ABSTRACT
We extended a mechanistic, physics-based framework of the dry down process, previously developed for liquids and electrolytes, to solids and coded it into the latest UB/UC/P&G skin permeation model, herein renamed DigiSkin. The framework accounts for the phase change of the permeant from dissolved in a solvent (liquid) to precipitated on the skin surface (solid). The evaporation rate for the solid is reduced due to lower vapor pressure for the solid state versus subcooled liquid. These vapor pressures may differ by two orders of magnitude. The solid may gradually redissolve and penetrate the skin. The framework was tested by simulating the in vitro human skin permeation of the 38 cosmetically relevant solid compounds reported by Hewitt et al., J. Appl. Toxicol. 2019, 1-13. The more detailed handling of the evaporation process greatly improved DigiSkin evaporation predictions (r2 = 0.89). Further, we developed a model reliability prediction score classification using diverse protein reactivity data and identified that 15 of 38 compounds are out of model scope. Dermal delivery predictions for the remaining chemicals have excellent agreement with experimental data. The analysis highlighted the sensitivity of water solubility and equilibrium vapor pressure values on the DigiSkin predictions outcomes influencing agreement with the experimental observations.
Subject(s)
Cosmetics , Keratins , Skin Absorption , Skin , Solvents , Solvents/chemistry , Humans , Hydrogen-Ion Concentration , Skin/metabolism , Keratins/chemistry , Cosmetics/chemistry , Cosmetics/pharmacokinetics , Administration, Cutaneous , Solubility , Models, Biological , Pharmaceutical Vehicles/chemistry , Phase TransitionABSTRACT
A novel magnetic dispersive solid phase extraction (MDSPE) procedure based on the deep eutectic solvent (DES) modified magnetic graphene oxide/metal organic frameworks nanocomposites (MGO@ZIF-8@DES) was established and used for the efficient enrichment of estradiol, estrone, and diethylstilbestrol in cosmetics (toner, lotion, and cream) for the first time. Then, the three estrogens were separated and determined by UHPLC-UV analysis method. In order to study the features and morphology of the synthesized adsorbents, various techniques such as FT-IR, SEM, and VSM measurements were executed. The MGO@ZIF-8@DES nanocomposites combine the advantages of high adsorption capacity, adequate stability in aqueous solution, and convenient separation from the sample solution. To achieve high extraction recoveries, the Box-Behnken design and single factor experiment were applied in the experimental design. Under the optimum conditions, the method detection limits for three estrogens were 20-30 ng g-1. This approach showed a good correlation coefficient (r more than 0.9998) and reasonable linearity in the range 70-10000 ng g-1. The relative standard deviations for intra-day and inter-day were beneath 7.5% and 8.9%, respectively. The developed MDSPE-UHPLC-UV method was successfully used to determine three estrogens in cosmetics, and acceptable recoveries in the intervals of 83.5-95.9% were obtained. Finally, three estrogens were not detected in some cosmetic samples. In addition, the Complex GAPI tool was used to evaluate the greenness of the developed pretreatment method. The developed MDSPE-UHPLC-UV method is sensitive, accurate, rapid, and eco-friendly, which provides a promising strategy for determining hormones in different complex samples.
Subject(s)
Cosmetics , Deep Eutectic Solvents , Estrogens , Graphite , Metal-Organic Frameworks , Nanocomposites , Solid Phase Extraction , Graphite/chemistry , Cosmetics/chemistry , Cosmetics/analysis , Nanocomposites/chemistry , Metal-Organic Frameworks/chemistry , Solid Phase Extraction/methods , Estrogens/analysis , Estrogens/isolation & purification , Estrogens/chemistry , Deep Eutectic Solvents/chemistry , Limit of Detection , Estradiol/chemistry , Estradiol/analysis , Estradiol/isolation & purification , Estrone/analysis , Estrone/chemistry , Estrone/isolation & purification , Adsorption , Diethylstilbestrol/analysis , Diethylstilbestrol/chemistry , Diethylstilbestrol/isolation & purification , Chromatography, High Pressure Liquid/methodsABSTRACT
The rise of polymer materials in modern life has drawn attention to renewable, easily biodegradable, environmentally-friendly bio-based polymers. Notably, significant research has been dedicated to creating green antimicrobial functional materials for the biomedical field using natural polymer materials. Cellulose is a rich natural biomass organic polymer material. Given its favorable attributes like film-forming capability, biodegradability, and biocompatibility, it is extensively employed to tackle a wide range of challenges confronting humanity today. However, its inherent drawbacks, such as insolubility in water and most organic solvents, hygroscopic nature, difficulty in melting, and limited antimicrobial properties, continue to pose challenges for realizing the high-value applications of cellulose. Achieving multifunctionality and more efficient application of cellulose still poses major challenges. In this regard, the current development status of cellulose materials was reviewed, covering the classification, preparation methods, and application status of cellulose-based antimicrobial materials. The application value of cellulose-based antimicrobial materials in biomedicine, textiles, food packaging, cosmetics and wastewater treatment was summarised. Finally, insights were provided into the developing prospects of cellulose-based antimicrobial materials were provided.
