PENCILLINS




            .BY
       T.SHIVAKUMR
Shiva.pharmacist@gmail.com
PENICILLINS

Beta- lactam antibiotics
Derivatives of 6- aminopenicillanic acid
 :Alteration of the side group resulted in cpds with
Broader spectrum of activity
Resistance to penicillinase
Stability in acid PH
Most widely effective antibiotics
Least toxic drugs known
MECHANISM OF ACTION
They act by inhibition of bacterial cell wall synthesis
Thus exposing the osmotically less stable
membrane
This cause lysis of bacterial cell wall
These agents are bactericidal
Active against multiplying and not resting bacteria
Inactive against mycobacteria, protozoa, fungi and
viruses
Classifications of penicillins


)Penicillin G ( Benzyl penicillin )(i.m ,slow i.v or infusion .1
.Highest activity against Gram-positive organisms but susceptible to Beta-lactamase
 :Effective against
Gram-positive aerobic cocci - Staph. aureus- not producing penicillinase,
                                    S.pneumoniae ( group A ) ,S.pyogenes
Gram-negative aerobic cocci -N.meningitidis
 N. gonorrhea-no longer of choice
Gram- positive bacilli : Bacillus anthracis

Spirochetes : T. pallidum – drug of choice
Anaerobes
Clostridium spp but inactive against B.fragilis
)Actinomycetes israelii ( actinomycosis
Repository penicillins
Developed to prolong duration of penicillin G in the
    blood
1. Penicillin G procaine
   Duration 12- 24 hr
   It is given i.m and not i.v( risk of procaine toxicity)
   Seldom used now ( increased frequency of
    penicillinase producing N. gonorrhea
Repository penicillins ( cont.)
2. Penicillin G benzathin ( i.m )
   Duration 3- 4 weeks
   Painful at the injection site ( limits its use )
   Uses
    1. Syphilis
    2. Rheumatic fever prophylaxis( inhibits
       group A beta- hemolytic streptococci)
    3. Streptococcal pharyngitis
. )Class. Of penicillins ( cont
Disadvantages of penicillin G
A. Destroyed by gastric HCL
B. Inactivated by penicillinase
C. Narrow spectrum of activity
. )Class. Of penicillins ( cont
Acid resistant penicillins. 2
.Phenoxy- methyl penicillin ( penicillin v), p.o
 )spectrum of activity is similar to penicillin G   (
Uses
Group A Streptococcal pharyngitis
Prophylaxis against group A streptococci in patients
.with history of rheumatic heart disease
Disadvantages
Readily hydroyzed by beta-lactamase
. )Class. Of penicillins ( cont
Penicillinase-resistant penicillins. 3
Methicillin       Oxacillin
Cloxacillin        Dicloxacillin
Floxacillin        Nafcillin
Lower activity against G+ compared to Penicllin G
but
.Are the choice for infections caused by penicillinase producing S. aureus
