16 results on '"Bizzi, Cezar Augusto"'
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2. New and feasible method for total phosphorus and sulfur determination in dietary supplements by ion chromatography
- Author
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Mesko, Marcia Foster, Crizel, Marcelo Guerreiro, Novo, Diogo La Rosa, Hartwig, Carla Andrade, Rondan, Filipe Soares, and Bizzi, Cezar Augusto
- Published
- 2020
- Full Text
- View/download PDF
3. Evaluation of oxygen pressurized microwave-assisted digestion of botanical materials using diluted nitric acid
- Author
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Bizzi, Cezar Augusto, Barin, Juliano Smanioto, Müller, Edson Irineu, Schmidt, Lucas, Nóbrega, Joaquim A., and Flores, Erico Marlon Moraes
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- 2011
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4. Ultrasonic _assisted extraction of phenolic compounds with evaluation of red onion skin (Allium cepa L.) antioxidant capacity.
- Author
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Bordin Viera, Vanessa, Piovesan, Natiéli, Mello, Renius De Oliveira, Barin, Juliano Smanioto, Fogaça, Aline De Oliveira, Bizzi, Cezar Augusto, De Moraes Flores, Érico Marlon, Dos Santos Costa, Ana Carolina, Pereira, Diego Elias, Soares, Juliana Késsia Barbosa, and Hashime Kubota, Ernesto
- Subjects
ONIONS ,OXIDANT status ,PHENOLS ,PLANT phenols ,CAROTENES ,ULTRASONICS ,ANTHOCYANINS - Abstract
This study aimed to determine the antioxidant activity of red onion peel extract using ultrasound extraction. Antioxidant activity was evaluated using DPPH, inhibition of β-carotene, ABTS and FRAP. The results indicated that the 130 W ultrasound power, in pulsed mode, and with 60% solvent favored flavonoids and total anthocyanins, FRAP and β-carotene. The highest levels of total phenolics were found using 60% solvent, at 130 W, and in continuous extraction mode. DPPH was influenced only by the 60% solvent, and the ABTS values were higher with the 80% solvent, in pulsed mode, and at 130 W of power. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
5. Solid sampling coupled to flame furnace atomic absorption spectrometry for Mn and Ni determination in petroleum coke
- Author
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Bizzi, Cezar Augusto, Paniz, José Neri Gottfried, Rodrigues, Luiz Frederico, Dressler, Valderi Luiz, and Flores, Érico Marlon de Moraes
- Published
- 2010
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6. Organic, inorganic and total mercury determination in fish by chemical vapor generation with collection on a gold gauze and electrothermal atomic absorption spectrometry
- Author
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Duarte, Fábio Andrei, Bizzi, Cezar Augusto, Antes, Fabiane Goldschmidt, Dressler, Valderi Luiz, and Flores, Érico Marlon de Moraes
- Published
- 2009
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- View/download PDF
7. Health risk assessment and soil and plant heavy metal and bromine contents in field plots after ten years of organic and mineral fertilization.
