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Antimicrobials
Mrs. Dipali Kulkarni
Assistant Professor,
Yash Institute of Pharmacy,
Aurangabad.
ANTIMICROBIALS
• Topical anti-infective
agents may be applied to
intact cutaneous & mucous
surface before surgery & to
treat minor cuts, abrasions
or burns.
• Koch (1865) had
established the relationship
between infection and
micro-organism till then the
need for topical anti-
infective agents was not
realized
. • Hospital disinfection,
sterilization of instruments
and the surgical handwash
are the general measures
which are being routinely
used to reduce the risk of
hospital acquired infections
and to minimize the transfer
of micro-organisms to the
susceptible patients.
• Keratolytic agents: Agents used to apply on the skin to soften
the keratin e.g. Sulphur & Aluminium oxide
• 2. Antiseptic agents
• 3. Disinfectants
• 4. Sanitizers
• 5. Germicides
• • Antimicrobials/topical anti-infective agents is an agent which
kill microorganisms or stop their growth.
• • Antibacterial agents can be further subdivided into
bactericidal agents, which kill bacteria, and bacteriostatic
agents, which slow down or stall bacterial growt
• Topical anti-infective agents may be categorized into
Antiseptic is any agent which either kills or inhibits the
growth of microorganisms when applied topically at
damaged tissue.
• Disinfectant agents destroy microorganisms but not
usually bacteria spores.
• Germicides agents kill microorganisms. it may be
classified as bacteriocides (bacteriostatic – inhibit the
growth of bacteria), sporicides, viricides and fungicides.
• Sterilization is total removal or destruction of all living
microorganisms which is done by chemical or mechanical
processes like heat or radiation (e.g. UV radiation) methods.
• Most of the
topical anti-
infective agents
exert
antimicrobial
activity through
either:
1. Oxidation
2.
Halogenations
3. Protein
precipitation
Mechanism of Action of Antimicrobials
Hydrogen peroxide
Physical properties
• In pure state hydrogen
peroxide is almost
colourless (very pale
blue) liquid, acidic in
taste.
• It melts at 272.4 K and
has a boiling point of
423 K.
• It is miscible in water in
all proportions and
forms hydrates.
Chemical properties
• It is
decomposed
rapidly
on
coming in contact with
oxidiable organic matter
and with certain metals
and also if allowed to
become alkaline.
into
• it decomposes
water and oxygen
H2O2 → H2O+O2
PREPARATION
1. From sodium peroxide (Merck’s method)
• Calculated amount of sodium peroxide (Na2O2) is
gradually added to an ice-cold solution of 20%
H2SO4 in small lots with constant stirring.
Na2O2 + H2SO4 → Na2SO4 + H2O2
Upon cooling, crystals of Na2SO4.10H2O separate out
and the resulting solution contains about 30% H2O2.
The solution also contains some dissolved Na2SO4, but
it does not interfere with the reactions of H2O2.
A pure sample of H2O2 may, however, be prepared by
vacuum distillation.
PREPARATION
FROM BARIUM PEROXIDE: treatment of thin aqueous
cream of barium peroxide with cold dilute sulphuric
acid forms hydrogen peroxide
BaO2 + H2SO4 → BaSO4 + H2O2
When CO2 is passed slowly through ice cold paste of
barium peroxide, hydrogen peroxide is formed
BaO2 +CO2 + H2O → BaCO3 + H2O2
Assay: oxidation-reduction titration
• hydrogen peroxide is titrated with a standard
solution of potassium permanganate in the
presence of sulphuric acid at room temperature.
potassium itself act as indicator. the end point is
appeared as a permanent pink colour
KMnO4 + H2SO4 + 5H2O → K2SO4 + MnSO4 + 8H2O + O2
Uses:
• hydrogen peroxide used as disinfectant, anti infective and
deodorant.
• Hydrogen peroxide ear drops have been used for the
removal of wax.
• Hydrogen peroxide solution is used as a mouth wash in
treatment of acute stomatitis and as deodorant gargle.
Potassium Permanganate
KMnO4
• The salt is also known as "permanganate of potash.
• The permanganate ion is a strong oxidizing agent. It
dissolves in water to give deep purple solutions,
evaporation of which gives prismatic purplish-black
glistening crystals. It has a sweet flavour with sweet
astingent taste.
Uses:
• Act as disinfectant, deodorant
• Act as astringent, antiinfective and bactericidal agent
• Solutions are used to clean ulcers or abscesses as
wet dressings and in baths in eczematous condition.
Preparation:
• Pottasium permanganate is prepared by heating
potassium hydroxide with manganeese dioxide in
the presence of air or an oxidising agent such as
potassium nitrate or potassium chlorate
2KOH + MnO2K2MnO4 +H2O
• The greenish product potassium manganate is
extracted with water and treated with carbon
dioxide. Or ozonized air to precipitate about one-
third of the manganese as the hydrated dioxide .
