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首页> 外文期刊>Drug development and industrial pharmacy >Formulation development and accelerated stability testing of a novel sunscreen cream for ultraviolet radiation protection in high altitude areas
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Formulation development and accelerated stability testing of a novel sunscreen cream for ultraviolet radiation protection in high altitude areas

机译:高海拔地区紫外线防晒霜新型防晒霜的配方开发和加速稳定性试验

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摘要

The present study is aimed at the development of a sunscreen cream for use in high altitude areas which have been found to possess superior sun protection factor (SPF) along with remarkable antioxidant activity. The topical formulation is a standard oil-in-water emulsion of a combination of United States Food and Drug Administration (US FDA) approved ultraviolet filters; along with melatonin and pumpkin seed oil. The in-silico optimized formulation was characterized using established methods and the stability study was carried out as per International Conference on Harmonization guidelines. The formulation was prepared after requisite pre-formulation analysis by Fourier-transform infrared spectroscopy, differential scanning calorimetric and thermogravimetric analyses; followed by characterization based on color, odor, phase separation, spreadability, specific gravity, homogeneicity, centrifugation and sensitivity. For the stability study, a total of three samples from three batches of the finished product were subjected to the stability study. The samples were analyzed for content uniformity, pH, in vitro SPF, rheology, zeta potential, droplet diameter and microbial analysis of the Oth day and also the the end of the storage period. Results obtained from the stability study indicated that the formulation possesses 50+ in vitro SPF value and remained stable for 6 months and 12 months under storage at 40±2°C and 75 ±5% relative humidity; and -20°C±5°C respectively.
机译:本研究旨在开发用于高海拔地区的防晒霜,这些研究已经发现具有优异的防晒系数(SPF)以及显着的抗氧化活性。局部配方是美国食品和药物管理局(美国FDA)批准的紫外线滤油的组合的标准油包装乳液;与褪黑激素和南瓜种子油一起。使用既定方法表征了二氧化硅优化配方,稳定性研究是根据统一指南的国际会议进行的。通过傅立叶变换红外光谱,差示扫描量热和热重分析进行必要的预制剂分析后制备制剂;其次是基于颜色,气味,相分离,铺展性,比重,均匀性​​,离心和敏感性的表征。对于稳定性研究,对三批成品的总共三个样品进行了稳定性研究。分析样品的含量均匀性,pH,体外SPF,流变学,Zeta电位,液滴直径和微生物的微生物分析以及储存周期的结束。从稳定性研究获得的结果表明,制剂具有50次体外SPF值,并在40±2°C和75±5%相对湿度下保持稳定6个月和12个月;和-20°C±5°C。

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