- Author
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da Rosa Couto, Rafael, Faversani, Jéssica, Ceretta, Carlos Alberto, Ferreira, Paulo Ademar Avelar, Marchezan, Carina, Basso Facco, Daniela, Garlet, Luana Paula, Silva, Jussiane Souza, Comin, Jucinei José, Bizzi, Cezar Augusto, Flores, Erico Marlon Moraes, and Brunetto, Gustavo
- Subjects
HEAVY metals & the environment ,BROMINE ,HEALTH risk assessment ,FLUORESCENCE ,PHOTOLUMINESCENCE - Abstract
Heavy metals and bromine (Br) derived from organic and industrialized fertilizers can be absorbed, transported and accumulated into parts of plants ingested by humans. This study aimed to evaluate in an experiment conducted under no-tillage for 10 years, totaling 14 applications of pig slurry manure (PS), pig deep-litter (PL), dairy slurry (DS) and mineral fertilizer (MF), the heavy metal and Br contents in soil and in whether the grains produced by corn ( Zea mays L.) and wheat ( Triticum aestivum L.) under these conditions could result in risk to human health. The total contents of As, Cd, Pb, Cr, Ni, Cu, Zn and Br were analyzed in samples of fertilizers, waste, soil, shoots and grains of corn and wheat. Afterwards, enrichment factor (EF), accumulation factor (AF), health risk index (HRI), target hazard quotient (THQ) and target cancer risk (TCR) were determined. Mineral fertilizer exhibited the highest As and Cr content, while the highest levels of Cu and Zn were found in animal waste. The contents of As, Cd, Cr, Cu, Ni, Pb and Zn in soil were below the limits established by environmental regulatory agencies. However, a significant enrichment factor was found for Cu in soil with a history of PL application. Furthermore, high Zn contents were found in shoots and grains of corn and wheat, especially when the plants were grown in soil with organic waste application. Applications of organic waste and mineral fertilizer provided high HRI and THQ for Br and Zn, posing risks to human health. The intake of corn and wheat fertilized with pig slurry manure, swine deep bed, liquid cattle manure and industrialized mineral fertilizer did not present TCR. [ABSTRACT FROM AUTHOR]
- Published
- 2018
- Full Text
- View/download PDF
8. Bromine and Chlorine determination in cigarette tobacco using microwave-induced combustion and inductively coupled plasma optical emission spectrometry
- Author
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Müller, Aline Lima Hermes, Bizzi, Cezar Augusto, Pereira, Juliana Severo Fagundes, Mesko, Márcia Foster, Moraes, Diogo Pompéu de, Flores, Erico Marlon de Moraes, and Müller, Edson Irineu
- Subjects
Espectrometria de emissão ótica com plasma indutivamente acoplado ,Tabaco ,Combustão induzida por micro-ondas ,Cloro ,Chlorine ,Cigarette ,Bromine ,Bromo ,Microwave-induced combustion ,ICP OES - Abstract
A combustão iniciada com micro-ondas (MIC) foi aplicada para decomposição de amostras de tabaco de cigarro e subsequente determinação de bromo e cloro por espectrometria de emissão óptica com plasma indutivamente acoplado (ICP OES). Massas de amostra de até 500 mg foram decompostas em frascos fechados e pressurizados com 20 bar de oxigênio. A combustão foi completada em menos de 30 s e os analitos foram absorvidos em solução diluída de (NH4)2CO3. A exatidão foi avaliada usando materiais de referência certificados e mediante a determinação utilizando ICP-MS. A concordância foi melhor do que 98% usando 50 mmol L-1 de (NH ) CO 4 2 3 como solução absorvedora e 5 min de refluxo. A temperatura durante a combustão foi superior a 1400 °C e o conteúdo de carbono residual nos digeridos após MIC foi menor que 1%. Até oito amostras podem ser decompostas simultaneamente. Limites de quantificação utilizando MIC e determinação por ICP OES foram de 12 e 6 µg g-1 para Br e Cl, respectivamente. The microwave-induced combustion (MIC) was applied for cigarette tobacco samples digestion and further determination of bromine and chlorine by inductively coupled plasma optical emission spectrometry (ICP OES). Samples masses up to 500 mg were combusted in closed vessels using 20 bar of oxygen. Combustion was complete in less than 30 s and analytes were absorbed in diluted (NH4)2CO3 solution. Accuracy was evaluated using certified reference materials with similar matrix composition and comparison with results obtained using ICP-MS. The agreement was better than 98% using 50 mmol L-1 (NH4)2CO3 as absorbing solution and 5 min of reflux. Temperature during combustion was higher than 1400 °C and the residual carbon content in digest obtained after MIC was lower than 1%. Up to eight samples could be processed simultaneously and a single absorbing solution was suitable for both Br and Cl. Limit of quantification by MIC and further ICP OES determination was 12 and 6 μg g-1 for Br and Cl, respectively.