The remaining manganese in converted into KMno4
3K2MnO4 + 2CO2 2KMnO4 +MnO2 + 2K2CO3
If chlorine is passed through the solution in place
or carbondioxide the whole of the manganese of
the manganate is converted into permanganate
• 2K2MnO4 + Cl2à 2KMnO4 +2KCL
Manganate can also be converted into the
permanganate by electrolyzing a warm solution
• 2KMnO4 +2H2O à 2KMnO4 +2KOH +H2
Assay of Potassium
Permanganate:
• The assay is based on the oxidation reduction
titration which is carried out with a standard
solution of oxalic acid in the presence of
sulphuric acid at 70oC throughout the entire
titration. In the assay potassium permanganate
itself serves as an indicator to give pink colour.
2KMNO4 + 5 H2C2O4.2H2O + 5H2SO4 →
K2SO4 + 2MnSO4 + 18H2O + 10CO2
Each ml of 0.1N oxalic acid is euivalent to 0.00316
g of KMnO4
It occursas an odourless, white crystals or white powder with slight
acidic and bitter taste.
Solubility: Freely soluble in glycerin & partially soluble in water &
alcohol.
various dehydration products obtained by heating boric acid with a
loss of water include :
Boric Acid (H3BO3)
Temperature ◦C Dehydration product
100 Metaboric acid (HBO2)
160 Tetraboric acid
(H2B4O7)
More than 160 Boron trioxide (2B2O3)
Preparation:
Boric acid can be prepared by
adding a mixture of conc.H2SO4
and water to a boiling solution
of borax
• Na2B4O7 + H2SO4 + 5H2O →
Na2SO4 + 4H3BO3
Preparation of boric acid involves the
reaction between borax (disodium
tetra borate decahydrate ) with a
mineral acid such as hydrochloric acid
(HCl). The obtained white crystals of
boric acid are completely insoluble in
cold water.
Na2B4O7.10H2O + 2 HCl → 4 B(OH)3 (or
H3BO3) + 2 NaCl+ 5 H2O
Assay: It is assayed by
titrimetric method.
Being a very weak acid, it
can not be directly titrated
accurately with strong
alkali.
When it is dissolved in a
mixture of water and
glycerin, it behaves like a
strong monobasic acid (i.e.
glyceroboric acid) and
then it can titrated with
alkali using
phenolphthalein as an
indicator till pink colour.
Factor: each ml of 1.0N
NaOH is euivalent to
0.06183 g of H3BO3.
Uses:
• it is used as a local anti-
ineffective agent, germicide &
dusting powder as an antiseptic.
Boric acid can be very
dangerous, "not for
internal use”.
It is also used in opthalmic
preparations as buffer.
Iodine & its Preparations
Iodine & its Preparations
Iodine & its preparations
Antimicrobial
Antimicrobial
Antimicrobial
Antimicrobial
Antimicrobial
Antimicrobial
Antimicrobial
Antimicrobial
Antimicrobial
Antimicrobial
Antimicrobial

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Antimicrobial

  • 1. Antimicrobials Mrs. Dipali Kulkarni Assistant Professor, Yash Institute of Pharmacy, Aurangabad.
  • 2. ANTIMICROBIALS • Topical anti-infective agents may be applied to intact cutaneous & mucous surface before surgery & to treat minor cuts, abrasions or burns. • Koch (1865) had established the relationship between infection and micro-organism till then the need for topical anti- infective agents was not realized . • Hospital disinfection, sterilization of instruments and the surgical handwash are the general measures which are being routinely used to reduce the risk of hospital acquired infections and to minimize the transfer of micro-organisms to the susceptible patients.
  • 3. • Keratolytic agents: Agents used to apply on the skin to soften the keratin e.g. Sulphur & Aluminium oxide • 2. Antiseptic agents • 3. Disinfectants • 4. Sanitizers • 5. Germicides • • Antimicrobials/topical anti-infective agents is an agent which kill microorganisms or stop their growth. • • Antibacterial agents can be further subdivided into bactericidal agents, which kill bacteria, and bacteriostatic agents, which slow down or stall bacterial growt • Topical anti-infective agents may be categorized into
  • 4. Antiseptic is any agent which either kills or inhibits the growth of microorganisms when applied topically at damaged tissue. • Disinfectant agents destroy microorganisms but not usually bacteria spores. • Germicides agents kill microorganisms. it may be classified as bacteriocides (bacteriostatic – inhibit the growth of bacteria), sporicides, viricides and fungicides. • Sterilization is total removal or destruction of all living microorganisms which is done by chemical or mechanical processes like heat or radiation (e.g. UV radiation) methods.
  • 5. • Most of the topical anti- infective agents exert antimicrobial activity through either: 1. Oxidation 2. Halogenations 3. Protein precipitation Mechanism of Action of Antimicrobials
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  • 11. Hydrogen peroxide Physical properties • In pure state hydrogen peroxide is almost colourless (very pale blue) liquid, acidic in taste. • It melts at 272.4 K and has a boiling point of 423 K. • It is miscible in water in all proportions and forms hydrates. Chemical properties • It is decomposed rapidly on coming in contact with oxidiable organic matter and with certain metals and also if allowed to become alkaline. into • it decomposes water and oxygen H2O2 → H2O+O2
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  • 15. PREPARATION 1. From sodium peroxide (Merck’s method) • Calculated amount of sodium peroxide (Na2O2) is gradually added to an ice-cold solution of 20% H2SO4 in small lots with constant stirring. Na2O2 + H2SO4 → Na2SO4 + H2O2 Upon cooling, crystals of Na2SO4.10H2O separate out and the resulting solution contains about 30% H2O2. The solution also contains some dissolved Na2SO4, but it does not interfere with the reactions of H2O2. A pure sample of H2O2 may, however, be prepared by vacuum distillation.
