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ANTIBIOTICS
CLASSIFICATION BASED ON MODE OF ACTION
AND INDUSTRIAL PRODUCTION
By : Aghera Raj
IMSC Biotechnology
Parul Instiute Of Applied Sciences
Introduction
 Substance derived from microorganism or produce
synthetically, that destroy or limits growth of living
organisms.
 One of the wonder discovery of 20th century.
 Antibiotics resistance is public health issue with a
significant impact on
• Morbidity
• Mortality
• Health-care associated costs
What is antibiotics?
 A medicine that inhibits growth of living organisms or
destroy microorganisms.
 Originally, an antibiotics was a substance produced by
one microorganism that selectively inhibits the growth of
another.
Antibiotic classification
 According to antimicrobial activity
 Bactericidal
 Bacteriostatic
 According to bacterial spectrum of activity
 Narrow spectrum
 Broad spectrum
 According to absorbability from the site of administration to
attain significant concentration for the treatment of systemic
infection
 Locally acting
 systemic
Mechanics of action
Classification of antibiotics based on mode of action
Nitu met | sultan | in ceptember with a fluid pen and a car
Nit- nitrofurans
Met- metronidazole
Sul- sulphonamides
Cep- cephalosporin
Flu- fluoroguinolones
Pen- penicillin
Car- carbapenem
DNA synthesis
inhibitor
Tetrahydro folate
synthesis inhibitor
Peptidoglycans
DNA gyras enzyme inhibition
Peptides synthesis inhibitors
Protein synthesis inhibitors
Ma Life At Cell
Ma- macrolides
Li- lincosamides
A- aminoglycosides
T- tetracyclins
30S
50S
C- clindamycin
E- erythromycin
L- linezolid
50S
30S
50S
Mechanism of major antibacterial agents
Antibiotic resistance
 Production of enzyme that inactivates drug
 β-lactamase
 S. aureus, Enterobacteriaceae, Pseudomanas, H. influenza
 Altered permeability to the drug result to decreased effective
intracellular concentration
 Synthesis of altered structural targets for the drug
 Streptomycin resistance – mutant protein in 30S ribosomal
subunit delete binding site Enterobacteriaceae
 Multi-drug resistance pump
• Bacteria actively export substances including drug in exchange for
protons
Industrial production of antibiotics
 Inoculum:
 A small amount of material containing bacteria, viruses,
or other microorganisms that is used to start a culture.
 A high yielding strain (Bacteria) is a prerequisite for
antibiotic production.
 The Inoculum is prepared usually in the form of a spore
suspension, which is transferred into the fermenter.
 Fermenter / Bioreactor:
 Antibiotic are generally produced in stainless steel
fermenters used in the batch or fed mode, see in figure
below.
 Water cooling is often used to maintain the temperature
between 24-26° C.
 Generally, the fermenter is maintained at above
atmospheric pressure which reduces contamination risk
and enhances O2 supply.
 The final stage fermenter is preferably used for antibiotic
production for the longest period.
Batch fermentation
 Initial stages of fermentation are designed for
considerable microbial growth; these are carried out in
seed stage fermenters of smaller size.
 One or more seed stages may be used, depending on the
process and the strain, to produce the maximum amount
of biomass.
Flow diagram
Process description
 The production fermenter is run in a fed batch mode in
which a nutrient e.g., glucose is added continuously
throughout the fermentation to enhance the duration of
antibiotic production.
 This is accompanied by withdrawal of small volumes of
broth to check increase in volume of the broth in the
fermenter.
 Antifoaming agents are added at the appropriate stage of
fermentation.
 Selected microbiological, physical and chemical features
are monitored during the fermentation in order to achieve
proper control.
 At the end of final production stage incubation, the broth
contains only a low concentration (3-35% If the total
solutes in the broth) of the antibiotic.
 Antibiotic recovery is done by separation of cells from the
broth by filtration or centrifugation which is followed by
purification.
 Removal of cells: The first step in product recovery is the
separation of whole cells and other insoluble ingredients
from the culture broth by technique such as filtration and
centrifugation.
 The product needs to be very pure, since it being used
as a therapeutic medical drug, so it is dissolved and then
precipitated as a potassium salt to separate it from other
substances in the medium.
Quality control
 Retained Sample
 Analysis of finished product
 Sampling
 Validation
 Records
 Batch inspection and sampling
 SOP
 GMP
Packaging
 Primary packaging
 Secondary packaging
 Tertiary packaging
Antibiotics classification on bases of mode of action and industrial production

