Related Experiment Video
Updated: May 18, 2026

07:22
Using a Laminating Technique to Perform Confocal Microscopy of the Human Sclera
Published on: May 6, 2016
Diffusion of macromolecules through sclera.
Heng Miao1, Bi-Dong Wu, Yong Tao
1Department of Ophthalmology, People's Hospital, Peking University, Beijing, China.
Acta Ophthalmologica
|September 25, 2012
Summary
Porcine sclera permeability to macromolecules is lower in thicker posterior regions. Permeability decreases with increasing molecular weight and scleral thickness, impacting drug delivery.
Area of Science:
- Ocular Pharmacology
- Biomaterials Science
- Drug Delivery Systems
Background:
- The sclera, a crucial outer layer of the eye, presents a significant barrier to drug delivery.
- Understanding scleral permeability is vital for developing effective transscleral drug delivery strategies.
Purpose of the Study:
- To quantify the in vitro permeability coefficient of porcine sclera to macromolecules.
- To investigate how topographical location and molecular weight influence scleral permeability.
Main Methods:
- Porcine sclera from equatorial and posterior regions was used in a two-chamber diffusion apparatus.
- Permeability to fluorescein isothiocyanate (FITC)-conjugated dextrans (40-150 kDa) was measured using fluorescence spectrophotometry.
- Scleral thickness and macromolecule surface enrichment were analyzed via microscopy.
Main Results:
- Scleral permeability coefficient (Pc) was significantly higher in the equatorial region compared to the posterior region.
- A significant negative relationship was observed between Pc and scleral thickness for all tested molecular weights.
- Permeability decreased significantly with increasing macromolecule molecular weight, with larger molecules accumulating on the scleral surface.
Conclusions:
- Scleral permeability is inversely related to scleral thickness and the molecular weight of macromolecules.
- Topographical variations in scleral thickness influence permeability, with potential pharmacokinetic implications for transscleral drug delivery.
- Macromolecule accumulation on the scleral surface increases with molecular size.
More Related Videos
Related Concept Videos
Protein Diffusion in the Membrane
Proteins show rotational as well as lateral diffusion across the membrane. The lateral diffusion of proteins was confirmed through the cell fusion experiment where mouse and human cells were fused, resulting in hybrid cells. When the human and mouse cells fused, the specific membrane proteins on human and mouse cells were marked with the red and green-fluorescent markers, respectively. Initially, the red and green fluorescence was located on the respective hemisphere of the cell. As time...
Diffusion
Diffusion is the passive movement of substances down their concentration gradients—requiring no expenditure of cellular energy. Substances, such as molecules or ions, diffuse from an area of high concentration to an area of low concentration in the cytosol or across membranes. Eventually, the concentration will even out, with the substance moving randomly but causing no net change in concentration. Such a state is called dynamic equilibrium, which is essential for maintaining overall...
Diffusion
Diffusion is a type of passive transport. In passive transport, a substance tends to move from an area of high concentration to an area of low concentration until the concentration is equal across the space. For example, take the diffusion of substances through the air. When someone opens a perfume bottle in a room filled with people, the perfume is at its highest concentration in the bottle and is at its lowest at the edges of the room. The perfume vapor will diffuse, or spread away, from the...
Passive Diffusion: Overview and Kinetics
Passive diffusion is a critical process that allows small lipophilic drugs to cross the cell membrane along a concentration gradient. This mechanism's efficiency depends on four primary factors: the membrane's surface area, the drug's lipid-water partition coefficient, the concentration gradient, and the membrane's thickness.
When administered orally, drugs establish a substantial concentration gradient between the gastrointestinal (GI) lumen and the bloodstream, expediting their diffusion into...
When administered orally, drugs establish a substantial concentration gradient between the gastrointestinal (GI) lumen and the bloodstream, expediting their diffusion into...
Mechanisms of Drug Absorption: Paracellular, Transcellular, and Vesicular Transport
Drugs need to permeate cell membranes to reach their target sites after administration. Orally administered drugs must transcend intestinal epithelial membrane barriers to infiltrate the systemic circulation. Drugs with a molecular weight of less than 500 Daltons diffuse through gaps between neighboring cells, called paracellular pathways.
However, most drugs use the transcellular route, traversing directly through the cell membranes via two mechanisms: passive and active transport. Passive...
However, most drugs use the transcellular route, traversing directly through the cell membranes via two mechanisms: passive and active transport. Passive...
Capillary Exchange
The cardiovascular system's chief role is to disseminate gases, nutrients, waste, and other substances to the body's cells. Small molecules like gases, lipids, and lipid-soluble substances directly diffuse through capillary wall endothelial cell membranes. Glucose, amino acids, and ions, including sodium, potassium, calcium, and chloride, use transporters for facilitated diffusion via membrane-specific channels. Glucose, ions, and bigger molecules may also pass through intercellular clefts.

