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Beta Lactam Antibiotic
Cephalosporin
Dr Lokendra Sharma
Professor
Beta Lactam Antibiotic ?
Major
Penicillins
Cephalosporins
Minor
Monobactum
Carbapenum
An ideal antibiotics ?
• Broad-spectrum ? Narrow ?
• Did not induce resistance
• Selective toxicity, low side effects
• Preserve normal microbial flora
For lecture only
CEPHALOSPORINS ?
• Cephalosporium fungus
• Dihydrothiazine ring + B lactum
• Semisynthetic B-lactams derived from
chemical side chains added to 7-
aminocephalosporanic acid.
• 4 generations CS add 5th
• Generally more resistant to B-lactamases.
.
SPECTRUM
1ST GENERATION gram(+). cefazolin (used
as prophylactic following surgery)
2ND GENERATION: gram (+) & gram (-)
3RD GENERATION: good against gram (-)
aerobes
some cross into CNS readily e.g. cefotaxime !
used to
treat meningitis
4TH GENERATION: like 3rd gen but more
resistant to betalactamases
5th
GENERATION
Fifth Generation
Ceftobiprole and ceftaroline both parental
Inhibit Bind to Penicillin binding protein -2a
produce by MRSA resistance S
Pneumonia
Ceftaroline 2010 for MRSA
Ceftobiprole – post antibiotic effect on
MRSA
Ceftolozane 5 GN
??
• All CEF = 1 GN (Except cefaclor 2GN)
• Pi = 4 GN (CefPime, CefPirome)
• ME end =3 rd generation (Exept
CefuroxiME)
• ROL (CeftibipRole,CeftaRoline) 5 GN
• ME,ONE,TEN (3 GN)
• OR oral (CefacLOr,)
• T Injectable (CefoTetan)
.
 Bactericidal
 Less susceptible to β-lactamases.
 Disrupt the synthesis of the peptidoglycan .
 The peptidoglycan layer =important structural integrity.
 The final transpeptidation step in the synthesis of the
peptidoglycan
 Facilitated by transpeptidases known as
penicillin-binding proteins (PBPs).
 PBPs bind to the D-Ala-D-Ala at the end of muropeptides
(peptidoglycan precursors) to crosslink the peptidoglycan.
 Beta-lactam antibiotics mimic the D-Ala-D-Ala site
 Irreversibly inhibiting PBP crosslinking of peptidoglycan.
1. drugs that affect the bacterial cell wall
Inhibit Transpeptidase &Carboxipeptidase
.Pharmacokinetics
• 7 aminocephalosporinic acid = active
nucleous
• New modification at position 3 & 7
• Modification position 3 PK & toxicity
• Modification position 7 Antibacterial
Spectrum
.
• Conc dependent killing(CDK)= FQ,Aminog
• Time dependent killing(TDK)= beta lactum
• postantibiotic effects(PAE)
• MIC
Cephalosporins
Antibacterial Spectrum 
First Generation Second Generation Third Generation Fourth Generation
+Cocci Ó¨ Cocci Ó¨ Cocci Ó¨ Cocci
Ó¨ Bacclli Ó¨ Bacclli Ó¨ Bacclli Ó¨ Bacclli
Anaerobes Anaerobes
Resistance
3GN
LESS LESS LESS LESS
+ Bacclli +Cocci +Cocci
Ó¨ Cocci
+ Bacclli + Bacclli
+Cocci
Cephalosporins
 
First Generation Second Generation Third Generation Fourth Generation
* Oral Agent
CEFADROXIL *
(tissue)
CEFACLOR * CEFDINIR
CEFEPIME
(100% renal)
CEFAZOLIN
(surgical
prophylaxis)
CEFAMANDOLE CEFOPERAXONE
CEFPIROME
Cefalidin
 
CEFELIXIN *
(bile)
CEFONICID
CEFOTAXIME
(prototype)
CEPHALOTHIN
(prototype)
(IM pain)
CEFORANIDE
CEFTAZIDIME
(Thrombocytopeni)
 
CEPHAPRIN
CEFOTETAN
(anaerobics)
CEFTIBUTEN  
CEPHRADINE *
(diarrhoea)
CEFOXITIN
(prototype )
CEFTIZOXIME  
CEFUROXIME
CEFTRIAXONE
First generation cephalosporins:
 CEPHALOTHIN, CEFAZOLIN,
CEFALEXIN. (Streptococcus,
pneumococcus but not or methicillin-
resistant Staphylococcus).
 + Cocci > - Bacilli > + Bacilli > - Cocci >
Anaerobics
 Do not cross  blood-brain barrier.