Subject(s)
Anti-Infective Agents , Cellulose , Cellulose/chemistry , Anti-Infective Agents/chemistry , Anti-Infective Agents/pharmacology , Humans , Food Packaging/methods , Textiles , Cosmetics/chemistry , Biocompatible Materials/chemistry , Biocompatible Materials/pharmacologyABSTRACT
Polyethylene glycols (PEGs) are used in industrial, medical, health care, and personal care applications. The cycling and disposal of synthetic polymers like PEGs pose significant environmental concerns. Detecting and monitoring PEGs in the real world calls for immediate attention. This study unveils the efficacy of time-of-flight secondary ion mass spectrometry (ToF-SIMS) as a reliable approach for precise analysis and identification of reference PEGs and PEGs used in cosmetic products. By comparing SIMS spectra, we show remarkable sensitivity in pinpointing distinctive ion peaks inherent to various PEG compounds. Moreover, the employment of principal component analysis effectively discriminates compositions among different samples. Notably, the application of SIMS two-dimensional image analysis visually portrays the spatial distribution of various PEGs as reference materials. The same is observed in authentic cosmetic products. The application of ToF-SIMS underscores its potential in distinguishing PEGs within intricate environmental context. ToF-SIMS provides an effective solution to studying emerging environmental challenges, offering straightforward sample preparation and superior detection of synthetic organics in mass spectral analysis. These features show that SIMS can serve as a promising alternative for evaluation and assessment of PEGs in terms of the source, emission, and transport of anthropogenic organics.
Subject(s)
Cosmetics , Polyethylene Glycols , Spectrometry, Mass, Secondary Ion , Cosmetics/analysis , Cosmetics/chemistry , Spectrometry, Mass, Secondary Ion/methods , Polyethylene Glycols/chemistry , Polyethylene Glycols/analysis , Principal Component AnalysisABSTRACT
PURPOSE: This study aimed to develop a novel exfoliating material with high efficacy and low irritation by synthesizing the Mandelic acid_Carnitine ion pairing complex (M_C complex) and evaluating its exfoliating properties. Additionally, the study assessed the skin improvement effects of the M_C complex through clinical evaluations. METHODS: The M_C complex was synthesized in a 1:1 molar ratio of Mandelic acid and Carnitine. Structural characterization was performed using dynamic light scattering and Fourier-transform infrared spectroscopy. Exfoliating efficacy was evaluated on porcine skin, and clinical assessments were conducted on human subjects to measure various skin improvement parameters. RESULTS: The formation of the M_C complex was confirmed through particle size analysis, zeta-potential measurements, and FT-IR spectroscopy. The M_C complex demonstrated superior exfoliating efficacy compared to Mandelic acid alone, especially at pH 4.5. Clinical evaluations showed significant improvements in blackheads, whiteheads, pore volume, depth, density, count, and affected area, as well as skin texture. No adverse reactions were observed. CONCLUSION: The M_C complex exhibits high exfoliating efficacy and minimal irritation, making it a promising cosmetic ingredient for improving skin health. These findings support its potential as a low-irritation exfoliating material under mildly acidic conditions, contributing to overall skin health enhancement.
