响应面分析法优化微波提取密蒙花总黄酮工艺

以水为介质,密蒙花总黄酮提取率为考察指标,优化微波强化提取密蒙花总黄酮的工艺.选取微波功率、微波工作时间和液料比为影响因子,在单因素试验的基础上,进行3因素3水平的Box-Behnken中心组合试验设计.以密蒙花总黄酮提取率为响应值,进行响应面(RSM)分析,优化微波强化提取密蒙花总黄酮的提取条件.试验结果表明,微波处...     

响应面分析法优化超声波提取密蒙花黄色素工艺

以水为介质、密蒙花黄色素水溶液的吸光度为考察指标,优化超声波强化提取密蒙花黄色素的工艺。选取超声波功率、提取时间和液料比为影响因素,在单因素试验基础上,进行三因素三水平的Box-Behnken 中心组合试验设计,以密蒙花黄色素的吸光度为响应值进行响应面(RSM)分析,优化超声波强化提取密蒙花黄色素的提取条件。结果表明：超声波处理密蒙花有利于黄色素的浸出,超声波强化提取最佳条件为提取功率800W、提取时间24min、液料比27:1(mL/g);在最佳提取条件下,密蒙花黄色素吸光度理论值可达0.257,验证值为0.259,验证值与理论值间的相对误差为0.78%。密蒙花黄色素得率达5.95%。     

Food colorants: anthocyanins

Interest in food colorants as shown by the number of patents has doubled in recent years with natural pigments outnumbering synthetics by five to one. The natural colorant area can be subdivided into anthocyanins, betalains, chlorophylls, carotenoids, flavonoids, polyphenols, Monascus, hemes, quinones, biliproteins, safflower, turmeric, and miscellaneous. All involve different groups of chemical compounds which may be used directly as colorants, or may be chemically modified to produce different hues or increased stability. All usually involve a method of collection, extraction, purification, possibly stabilization, and formulation. A variety of hues can be obtained ranging from green through yellow, orange, red, blue, and violet, depending on the source of colorant. Similarly, water or oil-soluble formulations can be prepared depending on the type of colorant.     

Natural Colorant from Marigold-Chemistry and Technology

Natural pigments offer an alternative to synthetic dyes, but for successful application, an understanding of the chemical and physical properties of the pigment is essential. With the growing legislative restrictions on the use of synthetic colors, a reappraisal of natural plant pigments is taking place with a view to use them as possible colorants in foods. For natural pigments to be accepted as food colorants, legal sanction is a must. With the application of new innovations, natural pigments can become more cost effective and increase their competitiveness against certified dye and dye products. Marigold flowers, which are yellow to orange red in color, are a rich source of lutein, a carotenoid pigment. This pigment has acquired greater significance because of its antioxidant property and for its eye health protection. Although marigold flower extract has been used in veterinary feeds, the potential use of marigold as a natural food colorant has not been exploited to the full extent due to the lack of information on its safety, stability, and compatibility in foods. This article deals with the chemistry, processing, and stability of the pigment and its applications.     

Colorants in cheese manufacture: Production,chemistry, interactions,and regulation

Colored Cheddar cheeses are prepared by adding an aqueous annatto extract (norbixin) to cheese milk; however, a considerable proportion (～20%) of such colorant is transferred to whey, which can limit the end use applications of whey products. Different geographical regions have adopted various strategies for handling whey derived from colored cheeses production. For example, in the United States, whey products are treated with oxidizing agents such as hydrogen peroxide and benzoyl peroxide to obtain white and colorless spray‐dried products; however, chemical bleaching of whey is prohibited in Europe and China. Fundamental studies have focused on understanding the interactions between colorants molecules and various components of cheese. In addition, the selective delivery of colorants to the cheese curd through approaches such as encapsulated norbixin and microcapsules of bixin or use of alternative colorants, including fat‐soluble/emulsified versions of annatto or beta‐carotene, has been studied. This review provides a critical analysis of pertinent scientific and patent literature pertaining to colorant delivery in cheese and various types of colorant products on the market for cheese manufacture, and also considers interactions between colorant molecules and cheese components; various strategies for elimination of color transfer to whey during cheese manufacture are also discussed.     

