pharmacology - iipharmasy.weebly.com/.../pharmacology_-_ii_1.pdf · pharmacology - ii dr shariq...
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![Page 1: Pharmacology - IIpharmasy.weebly.com/.../pharmacology_-_ii_1.pdf · PHARMACOLOGY - II Dr Shariq Syed Associate Professor AIKTC, SoP. PHARMACOLOGY !! EXCITING STUFF WE WILL EXPLORE](https://reader033.vdocuments.site/reader033/viewer/2022052306/5f0c75007e708231d4357f12/html5/thumbnails/1.jpg)
PHARMACOLOGY - IIDr Shariq Syed
Associate Professor
AIKTC, SoP
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PHARMACOLOGY !!
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EXCITING STUFF WE WILL EXPLORE THIS SEM
Chemotherapy
• 30 hrs
Immuno-modulators
• 9 hrs
Drugs for Endocrine systems
• 11 hrs
Hematological Disorders
• 10 hrs
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CHEMOTHERAPY
• Drugs to treat general infections
• Anti-fungal
• Anti-viral
• Drugs for TB, Leprosy, Malaria
• Drugs for Amoebiasis
• Anthelmentic Drugs
• Anti-cancer drugs
Chemotherapy
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IMMUNO-MODULATORS
• Understanding immune function
• Drugs use to stimulate or suppress immune function
• Immune modulators used to treat cancer, HIV
•
Immuno-modulators
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DRUGS TO TREAT ENDOCRINE DISORDERS
• Thyroid & Ant-thyroid drugs
• Drugs to treat diabetes
• Bone mineral homeostasis
• Oxytocics
• Oral contraceptives
Endocrine disorders
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DRUGS TO TREAT HEMATOLOGICAL DISORDERS
• Drugs used in Anemia
• Coagulants, Anti-coagulants
• Thrombolytic and Anti-platelet agents
Hematological disorders
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WHAT EXCITING STUFF WE WILL EXPLORE
Chemotherapy Immuno-modulators
Drugs for Endocrine systems
Hematological Disorders
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CHEMOTHERAPY
What is Chemotherapy ?
Use of CHEMICAL compounds in treatment of INFECTIOUSdiseases, so as to destroy offending ORGANISM and PARASITESwithout damaging the HOST tissue
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BRIEF HISTORY OF CHEMOTHERAPY
Pre-EhlrichEra before
1891
Period of Paul Ehlrich
Period after 1935,
Antibiotic Era
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BRIEF HISTORY OF CHEMOTHERAPY
Paul Ehlrich (Organic Chemist)
Certain Dyes specifically killed/stained certain bacterial cells
Generated a thought/Idea “Synthesize chemicals that can Kill organism” – Magic Bullet
Methylene Blue to treat Malaria
Arsenic compounds to treat other infections
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BRIEF HISTORY OF CHEMOTHERAPY
Paul Ehlrich proposed the concept of “RECEPTORS’
Specific chemical group on cell cell surface
Both Organisms/Human would have RECEPTORS
Drug + Human Receptor = BAD effect (Organotropic Compound)
Drug + organism Receptor = Killing Effect on Organism (Parasitotropic Compound)
Drug “ARSEPHENAMINE” designed to treat Syphillus
Awarded NOBLE PRIZE for his work in 1908
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BRIEF HISTORY OF CHEMOTHERAPY
Domag & His group continued ahead with Ehlrich’s work
Protonsil: Azo Dyes + Suphonamide side chain = treated Streptococci infection
Later, discovered that Sulphonamide get’s released in body, affects Streptococci
Domagg awarded Nobel Prize in 1939
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BRIEF HISTORY OF CHEMOTHERAPY
Early in last century an Interesting idea was floated
“Use one microorganism to cure infection by other organism”
Pasteur (1885) demonstrated the Proof of this concept
Common bacteria prevented growth of Anthrax bacilli
Another group: Emmerich found extracts of Pseudomonas Aeruginosa could destroy variety pathogens
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BRIEF HISTORY OF CHEMOTHERAPY
In 1928, Sir Fleming while working on Staphylococcal variants saw a fungal growth around
This fungus appeared to stop the growth of Staphylococcal
He cultivated the fungus, named it penicillin
Subsequent work by Florey, Chain & Abraham’s work: In 1941- Penicillin was established as potent drug during WW-II to treat infections
Florey, Chain & Abraham awarded Nobel prize in 1945
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BRIEF HISTORY OF CHEMOTHERAPY
Penicillin work led to screening of thousands of microrganism
Schatz et.al reported isolation of Streptomycin from S. griseus
Major advancement since Streptomycin was effective against G-ve
This group also coined word “Antibiotic”
Most of Antibiotics derived from Fungi but some from bacteria as well
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HOW TO TARGET THESE MICRO-ORGANISM ??