Subject(s)
Carnitine , Cosmetics , Mandelic Acids , Mandelic Acids/chemistry , Mandelic Acids/pharmacology , Humans , Carnitine/pharmacology , Carnitine/chemistry , Animals , Swine , Cosmetics/pharmacology , Cosmetics/chemistry , Female , Adult , Skin/drug effects , Skin/chemistry , Male , Middle Aged , Spectroscopy, Fourier Transform InfraredABSTRACT
Microalgae are gaining attention as they are considered green fabrics able to synthesize many bioactive metabolites, with unique biological activities. However, their use at an industrial scale is still a challenge because of the high costs related to upstream and downstream processes. Here, a biorefinery approach was proposed, starting from the biomass of the green microalga Pseudococcomyxa simplex for the extraction of two classes of molecules with a potential use in the cosmetic industry. Carotenoids were extracted first by an ultrasound-assisted extraction, and then, from the residual biomass, lipids were obtained by a conventional extraction. The chemical characterization of the ethanol extract indicated lutein, a biosynthetic derivative of α-carotene, as the most abundant carotenoid. The extract was found to be fully biocompatible on a cell-based model, active as antioxidant and with an in vitro anti-aging property. In particular, the lutein-enriched fraction was able to activate Nrf2 pathway, which plays a key role also in aging process. Finally, lipids were isolated from the residual biomass and the isolated fatty acids fraction was composed by palmitic and stearic acids. These molecules, fully biocompatible, can find application as emulsifiers and softener agents in cosmetic formulations. Thus, an untapped microalgal species can represent a sustainable source for cosmeceutical formulations. KEY POINTS: ⢠Pseudococcomyxa simplex has been explored in a cascade approach. ⢠Lutein is the main extracted carotenoid and has antioxidant and anti-aging activity. ⢠Fatty acids are mainly composed of palmitic and stearic acids.
Subject(s)
Cosmetics , Microalgae , Microalgae/metabolism , Microalgae/chemistry , Cosmetics/chemistry , Carotenoids/chemistry , Carotenoids/isolation & purification , Biomass , Antioxidants/chemistry , Antioxidants/pharmacology , Antioxidants/isolation & purification , Lutein/isolation & purification , Lutein/chemistry , Lutein/metabolism , Humans , Fatty Acids/chemistryABSTRACT
Nanotechnology is revolutionizing fields of high social and economic impact. such as human health preservation, energy conversion and storage, environmental decontamination, and art restoration. However, the possible global-scale application of nanomaterials is raising increasing concerns, mostly related to the possible toxicity of materials at the nanoscale. The possibility of using nanomaterials in cosmetics, and hence in products aimed to be applied directly to the human body, even just externally, is strongly debated. Preoccupation arises especially from the consideration that nanomaterials are mostly of synthetic origin, and hence are often seen as "artificial" and their effects as unpredictable. Melanin, in this framework, is a unique material since in nature it plays important roles that specific cosmetics are aimed to cover, such as photoprotection and hair and skin coloration. Moreover, melanin is mostly present in nature in the form of nanoparticles, as is clearly observable in the ink of some animals, like cuttlefish. Moreover, artificial melanin nanoparticles share the same high biocompatibility of the natural ones and the same unique chemical and photochemical properties. Melanin is hence a natural nanocosmetic agent, but its actual application in cosmetics is still under development, also because of regulatory issues. Here, we critically discuss the most recent examples of the application of natural and biomimetic melanin to cosmetics and highlight the requirements and future steps that would improve melanin-based cosmetics in the view of future applications in the everyday market.
Subject(s)
Hair Color , Melanins , Melanins/chemistry , Melanins/metabolism , Humans , Animals , Cosmetics/chemistry , Nanoparticles/chemistry , Skin Pigmentation/drug effects , Nanostructures/chemistry , Nanotechnology/methodsABSTRACT
The growing demand for phycobiliproteins from microalgae generates a significant volume of by-products, such as extraction cakes. These cakes are enriched with products of interest for the cosmetics market, namely free fatty acids, particularly polyunsaturated (PUFA). In this work, two cakes, one of spirulina and one of Porphyridium cruentum, were valorized using innovative natural hydrophobic deep eutectic solvents (NaDES) based on alkanediols. The most promising NaDES, as determined by physicochemical properties and screening, are mixtures of alkanediols and fatty acids. These include the mixtures of 1,3-propanediol and octanoic acid (1:5, mol/mol) and 1,3-propanediol and octanoic and decanoic acid (1:3:1, mol/mol). Two extractive processes were implemented: ultrasound-assisted extraction and an innovative mechanical process involving dual asymmetric centrifugation. The second process resulted in the production of extracts significantly enriched in PUFA, ranging from 65 to 220 mg/g dry matter with the two cakes. The extracts and NaDES demonstrated good safety with respect to epidermal keratinocyte viability (>80% at 200 µg/mL). The study of their impact on commensal and pathogenic cutaneous bacteria demonstrated significant effects on the viability of Staphylococcus aureus and Staphylococcus epidermidis (>50% decrease at 200 µg/mL) while preserving Corynebacterium xerosis and Cutibacterium acnes. These results highlight the potential of valorizing these co-products using alkanediol-based NaDES, in a strategy combining an active vector (NaDES) and a growth regulator extract, for the management of cutaneous dysbiosis involving staphylococci.