.However, MRSA & ORSA has emerged
Not effective against G- aerobes( E.coli, klebsiella,N.gonorrhea or
.)pseudomonas spp
.Less active than penicillin on anaerobes
High protein and food binders
)Class. Of penicillins ( cont
Broad- spectrum penicillins. 4
a) Ampicillin, Ampicillin- sulbactam,
Bacampicillin, Amoxicillin, Amoxicillin-
 ).clavulanic acid ( augmentin
Less active than penicillin G against G+ cocci.
.Active against G- organisms
)Broad-spectrum penicillins ( cont
Uses
H. Influenza infections ( otitis media, sinusitis, chronic bronchitis,
).pneumonia, bacterial meningitis
M.catarrhalis
).E. Coli infections ( Urinary & biliary infections
)Samonella infections ( typhoid fever
)Shigella infections ( ampicillin
Gonococcal infections ( alternative for penicillin in the treatment of
)gonorrhea
Prophlaxis of infective endocarditis
Disadvantages
Amoxicillin & ampicillin alone are readily destroyed by Staph.
.Penicillinase
)Broad spectrum penicillins ( cont
B ) Extended- spectrum : Ticarcillin-clavulanic acid,
 )piperacillin,piperacillin-tazobactam ( Tazocin
Uses
Pseud. aeruginosa. For pseud.septicemia, they
 should be given together with an aminoglycoside
 ).eg. Gentamicin(
Disadvantages
Ticarcillin and piperacillin alone are readily destroyed
by S. penicillinase. High dose may lead to
.hypernatraemia due to sodium content
Absorption,distribution & metabolism
Oral absorption of most penicillins is poor
Exception: penicillin v
Amoxicillin
Food interfer with absorption
:To increase GI absorption: give ester form
Bacampicillin
Carbenicillin indany
Distribution
Widely distributed
Relatively insoluble in lipid
Hence, have poor penetration into cells and BBB
Inflammation ( eg. Meningitis ) permits entrance into CSF
. )Absorp., metabolism ( cont
:Protein binding differs
Ampicillin and penicillin G    20% bound
Nafcillin, oxacillin,          90% bound
cloxacillin , dicloxacillin
Metabolism and excretion
Not metabolized in human
Excreted mostly unchanged in urine( except.
 ) Nafcillin,oxacillin, cloxacillin, dicloxacillin
Probenecid blocks their secretion
)   Half-life 30-60 min ( increased in renal failure
Adverse effects of penicillins
1.Hypersensitivity reactions ( occur in 1-10% of pts;
                                   fatality occur in 0.002%)
 ( immediate, accelerated & late allergic rxns) ** Cross-reactions
   Urticarial rash
   Fever
   Bronchspasm
   Serum sickness
   Exfoliative dermatitis
   Stevens- Johnson syndrome
   Anaphylaxis
2. Super infections
3. Diarrhoea
4. May cause convulsions after high doses by i.v or in
     renal failure
THANQ
                           