Removal of color from fruit candy waste by activated carbon adsorption

The research in this paper was aimed at finding a treatment method for recovery of fruit candy (fruit leathers) wastes. Fruit leather wastes were dissolved in water to investigate the efficacy of activated carbon adsorption to remove food colorants, which reduce recycling possibilities. The effects of initial pH (2.5-9), food colorant concentration (10-110 g fruit leather/L) and adsorbent dosage (1-12 g/L) on the adsorption process were investigated. Maximum adsorption was obtained at the original pH value of dissolved fruit candy waste in water. Maximum adsorbent capacities for red, yellow and blue food colorants were 4.4; 11.7 and 2 mg/g at pH 3.5 respectively. Regeneration of food colorant loaded activated carbon can be effected at 400 °C. Cost estimates indicate that red color removal would seem to be an economical proposition, costing about $19/ton fruit candy waste, yellow marginal at $70/ton waste, and blue uneconomical at $245/ton waste.     

Identification of acid-stable carmine in imported apple syrup product

An unknown red pigment was purified from an apple syrup product imported from Canada, using a DIAION HP-20 column with methanol as the eluent. By spectroscopic means and chemical synthesis, the isolated pigment was identified as 4-aminocarminic acid, which is the major pigment of acid-stable carmine (a red colorant illegal in Japan). In addition, HPLC and TLC methods were proposed to detect this illegal colorant. While the color of carminic acid changed from yellow to red in the pH range of McIlvaine buffer (3.0-7.0), the color of 4-aminocarminic acid was always red, and also the ultraviolet/visible (UV/Vis) spectra did not change. These characteristics are useful to distinguish 4-aminocarminic acid from carminic acid.     

DETERMINATION OF SYNTHETIC COLORANTS IN CONFECTIONERY AND INSTANT DRINK POWDERS CONSUMED IN TURKEY USING UV/VIS SPECTROPHOTOMETRY

One hundred and forty samples of Turkish confectionery and 96 instant drink powders marketed in Turkey, colored with a single colorant, were analyzed for colorants using both quantitative and qualitative UV/VIS spectrophotometer determinations. Six and five synthetic food colorants were determined in confectionery and instant drink powders, respectively. All the synthetic colorants determined in confectionery, except for Erythrosine, are permitted for use by the Turkish Food Codex and European Community (EC). The permitted colorant levels in 63 (43.7%) of 135 confectionery and in 35 (36.45%) of 96 instant drink powder samples were determined to be higher than the maximum tolerable limit in the Turkish Regulations. Continuous surveillance programs may be warranted to monitor regularly the level of colorant in confectionery and instant drink powder consumed, especially by children.     

Magnetic Mixed Hemimicelles Solid-Phase Extraction of Three Food Colorants from Real Samples

Introducing a specific clean extraction procedure with a minimal matrices effect for food colorant determination is still a challengeable topic and highly recommended. Mixed hemimicelle solid-phase extraction method, based on cetyltrimethylammonium bromide-coated Fe₃O₄/SiO₂ nanoparticles as a novel, simple, and fast preconcentration method, was applied for preconcentration and fast isolation of three synthetic food colorants in foodstuff matrices prior to HPLC-UV-vis determination. The influence of different parameters on extraction efficiency such as surfactant amount, sample pH, time of extraction, desorption condition, and nanoparticles concentration was optimized. Under the optimized conditions, a preconcentration factor of 100 was achieved by extracting 10 mL sample. The limit of detection for the three synthetic food colorants including Tartrazine, Sunset yellow FCF, and Quinoline yellow is 2.50, 1.25, and 2.12 μg/L, respectively. The proposed method was applicable for extraction and preconcentration of three food colorants in various food samples with the food dye contents in the range of 13–105 μg/L.     

