Journal List > J Korean Ophthalmol Soc > v.49(4) > 1008241

Park, Kim, and Choi: The Effect of Intracameral Triamcinolone Acetonide Injection on the Cornea in Rabbits

Abstract

Purpose

To evaluate the safety and effects of intracameral triamcinolone acetonide injection in rabbit corneas.

Methods

Triamcinolone acetonide in the amounts of 0.5, 1, and 2 mg was injected into the anterior chamber of rabbit eyes, and intraocular pressure, corneal thickness, and endothelial cell counts were evaluated on days 1, 3, 7, 14, and 28. Twenty-eight days after triamcinolone acetonide injection, the eyes were enucleated and examined after TUNEL staining.

Results

No statistically significant differences were found among control, 0.5, and 1 mg triamcinolone-injected eyes in central corneal thickness, endothelial cell density, pleomorphism, and polymegathism. There was no difference between 2 mg triamcinolone-injected eyes and control eyes for corneal thickness and cell density, but there were statistically significant differences between these two groups for pleomorphism (p<0.05) and polymegathism (p<0.05).

Conclusions

The results of this study suggested that intracameral injections of 0.5∼1 mg of triamcinolone acetonide are beneficial and cause no toxic effects on corneas.

References

1. Gordon DM. Prednisone and prednisolone in ocular disease. Am J Ophthalmol. 1956; 41:593–600.
2. Machemer R, Sugita G, Tano Y. Treatment of intraocular proliferations with intravitreal steroids. Trans Am Ophthalmol Soc. 1979; 77:171–80.
3. Kok H, Lau C, Maycock N, et al. Outcome of intravitreal triamcinolone in uveitis. Ophthalmology. 2005; 112:1916.
crossref
4. Arevalo JF, Garcia RA, Mendoza AJ. Indocyanine green-mediated photothrombosis with intravitreal triamcinolone acetonide for subfoveal choroidal neovascularization in age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol. 2005; 243:1180–5.
crossref
5. Chieh JJ, Roth DB, Liu M, et al. Intravitreal triamcinolone acetonide for diabetic macular edema. Retina. 2005; 25:828–34.
crossref
6. Cekic O, Chang S, Tseng JJ, et al. Intravitreal triamcinolone injection for treatment of macular edema secondary to branch retinal vein occlusion. Retina. 2005; 25:851–5.
crossref
7. Jonas JB, Kreissig I, Degenring RF. Intravitreal triamcinolone acetonide for pseudophakic cystoid macular edema. Am J Ophthalmol. 2003; 136:384–6.
crossref
8. Oh J-Y, Wee WR, Lee JH, Kim MK. Short-term effect of intracameral triamcinolone acetonide on corneal endothelium using the rabbit model. Eye. 2007; 21:812–8.
crossref
9. Hernaez‐ Ortega MC, Soto‐ Pedre E. Removal of benzyl alcohol from a commercially available triamcinolone acetonide suspension for intravitreal use. Ophthalmic Surg Lasers Imaging. 2006; 37:162–4.
crossref
10. Jonas JB, Degenring RF, Kreissig I, et al. Intraocular pressure elevation after intravitreal triamcinolone acetonide injection. Ophthalmology. 2005; 112:593–8.
crossref
11. Chan CK, Fan DS, Chan WM, et al. Ocular-hypertensive response and corneal endothelial changes after intravitreal triamcinolone injections in Chinese subjects: a 6-month follow-up study. Eye. 2005; 19:625–30.
crossref
12. Jonas JB, Kreissig I, Degenring RF. Intraocular pressure after intravitreal injection of triamcinolone acetonide. Br J Ophthalmol. 2003; 87:24–7.
crossref
13. Vajpayee RB, Sharma N, Dada T, et al. Management of posterior capsule tears. Surv Ophthalmol. 2001; 45:473–88.
crossref
14. Akura J, Hatta S, Kaneda S, et al. Management of posterior capsule rupture during phacoemulsification using the dry technique. J Cataract Refract Surg. 2001; 27:982–9.
crossref
15. Yamakiri K, Uchino E, Kimura K, Sakamoto T. Intracameral triamcinolone helps to visualize and remove the vitreous body in anterior chamber in cataract surgery. Am J Ophthalmol. 2004; 138:650–2.
crossref
16. Jonas JB. Intraocular availability of triamcinolone acetonide after intravitreal injection. Am J Ophthalmol. 2004; 137:560–2.
crossref
17. Chen TY, Yang CM, Liu KR. Intravitreal triamcinolone staining observation of residual undetached cortical vitreous after posterior vitreous detachment. Eye. 2006; 20:423–7.
crossref
18. Furino C, Micelli Ferrari T, Boscia F, et al. Triamcinolone-assisted pars plana vitrectomy for proliferative vitreoretinopathy. Retina. 2003; 23:771–6.
crossref
19. Walker TD. Benzalkonium toxicity. Clin Experiment Ophthalmol. 2004; 32:657.
20. Morrison VL, Koh HJ, Cheng L, et al. Intravitreal toxicity of the kenalog vehicle (benzyl alcohol) in rabbits. Retina. 2006; 26:339–44.
crossref
21. Garcia-Arumi J, Boixadera A, Giralt J, et al. Comparison of different techniques for purification of triamcinolone acetonide suspension for intravitreal use. Br J Ophthalmol. 2005; 89:1112–4.
crossref
22. Nishimura A, Kobayashi A, Segawa Y, et al. Isolating triamcinolone acetonide particles for intravitreal use with a porous membrane filter. Retina. 2003; 23:777–9.
crossref
23. Foster A, Resnikoff S. The impact of Vision 2020 on global blindness. Eye. 2005; 19:1133–5.
crossref
24. Misra A, Burton RL. Incidence of intraoperative complications during phacoemulsification in vitrectomized and nonvitrectomized eyes: prospective study. J Cataract Refract Surg. 2005; 31:1011–4.
crossref
25. Mason JO 3rd, Somaiya MD, Singh RJ. Intravitreal concentration and clearance of triamcinolone acetonide in nonvitrectomized human eyes. Retina. 2004; 24:900–4.
crossref
26. Zinn KM. Iatrogenic intraocular injection of depot corticosteroid and its surgical removal using the pars plana approach. Ophthalmology. 1981; 88:13–7.
27. Van Horn DL, Sendele DD, Seideman S, Buco PJ. Regenerative capacity of the corneal endothelium in rabbit and cat. Invest Ophthalmol Visual Sci. 1977; 10:597–613.

