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Ocular Pharmacology PDF

This document discusses ocular pharmacology and various drug groups used to treat eye conditions. It begins by explaining pharmacokinetic principles like drug absorption, distribution, and excretion that impact a drug's effectiveness. Common ocular drug administration routes are then described, including eye drops, ointments, and injections. Several drug classes are outlined, such as cholinergic agents, adrenergic agents, carbonic anhydrase inhibitors, prostaglandin analogs, anti-inflammatories, antibiotics, and antifungals. Each drug group's mechanisms of action and examples are provided.

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0% found this document useful (0 votes)
371 views54 pages

Ocular Pharmacology PDF

This document discusses ocular pharmacology and various drug groups used to treat eye conditions. It begins by explaining pharmacokinetic principles like drug absorption, distribution, and excretion that impact a drug's effectiveness. Common ocular drug administration routes are then described, including eye drops, ointments, and injections. Several drug classes are outlined, such as cholinergic agents, adrenergic agents, carbonic anhydrase inhibitors, prostaglandin analogs, anti-inflammatories, antibiotics, and antifungals. Each drug group's mechanisms of action and examples are provided.

Uploaded by

benny christanto
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Ocular pharmacology

Section 1
Pharmacologic principles
Especial forms and administrations
routes of eye drugs
Section 2
Ocular pharmacotherapeutics
Current and common drug groups
Pharmacokinetics
To achieve a therapeutic effect , a drug must
reach it's site of action in sufficient
concentration :
• Amount administered
• Extent & rate of absorption at the
administration site
• Distribution & binding in tissues
• Movement by bulk flow in circulating
fluids
• Transport between compartments
• Biotransformation
• Excretion
Eye drops
• Most ocular medications
• Adequate concentration in anterior
segment
• Without incurring unwanted effects in
other systems
Eye drops
Some features limit its effectiveness :
* Very little of an administered drop
When a 50 µl eye drop is delivered , the
volume of lachrymal fluid rises about 10 µl
in the blinking eye of an upright patient.
(20% of administered drug is retained )
* Rapid turnover of fluid , 16% per minute ,
and much more if the drop elicits reflex
tearing
Eye drop
Some measures improve ocular absorption:
• More than one eye drop → wait 5minutes
between drops
• Compress the nasolachrymal duct to prevent
egress of tears and to reduce systemic
absorption through the nasal mucosa
Eye drop
• Contact time of eye drop medication is short ,
• The rate of transfer from the tear fluid into the
cornea is critical .
• Corneal epitheliuum and endothelium have tight
intercellular junctions
• Drug concentration
• Solubility
• Viscosity
• Reflex tearing
Solubility
To traverse the cornea , a drug must pass in
turn through :
• Lipid rich environment of the epithelial cell
membrane
• Water rich environment of the stroma
• Lipid barrier at the endothelium
Reflex tearing
• Reduces the contact time of the drug with
the cornea
• Any physical contact that elicit blinking
reflex
• PH value very different from 7.4
Ointments
• Increasing the contact time of ocular
medications
• Consist of petrolatum and mineral oil
• Melt at body temperature
Periocualr injections
• Sub conjunctiva
• Sub tenon
• Retrobulbar
• Peribulbar
Intraocualr injections

• Intracameral
• Intravitreal
Systemic therapy
• Blood ocular barriers limit access through
vascular channels
• More readily penetrated by drugs with
higher lipid solubilities
• The unbound to plasma proteins drugs
can cross the blood ocular barriers
Cholinergic agents
• Affect the activity acetylcholine
receptors in synaps of the peripheral
nervous system
• parasympatetic effectors sites are in
the iris sphincter and ciliary body
Cholinergic agents
• Direct acting agonists act on the receptor
to elicit an excitatory postsynaptic
potential
• Indirect acting agonists inhibit the
acetylcholine esterase of the synaptic cleft
, preventing deactivation of endogenous
acetylcholine
• Antagonists block the action of
acetylcholine on the receptors
Cholinergic agents
• Parasympathomimetic agents :
• Contraction of the iris sphincter (miosis)
and changes the anatomical relationship
of the iris to the lens and chamber angle
• Contraction of the circular fibers of the
cilliary muscle ( accommodation)
• Contraction of the longitudinal fibers of
the cilliary muscle ( outflow facility ↑)
Parasympathomimetic
agents
• Miosis → narrow angle glaucoma
• Accommodation → accommodative
esotropia
• increasing outflow facility → open angle
glaucoma
accommodative esotropia
• The near response is a synkinetic of
accommodation , miosis and convergence
• Parasympathomimetic agents reduce the
need to accommodate , the patient not
only experience lees accommodation but
also less convergence
Parasympathomimetic
agents
• Acetylcholine ( miochol ) → intracameral
• Carbacol ( more effective and longer
lasting ) → intracameral
• Pilocarpine 0.12% confirm Adie tonic pupil
″ 1- 6% in the treatment
of glaucoma
Parasympathomimetic agents

