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Figure 2. The effect of applied pressure on the specific surface of sulfathiazole tablets.
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The specific surface of the starch and sulfathiazole granulation is 0.18 m2/ g; the tablet
compressed at a pressure of 1600 kg/cm2 had a specific surface of 0.9 m 2 /g.
With some materials fragmentation does not occur because the stresses are relieved by plastic
deformation. Plastic deformation may be thought of as a change in particle shape and as the
sliding of groups of particles in an attempt to relieve stress (viscoelastic flow). Such
deformation produces new, clean surfaces that are potential bonding areas.
D. Bonding
Several mechanisms of bonding in the compression process have been conceived. Three
theories are the mechanical theory, the intermolecular theory, and the liquid-surface film
theory.
The mechanical theory proposes that under pressure the individual particles undergo
elastic, plastic, or brittle deformation and that the edges of the particles intermesh, forming a
mechanical bond. If only the mechanical bond exists, the total energy of compression is equal
to the sum of the energy of deformation, heat, and energy adsorbed for each constituent.
Mechanical interlocking is not a major mechanism of bonding in pharmaceutical tablets.
According to the intermolecular forces theory, under pressure the molecules at the
points of true contact between new, clean surfaces of the granules are close enough so that
van der Waals forces interact to consolidate the particles. A microcrystalline cellulose
tablet has been described as cellulose fibrils in which the crystals are compressed close
enough together so that hydrogen bonding between them occurs. It appears that very little
deformation or fusion occurs in the compression of microcrystalline cellulose. Although
aspirin crystals undergo slight deformation and fragmentation at low pressure, it appears
that hydrogen bonding has strongly bonded the tablets, because the granules retain their
integrity with further increases in pressure.
The liquid-surface film theory attributes bonding to the presence of a thin liquid
film, which may be the consequence of fusion or solution, at the surface of the particle
induced by the energy of compression. During compression an applied force is exerted on
the granules; however, locally the force is applied to a small area of true contact so that a
very high pressure exists at the true contact surface. The local effect of the high pressure
on the melting point and solubility of a material is essential to bonding. The relation of
pressure and melting point is expressed by the Clapeyron equation:
dT /dP = T (V 1 – Vs)/ ΔH
in which dT/dP is the change in melting point with a change in pressure, T is the
absolute temperature, ΔH is the molar latent heat of fusion, and V 1 and Vs are the molar
volumes of the liquid melt and the solid, respectively.
The poor compressibility of most water-insoluble materials and the relative ease of
compression of water-soluble materials suggest that pressure-induced solubility is important in
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tableting. The moisture may be present as that retained from the granulating solution after
drying or that adsorbed from the atmosphere. Granulations that are absolutely dry have poor
compressional characteristics. Water or saturated solutions of the material being compressed
may form a film that acts as a lubricant, and if less force is lost to overcome friction, more force
is utilized in compression and bonding, and the ejection force is reduced.
Figure 3. The effect of applied pressure on the apparent density of tablets of sulfathiazole.
F. Decompression
The success or failure to produce an intact tablet depends on the stresses induced by
elastic rebound and the associated deformation processes during decompression and ejection.
Often, if capping or lamination of the ejected tablet has occurred, the individual pieces are
dense, hard, and strongly bonded indicating that sufficient areas of true contact existed
during compression. In such cases, the mechanism of failure is different from that of a
crumbly tablet. As the upper punch is withdrawn from the die cavity, the tablet is confined
in the die by a radial pressure. Consequently, any dimensional change during decompression
must occur in the axial direction.
Ideally, if only elastic deformation occurred, with the sudden removal of axial
pressure the granules would return to their original form breaking any bonds that may have
formed under pressure. Also the die wall pressure would be zero as the elastic material recovered
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axially and contracted radially. Actually under nonisostatic pressure, pharmaceutical materials
undergo sufficient plastic deformation to produce a die wall pressure in excess of that that may
be relieved by elastic recovery accompanying removal of the upper punch. As the movement
of the tablet is restricted by the residual die wall pressure and the friction with the die wall,
the stress from the axial elastic recovery and the radial contraction causes splitting (capping) of
the tablet unless the shear stress is relieved by plastic deformation.
