Diffusion takes place through higher concentration to lower concentration.

1. PRESENTED BY-
ATISH KHILARI
M.PHARM(1ST SEM)
(PHARMACEUTICS)
GUIDED BY-
MRS.SHILPA CHAUDHARI
DR.D.Y.PATIL COLLEGE OF
PHARMACY,AKURDI(PUNE)

2. CONTENTS
1.INTRODUCTION
2.STEADY STATE DIFFUSION
3.MECHANISM
4.FACTOR INFLUENCE THE DIFFUSION
5.TRANSPORT ACROSS THE MEMBRANE
6.METHODS & PROCEDURES
7.APPLICATIONS
8.REFERENCES
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3. INTRODUCTION
DEFINITION:
Diffusion:
 “The movement of particles in a solid from an area of
high concentration to an area of low concentration,
resulting in the uniform distribution of the substance.”
 During diffusion molecules move from an area of high
concentration to an area of low concentration.
 They are said to move down a concentration gradient.
 The material that undergoes the transport is known as
diffusant or permeant or penetrant.
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4. INTRODUCTION
 Diffusion is a passive process which means that no
energy is needed.
 Molecules diffuse until they are evenly spaced apart
and equilibrium is reached.
high
concentration
low
concentration
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5. INTRODUCTION
 In which states are molecules able to diffuse?
solid (e.g. ice) liquid (e.g. water) gas (e.g. steam)
Molecules in liquids and gases are constantly moving
and bumping into each other. This means that they tend
to spread out. By contrast, solids cannot diffuse.
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6. STEADY STATE DIFFUSION
 Diffusion is direct result of Brownian motion.
 Molecule diffuse spontaneously from region of higher
concentration to region of lower concentration until diffusion
equilibrium is established.
 Rate of diffusion independent of time.
 Flux proportional to concentration gradient =
C1
C2
x
C1
C2
x1 x2
Fick’s first law of diffusion
dx
dC
DJ 
D = diffusion coefficient6

7. STEADY- STATE DIFFUSION
 The flux J is expressed as either in number of atom per unit
time.
 Steady state diffusion means that J does not depend upon
time.
 In this case fick‘s 1st law hold that flux along direction “x” is-
Where, J is equal to rate of mass transfer across unit
surface area of barrier.
dx
dC
DJ 
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8. STEADY-STATE DIFFUSION
SINK CONDITION:
 State in which concentration in receptor compartment is
maintained at lower level compaired to its
concentration in donor compartment.
 During diffusion donor compartment act as source &
receptor compartment act as sink.
 Useful for maintaining concentration gradient nearly
constant.
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9. STEADY-STATE DIFFUSION
Fick´s 1st law:
 Mass get transported from 1 compartment to another
over period of time is Flux.
 Flux (J) = Rate of mass transfer across unit surface area
of barrier.
J= 1/S (dm/dt)
Where,
dm = change in mass of material.
S = barrier surface area.
dt = change in time.
1)
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10. STEADY-STATE DIFFUSION
Acc.to Fick‘s law,flux is directly proportional
to conc.gradient.
D=diffusion coefficient of penetrant.
dx=change in distance.
Combine equation 1) & 2) gives,
* This equation represent rate of mass transfer as per
fick‘s law.
dx
dC
DJ  2)
dm/dt= -DS (dc/dx)
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11. MECHANISM
Mechanisms:
 Gases & Liquids – random (Brownian) motion.
 Solids – vacancy diffusion or interstitial diffusion.
I. Vacancy diffusion:
 Only adjacent atoms can move into a vacancy.
 Vacancy moves in opposite direction of atomic
motion.
 Rate depends on concentration of vacancies.
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12. MECHANISM
• atoms exchange with vacancies .
 rate depends on:
 -- number of vacancies
 -- activation energy to exchange.
increasing elapsed time
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13. MECHANISM
Inter diffusion: Atoms tend to migrate from regions of
high conc. to regions of low concentration.
 – smaller atoms can diffuse between atoms.
Initially After some time
•Atom can move into any adjacent empty interstitial
position (usually smaller atoms).
•Rate depends on concentration of interstitial
atoms.
•(Usually faster than vacancy diffusion).
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14. Factors that Influence Diffusion
I. Diffusing Species:
 Magnitude of diffusion coefficient, D – indicates the rate
at which atoms diffuse.
 Both diffusing species and host material influence the
coefficient:
 Relative sizes of atoms.
 Openness of lattice.
 Ionic charges.
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15. Factors that Influence Diffusion
II. Temperature:
 Very strong effect on the diffusion coefficient:
• Diffusion coefficient increases with increasing T.
D  Do exp






