RESUMO
In this study, 241 vegetable-oil food samples were collected from the Hangzhou market in China and analysed for fatty acid esters of 3- and 2-monochloropropanediol (3-MCPD and 2-MCPD) using non-derivative gas chromatography tandem mass spectrometry (GC-MS/MS). Food consumption data were taken from a food consumption survey of urban and rural residents in Hangzhou city performed in 2010-2011. Levels of 3-MCPD esters in edible oil ranged from not detected to 7.98 mg/kg, and the highest mean levels were found in tea seed oil, with concentrations of 2.94 mg/kg. Esters of 2-MCPD levels ranged from not detected to 4.03 mg/kg, and the highest mean levels were also found in tea seed oil, containing 1.49 mg/kg. The range of mean dietary intake of 3-MCPD esters in different groups of edible oil was from 0.096 to 1.54 µg/kg body weight (bw) per day, which is lower than the tolerable daily intake (TDI) established by the European Food Safety Authority (EFSA) (2 µg/kg bw/day). For people aged above 6 years old, the dietary intake of 3-MCPD from edible oil was 0.42 µg/kg bw per day (mean) and 1.22 µg/kg bw per day (P97.5). The range of mean dietary intake of 2-MCPD esters in different groups of edible oil was from 0.025 to 0.79 µg/kg bw/day, and 2-MCPD esters intake was 0.20 µg/kg bw per day (mean) and 0.60 µg/kg bw per day (P97.5). In addition, the dietary intake exposure to 3-MCPD and 2-MCPD esters for urban residents was lower than that for rural residents. The findings indicate that the potential health risks caused by dietary 3-MCPD esters from edible oils were of low concern for most of the Hangzhou residents. However, the exposure risk for consumers with excessive consumption of certain kind of edible oil calls for attention.
Assuntos
Óleos de Plantas/química , Propilenoglicóis/química , China , Exposição Dietética , Análise de Alimentos , Contaminação de Alimentos , Humanos , Propilenoglicóis/análise , Medição de RiscoRESUMO
Caffeic acid phenethyl ester (CAPE), a major pharmacologically active component of poplar type propolis, is known for its proapoptotic, anti-inflammatory, antioxidant, antiviral, and enzyme inhibiting activities. The aim of this study was to perform an in vitro and in vivo safety assessment of a micellar system based on a newly synthesized copolymer, consisting of polyglycidol and poly(allyl glycidyl ether) (C12-PAGE-PG) as a drug delivery platform for CAPE. The in vitro studies on HepG2 and L929 cells by MTT and LDH assays after treatment with the empty and CAPE-loaded micelles showed no cytotoxic effects of the empty micelles and retained cytotoxic activity of CAPE loaded in the micelles. No hemolysis or stimulation of mouse lymphocytes or macrophages was observed in vitro. In vivo hematological, biochemical, and histological assays on rats, treated with the empty (2580 and 5160 µg/kg) or CAPE-loaded (375 and 750 µg CAPE/kg) micelles did not reveal pathological changes of any of the parameters assayed after 14-days' treatment. In conclusion, initial toxicological data characterize C12-PAGE-PG as a non-toxic and promising copolymer for development of micellar drug delivery systems, particularly for a hydrophobic active substance as CAPE.
Assuntos
Ácidos Cafeicos/administração & dosagem , Sistemas de Liberação de Medicamentos , Álcool Feniletílico/análogos & derivados , Polímeros/química , Animais , Ácidos Cafeicos/toxicidade , Linhagem Celular , Compostos de Epóxi/química , Células Hep G2 , Humanos , Interações Hidrofóbicas e Hidrofílicas , Masculino , Camundongos , Micelas , Álcool Feniletílico/administração & dosagem , Álcool Feniletílico/toxicidade , Propilenoglicóis/química , Ratos , Ratos WistarRESUMO
Nanostructured lipid carriers (NLC) and nanoemulsions (NE) are colloid carriers which could improve dermal delivery of tacrolimus. The aims of this study were to evaluate effects of different formulation and process parameters on physicochemical characteristics and stability of lecithin-based NLC with glyceryl palmitostearate as solid and propylene glycol monocaprylate as liquid lipid and to compare the influence of different inner structure of tacrolimus-loaded NLC and corresponding NE on physicochemical characteristics, stability, entrapment efficiency, in vitro drug release and overall skin performance. Solid/liquid lipid ratio, total amount of lipids, homogenization pressure and cooling after the preparation were identified as critical variables in NLC development. Moreover, tacrolimus-loaded NLC emerged as more stabile carrier than NE. Differential stripping performed on porcine ear skin revealed significantly higher tacrolimus amount in stratum corneum from nanocarriers compared to referent ointment (Protopic®). Similarly the highest amount of tacrolimus in hair follicles was obtained using NLC (268.54⯱â¯92.38â¯ng/cm2), followed by NE (128.17⯱â¯48.87â¯ng/cm2) and Protopic® (77.61⯱â¯43.25â¯ng/cm2). Contrary, the highest permeation rate through full-thickness porcine ear skin was observed for Protopic®, implying that the selection of experimental setup is critical for reliable skin performance assessment. Overall, developed NLC could be suggested as promising carrier in a form of lotion for tacrolimus dermal delivery.