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BOWEL ELIMINATION FACTORS AFFECTING AND TYPES

Antibiotics classification on bases of mode of action and industrial production

  • 1. ANTIBIOTICS CLASSIFICATION BASED ON MODE OF ACTION AND INDUSTRIAL PRODUCTION By : Aghera Raj IMSC Biotechnology Parul Instiute Of Applied Sciences
  • 2. Introduction  Substance derived from microorganism or produce synthetically, that destroy or limits growth of living organisms.  One of the wonder discovery of 20th century.  Antibiotics resistance is public health issue with a significant impact on • Morbidity • Mortality • Health-care associated costs
  • 3. What is antibiotics?  A medicine that inhibits growth of living organisms or destroy microorganisms.  Originally, an antibiotics was a substance produced by one microorganism that selectively inhibits the growth of another.
  • 4. Antibiotic classification  According to antimicrobial activity  Bactericidal  Bacteriostatic  According to bacterial spectrum of activity  Narrow spectrum  Broad spectrum  According to absorbability from the site of administration to attain significant concentration for the treatment of systemic infection  Locally acting  systemic
  • 6. Classification of antibiotics based on mode of action Nitu met | sultan | in ceptember with a fluid pen and a car Nit- nitrofurans Met- metronidazole Sul- sulphonamides Cep- cephalosporin Flu- fluoroguinolones Pen- penicillin Car- carbapenem DNA synthesis inhibitor Tetrahydro folate synthesis inhibitor Peptidoglycans DNA gyras enzyme inhibition Peptides synthesis inhibitors
  • 7. Protein synthesis inhibitors Ma Life At Cell Ma- macrolides Li- lincosamides A- aminoglycosides T- tetracyclins 30S 50S C- clindamycin E- erythromycin L- linezolid 50S 30S 50S
  • 8. Mechanism of major antibacterial agents
  • 9. Antibiotic resistance  Production of enzyme that inactivates drug  β-lactamase  S. aureus, Enterobacteriaceae, Pseudomanas, H. influenza  Altered permeability to the drug result to decreased effective intracellular concentration  Synthesis of altered structural targets for the drug  Streptomycin resistance – mutant protein in 30S ribosomal subunit delete binding site Enterobacteriaceae  Multi-drug resistance pump • Bacteria actively export substances including drug in exchange for protons
  • 10. Industrial production of antibiotics  Inoculum:  A small amount of material containing bacteria, viruses, or other microorganisms that is used to start a culture.  A high yielding strain (Bacteria) is a prerequisite for antibiotic production.  The Inoculum is prepared usually in the form of a spore suspension, which is transferred into the fermenter.
  • 11.  Fermenter / Bioreactor:  Antibiotic are generally produced in stainless steel fermenters used in the batch or fed mode, see in figure below.  Water cooling is often used to maintain the temperature between 24-26° C.  Generally, the fermenter is maintained at above atmospheric pressure which reduces contamination risk and enhances O2 supply.  The final stage fermenter is preferably used for antibiotic production for the longest period.
  • 13.  Initial stages of fermentation are designed for considerable microbial growth; these are carried out in seed stage fermenters of smaller size.  One or more seed stages may be used, depending on the process and the strain, to produce the maximum amount of biomass. Flow diagram
  • 14. Process description  The production fermenter is run in a fed batch mode in which a nutrient e.g., glucose is added continuously throughout the fermentation to enhance the duration of antibiotic production.  This is accompanied by withdrawal of small volumes of broth to check increase in volume of the broth in the fermenter.  Antifoaming agents are added at the appropriate stage of fermentation.
  • 15.  Selected microbiological, physical and chemical features are monitored during the fermentation in order to achieve proper control.  At the end of final production stage incubation, the broth contains only a low concentration (3-35% If the total solutes in the broth) of the antibiotic.  Antibiotic recovery is done by separation of cells from the broth by filtration or centrifugation which is followed by purification.  Removal of cells: The first step in product recovery is the separation of whole cells and other insoluble ingredients from the culture broth by technique such as filtration and centrifugation.
  • 16.  The product needs to be very pure, since it being used as a therapeutic medical drug, so it is dissolved and then precipitated as a potassium salt to separate it from other substances in the medium.
  • 17. Quality control  Retained Sample  Analysis of finished product  Sampling  Validation  Records  Batch inspection and sampling  SOP  GMP
  • 18. Packaging  Primary packaging  Secondary packaging  Tertiary packaging