RESUMEN
Abstract Objective: Perfume (Parfum) or fragrance is a natural or synthetic cosmetic ingredient added to emit a pleasant aroma or to improve the odor of a cosmetic formula. It is a mixture of substances, not revealed by the manufacturer, which may contain ingredients with allergenic potential, endocrine disruptors, and other possible harmful effects on human health. This study aims to analyze children's cosmetics labels to assess the presence of Perfume. Methods: The researchers randomly visited points of sale in Curitiba, the capital of a southern Brazilian state; in order to catalog the largest possible number of children's cosmetics items. Results: 398 children's cosmetics were analyzed and found Parfum on 295 (74.1 %) of the labels, including 90.4 and 79,1 % of the shampoos and wet wipes, respectively. Conclusion: Exposure of children's skin to fragrances can lead to local side effects such as allergies, but also to systemic effects, and the lack of knowledge of the general population and health professionals about its possible deleterious effects emphasizes the importance of changes in the regulation of cosmetics aiming to reduce the use of this ingredient.
RESUMEN
ObjectiveTo establish a UHPLC-MS/MS quantitative method for the determination of glucuronic acid, tartaric acid, glycolic acid, malic acid, lactic acid, citric acid, DL-2-hydroxybutyric acid sodium, mandelic acid, benzilic acid, hydroxycaprylic acid, lactobionic acid, gluconic acid and N-acetylneuraminic acid in cosmetics. MethodsSamples were prepared by ultrasonic extraction, cleansed by precipitating reagent and followed by high-speed centrifugation of the extraction solution. The supernatant was filtered by 0.22 μm Millipore filter. The continued filtrate was taken for analysis. A reversed phase column, Poroshell 120 EC-C18 (2.7 μm, 4.6 mm×1 000 mm) was used with 0.1% formic acid buffer and acetonitrile as the mobile phase under the condition of gradient elution. The analytes were detected with electrospray ionization source in negative ion mode (ESI-) and multiple reactions monitoring (MRM), and quantified by external standard curve. ResultsThe method showed a good linearity of glucuronic acid, tartaric acid, malic acid, DL-2-hydroxybutyric acid sodium, benzilic acid, hydroxycaprylic acid and N-acetylneuraminic acid within the concentration range of 50.0‒2 000.0 μg·L-1 (r>0.995). The method showed a good linearity of glycolic acid, lactic acid, citric acid and mandelic acid within the concentration range of 100.0‒5 000.0 μg·L-1 (r>0.995). The method showed a good linearity of lactobionic acid and gluconic acid within the concentration range of 50.0‒5 000.0 μg·L-1 (r>0.995). The recoveries were in the range of 92.3%‒114.1%; the relative standard deviations (RSD) were in the range of 0.9%‒6.0% (n=3). The detection limits of glucuronic acid, tartaric acid, malic acid, citric acid, DL-2-hydroxybutyric acid sodium, mandelic acid, benzilic acid, hydroxycaprylic acid, lactobionic acid, gluconic acid and N-acetylneuraminic acid were 0.003% while the detection limits of glycolic acid, lactic acid and mandelic acid were 0.006%. In 10 batches of commercially available cosmetics, eight batches showed positive result. ConclusionThe UHPLC-MS/MS method is efficient, sensitive and accurate and is applicable to the determination of 13 α-hydroxy acidic components in cosmetics.