Assuntos
Portadores de Fármacos/administração & dosagem , Imunossupressores/administração & dosagem , Lecitinas/administração & dosagem , Nanoestruturas/administração & dosagem , Tacrolimo/administração & dosagem , Administração Cutânea , Animais , Caprilatos/administração & dosagem , Caprilatos/química , Portadores de Fármacos/química , Composição de Medicamentos , Liberação Controlada de Fármacos , Emulsões , Imunossupressores/química , Lecitinas/química , Lipídeos/administração & dosagem , Lipídeos/química , Nanoestruturas/química , Pomadas , Propilenoglicóis/administração & dosagem , Propilenoglicóis/química , Pele/metabolismo , Absorção Cutânea , Suínos , Tacrolimo/químicaRESUMO
Electronic cigarette has the potential to serve as a tobacco cessation aid if the prerequisites which are safety and efficacy in term of nicotine delivery are achieved. The nicotine-based liquids are mainly composed by propylene glycol and glycerol playing the important role of airborne carriers. 1,3 propanediol is proposed as a propylene glycol substitute to potentially improve the thermal stability, nicotine delivery and to decrease inhaled flavors concentrations. We have implemented various thermal, physicochemical and computational methods to evaluate the use of 1,3 propanediol as a substitute (or additional ingredient) to propylene glycol in e-liquids compositions. Our results indicate that 1,3 propanediol is stable upon heating when electronic cigarette are used in recommended conditions. We demonstrate that 1,3 propanediol gave better thermic profile compared to propylene glycol and glycerol, showing less thermal decomposition by-products. In addition, 1,3 propanediol gives to nicotine a more basic environment ensuring a high level of free base nicotine form. We have also established a quantum mechanical based computational method to validate e-liquids as flavor enhancer. Our findings showed that globally 1,3 propanediol seems to have better flavoring properties than glycerol and propylene glycol. Finally, 1,3 propanediol seems to induce quite similar aerodynamic properties compared to propylene glycol and glycerol.
Assuntos
Sistemas Eletrônicos de Liberação de Nicotina/métodos , Aromatizantes/química , Nicotina/administração & dosagem , Propilenoglicol/química , Propilenoglicóis/química , Simulação por Computador , Aromatizantes/efeitos adversos , Glicerol/química , Temperatura Alta , Modelos Químicos , Propilenoglicol/efeitos adversos , Propilenoglicóis/efeitos adversos , Espectroscopia de Prótons por Ressonância Magnética , Dispositivos para o Abandono do Uso de TabacoRESUMO
The Cosmetic Ingredient Review (CIR) Expert Panel (Panel) reviewed the safety of tromethamine, aminomethyl propanediol, and aminoethyl propanediolas used in cosmetics. All 3 ingredients are reported to function in cosmetics as pH adjusters, and tromethamine and aminomethyl propanediol are also reported to function as fragrance ingredients. The Panel reviewed relevant animal and human data related to these ingredients, along with a previous safety assessment of aminomethyl propanediol. The Panel concluded that tromethamine, aminomethyl propanediol, and aminoethyl propanediol are safe in cosmetics in the practices of use and concentration as given in this safety assessment.
