• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

防晒霜——终极化妆品。

Sunscreens--the ultimate cosmetic.

作者信息

Wolf Ronni, Matz Hagit, Orion Edith, Lipozencić Jasna

机构信息

Dermatology Unit, Kaplan Medical Center, 76100 Rechovot, Israel.

出版信息

Acta Dermatovenerol Croat. 2003;11(3):158-62.

PMID:12967508
Abstract

One decade ago, a sun protection factor (SPF) of 15 was considered a complete blocker of ultraviolet radiation (UV). The logic behind that cutoff point was that sunscreens with this SPF number would always prevent erythema and that preventing erythema would prevent all the ill effects of UV exposure. Today, we know that both of these assumptions were wrong and we tend to recommend higher SPF. Consumers apply only about one-quarter to one-half thickness of the layer of sunscreen material used to measure the SPF in the laboratory. That means that less than 50% of the SPF number claimed on the label is spread on the consumer's skin, meaning that a sunscreen with an SPF 30 will give the real protection of an SPF of 15. Therefore, recommend 60 when you want a real protection of 30! Significant injury, DNA damage, mutations, and carcinogenesis can and do occur also with cumulative suberythemal UV exposure. Thus, erythema induction, a criterion that defines SPF, is not a good indicator of UV damage. We also need higher SPF values to prevent the damage caused by suberythemal doses of UV. The value of the SPF claimed on the label is diminished by environmental factors that are not taken into account during SPF measurements in the laboratory, such as sweating, water immersion, rubbing off, and photodegradation. There are some misunderstandings and confusion about the mode of action of physical sunscreens. It was originally considered that, in contrast to organic sunscreens, the inorganic metal oxides (zinc oxide and titanium dioxide) acted as scatterers or reflectors of UV light, as a mirror. This is not the case with modern micronized forms of metal oxides. It has been shown that both zinc oxide and titanium dioxide mobilize electrons within their atomic structure while absorbing UV radiation. Thus, although metallic oxides are not inert per se, in their coated form they are stable, non-toxic, and safe and they act as highly efficient UV attenuators. Therefore, we recommend our patients to use this type of sunscreens. We should exert all our influence upon our patients not to expose themselves to excessive sunlight, to routinely use generous layers of sunscreen agents, and to wear protective clothing. To wait for the dust to settle around the issue of the effectiveness of sunscreens in preventing melanoma, while the ideal sunscreens--topical, systemic, whatever--are at our disposal, is a luxury we cannot afford.

摘要

十年前,防晒系数(SPF)为15被认为是紫外线(UV)的完全阻挡剂。该临界点背后的逻辑是,具有此SPF值的防晒霜总能预防红斑,而预防红斑就能预防紫外线暴露的所有不良影响。如今,我们知道这两个假设都是错误的,我们倾向于推荐更高的SPF值。消费者涂抹的防晒霜材料层厚度仅为实验室测量SPF时所用厚度的约四分之一到二分之一。这意味着标签上声称的SPF值中,只有不到50%涂在了消费者的皮肤上,也就是说,一款标注SPF 30的防晒霜实际提供的防护效果相当于SPF 15。所以,若想要获得相当于SPF 30的实际防护效果,就应推荐使用SPF 60的产品!累积的亚红斑紫外线暴露也确实会导致严重损伤、DNA损伤、突变和致癌。因此,作为定义SPF的标准,红斑诱导并不是紫外线损伤的良好指标。我们还需要更高的SPF值来预防亚红斑剂量紫外线造成的损伤。标签上声称的SPF值会因实验室测量SPF时未考虑的环境因素而降低,如出汗、水浸、擦掉以及光降解。对于物理防晒霜的作用方式存在一些误解和混淆。最初人们认为,与有机防晒霜不同,无机金属氧化物(氧化锌和二氧化钛)像镜子一样起到紫外线的散射或反射作用。现代微粉化形式的金属氧化物并非如此。研究表明,氧化锌和二氧化钛在吸收紫外线时都会在其原子结构内激发电子。因此,尽管金属氧化物本身并非惰性物质,但以涂层形式存在时它们是稳定、无毒且安全的,并且能作为高效的紫外线衰减剂。所以,我们建议患者使用这类防晒霜。我们应尽全力影响患者,使其避免过度暴露在阳光下,日常使用足量的防晒剂,并穿着防护服。在有理想的防晒霜——局部用、全身用,无论哪种——可供我们使用的情况下,等待防晒霜预防黑色素瘤有效性问题的尘埃落定是我们承担不起的奢侈行为。

