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2014, Journal of Pharmaceutical Sciences
There is an urgent need for the analysis of melamine in the global pharmaceutical supply chain to detect economically motivated adulteration or unintentional contamination using a simple, nondestructive analytical technique that confirms the extent of adulteration in a shorter time period. In this work, different analytical techniques (thermal analysis, X-ray diffraction, Fourier transform infrared (FT-IR), FT-Raman, and near-infrared (NIR) spectroscopy) were evaluated for their ability to detect a range of melamine levels in gelatin. While FT-IR and FT-Raman provided qualitative assessment of melamine contamination or adulteration, powder X-ray diffraction and NIR were able to detect and quantify the presence of melamine at levels as low as 1.0% w/w. Multivariate analysis of the NIR data yielded the most accurate model when three principal components were used. Data were pretreated using standard normal variate transformation to remove multiplicative interferences of scatter and particle size. The model had a root-mean-square error of calibration of 2.4 (R 2 = 0.99) and root-mean square error of prediction of 2.5 (R 2 = 0.96). The value of the paired t test for actual and predicted samples (1%-50% w/w) was 0.448 (p < 0.05), further indicating the robustness of the model.
Journal of Food Processing and Preservation, 2015
In this work, a reasonable substitute with laborious and expensive liquid chromatography for quick melamine detection in milk and dairy products is outlined. To accomplish this aim, first-order multivariate calibration methods including partial least squares (PLS) and net analyte preprocessing-partial least squares (NAP/PLS) are adopted for melamine quantification in complex food extracts down to 0.07 mg/kg without the need for efficient sample clean up. Solution pH has a significant influence on the performance of the proposed method and poor prediction was observed at pH 2.0 and 4.0. NAP/PLS outperformed PLS for melamine quantification, where analysis was carried out over the spectral domain 215-260 nm and pH 2-8. By using NAP/PLS, melamine is accurately quantified in spiked milk and dairy products (0.5-2.0 mg/kg) containing varying levels of fat (0-29%) and protein (3-23%), which proves the workability of the proposed method for handling wide spectrum of foodstuffs. At spiking level of 0.5 mg/kg, the average recoveries were acceptable (91.2-105.3%). However, modest recoveries were observed for food items containing high levels of protein and fat. Statistical tests confirmed that (with few exceptions) the NAP/PLS is of comparable analytical performance for highly advanced liquid chromatography which gives more chance for the current method to be applied for quick melamine detection in milk and dairy products. The proposed methods would be applied in food laboratories, especially when advanced instruments are not available. PRACTICAL APPLICATIONS A new application of multivariate calibration for melamine detection (down to 0.07 mg/kg) in different types of milk and two dairy products is reported. The proposed analytical method would be of great importance from practical point of view considering the fact that chromatographic separation was avoided. The proposed methods would be applied in food laboratories, especially when advanced instruments are not available.
Food Chemistry, 2013
Melamine is a nitrogenous chemical substance used principally as a starting material for the manufacture of synthetic resins. Due to its very high proportion of nitrogen melamine has been added illegitimately to foods and feeds to increase the measured protein content, which determines the value of the product. These issues prompted private as well as governmental laboratories to develop methods for the analysis of melamine in a wide variety of food products and ingredients. Owing to this fact present study is aimed to use single bounce attenuated total reflectance (SB-ATR) Fourier transform infrared spectroscopy (FTIR) method as an effective rapid tool for the detection and quantification of melamine in milk (liquid and powder). Partial least-squares (PLS) models were established for correlating spectral data to melamine concentration with R 2 > 0.99, and RMSEC 0.370. Linear calibration curves were obtained over the calibration range of 25-0.0625%. The LOD and LOQ of the method was 0.00025% (2.5 ppm) and 0.0015% (15 ppm) respectively. Proposed SB-ATR-FTIR method requires little or no sample preparation with an assay time of 1-2 min.
Applied Spectroscopy, 2009
Journal of Chemistry, 2013
The study presents a fully validated simple high-performance liquid chromatography method with diode array detection (HPLC-DAD), able to accurately determine the melamine, fraudulently added, in protein supplements, commonly used from healthy adults to enhance exercise or sport performance. The validation strategy was intentionally oriented towards routine use and the reliability of the method rather than extreme performance. For this reason, validation by accuracy profile, including estimation of uncertainty, was chosen. This procedure, based on the concept of total error (bias + standard deviation), clearly showed that this method was able to determine melamine over the range of 0.05-3.0 mg Kg −1 , selected by taking into account the maximum residue levels (MRLs) proposed by European legislation to distinguish between the unavoidable background presence of melamine and unacceptable adulteration. The accuracy profile procedure established that at least 95% of the future results obtained with the proposed method would be within the ±15% acceptance limits of the validated HPLC-DAD method over the whole defined concentration range.
