冻干芦荟萃取物、光保护和延缓白化病损害索赔证明

J. Chifamba, A. J. Addae, S. Zengeni, M. Pomerai, N. Kurebgaseka
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引用次数: 0

摘要

引言紫外线辐射通过诱导光氧化损伤和光合作用抑制,对植物的生理结构和光合装置具有潜在危害。芦荟(Aloe excelsa)是一种生命力顽强的(亚)热带植物,已进化出各种光保护机制,以便在这些恶劣的环境中繁衍生息。目前,美国食品和药物管理局(FDA)的非处方专论 M020 将 16 种已获批准的防晒霜中的 14 种斥为对生态和人类健康 "不安全",因此,人们开始寻找更安全的防晒霜,而来自光弹性植物的植物成分可能就是下一代安全有效的防晒霜。目的:本研究通过植物筛选和体外评估其 SPF、UVAPF、UVA/UVB 比率、临界波长、抗氧化性和抗炎潜力,研究了冻干水乙醇芦荟提取物的光保护活性。研究方法从横向切割的新鲜芦荟中提取芦荟凝胶基质,用 70% 的乙醇浸泡,冻干,然后进行定量和定性植物化学筛选。抗氧化活性采用 DPPH 清除法测定,光保护研究采用 COLIPA 2011/FDA Final Rule 2011 的指导原则进行体外研究,抗炎能力采用蛋白质变性试验进行评估。结果:定性植物化学筛选证实了芦荟中存在大量具有药理作用的初级和次级代谢产物,定量植物分析表明,芦荟的总酚、单宁和类黄酮含量高于芦荟。抗炎能力与标准双氯芬酸密切相关,抗氧化能力几乎与抗坏血酸相当。制备的 50% 芦荟凝胶的 SPF 值为 7.6,UVAPF 值为 4,临界波长为 375。计算得出的光稳定性:%SPFeff 和 %UVAPFeff 均高于 97%。结论研究结果证实,芦荟是一种多功能光防护材料,具有抗氧化、消炎和紫外线防护特性。从技术上讲,50% 的冻干芦荟凝胶可归类为低 SPF 防晒霜。丰富的初级和次级代谢产物与本研究中观察和计算得出的光防护参数直接相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lyophilised Aloe excelsa Fractions, Photo-protection and Actinic Damage Retardation Claims Substantiation
Introduction: Ultraviolet radiation is potentially harmful to plants’ physiological structures and their photosynthetic apparatus through induction of photo-oxidative damage and photosynthetic inhibition. Aloe excelsa a resilient (sub) tropical plant has evolved various photo-protective mechanisms to proliferate in these harsh environments. With the current FDA, over-the-Counter Monograph M020 castigating 14 of the 16 approved sunscreens as “unsafe” to the ecology and human health, the hunt for safer sunscreens is on and phytoconstituents from photo-resilient plants may just  be the next generation, safe and efficacious sunscreens. Aims: This study investigated the photo-protective activity of lyophilized hydro-ethanolic Aloe excelsa extracts through phytoscreening and in-vitro estimations of their SPF, UVAPF, UVA/UVB ratio, critical wavelength, anti-oxidancy as well as anti-inflammatory potential. Methods: The Aloe excelsa gel matrix was physically extracted from transversely cut fresh rossetes, macerated in 70% ethanol, lyophilized and then subjected to both quantitative and qualitative phytochemical screening techniques. The antioxidant activity was measured using the DPPH scavenging assay, the photoprotection investigation was performed in-vitro using directives from COLIPA 2011/FDA Final Rule 2011 as guidelines and the anti-inflammatory capacity was evaluated using the protein denaturing test. Results: Qualitative phytochemical screening confirmed the presence of numerous primary and secondary metabolites of pharmacological interest, Quantitative phyto-analysis revealed that  Aloe excelsa has higher levels of total phenols, tannins and flavonoids than Aloe vera. Anti-inflammatory capacity was closely related to the standard Diclofenac and the anti oxidancy was almost equivalent to ascorbic acid. A prepared 50% Aloe excelsa gel had an SPF of 7.6 and a UVAPF of 4 and a critical wavelength of 375. The calculated photostabilities: %SPFeff and %UVAPFeff were both above 97%. Conclusion: The results confirm that Aloe excelsa is a multifunctional photoprotective material with confirmed anti-oxidancy, anti-inflammatory and UVR protection attributes. The 50% lyophilised Aloe excelsa gel can be technically classified as a low SPF sunscreen. The abundant primary and secondary metabolites correlate directly with the observed and calculated photoprotective parameters obtained in this study.
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