Assuntos
Cosméticos/efeitos adversos , Cosméticos/química , Propilenoglicóis/efeitos adversos , Trometamina/efeitos adversos , Animais , Linhagem Celular , Sobrevivência Celular/efeitos dos fármacos , Qualidade de Produtos para o Consumidor , Humanos , Estrutura Molecular , Propilenoglicóis/administração & dosagem , Propilenoglicóis/química , Propilenoglicóis/farmacocinética , Ratos , Trometamina/administração & dosagem , Trometamina/química , Trometamina/farmacocinéticaRESUMO
The stability and bio-distribution of genes or drug complexes with poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO, Pluronic F-68) polymeric micelles (PM) are essential for an effective nanosized PM delivery system. We used Förster resonance energy transfer (FRET) pairs with PM and measured the FRET ratio to assess the stability of PM in vitro and in vivo on the cornea. The FRET ratio reached a plateau at 0.8 with 3% PM. Differential scanning calorimetry measurement confirmed the complex formation of FRET pairs with PM. Confocal imaging with the fluorophores fluorescein isothiocyanate isomer I (FITC) and rhodamine B base (RhB) also showed the occurrence of FRET pairs in vitro. The fluorophores were mixed with 3% PM solution or the FITC-labeled PEO-PPO-PEO polymers (FITC-P) were mixed with RhB-labeled plasmids (RhB-DNA). In addition, the in vitro corneal permeation of FRET pair complexes with PM reached a 0.8 FRET ratio. One hour after eye drop administration, FRET pairs colocalized in the cytoplasm, and surrounded and entered the nuclei of cells in the cornea, and the polymers were located in the corneal epithelial layers, as detected through anti-PEG immunohistochemistry. Furthermore, fluorescence colocalization in the cytoplasm and cell nucleus of the corneal epithelium was confirmed in tissues where RhB or RhB-DNA complexed with FITC-P was found to accumulate. We demonstrate that at a concentration of 3%, PM can encapsulate FRET pairs or RhB-DNA and retain their integrity within the cornea 1 h after administration, suggesting the feasibility and stability of PEO-PPO-PEO polymers as a vehicle for drug delivery.
Assuntos
Córnea/química , Sistemas de Liberação de Medicamentos/métodos , Soluções Oftálmicas/química , Plasmídeos/química , Polietilenoglicóis/química , Propilenoglicóis/química , Animais , Córnea/efeitos dos fármacos , Córnea/metabolismo , Portadores de Fármacos/química , Portadores de Fármacos/metabolismo , Sistemas de Liberação de Medicamentos/instrumentação , Transferência Ressonante de Energia de Fluorescência , Interações Hidrofóbicas e Hidrofílicas , Masculino , Camundongos Endogâmicos BALB C , Camundongos Nus , Soluções Oftálmicas/metabolismo , Soluções Oftálmicas/farmacologia , Plasmídeos/metabolismo , Polietilenoglicóis/metabolismo , Propilenoglicóis/metabolismoRESUMO
The Cosmetic Ingredient Review (CIR) Expert Panel assessed the safety of 131 alkyl polyethylene glycol (PEG)/polypropylene glycol ethers as used in cosmetics, concluding that these ingredients are safe in the present practices of use and concentration described in this safety assessment when formulated to be nonirritating. Most of the alkyl PEG/PPG ethers included in this review are reported to function in cosmetics as surfactants, skin-conditioning agents, and/or emulsifying agents. The alkyl PEG/PPG ethers share very similar physiochemical properties as the alkyl PEG ethers, which were reviewed previously by the CIR Expert Panel and found safe when formulated to be nonirritating. The alkyl PEG ethers differ by the inclusion of PPG repeat units, which are used to fine-tune the surfactant properties of this group. The Panel relied heavily on data on analogous ingredients, extracted from the alkyl PEG ethers and PPG reports, when making its determination of safety.