Journal of Food Science, 2008
Melamine, a nitrogen-rich chemical, was implicated in pet and human food recalls in 2007, which caused enormous economic losses to the food industry. In this study, melamine concentration in wheat gluten, chicken feed, and processed foods (that is, cake and noodle) was measured by surface enhanced Raman spectroscopy (SERS) in combination with SERS-active substrates. SERS was able to rapidly detect 0.1% melamine in wheat gluten, 0.05% in chicken feed, 0.05% in cakes, and 0.07% in noodle, respectively. A partial least squares (PLS) model was established for the quantification of melamine in foods by SERS: R = 0.90, RMSEP = 0.33. In addition, SERS results were verified by HPLC analysis based on a simplified FDA method. Compared with HPLC, the SERS method is much faster and simpler, requires minimum sample preparation, but still yields satisfactory qualitative and quantitative results. These results demonstrate that it is an applicable approach to use SERS to screen foods, eliminate presumptive negative samples of melamine contamination from the sample population, and then verify presumptive positive samples using HPLC protocols. Combining these 2 methods could provide a more rapid and cost-effective way for monitoring melamine contamination in increasingly large numbers of imported foods and feed products.
Tandem Mass Spectrometry - Applications and Principles, 2012
jfoodpharmsci.com
An electronic nose (E-Nose) has been used as rapid analytical technique for melamine detection in food samples. The parameter used is melamine retention index (MRI) in E-Nose chromatogram. The value of MRI was also confirmed using two dimensional gas ...
Hyperspectral Raman imaging has the potential for rapid screening of solid-phase samples for potential adulterants. We can improve mixture analysis algorithms by defining a temperature range in which the contaminant spectrum changes dramatically and uniquely compared with unadulterated material. Raman spectra were acquired for urea, biuret, cyanuric acid, and melamine (pure and at 1% in dried milk powder) from 50 to 310 8C with a gradient of 1 8C min À1. Adulterants were clearly indentified in the milk powder. Specific frequencies that were mainly associated with ring breathing, stretching, and in-plane deformation shifted with respect to temperature up to 12 cm À1 in all four molecules. Specific frequencies significantly increased/decreased in intensity within narrow temperature ranges independent of whether the amine was mixed in milk. Correlation of Raman and differential scanning calorimetry data identified structural components and vibrational modes, which concur with or trigger phase transitions.
Analytical and Bioanalytical Chemistry, 2009
In the summer of 2008, serious illnesses and deaths of babies in China were linked to melamine-tainted powdered infant formula. Melamine contains several metabolites, such as ammeline, ammelide, and cyanuric acid, and has been used for the adulteration of foods or milk to increase their apparent protein content. It is assumed that melamine and its metabolites are absorbed in the gastrointestinal tract, and precipitate in the kidney to form crystals. A new tolerable daily intake of 0.2 mg kg−1 body weight was adapted by the World Health Organization in 2008. This paper reviews the variety of analytical methods that have been used for the analysis of melamine in food. The limit of detection of these various methods is 0.05–100 ppm. The maximum acceptable concentration in food has been set at 50 ppb by the US FDA. A fast and ultrasensitive procedure for screening, detection, and characterization of melamine and its derivative compounds needs to be established. Currently, mass-spectrometry technologies provide an alternative to derivatization for regulatory analysis of food.
Food Additives & Contaminants: Part A, 2018
Extensive research has been conducted on non-destructive and rapid detection of melamine in powdered foods in the last decade. While Raman and near-infrared hyperspectral imaging techniques have been successful in terms of non-destructive and rapid measurement, they have limitations with respect to measurement time and detection capability, respectively. Therefore, the objective of this study was to develop a mercury cadmium telluride (MCT)-based shortwave infrared (SWIR) hyperspectral imaging system and algorithm to detect melamine quantitatively in milk powder. The SWIR hyperspectral imaging system consisted of a customdesigned illumination system, a SWIR hyperspectral camera, a data acquisition module and a sample transfer table. SWIR hyperspectral images were obtained for melamine-milk samples with different melamine concentrations, pure melamine and pure milk powder. Analysis of variance and the partial least squares regression method over the 1000-2500 nm wavelength region were used to develop an optimal model for detection. The results showed that a melamine concentration as low as 50 ppm in melamine-milk powder samples could be detected. Thus, the MCT-based SWIR hyperspectral imaging system has the potential for quantitative and qualitative detection of adulterants in powder samples.
