Crashing
Bluelighter
Why has the presence of polymorphism never been mentioned when considering the classic 'good vs. bad' acid?
This, to me overthought is basically useless, and none of the studies have to due with MXE.... Until then let's get talking!Agreed with theacidtest. When the crystal dissolves any 'morphisms' are lost so it shouldn't matter anymore.
I guess a good suggestion, but the rest of the debate really belongs in the dirty acid debate / faq-in-progress (sigh) thread..
okay to close this or does anyone have grounds for further discussion?
In the case of the antiviral drug ritonavir, not only was one polymorph virtually inactive compared to the alternative crystal form, but the inactive polymorph was subsequently found to convert the active polymorph into the inactive form on contact, due to its lower energy and greater stability making spontaneous interconversion energetically favourable. Even a speck of the lower energy polymorph could convert large stockpiles of ritonivir into the medically useless inactive polymorph, and this caused major issues with production which ultimately were only solved by reformulating the medicine into gelcaps and tablets, rather than the original capsules.
The point is not whether polymorphism is real but whether it's relevant.
I guess it's an interesting discussion, but what practical implications are there for the average drug user?
See yes and no. Different drying techniques can yield wildly different shape do, sized, and even colored crystals when it comes to some drugs.Well i think the reason the crystals form differently is because the molecules are slightly warped, so they would lay into the receptor slightly differently, thus have slightly different effects.
And thank you for title change.