Identification of the Major Components of Buddleja officinalis Extract and Their Metabolites in Rat Urine by UHPLC‐LTQ‐Orbitrap

Buddleja officinalis Maxim, one of the most popular herbal medicines in China, is widely prescribed for curing eye diseases for centuries. In this study, the major components of B. officinalis extract (BOE) and their metabolites in rat urine were detected and identified by ultra‐high‐pressure liquid chromatography coupled with linear ion trap‐orbitrap tandem mass spectrometry (UHPLC‐LTQ‐Orbitrap). A total of 19 compounds, including 8 flavonoids and 11 phenylethanoid glycosides, were confirmed or tentatively identified from BOE. In vivo, 33 components, including 3 prototypes and 30 metabolies, were confirmed or tentatively identified in rat urine samples. The metabolic pathways of different types of compounds were also proposed. This study would effectively narrow the range of potentially bioactive constituents of BOE and shed light to its action mechanism.     

Exploring the antioxidant potential of Teucrium polium extracts by HPLC–SPE–NMR and on-line radical-scavenging activity detection

Teucrium polium is a popular medicinal plant that is used in the daily diet and the in vitro and in vivo antioxidant potency of its extracts has been widely investigated. In the present work, polar extracts from T. polium were analyzed in terms of its composition and radical-scavenging activity with the employment of the state-of-the-art HPLC-SPE-NMR and HPLC-DPPH techniques in the search of new antioxidant agents for food industry. NMR and MS data revealed the presence of phenylpropanoid glycosides verbascoside and poliumoside, the flavones apigenin and its derivatives and two methoxyflavones. The on-line DPPH experiments showed that poliumoside is the most active component of the extracts and the antioxidant potential of T. polium polar extracts is mainly attributed to phenylpropanoid glycosides (66–80%). Our results suggested that T. polium extracts could be a promising source of natural antioxidants. This holistic approach also revealed that poliumoside or polar extracts of T. polium can be used in food industry as antioxidant agents with natural origin. The HPLC-SPE-NMR and HPLC-DPPH analysis of the extracts was performed for first time in the same device without any modification of the instrumentation, avoiding the need for isolation of the individual components.     

Milk colloidal system as a reaction medium and carrier for the natural blue colorant obtained from the cross-linking between genipin and milk proteins

A promising natural blue colorant was obtained from the cross-linking between genipin and milk proteins. Milk was simultaneously used to extract genipin from the unripe genipap (Genipa americana L.) and evaluated as a reaction medium and carrier for the novel blue colorant. The effects of the milk composition (skimmed, semi-skimmed, and whole) on the kinetic of blue color formation in the colorant-loaded milk samples during their cold storage time for 96 h were evaluated using their color parameters and free-genipin content. The reaction between milk proteins and genipin were evaluated by FTIR spectroscopy. In addition, the blue colorant-loaded milk samples were characterized according to their droplet size distribution, microstructure, and phase separation kinetics. The milk fat content influenced the genipin recovery while the milk with higher protein content contributed to obtaining a more intense blue color. Using whole milk with 3.0 g/100 g fat content favored the light scattering and, thus, a blue colorant with a more intense −b¹ and L¹ values was obtained. On the other hand, the use of skimmed milk with 0.5 g/100 g fat content resulted in more consumption of genipin due to its more protein content for the reaction of blue color compounds formation. Thus, a more intense and darker blue coloration was observed with lower light scattering. The milk composition did not modify the phase separation kinetics of the blue colorant-loaded milk. Therefore, our results have demonstrated that the milk was a suitable medium for the reaction of blue color formation and also a good blue compounds carrier.Industrial relevanceConsumer demands for natural colorants have increased in the last years.Thus, the new food industry challenge is to develop novel healthy, safe and high-quality food products based on natural colorants. Currently, the colorant market does not have still available a natural blue colorant. Therefore, the development of a novel natural blue colorant from plant material could meet this worldwide demand increasing the added value of many products such as ice cream, dairy beverages, and candies.     

