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Implication and evaluation of
micromeritics in formulation
Introduction
The science and technology of small particles was
given by the name micromeritics by Dalla Valle
Micromeritics is the science and technology of small
particles . The unit of particle size most frequently used
in micromeritics is micrometer, also called as a micron.
Control of particle size and the size range of a drug can
be significantly related to its physical, chemical and
pharmacological properties. Bioavailability, and
physical stability in some dosage forms can also be
affected by particle size.
Micromeritics study in different
formulation
• Colloidal dispersion are characterized by particles
that are too small to be seen in the ordinary
microscope.
• The particles of pharmaceutical emulsion and
suspension and the “fines” of powder fall in the
range of the optical microscope.
• Particles having the size of coarser powder , tablet
granulation , and granular salts fall with in the
sieve range.
Applications
1) Release & Dissolution
Particle size & surface area influence the release of a drug
from a dosage form that is administered orally, rectally
parenterally & topically. Higher surface area brings about
intimate contact of the drug with the dissolution fluids
in vivo & increases the drug solubility & dissolution.
2) Absorption & Drug Action
Particle size & surface area influence the drug absorption
& subsequently the therapeutic action. Higher the
dissolution, faster the absorption & hence quicker &
greater the drug action.
3) Physical Stability
Micromeritc properties of a particle i.e the particle size in a
formulation influences the physical stability of the suspensions
& emulsions. Smaller the size of the particle, better the
physical stability of the dosage form owing to the brownian
movement of the particles in the dispersion
Factors influenced by particle size
Surface area :

increased S.A. affects the therapeutic

efficiency of medicinal compounds that possess a low solubility in
body fluids by increasing the area of contact between the solid and
the dissolving fluid. Thus compound dissolves in a shorter time.

Extraction : the time required for extraction is shortened by
the increased area of contact between the solvent and solid
and the reduced distance the solvent has to penetrate the
material.
Dissolution : the time required for dissolution of solid
chemicals is shortened by the use of smaller particles.
Drying : the drying of wet mass may be facilitated by
milling, which increase the S.A. and reduces the
distance the moisture must travel with in the
particle to reach the outer surface.
Mixing : the mixing of several solid ingredients of a
pharmaceutical is easier and more uniform if the
ingredients are approximately the same and
small size.
Lubrication : lubricant used in compressed tablets and
capsules function by virtue of their ability to
coat the surface of granulation or powder.
Properties of powder based on particle
size and shape
Porosity : the porosity or voids of powder is defined as the ratio
of the void volume to the bulk volume of packing.
(v)

Є = Vb-Vp

particle

Vb

Here ; Vb – Vp = void volume
Vb = bulk volume
Vp = true volume of

Packing arrangements ; powder beds of uniform sized
spheres can assume two ideal packing arrangement.
closest or rhombohedral most open ,loosest or cubic packing
the theoretical porosity of powder of uniform spheres in
closest packing is 26% and for loosest packing is 48%.
Density (ρ): density is universally defined as weight per unit volume.
Three type of densities can be defined
True density
Granule density
Bulk density

Bulkiness : Specific bulk volume ,the reciprocal of bulk density, it is often
called bulkiness or bulk.
Bulkiness increase with a decrease in particle size .
Flow properties : powder may be free flowing or cohesive.
Factors that
affect the Flow properties are particle size , shape ,
surface
texture, porosity and density.
Angle of repose (φ) have been used as indirect method
for quantifying
powder flowability.
φ = tan-1 (h/r)
Here: h = height of pile
r = radius of pile
Compression :The strength of compressed tablet dependson number of factor,
most important are which are particle size and compression. As the
compression increases the tablet hardness and fracture resistance also
increases.
Particle size and the lifetime of a drug
•

In production : particle size influences the production of formulated
medicines as solid dosage form both tablets and capsules are
produced
Powders with different particle size have different flow and packing
properties , which alter the volume of powder during each
encapsulation or table compression event .
In Body: after administration of the medicine, the dosage should
release the drug in to solution at optimum rate . This depends on
several factors, one of which will be particle size of drug.
Particles having small dimension will tend to increase the rate of solution
Conclusion
Particle size is an important parameter both for the
production of medicines containing particulate solids and in the efficacy of
the medicine administration

