Can cryoprotectant toxicity be crowd-sourced?

From the article The red blood cell as a model for cryoprotectant toxicity by Aschwin de Wolf

One simple model that allows for “high throughput” investigations of cryoprotectant toxicity are red blood cells (erythrocytes). Although the toxic effects of various cryoprotective agents may differ between red blood cells, other cells, and organized tissues, positive results in a red blood cell model can be considered the first experimental hurdle that needs to be cleared before the agent is considered for testing in other models. Because red blood cells are widely available for research, this model eliminates the need for animal experiments for initial studies. It also allows researchers to investigate human cells. Other advantages include the reduced complexity of the model (packed red blood cells can be obtained as an off-the-shelf product) and lower costs.

It sounds to me like this is a very cheap assay for viability. You don’t need much equipment. High toxicity compounds can be screened on visual appearance. More detailed analysis can be done by a light microscope or a spectrophotometer.

The biggest issue facing cryonics (and the holy grail of suspended animation with true biostasis) is the existence of cryoprotectant toxicity. Less toxic solutions can be perfused for a longer period of time, and thus penetrate the entire organism without triggering additional loss of viability. Vitrification already eliminates all ice formation—we know enough to know that without toxicity, it should work for trivially reversible forms of long-term suspended animation.

Thus if we want to ask what can be done cheaply by a lot of people to help cryonics move forward, one possibility is that they could perform empirical tests on the compounds most likely to prove effective for cryoprotection.

We can speculate about the brain being reparable at all kinds of levels of damage—but that is speculation. Sure we do have to make a decision to sign up or not based on that speculation. But the more hard evidence we can obtain, the more of a chance that we aren’t being distracted from the reality of the situation by wishful thinking—and the more likely we are to persuade our fellow self-identifying rational skeptics to take our side. Furthermore (and I know this sounds obvious, but it still needs to be said) in taking a more empirical approach to actually resolving the issues as quickly as possible, we are more likely to survive than otherwise.

There are still a lot of questions that are raised in my mind by this crowdsourcing idea. What kinds of mechanisms would be best for collaboration and publication of results? Are there many other dirt-cheap empirical testing methods that small unfunded groups of nonspecialists could employ for useful research? How many people and groups could/​should get involved in such a project? Aschwin mentions “theoretical work in organic chemistry” as the first step—how much of that has already been done, or needs to be done? What kind of a learning curve is there on learning enough organic chemistry to propose a useful test?