RESUMEN
The supervision of cosmetics started relatively late in China, and corresponding laws and regulations on ethical review are not yet perfect. The Cosmetics Supervision and Administration Regulations, which came into force on January 1, 2021, had stricter requirements for cosmetic efficacy claims, requiring that cosmetic efficacy claims should have a sufficient scientific basis. Cosmetic efficacy claims evaluation trials include human efficacy evaluation trials, consumer use tests, and laboratory trials. Human efficacy evaluation trials and consumer use tests should comply with the requirements of ethical principles, the necessary product safety evaluation should be completed before the tests are carried out, to ensure that there is no harm to the human health of research participants (or consumers) under normal, foreseeable circumstances. The Regulations on the Administration of Registration and Filing Materials for Cosmetics required that product test reports should include microbiological and physical-chemical tests, toxicological trials, human safety trial reports, and human efficacy trial reports. The key points of the ethics committee’s review of cosmetic efficacy claims evaluation trials include the reasonableness of the trial protocol, consumer survey and expert evaluation, selection of detection methods, study population and sample size, safety evaluation of the cosmetics, risk assessment of cosmetic raw materials, protection of privacy, and qualifications of the testing institutions and researchers. High-quality ethical review is conducive to safeguarding the safety and rights of research participants (or consumers), and will also promote the quality of cosmetic efficacy claims evaluation trails in China.
RESUMEN
Due to the high similarity with the lipid layer between human skin keratinocytes, functional cosmetics with layered liquid crystal structure prepared by liquid crystal emulsification technology encapsulating natural active substances have become a hot research topic in recent years. This type of functional cosmetic often has a fresh and natural skin feel, excellent skin barrier repair function and efficient moisturizing effect, etc., showing great potential in cosmetic application. However, the present research on the application of liquid crystal emulsification technology to functional cosmetics is still in the initial stage, and there are fewer relevant reports with reference values. Based on the mentioned above, this review provides a comprehensive summary of functional cosmetics with layered liquid crystal structures prepared by liquid crystal emulsification technology from the following aspects: the structure of human skin, the composition of lamellar liquid crystal, the advantages of liquid crystal emulsification technology containing natural active substances used in the field of functional cosmetics, the preparation process, main components, influencing factors during the preparation and the market functional cosmetics with lamellar liquid crystal structure. Finally, the prospect of the application of liquid crystal emulsification technology in functional cosmetics is presented, to provide useful references for those engaged in the research of liquid crystal emulsification technology-related functional cosmetics.
RESUMEN
A dermatite de contato pigmentada se destaca por sua raridade, sendo associada a inúmeros alérgenos cosméticos e têxteis. Acomete predominantemente mulheres de meia idade e fototipos altos. O teste de contato é imprescindível para a identificação do agente causal. O tratamento indicado consiste no afastamento do agente causal, no uso de fotoprotetores, clareadores tópicos e, por vezes, procedimentos dermatológicos abrasivos. Relatamos um caso de dermatite de contato pigmentada por cosmético motivado pela exuberância clínica e desfecho satisfatório, ressaltando a importância da suspeição diagnóstica e do manejo adequado impactando neste desfecho.
Pigmented contact dermatitis is a rare condition associated with numerous cosmetic and textile allergens. It predominantly affects middle-aged women with high phototypes. The patch test is essential to identify the causative agent. Treatment includes removal of the causative agent, sunscreen use, administration of topical bleaching agents, and occasionally abrasive dermatologic procedures. We report a case of pigmented cosmetic contact dermatitis motivated by its clinical exuberance and satisfactory outcome, emphasizing the importance of diagnostic suspicion and adequate management impacting this outcome.
Asunto(s)
Humanos , Femenino , Persona de Mediana EdadRESUMEN
Mercury is highly toxic and can be absorbed through skin contact. From December 5, 2020 to February 16, 2021, occupational disease laboratory of the First People's Hospital of Baiyin received 30 urine mercury test samples from a beauty salon in Lanzhou City. The test results showed that 28 samples exceeded the normal value (normal value: 4 μg/g Cr) . 15 patients were treated with sodium dimertopropyl sulfonate for mercury removal and tiopron for liver protection, and the prognosis was good.