.
Methods for determining particle
size:
• 1- Optical microscopy (range: 0.2 –100
um):
• The microscope eyepiece is fitted with a
micrometer by
• which the size of the particles may be
estimated.
• 2- Sieving (range: 40 – 9500μm ):
-Standard sized sieves are available to
cover a wide range of sizes. These sieves
are designed to sit in a stack so that
material falls through smaller and
smaller meshes until it reaches a mesh
which is too fine for it to pass through.
The stack of sieves is mechanically
shaken to promote the passage of the
solids.
The fraction of the material between pairs
of sieve sizes is determined by weighing
the residue on each sieve.
The result achieved will depend on the
duration of the agitation and the manner of
the agitation.
3- Sedimentation (range: .08 –300μm):
• by measuring the terminal settling
velocity of particles through a liquid
medium in a gravitational centrifugal
environment using
• Andreasen apparatus.
• 4- Particle volume measurement
(range: .5 - 300 um):
- In this type of machine the powder is
suspended in an electrolyte solution .
This suspension is then made to flow
through a short insulated capillary
section between two electrodes and
the resistance of the system is
measured. When a particle passes
through the capillary there is a
momentary peak in the resistance, the
amplitude of the peak is proportional
to the particle size. Counting is done
by a computer
Derived properties of powders:
Derived properties of powders:
1- Porosity:
Suppose a nonporous powder, is placed in a graduated
cylinder:
the total volume occupied is known as the bulk volume
Vb .
 bulk volume = true volume + volume of spaces between
particles.
The volume of the spaces, the void volume, V = Vb - Vp
Vp is the true volume of particles.
The porosity or voids ε of powder is determined as the ratio
Conti..
• of void volume to bulk volume.
• Porosity = ε = Vb – Vp/Vp = 1 – Vp/Vb
Porosity is frequently expressed in percent, ε x 100 .
Derived properties of powders:
• 2- Densities of particles:
Density is defined as weight per unit volume (W/V).
Types of densities:
• A- true density:The true density, or absolute density,of a
sample excludes the volume of the pores and voids within
the sample.
• B- bulk density (w/v) the bulk density :value includes
the volume of all of the pores within the sample.
Densities of particles
• During tapping, particles gradually
pack more efficiently, the powder
volume decreases and the tapped
density increases.
Derived properties of
powders:
3- Bulkiness = Specific bulk volume = reciprocal of
bulk density:
 It is an important consideration in the packaging of
powders.
 The bulk density of calcium carbonate vary from 0.1 to
1.3, and the lightest (bulkiest) type require a container
about 13 times larger than that needed for the heaviest
variety.
(Bulkiness increases with a decrease in particle size).
In mixture of materials of different sizes, the smalle
particles sift between the larger ones and tend to reduce
bulkiness.
Conti..
Derived properties of
powders:

• 4- Flow properties:
Powders may be free-flowing or cohesive (“sticky”).
Many common manufacturing problems are attributed to
powder flow:
• 1- Powder transfer through large equipment such as
hopper.
• 2- Uneven powder flow → excess entrapped air within
powders →capping or lamination.
• 3- Uneven powder flow → increase particle’s friction
with die wall causing lubrication problems, and increase
dust contamination risks during powder transfer.
Derived properties of
powders:
• 4- non-uniformity (segregation) in blending
powder flow problems
Tests to evaluate the
flowability of a powder:
• 1- Carr’s compressibility index
• A volume of powder is filled into a graduated glass
cylinder and repeatedly tapped for a known duration.
The volume of powder after tapping is measured.
• Carr’s index (%) =Tapped density – Poured or bulk
density x 100/Tapped density
• Bulk density = weight / bulk volume
• Tapped density = weight / true volume
Tests to evaluate the flowability of a
powder:
Flow discription

