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ROHIT MISHRA
M.PHARM
PHARMACEUTICS
GLA
The process of movement of
unchanged drug from the siteof
administration to systemic
circulation.
What is Drug Absorption
MECHANISMS OF
DRUG ABSORPTION
I. PassiveDiffusion
 Diffusion
 Movement fromhigh
low concentration
• Major process for absorption
of more than 90% of drugs
• Non ionic diffusion
• Driving force – concentration
or electrochemical gradient
• Difference in the drug
concentration on either side
of the membrane
• Drug movement is a result of
kinetic energy of molecules
Mathematically(Fick’s First law of
diffusion)
.................I
dQ/dt = rate of drug diffusion (amount/time)
D = diffusion coefficient of the drug
A= surface area of the absorbing membrane for drug diffusion
Km/w = partition coefficient of drug between the lipoidal membrane &
the aqueous GI fluids
(CGIT – C) = difference in the concentration of drug in the GI fluids &
the plasma (Concentration Gradient)
h = thickness of the membrane
Characteristics of Passive diffusion:
Energy independent
Greater the area & lesser the thickness of the membrane, faster
the diffusion
The process rapid over for short distances
Concentration equal on both the sides of the membrane -
Equilibrium is attained
Greater the PC of the drug faster the absorption
ii. PoreTransport
• It is also called as convective transport, bulk flow or filtration.
• Mechanism – through the protein channel present in the cell
membrane.
• Drug permeation through pore transport – renal excretion, removal
of drug from CSF & entry of drug into the liver
The driving force – hydrostatic or osmotic pressure differences across
the membrane. Thus, bulk flow of water along with the small solid
molecules through aqueous channels. Water flux that promotes such a
transport is called as solvent drag
The process is important in the absorption of low molecular weight
(<100D), low molecular size (smaller than the diameter of the pore)
& generally water soluble drugs through narrow, aqueous filled
channels or pores e.g. urea, water & sugars.
Chain like or linear compounds (upto 400D)- filtration
iii. Ion-PairTransport
Responsible for absorption of compounds which ionizes at all
pH values. e.g. quaternary ammonium, sulphonic acids
Ionized moieties forms neutral complexes with endogenous ions
which have both the required lipophilicity & aqueous solubility
for passive diffusion.
E.g. Propranolol, a basic drug that forms an ion pair with oleic
acid & is absorbed by this mechanism
Carrier MediatedTransport
• Involves a carrier
which reversibly
binds to the solute
molecules and forms a
solute-carrier
complex.
• This molecule
transverse across the
membrane to the other
side and dissociates,
yielding the solute
molecule.
• The carrier then
returns to the original
site to accept a new
molecule.
• There are two type of
carrier mediated
transport system
1) Facilitated
diffusion
2) Active transport
FacilitatedDiffusion
• Facilitated diffusion is a
form of carrier transport
that does not require the
expenditure of cellular
energy.
• Carriers are numerous in
number & are found
dissolved in cell
membrane .
• The driving force is
concentration gradient,
particles move from a
region of high conc to low
conc.
Contd…
• The transport is aided
by integral membrane
proteins.
• Facilitated diffusion
mediates the
absorption of some
simple sugars,
steroids, amino acids
and pyrimidines from
the small intestine and
their subsequent
transfer across cell
membranes.
ActiveTransport
• Requires energy, which is
provided by hydrolysis of
ATP for transportation.
• More commonly,
metabolic energy is
provided by the active
transport of Na+, or is
dependent on the
electrochemical gradient
produced by the sodium
pump, Na+/K+ ATPase
(secondary active
transport).
This transport requires energy in the form of ATP
Primary ActiveTransport
• Direct ATPrequirement
• The process transfers only one ion or molecule & only in
one direction. Hence, called as UNIPORT
• E.g. absorption of glucose
• ABC (ATP binding Cassette) transporters
Secondary ActiveTransport
• No direct requirement ofATP
• The energy required in transporting an ion aids transport of
another ion or molecule (co-transport or coupled transport)
either in the same direction or opposite direction.
• 2 types:
• Symport (co-transport)
• Antiport (counter transport)
symportantiport
ATP ATP
Antiport and Symport
Endocytosis
• It is a process in which
cell absorbs molecules
by engulfing them.
• Also termed as
vesicular transport.
• It occurs by 3
mechanisms:
Phagocytosis
Pinocytosis
Transcytosis
Phagocytosis
Pinocytosis
• It is a form of endocytosis in
which small particles are
brought to the cell, forming an
invagination.
• These small particles are
suspended in small vesicles.
• It requires energy in the form
ofATP.
• It works as phagocytosis, the
only difference being, it is non
specific in the substances it
transports.
