Peringatan Keamanan

The acute subcutaneous LD50 of structurally-related nicotinamide and nicotinic acid in rats were 1.68 and 5.0 g/kg bw, respectively F63. In humans, oral ingestion of 3-9 g of nicotinic acid per day resulted in "niacin hepatitis", gout, and impaired glucose intolerance within a short period of time F63.

Methyl nicotinate

DB13882

small molecule approved

Deskripsi

Methyl nicotinate is the methyl ester of DB00627 that is used as an active ingredient as a rubefacient in over-the-counter topical preparations indicated for muscle and joint pain. The action of methyl nicotinate as a rubefacient is thought to involve peripheral vasodilation. For veterinary purposes, methyl nicotinate is used to treat respiratory diseases, vascular disorders, rheumatoid arthritis, and muscle and joint pains F64.

Struktur Molekul 2D

Berat 137.136
Wujud solid

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) _In vitro_, the half-life of methyl nicotinate in the dermis was 3 to 10 minutes [A33028].
Volume Distribusi According to the animal studies, nicotinic acid is mainly concentrated in the liver, kidneys, and adipose tissue [F64].
Klirens (Clearance) No pharmacokinetic data available.

Absorpsi

The presence of methyl group facilitates the penetration of methyl nicotinate through the skin with good lipophilicity, allowing rapid absorption following topical administration F64. In vitro, about 80-90% of the polar compounds methyl nicotinate rapidly penetrated the skin F64. It was demonstrated in excised skin of hairless mice that methyl nicotinate can effectively bypass the stratum corneum layer of the skin F64. In humans, nicotinic acid and nicotinamide were shown to be rapidly absorbed from the stomach and intestine via a sodium carrier-mediated mechanism at low concentrations F64.

Metabolisme

Methyl nicotinate undergoes ester hydrolysis to form nicotinic acid and methanol F64. The hydrolysis is thought to be mediated by nonspecific ?-naphthylacetate-esterase at the dermis layer of the skin A33027.

Rute Eliminasi

Following epicutaneous administration of small radiolabelled dose of methyl nicotinate in human volunteers, approximately 15% of the dose was recovered in the urine within 108 hours after treatment F63. The excretion of nicotinic acid mainly takes place in the kidneys F63.

Interaksi Obat

0 Data
Tidak ada data.

Referensi & Sumber

Artikel (PubMed)
  • PMID: 14550884
    Muller B, Kasper M, Surber C, Imanidis G: Permeation, metabolism and site of action concentration of nicotinic acid derivatives in human skin. Correlation with topical pharmacological effect. Eur J Pharm Sci. 2003 Oct;20(2):181-95.
  • PMID: 2317445
    Roskos KV, Bircher AJ, Maibach HI, Guy RH: Pharmacodynamic measurements of methyl nicotinate percutaneous absorption: the effect of aging on microcirculation. Br J Dermatol. 1990 Feb;122(2):165-71.

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