Albendazole

Synonymes : Albendazole, 54965-21-8, Methyl 5-(propylthio)-2-benzimidazolecarbamate, Albendazolum, Zentel, Albenza, Eskazole

Albendazole is a synthetic benzimidazole derivative that acts as a broad-spectrum anthelmintic. Its molecular structure features a benzimidazole core with a propylthio side chain and a methyl carbamate group, which is essential for its interaction with β-tubulin. By binding to β-tubulin, albendazole inhibits microtubule polymerization, disrupting the cytoskeleton and leading to impaired glucose uptake and eventual parasite death. This mechanism is effective against a wide range of nematodes, cestodes, and trematodes.

Originally developed for veterinary use, albendazole has become a cornerstone in human medicine for treating soil-transmitted helminthiases, neurocysticercosis, and hydatid disease. It is included in the WHO Model List of Essential Medicines. The compound is poorly water-soluble, which poses formulation challenges; thus, various strategies such as micronization, solid dispersions, and lipid-based delivery systems are employed to enhance its bioavailability.

In pharmaceutical manufacturing, albendazole is typically produced in polymorphic forms, with Form I and Form II being the most common. The choice of polymorph can influence dissolution rate and, consequently, therapeutic efficacy. Our albendazole is manufactured under cGMP conditions and meets or exceeds the requirements of the current European Pharmacopoeia and United States Pharmacopeia. It is available with a purity of ≥98% (HPLC), ensuring consistent quality for both human and veterinary drug production.

Structure chimique et propriétés

Albendazole belongs to the benzimidazole class, characterized by a bicyclic system fused with an imidazole ring. The presence of the propylthio group enhances its lipophilicity, while the carbamate moiety contributes to its anthelmintic activity. The compound exists as a white to off-white crystalline powder, with a melting point range of 208–210°C (decomposition). It is practically insoluble in water but shows good solubility in aprotic polar solvents like dimethyl sulfoxide and dimethylformamide. Its logP value is approximately 3.5, indicating moderate lipophilicity, which facilitates membrane permeability in target organisms.

Mécanisme d'action

• β-Tubulin binding: Albendazole selectively binds to parasite β-tubulin, inhibiting microtubule assembly and causing structural disorganization within cells.
• Glucose uptake inhibition: Disruption of microtubules leads to decreased glucose absorption, depleting energy reserves in helminths.
• Immobilization and death: The combined effects result in paralysis and eventual death of susceptible parasites.
• Ovicidal activity: Albendazole also exhibits ovicidal effects by preventing embryonation of eggs.

Spécifications de qualité

Approvisionnement et documentation

• Capacité: 50 metric tons per year
• Délai de livraison: 3 à 5 jours ouvrés (articles en stock)
• Documentation: Certificat d'analyse (COA), fiche de données de sécurité (FDS) et fiche technique (TDS) disponibles sur demande
• Emballage: 25 kg fiber drum with double polyethylene liner, or as per customer requirements

Demande de devis

• LyvBio Co. — E-mail : info@lyvbio.com