Micromeritics, the science of small particles, is important for drug formulation and delivery. Particle size influences properties like surface area, dissolution rate, absorption and drug action. It also impacts physical stability of suspensions and emulsions. Various methods can determine particle size, including microscopy, sieving, and sedimentation. Derived powder properties like porosity, density, bulkiness, and flowability depend on particle size, shape, and surface properties. Tests like Carr's index and angle of repose evaluate powder flowability. Altering particle features and adding glidants can improve powder flow in formulations.
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli
III Semester.
UNIT-IV / Micromeritics
PHYSICAL AND CHEMICAL DEGRADATION OF PHARMACEUTICAL PRODUCTS.
Physical Factors
Loss of volatile constituents
Loss of water
Absorption of water
Crystal growth
Polymorphism changes
Colour changes
Chemical factors
Hydrolysis
Oxidation
Carboxylation
Decarboxylation
Isomerization
Polymerization
PHYSICAL PHARMACEUTICS II COARSE DISPERSION VijayaKumarR28
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli.
As per PCI syllabus for B Pharm / 2nd Year ,III Semester.
UNIT-III / Coarse dispersion
Powder Technology
Particle analysis in pharmaceuticals
Determination of particle size and surface area
Large scale equipment for powders
Types of powders
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli
III Semester.
UNIT-IV / Micromeritics
PHYSICAL AND CHEMICAL DEGRADATION OF PHARMACEUTICAL PRODUCTS.
Physical Factors
Loss of volatile constituents
Loss of water
Absorption of water
Crystal growth
Polymorphism changes
Colour changes
Chemical factors
Hydrolysis
Oxidation
Carboxylation
Decarboxylation
Isomerization
Polymerization
PHYSICAL PHARMACEUTICS II COARSE DISPERSION VijayaKumarR28
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli.
As per PCI syllabus for B Pharm / 2nd Year ,III Semester.
UNIT-III / Coarse dispersion
Powder Technology
Particle analysis in pharmaceuticals
Determination of particle size and surface area
Large scale equipment for powders
Types of powders
INCLUDES SPREADING COEFFICIENT AND ITS THEORY AND ALSO FEW OF ITS APPLICATION IN PHARMACEUTICAL FIELD
WILL BE HELPFUL FOR B PHARMACY STUDENTS
INCLUDES HOW IT IS DERIVED AND ALSO HOW IT IS RELATED TO SPREADING OF A CREAM OR OINTMENT ON OUR SKIN
IMPORTANCE OF SPREADING COEFFICIENT
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli
B Pharm / 2nd Year ,III Semester.
UNIT-I / Colloidal dispersion's
Decomposition and stabilization of pharmaceutical productsArshad Khan
Drug stability:Stabilization of medicinal agents against common reactions like hydrolysis & oxidation. Accelerated stability testing in expiration dating of pharmaceutical dosage forms. Photolytic degradation and its prevention.
Suspension, type of suspension, interracial property of suspended particles Dheeraj Saini
Here you find
Suspension , types of suspension, difference between flocculated and deflocculated suspension and interfacial properties of suspended particles
INCLUDES SPREADING COEFFICIENT AND ITS THEORY AND ALSO FEW OF ITS APPLICATION IN PHARMACEUTICAL FIELD
WILL BE HELPFUL FOR B PHARMACY STUDENTS
INCLUDES HOW IT IS DERIVED AND ALSO HOW IT IS RELATED TO SPREADING OF A CREAM OR OINTMENT ON OUR SKIN
IMPORTANCE OF SPREADING COEFFICIENT
R. VIJAYAKUMAR., M Pharm,
Research Scholar
department of Pharmaceutical Technology.
Anna university- BIT
Tiruchirappalli
B Pharm / 2nd Year ,III Semester.
UNIT-I / Colloidal dispersion's
Decomposition and stabilization of pharmaceutical productsArshad Khan
Drug stability:Stabilization of medicinal agents against common reactions like hydrolysis & oxidation. Accelerated stability testing in expiration dating of pharmaceutical dosage forms. Photolytic degradation and its prevention.
Suspension, type of suspension, interracial property of suspended particles Dheeraj Saini
Here you find
Suspension , types of suspension, difference between flocculated and deflocculated suspension and interfacial properties of suspended particles
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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. 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 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.
Micromeritics ,1. Micromeritics: Importance of particle size determination, different means of expressing particle size, methods of particle size determination: Optical and electron microscope studies, Coulter counter methods, laser beam technique, sieve analysis, sedimentation methods; particle shape and surface area. Measurement of particle surface area.
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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.
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