The IDEA is to find what is different between these organism & our cells !
Strategy or Plan then would be to target that difference
You can target
1. Biochemical Reactions
specific to bacteria
2. Specific Bacterial Structure
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HOW TO TARGET THESE MICRO-ORGANISM ??
Small to large
Macromolecules
(Proteins, Nucleic Acid,
Peptidoglycan)
Class III
Utilize Energy +
Class I products = small
molecules (AA,
Nucleotides)
Class II
Utilize Glucose to make ATP & Simple molecules
Class I
Biochemical
Reactions that are
specific to Bacteria
can be Potential
Targets
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HOW TO TARGET THESE MICRO-ORGANISM ??
Utilize Glucose to
make ATP & Simple
molecules
Class I
Biochemical
Reactions that are
specific to Bacteria
can be Potential
Targets
Class I Reactions:
• Not very Promising
• Both Host & bacteria use similar
pathways (TCA, Embden-
Meyerhof)
• Even if glucose oxd is blocked,
Bacteria are smart/adapt to
use other pathways
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HOW TO TARGET THESE MICRO-ORGANISM ??
Folate Biosynthesis
Humans get it from outside
Bacteria has to synthesize !
We can target this pathway, That’s what SULPHONAMIDES do !!
Utilize Energy &
Class I products = small
molecules (AA,
Nucleotides)
Class II
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HOW TO TARGET THESE MICRO-ORGANISM ??
Nucleotide Biosynthesis:
Purines & Pyrimidines Analogs
Strategy: To disrupt, block Nucleotide biosynthesis
This would prevent Bacterial DNA Replication
Bacteriostatic Effect !
Utilize Energy +
Class I products = small
molecules (AA,
Nucleotides)
Class II
Bacterial enzymes are more sensitive to inhibition compared to humans
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HOW TO TARGET THESE MICRO-ORGANISM ??
1. Peptidoglycan Synthesis (Bacterial Capsule)
1. Synthesis vulnerable, can be blocked at various steps
2. Wide range of antibiotics attack this step
3. Cycloserine, Vancomycin, Bacitracin, Penicillin's etc
Small to large
Macromolecules
(Proteins, Nucleic Acid,
Peptidoglycan)
Class IIIPathogens cannot take up macromolecules from environment
Potential targets for drugs
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HOW TO TARGET THESE MICRO-ORGANISM ??
1. Nucleic Acid Synthesis
1. Inhibit synthesis of Nucleotides
2. Alter base pairing
3. Inhibit DNA or RNA polymerase enzyme
4. Inhibit DNA Gyrase
5. Direct effect on DNA Itself
Small to large
Macromolecules
(Proteins, Nucleic Acid,
Peptidoglycan)
Class III
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HOW TO TARGET THESE MICRO-ORGANISM ??
Targeting “Formed Structures”
Plasma Membrane (PM):
Bacterial/Fungal PM similar to Humans but can be Easily disrupted
Polymixins (Cationic peptide antibiotics)
Act as detergents, disrupting PM
Fungal PM has large amounts of Ergosterol
Polyene Antibiotics (Nystatin, Amphotericin) leakage of ions (Act as ionophores)
Azoles block Ergosterol synthesis
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HOW TO TARGET THESE MICRO-ORGANISM ??
Target: INTRACELLULAR ORGANELLES
Microtubules or Microfilaments:
Drugs target parasitic tubulin (Albendazole)
Food vacuole:
Drug target malarial parasite polymerase reaction
Target: MUSCLE FIBRES:
Anthelmintic drugs have selective action on Helminth muscle cell