Subject(s)
Fatty Acids, Nonesterified , Spirulina , Spirulina/chemistry , Humans , Deep Eutectic Solvents/chemistry , Microalgae/chemistry , Keratinocytes/drug effects , Cosmetics/chemistry , Dermatologic Agents/pharmacology , Dermatologic Agents/chemistry , Aquatic OrganismsABSTRACT
Cannabis-based products have gained attention in recent years for their perceived therapeutic benefits (with cannabinoids such as THC and CBD) and widespread availability. However, these products often lack accurate labelling regarding their cannabinoid content. Our study, conducted with products available in Portugal, revealed significant discrepancies between label claims and actual cannabinoid compositions. A fully validated method was developed for the characterisation of different products acquired from pharmacies and street shops (beverages, herbal samples, oils, and cosmetic products) using high-performance liquid chromatography coupled with a diode array detector. Linearity ranged from 0.4 to 100 µg/mL (0.04-10 µg/mg) (THC, 8-THC, CBD, CBG, CBDA, CBGA), 0.1-100 µg/mL (0.01-10 µg/mg) (CBN), 0.4-250 µg/mL (0.04-25 µg/mg) (THCA-A), and 0.8-100 µg/mL (0.08-10 µg/mg) (CBCA). Among sampled beverages, none contained detectable cannabinoids, despite suggestive packaging. Similarly, oils often differed from the declared cannabinoid compositions, with some containing significantly higher CBD concentrations than labelled. These inconsistencies raise serious concerns regarding consumer safety and informed decision-making. Moreover, our findings underscore the need for stringent regulation and standardised testing protocols to ensure the accuracy and safety of cannabis-based products.
Subject(s)
Cannabinoids , Cannabis , Portugal , Cannabinoids/analysis , Cannabinoids/chemistry , Cannabis/chemistry , Chromatography, High Pressure Liquid , Humans , Cosmetics/analysis , Cosmetics/chemistry , Beverages/analysis , Medical Marijuana/analysis , Medical Marijuana/chemistryABSTRACT
Grape marc is a by-product resulting from the winemaking industry that still contains beneficial compounds that can be valorized. Thus, we report here the possibility of using polyphenolic extracts of grape marc origin to obtain sun protection creams. The extractions were performed in ethanol and acetone solutions using pomace from different grape varieties (Merlot, Bläufrankisch, Feteasca Neagra, Isabella) as a raw material. The obtained extracts were analyzed in order to determine the total phenolic content, the antioxidant activity, and the sun protection factor (SPF) via Mansur spectrophotometric assay. The best results were achieved using 70% ethanol in water as a solvent. The extracts with the highest potential photoprotective effects are from the Merlot variety (SPFspectrophotometric = 7.83 ± 0.76). The sunscreens were prepared using the 70% ethanolic extract of the Merlot variety evaporated to dryness, redissolved in either distilled water or ethanol. The SPF estimated in vitro via the COLIPA method showed values of 14.07 ± 1.50 and 11.46 ± 1.32 for the aqueous and ethanolic extracts, respectively, when working with a cream to polyphenolic extract a ratio of 1/1 (w/w). At the same time, the use of aqueous polyphenolic extracts ensures the better stability of creams compared with the ethanolic ones.