Qd
RT
= pre-exponential
= diffusion coefficient
= activation energy
= gas constant
= absolute temperature
D
Do
Qd
R
T
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16. DIFFUSION ACROSS MEMBRANE
Diffusion across membrane:
There are two ways in which
substances can enter or
leave a cell:
1) Passive
a) Simple Diffusion
b) Facilitated Diffusion
c) Osmosis
2) Active
a) Molecules
b) Particles
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17. DIFFUSION ACROSS MEMBRANE
This is the movement of specific molecules down a concentration
gradient, passing through the membrane via a specific carrier
protein
Selection is by size; shape; charge.
Common molecules entering/leaving cells include glucose & amino-
acids.
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18. DIFFUSION ACROSS MEMBRANE
It is passive and requires no energy from the cell.
If the molecule is changed on entering the cell (glucose + ATP
→ glucose phosphate + ADP), then the concentration gradient
of glucose will be kept high.
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19. DIFFUSION ACROSS MEMBRANE
Active Transport :
 Active transport is the energy-demanding transfer of a substance
across a cell membrane against its concentration gradient, i.e.,
from lower concentration to higher concentration.
 Special proteins within the cell membrane act as specific protein
‘carriers’. The energy for active transport comes from ATP.
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20. DIFFUSION ACROSS MEMBRANE
Passive Transport:
• Passive diffusion is the process by which
molecules spontaneously diffuse from a
region of higher concentration to a
region of lower concentration.
• Lipid-soluble drugs penetrate the lipid
cell membrane and can pass the cell
membrane by passive diffusion.
• Also, large molecules, such as proteins
and protein-bound drugs, cannot diffuse
through the cell membrane.
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21. METHODS & PROCEDURES
Two types:
A) horizontal transport cell:
a. wurester cell
b. Viles chein permeation cell
B) vertical transport cell:
a) Aquair and weiner diffusion cell
b) biber and rhodes cell
c) franz diffusion cell
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22. Horizontal Transport Cell
wurester cell:
Receptor and donor compartment
made of pyrex glass material.
Animal or human skin acts as
semi permeable cell and barrier
may be supported on a perforated
plate.
Drug sample solution taken in
donor compartment and solvent in
the receptor compartment.
Whole set up placed in constant
temperature bath to maintain the
temp of 37±0.2°C.
The liquid in receptor stirred by
using magnetic beads to obtain
uniform distribution.
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23. VERTICAL TRANSPORT CELL
Aquair and weiner diffusion cell:
Receptor and donor compartment
made of pyrex glass or plastic
material.
Animal or human skin acts as semi
permeable cell and barrier may be
supported on a perforated plate.
Drug sample solution taken in
upper compartment and solvent in
the lower compartment.
Whole set up placed in constant
temperature bath to maintain the
temp of 37±0.2°C.
The liquid in receptor stirred by
using magnetic beads to obtain
uniform distribution.
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24. APPLICATIONS
1) The release of drug from dosage form is diffusion
controlled,such dosage form available in market as
sustained & controlled release product.
2) The molecular weight of polymers can be estimated from
diffusion process.
3) The transport of drugs from GI tract,skin,etc., can be
understood & predicted from the principles of diffusion.
4) The diffusion of drugs into tissues & their excretion
through kidneys can be anticipated through diffusion
studies.
5) The process such as dialysis, microfiltration, ultrafiltration,
haemodialysis,osmosis,etc., use the principles of diffusion.
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25. REFERENCES
1. C.V.S. Subrahamanyam,Textbook of physical pharmaceutics,
2nd Edition, Vallabh prakashan, pg.no.110-127
2. D.M. Brahmankar ,Biopharmaceutics and Pharmacokinetics-A
Treatise”,2nd Edition, 2009,Vallabh Prakashan, pp- 10 to 22.
3. www.google.com
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