Since 2008, the detection of the adulterant melamine (2,4,6-triamino-1,3,5-triazine) in food products has become the subject of research due to several food safety scares. Near-infrared (NIR) hyperspectral imaging offers great potential for food safety and quality research because it combines the features of vibrational spectroscopy and digital imaging. In this study, NIR hyperspectral imaging was investigated for quantitative evaluation of melamine particles in nonfat and whole milk powders. Melamine was mixed into milk powders in a concentration range of 0.02e1.00% (w/w). A NIR hyperspectral imaging system was used to acquire images (938e1654 nm) of melamine powder, whole milk powder, nonfat milk powder, and mixtures of melamine and each of the milk powders. Two optimal bands (1447 nm and 1466 nm) were selected by a linear correlation algorithm with pure milk and pure melamine. Band ratio (B 1447/1466 ) images coupled with a single threshold were used to create resultant images to visualize identification and distribution of the melamine adulterant particles in milk powders. The identification results were verified by spectral feature comparison between separated mean spectra of melamine pixels and milk pixels. Linear correlations (r) were found between the number of pixels identified as containing melamine and melamine concentration in nonfat milk and whole milk powders, which were 0.980 and 0.970 or higher, respectively. The study demonstrated that the combination of NIR hyperspectral imaging and simple band ratioing was promising for rapid quantitative analysis of melamine in milk powders.
Chromatographia, 2009
A novel method for the determination of melamine residue in food was developed using solid-phase extraction and capillary zone electrophoresis with UV detection. Spiked samples were extracted with 1% trichloroacetic acid while 0.03 g sodium deoxycholate was used to precipitate protein in the real samples. After centrifuging and clean-up by solid-phase extraction cartridge, the extract was directly analyzed by CZE-UV. The method was validated and good results were obtained with respect to precision, repeatability and spiked recovery. The limit of detection for melamine varied between 0.25 and 0.5 mg kg -1 . The proposed method was successfully applied for the analysis of melamine in food with total recoveries ranging from 94 to 102% in the spiked range of 0.5-5 mg kg -1 , and the relative standard deviations were between 1.5 and 4.1%.
2009
Melamine Food and beverage Milk-based products Ion-pair liquid chromatography Tandem mass spectrometry Triple quadrupole a b s t r a c t This paper describes a fast method for the sensitive and selective determination of melamine in a wide range of food matrices, including several milk-based products. The method involves an extraction with aqueous 1% trichloroacetic acid before the injection of the 10-fold diluted extract into the liquid chromatography-electrospray tandem mass spectrometry (LC-ESI-MS/MS) system, using labelled melamine as the internal standard. As melamine is present in aqueous media in the cationic form, the chromatographic separation in reversed-phase LC requires the use of anionic ion-pair reagents, such as tridecafluoroheptanoic acid (THFA). This allows a satisfactory chromatographic retention and peak shape in all the types of food samples investigated. The method has been validated in six food matrices (biscuit, dry pasta and four milk-based products) by means of recovery experiments in samples spiked at 1 and 5 mg kg −1 . Average recoveries (n = 5) ranged from 77% to 100%, with excellent precision (RSDs lower than 5%) and limits of detection between 0.01 and 0.1 mg kg −1 . In addition, accuracy and robustness of the method was proven in different soya-based matrices by means of quality control (QC) sample analysis. QC recoveries, at 1 and 2.5 mg kg −1 , were satisfactory, ranging from 79% to 110%. The method developed in this work has been applied to the determination of melamine in different types of food samples. All detections were confirmed by acquiring two MS/MS transitions (127 > 85 for quantification; 127 > 68 for confirmation) and comparing their ion intensity ratio with that of reference standards. Accuracy of the method was also assessed by applying it to a milk-based product and a baking mix material as part of an EU proficiency test, in which highly satisfactory results were obtained.
Food Control, 2011
A simple and rapid ultra-performance liquid chromatographic (UPLC) method with tandem mass spectrometry has been developed and validated for the determination of melamine in milk, milk products, bakery goods, and flour. The method comprises a simple extraction step with a solution of acetonitrileewater, ultrasound treatment and a liquideliquid extraction with dichloromethane for fat removal. The purified extract is further diluted before injection on a ACQUITY BEH Hilic, with a total run of 2 min. Quantification of the results was performed with isotopic dilution ( 13 C 3 -labelled melamine). No matrix effect was observed. Consequently solvent-based standards could be used for the calibration curve witch ranges from 0.5 mg/kg to 40 mg/kg. The calibration function was linear with a determination coefficient of >0.999 (r 2 ). The limit of detection and the limit of quantification were respectively 0.2 and 0.5 mg/kg. Repeatability and within-lab reproducibility were <6% RSD. Average apparent recovery of melamine ranged from 97% to 99%. Accuracy of the method has been successfully tested by participating in two proficiency tests. The method is easily performed with confident quantification and provides a good alternative to solid phase extraction as well as to time-consuming derivatization prior to gas chromatography.
