kausar ahmad kulliyyah of pharmacy phm1153 physical pharmacy 1 2011/12 1 solids
TRANSCRIPT
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KAUSAR AHMADKULLIYYAH OF PHARMACY
PHM1153 Physical Pharmacy 1 2011/12
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Solids
http://staff.iium.edu.my/akausar
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Contents
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General properties
Types of solids Amorphous Crystalline
Crystal structureCrystallisation
• Crystal growth
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What is solid…..to pharmacy?
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Majority of drugs and excipients exist as solids
Various dosage forms are preparede.g. tablets, emulsions
Types of solids affect Processing Efficacy
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General Properties
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Maintain shape
Not fluid
Molecules/atoms/ions are held closely by
intermolecular
interatomic
ionic forces
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Intermolecular forces
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1. Van der Waals forces
i. Dipole-dipole (Keesom) e.g. HCl
ii. Dipole-induced dipole (Debye)
iii. Induced dipole-induced dipole (London)
2. Ion dipole and ion-induced dipole forces
3. Hydrogen bonds e.g. H2O
In solids, average kinetic energy << strength of intermolecular forcesHence, each molecule can only move short distances around a fixed position.
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Classification of Solids
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Amorphous
Crystalline
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Amorphous Solids
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E.g. silica gel, synthetic plastics/polymersIrregular shape
- molecules are arranged in a random mannerNo definite melting point
- no crystal lattice to breakExhibit characteristic glass transition temperature, TgFlow when subject to pressure over timeIsotropic i.e. same properties in all directionAffect therapeutic activity e.g. amorphous antibiotic
novobiocin is readily absorbed and therapeutically active compared to the crystalline form
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Crystalline Solids
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E.g. diamond, graphite
Regular shape i.e. fixed geometric patterns
Incompressible
Definite /specific boiling points
Diffract X-rays
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Crystal Structure
Crystals contain
highly ordered
molecules or atoms
held together by
non-covalent
interactions
E.g. NaCl has the
cubic structure
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Source: http://cst-www.nrl.navy.mil/lattice/spcgrp/cubic.html
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PHM1153 Physical Pharmacy 1 2011/12 10
TRICLINICboric acid
MONOCLINICsucrose
ORTHOROMBICiodine
TRIGONAL?
TETRAGONALurea
HEXAGONALiodoform
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Crystal Lattices in 3D
Crystal lattice End centred
Side centred
Face centred
Body centred
Bravais/ Total
Cubic 1 1 1 3
Triclinic 1 1
Monoclinic 1 1 2
Orthorhombic 1 1 1 1 4
Hexagonal 1 1
Rhombohedral 1 1
Tetragonal 1 1 2
Total unit cells 7 14
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Lattices for drugs
For drugs, only 3 types:
1. Triclinic
2. Monoclinic
3. Orthorombic
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FCC Structure of NaCl
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Small spheres represent Na+ ions, large spheres represent Cl- ions.
Each sodium ion is octahedrally surrounded by six chloride ions and vice versa.
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Binding Forces
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Solid Crystal structure
Binding force
NaCl cubic Electrostatic attraction
Diamond ? Covalent
Graphite hexagonal Covalent
Fatty acids ? Van der Waals & hydrogen bonding
Gold ? ?
Mefenamic acid
? ?
Salicylic acid ? ?
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Crystallisation
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Crystallisation steps from solution:-
1. Supersaturation of the solutione.g. cooling, evaporation, addition of precipitant or chemical reaction
2. Formation of crystal nucleie.g. collision of molecules, deliberate seeding
3. Crystal growth around the nuclei
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Crystal Growth
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Steps involved:
1. Transport of molecules to the surface Degree of agitation in the system affects the
diffusion coefficient, thus affects crystal growth.
Affinity of solute to solvent
2. Arrangement in the lattice
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Precipitation
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1. Induced by altering pH of solution to reach saturation solubility.
2. By chemical reaction to produce precipitate from a homogeneous solution.
The rate of reaction is important in determining habit.
