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Therapeutic Ultrasound for Topical Corneal Delivery of Macromolecules.
Almogbil, Hanaa H; Montecinos-Franjola, Felipe; Daszynski, Camille; Conlon, William J; Hachey, Justin S; Corazza, Giavanna; Rodriguez, Erik A; Zderic, Vesna.
Affiliation
  • Almogbil HH; Department of Biomedical Engineering, The George Washington University, Washington, DC, USA.
  • Montecinos-Franjola F; Department of Chemistry, The George Washington University, Washington, DC, USA.
  • Daszynski C; Department of Biomedical Engineering, The George Washington University, Washington, DC, USA.
  • Conlon WJ; Department of Chemistry, The George Washington University, Washington, DC, USA.
  • Hachey JS; Department of Chemistry, The George Washington University, Washington, DC, USA.
  • Corazza G; Department of Biomedical Engineering, The George Washington University, Washington, DC, USA.
  • Rodriguez EA; Department of Chemistry, The George Washington University, Washington, DC, USA.
  • Zderic V; Department of Biomedical Engineering, The George Washington University, Washington, DC, USA.
Transl Vis Sci Technol ; 11(8): 23, 2022 08 01.
Article in En | MEDLINE | ID: mdl-35998058
ABSTRACT

Purpose:

The objective of this study was to utilize therapeutic ultrasound in enhancing delivery of topical macromolecules into the cornea.

Methods:

Rabbit corneas were dissected and placed in a diffusion cell with a small ultra-red fluorescent protein (smURFP; molecular weight of 32,000 Da) as a macromolecule solution. The corneas were treated with continuous ultrasound application at frequencies of 400 or 600 kHz and intensities of 0.8 to 1.0 W/cm2 for 5 minutes, or sham-treated. Fluorescence imaging of the cornea sections was used to observe the delivery of macromolecules into individual epithelial cells. Spectrophotometric analysis at smURFP maximal absorbance of 640 nm was done to determine the presence of macromolecules in the receiver compartment. Safety of ultrasound application was studied through histology analysis.

Results:

Ultrasound-treated corneas showed smURFP delivery into epithelial cells by fluorescence in the cytoplasm, whereas sham-treated corneas lacked any appreciable fluorescence in the individual cells. The sham group showed 0% of subcellular penetration, whereas the 400 kHz ultrasound-treated group and 600 kHz ultrasound-treated group showed 31% and 57% of subcellular penetration, respectively. Spectrophotometry measurements indicated negligible presence of smURFP macromolecules in the receiver compartment solution in both the sham and ultrasound treatment groups, and these macromolecules did not cross the entire depth of the cornea. Histological studies showed no significant corneal damage due to ultrasound application.

Conclusions:

Therapeutic ultrasound application was shown to increase the delivery of smURFP macromolecules into the cornea. Translational Relevance Our study offers a clinical potential for a minimally invasive macromolecular treatment of corneal diseases.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ultrasonic Therapy / Corneal Diseases Limits: Animals Language: En Journal: Transl Vis Sci Technol Year: 2022 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ultrasonic Therapy / Corneal Diseases Limits: Animals Language: En Journal: Transl Vis Sci Technol Year: 2022 Document type: Article Affiliation country: Estados Unidos