Minocycline – chemistry and use MCQs With Answer

Minocycline is a semisynthetic tetracycline antibiotic important in pharmacy practice. This concise introduction for B. Pharm students explains minocycline chemistry — a tetracyclic (naphthacene) core with semisynthetic modifications that increase lipophilicity — and key pharmacology: mechanism of action (30S ribosomal binding), pharmacokinetics (high oral bioavailability, prolonged half‑life, hepatic metabolism), therapeutic uses (acne, rosacea, community‑acquired MRSA, atypical and intracellular pathogens), mechanisms of resistance, major adverse effects (vestibular symptoms, hyperpigmentation, hepatotoxicity), contraindications and drug interactions (chelation with divalent cations, intracranial hypertension risk with isotretinoin). MCQs focus on chemistry, mechanism of action, pharmacokinetics, clinical indications and safety to prepare for exams. ‘Now let’s test your knowledge with 30 MCQs on this topic.’

Q1. What is the chemical classification of minocycline?

  • Beta-lactam antibiotic
  • Aminoglycoside antibiotic
  • Semisynthetic tetracycline derivative
  • Macrolide antibiotic

Correct Answer: Semisynthetic tetracycline derivative

Q2. Which core ring system characterizes the tetracycline class to which minocycline belongs?

  • Beta-lactam four-membered ring
  • Five-membered furan ring system
  • Fused four-ring naphthacene (tetracyclic) nucleus
  • Aromatic quinolone bicyclic system

Correct Answer: Fused four-ring naphthacene (tetracyclic) nucleus

Q3. What is the primary mechanism of antibacterial action of minocycline?

  • Inhibition of DNA gyrase
  • Inhibition of peptidyl transferase on 50S subunit
  • Binding to 30S ribosomal subunit and blocking aminoacyl-tRNA binding
  • Inhibition of folic acid synthesis

Correct Answer: Binding to 30S ribosomal subunit and blocking aminoacyl-tRNA binding

Q4. Pharmacodynamically, minocycline is generally considered:

  • Bactericidal at all concentrations
  • Bacteriostatic, inhibiting bacterial growth
  • Fungicidal against Candida species
  • Only effective when combined with beta-lactams

Correct Answer: Bacteriostatic, inhibiting bacterial growth

Q5. Which resistance mechanisms commonly reduce minocycline activity?

  • Production of beta-lactamases and altered PBPs
  • Efflux pumps and ribosomal protection proteins
  • Altered DNA gyrase and topoisomerase IV
  • Increased permeability to drug uptake

Correct Answer: Efflux pumps and ribosomal protection proteins

Q6. Which statement best describes oral bioavailability of minocycline?

  • Poor oral bioavailability (<20%)
  • Moderate oral bioavailability (30–50%)
  • High oral bioavailability (>70%)
  • Absent—only parenteral administration is effective

Correct Answer: High oral bioavailability (>70%)

Q7. What is the typical elimination half-life range reported for minocycline in adults?

  • 1–3 hours
  • 6–8 hours
  • Approximately 11–22 hours
  • More than 48 hours

Correct Answer: Approximately 11–22 hours

Q8. Compared with older tetracyclines, minocycline’s relative lipophilicity is:

  • Lower, making tissue penetration poor
  • About the same as tetracycline
  • Higher, contributing to improved tissue and CNS penetration
  • Extremely hydrophilic and eliminated unchanged in urine

Correct Answer: Higher, contributing to improved tissue and CNS penetration

Q9. What is the predominant elimination route for minocycline?

  • Almost exclusively renal excretion of unchanged drug
  • Primarily hepatic metabolism with fecal/biliary excretion
  • Excreted unchanged in sweat
  • Elimination solely via pulmonary exhalation

Correct Answer: Primarily hepatic metabolism with fecal/biliary excretion

Q10. Which of the following is a principal licensed or common clinical use of minocycline?

  • First-line therapy for acute epiglottitis
  • Management of acne vulgaris and rosacea
  • Exclusive use in tuberculosis treatment
  • Routine prophylaxis for viral hepatitis

Correct Answer: Management of acne vulgaris and rosacea

Q11. Minocycline has activity against many strains of which problematic pathogen encountered in community infections?

  • Extended-spectrum beta-lactamase (ESBL) Enterobacteriaceae only
  • Community-acquired MRSA (methicillin-resistant Staphylococcus aureus)
  • Pseudomonas aeruginosa as a first-line agent
  • All anaerobes without exception

Correct Answer: Community-acquired MRSA (methicillin-resistant Staphylococcus aureus)

Q12. Minocycline is contraindicated in which of the following populations due to effects on bone and teeth?

  • Pregnant women and children under 8 years
  • Elderly patients over 65 only
  • Patients with controlled diabetes mellitus
  • Adults with hypertension

Correct Answer: Pregnant women and children under 8 years

Q13. Which adverse effect is classically associated with minocycline and may present as dizziness or vertigo?

  • Cardiac arrhythmia
  • Vestibular toxicity
  • Severe hypoglycemia
  • Acute renal colic

Correct Answer: Vestibular toxicity

Q14. Long-term use of minocycline may cause which distinctive dermatologic adverse effect?

  • Photosensitive blistering identical to porphyria
  • Progressive skin and mucosal hyperpigmentation
  • Immediate urticaria in all patients
  • Loss of all body hair (alopecia universalis)

Correct Answer: Progressive skin and mucosal hyperpigmentation

Q15. Which drug interaction reduces minocycline oral absorption significantly?

