mms - كلية الطب · 2018-10-18 · •tolnaftate is used to treat tinea pedis, tinea cruris,...
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Drugs dermatological conditions II
Dr Sura Al Zoubi
MMS
Pharmacology
Lecture 5
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TOPICAL CORTICOSTEROIDS
• Corticosteroids (glucocorticoids) have immunosuppressive and antiinflammatory properties.
• Topical corticosteroids are used for the treatment of psoriasis, eczema, contact dermatitis, and other skin conditions manifested by itching and inflammation.
• They are administered locally and via topical and intralesional routes.
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• Corticosteroids work via intracellular receptors and initiate several transcriptions and translations leading to their multiple effects.
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• The actions include inhibitory effects on the
arachidonic acid cascade, depression of production
of many cytokines, and effects on inflammatory
cells.
• In psoriasis, they inhibit epidermal cell mitosis.
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• Numerous topical corticosteroids are available,
with varying potencies and multiple vehicles
of delivery.
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• Tachyphylaxis (decrease in response after repetitive use, tolerance) can occur with continuous use.
• Substitution of a different corticosteroid or less frequent use can minimize tolerance.
• Adverse effects: skin atrophy (thinning of the skin), striae, purpura, acneiform eruptions, dermatitis, local infections, and hypopigmentation.
• In children, potent agents applied to a large surface area can cause systemic toxicity, including depression of the hypothalamic–pituitary–adrenal axis and growth retardation
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TRICHOGENIC AGENTS
• Minoxidil and finasteride are trichogenic
agents that are indicated for the treatment of
androgenic alopecia (“male pattern baldness”).
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Minoxidil
• Minoxidil, originally used as a systemic
antihypertensive, was noted to have the
adverse effect of increased hair growth.
• This adverse effect was turned into a
therapeutic application in the treatment of
alopecia.
• For hair loss, the drug is available as a
nonprescription topical foam or solution
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• MOA:
1. Antihypertensive: vasodilator, acts by opening adenosine triphosphate-sensitive potassium channels in vascular smooth muscle cells.
2. Trichogenic: Although the mechanism of action is not fully known, it is believed to act, at least in part, by shortening the rest phase of the hair cycle.
• Minoxidil is thought to promote the survival of human dermal papillary cells (DPCs) or hair cells by activating both extracellular signal-regulated kinase (ERK) and Akt and by preventing cell death. anti-apoptotic effects on DPCs.
• Minoxidil, when used as a This vasodilation may also improve the viability of hair cells or hair follicles.
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• As a topical therapy, it does not cause systemic
hypotension.
• Minoxidil is effective at halting hair loss in both men
and women and may produce hair growth in some
patients.
• The drug must be used continuously
to maintain effects on hair growth.
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Finasteride
• Finasteride is an oral 5-α reductase inhibitor that blocks conversion of testosterone to the potent androgen 5-α dihydrotestosterone (DHT).
• High levels of DHT can cause the hair follicle to miniaturize and atrophy.
• Finasteride decreases scalp and serum DHT concentrations, thus inhibiting a key factor in the etiology of androgenic alopecia. (Finasteride is used in higher doses for the treatment of benign prostatic hyperplasia).
• Adverse effects: decreased libido, decreased ejaculation, and erectile dysfunction.
• The drug should not be used or handled in pregnancy, as it can cause hypospadias in a male fetus.
• Like minoxidil, use must be continued to maintain therapeutic benefits.
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DRUGS FOR CUTANEOUS
MYCOTIC INFECTIONS • Mold-like fungi that cause cutaneous infections are
called dermatophytes or tinea.
• Tinea infections are classified by the affected site (for example, tinea pedis, which refers to an infection of the feet).
• Common dermatomycoses, such as tinea infections that appear as rings or round red patches with clear centers, are often referred to as “ringworm.” This is a misnomer because fungi rather than worms cause the disease.
• The three different fungi that cause the majority of cutaneous infections are Trichophyton, Microsporum, and Epidermophyton.
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1. Squalene epoxidase inhibitors
Terbinafine
Naftifine
Butenafine
2. Griseofulvin
3. Nystatin
4. Imidazoles
5. Ciclopirox
6. Tolnaftate
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DRUGS FOR CUTANEOUS MYCOTIC
INFECTIONS
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A. Squalene Epoxidase Inhibitors
• These agents act by inhibiting
squalene epoxidase, thereby
blocking the biosynthesis of
ergosterol, an essential
component of the fungal cell
membrane.
• Accumulation of toxic
amounts of squalene results in
increased membrane
permeability and death of the
fungal cell.
