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VeilleNanos - Nanos and drugs

Nanos and drugs

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Nanos and drugs

By the AVICENN team – Last updated April 2025

Nanos in drugs: research and applications

Reliable, up-to-date information on nanotechnology research and applications in the pharmaceuticals sector is scarce1See the references listed at the bottom of the page in the “Elsewhere on the web” section for more details.

Almost nothing from ANSM on nanos in drugs

The French National Agency for the Safety of Medicines and Health Products (ANSM) published a report in 2011 on the Biological Evaluation of medical devices containing nanomaterials.

Followed by silence… it took nearly ten years to obtain a new report, composed of information that was unfortunately relatively dated:

  • Article 60 of the law on the modernization of our health system stated that the government would submit a report on nanomaterials in drugs and medical devices to Parliament in the summer of 2017.
  • While the Department of Health announced its upcoming release in July 2018, by mid-2020, we still had no record of the report.
  • Despite its numerous reminders to the Ministry of Health, AVICENN did not manage to get more information, except that the report, carried out by ANSM, was being finalized and in the process of inter-ministerial validation… but this since at least December 2017…
  • In July 2020, AVICENN therefore sent a registered letter to the Prime Minister and the Minister of Solidarity and Health to demand the release of the government report on nanomaterials in drugs and medical devices that should have been made public three years before.
  • The report received on August 3, 2020 has no date or author(s), no details on methodology, has mostly old references and major limitations.

The recommendations of the latest ANSM report are nevertheless interesting and remain more relevant than ever:

  • developments in standardization and regulation for better identification and evaluation of nanomedicines and medical devices
  • modifications of the R-nano register (convergent with the demands of the precautionary and prevention actors)
  • increased involvement of ANSM on the subject
  • etc.

(Un)desired presence of nanoparticles in drugs

E71 in the spotlight

E171, banned in food since 2020, is present in many medicines2– In 2017, Que Choisir revealed that “4,000 drugs contain the dye E171” (composed in part of titanium dioxide nanoparticles).
– In 2018, 60 Millions de Consommateurs brought confirmation through tests of the presence of these nanoparticles in 6 widely used drugs: Efferalgan – Upsa, Spasfon – Teva, Zyrtecset – UCB Pharma, Nurofen – Reckitt Benckiser, Doliprane enfant – Sanofi, Euphytose – Bayer.
– In December 2021, in its exclusive issue on nanoparticles, Kali magazine published a list of the 800 most prescribed drugs that contain titanium dioxide
.
This excipient, composed of titanium dioxide nanoparticles, has no therapeutic purpose; it is used as a colorant and/or opacifier in the film coating of tablets or capsules for its protective properties against UV radiation. It is therefore to be dissociated from “nano-drugs”, which are voluntarily designed on a nano-scale with the aim of crossing physiological barriers and bringing active substances more rapidly and/or more precisely into the body.

Many voices in recent years have been calling for the removal of E171 from medicines.

Thomas Borel, Director of Scientific Affairs at LEEM, the professional organization of drug companies in France, believes that “the excipient E171 ensures the stability of the drug” and that it is therefore “indispensable” for example, to ensure protection and ingestion of the drug3Cf. Why titanium dioxide has been banned from plates, but not toothpastes, Challenges, June 7, 2019 and “Removing E171 from drugs would be extremely burdensome,” Rose Up, August 28, 2019.
That said, brands are now promoting TiO2-free drug coatings4See for example Biogrund’s marketing campaign launched in March 2019:
Challenges of TiO2 free film coatings, March 25, 2019
Titanium dioxide (TiO2) – a critical excipient, 19 March 2019
Replacement of titanium dioxide (TiO2) in tablet film coatings
Are you facing the challenge of replacing TiO₂ in your coating formulations?
and in 2019, Sanofi confirmed that it was considering substituting titanium dioxide in its drugs5See speech by René Labatut, Vice President, Technology Innovation Strategy, Sanofi, at the NanoResp Forum, Drugs and vaccines: what are their nanoparticles for?”, May 20, 2019. In May 2018, the TiO2 nanoparticle management plan implemented by Sanofi had been the subject of a presentation at the SOFHYT forum on emerging risks.. In subsequent years, this led to the effective elimination of E171 from Doliprane, among other drugs.

