A Novel Approach to Assessing Eye Irritation Potential Using the Bovine Corneal Opacity and Permeability Assay

1996 ◽  
Vol 15 (2) ◽  
pp. 147-163 ◽  
Author(s):  
P. L. Casterton ◽  
L. F. Potts ◽  
B. D. Klein
2015 ◽  
Vol 13 (1) ◽  
Author(s):  
Susanne N. Kolle ◽  
Ursula G. Sauer ◽  
Maria C. Rey Moreno ◽  
Wera Teubner ◽  
Wendel Wohlleben ◽  
...  

1993 ◽  
Vol 7 (4) ◽  
pp. 471-476 ◽  
Author(s):  
Ph. Vanparys ◽  
Gh. Deknudt ◽  
M. Sysmans ◽  
G. Teuns ◽  
W. Coussement ◽  
...  

2010 ◽  
Vol 196 ◽  
pp. S141
Author(s):  
J.H. Han ◽  
S.H. Seok ◽  
Y.R. Na ◽  
T.H. Kim ◽  
H. Jung ◽  
...  

1989 ◽  
Vol 16 (4) ◽  
pp. 344-352
Author(s):  
Paul J. Dierickx

Glutamic acid (GA) content was measured in cultured Hep G2 cells, after treatment of the cells with test compounds. The results with 37 chemicals were compared with their respective rabbit eye irritation data, of which 17 were determined according to the OECD test, and the other 20 in range-finding studies. The chemicals were mainly organic solvents (alcohols, esters, amines, acids and others). The xenobiotics were applied to the cells for 4 hours at 5 different concentrations. The cells were then incubated for 15 minutes with tritiated GA. GA uptake inhibition was measured by liquid scintillation counting, and the results were expressed as the GI50 value, which is the concentration of test compound required to induce a 50% reduction in GA uptake. A linear correlation coefficient r = 0.66 was found between the log GI50 and the mean corneal opacity scores. This value is comparable to that obtained in total protein and uridine uptake inhibition studies. However, r = 0.81 was found when the log GI50 was compared with range-finding scores, indicating that a closer relationship exists between cytotoxicity and the latter.


Pharmaceutics ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 801
Author(s):  
Abdelrahman Mohamed ◽  
Viktor Korzhikov-Vlakh ◽  
Nan Zhang ◽  
André Said ◽  
Iuliia Pilipenko ◽  
...  

A plethora of micro- and nanoparticle types are currently investigated for advanced ocular treatment due to improved drug retention times, higher bioavailability and better biocompatibility. Yet, comparative studies of both physicochemical and toxicological performance of these novel drug delivery systems are still rare. Herein, poly(L-lactic acid)- and poly(ε-caprolactone)-based micro- and nanoparticles were loaded with prednisolone as a model drug. The physicochemical properties of the particles were varied with respect to their hydrophilicity and size as well as their charge and the effect on prednisolone release was evaluated. The particle biocompatibility was assessed by a two-tier testing strategy, combining the EpiOcularTM eye irritation test and bovine corneal opacity and permeability assay. The biodegradable polyelectrolyte corona on the particles’ surface determined the surface charge and the release rate, enabling prednisolone release for at least 30 days. Thereby, the prednisolone release process was mainly governed by molecular diffusion. Finally, the developed particle formulations were found to be nontoxic in the tested range of concentrations.


1999 ◽  
Vol 18 (4) ◽  
pp. 349-358 ◽  
Author(s):  
Rosemarie Osborne ◽  
Greg J. Carr ◽  
Karen A. Kohrman ◽  
Katherjnea Stitzel

2015 ◽  
Vol 29 (6) ◽  
pp. 1283-1288 ◽  
Author(s):  
Gisele Augusto Rodrigues Oliveira ◽  
Rafael do Nascimento Ducas ◽  
Gabriel Campos Teixeira ◽  
Aline Carvalho Batista ◽  
Danielle Palma Oliveira ◽  
...  

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