Mode Of Action of Squalene Epoxidase
Inhibitors
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1. Terbinafine
• Oral terbinafine is the drug of choice for treating dermatophyte
onychomycoses (fungal infections of nails).
• It is better tolerated, requires a shorter duration of therapy, and is more
effective than either itraconazole or griseofulvin. Therapy is
prolonged (usually about 3 months) but considerably shorter than that
with griseofulvin.
• Oral terbinafine may also be used for tinea capitis (infection of the
scalp) as the topical antifungals are ineffective.
• Topical terbinafine (1% cream, gel or solution) is used to treat tinea
pedis, tinea corporis (ringworm), and tinea cruris (infection of the
groin).
• Duration of treatment is usually 1 week.
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Antifungal spectrum
• Terbinafine is active against Trichophyton.
• It may also be effective against Candida,
Epidermophyton, and Scopulariopsis, but the
efficacy in treating clinical infections due to
these pathogens has not been established.
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Pharmacokinetics
• Terbinafine is available for oral and topical administration, although its bioavailability is only 40% due to first-pass metabolism.
• Terbinafine is highly protein bound and is deposited in the skin, nails, and adipose tissue.
• Terbinafine accumulates in breast milk and should not be given to nursing mothers.
• A prolonged terminal half-life of 200 to 400 hours may reflect the slow release from these tissues.
• Oral terbinafine is extensively metabolized by several CYP450 isoenzymes and is excreted mainly via the urine.
• The drug should be avoided in patients with moderate to severe renal impairment or hepatic dysfunction.
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Adverse effects
• Common adverse effects of terbinafine include gastrointestinal disturbances (diarrhea, dyspepsia, and nausea), headache, and rash.
• Taste and visual disturbances have been reported, as well as transient elevations in serum hepatic transaminases.
• Terbinafine is an inhibitor of the CYP450 2D6 isoenzyme, and concomitant use with substrates of that isoenzyme may result in an increased risk of adverse effects with those agents.
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2. Naftifine
• Naftifine is active against Trichophyton,
Microsporum, and Epidermophyton.
• Naftifine 1% cream and gel are used for topical
treatment of tinea corporis, tinea cruris, and
tinea pedis.
• Duration of treatment is usually 2 weeks.
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3. Butenafine
• Butenafine [byoo-TEN-a-feen] is active
against Trichophyton rubrum,
Epidermophyton, and Malassezia.
• Like naftifine, butenafine 1% cream is used for
topical treatment of tinea infections.
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B. Griseofulvin • Griseofulvin causes disruption of the
mitotic spindle and inhibition of fungal
mitosis .
• It has been largely replaced by oral
terbinafine for the treatment of
onychomycosis, although it is still
used for dermatophytosis of the scalp
and hair.
• Griseofulvin is fungistatic and requires
a long duration of treatment (for
example, 6 to 12 months for
onychomycosis).
• Duration of therapy is dependent on
the rate of replacement of healthy skin
and nails.
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• Ultrafine crystalline preparations are absorbed adequately from the gastrointestinal tract, and absorption is enhanced by high-fat meals.
• The drug concentrates in skin, hair, nails, and adipose tissue.
• Griseofulvin induces hepatic CYP450 activity, which increases the rate of metabolism of a number of drugs, including anticoagulants.
• The use of griseofulvin is contraindicated in pregnancy and patients with porphyria.
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C. Nystatin • Nystatin is a polyene antifungal, and its structure,
chemistry, mechanism of action, and resistance profile resemble those of amphotericin B. (binds to ergosterol, a major component of the fungal cell membrane. When present in sufficient concentrations, it forms pores in the membrane that lead to K+ leakage, acidification, and death of the fungus.)
• It is used for the treatment of cutaneous and oral Candida infections.
• The drug is negligibly absorbed from the gastrointestinal tract, and it is not used parenterally due to systemic toxicity (acute infusion-related adverse effects and nephrotoxicity).
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• It is administered as an oral agent (“swish and swallow” or “swish and spit”) for the treatment of oropharyngeal candidiasis (thrush), intravaginally for vulvovaginal candidiasis, or topically for cutaneous candidiasis
• Adverse effects are rare after oral administration, but nausea and vomiting occasionally occur.
• Topical and vaginal forms may cause skin irritation.
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D. Imidazoles
• Imidazoles are azole derivatives, which currently include:
1. Butoconazole [byoo-toe-KON-a-zole],
2. clotrimazole [kloe-TRIM-a-zole],
3. Econazole [e-KONE-a-zole],
4. ketoconazole [kee-toe-KON-a-zole],
5. Miconazole [my-KON-a-zole],
6. oxiconazole [oks-i-KON-a-zole],
7. sertaconazole [serta-KOE-na-zole],
8. sulconazole [sul-KON-a-zole],
9. terconazole [ter-KONa-zole], and
10. tioconazole [tye-oh-KONE-a-zole].
