The US National Academy of Science today published its long-awaited Research Strategy for Environmental, Health, and Safety Aspects of Engineered Nanomaterials. I won’t comment extensively on the report as I was a member of the committee that wrote it. But I did want to highlight a number of aspects of it that I think are particularly noteworthy:
Great progress so far, but it’s time to change gears. Something we grappled with as a committee was what the value of yet another research strategy was going to be. After all, it wasn’t so long ago that the US federal government published a well received strategy of its own. A key driver behind our strategy was a sense that the past decade has been one of defining the challenges we face as the field of nanotechnology develops, while the next decade will require more focus as an ever greater number of nanotechnology-enabled products hit the market. In other words, from a research perspective it’s time to change gears, building on past work but focusing on rapidly emerging challenges.
Combining life cycle and value chain in a single framework for approaching nanomaterial risk research. As a committee, we spent considerable time developing a conceptual framework for approaching research addressing the health and environmental impacts of engineered nanomaterials. What we ended up using was a combination of value chain – ranging from raw materials to intermediate products to final products – and material/product life cycle at each stage of the value chain. This effectively allows risk hot spots to be identified at each point of a material and product’s development, use and disposal cycle.
Principles, not definitions. Rather than rely on a single definition of engineered nanomaterial to guide risk-related research, we incorporated a set of principles into our conceptual framework to help identify materials of concern from an environment, health and safety impact perspective. These build on the principles proposed by myself, Martin Philbert and David Warheit in a toxicology review published last year. From the National Academies report:
…the present committee focuses on a set of principles in lieu of definitions to help identify nanomaterials and associated processes on which research is needed to ensure the responsible development and use of the materials. The principles were adopted in part because of concern about the use of rigid definitions of ENMs that drive EHS research and risk-based decisions … The principles are technology-independent and can therefore be used as a long-term driver of nanomaterial risk research. They help in identifying materials that require closer scrutiny regarding risk irrespective of whether they are established, emerging, or experimental ENMs. The principles are built on three concepts: emergent risk, plausibility, and severity; …
Emergent risk, as described here, refers to the likelihood that a new material will cause harm in ways that are not apparent, assessable, or manageable with current risk-assessment and risk-management approaches. Examples of emergent risk include the ability of some nanoscale particles to penetrate to biologically relevant areas that are inaccessible to larger particles, the failure of some established toxicity assays to indicate accurately the hazard posed by some nanomaterials, scalable behavior that is not captured by conventional hazard assessments (such as behavior that scales with surface area, not mass), and the possibility of abrupt changes in the nature of material-biologic interactions associated with specific length scales. Identifying emergent risk depends on new research that assesses a novel material’s behavior and potential to cause harm.
Emergent risk is defined in terms of the potential of a material to cause harm in unanticipated or poorly understood ways rather than being based solely on its physical structure or physicochemical properties. Thus, it is not bound by rigid definitions of nanotechnology or nanomaterials. Instead, the principle of emergence enables ENMs that present unanticipated risks to human health and the environment to be distinguished from materials that probably do not. It also removes considerable confusion over how nanoscale atoms, molecules, and internal material structures should be considered from a risk perspective, by focusing on behavior rather than size.
Many of the ENMs of concern in recent years have shown a potential to lead to emergent risks and would be tagged under this principle and thus require further investigation. But the concept also allows more complex nanomaterials to be considered—those in the early stages of development or yet to be developed. These include active and self-assembling nanomaterials. The principle does raise the question of how “emergence” is identified, being by definition something that did not exist previously. However the committee recognized that in many cases it is possible to combine and to interpret existing data in ways that indicate the possible emergence of new risks. For example, some research has suggested that surface area is an important factor that affects the toxic potency of some ENMs; ENMs that have high specific surface area and are poorly soluble might pose an emergent risk.
Plausibility refers in qualitative terms to the science-based likelihood that a new material, product, or process will present a risk to humans or the environment. It combines the possible hazard associated with a material and the potential for exposure or release to occur. Plausibility also refers to the likelihood that a particular technology will be developed and commercialized and thus lead to emergent risks. For example, the self-replicating nanobots envisaged by some writers in the field of nanotechnology might legitimately be considered an emergent risk; if it occurs, the risk would lie outside the bounds of conventional risk assessment. But this scenario is not plausible, clearly lying more appropriately in the realm of science fiction than in science. The principle of plausibility can act as a crude but important filter to distinguish between speculative risks and credible risks.
The principle of severity refers to the extent and magnitude of harm that might result from a poorly managed nanomaterial. It also helps to capture the reduction in harm that may result from research on the identification, assessment, and management of emergent risk. The principle offers a qualitative reality check that helps to guard against extensive research efforts that are unlikely to have a substantial effect on human health or environmental protection. It also helps to ensure that research that has the potential to make an important difference is identified and supported.
Together, those three broad principles provide a basis for developing an informed strategy for selecting materials that have the greatest potential to present risks. They can be used to separate new materials that raise safety concerns from materials that, although they may be novel from an application perspective, do not present undetected, unexpected, or enhanced risks. They contribute to providing a framework for guiding a prioritized risk-research agenda. In this respect, the principles were used by the committee as it considered the pressing risk challenges presented by ENMs.
