Development And Evaluation of topical liposomal preparation of Walnut oil and tamarind seed oil against ageing

Aditya Singh , Vaseem Ahamad Ansari , Md Faheem Haider , Farogh Ahsan , Tarique Mahmood , Rufaida Wasim , Shubhrat Maheshwari
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引用次数: 0

Abstract

Background

Revamp of liposomal preparation inimical ageing by using a splendid treasure of herbal drugs includes non-prescription and prescription upshot. Liposomal therapy stands at the forefront of cutting-edge cosmeceutical innovation. It involves a sophisticated, bi-layered delivery system designed for the precise infusion of walnut oil and tamarind seed oil into the skin. This innovative approach effectively combats the signs of ageing, whether they are the result of a sedentary lifestyle or genetic factors within one's family history.

Purpose

The current study focuses on exploring the area of traditional systems of medicine in the field of pharmaceuticals to achieve the combined effect of walnut oil [F1] and tamarind seed oil [F2] in the form of liposomal preparation against ageing.

Methods

Liposomes of walnut oil and tamarind seed oil were developed by using a rotary vacuum evaporator, and microscopy of the formulated liposomes was done using a Digicam microscope, which provided a microscopic view that both formulated liposomes are spherical, but F1 liposomes are more dense and tactile than F2, and the F2 liposomal formulation has more vesicles than F1. In-vitro drug release studies of F1 and F2 were done by diffusion cells while using a dialysis membrane with buffer medium 6.8. Further characterization techniques like SEM and FTIR were used to investigate the size range with the clear shape of the particles and to obtain a clear peak that matched the pure drug, which shows that it has retained its pharmacological properties. The final step was directed towards the preparation of topical anti-ageing cream by combining F1 and F2 to obtain the synergistic effect, and the formulation cream was successfully visualised under a projection microscope at a magnification of 10x, which reveals that spherically droplet vacuoles are present with a soft texture and a creamy, whitish colour. Last but not least, a 14-day animal study was conducted on female Swiss mice from the authorised animal laboratory departmental animal house at Integral University. The studies were conducted in 3 groups: G1 was given saline as a control, G2 was given Olay as a topical application, and G3 was given the test cream. The anti-ageing potential of the formulated cream was evaluated by skin compliance studies using UV exposure.

Results

Walnut oil and tamarind seed oil-based liposomes were formulated after placebo selection, i.e., F1 and F2, and the microscopic view of F1 sphere-shaped vesicles is larger, brighter, and more dense than F2, and the sphere-shaped vesicles of F1 and F2 contain phospholipid bilayers composed of soyalecthin, which helps to deliver drugs at a specific site. The pH of two formulations, F1 and F2, was determined by storing them at different temperatures, 350°C and 450°C. The pH resultant values were in the range of 5.8 to 6.9, which means that the formulated liposomes are ideal for skin function. ​In-vitro ​drug release studies of F1 and F2 data revealed that F1 shows less drug release than F2 at 35 min, which is less than 100%. This specified study was done to identify the time that was taken to release the drug. The structural analysis of liposomes F1 and F2 was done by the highly characterised technique of SEM, and the result revealed that F1 and F2 were in a spherical shape. F1 liposome was 5 ​μm in diameter, while F2 liposome was 1 ​μm in diameter, which means that they lie in the bilayer liposomal range. FTIR is an important parameter to analyse the functional group and also to identify the peak of the pure drug that is similar to the excipient for retaining the pharmacological action, so here F1 and F2 liposomes are similar to the pure drug. The topical preparation of liposomes F1 and F2 was decided to formulate cream that is easy to use and store. The combining anti-ageing creams of F1 and F2 were visualised under a projection microscope, and the view of the liposomal cream revealed sphere-shaped vesicles. As a result of skin compliance studies, ∗∗G3 is significantly more significant than G1 and ∗G2 is significantly more significant than G1. The anti-ageing evaluation study stated that ∗∗G3 is much more significant than G2, and ∗G2 is much more significant than G1.

Conclusion

The present study indicates that walnut oil and tamarind seed oil were successfully entrapped in a liposomal formulation in the form of cream. The characterization studies reveal that they are potent against ageing.

核桃油和罗望子油局部脂质体抗衰老制剂的开发与评估
背景脂质体制剂的改良通过使用绚丽的中药宝藏来抑制衰老,包括非处方药和处方药。脂质体疗法是最前沿的药妆创新疗法。它采用精密的双层输送系统,将核桃油和罗望子油精确地注入皮肤。这项创新方法能有效对抗衰老迹象,无论这些迹象是由于久坐不动的生活方式还是家族遗传因素造成的。 目的 本研究重点探索传统医药系统在制药领域的应用,以实现核桃油 [F1] 和罗望子油 [F2] 以脂质体制剂形式对抗衰老的综合效果。方法使用旋转真空蒸发器研制核桃油和罗望子油的脂质体,并使用 Digicam 显微镜对配制的脂质体进行显微观察,结果显示两种配制的脂质体均为球形,但 F1 脂质体比 F2 更致密,触感更好,F2 脂质体制剂比 F1 有更多的囊泡。F1 和 F2 的体外药物释放研究是通过使用透析膜和 6.8 缓冲介质的扩散细胞进行的。扫描电镜和傅立叶变换红外光谱等进一步的表征技术用于研究颗粒的大小范围和清晰形状,并获得了与纯药物相匹配的清晰峰值,这表明它保留了其药理特性。最后一步是制备外用抗衰老乳膏,将 F1 和 F2 混合使用,以获得协同增效作用,并在投影显微镜下以 10 倍的放大倍数成功观察了制剂乳膏,结果显示存在球形液滴空泡,质地柔软,呈乳白色。最后,我们还对瑞士综合大学授权动物实验室的雌性瑞士小鼠进行了为期 14 天的动物实验。研究分 3 组进行:G1 组为生理盐水对照组,G2 组为玉兰油局部涂抹组,G3 组为测试面霜组。结果经过安慰剂选择后,配制出了以核桃油和罗望子油为基础的脂质体,即 F1 和 F2,显微镜下看,F1 的球形囊泡比 F2 的更大、更亮、更致密,F1 和 F2 的球形囊泡含有由苏亚拉酸组成的磷脂双分子层,有助于在特定部位递送药物。将 F1 和 F2 两种配方分别储存在 350°C 和 450°C 的不同温度下,测定了它们的 pH 值。得出的 pH 值在 5.8 至 6.9 之间,这意味着配制的脂质体非常适合皮肤功能。F1 和 F2 的体外药物释放研究数据显示,在 35 分钟内,F1 的药物释放量低于 F2,小于 100%。进行这项特定研究是为了确定药物释放所需的时间。脂质体 F1 和 F2 的结构分析采用了特征性很强的扫描电镜技术,结果显示 F1 和 F2 呈球形。F1 脂质体的直径为 5 μm,而 F2 脂质体的直径为 1 μm,这意味着它们属于双层脂质体范围。傅立叶变换红外光谱是分析官能团的重要参数,也是确定纯药与赋形剂相似的峰值以保留药理作用的重要参数,因此这里的 F1 和 F2 脂质体与纯药相似。脂质体 F1 和 F2 的外用制备方法是为了配制出易于使用和储存的面霜。在投影显微镜下观察 F1 和 F2 的组合抗衰老霜,发现脂质体霜呈球形囊泡。皮肤顺应性研究结果表明,∗∗G3 明显高于 G1,∗∗G2 明显高于 G1。抗衰老评价研究表明,∗∗G3 比 G2 明显更显著,∗G2 比 G1 明显更显著。表征研究表明,它们具有抗衰老的功效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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