% compressability

Excellent flow

5-15

good

16-18

fair

19-21

poor

22-35

Very poor

36-40

Extremly poor

>40
Tests to evaluate the flowability of a
powder:
2- Hausner ratio:
Hausner ratio=Tapped density /Poured or bulk density
Hausner ratio was related to interparticle friction:
Value less than 1.25 indicates good flow ( = 20% Carr ).
The powder with low interparticle friction, such as coarse
spheres.
Value greater than 1.5 indicates poor flow ( = 33% Carr ).
more cohesive, less free-flowing powders such as flakes.
Between 1.25 and 1.5, added glidant normally improves
flow. > 1.5 added glidant doesn’t improve flow.
Tests to evaluate the flowability of a
powder:
3- The angle of repose φ:
The frictional forces in a loose powder can
bemeasured by the angle of repose φ.
φ = the maximum angle possible between the
surface of a pile of powder and horizontal plane =
coefficient of friction μ between the particles:
tan φ = μ
tan φ = h / r
r = d / 2
3- The angle of repose φ:
The sample is poured onto a horizontal surface and the
angle of the resulting pyramid is measured.
 The user normally selects the funnel orifice through
which the powder flows slowly and reasonably
constantly.
 Angle of repose less than 20 (excellent flow)
 Angle of repose between 20-30 (good flow)
 Angle of repose between 30-34 (Pass flow)
 Angle of repose greater than 40 (poor flow)
***The rougher and more irregular the surface of
the particles,the higher will be the angle of repose.
• Alteration of Particle’s size & Distribution
There is certain particle size at which powder’s flow
ability is optimum.
 Coarse particles are more preferred than fine ones as
they are less cohesive.
 The size distribution can also be altered to improve
flowability by removing a proportion of the fine
particle fraction or by increasing the proportion of
coarser particles, such as occurs in granulation.
• Alteration of Particle Shape & texture
Particle’s Shape: Generally, more spherical particles
have better flow properties than more irregular
particles.
• Spherical particles are obtained by spray drying, or by
temperature cycling crystallization.
• Particle's texture: particles with very rough surfaces
will be more cohesive and have a greater tendency to
interlock than smooth surfaced particles.
Alteration of Surface Forces
 Reduction of electrostatic charges can improve powder
flowability. Electrostatic charges can be reduced by
altering process conditions to reduce frictional contacts.
 Moisture content of particle greatly affects powder’s
flowability.
Adsorbed surface moisture films tend to increase bulk
density and reduce porosity.
Drying the particles will reduce the cohesiveness and
improve the flow.
 Hygroscopic powders, stored and processed under low
humidity conditions.
• Formulation additives ( Flow activators):
• Flow activators are commonly referred as glidants.
• Flow activators improve the flowability of powders by
reducing adhesion and cohesion.
• e.g. talc, maize starch and magnesium stearate
THANK YOU
….