Subject(s)
Antioxidants , Plant Extracts , Sunscreening Agents , Vitis , Sunscreening Agents/chemistry , Sunscreening Agents/pharmacology , Vitis/chemistry , Plant Extracts/chemistry , Plant Extracts/pharmacology , Antioxidants/chemistry , Antioxidants/pharmacology , Cosmetics/chemistry , Polyphenols/chemistry , Polyphenols/pharmacology , Wine/analysis , Biological Products/chemistry , Biological Products/pharmacology , Sun Protection FactorABSTRACT
Phenolic compounds represent a group of secondary metabolites that serve essential functions in plants. Beyond their positive impact on plants, these phenolic metabolites, often referred to as polyphenols, possess a range of biological properties that can promote skin health. Scientific research indicates that topically using phenolics derived from plants can be advantageous, but their activity and stability highly depend on storage of the source material and the extraction method. These compounds have the ability to relieve symptoms and hinder the progression of different skin diseases. Because they come from natural sources and have minimal toxicity, phenolic compounds show potential in addressing the causes and effects of skin aging, skin diseases, and various types of skin damage, such as wounds and burns. Hence, this review provides extensive information on the particular crops from which by-product phenolic compounds can be sourced, also emphasizing the need to conduct research according to proper plant material storage practices and the choice of the best extracting method, along with an examination of their specific functions and the mechanisms by which they act to protect skin.
Subject(s)
Cosmetics , Crops, Agricultural , Phenols , Phenols/chemistry , Cosmetics/chemistry , Humans , Plant Extracts/chemistry , Plant Extracts/pharmacology , Polyphenols/chemistryABSTRACT
Hyperpigmentation disorders may result from inappropriate melanin deposition and/or excessive melanin synthesis. They are classified mainly as aesthetic problems, but they can significantly affect human health by decreasing self-esteem. There are available only limited treatment options for hyperpigmentation disorder, among others, cosmetic products applied topically. Depigmenting ingredients were found to be ineffective and characterized by various side effects. As a result, many efforts are made to discover novel, potent, and safe melanogenesis inhibitors for possible use in topical cosmetic depigmenting formulations. Cinnamic acid derivatives constitute a widely tested group for that purpose. This article reports research in the group of N-alkyl cinnamamide derivatives (un)substituted in phenyl ring. Among tested series, (E)-3-(4-chlorophenyl)-N-(5-hydroxypentyl)acrylamide (compound 21) showed the most promising inhibitory properties in mushroom tyrosinase assay (IC50 = 36.98 ± 1.07 µM for monophenolase activity, IC50 = 146.71 ± 16.82 µM for diphenolase activity) and melanin production inhibition in B16F10 mouse melanoma cell line at concentration 6.25 µM resulting probably from decreasing of Tyr, Mitf, Tyrp-1, and Tyrp-2 genes expression. This compound also showed melanin production inhibitory properties in pigmented reconstructed human epidermis when used in 1 % and 2 % solutions in 50 % PEG400. In vitro evaluation of its safety profile showed no cytotoxicity to human keratinocytes HaCaT, human skin fibroblasts BJ, and human primary epidermal melanocytes HEMa, no mutagenicity in the Ames test, no genotoxicity in micronucleus test, no phototoxicity, as well as no skin irritation potential tested in PEG400 solution. This compound was also shown to penetrate across the epidermis to reach the possible site of action. The performed research led to classify (E)-3-(4-chlorophenyl)-N-(5-hydroxypentyl)acrylamide as a novel potential depigmenting cosmetic ingredient.
Subject(s)
Cinnamates , Cosmetics , Hyperpigmentation , Melanins , Monophenol Monooxygenase , Humans , Animals , Hyperpigmentation/drug therapy , Mice , Monophenol Monooxygenase/antagonists & inhibitors , Monophenol Monooxygenase/metabolism , Cinnamates/chemistry , Cinnamates/pharmacology , Cinnamates/chemical synthesis , Structure-Activity Relationship , Molecular Structure , Cosmetics/chemistry , Cosmetics/pharmacology , Melanins/metabolism , Dose-Response Relationship, Drug , Acrylamide/chemistry , Acrylamide/pharmacology , Drug Discovery , Enzyme Inhibitors/pharmacology , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/chemical synthesis , AgaricalesABSTRACT
Skin yellowness is a hallmark of dull or unhealthy skin, particularly among Asians. Previous research has indicated a link between skin glycation and skin yellowness. However, the specific glycated chemicals contributing to yellowish skin appearance have not been identified yet. Using HPLC-PDA-HRMS coupled with native and artificially glycated human epidermal explant skin, we identified intensely yellow colored glycated chromophores "(1R, 8aR) and (1S, 8aR)-4-(2-furyl)-7-[(2-furyl)-methylidene]-2-hydroxy-2H,7H,8AH-pyrano-[2,3-B]-pyran-3-one" (abbreviated as AGEY) from human skin samples for the first time. The abundance of AGEY was strongly correlated with skin yellowness in the multiple skin explant tissues. We further confirmed the presence of AGEY in cultured human keratinocytes and 3D reconstructed human epidermal (RHE) models. Additionally, we demonstrated that a combination of four cosmetic compounds with anti-glycation properties can inhibit the formation of AGEY and reduce yellowness in the RHE models. In conclusion, we have identified specific advanced glycation end products with an intense yellow color, namely AGEY, in human skin tissues for the first time. The series of study results highlighted the significant contribution of AGEY to the yellow appearance of the skin. Furthermore, we have identified a potential cosmetic solution to mitigate AGEY formation, leading to a reduction in yellowness in the in vitro RHE models.