Asunto(s)
Humanos , Mercurio/efectos adversos , Cosméticos/efectos adversos , Intoxicación por Mercurio , PielRESUMEN
Objective:To analyse the skin clinical characteristics of adverse reactions to cosmetic products.Methods:A total of 132 patients suffered with the skin adverse reactions of cosmetics were collected in the Department of Dermatology in the First Affiliated Hospital of Xinxiang Medical University from January 2021 to December 2021. There were 5 males and 127 females, aged 2-66 (34.0±13.1) years. and the personal information, medical records, clinical characteristics and the cosmetic information as well as laboratory results were collected.Results:The major types of adverse reactions to cosmetic products were contact dermatitis (86.4%). Head was the most commonly affected site, The most common symptoms were pruritus and burning sensation (83.9%), and sores, dryness, tightness of the skin, and the common skin lesions included erythema and papula (92.9%). Suspected cosmetics were mostly skin care products (45 cases) and freckle removing products (30 cases). Only 7 patients accepted patch tests, 1 case had negative results and others were all tested positive.Conclusions:Adverse drug reactions affect young and middle-aged women mostly. Contact dermatitis is the most common adeverse reaction to cosmetic products and the patch test is still the most effective method in helping diagnosing contact dermatitis to cosmetic products.
RESUMEN
Introdução: os efeitos deletérios da radiação ultravioleta (UV) sobre os tecidos labiais podem desencadear diversas lesões, inclusive de caráter maligno. A utilização de produtos fotoprotetores tem sido a melhor opção contra os efeitos nocivos dessa radiação. Diversas marcas de fotoprotetores labiais (FPL) estão disponíveis no mercado, onde o consumo é diretamente influenciado por qualidade e preço. Objetivo: analisar e comparar FPLs disponíveis em farmácias quanto à composição, ao preço e às características de rotulagem, segundo regulamentações da ANVISA. Metodologia: foi realizado estudo descritivo, que avaliou FPLs, quanto a FPS, indicação, constituintes químicos, FPUVA, preço e rótulo. Informações sobre as substâncias presentes e suas funções foram obtidas no INCI (Comissão Europeia), e os filtros solares foram identificados na INN (Organização Mundial da Saúde). As avaliações de rotulagem foram baseadas nas Resoluções da Diretoria Colegiada da ANVISA de nº 30/12, nº 7/15 e nº 69/16. Resultados: dezessete FPLs foram avaliados. Cinco apresentaram FPS 15; três, FPS 20; seis, FPS 30; e três, FPS 50. Dez filtros UV foram identificados, estando o Ethylhexyl Methoxycinnamate presente em maior número de FPLs. Doze produtos informaram ter proteção UVA. As características dos rótulos se encontravam dentro das determinações da ANVISA, na grande maioria dos casos. Houve alta variação do preço. Conclusão: a partir deste estudo, foi possível conhecer mais sobre a composição e as características dos FPL, principalmente sobre FPS e FPUVA, bem como se estão de acordo com as normas estabelecidas pela ANVISA, propiciando um maior conhecimento dos produtos que estão sendo comercializados.
Introduction: the deleterious effects of ultraviolet (UV) radiation on lip tissues can trigger several lesions, including malignant ones. The use of photoprotective products has been the best option against the harmful effects of this radiation. Several brands of lip sunscreens (FPL) are available on the market, where consumption is directly influenced by quality and price. Objective: to analyze and compare SPFs available in pharmacies in terms of composition, price and labeling characteristics, according to ANVISA regulations. Methodology: a descriptive study was carried out, which evaluated FPLs, in terms of SPF, indication, chemical constituents, PPD, price and label. Information on the substances present and their functions were obtained from the INCI (European Commission), and the sunscreens were identified from the INN (World Health Organization). The labeling evaluations were based on the Resolutions of the Collegiate Board of Directors of ANVISA No. 30/12, No. 7/15 and No. 69/16. Results: seventeen FPLs were evaluated. Five had SPF 15; three, SPF 20; six, SPF 30; and three, SPF 50. Ten UV filters were identified, with Ethylhexyl Methoxycinnamate present in the highest number of FPLs. Twelve products reported having UV protection. The characteristics of the labels were within the determinations of ANVISA, in the vast majority of cases. There was a high price variation. Conclusion: from this study, it was possible to know more about the composition and characteristics of FPL, mainly about SPF and UV, as well as whether they are in accordance with the standards established by ANVISA, providing a greater knowledge of the products that are being marketed.
