RESUMO
The aim of this study was to assess the Al dietary exposure of young Chinese children aged 0-3 years via formulae, complementary foods and wheat-based foods. Al residue data were obtained from the national food contamination monitoring programme from 2013 to 2016, encompassing 13,833 samples of 12 food items with a detection rate of 76.0%. Food consumption data were gathered from the China National Food Consumption Survey conducted in 2015, comprising 20,172 children aged 0-3 years old. The mean dietary exposure to Al for the general population of young Chinese children was estimated at 0.76 mg/kg bw/week, which does not exceed the PTWI. The 97.5th percentile intakes of Al reached 3.42 mg/kg bw/week, more than 1.7 times the PTWI. Wheat-based foods contributed 80.5% of the Al intake for the general population of young Chinese children, while formulae and complementary foods accounted for 19.5% of the total intake. The dietary intake of Al from formulae and complementary foods accounted for 6.0% and 1.6% of PTWI, respectively. These findings suggested that dietary exposure to Al among the general population of young Chinese children was lower than the PTWI and that there are no health concerns related to this level of Al intake. However, more attention should be placed on the health risks associated with Al exposure from wheat-based foods for young consumers with high food consumption in China (97.5th percentile).
Assuntos
Alumínio/análise , Exposição Dietética/análise , Análise de Alimentos , Contaminação de Alimentos/análise , Alumínio/administração & dosagem , Pré-Escolar , Humanos , Lactente , Recém-NascidoRESUMO
A clinical pharmacokinetic study was performed in 12 healthy women to evaluate systemic exposure to aluminum following topical application of a representative antiperspirant formulation under real-life use conditions. A simple roll-on formulation containing an extremely rare isotope of aluminum (26 Al) chlorohydrate (ACH) was prepared to commercial specifications. A 26 Al radio-microtracer was used to distinguish dosed aluminum from natural background, using accelerated mass spectroscopy. The 26 Al citrate was administered intravenously (i.v.) to estimate fraction absorbed (Fabs ) following topical delivery. In blood samples after i.v. administration, 26 Al was readily detected (mean area under the curve (AUC) = 1,273 ± 466 hours×fg/mL). Conversely, all blood samples following topical application were below the lower limit of quantitation (LLOQ; 0.12 fg/mL), except two samples (0.13 and 0.14 fg/mL); a maximal AUC was based on LLOQs. The aluminum was above the LLOQ (61 ag/mL) in 31% of urine samples. From the urinary excretion data, a conservative estimated range for dermal Fabs of 0.002-0.06% was calculated, with a mean estimate of 0.0094%.
Assuntos
Alumínio/farmacocinética , Antiperspirantes/efeitos adversos , Radioisótopos/farmacocinética , Absorção Cutânea , Administração Cutânea , Administração Intravenosa , Adulto , Alumínio/administração & dosagem , Alumínio/efeitos adversos , Antiperspirantes/química , Área Sob a Curva , Qualidade de Produtos para o Consumidor , Feminino , Voluntários Saudáveis , Humanos , Parestesia/induzido quimicamente , Parestesia/epidemiologia , Prurido/induzido quimicamente , Prurido/epidemiologia , Radioisótopos/administração & dosagem , Radioisótopos/efeitos adversos , Eliminação Renal , Adulto JovemRESUMO
Inhalative exposure can occur accidentally when using cosmetic spray products. Usually, a tiered approach is applied for exposure assessment, starting with rather conservative, simplistic calculation models that may be improved with measured data and more refined modelling. Here we report on an advanced methodology to mimic in-use conditions for antiperspirant spray products to provide a more accurate estimate of the amount of aluminium possibly inhaled and taken up systemically, thus contributing to the overall body burden. Four typical products were sprayed onto a skin surrogate in defined rooms. For aluminium, size-related aerosol release fractions, i.e. inhalable, thoracic and respirable, were determined by a mass balance method taking droplet maturation into account. These data were included into a simple two-box exposure model, allowing calculation of the inhaled aluminium dose over 12 min. Systemic exposure doses were calculated for exposure of the deep lung and the upper respiratory tract using the Multiple Path Particle Deposition Model (MPPD) model. The total systemically available dose of aluminium was in all cases found to be less than 0.5 µg per application. With this study it could be demonstrated that refinement of the input data of the two-box exposure model with measured data of released airborne aluminium is a valuable approach to analyse the contribution of antiperspirant spray inhalation to total aluminium exposure as part of the overall risk assessment. We suggest the methodology which can also be applied to other exposure modelling approaches for spray products, and further is adapted to other similar use scenarios.