Thus, capping is due to uniaxial relaxation in the die cavity at the point where the
upper punch pressure is released and some may also occur at ejection. It has been demonstrated
that if decompression occurs simultaneously in all directions capping is reduced or eliminated.
Stress relaxation of plastic deformation is time dependent. Materials having slow rates of
stress relaxation crack in the die upon decompression. In Figure 4 the ratio of the pressure at
time t to the maximum pressure is plotted against the logarithm of the time. The change of the
initial slope suggests some prominent mechanism of bonding soon becomes negligible. The initial
slope reflects the ability of the materials to relieve stress during decompression. The rate of
stress relieve is slow for acetaminophen so cracking occurs while the tablet is within the die.
With microcrystalline cellulose the rate of stress relieve is rapid, and intact tablets result. If
stress relaxation is slow and cracking is a problem, a slower operational speed provides more
time for stress relaxation. A shape of tablet may be selected to reduce stress gradients within
the tablet. With deep oval punches the larger quantity of material in the dome is expanding
radially during ejection, and as the main body of the tablet can not expand radially but is
constrained by the die wall, larger shear stresses develop. Flat-faced punches would form tablets
that avoid this large shear stress.
Figure 5. Events of the process of compression in terms of applied pressure and relative
volume.
ln V/(V-V∝) = kP + V0/(V0-V∝)
in which V is the volume at pressure P, V o is the original volume of the powder including
voids, k is a constant related to the yield value of the powder, and V∝ is the volume of the
solid.
The Heckel relationship may be written in terms of relative density ρ rel rather than volume
in which P is the applied pressure, and K and A are constants. The Heckel constant K has
been related to the reciprocal of the mean yield pressure, which is the minimum pressure
required to cause deformation of the material undergoing compression. The intercept of the
curved portion of the curve at low pressure represents a value due to densifica tion by
particle rearrangement. The intercept obtained from the slope of the upper portion of the
curve is a reflection of the densification after consolidation. A large value of the Heckel
constant indicates the onset of plastic deformation at relatively low pressures.
A Heckel plot permits an interpretation of the mechanism of bonding. For dibasic
calcium phosphate dihydrate, which undergoes fragmentation during compression, the Heckel
plot in Figure 6 is nonlinear and has a small value for its slope (a small Heckel constant).
Figure 6. Density-applied pressure relationship according to the Heckel plot. Key: (●),
dibasic calcium phosphate dihydrate; and (ο ), with 4.5% starch.
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It appears that the concentration of binder has a greater influence in more porous
tablets than in those approaching zero voids. As the applied pressure is increased and the
porosity of the tablet is decreased, the interparticular distances through which bonding
forces operate are shorter. Thus, the bonding force of the material is stronger at lower
porosity, and a lesser quantity of binder is required to produce a tablet of desired strength.
The quotient of the applied force and the area of true contact is the applied
deformation pressure at the areas of true contact. Thus, under pressure a desired maximum
area of true contact is established merely by applying adequate pressure. However, when the
applied force is removed, the area of true contact may change. It has been stated that smaller
particles yield larger areas of true contact and thus bond more strongly. However, the
compression process is not independent of permanent deformation pressure (hardness) which
may vary with size. Also plastic deformation tends to increase the number of dislocations in a
crystal. In practice the magnitude of the permanent deformation pressure is unknown, and the
particle size and shape may alter the packing density. As a consequence of these unknowns, a
speculation on the effect of particle size on the strength of a tablet is questionable.
The materials compressed in pharmacy are nonmetallic and are generally mixtures of
organic compounds. The relative significance of each event in the process of compression
depends on the mechanical properties (plastic behavior, crushing strength) of the mixture, its
chemical nature and surface effects (friction, adsorbed films, lubrication).
