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Summary

Summary Pharmaceutical materials

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Industrial pharmacy - 1st semester Includes bullet points, key diagrams and images

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  • June 8, 2023
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  • 2019/2020
  • Summary
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Materials

 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

System Axes Angles
Cubic a=b=c α=β=γ=90o
Tetragonal a=b≠c α=β=γ=90o
Orthorhombic a≠b≠c α=β=γ=90o
Monoclinic a≠b≠c α= γ=90o≠β
Triclinic a≠b≠c α≠β≠γ
Trigonal a=b=c α≠β≠γ≠90o
Hexagonal a=b≠c α=β=90o, γ=120o


 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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