Caprylhydroxamic Acid: A Growing Allergen in Skincare Products

IF 4.6 1区 医学 Q2 ALLERGY
Valentine Theret, Estelle Burle, Françoise Giordano
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Thus, patch testing was performed with lotion's ingredients provided by the firm and revealed strong contact allergy 3+ for a component named SPECTRA STAT E, a commercial blend containing caprylhydroxamic acid (CHA), methylpropanediol (MP), and ethylhexylglycerin (EE). As the latter had previously tested negative, CHA and MP were suspected allergens.</p><p>Further patch testing was conducted using SPECTRA STAT E (CHA, MP and EE) and SPECTRA STAT (CHA alone) with three different concentrations in petrolatum (1%, 2% and 5% pet). All formulations tested positive for 1+ or 2+ at lower concentrations, and 3+ at higher concentrations on D3 (Figure 1B), confirming CHA as the responsible allergen. The results of the key patch tests are detailed in Table 1. 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This is, therefore, used in emulsions, creams, lotions and surfactant-based products such as shower gels, facial cleansers and shampoos.</p><p>In the published literature, there has been only one documented contact allergy being attributed to CHA related to Apobase moisturisers. This occurrence coincided with a modification in the formulation of cosmetic products, which included the preservative Phenostat between the years 2014 and 2016. This mixture contains phenoxyethanol, caprylhydroxamic acid and methylpropanediol [<span>3</span>]. The study, which was conducted on 39 patients in Finland, showed positive reactions to the novel Apobase formulas and to caprylhydroxamic acid. However, no positive reactions were observed to the old formulas or to the other components of Phenostat, thus confirming caprylhydroxamic acid as an emerging contact allergen. Following this contact allergy epidemic, Phenostat had been withdrawn from Apobase in 2016 in Finland. 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引用次数: 0

Abstract

A 70-year-old woman presented with bilateral upper and lower eyelid eczema and cheilitis persisting for 1 year despite dermocorticoids (Figure 1A).

Initial patch testing with European baseline series revealed contact allergy to methylchloroisothiazolinone and methylisothiazolinone (MCI/MI). However, the eczema persisted and spread despite MCI/MI avoidance.

A second-round of patch testing with the European baseline series, cosmetic series (Chemotechnique Diagnostics, Vellinge, Sweden) and 11 personal care products was carried out and found out to be positive 2+ on day 3 for the semi-open test with her cleaning lotion, universal lotion NOREVA (NOREVA laboratory, France), despite the absence of MCI/MI. Thus, patch testing was performed with lotion's ingredients provided by the firm and revealed strong contact allergy 3+ for a component named SPECTRA STAT E, a commercial blend containing caprylhydroxamic acid (CHA), methylpropanediol (MP), and ethylhexylglycerin (EE). As the latter had previously tested negative, CHA and MP were suspected allergens.

Further patch testing was conducted using SPECTRA STAT E (CHA, MP and EE) and SPECTRA STAT (CHA alone) with three different concentrations in petrolatum (1%, 2% and 5% pet). All formulations tested positive for 1+ or 2+ at lower concentrations, and 3+ at higher concentrations on D3 (Figure 1B), confirming CHA as the responsible allergen. The results of the key patch tests are detailed in Table 1. The contact allergy to the universal lotion NOREVA is, therefore, linked to caprylhydroxamic acid, although the responsibility of methylpropanediol cannot be ruled out as it is not available from the firm on its own.

Contact allergies to cosmetics are very common, with a wide variety of clinical presentations [1] and often leading to patch testing. The majority of these cases are caused by fragrances and preservatives [2].

Spectrastat E is a preservative system developed by INOLEX that contains caprylhydroxamic acid, a natural chelating agent inhibiting yeast and mould growth; ethylhexylglycerin, a skin-conditioning agent preventing bacterial proliferation; and methylpropanediol, a formulation carrier. This is, therefore, used in emulsions, creams, lotions and surfactant-based products such as shower gels, facial cleansers and shampoos.

In the published literature, there has been only one documented contact allergy being attributed to CHA related to Apobase moisturisers. This occurrence coincided with a modification in the formulation of cosmetic products, which included the preservative Phenostat between the years 2014 and 2016. This mixture contains phenoxyethanol, caprylhydroxamic acid and methylpropanediol [3]. The study, which was conducted on 39 patients in Finland, showed positive reactions to the novel Apobase formulas and to caprylhydroxamic acid. However, no positive reactions were observed to the old formulas or to the other components of Phenostat, thus confirming caprylhydroxamic acid as an emerging contact allergen. Following this contact allergy epidemic, Phenostat had been withdrawn from Apobase in 2016 in Finland. They also performed patch tests with different concentrations on patients and on healthy controls, determining that the ideal patch testing dilution for CHA for patch tests is 1%.

Whereas MP is used as a solvent and is not described in the literature as a potential allergen.

Our case is the first described since the removal of CHA from Apobase in 2016.

Caprylhydroxamic acid (INCI name: CAPRYLHYDROXAMIC ACID) seems to be an emerging allergen responsible for severe contact allergy. It is likely that it will be used more and more in cosmetics because it is considered to be derived from natural products.

It is currently used in skin and body creams, hair products, makeup, sunscreens, antiperspirants and deodorants and in a variety of cleaning products and facial cleansing gels, as in our case.

The patch tests conducted were positive for MI, MCI/MI and CHA. This could be the result of a coincidental discovery or the sign of a potential cross-reaction, necessitating further analysis with a larger sample size, even though the molecules in question do not share a similar chemical structure.