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• As a class of topical agents, they have a wide
range of activity against
1. Epidermophyton,
2. Microsporum,
3. Trichophyton,
4. Candida, and
5. Malassezia,
• depending on the agent.
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• The topical imidazoles have a variety of uses, including:
1. tinea corporis,
2. tinea cruris,
3. tinea pedis, and
4. oropharyngeal and vulvovaginal candidiasis.
• Topical use is associated with contact dermatitis, vulvar irritation, and edema.
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• Clotrimazole is also available as a troche (lozenge),
• miconazole is available as a buccal tablet for the treatment of thrush.
• Oral ketoconazole has historically been used for the treatment of systemic fungal infections but is rarely used today due to the risk for severe liver injury, adrenal insufficiency, and adverse drug interactions.
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E. Ciclopirox • Ciclopirox inhibits the transport of essential elements in the
fungal cell, disrupting the synthesis of DNA, RNA, and proteins.
• Ciclopirox is active against:
1. Trichophyton,
2. Epidermophyton,
3. Microsporum,
4. Candida, and
5. Malassezia.
• It is available in a number of formulations.
• Ciclopirox 1% shampoo is used for treatment of seborrheic dermatitis.
• Ciclopirox 0.77% cream, gel, or suspension can be used to treat tinea pedis, tinea corporis, tinea cruris, cutaneous candidiasis, and tinea versicolor.
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F. Tolnaftate • Tolnaftate distorts the hyphae and stunts mycelial
growth in susceptible fungi.
• Tolnaftate is active against:
1. Epidermophyton,
2. Microsporum, and
3. Malassezia furfur.
• Tolnaftate is not effective against Candida.
• Tolnaftate is used to treat tinea pedis, tinea cruris,
and tinea corporis.
• It is available as a 1% solution, cream, and powder 29
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Topical Antiviral Drugs
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Topical Antiviral Drugs
• Herpes viruses are associated with a broad
spectrum of diseases, for example,
1. cold sores,
2. viral encephalitis, and
3. genital infections.
• The drugs that are effective against these viruses
exert their actions during the acute phase of viral
infections and are without effect during the latent
phase. 31
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1. Acyclovir • Acyclovir (acycloguanosine) is the prototypic
antiherpetic therapeutic agent.
• Herpes simplex virus (HSV) types 1 and 2, varicella-zoster virus (VZV), and some Epstein-Barr virus–mediated infections are sensitive to acyclovir.
• It is the treatment of choice in HSV encephalitis.
• The most common use of acyclovir is in therapy for genital herpes infections.
• It is also given prophylactically to seropositive patients before bone marrow transplant and post–heart transplant to protect such individuals from herpetic infection.
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• Acyclovir, a guanosine analog, is
monophosphorylated in the cell by
the herpesvirus-encoded enzyme
thymidine kinase.
• Therefore, virus-infected cells are
most susceptible. The
monophosphate analog is converted
to the di- and triphosphate forms by
the host cell kinases.
• Acyclovir triphosphate competes
with deoxyguanosine triphosphate as
a substrate for viral DNA polymerase
and is itself incorporated into the
viral DNA, causing premature DNA
chain termination. 33
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2. Penciclovir • Penciclovir is an acyclic guanosine nucleoside
derivative that is active against HSV-1, HSV-2,
and VZV.
• Penciclovir is only administered topically
• It is monophosphorylated by viral thymidine
kinase, and cellular enzymes form the nucleoside
triphosphate, which inhibits HSV DNA
polymerase.
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3.Trifluridine • Trifluridine is a fluorinated pyrimidine nucleoside analog
that is structurally similar to thymidine.
• Once converted to the triphosphate, the agent is believed to
inhibit the incorporation of thymidine triphosphate into viral
DNA and, to a lesser extent, lead to the synthesis of
defective DNA that renders the virus unable to replicate.
• Trifluridine is active against HSV-1, HSV-2, and vaccinia
virus.
• It is indicated for treatment of HSV kerato-conjunctivitis
and recurrent epithelial keratitis.
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Trifluridine • Because the triphosphate form of trifluridine can also
incorporate to some degree into cellular DNA, the drug is considered to be too toxic for systemic use.
• Therefore, the use of trifluridine is restricted to a topical ophthalmic preparation.
• A short half-life necessitates that the drug be applied frequently.
• Adverse effects include a transient irritation of the eye and palpebral (eyelid) edema
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Thank you
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