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Crystallization of Sodium Acetate end lecture here
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Description: A supersaturated solution of sodium acetate is crystallized by pouring it onto a seed crystal, forming a stalagmite-like solid. Heat is radiated from the solid. Source: Shakhashiri, B.Z. Chemical Demonstrations: A Handbook for Teachers of Chemistry
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End of lecture 1 of 2
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Crystallisation
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Contents - 2
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Properties of solids and implications
Crystal habits
Types of crystal habit
Factors affecting habits
Polymorphism
Methods to characterise solids
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Crystal Habits
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Variation in size
Number of faces
Kind of faces
Habits describe the overall shape of the crystal e.g. acicular (needle), prismatic, pyramidal, tabular, equant, columnar & lamellar types.
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Factors affecting types of habits
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Temperature
Solvent/s
Crystal growth ratee.g. at high
rate, acicular form of
phenylsalicylate is formed
Viscositye.g. less viscous media favours
coarse and equidimensional
forms of minerals
Addition of impuritiese.g.sulfonic
acid dyes alter habits of
ammonium, sodium and potassium nitrates
Presence of surfactants
e.g. anionic & cationic
surfactants on adipic acid
crystals
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Types of Habits
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ACICULARLong and needle-like, thinner than prismatic but thicker than fibrous. e.g. Natrolite
EQUANTAny three perpendicular axis through the crystal are more or less equal. Can be used to describe rounded as well as angular crystals. e.g. Fluorite
PRISMATICCommon crystal habit. Prismatic crystals are "pencil-like", elongated crystals that are thicker than needles.
TABULARBook-like (tablets) that are thicker than platy but not as elongated as bladed. Wulfenite forms crystals that are a good example of tabular crystals.
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Sodium Chloride
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Exercise
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How many forms of adipic acid crystals exist?
Refer Florence & Attwood
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Polymorphisms
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When compounds crystallise as different polymorphs, properties change.
Molecules arrange in two or more ways in the crystal: packed differently in crystal lattice, different orientation, different in conformation of molecules at lattice site.
X-ray diffraction patterns change.
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Example: Polymorphism of Spironolactone
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A diuretic (no potassium loss)
2 polymorphic forms and 4 solvated crystalline
Form 1: spironolactone powder is dissolved in acetone at a temperature near boiling point and cooled to 0 deg. C within a few hours – needle-like
Form 2: powder dissolved in acetone or dioxane or chloroform at RT and acetone allowed to evaporate for several weeks - prism
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Polymorphs of Spironolactone
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1
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Properties of Spironolactone Polymorphs
Parameters Form 1 Form 2
Unit cell Orthorombic Orthorombic
Dimension of a, b, c axes
0.998, 3.557, 0.623
1.058, 1.900, 1.101
Crystal habit Needle-like Prisms
Melting point 205 deg. C 210 deg. C
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Polymorphism in Pharmaceutical Compounds
Drugs Crystalline Amorphous
Ampicillin 1 0
Cortisone acetate 8 0
Chloramphenicol palmitate
3 1
Erythromycin 2 0
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Solubility of Chloramphenicol Palmitate
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Form B
Form A
1: 1
Form B
Form A
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Characterisation of Solids
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1. Microscopy – polarised light
2. X-ray crystallography - single crystal- on the basis that crystals can diffract X-rays- wavelengths same magnitude as distance between atoms/molecules in crystal- enable the determination of the distances of various planes in crystals. Thus, structures.- e.g. penicillin
3. X-ray diffraction – powder sample >>polymorphic state
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Continue characterisation of solids
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4. Differential scanning calorimetry – Tg, Tc and Tm
5. Infrared spectrometry
6. Melting point – pure solid & liquid in equilibrium normal at 1 atm
7. Heat of fusion ( Hf) – heat required to melt
(increase intermolecular distance) 1 g of solid
8. Solubility
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References
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Atkins, P & de Paula, J. (2002). Atkins’ Physical Chemistry 7th Ed. New
York: Oxford.
Cartensen, J. T. (2001). Advance Pharmaceutical Solids. New York:
Marcel Dekker.
Cullity, B. D. & Stock, S. R. (2001). Elements of x-ray diffraction 3rd Ed.
New Jersey: Prentice Hall.
Florence, A. T. & Attwood, D. (1998). Physicochemical Principles of
Pharmacy 3rd. Ed. London: Macmillan.
Martin, A. (1993). Physical Pharmacy 4th Ed. Baltimore: Lippincott. Note:
The 6th edition is now available.
Smart, L. E. & Moore, E. A. (2005). Solid State Chemistry 3rd Ed. Boca
Raton: CRC
West, A. R. (1999). Basic Solid State Chemistry 2nd Ed. West Sussex:
Wiley