Asunto(s)
Protectores Solares , Cosméticos , Agencia Nacional de Vigilancia Sanitaria , Productos para Labios , Factor de Protección Solar , Epidemiología DescriptivaRESUMEN
Atualmente, as alterações estéticas faciais e a insatisfação com a autoimagem são influências que motivam a busca por procedimentos estéticos rápidos, não cirúrgicos e menos invasivos. Por esse motivo, a procura de pacientes que procuram por procedimentos estéticos orofaciais é crescente. O objetivo deste estudo foi elencar as complicações decorrentes dos procedimentos de harmonização orofacial por meio de uma revisão sistemática da literatura, identificando quais tipos de complicações e áreas são mais acometidas. As seguintes bases de dados foram pesquisadas: Medline (PubMed), SciELO, Scopus, Cochrane, Lilacs e Web of Science, de março a setembro de 2020, selecionando os estudos que apresentavam os seguintes critérios de inclusão: estudos originais em humanos sobre complicações após procedimentos de harmonização orofacial. Foram selecionados 33 estudos da literatura que apresentavam relatos de complicações em pacientes após o procedimento de harmonização orofacial na testa, nariz, olhos, região periocular e lábios. Mesmo a execução de procedimentos estéticos faciais menos invasivos pode acarretar possíveis complicações imediatas ou tardias após o procedimento, principalmente na região periocular e nos olhos. É importante alertar previamente os profissionais para essa possibilidade.
Currently, facial aesthetic changes and dissatisfaction with self-image are influences that motivate the search for quick, non-surgical and less invasive cosmetic procedures. For this reason, the demand for patients looking for orofacial aesthetic procedures is increasing. The objective of this study was List the complications resulting from orofacial harmonization procedures through a systematic literature review, identifying which types of complications and areas are most affected. The following databases were searched: Medline (PubMed), SciELO, Scopus, Cochrane, Lilacs and Web of Science, from March to September 2020, selecting the studies that presented the following inclusion criteria: original studies in humans, about complications after orofacial harmonization procedures. Thirty-three studies from the literature were selected that presented reports of complications in patients after the orofacial harmonization procedure in the forehead, nose, eyes, periocular region and lips. Even the execution of less invasive facial cosmetic procedures can cause possible immediate or late complications after the procedure, especially in the periocular region and eyes. It is important to make professionals aware of this possibility beforehand.
RESUMEN
INTRODUÇÃO: A fotobiomodulação associada a cosméticos despigmentantes e rejuvenescedores tem mostrado benefícios na melhora da flacidez e hiperpigmentação genital em mulheres. OBJETIVO: O objetivo do estudo foi descrever a percepção de profissionais acerca da melhora de flacidez e hiperpigmentação genital tratados por fotobiomodulação associada a cosméticos. MÉTODO: O estudo evidenciou percepção de melhora no aspecto geral, flacidez e pigmentação genital com uso da terapêutica proposta. RESULTADOS: Amostra composta por dez mulheres submetidas a quatro sessões de tratamento. A análise dos profissionais foi mediante a comparação dos registos fotográficos de antes e depois do tratamento da região genital. CONCLUSÃO: No entanto, é necessário que novos modelos de avaliação para evidenciar a efetividade terapêutica para tratamentos de flacidez e discromias na região genital sejam desenvolvidos ampliando assim os métodos de avaliação para além da percepção de melhora do aspecto geral.
INTRODUCTION: Photobiomodulation associated with depigmenting and rejuvenating cosmetics has shown benefits in improving sagging and genital hyperpigmentation in women. OBJECTIVE: The aim of the study was to describe the perception of professionals about the improvement of sagging and genital hyperpigmentation treated by photobiomodulation associated with cosmetics. METHOD: The study showed a perception of improvement in the general appearance, sagging and genital pigmentation with the use of the proposed therapy. RESULTS: Sample composed of ten women submitted to four treatment sessions. The analysis of the professionals was by comparing the photographic records of before and after the treatment of the genital region. CONCLUSION: However, it is necessary that new evaluation models to evidence the therapeutic effectiveness for treatments of flaccidity and dyschromias in the genital region are developed, thus expanding the evaluation methods beyond the perception of improvement in the general aspect.