 Primarily excreted = kidney
 Ineffective Pseudomonas aeruginosa,
Enterobacter, and indole-positive Proteus
species
Second generation
cephalosporins:
 CEFUROXIME, CEFAMANDOLE, CEFOXITIN, CEFACLOR.
 - Cocci
>+ Cocci > +Bacilli
- Bacilli
 Cefuroxime cross BBB ,Resistant to beta-
lactamase  
 Do not achieve adequate levels in the CSF.
Cephalosporins
 Third generation 
cefotaxime 
cefixime 
cefpodoxime 
ceftazidime 
cefdinir 
Fourth generation  (cefilidin,cefoselin,cefluprenam)    
    cefe Pime 
    cef Pirome
Fifth GN
      - CeftobipRole  
      - ceftaRoline 
Third generation
cephalosporins:
 MOXALACTAM, CEFAPERAZONE, CEFTAZIDIRNE,
CEFTRIAXONE.
 Extended Gram negative coverage, 
 resistant to non-Staphylococcus b-lactamase,
 Cross the blood-brain barrier. 
 Enterobacter, Pseudomonas (ceftazidime and 
cefaperazone only), Serratia, b-lactamase producing
Haemophillus influenza and Neisseria species.
 Ceftizoxime and moxalactam retain good activity against 
Bacteroides fragilis.
 - cocci & Bacilli & Anaerobes > + Cocci & Bacilli
Fourth generation
 CEFEPIME ,CEFPIROME . 
 Comparable to third-generation but more
resistant to some beta-lactamases.
 - Cocci & Bacilli (Resistant to 3rd
Gn) & > +
Cocci &
 + Bacilli & Anaerobes ----NO
Fifth Generation 
CeftobipRole and ceftaRoline both 
parental
Inhibit Bind to Penicillin binding protein -2a 
produce by MRSA  resistance S 
Pneumonia
CeftaRoline 2010  for MRSA 
CeftobipRole – post antibiotic effect on 
MRSA
Pharmacokinetics
 Some orally most parenterally (IM or IV).
 widely distributed .
 CEFOPERAZONE, CEFOTAXIME,
CEFUROXIME, CEFTRIAXONE, AND
CEFTAZIDIME (third generation) also cross the blood-
brain barrier
 Drugs of choice for meningitis due to Gram-
negative intestinal bacteria.
.
Almost all  eliminated via the kidneys and 
actively secreted by renal tubules. 
CEFAPERAZONE AND CEFTRIAXONE  
eliminated through  biliary tract----Q.
Nephrotoxicity increase with loop diurtics  
…..Q 
ADVERSE EFFECTS
 Hypersensitivity reactions =similar 
penicillins.
 Nephrotoxicity =CEPHALORIDINE----Q
 Intolerance to alcohol (disulfiram like 
reaction)(Q----cefamandole, cefotetan, 
moxalactam, cefoperazone=MTT group)
 Diarrhea= oral forms. cephaloridine ,third 
cefoperazone,cefixime
 Superinfection. resistant organisms , fungi, 
often proliferate 
ADVERSE EFFECTS
BLEEDING
 Hyperprothrombinemia= (Q-----MTT group= 
cefamandole, cefotetan, moxalactam, 
cefoperazone)
 Thrombocytopenia, Platelet dysfunction. 
Administration of vitamin K (10mg) twice a week can 
prevent this. 
 Neutropenia=Rare
 Serum sickness=cefaclor ----- Q
Coinfection and
Superinfection ?
CEPHALOSPORINS
• Adverse reactions.
– 5-10% cross-sensitivity
with pcn allergic pts.
– 1-2% hypersensitivity
reactions in non-pcn
allergic pts.
– Broader spectrum leads to
opportunistic infections
(candidiasis, C. difficile
colitis).
CEPHALOSPORINS
1. Identify this manifestation ?
2. What is Opportunistic
infection ?
3. What is the treatment and
Preventive Majors ?
4. Spectrum of Bacteria ?
Identify ?
Cause ?
Biliary
sludging
syndrome
?
USES:
 A cephalosporin with or without aminoglycoside
1st
Trt Klebsiella pneumococci.
 First GN surgical prophylaxis (Cefazolin) of wound
infection.
 Third GN meningitis due to, meningococci, and
Haemophillus influenza.
 CEFTRIAXONE = TOC beta-lactamase producing
Neisseria gonorrhea.