饮料中柠檬黄的测定能力验证情况分析

目的了解和评价全国食品检验系统实验室对人工合成着色剂柠檬黄的检测能力,促进各参加实验室在人工合成着色剂检测方面能力的提高。方法在全国食检系统内组织开展饮料中柠檬黄的测定能力验证项目。制备阳性及空白考核样品,完成均匀性稳定性实验,确保样品满足能力验证发样要求,向167家参加实验室随机发放样品,并在规定时间内回收有效数据,采用稳健(Robust)统计进行分析并给出结论。结果在反馈结果的163家实验室中,16家实验室的检测结果为不满意,8家实验室的检测结果为可疑,139家实验室的检测结果为满意,满意率为85.3%。结论本次能力验证活动中,85.3%的满意率表明绝大部分实验室具备饮料中柠檬黄的检测能力。但依然存在部分实验室的评价结果为可疑或不满意的情况,应分析原因并进一步提高实验室的检测能力。     

Determination of Synthetic Food Colorants in Water-Soluble Beverages Individually by HPLC and Totally by Ce(IV)-Oxidative Spectrophotometry

Food colorants are an important class of food additives that give the first impression to consumers about the quality of food. Ce(IV)-reducing antioxidant capacity assay originally developed in our laboratories was adapted to the determination of synthetic food colorants for the first time. This method allowing for total antioxidant capacity assay of dietary polyphenols, flavonoids, and ascorbic acid in plant extracts is based on the room temperature oxidation of antioxidant compounds with Ce(IV) sulfate in dilute H₂SO₄ solution and measurement of the absorbance of unreacted Ce(IV) at 320?nm. The results of the proposed method were correlated with high-performance liquid chromatography (HPLC) findings. Individual standard solutions, synthetic mixtures of synthetic colorants, and colorant extracts were identified and quantified with HPLC on a C₁₈ column equipped with a diode array detector, and slight modifications on the existing HPLC method were made to analyze synthetic colorant mixtures. This work proposes Ce(IV)-oxidative spectrophotometry as a complementary technique to HPLC in the analysis of food colorants.     

Development of Multiresidue Analysis for 21 Synthetic Colorants in Meat by Microwave-Assisted Extraction–Solid-Phase Extraction–Reversed-Phase Ultrahigh Performance Liquid Chromatography

A novel ultrahigh performance liquid chromatographic method is developed for analysis of 21 synthetic colorants with different acid–base property, solubility, and polarity. The meat samples were extracted by microwave-assisted extraction followed by cleanup with solid-phase extraction. The effective separation of the colorants in meat matrixes was achieved, and no interfering peaks could be detected at the retention time of the analytes. The calibration curves showed good linearity with correlation coefficients of 0.9940–0.9999. The limits of quantification were 0.48–7.19 μg/kg. The average recovery of the 21 analytes from meat samples spiked with 25 and 75 μg?kg^?1 was 61.29–116.1 % with relative standard deviation (RSD) of <11 %. For blank beef sausage spiked with 50 μg?kg^?1 for each analyte, the intraday precision (as RSD) for 21 analytes was 1.45–9.21 % for six determinations within a day. This method has the advantages of being rapid, sensitive, accurate, and with high-throughput and can be applied for multiresidue analysis of meat samples, including six allowable azo food colorants, ten banned azo food colorants, four banned triphenylmethanes, and rhodamin B food colorant.     

酿造酱油氨基酸态氮含量和级别的快速检测

建立快速检测酿造酱油中氨基酸态氮含量和级别的方法。以GB 18186—2000《酿造酱油》中的相关数据为依据，以国产酱油为样品，以天然食用色素为呈色剂，根据等物质的量的反应原则，设定检测各级酱油产品所需的NaOH浓度和物质的量。结果表明：紫薯食用色素为红色、橙红色和橙灰色时，酱油为合格产品。该法操作简单、便捷，判断直观、准确、实用，取样后数分钟内即可获得检测结果，与GB 2009.235—2016《食品中氨基酸态氮的测定》对照测定氨基酸态氮的结果完全吻合。     

Influence of copigment derived from Tasmannia pepper leaf on Davidson's plum anthocyanins