Asunto(s)
Cosméticos , Pigmentación , GenitalesRESUMEN
Nos últimos anos, cresce a tendência pela busca de cosméticos "amigos da natureza", sem ingredientes químicos ou sintéticos, impulsionando as vendas de produtos pertencentes a este nicho de mercado. Atualmente, o termo clean beauty refere-se a produtos que não contenham ingredientes sobre os quais não se conheça o impacto que terão em nosso organismo ou seu potencial dano ambiental. Entretanto, a definição do que é um cosmético verde, bem como vegano, natural e orgânico, não é regulamentada pela Agência Nacional de Vigilância Sanitária (Anvisa), sendo o objetivo deste artigo fazer uma revisão das definições para facilitar o entendimento médico sobre o tema.
In recent years, there has been an increasing trend toward the search for nature-friendly cosmetics without chemical or synthetic ingredients, thus boosting sales of products within this market niche. Currently, the term clean beauty refers to products that do not contain ingredients with unknown impacts on our bodies or that are potentially harmful to the environment. However, the definition of green beauty products, as well as vegan, natural, or organic products, is not regulated by ANVISA. Therefore, this study aimed to review these definitions to facilitate the medical understanding of the subject
RESUMEN
Abstract Formaldehyde is a carcinogenic compound used as preservative in cosmetic products. In this study, a derivatization procedure using MeOH, EtOH and HCl (25:25:1), and incubation at 60ºC for 4 hours was optimized, and the derivatized products - methylal, ethoxymethoxymethane (EMM), and ethylal - were directly analyzed by headspace-gas chromatography-mass spectrometry (HS-GC-MS) to determine formaldehyde concentrations. The validated method provided good linearity of the standard curve, selectivity, recovery (89.6-106.6%), repeatability, and intermediate precision (RSD < 12%), with an LOD of 0.0015% and an LOQ of 0.005% for all derivatized analytes. The validated method showed to be fast, clean, and easy to implement in a laboratory. To the best of our knowledge, this is the first reported HS-GC-MS procedure to determine formaldehyde as methylal, ethylal, and EMM as derivatized compounds. The method was satisfactorily applied for the analysis of nine hair-straightener cream samples seized by the Civil Police of the Federal District, Brazil. Eight samples contained formaldehyde, at levels ranging from 0.33 to 4.02 %, higher than the legal levels, indicating the need to control the levels of this toxic compound in cosmetic products
Asunto(s)
Cosméticos/análisis , Formaldehído/análisis , Cromatografía de Gases y Espectrometría de Masas/métodos , Policía Judicial/legislación & jurisprudencia , Acetales/agonistas , MétodosRESUMEN
Abstract The consumption of cosmetics has been increasing every year and is expected to reach $675 billion by 2020 at an estimated growth rate of 6.4% per year. Exposure to skin irritants is the major cause of non-immunological inflammation of the skin. Therefore, the safety evaluation of cosmetic preservatives should be increased. Thus, the present work aimed to evaluate the cytotoxicity as the viability endpoint and the eye irritation potential of preservatives used in cosmetics. Cytotoxicity assays were performed using MTT and NRU in human keratinocytes (HaCaT), human dermal fibroblasts, adult (HDFa), and human hepatoma cells (HepG2). The eye irritation potential was evaluated using the Hen's Egg Test-chorioallantoic membrane (HET-CAM). The evaluated preservatives were methylparaben (MP), propylparaben (PP), phenoxyethanol (PE), and a mixture of methylchloroisothiazolinone and methylisothiazolinone (CMI/MI). All preservatives showed cytotoxic potential within the permitted concentrations for use in cosmetic products. In the HET-CAM test, PE and CMI/MI, MP, and PP were classified as severe, moderate, and poor irritants, respectively. Our results indicate that proper safety evaluations are required to ensure the beneficial properties of preservatives on cosmetic products without exceeding exposure levels that would result in adverse health effects for consumers.