  • Co-administration with beta blockers
  • Co-administration with divalent cations (calcium, iron, magnesium, aluminum)
  • Co-administration with acetaminophen
  • Co-administration with topical corticosteroids

Correct Answer: Co-administration with divalent cations (calcium, iron, magnesium, aluminum)

Q16. Concurrent use of minocycline with which drug class is associated with increased risk of intracranial hypertension (pseudotumor cerebri)?

  • Systemic retinoids such as isotretinoin
  • Statins used for hyperlipidemia
  • Beta-lactam antibiotics
  • Topical antifungals

Correct Answer: Systemic retinoids such as isotretinoin

Q17. Photosensitivity is a known adverse effect of many tetracyclines. Which statement about minocycline’s photosensitivity risk is most accurate?

  • Minocycline never causes photosensitivity
  • Minocycline can cause photosensitivity reactions, though incidence varies
  • Minocycline causes photosensitivity only when given intravenously
  • Minocycline causes photosensitivity only in neonates

Correct Answer: Minocycline can cause photosensitivity reactions, though incidence varies

Q18. Which baseline laboratory test is most relevant to monitor during prolonged minocycline therapy?

  • Thyroid-stimulating hormone (TSH) only
  • Liver function tests (LFTs)
  • Fasting blood glucose every week
  • Serum amylase exclusively

Correct Answer: Liver function tests (LFTs)

Q19. Which formulations of minocycline are commonly available for systemic therapy?

  • Topical ointment only
  • Oral tablets/capsules and intravenous formulations
  • Inhalation aerosol only
  • Transdermal patch only

Correct Answer: Oral tablets/capsules and intravenous formulations

Q20. In patients with moderate renal impairment, how is minocycline dosing usually managed?

  • Requires significant dose reduction and strict dialysis removal
  • No routine dose adjustment is typically necessary for mild to moderate renal impairment
  • Contraindicated even in mild renal impairment
  • Must be switched to aminoglycoside therapy

Correct Answer: No routine dose adjustment is typically necessary for mild to moderate renal impairment

Q21. From a medicinal chemistry perspective, minocycline’s semisynthetic modifications primarily aim to:

  • Increase susceptibility to beta-lactamases
  • Enhance lipophilicity, tissue penetration and stability
  • Eliminate all antibacterial spectrum except Gram-positives
  • Convert the molecule into a prodrug activated by gut flora

Correct Answer: Enhance lipophilicity, tissue penetration and stability

Q22. On the bacterial ribosome, minocycline blocks which step during protein synthesis?

  • Initiation complex formation at the 50S subunit
  • Binding of aminoacyl-tRNA to the A site on the 30S subunit
  • Termination release factor binding at the 30S subunit
  • Ribosomal RNA methylation step

Correct Answer: Binding of aminoacyl-tRNA to the A site on the 30S subunit

Q23. Minocycline’s antimicrobial spectrum typically includes:

  • Only Gram-negative enteric bacilli
  • Broad spectrum: Gram-positive, Gram-negative and atypical organisms
  • Only anaerobic bacteria
  • Only mycobacteria

Correct Answer: Broad spectrum: Gram-positive, Gram-negative and atypical organisms

Q24. Which tet resistance gene is typically associated with ribosomal protection rather than efflux?

  • tet(A)
  • tet(K)
  • tet(M)
  • mecA

Correct Answer: tet(M)

Q25. Why does minocycline often achieve higher tissue concentrations than tetracycline?

  • Because it is pumped out of tissues by efflux transporters
  • Because increased lipophilicity enhances tissue penetration
  • Because it is highly ionized at physiologic pH and trapped in plasma
  • Because it binds exclusively to serum albumin and not tissues

Correct Answer: Because increased lipophilicity enhances tissue penetration

Q26. Which chronic adverse effect should be specifically discussed with patients starting long-term minocycline therapy?

  • Risk of immediate anaphylactic shock in all patients
  • Potential for skin, oral mucosal and bone hyperpigmentation over time
  • Guaranteed severe neutropenia within 24 hours
  • Permanent loss of hearing in 100% of patients

Correct Answer: Potential for skin, oral mucosal and bone hyperpigmentation over time

Q27. In case of acute oral overdose of minocycline, the initial management most often includes:

  • Immediate chelation with intravenous calcium
  • Supportive care and decontamination such as activated charcoal if early
  • Administration of naloxone as antidote
  • Hemodialysis as first-line removal method

Correct Answer: Supportive care and decontamination such as activated charcoal if early

Q28. Which therapeutic action best categorizes minocycline at the molecular level?

  • Inhibitor of cell wall synthesis (transpeptidation)
  • Protein synthesis inhibitor at the 30S ribosomal subunit
  • DNA intercalator causing double-strand breaks
  • Inhibitor of folate synthesis (dihydropteroate synthase)

Correct Answer: Protein synthesis inhibitor at the 30S ribosomal subunit

Q29. Which storage/chemical stability consideration is important for tetracycline-class drugs like minocycline?

  • They are completely stable under prolonged exposure to strong light
  • They may degrade with heat and light, requiring proper storage
  • They polymerize on contact with plastic packaging only
  • They spontaneously convert to inactive glycosides at room temperature

Correct Answer: They may degrade with heat and light, requiring proper storage

Q30. Why are tetracyclines, including minocycline, generally avoided during pregnancy?

  • They induce labor in the third trimester
  • They cross the placenta and can impair fetal bone growth and cause permanent tooth discoloration
  • They are completely inactivated by placental enzymes and therefore ineffective
  • They cause gestational diabetes in most women

Correct Answer: They cross the placenta and can impair fetal bone growth and cause permanent tooth discoloration

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