Higuchi and Train were probably the first pharmaceutical scientists to study the effect of
compression on tablet characteristics (density, disintegration, hardness, porosity, and
specific surface) and on distribution of pressure. The relationship between applied pressure
and weight, thickness, density, and the force of ejection are relatively independent of the
material being compressed. Hardness, tensile strength, friability, disintegration, and dissolution
are properties that depend predominately on the formulation.
As the porosity and apparent density are inversely proportional, the plot of porosity
against the logarithm of applied pressure is linear with a negative slope, as shown in Figure 9.
Figure 10. The effect of applied pressure on the hardness of various tablets.
The strength of a tablet may be expressed as a tensile strength (breaking stress of a solid
unit cross section in kg/cm 2). As shown in Figure 11, the radial tensile strength is proportional
to the applied pressure.
Figure 11. The effect of applied pressure on tensile strengths of tablets of dibasic
calcium phosphate dehydrate granulated with 1.2% starch. At each applied pressure,
the value is given for σz /σx .
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For an isotropic, homogeneous tablet, the radial and axial tensile strengths are equal. In
practice the distribution of pressure, differences in density within the tablet, and the
mixture of several ingredients contribute to the nonhomogeneity of the tablet and to the
nonuniformity of tensile strength.
When a brittle material is compressed axially, the stress upon each particle does not
necessarily compress the particles along the axial direction because of random packing and
alignment of the particles toward each other during the events of compression. A greater
probability exists for vertical stress on the particles during the arrangement and
fragmentation events due to the movement of the punch. The overall result is that more clean
surfaces are created when they are normal to the radial direction. As applied pressure is
increased, fragmentation results in a stronger, radial tensile strength than axial tensile
strength as shown in Figure 11. If more bonds are formed in the radial direction, the
potential for the presence of cracks or dislocations is greater in the axial than in the radial
direction.
σx = 2 Fσ / Dt π
The axial tensile strength is determined by measurement of the maximum force Fσ to pull
the tablet apart in tensile failure. The axial tensile strength is then calculated by
σz = 4 F σ / D2 π
The radial strength is little affected by the concentration of povidone, but the axial
tensile strength is increased by increased concentrations of povidone to a strength greater
than the radial strength. The influence of applied pressure on the tensile strengths of lactose
with 1 and 9% povidone is shown in Figure 13.
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Figure 12. The effect of povidone on the tensile strengths of tablets of hydrous lactose
compressed at 890 kg/cm2. At each applied pressure the value is given for σz /σx .
Figure 13. The effect of applied pressure on the tensile strengths of tablets of hydrous lactose
granulated with 1% ( ________ ) and 9% (- - - - - - - -) povidone.
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The relationship of the crushing strength of granulations of lactose with povidone to the axial
and radial tensile strengths of tablets compressed at 890 kg/cm2 from the granulations is shown
in Figure 14.
Figure 14. Relationship of binder concentration to granule strength and tensile strengths
of tablets compressed at 890 kg/cm2 from lactose monohydrate granulated with
povidone. ( ) granule strength, (O) axial, and (●) radial tensile strength.
Figure 15. The relationship of hardness and axial tensile strength for dibasic calcium
phosphate dihydrate with various concentrations of magnesium stearate. (●) 0%, (Δ)
0.075%, ( ) 0.125%, (O) 0.25%, (◊) 0.5%, (∗ ) 1.0%, and (+) 2.0%.
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The tensile strengths of the tablet are increased as the resistance to crushing of the
granules is increased. The strength of the granule is increased as the concentration of the
binder is increased; thus, the effect of the strength of the granule on the tensile strengths of
the tablet is inseparable from the effect of concentration. Although the crushing strength of
granules is important in the handling of the granulation in the tableting process, the applied
pressure and the concentration of the binder determine the tensile strengths of a tablet.
With a hardness tester of the diametral compression type, weak tablets tend to fail due
to tensile stresses, and strong tablets tend to fail due to compressive stresses. Hardness is
proportional to radial tensile strength. As shown in Figure 15, the relationship of hardness to
axial tensile strength is nonlinear.