Maintaining current research and development funding levels. As a committee, we felt that the current US federal government of ~$120 million into environment, health and safety-specific nanotechnology research was reasonable, especially given the current economic climate. However, we did recommend that, as knowledge develops and commercialization of products using nanomaterials increases, funded research is aligned with areas and priorities identified within the strategy.
Developing cross-cutting activities. There were five areas where the committee felt that further funding was needed to ensure the value of nano-risk research was fully realized. Each of these cuts across areas of research, and provides the means to maximize the benefit of the science being supported. From the report:
Informatics: $5 million per year in new funding for the next 5 years should be used to support the development of robust informatics systems and tools for managing and using information on the EHS effects of ENMs. The committee concluded that developing robust and responsive informatics systems for ENM EHS information was critical to guiding future strategic research, and translating research into actionable intelligence. This includes maximizing the value of research that is EHS-relevant but not necessarily EHS-specific, such as studies conducted during the development of new therapeutics. Based on experiences from other areas of research, investment in informatics of the order of $15 million is needed to make substantial progress in a complex and data rich field. However, within the constraints of nanotechnology R&D, the committee concluded that the modest investment proposed would at least allow initial informatics systems to be developed and facilitate planning for the long-term.
Instrumentation: $10 million per year in new funding for the next 5 years should be invested in translating existing measurement and characterization techniques into platforms that are accessible and relevant to EHS research and in developing new EHS- specific measurement and characterization techniques for assessing ENMs under a variety of conditions. The committee recognized that the proposed budget is insufficient for substantial research into developing new nanoscale characterization techniques— especially considering the cost of high-end instruments such as analytic electron microscopes—in excess of $2 million per instrument. However, the proposed budget was considered adequate to support the translation of techniques developed or deployed in other fields for the EHS characterization of ENMs.
Materials: Investment is needed in developing benchmark ENMs over the next 5 years, a long-standing need that has attracted little funding to date. The scope of funding needed depends in part on the development of public-private partnerships. However, to assure that funding is available to address this critical gap, the committee recommends that $3-5 million per year be invested initially in developing and distributing benchmark ENMs. While more funds could be expended on developing a library of materials, this amount will assure that the most critically needed materials are developed. These materials will enable systematic investigation of their behavior and mechanisms of action in environmental and biologic systems. The availability of such materials will allow benchmarking of studies among research groups and research activities. The committee further recommends that activities around materials development be supported by public- private partnerships. Such partnerships would also help to assure that relevant materials are being assessed.
Sources: $2 million per year in new funding for the next 5 years should be invested in characterizing sources of ENM release and exposure throughout the value chain and life cycle of products. The committee considered that this was both an adequate and reasonable budget to support a comprehensive inventory of ENM sources.
Networks: $2 million per year in new funding for the next 5 years should be invested in developing integrated researcher and stakeholder networks that facilitate the sharing of information and the translation of knowledge to effective use. The networks should allow participation of representatives of industry and international research programs and are a needed complement to the informatics infrastructure. They would also facilitate dialogue around the development of a dynamic library of materials. The committee concluded that research and stakeholder networks are critical to realizing the value of federally funded ENM EHS research and considered this to be an area where a relatively small amount of additional funding would have a high impact—both in the development of research strategies and in the translation and use of research findings. Given the current absence of such networks, the proposed budget was considered adequate.
Authority and accountability. In our report, we talk quite a bit about the need for an entity within the federal government to take the lead in implementing a risk research strategy. While the US National Nanotechnology Initiative have done a great job coordinating interagency activities, we felt that there is only so far coordination without authority can go if socially and economically important research is to be conducted in a timely and relevant manner. What this “entity” might look like – we left that to the federal government to chew over.
There’s a lot more to the report – including (as you would expect) a broad assessment of research areas that need attention if the science of nanomaterial human health and environmental impacts is to continue to develop effectively.
This is the first of two reports- the second is due in around 18 months, and will look at progress toward implementing a relevant and effective research strategy.
The National Academies report “A Research Strategy for Environmental, Health, and Safety Aspects of Engineered Nanomaterials” can be downloaded here.
Very helpful Andrew, look forward to getting a similarly coherent and thought through approach in the UK from the government, or someone!
I like your principles, but looking at it from the perspective of industry, I can foresee some room for interpretation. For example, I could imagine the Nano Salt people for example, arguing that their product doesn’t fall within your principles, and because of clumping isn’t nano anyway and so doesn’t need any new tox. (I have not asked them btw, though have heard presentations saying similar things. I have no idea personally if that is correct, though can understand their reasoning.) What is your view on independent oversight of such areas where companies have chosen to interpret the guidance to assume no potential for harm and so no new tox?
I am assuming, as we are calling for, that a new focus on transparency about such decisions from companies will be the starting point. However, our very broad definition in the EU will cover it anyway from our point of view, whether that is a good thing for innovation or not, I am not sure!
Thanks Hilary.
For more background on the concept of principles rather than a definition, check out the Tox Sci paper linked to above. The aim there was to effectively take “nano” out of the equation, and enable people to focus on materials that presented an emergent and plausible health risk, irrespective of what they were called. If they were to be applied to a regulatory context rather than helping develop research directions, they would need quite a bit more work. But in principle, they remove some of the hiding places for organizations to hunker down in that don’t want to evaluate and respond to the potential impacts of new products.