clinical chemistry (antibiotics)

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Toxicology: Therapeutic Drugs: ANTIBIOTICS Presented by: Flores, Lanie Grace P. Gongora, Erica Mae S.

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Antibiotics

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Page 1: Clinical Chemistry (Antibiotics)

Toxicology: Therapeutic Drugs: ANTIBIOTICS

Presented by:Flores, Lanie Grace P.Gongora, Erica Mae S.

Page 2: Clinical Chemistry (Antibiotics)

What are antibiotics?

•Antimicrobial agents that kill or inhibit the growth of bacteria

•Produced naturally by a bacterium or fungus

Page 3: Clinical Chemistry (Antibiotics)

How do antibiotics work?

WIS

•Weakening the bacteria’s cell wall until it bursts

•Interfering with the bacteria’s ability to repair its damaged DNA

•Stopping the bacteria’s ability to make what it needs to grow

Page 4: Clinical Chemistry (Antibiotics)

AMINOGLYCOSIDES• Group of chemically related antibiotics• Treatment of infections with Gram (–) bacteria that are

resistant to less toxic antibiotics• Act synergistically against certain Gram (+) organisms• Used in treatment of:

– Severe infections of abdomen and UT– Bacteremia– Endocarditis

• Require trough and peak measurements

Page 5: Clinical Chemistry (Antibiotics)
Page 6: Clinical Chemistry (Antibiotics)

ROUTES OF ADMINISTRATION

Not well absorbed from the GI tract, it is limited to:– Intravenous (IV)– Intramuscular (IM)

Not used in an outpatient setting

Page 7: Clinical Chemistry (Antibiotics)

GENTAMICIN

• Most commonly used– Low cost– Reliable activity against Gram (-) aerobes

• Isolated from Micromonospora– Breakthrough in the treatment of bacillary

infections ( Pseudomonas aeruginosa)

Page 8: Clinical Chemistry (Antibiotics)

TOBRAMYCIN

• Has greater in vitro activity against Pseudomonas aeruginosa

Page 9: Clinical Chemistry (Antibiotics)

AMIKACIN

• Effective against resistant organisms– Its chemical structure makes it less susceptible to

inactivating enzymes• Preferred agent for serious nosocomial

infections caused by Gram (-) bacilli

Page 10: Clinical Chemistry (Antibiotics)

KANAMYCIN

• Used to treat serious bacterial infections in many different parts of the body

• Short-term use only• Toxic effects more likely to occur in elderly

patients and newborn infants

Page 11: Clinical Chemistry (Antibiotics)

STREPTOMYCIN

• The first aminoglycoside– Isolated from Streptomyces griseus

• Used for:– Tuberculosis– Infections caused by certain bacteria

Page 12: Clinical Chemistry (Antibiotics)

NEOMYCIN

• Had better activity than Streptomycin against aerobic Gram (-) bacilli

• Could not safely be used systemically due to its formidable toxicity

• Isolated from Streptomyces fradiae

Page 13: Clinical Chemistry (Antibiotics)

TOXIC EFFECTS

• Ototoxic effect – Disrupts inner ear cochlear and vestibular membrane

o Hearing and balance impairmento Irreversible

• Nephrotoxic effect– Increase in serum creatinine and BUN– Impairs the function of the PCT

o Electrolyte imbalanceo Possibly proteinuria

Page 14: Clinical Chemistry (Antibiotics)

TOXIC EFFECTS

• Neuromuscular blockade– Administration of neuromuscular blocking drugs and

anesthetics– Hypocalcemia– Myasthenia gravis

• Hypersensitivity reactions• Superinfections• CNS effects• GI disturbances

Page 15: Clinical Chemistry (Antibiotics)

ELIMINATION

• Renal filtration– Patients with compromised renal function,

adjustments must be made based on serum concentration

Page 16: Clinical Chemistry (Antibiotics)

METHODS

• Chromatography• Immunoassay

Page 17: Clinical Chemistry (Antibiotics)

VANCOMYCIN

• Glycopeptide antibiotic• Effective against Gram (+) cocci and bacilli• Skipping doses may increase risk of further

infection that is resistant to antibiotics• Used against resistant strains of Streptococcus

and Staphylococcus• Only trough levels are monitored to ensure the

serum drug concentration is within the therapeutic range

Page 18: Clinical Chemistry (Antibiotics)

ROUTE OF ADMINISTRATION

Because of poor oral absorption, it is administered by:– IV infusion

Page 19: Clinical Chemistry (Antibiotics)

TOXIC EFFECTS

• “Red-man syndrome”– Erythemic flushing of the extremities

• Ototoxic and Nephrotoxic effects are similar to aminoglycosides

Page 20: Clinical Chemistry (Antibiotics)
Page 21: Clinical Chemistry (Antibiotics)

ELIMINATION

• Renal filtration• Excretion

Page 22: Clinical Chemistry (Antibiotics)

METHODS

• Chromatography• Immunoassay

Page 23: Clinical Chemistry (Antibiotics)

CHLORAMPHENICOL

• Distributes to all tissues• Concentrates in the CSF• Isolated from Streptomyces venezuelae• 50% protein bound; rapidly absorbed in the GIT• No longer drug of choice due to BM toxicity• Used against:– Gram (+) and Gram (-) cocci and bacilli (including

anaerobes)– Ricketssia, Mycoplasma, Chlamydia, and Chlamydophila spp.

Page 24: Clinical Chemistry (Antibiotics)

ROUTES OF ADMINISTRATION

• Well absorbed orally• Intravenous (IV)

Page 25: Clinical Chemistry (Antibiotics)

TOXIC EFFECTS

• Blood dyscrasia• “Gray baby syndrome”– Condition that occurs in newborns (especially

premature babies) who are given the drug chloramphenicol

• Cytoplasmic vacuolation– Erythroid cells– Myeloid cells

Page 26: Clinical Chemistry (Antibiotics)
Page 27: Clinical Chemistry (Antibiotics)

ELIMINATION

• 68%-99% – Excreted in the urine

• 8% - 12%– Excreted as free chloramphenicol

• Remainder is excreted as inactive metabolites

Page 28: Clinical Chemistry (Antibiotics)

REFERENCES:

Bishop, Michael (2010). Clinical Chemistry 6th Edition: Techniques, Principles, Correlations.Rodriguez, M.T. (2014). Clinical Chemistry Review Handbook for Medical Technologists.Tortora et al. (1998). Microbiology: An Introduction 6th Edition.

http://www.aafp.org/afp/1998/1115/p1811.htmlhttp://www.drugs.com/cdi/streptomycin.htmlhttp://campus.usal.es/~galenica/clinpkin/Aminoglycosides.htmhttp://www.nlm.nih.gov/medlineplus/druginfo/meds/a604038.htmlhttps://www.merckmanuals.com/professional/infectious-diseases/bacteria-and-antibacterial-drugs/chloramphenicolhttp://www.medicinenet.com/chloramphenicol-oral/article.htm