Figure 1.
Anterior segment photographs after different concentrations of intracameral triamcinolone acetonide injections at 1, 7, and 28 days after 0.5 mg (A, B, C), 1 mg (D, E, F) and 2 mg (G, H, I) triamcinolone acetonide injection into the anterior chamber.
jkos-49-634f1.tif
Figure 2.
Specular micrographs at one day after 1 mg (A) and 2 mg (B) triamcinolone acetonide injection; CD=cell density; CV=coefficient of variation; 6A=hexagonality.
jkos-49-634f2.tif
Figure 3.
Hematoxylin & eosin staining (A) and TUNEL staining (B) of the central cornea in control, and in rabbit with 0.5, 1, and 2 mg of triamcinolone acetonide injection at 28 days. (×200)
jkos-49-634f3.tif
Table 1.
The average corneal thickness (µm) according to triamcinolone acetonide injection dose and time
Pre-operative Day 1 Day 3 Day 7 Day 14 Day 28 Statistical significance
BSS (n=5) 342.6±11.7 349.6±20.9 342.6±14.9 354.8±24.0 353.4±19.4 335.2±13.6 NS
TA 0.5 mg (n=5) 324.4±21.2 361.8±17.7 329.4±20.5 360.4±14.2 349.6±30.2 343.0±13.4 NS
TA 1.0 mg (n=5) 348.2±27.1 362.6±15.8 353.8±23.0 358.0±28.6 351.8±28.6 343.2±18.4 NS
TA 2.0 mg (n=5) 337.6±15.6 335.8±9.8 344.8±20.1 351.6±17.6 347.2±24.4 343.6±16.9 NS

Mean±SD (standard deviation); Ta=triamcinolone acetonide; BSS=balanced salt solution; NS=not significant. (p>0.05)

Table 2.
The average corneal endothelial cell density (cell/mm2) according to triamcinolone acetonide injection dose and time
Pre-operative Day 1 Day 3 Day 7 Day 14 Day 28 Statistical significance
BSS (n=5) 2941±261 2929±392 2846±201 2903±132 3027±190 2923±223 NS
TA 0.5 mg (n=5) 3028±134 2996±210 2964±100 2929±86 3030±172 2973±126 NS
TA 1.0 mg (n=5) 2978±210 3062±135 2860±213 2928±151 2977±249 2926±234 NS
TA 2.0 mg (n=5) 3006±246 3048±284 2912±197 2871±165 2833±194 2839±188 NS

Mean±SD (standard deviation); Ta=triamcinolone acetonide; BSS=balanced salt solution; NS=not significant. (p>0.05)

Table 3.
The average corneal endothelial polymegathism (coefficient of variation) according to triamcinolone acetonide injection dose and time
Pre-operative Day 1 Day 3 Day 7 Day 14 Day 28 Statistical significance
BSS (n=5) 18.0±1.2 22.8±3.4 19.6±4.6 18.2±2.0 18.0±1.5 19.8±3.1 NS
TA 0.5 mg (n=5) 19.4±0.8 25.0±5.7 21.2±3.9 20.2±3.2 20.5±2.4 20.2±4.2 NS
TA 1.0 mg (n=5) 21.0±1.8 27.4±5.5 21.4±4.0 22.0±3.2 21.4±2.8 19.8±2.6 NS
TA 2.0 mg (n=5) 19.8±1.3 37.0±4.8 26.0±3.1 21.4±2.0 21.8±2.2 20.8±2.9 P=0.007* P=0.02

Mean±SD (standard deviation); TA=triamcinolone acetonide; BSS=balanced salt solution; NS=not significant (p>0.05)

* Test of within-subject (time)

Test of between-subjects (concentration).

Table 4.
The average corneal endothelial pleomorphism (%, hexagonality) according to triamcinolone acetonide injection dose and time
Pre-operative Day 1 Day 3 Day 7 Day 14 Day 28 Statistical significance
BSS (n=5) 67.6±7.9 72.6±4.9 72.2±3.8 72.0±4.1 70.6±3.9 71.2±3.1 NS
TA 0.5 mg (n=5) 66.6±6.9 72.8±7.4 68.8±4.4 68.8±3.2 69.0±1.7 69.4±2.0 NS
TA 1.0 mg (n=5) 67.6±8.0 68.6±4.5 68.6±6.1 69.0±6.2 70.4±5.3 68.6±4.2 NS
TA 2.0 mg (n=5) 70.0±11.0 57.8±5.4 61.6±4.8 63.8±3.4 63.4±3.8 69.6±4.8 P=0.036* P=0.02

Mean±SD (standard deviation); TA=triamcinolone acetonide; BSS=balanced salt solution; NS=not significant (p>0.05)

* Test of within-subject (time)

Test of between-subjects (concentration).

TOOLS
Similar articles