Asunto(s)
Técnicas In Vitro/métodos , Cosméticos/análisis , Aditivos para Cosméticos , Seguridad , Piel/lesiones , Células/clasificación , Salud , Inflamación/complicaciones , Irritantes/farmacologíaRESUMEN
Abstract The effectiveness of sun protection depends directly on the photo-protective product employed, the way it is used and the amount applied. Many studies report that sunscreens are often applied incorrectly, at amounts much lower than those recommended for the sun protection factor (SPF) specified on the label. When not used properly, the effectiveness of the product against sun exposure damage is reduced. Currently, sunscreens are available in a variety of different formulations and types, such as stick (bar), aerosol, cream, lotion, oil, tanning formulations and makeup. However, developing an effective stable photo-protective formula that can be correctly applied regardless of type poses a challenge, as effectiveness is dependent on several factors. Factors influencing effectiveness include sun exposure conditions (direct or indirect), level of protection (SPF), amount of product applied, maximum exposure period before reapplication, product type (spray, lotion, etc.), layer thickness required, coverage, and ability to spread and permeate into the skin. Studies comparing the effectiveness of different forms of sunscreens, the amount of product applied by consumers and SPF and UVA protection determined by validated methodologies, are lacking. Therefore, the objective of this study was to review the available literature on the topic and discuss the effectiveness of sunscreen formulations and factors influencing sun protection. This review was carried out on the scientific databases MEDLINE, PubMed and Scielo. Of the many publications retrieved, thirty-nine articles most relevant for this review were selected.
RESUMEN
ABSTRACT Alternative methods to the use of animals in research have been a global trend, mainly after the publication of the 3R's principle (Replacement, Reduction, and Refinement), proposed by Russel and Burch. In the cosmetic sector, safety and efficacy assessments using animals have generated controversial debates. For this reason, in vitro research techniques are widely used to assess acute toxicity; corrosivity and irritation; skin sensitization; dermal and percutaneous absorption; repeated dose toxicity; reproductive toxicity; mutagenicity and genotoxicity; carcinogenicity; toxicokinetic studies; photo-induced toxicity; and human data. Although there are many methodologies described, validated, and widely used in the cosmetic area, the evaluation of the safety of cosmetic ingredients and products is still an expanding field. It needs global collaboration among regulatory agencies, universities, and industry, to meet several unmet needs in the fields of sensitization, carcinogenicity, systemic action, among other issues involving safety of users of cosmetic products. This review article will cover the currently most relevant in vitro models regarding irritation, corrosion, sensitization, mutagenicity, genotoxicity, and phototoxicity, to help to choose the most appropriate test for evaluating the safety and toxicity of cosmetic ingredients and products.
Asunto(s)
Humanos , Animales , Cosméticos/toxicidad , PielRESUMEN
The evolution of beauty market and personal care is constant in Brazil as well in the rest of the world. Technological advances have brought up nanotechnology to the cosmetological field, employing active principles at atoms enveloped by vesicles, in order to take the active principle precisely to the target tissue to optimize the results achieved because of the considerable ease to cross skin barriers. Manufacturing of nanotechnology cosmetics is confronted with low absorption capacity. One of the many active principle found in cosmetic industry is caffeine, a pseudoalkaloid from the xanthine group used as a stimulant with the mechanism of the lipolytic action. This active is widely used in a esthetics and cosmetics field in treatments involving dysfunctions such as localized fat and fibroedema geloid. To work out perfectly, the principle active need to interact and create a set of factors that includes lipolysis intensification. The caffeine encapsulation in gel-based nanocosmetics has the purpose of taking this active up to the adipocyte, the target cell, for mentioned dysfunctions treatment. Thus, we aim to present a review of how has been, the use of caffeine in the production of cosmetics.