- Published
- 2011
9. Are Infrared and Microwave Drying Suitable Alternatives for Moisture Determination of Meat Products?
- Author
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Marques, Ítalo Engers, Lucion, Fernanda Bortoluzzi, Bizzi, Cezar Augusto, Cichoski, Alexandre José, Wagner, Roger, de Menezes, Cristiano Ragagnin, and Barin, Juliano Smanioto
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MOISTURE content of meat ,MICROWAVE drying ,INFRARED heating ,THERMOGRAPHY ,MEAT quality - Abstract
The analytical methods used for routine moisture determination are based on a loss on drying (LOD) approach performed by conventional heating in ovens, but infrared loss on drying (IRLOD) and microwave-assisted loss on drying (MALOD) drying methods have been used to reduce the analysis time. MALOD speeds up water removal from meat products 64 times in comparison to LOD and provided similar results (agreement between 98 and 101%), but with lower energy consumption (<1 and 31 kWh for MALOD and LOD, respectively) and higher sample throughput (60 samples/h). Infrared thermographies showed temperature of 107.8C in MALOD, which is similar to those used in conventional ovens (105 and 120C). For IRLOD the results were generally lower and its use for meat products should be carefully considered. A fast and accurate analysis of moisture in meat products could be achieved using microwaves, saving time and energy expenditure in agreement to green analytical chemistry. Practical Applications Moisture is a routine analysis performed in every industrial and academic laboratory interested on the study of meat and its products. However, different analytical methods are used for this purpose, and often different results are obtained. Therefore, in this study the performance of three methods based on loss on drying (using conventional, infrared or microwave heating) were evaluated. The results showed lower moisture content by the use of infrared balances for all samples and its use should be carefully evaluated to avoid systematic errors. Contrarily, the results obtained by the use of microwaves were comparable with those of conventional heating, but several advantages were found. The energy consumption was reduced at least 31 times and 15 samples could be processed simultaneously in only 15 min opening the possibility of use of this method to improve routine analysis or as an analytical technique for processing control. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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10. Determination of Propranolol Hydrochloride in Pharmaceutical Preparations Using Near Infrared Spectrometry with Fiber Optic Probe and Multivariate Calibration Methods.
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Marques Junior, Jucelino Medeiros, Muller, Aline Lima Hermes, Foletto, Edson Luiz, da Costa, Adilson Ben, Bizzi, Cezar Augusto, and Irineu Muller, Edson
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PROPRANOLOL ,DRUG development ,NEAR infrared spectroscopy ,FIBER optics ,MULTIVARIATE analysis ,CALIBRATION - Abstract
A method for determination of propranolol hydrochloride in pharmaceutical preparation using near infrared spectrometry with fiber optic probe (FTNIR/PROBE) and combined with chemometric methods was developed. Calibration models were developed using two variable selection models: interval partial least squares (iPLS) and synergy interval partial least squares (siPLS). The treatments based on the mean centered data and multiplicative scatter correction (MSC) were selected for models construction. A root mean square error of prediction (RMSEP) of 8.2 mg g
−1 was achieved using siPLS (s2i20PLS) algorithm with spectra divided into 20 intervals and combination of 2 intervals (8501 to 8801 and 5201 to 5501 cm−1 ). Results obtained by the proposed method were compared with those using the pharmacopoeia reference method and significant difference was not observed. Therefore, proposed method allowed a fast, precise, and accurate determination of propranolol hydrochloride in pharmaceutical preparations. Furthermore, it is possible to carry out on-line analysis of this active principle in pharmaceutical formulations with use of fiber optic probe. [ABSTRACT FROM AUTHOR]- Published
- 2015
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- View/download PDF
11. Microwave-Assisted Solid Sampling Analysis Coupled to Flame Furnace Atomic Absorption Spectrometry for Cd and Pb Determination in Food-Contact Polymers.
- Author
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Henn, Alessandra Schneider, Frohlich, Angelica Chaiani, Pedrotti, Matheus Felipe, Cauduro, Vitoria Hagemann, Oliveira, Marcos Leandro Silva, Flores, Erico Marlon de Moraes, and Bizzi, Cezar Augusto
- Abstract
Microwave-assisted solid sampling analysis coupled to flame furnace atomic absorption spectrometry (MW-SS-FF-AAS) was used for Cd and Pb determination in food-contact polymer samples, with the aim of minimizing reagents and laboratory waste. Operational parameters, such as the FF tube design, the oxygen flow rate, the flame stoichiometry, the sample mass, among others, were evaluated and optimized. Calibration was performed using only reference solutions, and the limits of quantification were 1.7 and 4.6 μg g
−1 for Cd and Pb, respectively. Accuracy was assessed by the analysis of certified reference materials (CRMs), and by comparison with the results obtained by inductively coupled plasma mass spectrometry after microwave-assisted wet digestion. The MW-SS-FF-AAS results for the CRMs showed no statistical difference with the certified values, and good agreement was observed with the results of the digestion method. The MW-SS-FF-AAS method was considered suitable for Cd and Pb determination in food-contact polymers. The concentrations of Cd and Pb in the analyzed samples varied from <1.7 to 628 μg g−1 , and from <4.6 to 614 μg g−1 , respectively. As sample digestion is not necessary, the use of concentrated acids can be avoided by using the proposed MW-SS-FF-AAS method, greatly reducing waste generation. [ABSTRACT FROM AUTHOR]- Published
- 2022
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12. Evaluation of the mineral content of infant formulas consumed in Brazil.
