Op11 Ocular Pharmacology

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OCULAR PHARMACOLOGY – OP011

January, 2007

At the end of this session, the student will be able to:

1. List at least 5 factors affecting drug delivery to


the eye and four formulations that may be used to
increase drug exposure time to the eye.

2. Define glaucoma and distinguish between closed


and open angle glaucoma.

3. List at least five major drug types used in


glaucoma and know mechanism of action and
possible side effects.

4. List two classes of drugs used as mydriatics and


possible side effects.

Typical drugs to know: pilocarpine, carbachol, echothiophate,


epinephrine, brimonidine, timolol, acetazolamide, brinzolamide,
dorzolamide, lanaprost, isosorbide, mannitol, atropine,
tropicamide, phenylephrine.
January 2002

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TOPICAL DRUG DELIVERY TO THE EYE

Bioavailability:
• pH, tonicity, concentration,
• lipid solubility, partition coefficient,
• vehicle, additives, compliance,
• melanin affinity.

Formulations:
• gels,
• ointments,
• solid inserts,
• soft contact lenses, collagen shields.

tear layer
/ epithelial (hydrophobic)
Cornea < stroma (hydrophilic)
\ endothelial (hydrophobic)

Remember: drugs at this site are also very


accessible to the peripheral circulation.
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GLAUCOMA

• increased intraocular pressure (risk factor?)


- normally 12-20 mm Hg.
- when to Tx – no fixed level.
- literature sets ~21 mm Hg as upper limit of
normal.
- some safe at 30 mm Hg
- some may have damage at 20 mm Hg.
- General rule - if glaucomatous damage –
lower pressure.

• pressure due to balance of aqueous humor:


- production
- (ciliary body).
- drainage.
- Canal of Schlemm.
- uveoscleral outflow (up to 15%).

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Closed angle glaucoma (CAG)
• ballooning of iris decreases aqueous humor flow
– increases pressure.
• emergency situation.
• acute drug treatment followed by surgery.

Open angle glaucoma (OAG)


• chronic disease
• primary defect usually decreased drainage (canal
of Schlemm).
• Tx: ↑ drainage and/or ↓ humor production.

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DRUGS FOR GLAUCOMA

1. Parasympathomimietics (miotics):
• earliest used -
• pilocarpine, carbachol (receptor agonists).
• echothiophate (acetylcholinesterase inhibitor).

• increased outflow of aqueous humor.


- pilocarpine for OAG and CAG.
• poor night vision, blurred vision and aching.
- less accommodative spasm with pilocarpine.
- brow ache clears after 2 weeks.
• contraindicated when miosis undesirable (iritis).
• avoid strong miotics in retinal detachment.

• drops (2-4x’s/d); gels (1 day); inserts (7 days).

• Side effects – GI, salivation

• echothiophate – due to iris cysts and cataracts,


used only when other miotics not successful.

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DRUGS FOR GLAUCOMA (continued)

2. Sympathomimetics:
• epinephrine – better drugs now available
- acts on α and β-adrenoceptors in ciliary body
to improved outflow (uveoscleral).
- increased outflow (yet mydriasis?) but may
actually increase aqueous humor production.
- systemic problems – avoid in hypertension and
heart disease. High allergic toxic rate.
- avoid in CAG.
- dipivefrine – better penetration and converted
to epinephrine in the eye.

• α2-adrenoceptor agonists - topical


apraclonidine - used post eye surgery
- decreased aqueous humor production?
brimonidine – most common of this class
- decreases aqueous humor production and
increases outflow (uveosceral).
- lowers IOP with minimal systemic effects.

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DRUGS FOR GLAUCOMA (continued)

3. β-Adrenoceptor blockers:
• mainstay
• timolol (decreased MSA effect).
• useful in OAG and CAG.
• decreased aqueous humor production.
• most frequently used (no miosis or mydriasis).
• contraindications – heart failure, asthma,
diabetes, heart block, sinus bradycardia.

4. Carbonic anhydrase inhibitors:


• acetazolamide (topical most frequent, oral or iv).
• oral not for chronic use.
• inhibits HCO3 formation in ciliary body.
- decreased aqueous humor production.
• iv useful for emergencies.
• side effects - metabolic acidosis, potassium
depletion, fatigue, depression.
• brinzolamide (Azopt) and dorzolamide
(Trusopt) are topical agents used commonly.

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DRUGS FOR GLAUCOMA (continued)

5. Prostaglandin Analoques

• novel class of drugs for glaucoma

• prostaglandins decrease IOP by increasing


uveoscleral outflow.
- in humans < 15% of aqueous humor drained
by this route.
- ciliary muscle contraction (pilocarpine)
decreases outflow and relaxation (atropine)
increases outflow.
- increase outflow by both the relaxing ciliary
muscle and directly altering extracellular
maitrix to decrease outflow resistance.

• latanoprost is a topically applied prostaglandin


F2α analoque.
- may increase/change iris pigmentation
(brown), produce eyelid darkening and growth
of eyelashes. May be permanent.

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6. Hypertonic solutions:
• isosorbide (oral), mannitol (iv).
• emergency management of angle closure.
• may be used to decrease pressure pre-
operatively.
• avoid in severe dehydration, anuria, pulmonary
edema.

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SUMMARY

pupil outflow AH

parasympathomometic miosis ↑ -

Sympathomimetic
epinephrine mydriasis? ↑ ↑?
α2 agonist neutral ↑ ↓

β-blocker neutral - ↓
CA inhibitor neutral - ↓

PG analogue neutral ↑ -

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Treatment

1. β-blocker – mainstay
- if contraindicated or ineffective

2. try monotherapy with


- prostaglandins
- local CAI’s
- α2 adrenergic agonists
- if monotherapy ineffective

3. try combinations
- β-blocker + (prostaglandin or topical CAI’s)
- prostaglandin + (β-blocker or topical
adrenergic agent or CAI’s)

4. parasympathomimetics
- newer drugs better
- third line drugs due to side effects
- may use as miotic with prostaglandin or β-
blocker

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CYCLOPLEGIC AND MYDRIATIC AGENTS

Mydriatic - useful for examination of the eye.

Cycloplegic - useful for accurate refractions and


providing relief from ciliary spasm
during inflammation.

Parasympathoplegic Drugs:
• atropine (7-10 days); tropicamide (~1-6 hours).
• produce both mydriasis and cycloplegia.
• note duration of action.
• contraindicated in glaucoma.
• avoid in young children and infants (very
sensitive to CNS effects).

Sympathomimetic Drugs
• phenylephrine (3-7 h).
• mydriatic with little/no cycloplegia.
• use with caution in glaucoma (short t½), heart
disease and hypertension.

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