A evolução do mercado de beleza e cuidados pessoais é constante no Brasil e no resto do mundo. Os avanços tecnológicos trouxeram a nanotecnologia para o campo cosmetológico, empregando princípios ativos em átomos envolvidos por vesículas, a fim de levar o princípio ativo precisamente ao tecido alvo para otimizar os resultados alcançados devido à considerável facilidade de atravessar barreiras cutâneas. A fabricação de cosméticos nanotecnológicos é confrontada com baixa capacidade de absorção. Um dos muitos princípios ativos encontrados na indústria cosmética é a cafeína, um pseudoalocalóide do grupo xantina usado como estimulante no mecanismo da ação lipolítica. Este ativo é amplamente utilizado no campo da estética e dos cosméticos em tratamentos que envolvem disfunções, como gordura localizada e fibroedema gelóide. Para funcionar perfeitamente, o princípio ativo precisa interagir e criar um conjunto de fatores que inclui a intensificação da lipólise. O encapsulamento de cafeína em nanocosméticos à base de gel tem o objetivo de levar esse ativo até o adipócito, a célula alvo, para o tratamento de disfunções mencionado. Assim, objetivamos apresentar uma revisão de como tem sido o uso de cafeína na produção de cosméticos.
Asunto(s)
Cafeína/uso terapéutico , Cosméticos/análisis , Nanoestructuras/uso terapéutico , NanotecnologíaRESUMEN
Abstract The evolution of beauty market and personal care is constant in Brazil as well in the rest of the world. Technological advances have brought up nanotechnology to the cosmetological field, employing active principles at atoms enveloped by vesicles, in order to take the active principle precisely to the target tissue to optimize the results achieved because of the considerable ease to cross skin barriers. Manufacturing of nanotechnology cosmetics is confronted with low absorption capacity. One of the many active principle found in cosmetic industry is caffeine, a pseudoalkaloid from the xanthine group used as a stimulant with the mechanism of the lipolytic action. This active is widely used in a esthetics and cosmetics field in treatments involving dysfunctions such as localized fat and fibroedema geloid. To work out perfectly, the principle active need to interact and create a set of factors that includes lipolysis intensification. The caffeine encapsulation in gel-based nanocosmetics has the purpose of taking this active up to the adipocyte, the target cell, for mentioned dysfunctions treatment. Thus, we aim to present a review of how has been, the use of caffeine in the production of cosmetics.
Resumo A evolução do mercado de beleza e cuidados pessoais é constante no Brasil e no resto do mundo. Os avanços tecnológicos trouxeram a nanotecnologia para o campo cosmetológico, empregando princípios ativos em átomos envolvidos por vesículas, a fim de levar o princípio ativo precisamente ao tecido alvo para otimizar os resultados alcançados devido à considerável facilidade de atravessar barreiras cutâneas. A fabricação de cosméticos nanotecnológicos é confrontada com baixa capacidade de absorção. Um dos muitos princípios ativos encontrados na indústria cosmética é a cafeína, um pseudoalocalóide do grupo xantina usado como estimulante no mecanismo da ação lipolítica. Este ativo é amplamente utilizado no campo da estética e dos cosméticos em tratamentos que envolvem disfunções, como gordura localizada e fibroedema gelóide. Para funcionar perfeitamente, o princípio ativo precisa interagir e criar um conjunto de fatores que inclui a intensificação da lipólise. O encapsulamento de cafeína em nanocosméticos à base de gel tem o objetivo de levar esse ativo até o adipócito, a célula alvo, para o tratamento de disfunções mencionado. Assim, objetivamos apresentar uma revisão de como tem sido o uso de cafeína na produção de cosméticos.
RESUMEN
The evolution of beauty market and personal care is constant in Brazil as well in the rest of the world. Technological advances have brought up nanotechnology to the cosmetological field, employing active principles at atoms enveloped by vesicles, in order to take the active principle precisely to the target tissue to optimize the results achieved because of the considerable ease to cross skin barriers. Manufacturing of nanotechnology cosmetics is confronted with low absorption capacity. One of the many active principle found in cosmetic industry is caffeine, a pseudoalkaloid from the xanthine group used as a stimulant with the mechanism of the lipolytic action. This active is widely used in a esthetics and cosmetics field in treatments involving dysfunctions such as localized fat and fibroedema geloid. To work out perfectly, the principle active need to interact and create a set of factors that includes lipolysis intensification. The caffeine encapsulation in gel-based nanocosmetics has the purpose of taking this active up to the adipocyte, the target cell, for mentioned dysfunctions treatment. Thus, we aim to present a review of how has been, the use of caffeine in the production of cosmetics.