Assuntos
Alumínio/análise , Antiperspirantes/química , Exposição por Inalação/análise , Aerossóis , Alumínio/administração & dosagem , Qualidade de Produtos para o Consumidor , Humanos , Pulmão , Tamanho da Partícula , Medição de RiscoRESUMO
In order to address the issue of excessive intake of aluminium (Al) from Al-containing food additives in the Chinese diet, this study conducted a dietary exposure assessment of Al in the general population based on the national surveillance data of Al content in foods and national food consumption data. It was found that the mean dietary exposure of the whole Chinese population to Al from Al-containing food additives was 1.795 mg kgâ1 bw weekâ1, not exceeding the PTWI, while high dietary exposures (e.g., 97.5th percentile) to Al were 7.660 and 2.103-2.903 mg kgâ1 bw weekâ1 for children, respectively, both exceeding the PTWI. It was found that the dietary exposure to Al for 32.5% of the total Chinese population and 42.6% of children aged 4-6 years exceeded the PTWI. Wheat flour and wheat-based products are the main source of dietary A l exposure (85% of the total intake); and puffed foods are the major source of Al intake for children. These findings suggested that consumption of Al-containing food additives could be a health concern for consumers with high food consumption (97.5th percentile) and children under the age of 14 years.
Assuntos
Alumínio/administração & dosagem , Alumínio/análise , Dieta , Exposição Ambiental/análise , Aditivos Alimentares/química , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Alumínio/efeitos adversos , Criança , Pré-Escolar , China , Exposição Ambiental/efeitos adversos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Medição de Risco , Triticum , Adulto JovemAssuntos
Alumínio/efeitos adversos , Indústria Farmacêutica , Farmacêuticos , United States Food and Drug Administration/legislação & jurisprudência , Alumínio/administração & dosagem , Alumínio/química , Indústria Farmacêutica/normas , Rotulagem de Medicamentos/legislação & jurisprudência , Hidratação/normas , Humanos , Concentração Máxima Permitida , Preparações Farmacêuticas/normas , Serviço de Farmácia Hospitalar/normas , Estados UnidosRESUMO
The rabbit has been used for decades for predictive testing of skin irritancy, but in recent years, the guinea pig has been suggested as an alternative, especially for assessment of one of the components of the irritant reaction: edema (fluid accumulation). A method based on skin-fold measurements with Harpenden calipers has been developed and modified. In previous papers, experience with sodium lauryl sulphate, nonanoic acid and industrial solvents was reported. The present results concern the use of cutting fluids, buffered and unbuffered acid and alkaline solutions, formalin and dimethyl sulfoxide. This inexpensive and comparatively unsophisticated method afforded clear dose-response relationships and good discriminating power. The only exception was the acid and alkaline solutions, where no changes in skin-fold thickness were observed despite their documented irritant potential. The appearance of erythema (visual scoring) and the increase in skin-fold thickness, and their relationship, are discussed with some illustrative examples. The method described is now well standardized and is suited for predictive testing of the edema-inducing capacity of chemicals and products.