- Author
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Silva, Sabrina Vieira da, Mattanna, Paula, Bizzi, Cezar Augusto, Dos Santos Richards, Neila Silvia Peireira, and Barin, Juliano Smanioto
- Subjects
- *
INFANT formulas , *INFANT nutrition , *SPECTROMETRY , *TRACE elements , *MILK , *MINERAL content of food - Abstract
The mineral content of 10 commercially available milk-based infant formulas widely consumed in Brazil was investigated. The levels of elements (Ca, Cu, Fe, K, Mg, Mn, Na, and Zn) were determined by inductively coupled plasma optical emission spectrometry after microwave-assisted wet digestion. The results were compared with the producers' label declarations and levels proposed by the Codex Alimentarius and the Brazilian National Health Surveillance Agency. The obtained results were in good agreement with certified reference materials, and the relative standard deviation of the measurements was always below 10%, with the exception of Cu (up to 14%). A high degree of variation between the experimental and producers' data was found for trace elements among different brands, with differences as high as 41 and 68% for Cu and Zn, respectively. The content of minerals in the starting formulas was in accordance with levels established by the Codex Alimentarius, with the exception of 1 brand that had a Zn level that was not in agreement with the Codex minimum value. Among follow-up formulas, 2 brands contained levels of Ca and K that were higher than the maximum established by Brazilian standards, and 1 brand contained less than the minimum value recommended for Zn. The guidance upper levels have not been established in the Codex Alimentarius for follow-up formulas, and the maximum value has been established for only 2 of the analyzed minerals. This lack of a standard could be a problem; as shown in the present study, if the Brazilian standard is used, several formulas could be considered out of specification. Despite the limited number of samples evaluated in this work, the levels of some elements were out of specification and special attention by the Brazilian government on the content of minerals in infant formulas is needed. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
13. Desenvolvimento de métodos para análise isotópica de Mg, Sr e Pb de petróleo por MC-ICP-MS
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Henn, Alessandra Schneider, Flores, Érico Marlon de Moraes, Mello, Paola Azevedo, Mesko, Márcia Foster, Vanhaecke, Frank, Mester, Zoltan, Müller, Edson Irineu, and Bizzi, Cezar Augusto
- Subjects
Petróleo ,Lead determination ,Magnesium determination ,Determinação de chumbo ,Strontium determination ,CIENCIAS EXATAS E DA TERRA::QUIMICA [CNPQ] ,Determinação de estrôncio ,Isotopic analysis ,Análise isotópica ,MC-ICP-MS ,Crude oil ,Determinação de magnésio - Abstract
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES Neste trabalho, foi feita a determinação das razões isotópicas de Mg, Sr e Pb em petróleo por espectrometria de massa com plasma indutivamente acoplado e multi-coletor (MC-ICP-MS). Dois métodos de preparo de amostra foram avaliados: (i) digestão por via úmida assistida por micro-ondas com cavidade de digestão pressurizada (MAWD-PDC) e (ii) solubilização de sólidos inorgânicos após a norma ASTM D4807. Usando a MAWD-PDC, até 0,5 g de petróleo foram eficientemente digeridos usando apenas 6 mL de HNO3 14,4 mol L-1 (75 min, temperatura de até 250 ° C). A MAWD-PDC mostrou ser um método de preparo de amostras adequado para a subsequente determinação da concentração e das razões isotópicas de Mg, Sr e Pb. Por outro lado, o método baseado na ASTM não requer nenhum equipamento