Ocular med Flashcards
(36 cards)
agents that release drugs by diffusion following erosion of soluble polymers.
Opthalmic gels
usually contain mineral oil and a petrolatum base.
Ointments
They are helpful in delivering antibiotics, cycloplegic drugs, or miotic agents.
Ointments
provide a zero-order rate of delivery by steady-state diffusion, whereby the drug is released at a more constant rate over a prolonged period of time rather than as a bolus
Solid inserts
are made of soft, flexible plastics that allow oxygen to pass through to the cornea and may carry medications along with it.
Soft contact lenses
are developed as a corneal bandage lens and are currently indicated for ocular surface protection following surgery and in traumatic and nontraumatic corneal conditions.
Collagen shields
Six Ocular routes of drug administration
topical, subconjunctival, sub-Tenon, and retrobulbar injections, intraocular/intracameral injections, and intravitreal injections.
This route includes administration of topical agents such as ointments, creams, and other similar preparations directly into the eye surface.
Topical administration
- It has a prompt absorption pattern relative to its preparation (Route)
Topical administration
- It is convenient, economical, and relatively safe, however, may cause mucosal
irritation. (Route)
Topical administration
- It has prompt absorption and is used for anterior segment surgery and infections.
Intraocular/Intracameral Injection
It has a relatively short duration of action and may cause intraocular toxicity.
Intraocular/Intracameral Injection
It refers to the administration of agents into the vitreous cavity of the eye.
Intravitreal injection
It circumvents absorption and displays immediate local and potential sustained effect
Intravitreal Injection
Intravitreal injection
- It is used in conditions such as retinitis, but may also cause retinal toxicity.
What are the factors affecting absorption to systemic circulation include:
a. Precorneal fluid drainage
b. Drug binding to tear proteins
c. Systemic drug absorption
d. Corneal factors
e. Melanin binding
f. Drug metabolism
This is the main reason for low ocular drug absorption
Precorneal fluid drainage
may result in a reduction in concentration of total available free drug for required pharmacological action at target site.
Drug binding to tear proteins
It is nonproductive due to the presence of conjunctival capillaries and lymphatics causing significant drug loss into the systemic circulation decreasing drug bioavailability.
Systemic drug absorption
- The epithelial layer of the cornea is lipoidal in nature and the stroma is hydrophilic, thus affecting the absorption of drug relative to its composition.
Corneal factors
The melanin pigment present in the iris and the ciliary body may also change the ocular bioavailability of a topically administered drug.
Melanin binding
Enzymes such as CYP P450, aldehyde oxidase, hydrolase, transferase, and monoamine oxidase, are expressed in the ocular tissues and metabolized the ocular drug leading to decreased bioavailability.
Drug metabolism
It inhibits RnA-dependent protein synthesis by binding to the 50s ribosomal subunit, preventing the translocation of peptide chains.
Azithromycin
It inhibits bacterial cell wall synthesis by preventing transfer of mucopeptides into the growing cell wall and damages bacterial plasma membrane and active against protoplasts
Bacitracin