Formulation and Evaluation of In-situ Ophthalmic Gel of Ketorolac Tromethamine

Authors

  • Dipen R. Bhimani
  • Daya L. Chothani

Keywords:

Ketorolac tromethamine, In-situ gel, Sustained release, Ophthalmic delivery

Abstract

Low bioavailability, frequent dosage, and rapid precorneal excretion are the drawbacks of conventional ketorolac tromethamine eye drops. These drawbacks can be overcome by in-situ ophthalmic gels, which extend ocular residence and offer prolonged drug release. Using poloxamer 188 and poloxamer 407 as thermos-responsive gelling agents, the current study sought to create and assess a sustained release in-situ ocular gel containing ketorolac tromethamine. Using varying concentration of poloxamer 188 and poloxamer 407 integrated as a gelling agent, several formulations were created. Clarity, pH, gelling capacity, and in-vitro drug release were assessed for the produced gels. To ensure gelation at ocular physiological temperature, the optimized formulation including poloxamer 407 and poloxamer showed a sol-to-gel transition at approximately 34.7°C. For long-term precorneal retention, the gel displayed pseudoplastic flow with sufficient viscosity. According to in-vitro release experiments, ketorolac tromethamine exhibits a sustained release that can last for up to 12 hours. The work shows that ketorolac tromethamine can be safely and effectively delivered using in-situ gels based on poloxamers 188 and 407. These formulations are a possible substitute for traditional eye drops in the treatment of ocular inflammation and pain because they can increase ocular bioavailability, decrease dose frequency, and improve patient compliance

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Published

2023-12-20

How to Cite

1.
R. Bhimani D, Chothani DL. Formulation and Evaluation of In-situ Ophthalmic Gel of Ketorolac Tromethamine. J Neonatal Surg [Internet]. 2023 Dec. 20 [cited 2026 Sep. 22];12(1):248-60. Available from: https://jneonatalsurg.com/index.php/jns/article/view/10480

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