Assuntos
Alérgenos/efeitos adversos , Dermatite Irritante/etiologia , Edema/induzido quimicamente , Dermatopatias/induzido quimicamente , Dobras Cutâneas , Alérgenos/administração & dosagem , Alumínio/administração & dosagem , Alumínio/efeitos adversos , Animais , Peso Corporal/efeitos dos fármacos , Dermatite Irritante/diagnóstico , Dimetil Sulfóxido/administração & dosagem , Dimetil Sulfóxido/efeitos adversos , Relação Dose-Resposta a Droga , Edema/diagnóstico , Formaldeído/administração & dosagem , Formaldeído/efeitos adversos , Cobaias , Ácido Clorídrico/administração & dosagem , Ácido Clorídrico/efeitos adversos , Óleos Industriais/efeitos adversos , Oxalatos/administração & dosagem , Oxalatos/efeitos adversos , Ácido Oxálico , Valor Preditivo dos Testes , Dermatopatias/diagnóstico , Hidróxido de Sódio/administração & dosagem , Hidróxido de Sódio/efeitos adversosRESUMO
The primary purpose of this study was to determine the relative usefulness of various measures to monitor body aluminum burden in weanling rats fed various amounts of aluminum (0.39 mumol Al/g diet for 29 days, approximately 40 mumol Al/g diet with or without citrate for 29 days and approximately 100 mumol Al/g diet with citrate for 12 or 29 days) or injected intraperitoneally with graded doses of aluminum (0.01, 4.6, 11.8, 23.5 or 94 mumol Al). Twenty-four hours prior to sacrifice, all rats were injected intraperitoneally with either desferrioxamine (75 mg DFO) or buffer. All seven indices of aluminum exposure monitored (i.e. tibia, liver, kidney and serum aluminum concentrations; changes in serum aluminum concentrations in response to DFO; urinary aluminum excretion with and without DFO treatment) were highly (P < 0.001) correlated to parenteral aluminum exposure. Five of these measures (i.e. tibia, liver and serum aluminum concentrations and urinary aluminum excretion with and without DFO treatment) were also highly (P < 0.001) correlated to oral aluminum loads. Changes induced by DFO were very small. Moreover, the 'DFO stimulated' serum and urine aluminum concentrations were not more correlated to the body load of aluminum, as indicated by tibia aluminum concentrations, than baseline values. Comparisons of aluminum exposure in tibias and sera of rats exposed to parenteral and oral aluminum indicated that only 0.01-0.04% of dietary aluminum was absorbed. Ingestion of citrate had small but significant effects on aluminum retention.
Assuntos
Alumínio/análise , Citratos/farmacologia , Desferroxamina , Exposição Ambiental , Absorção , Administração Oral , Alumínio/administração & dosagem , Alumínio/farmacocinética , Ração Animal , Animais , Carga Corporal (Radioterapia) , Ácido Cítrico , Hematócrito , Injeções Intraperitoneais , Ferro/análise , Rim/química , Rim/metabolismo , Fígado/química , Fígado/metabolismo , Masculino , Ratos , Ratos Sprague-Dawley , Tíbia/química , Tíbia/metabolismoRESUMO
The efficacy of topical aluminium chloride hexahydrate 20% W/W ethanol (ACH) in the treatment symptomatic palmar hyperhidrosis was studied in 12 patients. A half-sided control single blind (assessor blind) study was done. Patients applied ACH on one palm daily for 4 weeks. The response to treatment was measured objectively with an evaporimeter. There was significant fall of skin water vapor loss (SVL) on treated palms compared with untreated palms. The basal mean SVL of treated palms and untreated palms were 79.9 and 77.9 g water/m2/h, respectively (n.s.). The mean SVLs of treated vs. untreated palms at week 1, 2, 3, and 4 were 66.4 vs. 79.7 (p less than 0.05), 56.6 vs. 72.2 (p less than 0.001), 58.2 vs. 72.5 (p = 0.1), and 51.4 vs. 72.7 (p less than 0.001) g water/m2/h, respectively. The mean SVL of treated palms returned near basal rate within 1 week of stopping treatment. Four patients developed skin irritation from ACH; in three this disappeared after 1 week and they were able to continue with treatment; one withdrew from the study because of the severe irritation. All patients reported that the ACH reduced palmar sweating within 48 hours of application; its effect disappeared within 48 hours after stopping treatment. ACH appeared to be useful in rapid control of palmar hyperhydrosis.