Comment by cogman10
3 days ago
> only take action when there is actual evidence and proof of harm being done
I agree with most of what you are saying. However, I think it's valid to also apply heavy scrutiny on new chemicals being added to the food chain. The default being to not allow it if it's not proven safe.
Red dye 3 probably shouldn't have been added to the food supply chain with that criteria but since it's already been there for decades with no strong link to negative outcomes there's little reason to ban it now.
You really don't want to know about GRAS (Generally recognized as safe) then. 700 food substances were grandfathered into the food supply chain and most new things are self-affirmed by the company selling them.
This is like the whole bugs in food thing.
Sometimes no bugs are allowed at all, people be getting upset if their pop tarts have bugs in them.
Sometimes it's like some bugs are allowed and just part of it like when I buy organic broccoli at the farmers market and need to soak it to get whatever those things are in there out. Or when I get those little mummified bugs in the bottom of oatmeal tins.
Sometimes it's like the food is literally coated in bugs like all that stuff that's coated on schellac. Which, finally to bring it back to a callback to your point, is both GRAS and also made of bugs.
Shellac isn't made of bugs - it's made by bugs. Specifically, it's the resin secreted by a female lac beetle onto the branch of the trees that they live and feed on.
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I don't disagree with you, but we don't have heavy scrutiny on the existing and natural chemicals that are in the food chain from all of the plants that we eat.
You could build a heuristic risk score against each molecule:
- What functional groups does it have?
- How many functional groups does it have?
- How much electron delocalization does it have?
- How much of that electron delocalization is PAHs?
- Does the molecule participate in redox reactions?
Etc.
Basically check to see which molecules can generate free radicals, strip DNA, convert to dangerous metabolites, etc.
It's call QSAR https://en.wikipedia.org/wiki/Quantitative_structure%E2%80%9... They may use a hundred of properties to guess the effect of the molecule.
Once you have that trained, you'll be able to publish it and dramatically improve the current SoTA!
I wish it was as easy as this - while there are known toxicophores/no-go functional groups in medchem, there is going to be a big dearth of data on non-acute (e.g. not hERG, hepatotoxicity, etc) toxicity, which is really what the question is here: what are the marginal risks/rewards from eating existing food X (since we know it's probably not acutely toxic).