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Take home messages Session 1
1. Approaches to the determination of NIAS as part of safety by design
It showed the capabilities of modern instrumental methods of analysis and
the benefits of close-working in the packaging chain since this helps
identify, understand, and limit the migration of IAS and NIAS. But detecting
and identifying more-and-more of less-and-less has to be backed up with
tox evaluation, as the presentation described.
The work on migration from can coatings into foods is still in progress and
no firm conclusions can yet be drawn. But it does illustrate that the food
simulating system must be questioned at regular intervals to check that it is
reliable with regards to migration (identity and quantity) into ‘real’ foods.
Since these data are used to estimate exposure.
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Take home messages Session 1
2. TTC in safety assessment of FCMs
This presentation described a number of tools that are
bundled together as the CoMSAS - Complex Mixture
Safety Assessment Strategy. They include analytical
chemistry, bioassays and application of the TTC approach.
Going from Theory to Practice, some test cases were
outlined. This is a key activity. The importance of general
acceptance was stressed and is underway.
.
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Take home messages Session 1
3. Bioassays and packaging safety assessment
Here were described several in vitro tests covering
different end-points and used to evaluate mixtures.
A very impressive battery of tests. The key
question for me was the sentence ‘when you cross
a certain threshold you can consider the result as
positive”.
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Take home messages Session 1
There was also an excellent slide comparing the results for several
tests applied to extracts of can coatings. Of course one will choose
the coating that gives the fewest responses.
But if that coating is twice as expensive and also does not perform
so well in pack tests, maybe the 2nd best coating is still OK - in fact
better than OK if it maintains better pack integrity, food microbiology
and limits metals release.
So how can we set a threshold that can get accepted generally?
Making the link between in vitro tests and human health is needed.
But I am confident that this research will continue from strength to
strength.
.
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Take home messages Session 1
4. Prioritisation of potentially genotoxic substances migrating from
printed paper and board using in silico tools.
This described a very pragmatic application of 4 (Q)SAR tools
to the approximately 1769 substances that are potentially used
in printed P/B. What struck me was the lower than expected
degree of agreement (‘overlap) between the different tools.
Especially since about half (50/100) of the highest prioritised
substances were in the training set (i.e. actual gentox data
were available and used to construct the models) in which
case the degree of overlap was even weaker. This was a
useful reminder that these tools should be used with caution.
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Take home messages Session 1
What also struck me (and was mentioned
the following session) is that in the
prioritisation exercise it would be useful to
know just how many of these 1769 listed
substances are actually used?
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Take home messages Session 1
5. Hydrocarbons from FCMs - focus on polyolefins and hot-melt
adhesives
This presentation showcased the power of LC-GC and GC-MS
when applied to these fiendishly complex hydrocarbon
mixtures. Some of the mixtures can be unpicked almost
completely whereas other mixtures are too complex even for
these techniques to resolve them into individual component
parts. In any case, perhaps they have to be evaluated as a
whole, as complex mixtures. Since there are many potential
sources of contamination in foods of which FCMs is only one, a
common regulation for hydrocarbon contaminants in foods was
suggested.
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Take home messages Session 1
.
Overall I found it to be a fantastic, well balanced
session in which I learned a lot and which set me
thinking.
Thank you for the opportunity to share these short
thoughts and reflection with you.
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Session 2: Safety Challenges
Arising From Renewable and
Recycling Food Contact
Materials
Lionel Spack
Take home messages Session 2
Lionel Spack 1. Eco-design tools
1. Environmental performance
2. Quantification of improvement when renewable or
recycled materials are used
2. Safety & Compliance
1. Bioassay mapping
2. Low migration
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Take home messages Session 2
Lionel Spack 4. Functional barrier evaluation
Protection of food in bag-in-box design
Simple and pragmatic approach/testing
5. On-line detection
Fast detection of main contaminants
Quality monitoring “on-time”
6. Modified PLA-Nanoclay
Oxygen barrier improvement
Improve mechanical behavior: stiffness, resistance
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Take home messages Session 3
Roland Franz
1. It was generally found and appreciated
that scientific knowledge in the area of
molecular mass transport in and migration
from FCMs as well as evaluation tools like
migration modeling and sophisticated
analytical tools have made tremendous
progress in support of safety-by-design.
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Take home messages Session 3
Roland Franz
2. As a direct consequence it was found that
the currently recognised migration model in
use is in many cases not only
overconservative but even too far away from
real migration and therefore needs
refinements in terms of updating the
underlying modeling parameters (diffusion
coefficients in polymers and partition
coefficients between polymer and foods).
3. Zzz
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Take home messages Session 3
Roland Franz
3. Studies have been carried out and are still
in hands to update modeling parameters in
particular for small molecules in polymer
systems like PET, Nylon, EVOH and similar
to allow more precise migration and
exposure modeling.
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Take home messages Session 3
Roland Franz
4. An empirical, semi-scientific model for
derivation of diffusion coefficients from
polymer properties such as glass transition
temperatures was presented as another
promising tool with the perspective for
broader applicability to any polymer type.
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Take home messages Session 3
Roland Franz
5. Concerning partition coefficients either
between food contact polymer and food or
between different polymers in multilayers
knowledge and data gaps were identified
and more research in that direction was felt
to needed.
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Take home messages Session 3
Roland Franz
6. Simulation of mass transport processes
on the basis of molecular dynamics can be
used to proactively scrutinize intended food
packaging applications in support of safety-
by-design. However, it was felt that
experimental data are still missing to
validate these calculations and generate
confidence in their applicability.
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Take home messages Session 4
Cristina Nerín
1. Most of the research done is on ACTIVE Packaging.
Only two posters and one oral on INTELLIGENT Packaging.
2. Active agents are mainly plant extracts and EOs.
Only one uses TiO2 as antimicrobial after activation UV-VIS.
3. Three posters on the mode of action of active packaging.
4. Technologies for active packaging: a) substances
encapsulation (PVOH, Cyclodextrins, liposoms) and b)
production (flexography, electrospinning).
5. Most of the studies use Biopolymers (PLA, gelatine-
starch) with improved properties.
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Take home messages Session 4
Cristina Nerín
6. Only a few organoleptic studies even though active agents
have strong odour and/or taste.
7. Studies on Migration of nanoparticles (three posters, one
oral).
8. Barrier to gases: Two posters on O2 scavengers and two
posters for improving the barrier properties.
9. Effect of food processing on migration.
10. Most of the presentations are far from the market.
More interaction between academia and industry
is required.
11. Food industry is not using the innovations, even
though there are some good materials on the market.
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Session 5: Future Challenges in
Food Packaging Processing
and Food Processing
Equipment
Mauro Fedeli
Take home messages Session 5
Mauro Fedeli
Sustainability:
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Reduction of plastic
packaging waste
Reduction of food waste
Compostable materials
Active packaging: oxygen
scavengers ethylene
inhibitors
Different portion sizes
Increasing the barrier properties of packaging
Increasing shelf life of products