Ocular med Flashcards

(36 cards)

1
Q

agents that release drugs by diffusion following erosion of soluble polymers.

A

Opthalmic gels

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2
Q

usually contain mineral oil and a petrolatum base.

A

Ointments

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3
Q

They are helpful in delivering antibiotics, cycloplegic drugs, or miotic agents.

A

Ointments

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4
Q

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

A

Solid inserts

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5
Q

are made of soft, flexible plastics that allow oxygen to pass through to the cornea and may carry medications along with it.

A

Soft contact lenses

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6
Q

are developed as a corneal bandage lens and are currently indicated for ocular surface protection following surgery and in traumatic and nontraumatic corneal conditions.

A

Collagen shields

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7
Q

Six Ocular routes of drug administration

A

topical, subconjunctival, sub-Tenon, and retrobulbar injections, intraocular/intracameral injections, and intravitreal injections.

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8
Q

This route includes administration of topical agents such as ointments, creams, and other similar preparations directly into the eye surface.

A

Topical administration

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9
Q
  • It has a prompt absorption pattern relative to its preparation (Route)
A

Topical administration

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10
Q
  • It is convenient, economical, and relatively safe, however, may cause mucosal
    irritation. (Route)
A

Topical administration

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11
Q
  • It has prompt absorption and is used for anterior segment surgery and infections.
A

Intraocular/Intracameral Injection

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12
Q

It has a relatively short duration of action and may cause intraocular toxicity.

A

Intraocular/Intracameral Injection

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13
Q

It refers to the administration of agents into the vitreous cavity of the eye.

A

Intravitreal injection

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14
Q

It circumvents absorption and displays immediate local and potential sustained effect

A

Intravitreal Injection

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15
Q

Intravitreal injection

A
  • It is used in conditions such as retinitis, but may also cause retinal toxicity.
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16
Q

What are the factors affecting absorption to systemic circulation include:

A

a. Precorneal fluid drainage
b. Drug binding to tear proteins
c. Systemic drug absorption
d. Corneal factors
e. Melanin binding
f. Drug metabolism

17
Q

This is the main reason for low ocular drug absorption

A

Precorneal fluid drainage

18
Q

may result in a reduction in concentration of total available free drug for required pharmacological action at target site.

A

Drug binding to tear proteins

19
Q

It is nonproductive due to the presence of conjunctival capillaries and lymphatics causing significant drug loss into the systemic circulation decreasing drug bioavailability.

A

Systemic drug absorption

20
Q
  • 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.
A

Corneal factors

21
Q

The melanin pigment present in the iris and the ciliary body may also change the ocular bioavailability of a topically administered drug.

A

Melanin binding

22
Q

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.

A

Drug metabolism

23
Q

It inhibits RnA-dependent protein synthesis by binding to the 50s ribosomal subunit, preventing the translocation of peptide chains.

24
Q

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

25
acts by inhibiting DNA synthesis in susceptible organisms via inhibition of both topoisomerase IV and DNA gyrase, inhibiting bacterial reproduction and bacterial cell division.
Besifloxacin
26
It inhibits bacterial protein synthesis by binding to 50s subunit of the bacterial ribosome, thus preventing peptide bond formation by peptidyl transferase.
Chloramphenicol
27
It acts by inhibiting DNA gyrase and topoisomerase IV, both essential in bacterial DNA replication, transcription, repair and recombination
Ciprofloxacin
28
It inhibits protein synthesis by irreversibly binding to the 50S ribosomal subunit thus blocking the transpeptidation or translocation reactions of susceptible organisms resulting in stunted cell growth.
Erythromycin
29
It acts by inhibiting DNA synthesis in susceptible organisms via inhibition of both DNA gyrase and topoisomerase IV, causing inhibitiom of bacterial reproduction and bacterial cell division.
Gatifloxacin
30
It interferes w/ bacterial protein synthesis by binding to 30S and 50S ribosomal subunits resulting in a defective bacterial cell membrane.
Gentamicin
31
It inhibits bacterial topoisomerase IV and DNA- gyrase, the enzymes required for DNA replication, transcription, repair, recombination and transposition, thereby inhibiting the relaxation of supercoiled DNA and promoting breakage of bacterial DNA strands.
LEVOFLOXACIN
32
It inhibits bacterial topoisomerase IV and DNA gyrase (topoisomerase II) enzymes which are essential for bacterial DNA replication, transcription, repair and recombination thereby impeding bacterial growth
Moxifloxacin
33
it inhibits bacterial topoisomerase IV and DNA gyrase enzymes required for DNA replication, transcription, repair, transposition and recombination.
Ofloxacin
34
It interferes with nucleic acid synthesis thus blocking conversion of PABA to the coenzyme dihydrofolic acid.
Sulfacetamide
35
It disrupts the bacterial cytoplasmic membrane of mostly gram negative organisms allowing leakage of intracellular constituents by binding to membrane phospholipids.
Polymixin B combination
36
It interferes with bacterial protein synthesis by binding 30S and 50s ribosomal subunits, resulting in a defective bacterial cell membrane.
Tobramycin