相似文献

1
Sunscreens--the ultimate cosmetic.防晒霜——终极化妆品。
Acta Dermatovenerol Croat. 2003;11(3):158-62.
2
Sunscreens - which and what for?防晒霜——哪种及用于何种情况?
Skin Pharmacol Physiol. 2005 Nov-Dec;18(6):253-62. doi: 10.1159/000087606. Epub 2005 Aug 19.
3
Sun protection factors: world wide confusion.防晒因子:全球混淆。
Br J Dermatol. 2009 Nov;161 Suppl 3:13-24. doi: 10.1111/j.1365-2133.2009.09506.x.
4
Broad-spectrum sunscreens provide better protection from solar ultraviolet-simulated radiation and natural sunlight-induced immunosuppression in human beings.广谱防晒霜能为人类提供更好的防护,抵御太阳紫外线模拟辐射和自然阳光引起的免疫抑制。
J Am Acad Dermatol. 2008 May;58(5 Suppl 2):S149-54. doi: 10.1016/j.jaad.2007.04.035.
5
Effect of daily versus intermittent sunscreen application on solar simulated UV radiation-induced skin response in humans.每日涂抹防晒霜与间歇性涂抹防晒霜对人体模拟太阳紫外线辐射引起的皮肤反应的影响。
J Am Acad Dermatol. 2000 Oct;43(4):610-8. doi: 10.1067/mjd.2000.107244.
6
Photoprotective efficacy and photostability of fifteen sunscreen products having the same label SPF subjected to natural sunlight.十五种标签 SPF 值相同的防晒产品在自然阳光下的光保护功效和光稳定性。
Int J Pharm. 2011 Apr 15;408(1-2):27-38. doi: 10.1016/j.ijpharm.2011.01.040. Epub 2011 Jan 26.
7
Randomized controlled trial testing the impact of high-protection sunscreens on sun-exposure behavior.一项随机对照试验,旨在测试高防护性防晒霜对阳光暴露行为的影响。
Arch Dermatol. 2005 Aug;141(8):950-6. doi: 10.1001/archderm.141.8.950.
8
Sunscreens containing the broad-spectrum UVA absorber, Mexoryl SX, prevent the cutaneous detrimental effects of UV exposure: a review of clinical study results.含有广谱UVA吸收剂麦素宁滤光环SX的防晒霜可预防紫外线暴露对皮肤的有害影响:临床研究结果综述
Photodermatol Photoimmunol Photomed. 2008 Aug;24(4):164-74. doi: 10.1111/j.1600-0781.2008.00365.x.
9
Partial protection against epidermal IL-10 transcription and Langerhans cell depletion by sunscreens after exposure of human skin to UVB.人体皮肤暴露于中波紫外线后,防晒霜对表皮白细胞介素-10转录及朗格汉斯细胞耗竭具有部分保护作用。
Photochem Photobiol. 1999 Nov;70(5):766-72.
10
Clothing reduces the sun protection factor of sunscreens.衣物会降低防晒霜的防晒因子。
Br J Dermatol. 2010 Feb 1;162(2):415-9. doi: 10.1111/j.1365-2133.2009.09478.x. Epub 2009 Aug 29.

引用本文的文献

1
Pre-Clinical Investigations of the Pharmacodynamics of Immunogenic Smart Radiotherapy Biomaterials (iSRB).免疫原性智能放射治疗生物材料(iSRB)的药效学临床前研究。
Pharmaceutics. 2023 Dec 14;15(12):2778. doi: 10.3390/pharmaceutics15122778.
2
Global Trends of Sunscreen Research Literature: A Bibliometric Analysis over the Period of 2010-2020.防晒研究文献的全球趋势:2010 - 2020年文献计量分析
J Cutan Aesthet Surg. 2022 Apr-Jun;15(2):161-167. doi: 10.4103/JCAS.JCAS_110_21.
3
Ingestion of titanium dioxide nanoparticles: a definite health risk for consumers and their progeny.
摄入二氧化钛纳米颗粒:对消费者及其后代明确存在的健康风险。
Arch Toxicol. 2022 Oct;96(10):2655-2686. doi: 10.1007/s00204-022-03334-x. Epub 2022 Jul 27.
4
Repeated-dose 90-day oral toxicity study of GST in Sprague-Dawley rats.谷胱甘肽S-转移酶(GST)对Sprague-Dawley大鼠的重复给药90天口服毒性研究。
Environ Anal Health Toxicol. 2022 Jun;37(2):e2022013-0. doi: 10.5620/eaht.2022013. Epub 2022 May 11.
5
Repeated-dose 28-day dermal toxicity study of TiO2 catalyst (GST) in Sprague-Dawley rats.二氧化钛催化剂(GST)对斯普拉格-道利大鼠的重复给药28天皮肤毒性研究。
Environ Anal Health Toxicol. 2022 Jun;37(2):e2022010-0. doi: 10.5620/eaht.2022010. Epub 2022 May 10.
6
Physico-Chemical Properties of Inorganic NPs Influence the Absorption Rate of Aquatic Mosses Reducing Cytotoxicity on Intestinal Epithelial Barrier Model.无机纳米颗粒的物理化学性质影响水生苔藓的吸收速率,降低对肠道上皮屏障模型的细胞毒性。
Molecules. 2021 May 13;26(10):2885. doi: 10.3390/molecules26102885.
7
Oral toxicity of titanium dioxide P25 at repeated dose 28-day and 90-day in rats.二氧化钛 P25 经口重复 28 天和 90 天给药的大鼠毒性。
Part Fibre Toxicol. 2020 Jul 17;17(1):34. doi: 10.1186/s12989-020-00350-6.
8
Titanium dioxide nanoparticles oral exposure to pregnant rats and its distribution.二氧化钛纳米颗粒经口暴露于怀孕大鼠及其分布。
Part Fibre Toxicol. 2019 Jul 18;16(1):31. doi: 10.1186/s12989-019-0313-5.
9
Comparative study of the cytotoxic and genotoxic potentials of zinc oxide and titanium dioxide nanoparticles.氧化锌和二氧化钛纳米颗粒的细胞毒性和遗传毒性潜力的比较研究
Toxicol Rep. 2015 Feb 19;2:765-774. doi: 10.1016/j.toxrep.2015.02.004. eCollection 2015.
10
Mechanism of N-acetyl-cysteine inhibition on the cytotoxicity induced by titanium dioxide nanoparticles in JB6 cells transfected with activator protein-1.N-乙酰半胱氨酸对转染激活蛋白-1的JB6细胞中二氧化钛纳米颗粒诱导的细胞毒性的抑制机制。
Exp Ther Med. 2017 Jun;13(6):3549-3554. doi: 10.3892/etm.2017.4415. Epub 2017 May 2.