Altering solid form alters- bioavailability, stability, manufacturing and
regulatory processes
Bioavailability- drug must be in solution to cross GI tract and rate limiting
step is usually rate of dissolution
Stability- chemical reactivity, conversion to other compounds and forms
may have different flow, compression and water sorption properties
Regulation- can patent different forms of drug and first steps of drug is to
characterise its form
Arrangement of molecules:
Crystalline materials-ordered and periodic arrangement, unit cell
repeated in all directions and have a melting point
Amorphous materials- no long range order, non-
random local structure and have a glass transition
temperature (Tg)
Crystal systems- symmetrical arrangement
Polymorphism- can have different crystal structures of
the same compound
Have different melting points and solubilities
Same solution/melt
Polymorphic stability- at a given temperature and pressure only 1 form is
stable (with lowest free energy) but others can be meta stable (kinetically
stable)
Monotropic- same form is stable irrespective of temperature
Enantiotropic- either of 2 forms can be stable depending on temperature
(critical temperature +n=form 1 or –n=form 2
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