Moreover, this report highlights the need for testing patient-used cosmetics alongside commercial patch series when investigating contact allergies, especially in reformulated products.

Valentine Theret: conceptualization, investigation, writing – original draft, writing – review and editing. Estelle Burle: writing – original draft, writing – review and editing, supervision. Françoise Giordano: conceptualization, supervision, writing – original draft, writing – review and editing.

The patient in this manuscript has given written informed consent to publication of their case details and photographs.

The authors declare no conflicts of interest.

Abstract Image

甲基羟肟酸:护肤品中日益增长的过敏原。
一名70岁女性,尽管使用了真皮皮质激素,但仍表现为双侧上、下眼睑湿疹和唇炎,持续1年(图1A)。欧洲基线系列的初步斑贴试验显示对甲基氯异噻唑啉酮和甲基异噻唑啉酮(MCI/MI)接触性过敏。然而,尽管避免了MCI/MI,湿疹仍然存在并扩散。对欧洲基线系列、化妆品系列(Chemotechnique Diagnostics,瑞典Vellinge)和11种个人护理产品进行了第二轮斑贴测试,尽管没有MCI/MI,但在第3天使用她的清洁乳液、通用乳液NOREVA(法国NOREVA实验室)进行的半开放式测试中发现阳性2+。因此,用该公司提供的乳液成分进行了斑贴试验,发现对一种名为SPECTRA STAT E的成分有强烈的接触过敏3+,这是一种含有卡普羟肟酸(CHA)、甲基丙二醇(MP)和乙基己基甘油(EE)的商业混合物。由于后者先前检测呈阴性,CHA和MP被怀疑是过敏原。进一步使用SPECTRA STAT E (CHA, MP和EE)和SPECTRA STAT (CHA单独)与三种不同浓度的凡士林(1%,2%和5% pet)进行贴片试验。所有配方在较低浓度下测试1+或2+阳性,在较高浓度下测试3+阳性(图1B),证实CHA是负责任的过敏原。表1详细列出了关键补丁测试的结果。因此,对通用洗剂NOREVA的接触性过敏与甲基羟肟酸有关,尽管甲基丙二醇的责任不能排除,因为该公司本身没有甲基丙二醇。化妆品接触性过敏非常常见,临床表现多种多样,通常需要进行贴片试验。这些情况大多是由香水和防腐剂引起的。Spectrastat E是一种由INOLEX开发的防腐剂系统,含有卡己基羟肟酸,一种抑制酵母和霉菌生长的天然螯合剂;乙基己基甘油,一种防止细菌增殖的皮肤调理剂;甲基丙二醇,一种配方载体。因此,它被用于乳液、面霜、乳液和基于表面活性剂的产品,如沐浴露、洗面奶和洗发水。在已发表的文献中,只有一个记录的接触性过敏归因于与Apobase保湿霜相关的CHA。这一事件与化妆品配方的修改相吻合,其中包括2014年至2016年期间的防腐剂Phenostat。这种混合物含有苯氧乙醇、癸羟肟酸和甲基丙二醇[3]。这项研究对芬兰的39名患者进行了研究,结果显示,新型Apobase配方和甲基羟肟酸对患者有积极反应。然而,未观察到对旧配方或表型stat的其他成分的阳性反应,从而证实了甲基羟肟酸是一种新兴的接触性过敏原。在这次接触性过敏流行之后,芬兰于2016年从Apobase撤出了Phenostat。他们还对患者和健康对照者进行了不同浓度的贴片试验,确定贴片试验中CHA的理想稀释度为1%。然而,MP被用作溶剂,在文献中没有被描述为潜在的过敏原。我们的案例是自2016年从Apobase移除CHA以来第一个被描述的案例。旋甲羟肟酸(INCI名称:旋甲羟肟酸)似乎是一种新兴的过敏原负责严重的接触性过敏。它很可能会越来越多地用于化妆品,因为它被认为是从天然产品中提取的。它目前被用于皮肤和身体乳霜、护发产品、化妆品、防晒霜、止汗剂和除臭剂,以及各种清洁产品和面部清洁凝胶,就像我们的情况一样。进行的斑贴试验对MI、MCI/MI和CHA均呈阳性。这可能是偶然发现的结果,也可能是潜在交叉反应的迹象,需要用更大的样本量进行进一步分析,即使所讨论的分子没有相似的化学结构。此外,本报告强调,在调查接触性过敏时,特别是在重新配制的产品中,需要对患者使用的化妆品和商业贴片系列进行测试。瓦伦丁·特雷特:构思,调查,写作-原稿,写作-审查和编辑。埃斯特尔·伯勒:写作-原稿,写作-审查编辑,监督。法语:构思,监督,写作-原稿,写作-审查和编辑。本手稿中的患者已书面知情同意其病例细节和照片的出版。作者声明无利益冲突。
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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来源期刊
Contact Dermatitis
Contact Dermatitis 医学-过敏
CiteScore
4.60
自引率
30.90%
发文量
227
审稿时长
4-8 weeks
期刊介绍: Contact Dermatitis is designed primarily as a journal for clinicians who are interested in various aspects of environmental dermatitis. This includes both allergic and irritant (toxic) types of contact dermatitis, occupational (industrial) dermatitis and consumers" dermatitis from such products as cosmetics and toiletries. The journal aims at promoting and maintaining communication among dermatologists, industrial physicians, allergists and clinical immunologists, as well as chemists and research workers involved in industry and the production of consumer goods. Papers are invited on clinical observations, diagnosis and methods of investigation of patients, therapeutic measures, organisation and legislation relating to the control of occupational and consumers".
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