Advanced Drug Delivery Systems: Ophthalmic Preparations

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Vocabulary practice flashcards covering ocular drug delivery forms, ocular anatomy and physiology, drug loss and absorption kinetics, insert technologies, contact lenses, and packaging requirements.

Last updated 8:26 AM on 10/10/26
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31 Terms

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Ophthalmic Drug Delivery Systems

Sterile preparations essentially free from foreign particles, compounded and packaged for instillation into the eye to treat ocular surface or intraocular conditions.

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Miotics

Ophthalmic pharmacological agents that cause constriction of the pupil, exemplified by pilocarpine hydrochloride.

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Mydriatics

Ophthalmic pharmacological agents that cause dilation of the pupil, exemplified by atropine.

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Sclera

The protective outer fibrous layer of the human eye, commonly referred to as the white of the eye.

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Iris

The pigmented muscular ocular tissue that responds to ambient light intensity by adjusting the diameter and size of the pupil.

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Crystalline Lens

A transparent, biconvex internal structure of the eye responsible for focusing incoming light onto the retina.

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Cornea

The transparent anterior continuation of the sclera that allows light penetration and supplies a major portion of the eye's refractive focusing power.

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Conjunctiva

A thin, vascularized, transparent mucous membrane that lines the interior of the eyelids and covers the visible surface of the sclera.

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Choroid

The vascular layer located between the sclera and the retina that supplies blood and nutrients to ocular structures.

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Retina

The innermost photoreceptive layer of the eye that converts light images into electrical signals conveyed via the optic nerve to the brain.

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Aqueous Humor

A clear, watery fluid filling the anterior chamber of the eye between the cornea and the lens.

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Vitreous Humor

A clear, colorless gelatinous mass that fills the posterior cavity of the eye behind the crystalline lens.

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Precorneal Tear Capacity

The normal physiological fluid capacity of the tear sac, which measures 10–30 μl10\text{–}30\,\mu\text{l}; instillation beyond 30 μl30\,\mu\text{l} triggers rapid dose loss via overflow.

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<p>Nasolacrimal Canal Drainage</p>

Nasolacrimal Canal Drainage

The physiological drainage route of instilled ocular solutions into the tear ducts and gastrointestinal tract, causing bitter or salty sensations and potential systemic absorption.

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Transcorneal Absorption

The primary pathway of intraocular drug transport requiring dual solubility to traverse both the lipophilic corneal epithelium and the hydrophilic stroma into the aqueous humor.

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Ophthalmic Solutions

Sterile, particulate-free liquid preparations containing completely dissolved active drugs, characterized by high dosing uniformity but short corneal residence time.

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Ophthalmic Suspensions

Sterile liquid preparations consisting of micronized insoluble drug particles dispersed in a liquid vehicle to prevent corneal scratching and prolong drug dissolution.

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Ophthalmic Powders for Reconstitution

Sterile lyophilized solid drug preparations packaged separately from the reconstitution vehicle to ensure chemical stability and extended shelf life.

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Gel-Forming Solutions (In Situ Gels)

Liquid ocular formulations that remain liquid in their container and undergo phase transition into a viscous gel upon contacting physiological tear fluid.

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Cellulose Acetate Phthalate

A pH-sensitive in situ gelling polymer that maintains liquid form at pH 4.54.5 and undergoes sol-to-gel transition at the tear fluid pH of 7.47.4.

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Timolol GFS

A commercial gel-forming solution of timolol maleate that extends intraocular pressure-lowering efficacy from 12 hours12\,\text{hours} to 24 hours24\,\text{hours}, permitting once-daily administration.

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Ophthalmic Ointments

Semisolid sterile preparations packed in collapsible tubes of 3–5 g3\text{–}5\,\text{g} that soften at ocular temperature to enhance contact time, predominantly administered at bedtime due to causing blurred vision.

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Nonerodible Ocular Inserts

Insoluble, flexible solid drug delivery devices placed in the conjunctival cul-de-sac to deliver medication at a controlled steady state without dissolving.

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<p>Ocusert</p>

Ocusert

A nonerodible ocular insert containing a pilocarpine reservoir enclosed by rate-controlling copolymer membranes and a white annular ring, delivering drug for 1 week1\,\text{week} to treat glaucoma.

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Soluble Ocular Inserts

Biodegradable solid ocular devices compounded with erodible matrices (such as hydroxypropyl cellulose or carbomer) that completely dissolve within 12–24 hours12\text{–}24\,\text{hours}, precluding removal.

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Lacrisert

A sterile, translucent, rod-shaped soluble insert composed of hydroxypropyl cellulose (HPC) that dissolves in 12–24 hours12\text{–}24\,\text{hours} to stabilize and thicken the precorneal tear film in dry eye syndrome.

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Rigid Contact Lenses

Durable, low-cost optical or therapeutic discs fabricated from polymethyl-methacrylate (PMMA) that require an adaptation period and may cause corneal scratching.

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Soft Contact Lenses

Flexible and immediately comfortable corneal discs manufactured from hydrophilic hydrogels such as hydroxyethylmethyl-methacrylate (HEMA).

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Soaking Solutions

Contact lens maintenance liquids formulated with antimicrobials such as chlorhexidine gluconate, benzalkonium chloride, or cetylpyridinium chloride to store and hydrate hard lenses.

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Artificial Tears (Rewetting Solutions)

Formulations containing polymers such as polyvinyl alcohol or Tween 80 formulated to rewet contact lenses in situ and augment the physiological tear film.

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ABAK System

A preservative-free multidose delivery container incorporating a 0.2 μm0.2\,\mu\text{m} microporous membrane filter that delivers calibrated, unpreserved sterile eye drops.