Evaluation of therapeutic effect of a new hypotensive formulation in a glaucoma model in rabbits

Authors

  • Mariana Andrea Guaycochea Cátedra de Física Biomédica, Facultad de Ciencias Médicas, Universidad Nacional de Córdoba.
  • Carolina del Valle Bessone Unidad de Investigación y Desarrollo en Tecnología Farmacéutica (UNITEFA-CONICET), Departamento de Ciencias Farmacéuticas, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba.
  • Lucía Bacigalupo Cátedra de Física Biomédica, Facultad de Ciencias Médicas, Universidad Nacional de Córdoba.
  • David Cremonezzi 1º Cátedra de Patología, Hospital Nacional de Clínicas, Facultad de Ciencias Médicas, Universidad Nacional de Córdoba.
  • Daniel Allemandi Unidad de Investigación y Desarrollo en Tecnología Farmacéutica (UNITEFA-CONICET), Departamento de Ciencias Farmacéuticas, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba.
  • Vilma Campana Cátedra de Física Biomédica, Facultad de Ciencias Médicas, Universidad Nacional de Córdoba.
  • Luis Ignacio Tártara Cátedra de Física Biomédica, Facultad de Ciencias Médicas, Universidad Nacional de Córdoba.

DOI:

https://doi.org/10.70313/2718.7446.v14.n3.76

Keywords:

experimental glaucoma, ocular drug therapy, cubosomes, latanoprost, ocular hypertension

Abstract

Purpose: To evaluate and compare the efficacy and toxicity of an ocular hypotensive formulation composed of nanometric lyotropic liquid crystals (cubosomes) (CLL) and latanoprost 0.005% (LT) in a glaucoma model in rabbits.
Materials and methods: 24 female rabbits were used, divided into 4 groups: 1. Ocular normotensive (NTO) treated with CLL-LT; 2. NTO treated with commercial LT (Louten® solution); 3. With ocular hypertensive (HTO) treated with CLL-LT and 4. With HTO treated with commercial LT. The induction of the glaucoma model was performed with an injection of 0.1 ml of α-chymotrypsin (3 mg/ml) in the posterior chamber of the right eye. The treatment administration method was with a single subconjunctival injection (50 µl) of the study formulations. They were evaluated by measuring the IOP once a day for a week as well as the clinical assessment. The data were analyzed using the t test for independent samples, considering p <0.05 for significant differences.
Results: The CLL-LT decreased IOP in rabbits HTO ~ 20%, and in NTO ~ 25%. Compared with the commercial solution, CLL-LT generated a greater decrease (p <0.05). The initial post-injection irritation subsided within 24 hours.
Conclusion: CLL-LT turned out to be more effective in reducing IOP than the commercial solution in NTO and OHT rabbits, without presenting permanent damage to the ocular surface.

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Published

2021-09-22

Issue

Section

Original Articles

How to Cite

[1]
2021. Evaluation of therapeutic effect of a new hypotensive formulation in a glaucoma model in rabbits. Oftalmología Clínica y Experimental. 14, 3 (Sep. 2021). DOI:https://doi.org/10.70313/2718.7446.v14.n3.76.

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