shiva.pharmacist@gmail.com 

Pencilins

  • 1.
    PENCILLINS .BY T.SHIVAKUMR Shiva.pharmacist@gmail.com
  • 2.
    PENICILLINS Beta- lactam antibiotics Derivativesof 6- aminopenicillanic acid :Alteration of the side group resulted in cpds with Broader spectrum of activity Resistance to penicillinase Stability in acid PH Most widely effective antibiotics Least toxic drugs known
  • 4.
    MECHANISM OF ACTION Theyact by inhibition of bacterial cell wall synthesis Thus exposing the osmotically less stable membrane This cause lysis of bacterial cell wall These agents are bactericidal Active against multiplying and not resting bacteria Inactive against mycobacteria, protozoa, fungi and viruses
  • 5.
    Classifications of penicillins )PenicillinG ( Benzyl penicillin )(i.m ,slow i.v or infusion .1 .Highest activity against Gram-positive organisms but susceptible to Beta-lactamase :Effective against Gram-positive aerobic cocci - Staph. aureus- not producing penicillinase, S.pneumoniae ( group A ) ,S.pyogenes Gram-negative aerobic cocci -N.meningitidis N. gonorrhea-no longer of choice Gram- positive bacilli : Bacillus anthracis Spirochetes : T. pallidum – drug of choice Anaerobes Clostridium spp but inactive against B.fragilis )Actinomycetes israelii ( actinomycosis
  • 6.
    Repository penicillins Developed toprolong duration of penicillin G in the blood 1. Penicillin G procaine Duration 12- 24 hr It is given i.m and not i.v( risk of procaine toxicity) Seldom used now ( increased frequency of penicillinase producing N. gonorrhea
  • 7.
    Repository penicillins (cont.) 2. Penicillin G benzathin ( i.m ) Duration 3- 4 weeks Painful at the injection site ( limits its use ) Uses 1. Syphilis 2. Rheumatic fever prophylaxis( inhibits group A beta- hemolytic streptococci) 3. Streptococcal pharyngitis
  • 8.
    . )Class. Ofpenicillins ( cont Disadvantages of penicillin G A. Destroyed by gastric HCL B. Inactivated by penicillinase C. Narrow spectrum of activity
  • 9.
    . )Class. Ofpenicillins ( cont Acid resistant penicillins. 2 .Phenoxy- methyl penicillin ( penicillin v), p.o )spectrum of activity is similar to penicillin G ( Uses Group A Streptococcal pharyngitis Prophylaxis against group A streptococci in patients .with history of rheumatic heart disease Disadvantages Readily hydroyzed by beta-lactamase
  • 10.
    . )Class. Ofpenicillins ( cont Penicillinase-resistant penicillins. 3 Methicillin Oxacillin Cloxacillin Dicloxacillin Floxacillin Nafcillin Lower activity against G+ compared to Penicllin G but .Are the choice for infections caused by penicillinase producing S. aureus .However, MRSA & ORSA has emerged Not effective against G- aerobes( E.coli, klebsiella,N.gonorrhea or .)pseudomonas spp .Less active than penicillin on anaerobes High protein and food binders
  • 11.
    )Class. Of penicillins( cont Broad- spectrum penicillins. 4 a) Ampicillin, Ampicillin- sulbactam, Bacampicillin, Amoxicillin, Amoxicillin- ).clavulanic acid ( augmentin Less active than penicillin G against G+ cocci. .Active against G- organisms
  • 12.
    )Broad-spectrum penicillins (cont Uses H. Influenza infections ( otitis media, sinusitis, chronic bronchitis, ).pneumonia, bacterial meningitis M.catarrhalis ).E. Coli infections ( Urinary & biliary infections )Samonella infections ( typhoid fever )Shigella infections ( ampicillin Gonococcal infections ( alternative for penicillin in the treatment of )gonorrhea Prophlaxis of infective endocarditis Disadvantages Amoxicillin & ampicillin alone are readily destroyed by Staph. .Penicillinase
  • 13.
    )Broad spectrum penicillins( cont B ) Extended- spectrum : Ticarcillin-clavulanic acid, )piperacillin,piperacillin-tazobactam ( Tazocin Uses Pseud. aeruginosa. For pseud.septicemia, they should be given together with an aminoglycoside ).eg. Gentamicin( Disadvantages Ticarcillin and piperacillin alone are readily destroyed by S. penicillinase. High dose may lead to .hypernatraemia due to sodium content
  • 14.
    Absorption,distribution & metabolism Oralabsorption of most penicillins is poor Exception: penicillin v Amoxicillin Food interfer with absorption :To increase GI absorption: give ester form Bacampicillin Carbenicillin indany Distribution Widely distributed Relatively insoluble in lipid Hence, have poor penetration into cells and BBB Inflammation ( eg. Meningitis ) permits entrance into CSF
  • 15.
    . )Absorp., metabolism( cont :Protein binding differs Ampicillin and penicillin G 20% bound Nafcillin, oxacillin, 90% bound cloxacillin , dicloxacillin Metabolism and excretion Not metabolized in human Excreted mostly unchanged in urine( except. ) Nafcillin,oxacillin, cloxacillin, dicloxacillin Probenecid blocks their secretion ) Half-life 30-60 min ( increased in renal failure
  • 16.
    Adverse effects ofpenicillins 1.Hypersensitivity reactions ( occur in 1-10% of pts; fatality occur in 0.002%) ( immediate, accelerated & late allergic rxns) ** Cross-reactions Urticarial rash Fever Bronchspasm Serum sickness Exfoliative dermatitis Stevens- Johnson syndrome Anaphylaxis 2. Super infections 3. Diarrhoea 4. May cause convulsions after high doses by i.v or in renal failure
  • 17.
    THANQ  shiva.pharmacist@gmail.com 