羟丙甲纤维素改善苯肾上腺素在兔实验模型中的散瞳动力学

E. Blinova, G. K. Poluosmak, E. Litvin, D. S. Blinov, M. V. Shiсh, O. S. Vavilova, O. Vasilkina, E. Shich
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引用次数: 1

摘要

目的:在体内比较研究中,确定含有和不含有羟丙甲纤维素、透明质酸作为辅助成分的苯肾上腺素药物制剂的散瞳作用的主要特征,并研究其局部生物利用度和对眼睛粘膜的影响。材料和方法。这项研究是在40只成年雄性苏联龙猫兔身上进行的。该研究模型涉及药物滴入清醒兔结膜囊时的散瞳影响和局部刺激作用。苯肾上腺素是所研究的所有制剂的一部分,通过高效液相色谱-串联质谱检测法在动物眼睛前房房水中测定了5分钟时的峰值浓度。后果单次滴注1滴含有羟丙甲纤维素作为赋形剂的2.5%盐酸苯肾上腺素溶液在深度、达到最大散瞳效果的速率及其持续时间方面优于不含羟丙甲纤维素的制剂。只有在少数情况下,含有羟丙甲纤维素的药物制剂引起了轻微的眼睑闭合反应,而滴注不含羟丙甲醇的苯肾上腺素溶液时会引起兔子眼睛的中度局部刺激反应。滴注1滴含有羟丙甲纤维素的2.5%苯肾上腺素溶液5分钟后测定的眼前房房水中苯肾上腺素的峰值浓度显著超过滴注不含羟丙甲纤维素相同浓度的苯肾上腺素药物时的峰值浓度。结论将羟丙甲纤维素作为辅助物质纳入苯肾上腺素滴眼液的配方中,优化了活性物质的药效学和药代动力学,因为活性物质更快地渗透到眼前房房水中,增加了局部生物利用度并延长了暴露时间。此外,这种形式对眼睛组织没有局部刺激作用也可以通过羟丙甲纤维素的存在来解释。
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Hypromellose improves mydriasis dynamics by phenylephrine in a rabbit experimental model
Purpose: to determine the main characteristics of the mydriatic effect of drug formulations of phenylephrine, containing and not containing hypromellose, hyaluronic acid as an auxiliary component, in a comparative in vivo study, as well as to study their local bioavailability and the effect on the mucous membrane of the eye. Materials and methods. The studies were carried out on 40 adult male Soviet Chinchilla rabbits. The research model involved the mydriatic impact and the local irritant effect of the drug when instilled into the awake rabbit’s conjunctival sac. The peak concentration of phenylephrine, which is part of all formulations studied, was determined in the aqueous humor of the anterior chamber of the animal's eye at the 5-minute point by high-performance liquid chromatography with tandem mass spectrometric detection. Results. A single instillation of 1 drop of a 2.5% solution of phenylephrine hydrochloride containing hypromellose as an excipient is superior in depth, rate of reaching the maximum mydriatic effect and its duration to the formulation that does not contain hypromellose as an excipient. Only in a few cases, drug formulations containing hypromellose caused an insignificant weak reaction of eyelid closure, in contrast to a moderate local irritant reaction of the rabbit's eye occurring when phenylephrine solution without hypromellose is instilled. Peak concentrations of phenylephrine in the aqueous humor of the anterior chamber of the eye determined 5 minutes after instillation of 1 drop of 2.5% phenylephrine solutions containing hypromellose significantly exceed those occurring when phenylephrine drugs of the same concentration that do not contain hypromellose are instilled. Conclusion. The inclusion of hypromellose as an auxiliary substance into the formulation of phenylephrine eye drops optimizes the pharmacodynamics and pharmacokinetics of the active substance due to faster penetration into the eye anterior chamber aqueous humor, increasing local bioavailability and prolonging the exposure time. In addition, the absence of a local irritating effect of such forms on the eye tissues may also be explained by the presence of hypromellose.
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16 weeks
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