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Related Concept Videos

Ophthalmic Drug Delivery Systems01:23

Ophthalmic Drug Delivery Systems

Ophthalmic drug delivery faces major limitations due to poor absorption across the corneal membrane. This process is primarily driven by diffusion and is influenced by two main factors: the physicochemical properties of the drug and tear drainage. Most ophthalmic drugs, such as pilocarpine, epinephrine, atropine, and local anesthetics, are weak bases. They are typically formulated at an acidic pH to enhance chemical stability. However, this leads to high ionization, reducing their ability to...
Angle Closure Glaucoma: Treatment01:28

Angle Closure Glaucoma: Treatment

Angle-closure glaucoma, or closed-angle glaucoma, is an eye condition where the iris bulges out and blocks the iridocorneal angle, resulting in a buildup of aqueous humor and increased intraocular pressure. Immediate medical attention is necessary due to the sudden onset of symptoms. The treatment for angle-closure glaucoma includes short-term and long-term approaches. Short-term treatment involves using eye drops like pilocarpine to lower intraocular pressure by increasing aqueous humor...
Open Angle Glaucoma: Treatment01:27

Open Angle Glaucoma: Treatment

In open-angle glaucoma, the iridocorneal angle remains open, but the trabecular meshwork becomes stiff, slowing down the outflow of aqueous humor. This causes a buildup of aqueous humor in the anterior chamber, leading to a sudden increase in intraocular pressure. The treatment for open-angle glaucoma focuses on reducing the elevated intraocular pressure by either decreasing the secretion of aqueous humor or increasing its outflow.
Drugs such as carbonic anhydrase inhibitors, α2- and...
Microbiome of the Eye01:22

Microbiome of the Eye

The human eye has a specialized microbiota that reflects its unique anatomical and immunological environment. This low-biomass microbial community predominantly colonizes the conjunctiva and eyelid margins, playing a vital role in ocular surface homeostasis and defense. Despite its proximity to the richly colonized facial skin, the ocular surface maintains a distinct microbial profile due to continuous mechanical and biochemical defense mechanisms.The conjunctival surface hosts fewer microbial...

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Validation and extension of the SUCCESS score for Fuchs dystrophy after cataract surgery.

Eye and vision (London, England)·2026
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Related Experiment Video

Updated: Jun 18, 2026

Clinical Application of Intense Pulsed Light Therapy and Radio Frequency for Treatment of Ocular Surface Diseases
07:36

Clinical Application of Intense Pulsed Light Therapy and Radio Frequency for Treatment of Ocular Surface Diseases

Published on: July 3, 2025

Cornea and ocular surface treatment.

Maria P De Miguel1, Jorge L Alio, Francisco Arnalich-Montiel

  • 1Cell Engineering Laboratory, La Paz Hospital IdiPAZ, Maternity Building, Paseo Castellana 261, Madrid 28046 Spain. mariapdemiguel@gmail.com

Current Stem Cell Research & Therapy
|November 28, 2009
PubMed
Summary
This summary is machine-generated.

Developing artificial corneas addresses challenges in corneal transplantation, like immune rejection and donor shortages. Future strategies combine advanced biomaterials with alternative cell sources for tissue regeneration.

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Ex Vivo and In Vivo Animal Models for Mechanical and Chemical Injuries of Corneal Epithelium

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Ex Vivo and In Vivo Animal Models for Mechanical and Chemical Injuries of Corneal Epithelium

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Area of Science:

  • Ophthalmology
  • Biomaterials Science
  • Regenerative Medicine

Background:

  • The cornea, crucial for vision and protection, can be damaged by pathology, leading to opacity.
  • Current corneal transplantation faces hurdles like immune rejection and limited donor availability.
  • Replacing only the damaged corneal layer is the ideal therapeutic strategy.

Purpose of the Study:

  • To review advances in bioengineered corneas and artificial cornea development.
  • To explore novel strategies for corneal tissue regeneration and replacement.
  • To identify promising biomaterials and alternative cell sources for future corneal therapies.

Main Methods:

  • Review of current literature on corneal pathology, transplantation, and bioengineering.
  • Analysis of stem cell biology and biomaterial advancements in corneal research.
  • Evaluation of alternative cell sources for epithelial, stromal, and endothelial corneal regeneration.

Main Results:

  • Bioengineered corneas include prosthetic devices and tissue-engineered hydrogels.
  • Corneal stem cell therapies face limitations due to damaged stem cell compartments and extensive culture needs.
  • Magnetically aligned collagen shows promise as an advanced biomaterial.
  • Alternative cell sources like oral mucosal epithelium, ear epidermis, bone marrow-derived mesenchymal stem cells, and adipose-derived stem cells are identified.

Conclusions:

  • Artificial corneas and tissue engineering offer solutions to corneal transplantation limitations.
  • Combining advanced biomaterials, such as magnetically aligned collagen, with alternative cell sources is a promising future direction.
  • Adipose-derived stem cells present a versatile option, particularly for endothelial replacement through directed differentiation.