Assuntos
Qualidade de Produtos para o Consumidor , Cosméticos , Éteres/toxicidade , Polietilenoglicóis/toxicidade , Propilenoglicóis/toxicidade , Alquilação , Animais , Fármacos Dermatológicos/química , Fármacos Dermatológicos/farmacocinética , Fármacos Dermatológicos/toxicidade , Emulsificantes/química , Emulsificantes/farmacocinética , Emulsificantes/toxicidade , Éteres/química , Éteres/farmacocinética , Humanos , Polietilenoglicóis/química , Polietilenoglicóis/farmacocinética , Propilenoglicóis/química , Propilenoglicóis/farmacocinética , Tensoativos/química , Tensoativos/farmacocinética , Tensoativos/toxicidade , Testes de ToxicidadeRESUMO
Propylene glycol is an aliphatic alcohol that functions as a skin conditioning agent, viscosity decreasing agent, solvent, and fragrance ingredient in cosmetics. Tripropylene glycol functions as a humectant, antioxidant, and emulsion stabilizer. Polypropylene glycols (PPGs), including PPG-3, PPG-7, PPG-9, PPG-12, PPG-13, PPG-15, PPG-16, PPG-17, PPG-20, PPG-26, PPG-30, PPG-33, PPG-34, PPG-51, PPG-52, and PPG-69, function primarily as skin conditioning agents, with some solvent use. The majority of the safety and toxicity information presented is for propylene glycol (PG). Propylene glycol is generally nontoxic and is noncarcinogenic. Clinical studies demonstrated an absence of dermal sensitization at use concentrations, although concerns about irritation remained. The CIR Expert Panel determined that the available information support the safety of tripropylene glycol as well as all the PPGs. The Expert Panel concluded that PG, tripropylene glycol, and PPGs ≥3 are safe as used in cosmetic formulations when formulated to be nonirritating.
Assuntos
Qualidade de Produtos para o Consumidor , Cosméticos/química , Fármacos Dermatológicos/toxicidade , Polímeros/toxicidade , Propilenoglicol/toxicidade , Propilenoglicóis/toxicidade , Administração Cutânea , Animais , Antioxidantes/administração & dosagem , Antioxidantes/química , Antioxidantes/farmacocinética , Antioxidantes/toxicidade , Cosméticos/toxicidade , Fármacos Dermatológicos/administração & dosagem , Fármacos Dermatológicos/química , Fármacos Dermatológicos/farmacocinética , Humanos , Polímeros/administração & dosagem , Polímeros/química , Polímeros/farmacocinética , Propilenoglicol/administração & dosagem , Propilenoglicol/química , Propilenoglicol/farmacocinética , Propilenoglicóis/administração & dosagem , Propilenoglicóis/química , Propilenoglicóis/farmacocinética , Higiene da Pele/efeitos adversos , Testes de Toxicidade , ViscosidadeRESUMO
Low-density polyethylene (LDPE) samples were treated in air plasma discharge, coated by polyallyamine brush thought copolymeric grafting surface-from reaction and deposited four common antibacterial agents (benzalkonium chloride, bronopol, chlorhexidine and triclosan) to gain material with active antibacterial properties. Surface characteristics were evaluated by static contact angle measurement with surface energy evaluation ATR-FTIR, X-ray Photoelectron Spectroscopy (XPS) and SEM analysis. Inhibition zone on agar was used as in vitro test of antibacterial properties on two representative gram positive Staphylococcus aureus (S. aureus) and gram negative Escherichia coli (E. coli) strains. It was confirmed, that after grafting of polyallyamine, more antibacterial agent is immobilized on the surface. The highest increase of antibacterial activity was observed by the sample containing triclosan. Samples covered by bronopol did not show significant antibacterial activity.
Assuntos
Alilamina/química , Antibacterianos/química , Polietileno/química , Antibacterianos/farmacologia , Compostos de Benzalcônio/química , Clorexidina/química , Testes de Sensibilidade Microbiana , Estrutura Molecular , Espectroscopia Fotoeletrônica , Poliaminas/química , Propilenoglicóis/química , Espectroscopia de Infravermelho com Transformada de Fourier , Triclosan/químicaRESUMO
Medical-grade polyvinyl chloride was surface modified by a multistep physicochemical approach to improve bacterial adhesion prevention properties. This was fulfilled via surface activation by diffuse coplanar surface barrier discharge plasma followed by radical graft copolymerization of acrylic acid through surface-initiated pathway to render a structured high density brush. Three known antibacterial agents, bronopol, benzalkonium chloride, and chlorhexidine, were then individually coated onto functionalized surface to induce biological properties. Various modern surface probe techniques were employed to explore the effects of the modification steps. In vitro bacterial adhesion and biofilm formation assay was performed. Escherichia coli strain was found to be more susceptible to modifications rather than Staphylococcus aureus as up to 85% reduction in adherence degree of the former was observed upon treating with above antibacterial agents, while only chlorhexidine could retard the adhesion of the latter by 50%. Also, plasma treated and graft copolymerized samples were remarkably effective to diminish the adherence of E. coli.