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MICROMERITICS

  • 1. Implication and evaluation of micromeritics in formulation
  • 2. Introduction The science and technology of small particles was given by the name micromeritics by Dalla Valle Micromeritics is the science and technology of small particles . The unit of particle size most frequently used in micromeritics is micrometer, also called as a micron. Control of particle size and the size range of a drug can be significantly related to its physical, chemical and pharmacological properties. Bioavailability, and physical stability in some dosage forms can also be affected by particle size.
  • 3. Micromeritics study in different formulation • Colloidal dispersion are characterized by particles that are too small to be seen in the ordinary microscope. • The particles of pharmaceutical emulsion and suspension and the “fines” of powder fall in the range of the optical microscope. • Particles having the size of coarser powder , tablet granulation , and granular salts fall with in the sieve range.
  • 4.
  • 5. Applications 1) Release & Dissolution Particle size & surface area influence the release of a drug from a dosage form that is administered orally, rectally parenterally & topically. Higher surface area brings about intimate contact of the drug with the dissolution fluids in vivo & increases the drug solubility & dissolution. 2) Absorption & Drug Action Particle size & surface area influence the drug absorption & subsequently the therapeutic action. Higher the dissolution, faster the absorption & hence quicker & greater the drug action.
  • 6. 3) Physical Stability Micromeritc properties of a particle i.e the particle size in a formulation influences the physical stability of the suspensions & emulsions. Smaller the size of the particle, better the physical stability of the dosage form owing to the brownian movement of the particles in the dispersion
  • 7. Factors influenced by particle size Surface area : increased S.A. affects the therapeutic efficiency of medicinal compounds that possess a low solubility in body fluids by increasing the area of contact between the solid and the dissolving fluid. Thus compound dissolves in a shorter time. Extraction : the time required for extraction is shortened by the increased area of contact between the solvent and solid and the reduced distance the solvent has to penetrate the material. Dissolution : the time required for dissolution of solid chemicals is shortened by the use of smaller particles.
  • 8. Drying : the drying of wet mass may be facilitated by milling, which increase the S.A. and reduces the distance the moisture must travel with in the particle to reach the outer surface. Mixing : the mixing of several solid ingredients of a pharmaceutical is easier and more uniform if the ingredients are approximately the same and small size. Lubrication : lubricant used in compressed tablets and capsules function by virtue of their ability to coat the surface of granulation or powder.
  • 9. Properties of powder based on particle size and shape Porosity : the porosity or voids of powder is defined as the ratio of the void volume to the bulk volume of packing. (v) Є = Vb-Vp particle Vb Here ; Vb – Vp = void volume Vb = bulk volume Vp = true volume of Packing arrangements ; powder beds of uniform sized spheres can assume two ideal packing arrangement. closest or rhombohedral most open ,loosest or cubic packing the theoretical porosity of powder of uniform spheres in closest packing is 26% and for loosest packing is 48%.
  • 10. Density (ρ): density is universally defined as weight per unit volume. Three type of densities can be defined True density Granule density Bulk density Bulkiness : Specific bulk volume ,the reciprocal of bulk density, it is often called bulkiness or bulk. Bulkiness increase with a decrease in particle size .
  • 11. Flow properties : powder may be free flowing or cohesive. Factors that affect the Flow properties are particle size , shape , surface texture, porosity and density. Angle of repose (φ) have been used as indirect method for quantifying powder flowability. φ = tan-1 (h/r) Here: h = height of pile r = radius of pile
  • 12. Compression :The strength of compressed tablet dependson number of factor, most important are which are particle size and compression. As the compression increases the tablet hardness and fracture resistance also increases.
  • 13. Particle size and the lifetime of a drug • In production : particle size influences the production of formulated medicines as solid dosage form both tablets and capsules are produced Powders with different particle size have different flow and packing properties , which alter the volume of powder during each encapsulation or table compression event . In Body: after administration of the medicine, the dosage should release the drug in to solution at optimum rate . This depends on several factors, one of which will be particle size of drug. Particles having small dimension will tend to increase the rate of solution
  • 14. Conclusion Particle size is an important parameter both for the production of medicines containing particulate solids and in the efficacy of the medicine administration .
  • 15. Methods for determining particle size: • 1- Optical microscopy (range: 0.2 –100 um): • The microscope eyepiece is fitted with a micrometer by • which the size of the particles may be estimated.
  • 16.
  • 17. • 2- Sieving (range: 40 – 9500μm ): -Standard sized sieves are available to cover a wide range of sizes. These sieves are designed to sit in a stack so that material falls through smaller and smaller meshes until it reaches a mesh which is too fine for it to pass through.
  • 18. The stack of sieves is mechanically shaken to promote the passage of the solids. The fraction of the material between pairs of sieve sizes is determined by weighing the residue on each sieve. The result achieved will depend on the duration of the agitation and the manner of the agitation.
  • 19.
  • 20. 3- Sedimentation (range: .08 –300μm): • by measuring the terminal settling velocity of particles through a liquid medium in a gravitational centrifugal environment using • Andreasen apparatus.