Side effects :

• Miosis
• Induced myopia and accommodation
• Cataractogenesis
• Retinal tear or even rhegmatogenous
detachment
Parasympathomimetic
agents
Indirect agonist such as echothiophate
( phospholine iodide )
• Longer duration of action
• Frequently more potent
• Twice daily treatment is sufficient
Parasympathomimetic
antagonist
• Paralysis of the iris sphincter → mydriasis
→ facilitating fundus examination ,
preventing posterior synechia
• Paralyze the ciliary muscle → inhibit
accommodation , relieve pain associated
with iridocyclitis , accurate refraction
Parasympathomimetic
antagonist

• Atropine 7- 14 days lasting


7-
• Homatropine 3 days
• Cyclopentolate 1-
1- 2 days
• Tropicamide 4- 6hours
4-
Parasympathomimetic
antagonist
Side effects :
• Ocular
Ocular→
→ due to midriasis
• Systemic → dose related toxicity
Flashing , fever , tachycardia , ……
Adrenergic receptors
• α1 mediate smooth muscle contraction
• α2 mediate feedback inhibition of
presynaptic sympathetic
• β1 predominantly in the heart
• β2 mediate relaxation of smooth
muscle in most blood vessels and in the
bronchi
α1 adrenergic agonist
• Stimulation of the iris dilator muscle
⇒ mydriasis
• Systemic absorption may elevate
systemic blood pressure
• Such as phenylephrine
α2 adrenergic agonist
• prevents release of norepinephrine at
nerve terminals
• Decrease aqueous production as well as
episcleral venous pressure & improves
trabecular outflow
• Such as apraclonidine hydrochloride
α1 adrenergic antagonist
• Inhibit adrenergic tone to the dilator
muscle ⇒ miosis
• Differentiating angle closure glaucoma
from POAG
• Such as thymoxamine
β2 adrenergic agonist
• Lower IOP by increasing uveoscleral
outflow and perhaps through the
trabecular meshwork
• L- epinephrine (α
(α, β agonist)
• Side effects : black deposits in the
conjunctiva
Reversible cystoid maculopathy ( 25% of
aphakic eyes )
β adrenergic antagonist
β blocker
• Lower IOP by reducing aqueous humor
production as much as 50%
• Timolol maleate ( timoptic ) and
levobunolol ( betagan ) are mixed β1 ,β2
antagonists
β1 adrenergic antagonist
• Significantly safer when pulmonary ,
cardiac , CNS or other systemic conditions
are considered
• Such as Betaxolol ( a selective drug )
Carbonic anhydrase inhibitor
• Mechanisms of aqueous secretion are not
fully understood
• Decrease of aqueous secretion depend
active transport Na by Na+ ,K+ , ATP ase on
the surface of nonpigmented epithelial
cells
_
• +
Na transport partially linked to Hco3
formation
_
• Hco3 formation reduced by inhibition of
the enzyme carbonic anhydrase
CAIs drugs
• Systemic : Acetazolamide
( diamox ) 250-
250- 500mg 4 - 6h
duration of action
Methazolamide
• Topical : Dorzolamide ( trusopt )
Brinzolamide ( azopt)
Treatment of all glaucomas
CAIs drugs side effects
• Metabolic acidosis
• Urinary tract stone formation
• Numbness and tingling of the hands ,
feet and lips
• Malaise
• Anorexia and weight loss , nausea
• Depression
Prostaglandin analogs
• New class of ocular hypertensive agents
• Latanoprost ( Xalatan)
Lower IOP by enhancing uveoscleral outflow
– reduce the pressure ( 25-
25- 35% )
Once daily dosing
Lack of cardiopulmonary effects
Ocular side effects : darkening of the iris
and periocular skin , cystoid macular
edema , uveitis
Osmotic agents
• Reduce IOP and vitreous volume by
drawing fluid out of the eye across
vascular barriers
• Used in the short management of acute
glaucoma and prior to cataract surgery
• Used with care in cardiovascular disorders:
CHF , hypertension , recent MI
Anti inflammatory agents
• glucocorticoids
• Non Steroidal Anti-
Anti-Inflammatory Agents
( NSAIDs )
• Antihistamine
• Histamine release blocker
• Anti fibrotics
Glucocorticoids