A evolução do mercado de beleza e cuidados pessoais é constante no Brasil e no resto do mundo. Os avanços tecnológicos trouxeram a nanotecnologia para o campo cosmetológico, empregando princípios ativos em átomos envolvidos por vesículas, a fim de levar o princípio ativo precisamente ao tecido alvo para otimizar os resultados alcançados devido à considerável facilidade de atravessar barreiras cutâneas. A fabricação de cosméticos nanotecnológicos é confrontada com baixa capacidade de absorção. Um dos muitos princípios ativos encontrados na indústria cosmética é a cafeína, um pseudoalocalóide do grupo xantina usado como estimulante no mecanismo da ação lipolítica. Este ativo é amplamente utilizado no campo da estética e dos cosméticos em tratamentos que envolvem disfunções, como gordura localizada e fibroedema gelóide. Para funcionar perfeitamente, o princípio ativo precisa interagir e criar um conjunto de fatores que inclui a intensificação da lipólise. O encapsulamento de cafeína em nanocosméticos à base de gel tem o objetivo de levar esse ativo até o adipócito, a célula alvo, para o tratamento de disfunções mencionado. Assim, objetivamos apresentar uma revisão de como tem sido o uso de cafeína na produção de cosméticos.
Asunto(s)
Absorción Cutánea , Cosméticos , Brasil , Cafeína , NanotecnologíaRESUMEN
ObjectiveTo establish a high⁃performance liquid chromatography (HPLC) quantitative method for the determination of epicatechin (EC), (-)⁃epicatechin gallate (ECG), (-)⁃epigallocatechin (EGC), (-)⁃epigallocatechin gallate (EGCG), (-)⁃gallocatechin (GC), (-)⁃gallocatechin gallate (GCG), (-)⁃catechin gallate (CG), cianidanol (CD) and gallic acid (GA) in cosmetics. MethodsSamples were prepared by ultrasonic extraction and followed by high-speed centrifugation of the extraction solution. The supernatant was filtered by 0.45 μm Millipore filter. The continued filtrate was taken for analysis. A reversed phase column, Kromasil 100-5 C18 (5 μm, 4.6 mm×250 mm) was used with 0.05% trifluoroacetic acid buffer and methanol as mobile phase under the condition of gradient elution. Diode array detection (DAD) method was used for the determination. Qualitative and quantitative determination was conducted in 10 batches of commercially available cosmetics. ResultsThe relative standard deviations (RSD) were in the range of 0.11%-6.30% (n=3); the recoveries were in the range of 84.4%-114.7%. The method showed a good linearity within the concentration range of 0.49-105.39 mg·L-1 (r>0.995). The detection limit was 5 μg·g-1. In 10 batches of commercially available cosmetics, three batches showed positive result, which was consistent with the UV spectrum of the standard. ConclusionThis method is efficient, sensitive and accurate. It is applicable to the determination of EC, ECG, EGC, EGCG, GC, GCG, CG, CD and GA in cosmetics.
RESUMEN
Natural collagen peptides are collagen hydrolysates. Because of their unique physicochemical properties and excellent biological activities, collagen peptides have been a research hotspot of cosmetic raw materials development and skincare efficacy improvement. Combined with the needs of the skincare efficacy and the development trends of cosmetics, the extraction methods and their structural characteristics of natural collagen peptides were summarized in detail. The applications and its research progress in skincare efficacy of collagen peptides, such as moisturizing and anti-wrinkle, trophism and anti-aging, filling and skin regeneration were expressed with emphasis. Finally, the development and practical applications in cosmetics of natural collagen peptides were adequately prospected.