New Spectrophotometric Methods for Determination of Albendazole in Presence of Cerium as Oxidant and Both Indigo Carmine and Alizarin Red Dyes in Bulk and Dosage Forms

Albendazole (ABZ), chemically known as methyl5-(propylthio)-2-benzimidazole carbamate [1] (Fig. 1), is widely used as an anthelmintic with a broad spectrum of activity [2]. ABZ is an inactive moiety but it readily gets metabolized to an active metabolite, albendazole sulfoxide (ABZSO) which is then further metabolized to an inactive metabolite, albendazole sulfone (ABZSO2) [3]. As ABZ is metabolized extensively, therefore, the plasma concentration of ABZ is also very low, as a result, the pharmacokinetic studies were done using ABZSO as an active metabolite and ABZSO2 as an inactive metabolite [4-8]. As such, the therapeutic importance of this compound justifies research to develop analytical methods for its determination in bulk form, pharmaceutical formulations and in biological samples. Several techniques can be found in the literature for monitoring ABZ therapy such as UV-vis spectrophotometry [9-12], spectroflourimetry [13], HPLC [14], HPTLC [15], LC/MS [16], capillary electrophoresis [17] and voltammetry [18].

[1]  P. Shrivastav,et al.  Simultaneous densitometric determination of anthelmintic drug albendazole and its metabolite albendazole sulfoxide by HPTLC in human plasma and pharmaceutical formulations. , 2017, Biomedical chromatography : BMC.

[2]  Mohamed S. Emara,et al.  Determination of Albendazole in the Presence of its Alkaline Degradation Product Using TLC-Densitometric and Chemometric Methods: A Comparative Study , 2017 .

[3]  Mohamed S. Emara,et al.  Application of a quinone-based fluorophore for spectrofluorimetric determination of albendazole in pure form and pharmaceutical formulations , 2016 .

[4]  Joachim Müller,et al.  Treatment of echinococcosis: albendazole and mebendazole – what else? , 2014, Parasite.

[5]  K. Basavaiah,et al.  Simple and rapid spectrophotometric assay of albendazole in pharmaceuticals using iodine and picric acid as CT complexing agents , 2014 .

[6]  R. Rocha‐Filho,et al.  Differential pulse voltammetric determination of albendazole in pharmaceutical tablets using a cathodically pretreated boron-doped diamond electrode , 2013 .

[7]  K. Basavaiah,et al.  Use of Two Sulfonphthalein Dyes for the Sensitive and Selective Extraction-Free Spectrophotometric Assay of Albendazole in Bulk Drug and in Tablets , 2013 .

[8]  A. Fathi,et al.  Spectrophotometric Determination of Albendazole Drug in Tablets: Spectroscopic Characterization of the Charge‐transfer Solid Complexes , 2011 .

[9]  Xiaoyan Chen,et al.  Simultaneous determination of albendazole and its major active metabolite in human plasma using a sensitive and specific liquid chromatographic-tandem mass spectrometric method. , 2004, Journal of pharmaceutical and biomedical analysis.

[10]  K. Pengsaa,et al.  Pharmacokinetic investigation of albendazole and praziquantel in Thai children infected with Giardia intestinalis , 2004, Annals of tropical medicine and parasitology.

[11]  A. Goudah Aspects of the Pharmacokinetics of Albendazole Sulphoxide in Sheep , 2003, Veterinary Research Communications.

[12]  L. Fleckenstein,et al.  HPLC assay for albendazole and metabolites in human plasma for clinical pharmacokinetic studies. , 2002, Journal of pharmaceutical and biomedical analysis.

[13]  P. S. Bonato,et al.  Enantioselective distribution of albendazole metabolites in cerebrospinal fluid of patients with neurocysticercosis. , 2002, British journal of clinical pharmacology.

[14]  E. Formentini,et al.  Pharmacokinetics of ricobendazole in calves. , 2001, Journal of veterinary pharmacology and therapeutics.

[15]  W. Thormann,et al.  Therapeutic drug monitoring of albendazole: Determination of albendazole, albendazole sulfoxide, and albendazole sulfone in human plasma using nonaqueous capillary electrophoresis , 2000, Electrophoresis.

[16]  J. Prieto,et al.  Small intestinal sulphoxidation of albendazole. , 1995, Xenobiotica; the fate of foreign compounds in biological systems.

[17]  V. E. Bower,et al.  pH values of the Clark and Lubs buffer solutions at 25 C , 1955 .

[18]  M. Raghunath,et al.  BENZIMIDAZOLE-2-CARBAMIC ACID AS A PRIVILEGED SCAFFOLD FOR ANTIFUNGAL, ANTHELMINTIC AND ANTITUMOR ACTIVITY A REVIEW , 2014 .

[19]  V. Lanchote,et al.  Enantioselective renal excretion of albendazole metabolites in patients with neurocysticercosis. , 2004, Chirality.

[20]  Julius Ju Lurje,et al.  Handbook of analytical chemistry , 1975 .

[21]  H. L. Riley Hydrogen Ions , 1942, Nature.