  • 21. • 4- Particle volume measurement (range: .5 - 300 um): - In this type of machine the powder is suspended in an electrolyte solution . This suspension is then made to flow through a short insulated capillary section between two electrodes and the resistance of the system is measured. When a particle passes through the capillary there is a momentary peak in the resistance, the amplitude of the peak is proportional to the particle size. Counting is done by a computer
  • 23. Derived properties of powders: 1- Porosity: Suppose a nonporous powder, is placed in a graduated cylinder: the total volume occupied is known as the bulk volume Vb .  bulk volume = true volume + volume of spaces between particles. The volume of the spaces, the void volume, V = Vb - Vp Vp is the true volume of particles. The porosity or voids ε of powder is determined as the ratio
  • 24. Conti.. • of void volume to bulk volume. • Porosity = ε = Vb – Vp/Vp = 1 – Vp/Vb Porosity is frequently expressed in percent, ε x 100 .
  • 25. Derived properties of powders: • 2- Densities of particles: Density is defined as weight per unit volume (W/V). Types of densities: • A- true density:The true density, or absolute density,of a sample excludes the volume of the pores and voids within the sample. • B- bulk density (w/v) the bulk density :value includes the volume of all of the pores within the sample.
  • 26. Densities of particles • During tapping, particles gradually pack more efficiently, the powder volume decreases and the tapped density increases.
  • 27. Derived properties of powders: 3- Bulkiness = Specific bulk volume = reciprocal of bulk density:  It is an important consideration in the packaging of powders.  The bulk density of calcium carbonate vary from 0.1 to 1.3, and the lightest (bulkiest) type require a container about 13 times larger than that needed for the heaviest variety. (Bulkiness increases with a decrease in particle size). In mixture of materials of different sizes, the smalle particles sift between the larger ones and tend to reduce bulkiness.
  • 29. Derived properties of powders: • 4- Flow properties: Powders may be free-flowing or cohesive (“sticky”). Many common manufacturing problems are attributed to powder flow: • 1- Powder transfer through large equipment such as hopper. • 2- Uneven powder flow → excess entrapped air within powders →capping or lamination. • 3- Uneven powder flow → increase particle’s friction with die wall causing lubrication problems, and increase dust contamination risks during powder transfer.
  • 31. • 4- non-uniformity (segregation) in blending
  • 33. Tests to evaluate the flowability of a powder: • 1- Carr’s compressibility index • A volume of powder is filled into a graduated glass cylinder and repeatedly tapped for a known duration. The volume of powder after tapping is measured. • Carr’s index (%) =Tapped density – Poured or bulk density x 100/Tapped density • Bulk density = weight / bulk volume • Tapped density = weight / true volume
  • 34. Tests to evaluate the flowability of a powder: Flow discription % compressability Excellent flow 5-15 good 16-18 fair 19-21 poor 22-35 Very poor 36-40 Extremly poor >40
  • 35. Tests to evaluate the flowability of a powder: 2- Hausner ratio: Hausner ratio=Tapped density /Poured or bulk density Hausner ratio was related to interparticle friction: Value less than 1.25 indicates good flow ( = 20% Carr ). The powder with low interparticle friction, such as coarse spheres. Value greater than 1.5 indicates poor flow ( = 33% Carr ). more cohesive, less free-flowing powders such as flakes. Between 1.25 and 1.5, added glidant normally improves flow. > 1.5 added glidant doesn’t improve flow.
  • 36. Tests to evaluate the flowability of a powder: 3- The angle of repose φ: The frictional forces in a loose powder can bemeasured by the angle of repose φ. φ = the maximum angle possible between the surface of a pile of powder and horizontal plane = coefficient of friction μ between the particles: tan φ = μ tan φ = h / r r = d / 2
  • 37. 3- The angle of repose φ: The sample is poured onto a horizontal surface and the angle of the resulting pyramid is measured.  The user normally selects the funnel orifice through which the powder flows slowly and reasonably constantly.  Angle of repose less than 20 (excellent flow)  Angle of repose between 20-30 (good flow)  Angle of repose between 30-34 (Pass flow)  Angle of repose greater than 40 (poor flow) ***The rougher and more irregular the surface of the particles,the higher will be the angle of repose.
  • 38. • Alteration of Particle’s size & Distribution There is certain particle size at which powder’s flow ability is optimum.  Coarse particles are more preferred than fine ones as they are less cohesive.  The size distribution can also be altered to improve flowability by removing a proportion of the fine particle fraction or by increasing the proportion of coarser particles, such as occurs in granulation.
  • 39. • Alteration of Particle Shape & texture Particle’s Shape: Generally, more spherical particles have better flow properties than more irregular particles. • Spherical particles are obtained by spray drying, or by temperature cycling crystallization. • Particle's texture: particles with very rough surfaces will be more cohesive and have a greater tendency to interlock than smooth surfaced particles.
  • 40. Alteration of Surface Forces  Reduction of electrostatic charges can improve powder flowability. Electrostatic charges can be reduced by altering process conditions to reduce frictional contacts.  Moisture content of particle greatly affects powder’s flowability. Adsorbed surface moisture films tend to increase bulk density and reduce porosity. Drying the particles will reduce the cohesiveness and improve the flow.  Hygroscopic powders, stored and processed under low humidity conditions.
  • 41. • Formulation additives ( Flow activators): • Flow activators are commonly referred as glidants. • Flow activators improve the flowability of powders by reducing adhesion and cohesion. • e.g. talc, maize starch and magnesium stearate