百里香酚负载口腔原位凝胶的设计体外评价

H. K. Polat, S. Gözcü, Huseyin Aksit
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引用次数: 1

摘要

目的:制备百里香酚热敏原位凝胶,以延长口腔接触时间,控制药物释放,提高口腔生物利用度。材料与方法:采用不同用量的poloxam188 (P188)和poloxam407 (P407)设计原位凝胶。黏附赋形剂,如羟丙基甲基纤维素(HPMC),被转移到原位凝胶中,以提高制剂粘附生物表面的能力。对所制备的制剂进行了体外药物释放度、pH值、透明度和溶胶-凝胶转变温度的评估。结果:开发的配方的所有原位凝胶凝胶化温度范围为33至37°C, pH值约为7,注射器的可注射性定义为从装有20号针的注射器中排出每种配方所需的力。P407和HPMC的含量随制剂的增加而降低体外爆发释放,同时增加黏度,但每个原位凝胶制剂释放时间为6小时。结论:含P407和P188的百里酚原位凝胶具有良好的口腔应用前景。
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Design of Thymol Loaded Dental In Situ Gels; In Vitro Evaluation
Objetive: The aim of the study was to develop thymol thermosensitive in situ gels based on poloxamers in order to prolong dental contact time, control drug release, and enhance dental bioavailability. Materials and Methods: Poloxamer 188 (P188) and poloxamer 407 (P407) were used in varying amounts to designed the in situ gels. Mucoadhesive excipient, like hydroxypropyl methylcellulose (HPMC), was transferred to the in situ gels to improve the formulation's ability to adhere to biological surfaces. For the created formulations, in vitro drug release, pH, clarity, and sol-gel transition temperature were all evaluated.Results: The all of in situ gels gelation temperatures of the developed formulations range from 33 to 37°C, pH values are around 7, and syringeability is defined as the amount of force necessary to discharge each formulation from a syringe fitted with a 20-gauge needle. The quantities of P407 and HPMC with the preparations, decreasing in vitro burst release while also increasing the viscosity but every in situ gel formulation releases for six hours. Conclusion:The results show that in situ gels containing P407 and P188 show promise for thymol dental application.
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