Food Research International, 2013
Major advances in the field of chemometrics combined with the use of vibrational spectroscopy have proven essential for the identification and quantification of food contaminants. These techniques, which have guided the work of regulatory agencies overlooking the food industry, can be readily applied to monitor food processing, quality control, and quality assurance. These processes can ensure product authenticity with respect to variety, geographical origin, and presence or absence of contaminants. Food analysis by vibrational spectroscopy provides overall chemical composition of the tested food sample; therefore, it is widely considered to be a highly reliable and empirical fingerprints of that samples. In 2008, melamine adulteration of milk powder in China resulted in devastatingly adverse effects for both consumers and the overall Chinese economy at large. As a result, regulatory agencies have markedly increased their interest in using fast, reliable, and accurate methods for identifying food contaminants. In this article, we provide a detailed overview of the uses of vibrational spectroscopy methods and chemometrics for the detection and quantification of melamine in dairy products.
Interdisciplinary Toxicology
Melamine-ware is widely used around the world. There is a public health concern as regards the safety of melamine when exposed to food. This study was carried out to measure the level of melamine migration in melamine-ware products by HPLC method and the effect of food-type on the level of melamine migration. In food control laboratories in Iran, there is no common method to measure and monitor melamine migration, hence a method using HPLC technique was adopted and validated to solve this problem. The validation results showed the reliability with 94.9% accuracy and 95.3% precision. Furthermore, the limit of detection (LOD) and quantification (LOQ) were 0.145 and 0.435 µg/ml, which for a new method were within acceptable ranges. Melamine migrations from 4 most available melamine wares were measured. Distilled water, 3% acetic acid and 15% ethanol were used as food simulant at 30 °C for 90 min. Although melamine migration occurred in all samples and acidic conditions had a significan...
Data in Brief, 2018
Nowadays, Melamine-containers is widely use to because of heatresistant. Due to the effects of Melamine-on human health, constant and long-term usage of Melamine-containers can be a source of Melamine-exposure to human body. The objective of this research was to measure the levels of Melamine-migration from Melamine-ware-products into foods at different test conditions and Effect of food type and Time on it. Spectrophotometer UV/VIS method was used to detect the limits of Melamine-and the method was based on the in the complex of Melamine-formaldehyde and Uranin (a ketone group).The limit of detection (LOD) of the method was 0.2 (mg/ml) which is functional for measuring. Migration was less than the standard level of European Union (30 mg/ml). In this study, 3% acetic acid, distilled water and 15% ethanol were used as simulants. The results showed the temperature is an important factor in Melamine-migration and in 97% of cases, with increasing temperature from 30 to 90 there is a significant increase (P o 0.05) in Melamine-migration furthermore migration from acidic simulants was more than alcoholic and neutral ones (p o 0.001).
2018
Melamine-based tableware has the advantage such lighter, stronger, and not broken easily. However, it’s not recommended for heat storage for long periods of time. Melamine migration in tableware results from the effect of food heating temperature, storage time, pH and processing. Melamine is dangerous if taken, inhaled, or absorbed through the skin. The maximum limit for melamine migration from food packaging is 30 ppm. Melamine migration studies have been carried out from the types of bowl and cup samples. In this study the sample was made in a simulation solution in the form of water and acetic acid pH 4.5 which was heated at 100 °C and 70 °C. Determination of melamine migration was carried out using HPLC method with condition: UV detection (λ 236), mobile phase acetonitrile: water (20:80), flow rate of 0.4 mL/minute, and C18 column with validation method results: correlation coefficient was 0.9993, detection limit and quantization limit were 0.00136 ppm and 0.00455 ppm, relative ...
Food Control, 2010
The general term "pesticide" includes a large number of substances that belong to many different chemical classes. Pesticides are applied to crops at various stages of cultivation to provide protection against weeds and pests, and during post-harvest storage to preserve quality. The list of which pesticides are authorized for use in Europe is available on EU pesticides Database. The QuEChERS approach is a method designed for the analysis of pesticides in fruits and vegetables. This method is based on an extraction and clean-up step; it has been designed to be Quick Easy Cheap Effective Rugged and Safe. The aim of this study was to modify the QuEChERS method to be applied in the analysis of 9 organophosphate and 1 pyrethroid pesticides in raw materials for animal feeding introducing an additional liquid eliquid partition step. This additional step allowed us to concentrate the samples, avoiding any solvent evaporation, prior to the instrumental analysis. Once the method was optimized, it was carried out a pesticides quantization study using a GCeMS SIM multi-residue analysis. 45 samples of maize and soy coming from Northern Italy (Piedmont Region) were analysed during ten months. In 30 samples organophosphate pesticides were found up to 12.4 mg kg À1 of Chlorpyrifos, while no Deltamethrin was detected.
Journal of Environmental & Analytical Toxicology, 2012
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