• Prevent or suppress corneal graft


rejection
Anterior chamber reaction
Immune or traumatic
uveitis Severe ocular
inflammation:
Subconj, retrobulbar , systemic
Glucocorticoids
Adverse effects of
glucocorticoids
• Glaucoma
• Post subcapsualr cataract
• Exacerbation of bacterial and
viral infection
• Ptosis , mydriasis , scleral
melting
• Suppression of the pituitary
adrenal axis
• Gluconeogenesis
• Peptic ulcer
NSAIDs
• Salicylates : aspirin , mefenamic acid
• Indoles : indomethacin
• Phenyl alkanoic acid : diclofenac ,
ibuperofen , naproxen
• Pyrazolones : phenylbutazone
Mast cell stabilizer &
antihistamine
• Allergic conjunctivitis : an immediate
hypersensivity reaction ( IgE)
• Released histamine : capillary
dilation & increased permeability →
injection & swelling
• Topical antihistamine : antazoline →
mild allergic symptoms
Cromolyn sodium

• Blocker of histamine release


• The therapy of choice for severe
vernal & atopic conjunctivitis
Anti proliferative agents
• In the treatment of severe ocular
inflammatory diseases :
Behjet syndrome
sympathetic ophthalmia

• Fluorouracil – mitomycine C
Antibiotic therapy
• Drug penetration in cornea
• Blood ocular barriers
• Select effective antibiotics
• Gram stain , culture and antibiogram
• Immediate intravitreal injection of
broad spectrum antibiotics in severe
endophthalmitis
Antibacterial agents
• Penicillin's
• Cephalosporine
• Sulfonamids
• Tetracyclin
• Chloramphenicol
• Aminoglycosids
• Fluoroquinolonbs
Antifungal
• Polyenes : natamycine 5% suspension for
topical ophthalmic use
• Amphotericine B at .25% - 0.5% in sterile
water
• These agents penetrate the cornea poorly
• Active topically against a variety of
filamentous fungi : aspergillus ,
cephalosporium, fusarium , penicillium ,
yeast candida albicans
Antifungal
• Imidazols : miconazole 1% solution
subconjunctivally or topically
• Miconazole penetrate the cornea
poorly
• Ketoconazole 200 mg tablet
( every 6-
6- 8h)
• Penetrates the blood – ocular barrier
poorly but therapeutic levels can be
achieved in inflamed eyes
• Aspergillus , coccidioides ,
cryptococus & candida
Antifungal
• Flucytosine: orally at 50 -150 mg/kg daily
divided into four doses
• Penetrates the blood ocular barrier well
• Use primarily as an adjunct to systemic
amphotericin B therapy
Antiviral agents
• Topical :
idoxuridine
trifluridine ( TFT)
vidarabine
Antiviral agents
• Systemic :
Acyclovir → herpes zoster,
prevent of HSV kratitis
Can be used topically , orally or
intravenously
Medication for
acanthamoeba infection
• A corneal pathogen → contact lens
users
• No single drug is effective in treating
all acanthamoeba keratitis
• Polyhexamethylene biguanid
( 0.02% solution ) first line agent
• Chlorhexidine , neomycine
,polymyxin, B gramicidine
mixtures , natamycine 5%
Anesthetics agents
• Topical : for tonometery , gonioscopy
, removal of superficial Fb ,
corneal scraping , laser procedures
• Local : retrobubar and eyelid blocks
→ excellent anesthesia for surgery
Anesthetics agents

• Esters : proparacaine , tetracaine


• Amides : lidocaine 40 – 60 min
bupivacain ( marcaine ) long
acting several hours

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