sofisticado ou o uso de solventes halogenados. Com este método, até 10 g de petróleo podem ser dissolvidos em tolueno e filtrados através de uma membrana de nylon. Elementos presentes na forma de sólidos inorgânicos, como Mg e Sr, são retidos nessa membrana e podem ser facilmente recuperados em água. No entanto, Pb não foi recuperado usando esse método, possivelmente porque ele está presente no petróleo na forma de complexos orgânicos que não ficam retidos na membrana. Quatro procedimentos de isolamento usando cromatografia em coluna foram avaliados para o isolamento de Mg, Sr e Pb da matriz do petróleo. Para o Mg, o isolamento foi realizado usando a resina de troca catiônica AG 50W-X8. O isolamento de Sr e Pb foi feito utilizando um protocolo de isolamento sequencial com base no uso da resina Sr-spec. Ambos os protocolos de isolamento foram caracterizados por rendimentos quantitativos e remoção de elementos da matriz. Não foi observada diferença estatística significativa entre os resultados para as razões isotópicas de Mg e Sr obtidos usando ambos os métodos de preparo de amostra (MAWD-PDC e solubilização). Assim, os dois métodos de preparo de amostra podem ser usados para análise isotópica de Mg e Sr em petróleo. A composição isotópica Mg-Sr-Pb dos petróleos brasileiros avaliados neste trabalho está dentro da faixa observada para a água do mar e o leito rochoso do depósito. Os métodos desenvolvidos neste trabalho podem ser considerados ferramentas promissoras para decifrar a história de formação de reservatórios de petróleo. In this work, the determination of isotope ratios of Mg, Sr and Pb in crude oil by multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS) was performed. Two sample preparation methods were evaluated: (i) microwave-assisted wet digestion with a pressurized digestion cavity (MAWD-PDC); and (ii) solubilization of inorganic solids after the ASTM D4807 test method. Using MAWD-PDC, up to 0.5 g of crude oil was efficiently digested using just 6 mL of 14.4 mol L-1 HNO3 (75 min, temperature up to 250 °C). MAWD-PDC was shown to be a suitable sample preparation method for subsequent determination of Mg, Sr and Pb concentration and their isotope ratios. On the other hand, the ASTM based method does not require any sophisticated equipment or the use of halogenated solvents. With this method up to 10 g of oil can be dissolved in toluene and filtered through a nylon membrane. Elements present as inorganic solids, such as Mg and Sr, are retained on the nylon membrane and can be easily recovered in water. However, Pb was not recovered using this method, possibly because this analyte is present in crude oil as organic complexes that are not retained on the membrane. Four isolation protocols using column chromatography were evaluated for Mg, Sr and Pb isolation from crude oil matrix. For Mg, isolation was successfully carried out using the cation exchange resin AG 50W-X8. The isolation of Sr and Pb was performed using a sequential isolation protocol relying on the use of the Sr-spec resin. Both isolation protocols were characterized by quantitative yields and matrix elements removal. No statistical difference was observed between the results for Mg and Sr isotope ratios obtained using both sample preparation methods (MAWD-PDC and solubilization). Thus, both sample preparation methods can be used for Mg and Sr isotopic analysis of crude oil. The Mg-Sr-Pb isotopic composition of the Brazilian crude oils evaluated in this work was within the range observed for seawater and the deposit bedrock. The methods developed in this work can be considered as promising tools to decipher the formation history of oil reservoirs.
