Cyclosporine release and distribution in ophthalmic emulsions determined by pulsatile microdialysis

肺表面活性物质 微透析 色谱法 超声 化学 乳状液 脉动流 控制释放 剂型 粘度 Zeta电位 材料科学 纳米技术 生物化学 纳米颗粒 复合材料 细胞外 医学 心脏病学
作者
Robert A. Bellantone,Kosha B. Shah,Piyush Patel,Marissa Kaplan,Xiaoming Xu,Vincent Li,Bryan Newman,Md Abul Kaisar
出处
期刊:International Journal of Pharmaceutics [Elsevier]
卷期号:615: 121521-121521 被引量:6
标识
DOI:10.1016/j.ijpharm.2022.121521
摘要

An in vitro release test based on pulsatile microdialysis (PMD) is presented for the purpose of measuring the release of cyclosporine from ophthalmic emulsions, along with a method to determine the drug distribution within the oil-rich globule, surfactant-rich micelle and aqueous phases of the emulsion formulation. Compositionally equivalent formulations containing 0.05% cyclosporine were prepared with similar physical parameters (globule size, viscosity, surface tension zeta potential, osmolality, pH) but made with different manufacturing conditions. Emulsions were made by ultrasonication, using different ultrasonication times (22-49 min) and temperatures (50-82 °C). Formulations were stored at room temperature (20 °C) and PMD was performed under two conditions, one in which the receiving medium temperature was 20 °C, and another in which the receiving medium temperature was 35 °C to mimic the temperature change expected when a drop of formulation is administered to the eye. The PMD release data were taken at release times of 20, 40, 60, 90, 120, 180, 300 and 600 s. All experiments showed a qualitatively similar release pattern, with a rapid initial rate of drug release (Release-1) for the first few minutes, followed by a much slower release (Release-2). In addition, imposing a sudden temperature change on the formulation was observed to affect the release, with some formulations releasing faster into receiver media at 35 °C than at 20 °C, while others released faster into 20 °C than 35 °C receiver media. The drug distribution was also calculated from PMD release data into 20 °C receiver media using a novel release kinetics model. The drug distribution varied among the formulations, with 54-77% of the cyclosporine in the oil phase of the emulsions. PMD is a promising method to evaluate how manufacturing-induced differences affect the distribution and release kinetics of cyclosporine within the emulsion formulation.
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