Assuntos
Materiais Biocompatíveis/química , Cloreto de Polivinila/química , Anti-Infecciosos/farmacologia , Aderência Bacteriana , Compostos de Benzalcônio/química , Biofilmes , Clorexidina/química , Desenho de Fármacos , Escherichia coli/metabolismo , Modelos Químicos , Propilenoglicóis/química , Staphylococcus aureus/metabolismo , Propriedades de Superfície , MolhabilidadeRESUMO
This study aimed to develop a biofilter packed only with fern chips for the removal of airborne propylene glycol monomethyl ether acetate (PGMEA). Fern chips could avoid the shortcomings of traditional media, such as compaction, drying, and breakdown, which lead to the performance failure of the biofilters. In addition, the fern chip medium has the following merits: (1) simplicity in composition; (2) low pressure drop for gas flow (<20 mmH2O x m(-1)); (3) simple in humidification, nutrient addition, pH control, and metabolite removal; (4) economical (US$174-385 x m(-3)), and (5) low weight (wet basis around 290 kg x m(-3)). A two-stage downflow biofilter (2.18 m in height and 0.4 x 0.4 m in cross-sectional area) was constructed for the performance test. Both stages were packed with fern chips of 0.30 m in height and 0.40 x 0.40 m in cross-section. Results indicate that with operation conditions of media moisture content controlled in the range of 50-74%, media pH of 6.5-8.3, empty bed retention time (EBRT) of 0.27-0.4 min, influent PGMEA concentrations of 100-750 mg x m(-3), volumetric organic loading of <170 g x m(-3) x hr(-1), and nutrition rates of Urea-nitrogen 66 g x m(-3) x day(-3), potassium dihydrogen phosphate (KH2PO4)-phosphorus 13.3 g x m(-3) x day(-3), and milk powder 1.00 g x m(-3) x day(-1), the fern-chip-packed biofilter could achieve an overall PGMEA removal efficacy of around 94%. Instant milk powder or liquid milk was essential to the good and stable performance of the biofilter for PGMEA removal.
Assuntos
Poluentes Atmosféricos/química , Gleiquênias/química , Filtração/instrumentação , Filtração/métodos , Propilenoglicóis/química , Poluição do Ar/prevenção & controle , Filtração/economia , EsgotosRESUMO
Little information is yet available on the economic viability of the production of bio-based bulk chemicals and intermediates from white biotechnology (WB). This paper details a methodology to systematically evaluate the techno-economic prospects of present and future production routes of bio-based bulk chemicals produced with WB. Current and future technology routes are evaluated for 15 products assuming prices of fermentable sugar between 70 euro/t and 400 euro/t and crude oil prices of US $25/barrel and US $50/barrel. The results are compared to current technology routes of petrochemical equivalents. For current state-of-the-art WB processes and a crude oil price of US $25/barrel, WB-based ethanol, 1,3-propanediol, polytrimethylene terephthalate and succinic acid are economically viable. Only three WB products are economically not viable for future technology: acetic acid, ethylene and PLA. Future-technology ethylene and PLA become economically viable for a higher crude oil price (US $50/barrel). Production costs plus profits of WB products decrease by 20-50% when changing from current to future technology for a crude oil price of US $25 per barrel and across all sugar prices. Technological progress in WB can thus contribute significantly to improved economic viability of WB products. A large-scale introduction of WB-based production of economically viable bulk chemicals would therefore be desirable if the environmental impacts are smaller than those of current petrochemical production routes.