- Published
- 2021
14. Activity of Free and Liposomal Antimony Trioxide in the Acute Promyelocytic Leukemia Cell Line NB4.
- Author
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Viana AR, Davidson CB, Salles B, DE Almeida LY, Krause A, Bizzi CA, Rego EM, Fontanari Krause LM, and Mortari SR
- Subjects
- Apoptosis drug effects, Cell Line, Tumor, Cell Proliferation drug effects, Cell Survival drug effects, Drug Carriers, Humans, Leukemia, Promyelocytic, Acute, Nanoparticle Drug Delivery System, Reactive Oxygen Species metabolism, Antimony administration & dosage, Antimony pharmacology, Liposomes
- Abstract
Background/aim: Antimony is a chemical element used in the therapy of parasitic diseases with a promising anticancer potential. The aim of this study was to evaluate in vitro activity of free or liposomal vesicle-packed antimony trioxide (AT or LAT) in the t(15;17)(q22;q21) translocation-positive acute promyelocytic leukemia (APL) cell line NB4., Materials and Methods: Cytotoxicity was analysed with trypan blue exclusion, the MTT assay and neutral red exclusion assay; cell proliferation with PicoGreen
® ; and reactive oxygen species (ROS) production with DCFDA., Results: Liposomal particles did not change the pH of the cell culture medium and entered the cells. Both formulations resulted in a time- and concentration-dependent cytotoxicity and production of ROS. LAT showed higher toxicity at lower concentrations compared to AT., Conclusion: LAT may be used to decrease drug dosage and maintain high anti-tumoral effects on APL cells., (Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)- Published
- 2021
- Full Text
- View/download PDF
15. Effects of zinc against mercury toxicity in female rats 12 and 48 hours after HgCl2 exposure.
- Author
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Mesquita M, Pedroso TF, Oliveira CS, Oliveira VA, do Santos RF, Bizzi CA, and Pereira ME
- Abstract
This work investigated the toxicity of inorganic mercury and zinc preventive effects in female rats sacrificed 12 or 48 h after HgCl2 exposure. Female Wistar rats were subcutaneously injected with ZnCl2 (27 mg/kg) or saline (0.9 %), and 24 h later they were exposed to HgCl2 (5 mg/kg) or saline (0.9 %). Rats sacrificed 12 hours after Hg administration presented an increase in kidney weight and a decrease in renal ascorbic acid levels. Zinc pretreatment prevented the renal weight increase. Rats sacrificed 48 h after Hg exposure presented a decrease in body weight gain, an increase in renal weight, a decrease in renal δ-aminolevulinic acid dehydratase activity, an increase in serum creatinine and urea levels, and a decrease in kidney total thiol levels. Zinc pretreatment partly prevented the decrease in body weight gain and increase in creatinine levels, in addition to totally preventing renal δ-aminolevulinic acid dehydratase inhibition. Mercury accumulation in the kidney and liver in both periods was observed after Hg administration. These results show the different Hg effects along the time of intoxication, and a considerably preventive effect of zinc against Hg toxicity.
- Published
- 2016
- Full Text
- View/download PDF
16. Evaluation of the mineral content of infant formulas consumed in Brazil.
- Author
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Vieira da Silva S, Mattanna P, Bizzi CA, Richards NS, and Barin JS
- Subjects
- Animals, Brazil, Calcium analysis, Humans, Infant, Microwaves, Milk chemistry, Nitric Acid, Potassium analysis, Reference Standards, Spectrum Analysis methods, Zinc analysis, Infant Formula chemistry, Infant Formula standards, Minerals analysis
- Abstract
The mineral content of 10 commercially available milk-based infant formulas widely consumed in Brazil was investigated. The levels of elements (Ca, Cu, Fe, K, Mg, Mn, Na, and Zn) were determined by inductively coupled plasma optical emission spectrometry after microwave-assisted wet digestion. The results were compared with the producers' label declarations and levels proposed by the Codex Alimentarius and the Brazilian National Health Surveillance Agency. The obtained results were in good agreement with certified reference materials, and the relative standard deviation of the measurements was always below 10%, with the exception of Cu (up to 14%). A high degree of variation between the experimental and producers' data was found for trace elements among different brands, with differences as high as 41 and 68% for Cu and Zn, respectively. The content of minerals in the starting formulas was in accordance with levels established by the Codex Alimentarius, with the exception of 1 brand that had a Zn level that was not in agreement with the Codex minimum value. Among follow-up formulas, 2 brands contained levels of Ca and K that were higher than the maximum established by Brazilian standards, and 1 brand contained less than the minimum value recommended for Zn. The guidance upper levels have not been established in the Codex Alimentarius for follow-up formulas, and the maximum value has been established for only 2 of the analyzed minerals. This lack of a standard could be a problem; as shown in the present study, if the Brazilian standard is used, several formulas could be considered out of specification. Despite the limited number of samples evaluated in this work, the levels of some elements were out of specification and special attention by the Brazilian government on the content of minerals in infant formulas is needed., (Copyright © 2013 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.)
- Published
- 2013
- Full Text
- View/download PDF
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