Abstract
Organic compounds can crystallise in different forms known as polymorphs. Some polymorphs have
disappeared from the physical world, never to be recrystallised again under the same conditions. The
most infamous of these cases is that of the HIV drug ritonavir: once its reluctant stable form II was
unwillingly nucleated for the first time, its desired but metastable form I could never be produced again
with the same manufacturing process. The disappearance of metastable polymorphs remains a
mysterious phenomenon, and the lack of control over it can be frustrating and costly for drug
development. Here we show that Ritonavir’s extraordinary disappearing polymorph can be consistently
produced by ball-mill grinding. Our work shows that not only crystal size, but also crystal shape and
molecular conformation dictate polymorph stability switches in the mill. Through population balance
modelling simulations, we also demonstrate how the size and shape of crystals at the steady state are
determined by crystal breakage, dissolution and growth kinetics in the mill, which in turn can be
controlled by the milling conditions. This work highlights the huge potential of mechanochemistry in
polymorph discovery, and the manufacturing and control of complex flexible drug compounds such as
Ritonavir.
Supplementary materials
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