Subject(s)
Glycation End Products, Advanced , Keratinocytes , Skin , Humans , Glycation End Products, Advanced/metabolism , Skin/metabolism , Keratinocytes/metabolism , Keratinocytes/drug effects , Chromatography, High Pressure Liquid , Glycosylation , Epidermis/metabolism , Cosmetics/chemistry , Female , Adult , Skin Pigmentation/drug effectsABSTRACT
Pharmaceuticals, personal care products (PPCPs), and endocrine-disrupting compounds (EDCs) have seen a recent sustained increase in usage, leading to increasing discharge and accumulation in wastewater. Conventional water treatment and disinfection processes are somewhat limited in effectively addressing this micropollutant issue. Ultrasonication (US), which serves as an advanced oxidation process, is based on the principle of ultrasound irradiation, exposing water to high-frequency waves, inducing thermal decomposition of H2O while using the produced radicals to oxidize and break down dissolved contaminants. This review evaluates research over the past five years on US-based technologies for the effective degradation of EDCs and PPCPs in water and assesses various factors that can influence the removal rate: solution pH, temperature of water, presence of background common ions, natural organic matter, species that serve as promoters and scavengers, and variations in US conditions (e.g., frequency, power density, and reaction type). This review also discusses various types of carbon/non-carbon catalysts, O3 and ultraviolet processes that can further enhance the degradation efficiency of EDCs and PPCPs in combination with US processes. Furthermore, numerous types of EDCs and PPCPs and recent research trends for these organic contaminants are considered.
Subject(s)
Cosmetics , Endocrine Disruptors , Water Pollutants, Chemical , Water Purification , Endocrine Disruptors/chemistry , Water Pollutants, Chemical/chemistry , Water Pollutants, Chemical/radiation effects , Pharmaceutical Preparations/chemistry , Cosmetics/chemistry , Water Purification/methods , Ultrasonics , Ultrasonic WavesABSTRACT
A peroxymonosulfate oxidation system was developed via modification of ß-cyclodextrin (ß-CD) on the surface of Fe2+-doped ZIF-67 (CD/Fe@ZIF-67) as an activator. The 99.7% carbamazepine, 91.3% bisphenol A (BPA), and 95.4% diclofenac (DCF) degradation efficiency were achieved within 10 min, 60, and 1 min, respectively. The hydrophobicity of these three pollutants is positively correlated with their adsorption kinetic constants by CD/Fe@ZIF-67 due to the introduction of ß-CD. Scavenger experiments and electron spin resonance spectra confirmed that carbamazepine was preferentially oxidized by SO4â¢- [λ(SO4â¢-)(70.5%) > λ(â¢OH)(28.2%) > λ(O2â¢-)(1.3%)], where SO4â¢- and O2â¢- played dominant roles in the degradation of BPA [λ(SO4â¢-)(71.7%) > λ(O2â¢-)(22.8%) > λ(â¢OH)(5.5%)], and O2â¢- was responsible for DCF removal [λ(O2â¢-) = 93.2%]. Additionally, the particulate catalyst was immobilized in the shell side of a ceramic membrane in a membrane reactor for catalyst recovery. This reactor achieved nearly 100% removal efficiency under optimal conditions: 0.036 wt % catalyst loading, 0.5 mM peroxymonosulfate concentration, 1 L inflow, 10 mg/L initial carbamazepine concentration, and 0.012 L/min hydraulic retention time. In summary, this study elucidates the active role of ß-CD in a polymetallic/peroxymonosulfate system and provides valuable insights into the development of effective oxidation methods for pharmaceutical and personal care products in wastewater.
