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The definitions of food additives vary from country to country. The Food and Agricultural Organization (FAO) and the World Health Organization (WHO) Joint Food Rules Committee define it as follows: Food additives are non-nutritive substances that are consciously added to foods in small amounts to improve the appearance, flavor and texture or storage properties of the food. Common food additives include colorants, sweeteners, preservative, antioxidants, etc. Although food additives can improve the color, aroma, taste and other qualities of foods, there are some problems with food additives, such as unknown sources or improper materials, and the most prone problem is abuse.
As an important means to guarantee the dietary safety, food additives testing is playing an increasingly important role. Alfa Chemistry offers a strong array of capabilities and testing services to food additives. From colorants to antioxidants testing, Alfa Chemistry provides incredible service and credible results and follows FDA and ISO standards. Alfa Chemistry is your one-stop-shop laboratory performing all of food additives analysis.
Category | Item |
---|---|
Colorants | Carmine, amaranth, lemon yellow, sunset yellow, brilliant blue, erythrosine, allura red, etc. |
Sweeteners | Acesulfame, cyclamate, saccharin sodium, aspartame, etc. |
Preservative | Sorbic acid, potassium sorbate, benzoic acid, sodium benzoate, dehydroacetic acid, natamycin, propionate, etc. |
Antioxidants | Beta hydroxy acid, butylated hydroxytoluene, tertiary butylhydroquinone, propyl gallate, BHA, TBHQ, etc. |
Banned food additives | Melamine, clenbuterol hydrochloride, diethylstilbestrol, malachite green, crystal violet, β-lactamase, sodium thiocyanate, leather hydrolyzed proteins, sudan red, basic orange II, rhodamine B, pigment green, auramine, acid orange, rongalit, boric acid, borax, potassium bromate, dimethyl fumarate, cyprohetadine, etc. |
Other | Sulfur dioxide, nitrite, nitrate, etc. |
Food Additive Detector
The food additive detector is a specialized device for rapid detection of additive levels in food. It can analyze various additives such as formaldehyde, nitrites, sulfur dioxide, proteins, borax, hydrogen peroxide, and nitrates. Using standard national methods, the device processes samples, applies them to a test card, and determines the residual additive levels based on color intensity.
High-Performance Liquid Chromatography (HPLC)
HPLC is used for the qualitative and quantitative analysis of food additives. It is characterized by its high sensitivity and high resolution.
Gas Chromatography (GC) and Mass Spectrometry (MS)
The combination of GC and MS enables precise determination of the chemical composition and structure of food additives.
UV-Visible Spectrophotometer
This instrument is used to measure the concentration of specific food additives.
Electrochemical Analyzer
The electrochemical analyzer evaluates the redox properties of certain additives, such as antioxidants.
Wang, Jianghua, et al. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 324 (2025): 125036.
Sodium tripolyphosphate (STPP) is a common food additive that, when ingested, can cause gastrointestinal discomfort and various adverse reactions, posing a potential health risk. Therefore, developing a fast, sensitive, and simple method to detect STPP in food is crucial.
In this study, nitrogen-doped carbon quantum dots (N-CQDs) were found to exhibit a gradual increase in emission peaks upon the addition of STPP, with a good linear response in the concentration range of 0.067–1.96 μM and a low detection limit of 0.024 μM. To the best of our knowledge, this is the first report of using carbon quantum dots for the direct detection of STPP. Additionally, the addition of Al3+ significantly reduced the fluorescence intensity of the N-CQDs@STPP solution, showing a good linear correlation in the 0.33–6.25 μM range, with a detection limit of 0.24 μM. This fluorescent probe was successfully applied to detect STPP and Al3+ in bread samples, demonstrating its great potential for practical application.
Zhang, Yumiao, et al. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 323 (2024): 124879.
A novel composite SERS substrate, consisting of AuNPs and NPG, has been developed for the rapid detection of 6-BA in food samples, offering a simple, sensitive, and reproducible method.
In this study, AuNPs with a particle size range of 60-90 nm were synthesized for SERS detection of varying concentrations of 6-BA solutions. SERS spectra were collected from 6-BA solutions at different concentrations, with the minimum detection concentration of 6-BA being 10−6 M. When compared to the conventional Raman spectra of 6-BA powder, the SERS spectra obtained using AuNPs as the substrate revealed distinct characteristic peaks at 740 cm−1 (symmetric deformation breathing vibration of the amidopurine ring), 813 cm−1 (ring respiration vibration), 1000 cm−1 (stretching breathing vibration of monosubstituted benzene ring skeleton), 1128 cm−1 (R2NH symmetric stretching vibration), 1314 cm−1 (C-N axial stretching vibration), 1403 cm−1 (CH deformation vibration), and 1465 cm−1 (ring stretching vibration). The strongest peak at 1000 cm−1 was identified as the characteristic peak for 6-BA.
Kamaraj, Jeffrey Joseph John Jeya, et al. Journal of the Taiwan Institute of Chemical Engineers 162 (2024): 105601.
The use of synthetic phenolic antioxidants, such as Propyl gallate (PG), in food products has raised concerns due to their potential impact on the nutraceutical properties of various foods. PG is commonly added to cooking oils, cheese, cookies, and other oil-based products to prevent fatty acid peroxidation, thus reducing fatty acid degradation and rancidity. However, excessive PG consumption can lead to serious health issues, including mitochondrial dysfunction and damage to the liver and kidneys. Therefore, monitoring PG levels in food products is crucial.
In this study, CoSe2 nano corals and FeS2 nanosheets were synthesized through a hydrothermal process and combined to create an electrochemical sensor for PG detection. The effect of PG concentrations ranging from 50 to 500 μM on the current response was measured using cyclic voltammetry (CV) in 0.01 M phosphate buffer (pH 7.0) at a scan rate of 50 mVs-1. The results demonstrated a gradual increase in current response with higher PG concentrations, indicating faster electron transfer kinetics at the modified glassy carbon electrode (GCE). The corresponding linear relationship between current and PG concentration was established, with the equation Ipa = 0.03095x(μM) + 1.824 and a coefficient of determination (R²) of 0.99783.
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