbed.

� usually given ......................... or ..........................

� all aminoglycosides are

- ototoxic (..........)

- nephrotoxic (.................)

Aminoglycosides

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Question:

If macrolides, tetracyclines and

aminoglycosides all block protein synthesis in bacteria, why are they different in use?

Answer:

1. They’re different chemically, which affects

things like their .............. and ...................

2. They interfere at different sites on the

bacterial ribosomes, which means they have

different .................................

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Where else can we attack the bacterium?

© Page, 2002

… by interfering with the bacterium’s ability

to form ........ or what it needs to do so.

Helps make

new DNA

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1. Drugs that inhibit DNA gyrase enzymes

DNA is made up

of ....................

To be able to

‘untangle’ all of the DNA in a cell you need to cut it

temporarily:

The protein that

does this is called a ......................

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(Drugs that inhibit DNA gyrase enzymes)

Fluoroquinolones block this DNA gyrase enzyme.

One example is ciprofloxacin

These drugs stop the bacterium from using its DNA.

But overuse has led to the widespread resistance!

Many respiratory pathogens are now resistant.

Not used in dentistry unless indicated by sensitivity testing – other drug classes have a better spectrum of activity and pharmacokinetics.

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2. Drugs that block the folic acid pathway

The story goes like this:

DNA is made of several different

kinds of molecules.

One thing that is needed for

several different purposes is

THF (..............................).

Blocking THF production

suppresses DNA synthesis.

Humans use folic acid from the

..... and can do this in one step.

Bacteria have first to ................

.........folic acid, so there are two

steps that can be blocked.

© Rang, 2003

Humans

‘Bugs’

Dietary

folate

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e.g. sulfamethoxazole

© Rang, 2003

DHPS

DHFR

(Drugs that block the folic acid pathway)

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The combination sulfamethoxazole/trimethoprim:

- More effective than either drug alone

- Still works if resistance develops to one drug

Used at a dose ratio of ..........

This gives a plasma concentration ratio of ...........

This is .............. for the drugs.

e.g. Septra®

(Drugs that block the folic acid pathway)

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So, to summarize all of the drugs we’ve covered:

Drugs that ................................................

- penicillins, cephalosporins, vancomycin, bacitracin

Drugs that ....................................................

- macrolides, tetracyclines, aminoglycosides

Drugs that ................................................

- fluoroquinolones, sulfonamides, trimethoprim

Let’s go on to a few more general things…

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Therapeutics: Keeping above the MIC

© Page, 2002

Antibiotic level has fallen ..................... ................................. ....................

Successive doses of drugAntibiotic concentration

in serum

MIC: Minimal

Inhibitory Concentration

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Antibiotics are generally very safe drugs

Therapeutic window

is .............................

Toxic effect

1 10 100

Dose of drug

0.1

0

20

40

60

80

100

% o

f patients

resp

ondin

g

Antibacterial effect

Therapeutic index (TI) = Toxic Dose ED50 = TD50 … is ................

Effective Dose ED50 ED50

TD50

50% effect

ED50

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In fact, many of the adverse effects

of antibiotics are ...............

responses, rather than toxicity at

high doses…

e.g. penicillins, sulfonamides

… or disturbances of the ..............

microbial .........., as for example in

‘antibiotic-associated diarrhea’.

e.g. erythromycin, tetracycline

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Bactericidal versus Bacteriostatic drugs

Number of

bacteria

Progressive growth

Growth is arrested

Cells are killed

e.g. sulfonamides

e.g. penicillins

DRUG

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Bactericidal drugs e.g. penicillins

• Drugs that cause the .............of the bacteria.

• Required if the patient is ....................................

Bacteriostatic drugs e.g. sulfonamides

• Drugs that .............................. of the bacteria.

• ........................... when the drug is removed.

• Success depends on there being an effective ...............................

(Bactericidal versus bacteriostatic drugs)

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Using antimicrobial drugs in combinations

Advantages:

� Wider ................. for mixed infections.

� Reduced .......... for individual agents.

� .................... between antibiotics.

Risks:

� Increased possibility of ................................

� ..................... between antibiotics.

� Greater risk of antibiotic ......................

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Synergism, antagonism and indifference

© Page, 2002

AA

A

B

BB

A+BA+B

A+B

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Remember Septra® ?

The combination sulfamethoxazole/trimethoprim:

Sulfamethoxazole = bacteriostatic

+

Trimethoprim = bacteriostatic

Synergism - ‘..............................’

Septra® = bactericidal

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The problem of antibiotic resistance

A substantial risk of antibiotics are used too freely.

Happens because bacteria are genetically ‘agile’ and can adapt to survive a toxin such as an antibiotic.

The bacteria adapt so that there is, for example:

1. Reduced ........... of the antibiotic into the bacteria.

2. Increased .............. of the target protein.

3. Lower binding of drug to an ............ target protein.

4. Enzyme ..................... of the drug.

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Candidiasis of the buccal mucosa and tongue

Acute

Chronic

(Laskaris, George. Color Atlas of Oral Diseases in Children and Adolescents:. Thieme Medical Publishers).

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• Candidiasis is the most common type of

oral fungal infection.

• Regardless of which drug is used,

therapy for at least 2 weeks is required.

• Clotrimazole, in the form of oral troches

(lozenges), is highly effective in most cases.

• On swallowing, however, clotrimazole

can cause liver problems.

Uses of antifungals in dentistry

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• Nystatin oral pastilles or rinses can be used if liver damage is a concern.

• For more extensive disease or difficult cases, such as patients with AIDS, systemic antifungal therapy may be indicated.

• Oral ketoconazole can be used; however, it is also potentially hepatotoxic.

• Oral fluconazole is an alternative to ketoconazole that is less hepatotoxic.

Uses of antifungals in dentistry

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• In extreme cases, intravenous

amphotericin B may be considered.

• This is significantly toxic and may cause renal damage.

• Surgery may be helpful to remove a

condensed lesion after medical therapy.

(Yagiela, John A.. Pharmacology and Therapeutics

for Dentistry, 5th Edition. C.V. Mosby).

Uses of antifungals in dentistry

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• Mostly they target ................., a lipid in the

fungal cell membrane that is equivalent to

the cholesterol in ours.

• They may bind to ergosterol and .................. that leak out cell contents (e.g. amphotericin B)

• They may .......................... that are important in making ergosterol (e.g. ketoconazole)

How do these antifungals work?

Common Reasons for Antibiotic Failure – In Decreasing Order of Probable Importance

1) Failure to surgically eradicate the source of the infection

2) Too low a blood antibiotic concentration

3) Inability of the antibiotic to penetrate to the site of infection

4) Impaired/inadequate host defenses

5) Patient failure to take the antibiotic

6) Inappropriate choice of antibiotic

7) Limited vascularity or blood flow

8) Decreased tissue pH or oxygen tension

9) Slow microbial growth

10) Emergence of antibiotic resistance

11) Delay in diagnosis

12) Incorrect diagnosis

13) Antibiotic antagonism

(Yagiela, John A.. Pharmacology and Therapeutics

for Dentistry, 5th Edition. C.V. Mosby).

For information only– not on the exam