Subject(s)
Carbamazepine , Nanocomposites , Water Pollutants, Chemical , beta-Cyclodextrins , beta-Cyclodextrins/chemistry , Water Pollutants, Chemical/chemistry , Carbamazepine/chemistry , Nanocomposites/chemistry , Water Purification/methods , Metal-Organic Frameworks/chemistry , Benzhydryl Compounds/chemistry , Oxidation-Reduction , Phenols/chemistry , Pharmaceutical Preparations/chemistry , Diclofenac/chemistry , Adsorption , Cosmetics/chemistry , Zeolites/chemistry , ImidazolesABSTRACT
The certification of cosmetic products has always been a prominent concern. Here, we have developed a pH sensor and applied it in the field of cosmetic safety. Initially, we designed two probes, CH with aggregation-induced emission (AIE) effect and the near-infrared fluorophore derivative CYTYR. By encapsulating them with DSPE-PEG2000-NH2, we obtained the CHCY-lipo nano-micelles with fluorescence resonance energy transfer (FRET) response. By combining them into a sensor array called pC, we achieved sensitive detection of a wide pH range, ranging from 4.69 to 9.25. To validate the performance of the pC sensor array, we employed a multi-channel mode and applied it to differentiate commercial anti-aging creams. Through linear discriminant analysis and 3D fingerprint analysis, the pC sensor array successfully distinguished anti-aging creams from different countries, providing a rapid and accurate method for cosmetic safety identification. The results of this study demonstrate the potential of the pC sensor array for quick authentication of cosmetic products, offering significant support and application prospects in safeguarding consumer health.
Subject(s)
Cosmetics , Hydrogen-Ion Concentration , Cosmetics/analysis , Cosmetics/chemistry , Humans , Fluorescence Resonance Energy Transfer/methods , Fluorescent Dyes/chemistry , Skin Cream/chemistryABSTRACT
Bacterial cellulose (BC) emerges as a versatile biomaterial with a myriad of industrial applications, particularly within the cosmetics sector. The absence of hemicellulose, lignin, and pectin in its pure cellulose structure enables favorable interactions with both hydrophilic and hydrophobic biopolymers. This enhances compatibility with active ingredients commonly employed in cosmetics, such as antioxidants, vitamins, and botanical extracts. Recent progress in BC-based materials, which encompasses membranes, films, gels, nanocrystals, and nanofibers, highlights its significant potential in cosmetics. In this context, BC not only serves as a carrier for active ingredients but also plays a crucial role as a structural agent in formulations. The sustainability of BC production and processing is a central focus, highlighting the need for innovative approaches to strengthen scalability and cost-effectiveness. Future research endeavors, including the exploration of novel cultivation strategies and functionalization techniques, aim to maximize BC's therapeutic potential while broadening its scope in personalized skincare regimes. Therefore, this review emphasizes the crucial contribution of BC to the cosmetics sector, underlining its role in fostering innovation, sustainability, and ethical skincare practices. By integrating recent research findings and industry trends, this review proposes a fresh approach to advancing both skincare science and environmental responsibility in the cosmetics industry.
Subject(s)
Cellulose , Cosmetics , Cosmetics/chemistry , Cellulose/chemistry , Humans , Bacteria , Biocompatible Materials/chemistryABSTRACT
BACKGROUND: The ongoing infusion of pharmaceutical and personal care products (PPCPs) into ecosystems sustains a perpetual life cycle and leads to multi-generational exposures. Limited understanding of their environmental impact and their intrinsic ability to induce physiological effect in humans, even at low doses, pose great risks to human health. Few scholarly works have conducted systematic research into the occurrence of PPCPs within potable water systems. Concurrently, the associated monitoring techniques have not been comprehensively examined with regards to the specific nature of drinking water, namely whether the significant presence of disinfectants may influence the detection of PPCPs. RESULTS: A modified approach in terms of detailed investigation of sample preservation and optimization of an in-lab fabricated solid phase extraction (SPE) cartridge filled with DVB-VP and PS-DVB sorbent was proposed. Favorable methodological parameters were achieved, with correlation coefficients spanning from 0.9866 to 0.9998. The LODs of the PPCPs fluctuated from 0.001 to 2 µg L-1, while the LOQs varied from 0.002 to 5 µg L-1. The analysis of spiked samples disclosed a methodological precision of 2.31-9.86 % and a recovery of 52.4-119 %. We utilized the established method for analyzing 14 water samples of three categories (source water, finished water and tap water) from five centralized water supply plants. A total of 24 categories encompassing 72 PPCPs were detected, with the concentrations of PPCPs manifested a marked decrease from source water to finished water and finally to tap water. SIGNIFICANCE: Our research meticulously examined the enhancement and purification effects of widely used commercial SPE cartridges and suggested the use of in-lab fabricated SPE cartridges packed with DVB-VP and PS-DVB adsorbents. We also conducted a systematic evaluation of the need to incorporate ascorbic acid and sodium thiosulfate as preservatives for PPCP measurement, in consideration of the unique characteristics of drinking water matrices, specifically, the significant concentration levels of disinfectants. Furthermore, the proposed method was effectively employed to study the presence of PPCPs in source water, finished water, and tap water collected from centralized water supply plants.
