Non-steroidal anti inflammatory agents decrease bacterial colonisation of contact lenses and prevent adhesion to human corneal epithelial cells

被引:35
作者
Bandara, BMK
Sankaridurg, PR [1 ]
Willcox, MDP
机构
[1] Univ New S Wales, Vision Cooperat Res Ctr, Sydney, NSW 2052, Australia
[2] Cooperat Res Ctr Eye Res & Technol, Sydney, NSW, Australia
[3] Univ New S Wales, Cornea & Contact Lens Res Unit, Sch Optometry & Vis Sci, Sydney, NSW, Australia
关键词
non-steroidal anti-inflammatory agent; NSAID; contact lens; colonization; corneal epithelial cells;
D O I
10.1080/02713680490516729
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose. To investigate non-steroidal anti-inflammatory agents (NSAIDs), salicylic acid, sodium diclofenac and ketorolac for inhibition of bacterial colonization of contact lenses (CL) and human corneal epithelial cells (HCE). Methods. CLs pre-colonised with Pseudomonas aeruginosa, Haemophilus influenzae, Staphylococcus epidermidis and Streptococcus pneumoniae were exposed overnight to NSAIDs and the number of viable bacteria on the CLs were calculated. Cytotoxicity of NSAIDs to HCE cells was evaluated with the MTT assay. Viable counts were used to measure the adhesion of P aeruginosa and S. epidermidis to HCE cells in the presence of the least cytotoxic NSAID. Results. All NSAIDs significantly decreased bacterial colonization of CLs in a dose-dependent manner. Salicylic acid (100mM) completely inhibited colonisation of all species tested and was the least cytotoxic. Salicylic acid also prevented adhesion of P aerugainosa and S. epidermidis to HCE (60% and 58% inhibition at 60 mM at 2 hours). Conclusions. Salicylic acid demonstrated potential as a compound for incorporation into anti-bacterial strategies to prevent bacterial contamination of contact lenses. This stud), highlighted the potential for NSAIDs as anti-bacterial agents and indicates that this class of compound should be investigated for other suitable candidates.
引用
收藏
页码:245 / 251
页数:7
相关论文
共 29 条
[1]   ULCERATIVE KERATITIS ASSOCIATED WITH CONTACT-LENS WEAR [J].
ALFONSO, E ;
MANDELBAUM, S ;
FOX, MJ ;
FORSTER, RK .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1986, 101 (04) :429-433
[2]  
ARAKISASAKI K, 1995, INVEST OPHTH VIS SCI, V36, P614
[3]  
ARBER BF, 1992, J INFECT DIS, V166, P861
[4]  
Arciola CR, 1998, J BIOMED MATER RES, V42, P1
[5]   REDUCTION OF CAPSULAR POLYSACCHARIDE PRODUCTION IN KLEBSIELLA-PNEUMONIAE BY SODIUM-SALICYLATE [J].
DOMENICO, P ;
SCHWARTZ, S ;
CUNHA, BA .
INFECTION AND IMMUNITY, 1989, 57 (12) :3778-3782
[6]   A NOVEL ANTIBIOFILM TECHNOLOGY FOR CONTACT-LENS SOLUTIONS [J].
FARBER, BF ;
HSIEH, HC ;
DONNENFELD, ED ;
PERRY, HD ;
EPSTEIN, A ;
WOLFF, A .
OPHTHALMOLOGY, 1995, 102 (05) :831-836
[7]  
FARBER BF, 1993, J BIOMED MATER RES, V27, P559
[8]  
Flach A J, 2001, Trans Am Ophthalmol Soc, V99, P205
[9]   Late corneal perforation after photorefractive keratectomy associated with topical diclofenac - Involvement of matrix metalloproteinases [J].
Gabison, EE ;
Chastang, P ;
Menashi, S ;
Mourah, S ;
Doan, S ;
Oster, M ;
Mauviel, A ;
Hoang-Xuan, T .
OPHTHALMOLOGY, 2003, 110 (08) :1626-1631
[10]   Possible role of the vitamin E solubilizer in topical diclofenac on matrix metalloproteinase expression in corneal melting - An analysis of postoperative keratolysis [J].
Hargrave, SL ;
Jung, JC ;
Fini, ME ;
Gelender, H ;
Cather, C ;
Guidera, A ;
Udell, I ;
Fisher, S ;
Jester, JV ;
Bowman, RW ;
McCulley, JP ;
Cavanagh, HD .
OPHTHALMOLOGY, 2002, 109 (02) :343-350