 E coli (G1),
 Salmonella Typhoid,Parathyphoid = CEFTRIAXONE
 H .Ducreyi = CEFTRIAXONE
 Pseudo Pseudomalli = CEFTRIAXONE
1.Antimicrobial agent acting by inhibition of cell wall synthesis is
a.Erythromycin
b.Tetracycline
c.Lomefloxacin
d.Cefepime
(d)
2.Which one of the following drugs is an antipseu-domonal
penicillin?
a.Cephalexin
b.Cloxacillin
c.Piperacillin
d.Dicloxacillin
(c)
3.All of the following drugs can cause renal failure EXCEPT
a.Cephaloridine
b.Amphotericin B
c.Cefoperazone
d.Gentamicin
(c)
4.Which of the following drug is NOT used for the treatment of
methicillin resistant staphylococcus aureus (MRSA)?
a.Cefaclor
b. Cotrimoxazole
c.Ciprofloxacin
d.Vancomycin
(a)
5. Which of the following is a fourth generation cephalosporin?
a.Ceftriaxone
b.Cefaclor
c.Cefepime
d.Cefuroxime
(c)
6. All of the following cephalosporins have good activity against pseudomonas
aeruginosa EXCEPT
a.Cephadroxil
b.Cefepime
c.Cefoperazone
d.Ceftazidime
(a)
7. Treatment of penicillin producing Neisseria gonorrhoeae is /are
a.Amoxicillin
b.Ciprofloxacin
c.Cefotaxime
d.Doxycycline
e.Azithromycin
(b) (c)
8.Which of these antibiotics are safe in renal
failure?
a.Cephalexin
b.Tetracycline
c.Nitrofurantion
d.Gentamicin
e.Doxycycline
(a)
9. Which of the following statement are true regarding cefepime
a.It is a fourth generation cephalosporin
b.Once a day dose is sufficient
c.It possess antipseudomonal action
d.Its dose should not be reduced in renal pathology
e.It is a prodrug
(a)
10.The mechanism of antibacterial action of cephalosporins involves
a.Inhibition of the synthesis of precursors of peptidoglycan
b.Interference with the synthesis of ergosterol
c.Inhibition of transpeptidation reaction
d.Inhibition of beta lactamase
(c)
11.Second generation cephalosporin that can be used orally is
a.Cefepime
b.Cefalothin
c.Cefaclor
d.Cefadroxil
(b)
12.Third generation cephalosporin that can be given orally is
a.Cefixime
b.Cefpirome
c.Cefaclor
D.Cefadroxil
(a)
13. The antibiotic which can be given safely in
a pregnant women is
a.Ciprofloxacin
b.Cefuroxime
c.Metronidazole
d.Chloramphenicol
(b)
14. Linezolid is best used for
a.MRSA
b.VRSA
c,.K.pneumoniae
d.E.coli
(b)
15.Which one of the following is a fourth generation cephalosporin?
a.Cefuroxime
b.Ceftazidime
c.Cefepime
d.Cefamandole
(c)
16.Neutropenia is associated with
a.Nafcillin
b.Methicillin
c.Carbencillin
d.Ampicillin
(a)
17.Which of the following antimicrobials has
antipseudomonal action?
(a)Cefopodoxime
(b)Cephradine
(c)Cefotetan
(d)Cefoperazone
(d)
18.Treatment of penicillinase producing
neisseria gonarrhoeae is/are
(a)Amoxycillin
(b)Ciprofloxacin
(c)Cefotaxime
(d)Doxycycline
(e)Azithromycin
(b)*(c)
19.Which of the following antimicrobials has
antipseudomonal action?
(a)Cefopodoxime
(b)Cephradine
(c)Cefotetan
(d)Cefoperazone
(d)
20.All are first generation cephalosporins
except
a.Cefadroxil
b.Cefazolin
c.Cephalexin
d.Cefaclor
D
21.A patient develops an infection of
methicillin resistant Staphylococcus
aureus.All of the following can be used to
treat this infection except.
a.Cotrimoxazole
b.Cefaclor
c.Ciprofloxacin
d.Vancomycin
(b)
22.All are true about cephalosporins,EXCEPT
a.Ceftazidime is a 3rd
generation cephalosporin.
b.Cefoperazone has got antipseudomonal
effect.
c.Cefoxitin has got no activity against
anaerobes.
d.Cephalosporins act by inhibiting cell wall
synthesis.
