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Q: What is local half-life in topical drug therapy?
the time the drug remains active at the site of absorption
Q: How does a long local half life affect dosing frequency?
Allows for daily dosing or reduced dosing frequency due to skin acting as a drug reservoir.
A: It increases absorption by trapping heat and moisture over the application site.
A: Cryotherapy and topical salicylic acid (Compound W).
A: Weakens wart tissue’s adherence to the epidermis, promoting removal.
Q: First line OTC treatment for eczema?
Emollients, topical steroids, topical antihistamines.
A: Topical immunosuppressants (tacrolimus, pimecrolimus) and PDE4 inhibitors (crisaborole).
A: Add topical antibiotics.
A: Benzoyl peroxide, salicylic acid, antimicrobials.
A: Converted to benzoic acid in skin → indirect antimicrobial activity + increased epidermal turnover.
A: Yes, often combined with erythromycin or clindamycin.
A: Tretinoin, isotretinoin, other Vitamin A derivatives.
A: Increases epidermal turnover, reduces cell cohesion, stabilizes lysosomes, increases RNA polymerase activity, increases PGE₂/cAMP/cGMP.
A: Inflammation, peeling, dryness, photosensitivity; acne may worsen first 4–6 weeks.
A: Teratogenic (contraception required before and after therapy), can cause skin dryness, lipid changes, IBD, headaches.
Q: 1st gen antihistamine role in sleep aids?
A: Anti-wakefulness effect (H1 + muscarinic blockade), common in nighttime cold meds.
A: Neurohormone derived from tryptophan, released mainly between 9 PM–4 AM.
A: MT1 (Gi): promotes sleep; MT2 (Gq): coordinates light–dark cycle.
A: Anticholinergic drugs, smoking, mouth breathing, dehydration.
A: Mouthwashes, sprays, lozenges, toothpaste, cholinergic agonists.
A: Benzocaine, corticosteroids, hydrogen peroxide.
A: Systemic analgesics, corticosteroids, cauterization (Debacterol).
A: Antihistamines, mast cell stabilizers.
A: Polymyxin B, protein synthesis inhibitors.
A: α₁ receptor agonists → reduce redness/swelling.
A: HSV-1 virus.
A: Prevents HSV fusion with host cell.
A: Guanine analogue → activated by viral thymidine kinase → inhibits viral DNA polymerase → chain termination.
A: Valacyclovir is an ester prodrug of acyclovir.
A: Prodrug of penciclovir, guanosine analogue.
A:
Azoles: inhibit ergosterol synthesis
Naftifine/Terbinafine/Tolnaftate: inhibit ergosterol synthesis
Nystatin/Amphotericin B: bind ergosterol, disrupt membrane
Ciclopirox: binds metal ions, disrupts enzymes.
A: Permethrin, lindane, crotamiton, sulfur, malathion, tea tree oil.
A: Binds glutamate-gated Cl⁻ channels → hyperpolarization → paralysis of parasite.
A: Prevents viral protein entry into host cell (requires high concentrations not achievable in humans).
Q: High dose ivermectin AEs?
A: Dizziness, confusion, hypotension, seizures, blurred vision, GI upset.
A: TMP-SMX, fluoroquinolones, amoxicillin-clavulanate, cephalosporins, nitrofurantoin, fosfomycin.