Assuntos
Biotecnologia/métodos , Biotecnologia/tendências , Indústria Química/tendências , Biotecnologia/economia , Carboidratos/química , Carboidratos/economia , Indústria Química/economia , Fermentação , Petróleo/classificação , Petróleo/economia , Ácidos Ftálicos/química , Ácidos Ftálicos/economia , Propilenoglicóis/química , Propilenoglicóis/economia , Ácido Succínico/química , Ácido Succínico/economiaRESUMO
The Polypropylene Glycol (PPG) Butyl Ethers function as skinand hair-conditioning agents in cosmetics. Intestinal absorption of the PPG Butyl Ethers was inversely proportional to the molecular weight. In general, the toxicity of the PPG Butyl Ethers decreased as the molecular weight increased. In acute studies, moderate intraperitoneal (IP) doses of various PPG Butyl Ethers caused convulsive seizures in mice and anesthetized dogs, and large oral doses caused decreased activity, anuria, renal tubular swelling and necrosis, and hepatic swelling and necrosis. PPG-2 Butyl Ether vapors were nontoxic by the inhalation route. PPG-2 Butyl Ether was nontoxic in short-term feeding and dermal exposure studies in rats. In animal irritation studies, PPG-2 Butyl Ether caused minor, transient erythema and desquamation; in addition, erythema, edema, ecchymosis, necrosis, and other changes were observed during an acute percutaneous study. PPG-2 Butyl Ether also caused minor to moderate conjunctival irritation and minor corneal injury. PPG-2 Butyl Ether when dermally applied was nontoxic to pregnant rats and was nonteratogenic at doses up to 1.0 ml/kg/day. PPG BE800 at concentrations of 0.001% to 0.26% in feed was noncarcinogenic to rats after 2 years of treatment. In clinical studies, PPG BE800 was nonirritating and nonsensitizing to the skin when tested using 200 subjects. PPG-40 Butyl Ether was neither an irritant nor a sensitizer in a repeat-insult patch test using 112 subjects. Although clinical testing did not indicate significant skin irritation is produced by these ingredients, the animal test data did indicate the potential that these ingredients can be irritating. Therefore, it was concluded that the PPG Butyl Ethers can be used safely in cosmetic products if they are formulated to avoid irritation. Data on the component ingredients, Propylene Glycol, PPG, and n-Butyl Alcohol, from previous cosmetic ingredient safety assessments were also considered and found to support the safety of PPG Butyl Ethers.
Assuntos
Qualidade de Produtos para o Consumidor , Cosméticos/toxicidade , Propilenoglicóis/toxicidade , Testes de Toxicidade , Animais , Cosméticos/química , Vias de Administração de Medicamentos , Humanos , Propilenoglicóis/químicaRESUMO
The Polypropylene Glycol (PPG) Stearyl Ethers are polypropylene ethers of stearyl ether that function as skin-conditioning agent in cosmetic formulations. Few data on the PPG Stearyl Ethers were available. Data on chemically related PPG Butyl Ethers were reviewed as a further basis for the assessment of safety. The amounts of PPG Butyl Ethers absorbed from the digestive tract were inversely proportional to the molecular weights on the compounds; skin penetration was slow to nil. During metabolism, the butyl group was removed and oxidized, and the chains were fragmented, oxidized to weak acids, and eliminated in the urine. Little acute oral toxicity was seen in animal studies. In general, the PPG Butyl Ethers were very toxic by the intravenous route and were slightly toxic to nontoxic by the intraperitoneal and subcutaneous routes. The smaller molecular weight ethers were generally more toxic than the larger molecular weight ethers. PPG-2 Butyl Ether vapor was nontoxic by the inhalation route. Undiluted PPG-15 Stearyl Ether was practically nonirritating to the eyes of rabbits, and PPG Butyl Ethers had minor to moderate conjunctival irritation, opacity, and iritis. PPG-15 Stearyl Ether was slightly irritating to rabbit skin. PPG-2 Butyl Ether caused minor, transient erythema and desquamation during a 4-hour occlusive patch test. PPG-2 Butyl Ether did not irritate the skin of pregnant mice, was nontoxic to dams, and was not teratogenic. PPG-9-13 Butyl Ether was noncarcinogenic when fed to rats. PPG-40 Butyl Ether was nonsensitizing in clinical tests. These data were considered by the Cosmetic Ingredient Review Expert Panel to support the safety of PPG Stearyl Ethers at their current use concentrations (2% to 10%, but not greater than 25%). Data on the component ingredients, Propylene Glycol, PPG, and Steraryl Alcohol, from previous cosmetic ingredient safety assessments were also considered and found to support the safety of PPG Stearyl Ethers.