Certain nanomaterials can be used in food and food products for various purposes. In the form of approved food additives, they alter properties such as taste, appearance or shelf life of the food. They are also used to encapsulate essential trace substances, making them more stable and easier for humans to absorb. At present, however, nanomaterials are usually only used as a by-product in our food.
Food additives and nanomaterials
The food industry uses food additives to specifically influence the properties of food, i.e. to optimise shelf life, processability, taste or appearance. These include colorants, preservatives, antioxidants, sweeteners, stabilizers, flavour enhancers and other substances. In the European Union, such additives may only be used after their official approval according to Regulation (EC) No. 1333/2008 with a labelling obligation for packaged and bulk foodstuffs in the form of E-numbers .
Since 13th December 2014, nanomaterials intentionally added to food also have to be labelled by adding the term “nano” to the respective substance (Regulation (EU) No 1169/2011) . According to this regulation, this specifically applies to novel nano-sized additives intentionally produced for this purpose. As of November 2019, no intentionally manufactured nanomaterials are used as food additives in the EU and therefore there are no “nano”-labelled food products on the market. Nanomaterials that occur as part of the food additives’ manufacturing process and that are not deliberately added to the food product do not require an additional “nano” labelling.
Use of nanomaterials in food and food products
As mentioned before, no intentionally engineered nanomaterials are currently used as food additives in the EU. However, some nanomaterials can be detected in food products. These nanomaterials either occur as a by-product of the food additives’ manufacturing process or they originate from natural sources. In contrast, nanomaterials are already used in food contact materials (see cross-cutting issue – nanomaterials in food packaging).
Materials that may contain nanoparticles and are used in food products can be divided into two groups: (1) inorganic compounds such as silicon dioxide or silver and (2) organic compounds based on proteins, fats or sugars.
Inorganic compounds for food application
The most prominent representatives of this group are silicon dioxide (E 551) and silver (E 174) . These approved food additives are not produced as nanomaterials and usually fulfil their purpose as significantly larger particles. During production however, it cannot be prevented that a certain proportion of nano-sized particles are formed which can be considered as nanomaterials [3-10]. The usage of such food additives is restricted to certain food products/groups and the maximal amount to be added is subject to official daily intake rates, e.g. only 10g/kg (corresponds to 10 per thousand) silicon dioxide in cheese are allowed.
Until August 2022, titanium dioxide was approved as E 171 for various applications in food. However, a re-evaluation of the studies on the toxicity of TiO2 independent of the size of the particles led to the suspension of its use due to some concerns .
Organic nanomaterials in food & food products
Another group consists of organic materials, as well as combinations of organic and inorganic substances, which may be present in nanoscale form and which are mainly used for the modification of surfaces . Role models for organic nanomaterials to be used in food products are endogenous substances such as proteins, fats or sugars. These organic nanoscale substances are used as nano-sized capsule materials facilitating the controlled release of e.g. vitamins or minerals (e.g. encapsulation of menthol by amylose) [3, 9]. In form of liposomal structures, they improve the solubility of e.g. vitamins or omega-3 fatty acids . Despite the numerous possible applications of nanomaterials, such encapsulants are not permitted in Europe.
Effects of nanomaterials in food on humans
All substances ingested via the food chain enter the intestine where they are either taken up into the body or are retained by the intestinal mucosa and subsequently excreted. The intestinal mucosa represents an internal barrier, which is generally only permeable for food-relevant substances (cf. body barriers – Nanoparticles and the Gastro-Intestinal Tract). Due to their small size, nanomaterials present in food products may potentially migrate through the intestinal mucosa. Furthermore, nanoscale particles can influence the gut bacteria present in the intestine. In order to exclude a health risk, the respective nanomaterials are typically examined by in vitro studies with different cell strains (cf. cross-sectional topics – In vitro tests for the benefit of nanosafety). Furthermore, in vivo studies with small mammals such as mice or rats serve to draw conclusions about their effects on the human body.
Studies on rats confirmed that synthetic amorphous silicon dioxide particles do not pose a major health risk to humans independent of the particles’ size, i.e. nanoscale or microscale. However, the data available for nanoscale silicon dioxide particles is incomplete and local effects on the digestive tract have yet to be investigated. EFSA therefore points out that further toxicological studies are necessary for nanoscale silica. Nevertheless, the existing studies are sufficient to exclude a toxic effect of silicon dioxide E551 as it is currently approved for usage in the EU .
