Validating a stability indicating HPLC method for kinetic study of cetirizine degradation in acidic and oxidative conditions

A stability indicating High-Performance Liquid Chromatography [HPLC] method was validated and used to study the degradation of cetirizine dihydrochloride in acidic and oxidative conditions. The separation was carried out on a Symmetry C18 column and a mixture of 50 mM KH[2]PO[4] and acetonitrile [60:40 v/v, pH = 3.5] was used as the mobile phase. The method was linear over the range of 1-20 micro g/mL of cetirizine dihydrochloride [r[2] > 0.999] and the within-day and between-day precision values were less than 1.5%. The results showed that cetirizine dihydrochloride was unstable in 2 M HCl and 0.5% H[2]O[2]. The kinetics of the acidic degradation showed a pseudo-first-order reaction in the temperature range of 70-90[degree sign]C. In addition, the kinetics of hydrogen peroxide mediated degradation was pseudo-first-order in the temperature range of 50-80[degree sign]C

comparative study of different brands of cetirizine hydrochloride tablets available in Karachi, Pakistan

The development of a formulation requires expertise during each manufacturing stage. Tablets are the most commonly used oral, solid dosage forms in which various excipients are used and various methods are employed for their preparation. Quality of tablets should fulfill certain specifications. If the formulations are not manufactured properly and are not optimized, they will not render the desired effects. This study shows the analysis and evaluation of various pharmaceutical parameters, i.e. thickness, hardness, weight variation, disintegration and dissolution, on different brands of cetirizine hydrochloride tablets available in the local market. Cetirizine hydrochloride is an orally administered drug used as anti-histaminic with almost no sedation. The analysis done can conveniently give a general survey of different brands of cetirizine hydrochloride tablets where the difference in parameters tested can relate to difference in the bioavailability of drugs

Comparative efficacy of wheal-and-flare suppression among various non-sedating antihistamines and the pharmacologic insights to their efficacy.

BACKGROUND AND OBJECTIVE: Non-sedating antihistamines (loratadine, fexofenadine, and cetirizine) have been widely used in Thailand. This study examined the time-of-onset and compared the 95% inhibitory effect of these agents on histamine-induced cutaneous reaction so as to understand the diversity of their efficacy. PATIENTS AND METHOD: Thirty-one atopic patients were randomized into 4 treatment groups, placebo (n = 7), loratadine (n = 8), fexofenadine (n = 8), and cetirizine (n = 8). They were pricked with histamine every 30 min for 4 hrs. The percentage change of the wheal/flare area was calculated. RESULTS: All active treatments showed wheal suppression superior to placebo after 210 min for loratadine (P = 0.04); 90 min for fexofenadine (P = 0.009); and 60 min for cetirizine (P = 0.02), while flare suppression was significantly marked after 150 min (P = 0.0008) for loratadine; 90 min for fexofenadine (P = 0.0001), and 60 min for cetirizine (P = 0.006). All drugs except loratadine demonstrated a 95% suppression of wheal superior to the placebo (P = 0.001 for fexofenadine; P = 0.0001 for cetirizine). Only fexofenadine exhibited a 95% suppression of flare statistically superior to placebo (P = 0.02). Discrepancies among the effects of these 3 antihistamines were also detected. DISCUSSION AND CONCLUSION: All antihistamines tested repressed the wheal-and-flare area superbly over the placebo within 4 hours. Cetirizine exerted the fastest onset, and it also appeared to be the most efficacious inhibitor. The heterogeneity of their efficacy probably stems from their diverse physicochemical properties, which have also been discussed.

Estado actual de antihistamínicos / Current state of antihistamine drugs

El aumento de la prevalencia mundial de las patologías respiratorias alérgicas conlleva un aumento simultáneo en la prescripción de antihistamínicos orales. Los efectos adversos que dichos medicamentos provocan en el sistema nervioso central son muy frecuentes(1), por lo que se presenta una revisión actualizada de los antihistamínicos sistémicos bajo el clásico adagio de la Medicina: "Primum non nocere" ("antes que nada no dañar"). En esta revisión se describe las generalidades de la acción de la histamina en el organismo. Los efectos terapéuticos y secundarios de los antihistamínicos de primera y segunda generación y finalmente se presenta una descripción acabada del nuevo antialérgico epinastina