Subject(s)
Solid Phase Extraction , Water Pollutants, Chemical , Solid Phase Extraction/methods , Water Pollutants, Chemical/analysis , Water Pollutants, Chemical/isolation & purification , Pharmaceutical Preparations/analysis , Water Supply , Drinking Water/analysis , Cosmetics/analysis , Cosmetics/chemistry , Environmental Monitoring/methodsABSTRACT
Pharmaceuticals and personal care products (PPCPs) are emerging contaminants in aqueous systems, posing threat to both human health and environment. In prior research, predominant focus has been on examining various adsorbents for removing PPCPs from single-pollutant systems. However, no study has delved into simultaneous adsorption of PPCPs multi-pollutant mixture. This study evaluates performance of Azadirachta indica leaf extract-based green-synthesized ZnO nanoparticles coated on spent tea waste activated carbon (ZTAC) for removing sulfadiazine (SZN) and acetaminophen (ACN). Adsorption investigations were conducted in single-component (ACN/SZN) and binary-component (ACN + SZN) systems. The synthesized ZTAC was characterized using SEM, XRD, FTIR, EDX, porosimetry and pHpzc analysis. The study examines impact of time (1-60 min), dose (0.2-4 g/L), pH (2-12) and PPCPs concentration (1-100 mg/L) on ACN and SZN removal. Various kinetic and isotherm models were employed to elucidate mechanisms involved in sorption of PPCPs. Furthermore, synergistic and antagonistic aspects of sorption process in multi-component system were investigated. ZTAC, characterized by its crystalline nature and surface area of 980.85 m2/g, exhibited maximum adsorption capacity of 47.39 mg/g for ACN and 34.01 mg/g for SZN under optimal conditions of 15 min, 3 g/L and pH 7. Langmuir isotherm and pseudo-second-order kinetic model best-fitted the experimental data indicating chemisorption mechanism. Removal of ACN and SZN on ZTAC demonstrated synergistic nature, signifying cooperative adsorption. Overall, valorization of ZTAC offers effective and efficient adsorbent for elimination of PPCPs from wastewater.
Subject(s)
Azadirachta , Plant Extracts , Plant Leaves , Water Pollutants, Chemical , Zinc Oxide , Azadirachta/chemistry , Zinc Oxide/chemistry , Plant Extracts/chemistry , Plant Leaves/chemistry , Adsorption , Water Pollutants, Chemical/chemistry , Charcoal/chemistry , Cosmetics/chemistry , Pharmaceutical Preparations/chemistry , Green Chemistry Technology/methods , Tea/chemistry , Metal Nanoparticles/chemistryABSTRACT
RATIONALE: Illegal addition of anti-infective drugs to cosmetics at low concentrations has been found. The illicit addition of anti-infective drugs encompasses a wide variety of medications. The current sample purification methods are inadequate to detect all these compounds. A sensitive, wide-coverage, and weak-matrix-effect measurement method needs to be established to address this issue. METHODS: Samples were extracted using acetonitrile, diluted 25 times, and then analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS) to detect 111 anti-infective drugs. The method was validated and assessed for matrix effect before being applied to cosmetic products. RESULTS: The calibration curves for the analytes exhibited a strong correlation coefficient (r > 0.995). The limit of detection ranged from 0.006 to 0.6 mg/kg. Matrix effects were significantly improved after a 25-fold dilution. The method was successfully applied to various cosmetics. Two of 82 samples tested contained lincomycin and miconazole, respectively. CONCLUSIONS: The developed method is quick and reliable to analyze anti-infective drugs in cosmetics, with potential for both qualitative and quantitative analyses. It is a valuable tool for cosmetic research and development, contributing to safer and more effective cosmetic products.