For the food additives silver (E 174) and gold (E 175), no final risk assessment can be performed by EFSA. This is justified by a lack of information on the occurring particle sizes [6,8]. In vitro studies showed that silver nanoparticles or the subsequently formed silver ions are able to migrate through the intestinal wall thus causing inflammatory reactions [10,11]. Due to these findings, the usage of both precious metals in food products is only approved for very few special applications, e.g. as a coating for confectionery.
In the EU, the approval of food additives is described in Regulation (EU) No. 234/2011 and novel foods are covered in Regulation (EU) No. 2015/2283. The Novel Foods Regulation specifies the information the applicant of a novel food product has to submit for the risk assessment of the respective product (e.g. toxicological data, particle size or manufacturing process). In addition, the applicant also has to list the food additives’ advantages and disadvantages for the consumer. Furthermore, Regulation (EU) No. 1169/2011 contains a precise description on how to label food/food products and additives to be consumer-compliant. According to Article 18 of the Regulation, intentionally added engineered nanomaterials must be labelled with the term “nano” as indicated on the list of ingredients. Nanomaterials occurring as a result of the manufacturing process are excluded [2,12,13].
In 2018, EFSA published a guidance document for the risk assessment of engineered nanomaterial and nanotechnology applications in food and feed. The practical guidance documents provides manufacturers with a catalogue of criteria for classifying nanomaterials. Building on this, the necessary characterisation methods and toxicological tests required to determine the risk are listed .
Food and food products may contain nanomaterials. In Europe however, currently no intentionally produced nanomaterials are used in food & feed applications; the occurring nanomaterials are by-products of the production process of approved food additives. In Asia and North America, on the other hand, nanomaterials are used specifically in food products, e.g. for the encapsulation of vitamins. Based on the majority of existing studies, current approved food additives pose no health risk for humans.
- Regulation (EC) No 1331/2008 of the European Parliament and of the Council of 16 December 2008 establishing a common authorisation procedure for food additives, food enzymes and food flavourings. OJ L 354, 31.12.2008, p. 1–6.
- Regulation (EU) No 1169/2011 of the European Parliament and of the Council of 25 October 2011 on the provision of food information to consumers, amending Regulations (EC) No 1924/2006 and (EC) No 1925/2006 of the European Parliament and of the Council, and repealing Commission Directive 87/250/EEC, Council Directive 90/496/EEC, Commission Directive 1999/10/EC, Directive 2000/13/EC of the European Parliament and of the Council, Commission Directives 2002/67/EC and 2008/5/EC and Commission Regulation (EC) No 608/2004 Text with EEA relevance. OJ L 304, 22.11.2011, p. 18–63.
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- EFSA ANS Panel (EFSA Panel on Food Additives and Nutrient Sources Added to Food),EFSA Journal, 16(1): 5088, 70 pp. et al. (2018),
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- Zimmermann, MB et al. (2011), Nanoscale, 3(6): 2390-2398.
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- Bohmert, L et al. (2014), Nanotoxicology, 8(6): 631-642.
- Gaiser, BK et al. (2013), Toxicol Sci, 131(2): 537-547.
- Commission Regulation (EU) No 234/2011 of 10 March 2011 implementing Regulation (EC) No 1331/2008 of the European Parliament and of the Council establishing a common authorisation procedure for food additives, food enzymes and food flavourings Text with EEA relevance OJ L 64, 11.3.2011, p. 15–24.
- Regulation (EU) 2015/2283 of the European Parliament and of the Council of 25 November 2015 on novel foods, amending Regulation (EU) No 1169/2011 of the European Parliament and of the Council and repealing Regulation (EC) No 258/97 of the European Parliament and of the Council and Commission Regulation (EC) No 1852/2001 (Text with EEA relevance). OJ L 327, 11.12.2015, p. 1–22.
- EFSA Scientiﬁc Committee, EFSA Journal 2018;16(7):5327, 95 pp. et al. (2018),
- Younes, M et al. (2021), EFSA J, 19(5): e06585