  • 16. PREPARATION FROM BARIUM PEROXIDE: treatment of thin aqueous cream of barium peroxide with cold dilute sulphuric acid forms hydrogen peroxide BaO2 + H2SO4 → BaSO4 + H2O2 When CO2 is passed slowly through ice cold paste of barium peroxide, hydrogen peroxide is formed BaO2 +CO2 + H2O → BaCO3 + H2O2
  • 17. Assay: oxidation-reduction titration • hydrogen peroxide is titrated with a standard solution of potassium permanganate in the presence of sulphuric acid at room temperature. potassium itself act as indicator. the end point is appeared as a permanent pink colour KMnO4 + H2SO4 + 5H2O → K2SO4 + MnSO4 + 8H2O + O2 Uses: • hydrogen peroxide used as disinfectant, anti infective and deodorant. • Hydrogen peroxide ear drops have been used for the removal of wax. • Hydrogen peroxide solution is used as a mouth wash in treatment of acute stomatitis and as deodorant gargle.
  • 18. Potassium Permanganate KMnO4 • The salt is also known as "permanganate of potash. • The permanganate ion is a strong oxidizing agent. It dissolves in water to give deep purple solutions, evaporation of which gives prismatic purplish-black glistening crystals. It has a sweet flavour with sweet astingent taste. Uses: • Act as disinfectant, deodorant • Act as astringent, antiinfective and bactericidal agent • Solutions are used to clean ulcers or abscesses as wet dressings and in baths in eczematous condition.
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  • 20. Preparation: • Pottasium permanganate is prepared by heating potassium hydroxide with manganeese dioxide in the presence of air or an oxidising agent such as potassium nitrate or potassium chlorate 2KOH + MnO2K2MnO4 +H2O • The greenish product potassium manganate is extracted with water and treated with carbon dioxide. Or ozonized air to precipitate about one- third of the manganese as the hydrated dioxide . The remaining manganese in converted into KMno4 3K2MnO4 + 2CO2 2KMnO4 +MnO2 + 2K2CO3
  • 21. If chlorine is passed through the solution in place or carbondioxide the whole of the manganese of the manganate is converted into permanganate • 2K2MnO4 + Cl2à 2KMnO4 +2KCL Manganate can also be converted into the permanganate by electrolyzing a warm solution • 2KMnO4 +2H2O à 2KMnO4 +2KOH +H2
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  • 23. Assay of Potassium Permanganate: • The assay is based on the oxidation reduction titration which is carried out with a standard solution of oxalic acid in the presence of sulphuric acid at 70oC throughout the entire titration. In the assay potassium permanganate itself serves as an indicator to give pink colour. 2KMNO4 + 5 H2C2O4.2H2O + 5H2SO4 → K2SO4 + 2MnSO4 + 18H2O + 10CO2 Each ml of 0.1N oxalic acid is euivalent to 0.00316 g of KMnO4
  • 24. It occursas an odourless, white crystals or white powder with slight acidic and bitter taste. Solubility: Freely soluble in glycerin & partially soluble in water & alcohol. various dehydration products obtained by heating boric acid with a loss of water include : Boric Acid (H3BO3) Temperature ◦C Dehydration product 100 Metaboric acid (HBO2) 160 Tetraboric acid (H2B4O7) More than 160 Boron trioxide (2B2O3)
  • 25. Preparation: Boric acid can be prepared by adding a mixture of conc.H2SO4 and water to a boiling solution of borax • Na2B4O7 + H2SO4 + 5H2O → Na2SO4 + 4H3BO3 Preparation of boric acid involves the reaction between borax (disodium tetra borate decahydrate ) with a mineral acid such as hydrochloric acid (HCl). The obtained white crystals of boric acid are completely insoluble in cold water. Na2B4O7.10H2O + 2 HCl → 4 B(OH)3 (or H3BO3) + 2 NaCl+ 5 H2O
  • 26. Assay: It is assayed by titrimetric method. Being a very weak acid, it can not be directly titrated accurately with strong alkali. When it is dissolved in a mixture of water and glycerin, it behaves like a strong monobasic acid (i.e. glyceroboric acid) and then it can titrated with alkali using phenolphthalein as an indicator till pink colour. Factor: each ml of 1.0N NaOH is euivalent to 0.06183 g of H3BO3. Uses: • it is used as a local anti- ineffective agent, germicide & dusting powder as an antiseptic. Boric acid can be very dangerous, "not for internal use”. It is also used in opthalmic preparations as buffer.
  • 27. Iodine & its Preparations
  • 28. Iodine & its Preparations
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  • 35. Iodine & its preparations