(c)
23.Which of the following cephalosporins can be used in patients
with low GFR?
a.Cefuroxime
b.Cefixime
c.Ceftazidime
d.Cefoperazone
(d)
24.Cephalosporin that does not require
dose reduction in patient with any degree
of renal impairment is
a.Cefuoxime
b.Cefoperazone
c.Ceftazidime
d.Cefotaxime
(b)
25.Which of the following drugs is not
used for MRSA?
a.Cefaclor
b.Cotrimoxazole
c.Ciprofloxacin
d.Vancomycin
(a)
Cephalosporin vs Penicillin
• Cephalosporin advantages
– cover staphylococci
– better vs. Klebsiella, enteric gram-neg.
bacilli, gonococci
• Cephalsporin disadvantages
– cost
– poor distribution to CSF (1st & 2nd
gen)
– not cover enterococcus
Learning objective achieved ?
• Classification
• ABS
• Mechanism of Action
• AE
• Use
Thank You
Dr Lokendra Sharma

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Beta lactam antibiotic cephalosporin

Editor's Notes

  1. Ceftobiprole, ceftaroline, ceftolozane Ceftobiprole has been described as "fifth-generation" cephalosporin,[20][21] though acceptance for this terminology is not universal. Ceftobiprole has powerful antipseudomonal characteristics and appears to be less susceptible to development of resistance. Ceftaroline has also been described as "fifth-generation" cephalosporin, but does not have the antipseudomonal or VRE coverage of ceftobiprole.[22] Ceftolozane is a new option for treatment of Complicated Intra-abdominal Infections (cIAI), and Complicated Urinary Tract Infections (cUTI). Ceftolozane is combined with the β-lactamase inhibitor tazobactam, as multi-drug resistant bacterial infections will generally show resistance to all β-lactam antibiotics unless this enzyme is inhibited.[23][24][25][26][27]
  2. bactericidal and have the same mode of action as other β-lactam antibiotics (such as penicillins), but are less susceptible to β-lactamases. Cephalosporins disrupt the synthesis of the peptidoglycan layer forming the bacterial cell wall. The peptidoglycan layer is important for cell wall structural integrity. The final transpeptidation step in the synthesis of the peptidoglycan is facilitated by transpeptidases[disambiguation needed] known as penicillin-binding proteins (PBPs). PBPs bind to the D-Ala-D-Ala at the end of muropeptides (peptidoglycan precursors) to crosslink the peptidoglycan. Beta-lactam antibiotics mimic the D-Ala-D-Ala site, thereby irreversibly inhibiting PBP crosslinking of peptidoglycan.
  3. bactericidal and have the same mode of action as other β-lactam antibiotics (such as penicillins), but are less susceptible to β-lactamases. Cephalosporins disrupt the synthesis of the peptidoglycan layer forming the bacterial cell wall. The peptidoglycan layer is important for cell wall structural integrity. The final transpeptidation step in the synthesis of the peptidoglycan is facilitated by transpeptidases[disambiguation needed] known as penicillin-binding proteins (PBPs). PBPs bind to the D-Ala-D-Ala at the end of muropeptides (peptidoglycan precursors) to crosslink the peptidoglycan. Beta-lactam antibiotics mimic the D-Ala-D-Ala site, thereby irreversibly inhibiting PBP crosslinking of peptidoglycan.
  4. First generation Cephazolin= Surgical prophylaxis Cephalothin = Prototype,  IM pain Cefadroxil = More tissue penetration Cephalexin= Bile conc Cephradine= Diarrhoea Second generation cefaclor cefuroxime cefprozil loracarbef Active against Gram negative organisms (Escherichia co1i Kiebsiella pneumoniae, and the indole negative Proteus mirabilis). Effective against some anaerobic cocci (Peptococcus and Peptosteptococcus, but NOT Bacteroides fragilis).
  5. The spectrum is extended to more Gram negative bacteria Enterobacter species, Klebsiella species, and indole-positive Proteus species. Also, Haemophilus influenza is covered by cefuroxime, cefamandole, cefaclor; Bacteroides fragilis by cefoxitin
  6. Cefclidine, cefepime (Maxipime), cefluprenam,cefoselis, cefozopran, cefpirome (Cefrom),cefquinome  These cephems are also sometimes grouped with fourth-generation cephalosporins: oxacephems: flomoxefNote:Cefquinome is not approved for human use. It is for veterinary medicine. Gram-positive: They are extended-spectrum agents with similar activity against Gram-positive organisms as first-generation cephalosporins.Gram-negative: Fourth-generation cephalosporins are zwitterions that can penetrate the outer membraneof Gram-negative bacteria.[19] They also have a greater resistance to β-lactamases than the third-generation cephalosporins. Many can cross the blood–brain barrier and are effective in meningitis. They are also used against Pseudomonas aeruginosa.
  7. Biliary sludging syndrome ?