Davanço Marcelo Gomes, Campos Michel Leandro, Rosa Talita Atanazio, Padilha Elias Carvalho, Alzate Alejandro Henao, Rolim Larissa Araújo, Rolim-Neto Pedro José, Peccinini Rosângela Gonçalves
Faculdade de Ciências Farmacêuticas, Universidade Estadual Paulista (UNESP), Campus Araraquara, Departamento de Princípios Ativos Naturais e Toxicologia, Araraquara, São Paulo, Brazil
Faculdade de Ciências Farmacêuticas, Universidade Estadual Paulista (UNESP), Campus Araraquara, Departamento de Princípios Ativos Naturais e Toxicologia, Araraquara, São Paulo, Brazil.
Antimicrob Agents Chemother. 2016 Mar 25;60(4):2492-8. doi: 10.1128/AAC.02506-15. Print 2016 Apr.
Benznidazole (BNZ) is the first-line drug for the treatment of Chagas disease. The drug is available in the form of immediate-release tablets for 100-mg (adult) and 12.5-mg (pediatric) doses. The drug is administered two or three times daily for 60 days. The high frequency of daily administrations and the long period of treatment are factors that significantly contribute to the abandonment of therapy, affecting therapeutic success. Accordingly, this study aimed to evaluate the preclinical pharmacokinetics of BNZ administered as extended-release tablets (200-mg dose) formulated with different types of polymers (hydroxypropyl methylcellulose K4M and K100M), compared to the tablets currently available. The studies were conducted with rabbits, and BNZ quantification was performed in plasma and urine by ultraperformance liquid chromatography methods previously validated. The bioavailability of BNZ was adequate in the administration of extended-release tablets; however, with the administration of the pediatric tablet, the bioavailability was lower than with other tablets, which showed that the clinical use of this formulation should be monitored. The pharmacokinetic parameters demonstrated that the extended-release tablets prolonged drug release from the pharmaceutical matrix and provided an increase in the maintenance of the drug concentrationin vivo, which would allow the frequency of administration to be reduced. Thus, a relative bioavailability study in humans will be planned for implementation of a new product for the treatment of Chagas disease.
苯硝唑(BNZ)是治疗恰加斯病的一线药物。该药物有100毫克(成人)和12.5毫克(儿童)剂量的速释片剂型。药物每日给药两到三次,持续60天。每日给药频率高和治疗周期长是导致治疗中断的重要因素,影响治疗效果。因此,本研究旨在评估与现有片剂相比,用不同类型聚合物(羟丙基甲基纤维素K4M和K100M)制成的缓释片(200毫克剂量)形式给药的BNZ的临床前药代动力学。研究在兔子身上进行,通过先前验证的超高效液相色谱法对血浆和尿液中的BNZ进行定量。BNZ在缓释片给药中的生物利用度是足够的;然而,儿童片剂给药时,生物利用度低于其他片剂,这表明该制剂的临床应用应受到监测。药代动力学参数表明,缓释片延长了药物从药物基质中的释放,并增加了体内药物浓度的维持时间,这将允许减少给药频率。因此,将计划在人体中进行相对生物利用度研究,以实施一种治疗恰加斯病的新产品。