Davidson's plum (Davidsonia pruriens, F. Muell.), a native to Australian rainforests, large, crimson-red fruit, which superficially resembles plum, has been commercially cultivated in Australia since 1990s. The current production volume exceeds market demands therefore this study was designed to evaluate the suitability of Davidson's plum extract as a source of anthocyanin-based food colorant. The stability of the Davidson's plum extract towards heat treatment at 95 °C was higher than that of commercial mulberry colorant, but inferior to colorants derived from red cabbage and purple sweetpotato. An addition of a variety of phenolic acids significantly increased color intensity indicating the formation of copigmentation complexes. Commercial chlorogenic acid as well as extract from a native Australian herb rich in chlorogenic acid, Tasmannia pepper leaf (Tasmannia lanceolata, R. Br.), were both tested in model soft drink solutions subjected to light irradiation and heat treatment. In both cases, the addition of the copigment resulted in a lasting increase in color intensity. In conclusion, Davidson's plum extract can successfully be utilized as a source of natural food color. Extract from Tasmania pepper leaf can be used as a co-pigment for Davidson's plum anthocyanins. PRACTICAL APPLICATION: The color properties of an anthocyanin colorant derived from the native Australian fruit Davidson's plum are comparable to those of mulberry, which is currently applied as a food colorant in Australian food products. Utilization of Davidson's plum fruit as a source of natural color will allow the industry to increase the range of natural pigments and will create new opportunities for the emerging native food industry.     

Detection of the color adulteration of green table olives with copper chlorophyllin complexes (E-141ii colorant)

The present work proposes a procedure for the detection of the color adulteration of green table olives with E-141ii colorant. Addition of this colorant to table olives to obtain a green permanent color in the product is a fraudulent practice, because the FDA allows its use only in citrus-based dry beverage mixes and European Union regulations do not permit the addition of colorants to table olives. The method consists of a pigment extraction in liquid phase and subsequent analysis by HPLC-DAD. The fraudulent addition of E-141ii is determined from the detection in fruit and/or packing solution, of peaks identified as copper chlorophyllin complexes, which are compounds completely foreign to the natural pigment profile of green table olives. The proposed methodology allows controlling the color quality of green table olives.     

Determination of green,blue and yellow artificial food colorants and their abuse in herb-coloured green Easter beers on tap

Beer is one of the most popular alcoholic beverages worldwide. For consumer acceptance, significant factors are its taste, flavour and colour. This study determines selected synthetic green, blue and yellow food colorants in popular Easter herb-coloured green beers on tap produced in breweries on Holy Thursday. The abuse of beer colouring with Tartrazine (E 102), Quinoline yellow (E 104), Sunset yellow (E 110), Patent blue (E 131), Indigo carmine (E 132), Brilliant blue FCF (E 133), Green S (E 142) and Fast green FCF (E 143) was assessed in 11 green beer samples purchased in local restaurants. HPLC was used for the separation and detection of artificial colorants with diode-array detection and a Chromolith Performance CN 100 × 4.6 mm column with guard pre-column Chromolith CN 5 × 4.6 mm. Separation was performed in gradient elution with mobile phase containing methanol–aqueous 2% ammonium acetate at pH 7.0. The study showed that eight beers (70%) marketed in the Czech Republic contained artificial colorants (Tartrazine and Brilliant blue FCF). The concentration of colorants found in analysed green herb-coloured beers ranged from 1.58 to 3.49 mg l^–1 for Tartrazine, 0.45–2.18 mg l^–1 for Brilliant blue, while Indigo carmine was detected only once at concentration 2.36 mg l^–1. Only three beers showed no addition of the synthetic colorants. However, the levels of artificial colorants found in beers marketed in the Czech region were very low and did not show a serious risk for consumers’ health.     

固相萃取-HPLC法同时测定肉制品中苋菜红、胭脂红、日落黄和诱惑红的含量

建立了利用固相萃取-高效液相色谱法同时测定肉制品中4种合成色素的检测方法.样品经乙醇、氨水和水溶液(7∶2∶1,mlm)提取后,固相萃取净化,经C18柱分离,用紫外检测器检测.结果表明:4种合成色素分离良好,加标平均回收率为66.7％～99.7％,相对标准偏差1.9％～3.6％.该方法准确度和精密度较高,可应用于测定肉制品中的合成色素.