In February 2025, the European Commission should decide whether to delete – or if not, to extend for a period to be determined – the authorization for the use of titanium dioxide (E171) in medicinal products6cf. recitals 14 to 18 and article 3 of European Regulation 2022/63. Several weeks later, still nothing… : to be continued!

Other nanoparticles of concern in drugs

Titanium dioxide (E171) nanoparticles are not the only problem. The safety of other nanoparticles also present in drugs is questionable – in particular those used as colorants (iron oxides in particular7In December 2022, AVICENN’s report Searching for [nanos] in every day products noted the presence of nanoparticles of titanium dioxide and iron oxides in Bayer’s drug Xarelto) or silica. Will the work carried out by ANSES on the risks of nanos in food quickly shed light on these questions?

Stay tuned…

Elsewhere on the web

– In French :

– In English:

Any questions or comments? This information sheet compiled by AVICENN is intended to be completed and updated. Please feel free to contribute.

Upcoming Nano Agenda

5
Oct.
2025
NaMasTE thematic school (CNRS, Ile d’Oléron – France)
Ile d'Oléron
Training
  • Thematic school of the NaMasTE research group (Manufactured Nanomaterials, Toxicology, Ecotoxicology and Risks: towards controlled development)
  • Public: engineers, researchers (contract and permanent), PhD students, industrialists and members of associations working on nanomaterials.
  • The program includes the physical chemistry, biology and environmental sciences needed to understand the key aspects involved in the controlled development of nanomaterials.
    → Safer-by-design approaches, which integrate analysis of the production, characterization of properties, fate, and impacts (beneficial or harmful) of nanomaterials and products containing them throughout their life cycle
  • Dates: October 5 to 10, 2025
  • Organizers: CNRS
  • Website: https://namaste.sciencesconf.org
6
Oct.
2025
Characterizing and preventing risks related to manufactured nanomaterials and ultrafine particles (INRS, Vandœuvre-Lès-Nancy – France)
Nancy
Training
  • Training intended for occupational physicians, occupational risk prevention specialists (IPRP), company prevention specialists, prevention department staff from Carsat, Cramif and CGSS, institutional prevention specialists (Dreets, Dreal, MSA…).
  • Organizer: French National institute of research and security (INRS)
  • October 6 to 10, 2025
  • Website: www.inrs.fr/…/formation/…JA1030_2025
6
Oct.
2025
Scientific integrity, manipulation of scientific information, industry influence strategies and whistleblower protection (Université Paris Cité, Paris – France)
Paris
Conference
health
conflicts of interest
health
information
research
risks
science and society
  • 3pm – Conference by Irène Frachon on her fight to reveal the dangers of Mediator, the difficulties encountered by whistleblowers in the face of institutional and industrial pressure, and the importance of their role in defending public health.
  • 4pm – Round table on the manipulation of scientific information and the defense of whistleblowers moderated by Raphaël Lévy (professor of physics at Sorbonne Paris Nord University, specialist in nanoparticles and their uses in biology, coordinator of the ERC NanoBubbles project dedicated to research into the corrective mechanisms of science), with :
    • Maud Bernisson, post-doctoral fellow at LISIS (CNRS), member of the ERC NanoBubbles project, on the mechanisms of influence of pharmaceutical companies in the scientific field.
    • Marc Samama, professor, anesthesiologist, co-chairman of the Commission des blocs et plateaux techniques de la CME de l’AP-HP, past Editor-in-Chief of the European Journal of Anaesthesiology, director of the Office de l’Intégrité Scientifique de l’AP-HP.
    • Solène Lellinger, Senior Lecturer in the History and Philosophy of Health at Paris Cité University, specializing in the socio-history of medicines and their intersection with medical practices, and in particular the ways in which knowledge and information about medicines are produced.
    • Cécile Barrois de Sarigny, Deputy Ombudsman in charge of whistleblower protection.
  • With the support of the ERC Synergy NanoBubbles project
  • Website: https://u-paris.fr/sante/irene-frachon-a-paris-une-conference-et-une-table-ronde-sur-lintegrite-scientifique

This sheet was originally created in February 2019


Notes and references

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