• This process is important in
the absorption of oil soluble
vitamins & in the uptake of
nutrients
References
D.M Brahmankar and Sunil B. Jaiswal, Biopharmaceutics and
Pharmacokinetics: A Treatise 2009 second edition Published by
M.K Jain for Vallabh Prakashan New Delhi Page number 1-23
Mechanism rohit mishra

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Mechanism rohit mishra

  • 2. The process of movement of unchanged drug from the siteof administration to systemic circulation. What is Drug Absorption
  • 4. I. PassiveDiffusion  Diffusion  Movement fromhigh low concentration • Major process for absorption of more than 90% of drugs • Non ionic diffusion • Driving force – concentration or electrochemical gradient • Difference in the drug concentration on either side of the membrane • Drug movement is a result of kinetic energy of molecules
  • 5.
  • 6. Mathematically(Fick’s First law of diffusion) .................I dQ/dt = rate of drug diffusion (amount/time) D = diffusion coefficient of the drug A= surface area of the absorbing membrane for drug diffusion Km/w = partition coefficient of drug between the lipoidal membrane & the aqueous GI fluids (CGIT – C) = difference in the concentration of drug in the GI fluids & the plasma (Concentration Gradient) h = thickness of the membrane
  • 7. Characteristics of Passive diffusion: Energy independent Greater the area & lesser the thickness of the membrane, faster the diffusion The process rapid over for short distances Concentration equal on both the sides of the membrane - Equilibrium is attained Greater the PC of the drug faster the absorption
  • 8. ii. PoreTransport • It is also called as convective transport, bulk flow or filtration. • Mechanism – through the protein channel present in the cell membrane. • Drug permeation through pore transport – renal excretion, removal of drug from CSF & entry of drug into the liver
  • 9. The driving force – hydrostatic or osmotic pressure differences across the membrane. Thus, bulk flow of water along with the small solid molecules through aqueous channels. Water flux that promotes such a transport is called as solvent drag The process is important in the absorption of low molecular weight (<100D), low molecular size (smaller than the diameter of the pore) & generally water soluble drugs through narrow, aqueous filled channels or pores e.g. urea, water & sugars. Chain like or linear compounds (upto 400D)- filtration
  • 10. iii. Ion-PairTransport Responsible for absorption of compounds which ionizes at all pH values. e.g. quaternary ammonium, sulphonic acids Ionized moieties forms neutral complexes with endogenous ions which have both the required lipophilicity & aqueous solubility for passive diffusion. E.g. Propranolol, a basic drug that forms an ion pair with oleic acid & is absorbed by this mechanism
  • 11. Carrier MediatedTransport • Involves a carrier which reversibly binds to the solute molecules and forms a solute-carrier complex. • This molecule transverse across the membrane to the other side and dissociates, yielding the solute molecule. • The carrier then returns to the original site to accept a new molecule. • There are two type of carrier mediated transport system 1) Facilitated diffusion 2) Active transport
  • 12. FacilitatedDiffusion • Facilitated diffusion is a form of carrier transport that does not require the expenditure of cellular energy. • Carriers are numerous in number & are found dissolved in cell membrane . • The driving force is concentration gradient, particles move from a region of high conc to low conc.
  • 13. Contd… • The transport is aided by integral membrane proteins. • Facilitated diffusion mediates the absorption of some simple sugars, steroids, amino acids and pyrimidines from the small intestine and their subsequent transfer across cell membranes.
  • 14. ActiveTransport • Requires energy, which is provided by hydrolysis of ATP for transportation. • More commonly, metabolic energy is provided by the active transport of Na+, or is dependent on the electrochemical gradient produced by the sodium pump, Na+/K+ ATPase (secondary active transport).
  • 15. This transport requires energy in the form of ATP
  • 16. Primary ActiveTransport • Direct ATPrequirement • The process transfers only one ion or molecule & only in one direction. Hence, called as UNIPORT • E.g. absorption of glucose • ABC (ATP binding Cassette) transporters
  • 17. Secondary ActiveTransport • No direct requirement ofATP • The energy required in transporting an ion aids transport of another ion or molecule (co-transport or coupled transport) either in the same direction or opposite direction. • 2 types: • Symport (co-transport) • Antiport (counter transport)
  • 19. Endocytosis • It is a process in which cell absorbs molecules by engulfing them. • Also termed as vesicular transport. • It occurs by 3 mechanisms: Phagocytosis Pinocytosis Transcytosis
  • 21. Pinocytosis • It is a form of endocytosis in which small particles are brought to the cell, forming an invagination. • These small particles are suspended in small vesicles. • It requires energy in the form ofATP. • It works as phagocytosis, the only difference being, it is non specific in the substances it transports. • This process is important in the absorption of oil soluble vitamins & in the uptake of nutrients
  • 22. References D.M Brahmankar and Sunil B. Jaiswal, Biopharmaceutics and Pharmacokinetics: A Treatise 2009 second edition Published by M.K Jain for Vallabh Prakashan New Delhi Page number 1-23