As the hardness is increased, at higher values of hardness, there is a progressive
lessening of the rate of increase of the axial tensile strength until a limiting axial tensile
strength is attained. Thus, if the mechanical strength of a tablet is considered only in terms
of its hardness, nothing is known of its axial strength; and if the axial tensile strength were
weak, the tablet would laminate under stress.
C. Specific Surface
Specific surface is the surface area of 1 g of material. The influence of applied pressure on
the specific surface area of a tablet is typified by Figure 16.
Figure 16. The effect of applied pressure on the specific surface of various tablets.
As the lactose granules, which were granulated by adding 10% starch paste, are compressed,
the specific surface is increased to a maximal value (four times that of the initial granules),
indicating the formation of new surfaces due to fragmentation of the granules. Further
increases in applied pressure produce a progressive decrease in specific surface as the
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particles bond. A similar relation is shown for aspirin containing 10% starch. When an equal weight
of aspirin and lactose is blended with 10% starch and then compressed, the specific surface is
between that of the aspirin and lactose tablets individually. As the relationship between applied
pressure and apparent density is independent of the material being compressed, the influence
of starch on the specific surface and porosity is not significant.
For these aspirin, lactose, and aspirin-lactose tablets, the maximum specific surface
occurs at a porosity of approximately 10%, even though the applied pressures at which the
maxima occur vary with the different materials.
D. Disintegration
Usually, as the applied pressure used to prepare a tablet is increased, the
disintegration time is longer. Frequently, there is an exponential relationship between the
disintegration time and the applied pressure, as shown for aspirin and lactose in Figure 17.
Figure 17. The effect of applied pressure on disintegration time of various tablets.
In other formulations there is a minimum value when the applied pressure is plotted
against the logarithm of disintegration time, as shown in Figures 17 and 18 with 10% starch.
For tablets compressed at low pressures, there is a large void, and the contact of
starch grains in the interparticular space is discontinuous. Thus, there is a lag time before the
starch grains, which are swelling due to imbibitions of water, contact and exert a force on the
surrounding tablet structure. For tablets compressed at a certain applied pressure, the
contact of the starch grains is continuous with the tablet structure, and the swelling of the
starch grains immediately exerts pressure, causing the most rapid disintegration, as dem-
onstrated by a minimum in a plot of applied pressure against the logarithm of disintegration
time. For tablets compressed at pressures greater than that producing the minimum
disintegration time, the porosity is such that more time is required for the penetration of water
into the tablet, with a resulting increase in disintegration time.
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Figure 18. The effect of applied pressure on the disintegration time of sulfadiazine tablets with
various percentages of dried corn starch.
E. Dissolution
The effect of applied pressure on dissolution rate may be considered from the viewpoint
of non-disintegrating tablets and disintegrating tablets. Under sink conditions, the dissolution
rate is independent of applied pressures from 53 to 2170 kg/cm 2 for non-disintegrating
spheres of aspirin, benzoic acid, salicylic acid, an equimolar mixture of aspirin and salicylic
acid, and an equimolar mixture of aspirin and caffeine.
In another study it is found that the dissolution rate of aspirin disks to be independent of
the pressure over the range 2000 to 13,000 kg/ cm2 and independent of the particle size of
the granules used to prepare the disks. The dissolution rate of benzoic acid disks is
independent of particle size and applied pressure.
The effect of applied pressure on the dissolution of disintegrating tablets is difficult to
predict; however, for a conventional tablet it is dependent on the pressure range, the
dissolution medium, and the properties of the medicinal compound and the excipients. If
fragmentation of the granules occurs during compression, the dissolution is faster as the
applied pressure is increased, and the fragmentation increases the specific surface. If the
bonding of the particles is the predominate phenomena in compression, the increase in
applied pressure causes a decrease in dissolution.
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The four most common dissolution-pressure relations are:
1. The dissolution is more rapid as the applied pressure is increased.
2. The dissolution is slowed as the applied pressure is increased.
3. The dissolution is faster, to a maximum, as the applied force is increased, and then a
further increase in applied pressure slows dissolution.
4. The dissolution is slowed to a minimum as the applied pressure is increased, and then
further an increase in applied pressure speeds dissolution.