Abstract
The objective of the present study is to investigate the confounding effects, if any, of beta-cyclodextrins (βCDs) on corneal permeability coefficients obtained from in vitro transmembrane diffusion studies. Transcorneal permeability studies were carried out with 2-hydroxypropyl-beta-cyclodextrin (HPβCD) and randomly methylated-beta-cyclodextrin (RMβCD) at 5 and 2.5%w/v in isotonic phosphate-buffered solution (IPBS) (pH 7.4). Rabbit corneas received from Pel-Freez Biologicals® were used for these studies. Propranolol hydrochloride (PHCl) (1 mg/mL) was used as the paracellular permeability marker. A series of permeation studies were carried out with IPBS as the control, with CDs on the donor side only, CDs on the receiver side only, and CDs on both the donor and receiver sides. At the end of 1 or 3 h, corneas were collected and fixed using a solution containing 2%v/v glutaraldehyde + 2%w/v paraformaldehyde + IPBS and histological examinations were performed (Excalibur Pathology, Inc). The order of transcorneal permeability of PHCl was found to be CDs on the receiver side > control (no CDs) ≈ CDs on both the receiver and donor sides > CDs on the donor side. Histology studies revealed that the corneal epithelial and endothelial layers remained intact in the control sets. Damage to the cornea was observed in the order of CDs on the receiver side > CDs on the donor side > CDs on both sides > control. The use of CDs in solutions for in vitro permeation experiments with rabbit corneas needs to be carefully considered to avoid confounding effects in the data obtained.
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ACKNOWLEDGEMENTS
This work was supported by the National Institute of General Medical Sciences, National Institutes of Health Grant P20GM104932 and SBAHQ-10-I-0309. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
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Adelli, G.R., Balguri, S.P. & Majumdar, S. Effect of Cyclodextrins on Morphology and Barrier Characteristics of Isolated Rabbit Corneas. AAPS PharmSciTech 16, 1220–1226 (2015). https://doi.org/10.1208/s12249-015-0315-z
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DOI: https://doi.org/10.1208/s12249-015-0315-z