Eye Diseases and Pharmacology
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Eye Diseases and Pharmacology

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Questions and Answers

What is the acceptable range of osmolality for an ocular preparation to avoid irritation?

  • 100-640 mOsm/kg
  • 231-446 mOsm/kg (correct)
  • Less than 100 mOsm/kg or greater than 640 mOsm/kg
  • Greater than 640 mOsm/kg or less than 231 mOsm/kg
  • What is the primary purpose of ocular retention in ocular nanosystems?

  • To enhance the irritation consequences of the nanosystem
  • To increase the frequency of doses
  • To reduce the frequency of doses and improve drug bioavailability (correct)
  • To reduce the bioavailability of the drug
  • What is the primary method used to evaluate the safety of nanoemulsions in terms of irritation consequences?

  • In vivo tests
  • Ex vivo tests
  • Visual inspection (correct)
  • In vitro tests
  • What is the primary application of corneal permeation in ocular nanosystems?

    <p>To demonstrate the ability of the nanosystem to penetrate through the cornea</p> Signup and view all the answers

    What is the reason for the temporary change in osmolality of the ocular preparation after administration?

    <p>Fluid evaporation</p> Signup and view all the answers

    Study Notes

    Ocular Anatomy and Drug Delivery

    • Conjunctiva, AMD, diabetic retinopathy, and retinoblastoma represent conditions with varying effects on drug absorption, notably less impactful compared to the cornea.
    • Certain macromolecular nanomedicines, peptides, and oligonucleotides can penetrate deeply into the eye through conjunctiva.
    • Blood-ocular barriers, which include the blood-aqueous barrier (BAB) and blood-retinal barrier (BRB), limit the passage of xenobiotic compounds into the bloodstream.

    Ocular Formulations and Administration

    • Ocular formulations can be delivered via topical, intraocular, and periocular routes, or through ocular devices.
    • Dosage forms include liquid, semi-solid (ointments and gels), solid (powders and inserts), or mixed (in situ gels).
    • Most marketed ocular products (over 95%) are in liquid form.

    Challenges in Ocular Drug Delivery

    • Significant challenges include precorneal, corneal, and blood-corneal barriers that impede effective drug penetration.
    • Prolonging drug residence time and ensuring proper ocular permeation have been ongoing scientific pursuits.

    Nanotechnology and Ocular Drug Delivery

    • Nanotechnology is becoming increasingly appealing for ocular drug delivery due to its ability to encapsulate both hydrophilic and lipophilic drugs.
    • Advantages of nanocarriers include enhanced ocular permeability, increased drug stability, sustained residence time, and improved bioavailability.

    Characterization Approaches

    • Various in vitro, ex vivo, and in vivo characterization techniques help predict the performance of nanocarriers in drug delivery.
    • Common in vivo models include rodents (rabbit, rat, mouse), while in vitro models utilize epithelial cells, reconstructed corneas, or excised corneas along with permeation chambers (Franz-type diffusion cell).

    Ocular Retention and Bioavailability

    • Ocular retention is critical as it minimizes dosing frequency and enhances bioavailability of ophthalmic drugs.

    Safety and Irritation Metrics

    • Ocular preparations with osmolality lower than 100 mOsm/kg or greater than 640 mOsm/kg are considered irritants.
    • The normal range for osmolality in open eyes is between 231 to 446 mOsm/kg, restored shortly (within minutes) after administration of non-isotonic solutions.

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    Description

    This quiz covers various eye diseases such as age-related macular degeneration, diabetic retinopathy, and retinoblastoma, as well as the absorption of medications in the eye.

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