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Formulation and Evaluation of Thermoreversible in-situ Nasal Gel of Rizatriptan Benzoate and Caffeine

机译:利扎曲普坦苯甲酸酯和咖啡因的热可逆原位鼻凝胶的制备和评价

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Rizatriptan benzoate undergo hepatic first pass metabolism. Aim of present research work is to overcome hepatic first pass metabolism by formulating in-situ nasal gel along with caffeine to get cumulative effect. Formulation was developed to decrease the mucociliary authorization by using thermo-reversible polymer in gel, thus increase the contact time with nasal mucosa and humanizing the absorption of drug. Gels were prepared by cold technique process and evaluate by Appearance, Viscosity, Gelation Temperature, Permeation Studies, Drug Content, Gel strength etc. The gelation temperature of all studied gel formulations were found in range. pH of gel was in the range and drug content was found between 90-98.86%. Gel strength was found in range of 60-120 sec.
机译:利扎曲普坦苯甲酸酯经历肝首过代谢。目前研究工作的目的是通过与咖啡因一起配制原位鼻腔凝胶来克服肝首过代谢,从而获得累积效应。通过在凝胶中使用热可逆聚合物来开发配方以减少粘膜纤毛授权,从而增加与鼻粘膜的接触时间并人性化药物吸收。通过冷技术制备凝胶,并通过外观,粘度,胶凝温度,渗透研究,药物含量,胶凝强度等进行评估。所有研究的凝胶制剂的胶凝温度均在一定范围内。凝胶的pH在该范围内,并且发现药物含量在90-98.86%之间。发现凝胶强度在60-120秒的范围内。

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