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Substandard and falsified (SF) antimicrobials are gaining popularity in both developing and developed countries, posing a growing threat to public health. In general, the evaluation of SF antimicrobial drugs mainly focuses on the identification and quantification of the pharmaceutical active ingredients, ignoring other parameters of drug quality control. This study performed an in-depth characterization and hazard identification of suspected SF antimicrobial medicinal products encountered in Belgium. In this comprehensive evaluation, impurity tests and dissolution studies were carried out. The dissolution profiles of illegal SF antimicrobials were mathematically compared to their genuine counterparts using the f1 and f2 -factor. The results indicated that 17 out of 57 illegal samples contained higher than permitted amounts of impurities and clearly demonstrated low equivalences of dissolution profiles between SF antimicrobials and genuine products. The variations between tablets at the different time points of the dissolution curves were also higher for the SF medicines. Moreover, 11 out of 19 illegal samples failed to meet the dissolution criteria prescribed by the United States Pharmacopeia. As impurities may induce adverse reactions and improper dissolution patterns may be the cause of insufficient drug efficacy, aggravation of illness and even promotion of antimicrobial resistance can be expected. ispartof: DRUG TESTING AND ANALYSIS vol:12 issue:1 pages:53-66 ispartof: location:England status: published

Submitted by Vitor Silverio Rodrigues (vitorsrodrigues@reitoria.unesp.br) on 2014-05-27T11:25:55Z No. of bitstreams: 0Bitstream added on 2014-05-27T14:41:46Z : No. of bitstreams: 1 2-s2.0-79959529864.pdf: 404547 bytes, checksum: 3dd112d0ead1a181b75b1f2328b2f7f9 (MD5) Made available in DSpace on 2014-05-27T11:25:55Z (GMT). No. of bitstreams: 0 Previous issue date: 2011-06-28 A água é a matéria-prima mais utilizada na produção de várias formas farmacêuticas, sendo um constituinte da própria formulação e exigindo para tal uma série de especificações físico-químicas e microbiológicas. Além disso, é um insumo de utilização imprescindível para testes laboratoriais e procedimentos de limpeza de equipamentos e utensílios. O presente trabalho teve como objetivo verificar o grau de contaminação química e microbiana em água purificada utilizada em farmácias magistrais da região de São José do Rio Preto, SP. As coletas foram realizadas segundo recomendações da USP Pharmacopeia, com os devidos cuidados de assepsia, e as amostras encaminhadas imediatamente ao laboratório de controle de qualidade. Foram analisados vários parâmetros físico-químicos, tais como aspecto, pH, condutividade, resíduo por evaporação, amônia, cálcio, cloreto, metais pesados, sulfato e substâncias oxidáveis, além de parâmetros microbiológicos, como contagem total de aeróbios e pesquisa de coliformes totais e termotolerantes e Pseudomonas aeruginosa. Os resultados indicaram alguns parâmetros de não conformidade: em 10% das amostras analisadas para o pH e pesquisa de impurezas inorgânicas, em 17% para condutividade, em 14% para substâncias oxidáveis e em 20% para análise microbiológica, ressaltando a necessidade de maior rigor na produção e qualidade da água purificada produzida e/ou armazenada nesses estabelecimentos farmacêuticos. Water is the raw material used most in the production of diverse pharmaceutical forms and, being a constituent of the formulation itself, is subject to a number of physico-chemical and microbiological specifications. In addition, it is indispensable for laboratory tests and the cleaning of equipment and apparatus. The aim of this study was to ascertain the degree of physicochemical and microbiological contamination of purified water used in compounding pharmacies in the city of São José do Rio Preto, SP, Brazil. Samples were taken as recommended in the USP Pharmacopeia, with careful aseptic technique, and sent immediately the to quality control laboratory. Physicochemical properties were analyzed, including appearance, pH, conductivity, residue after evaporation, ammonia, calcium, chloride, heavy metals, sulfate and oxidizable substances, and microbiological tests were performed: total aerobic microbial count and detection of total and thermotolerant coliforms and Pseudomonas aeruginosa. Results showed that some parameters did not conform to the standards, especially pH, conductivity, inorganic impurities, oxidizable substances and microbiological test data, in 10%, 17%, 10%, 14% and 20% of the analyzed samples, respectively, This points to the need for greater care in the production and/or storage of purified water in these pharmaceutical establishments. Departamento de Fármacos e Medicamentos Faculdade de Ciências Farmacêuticas UNESP, Rodovia Araraquara-Jaú, km 1, Araraquara, SP, CEP 14801-902 Departamento de Fármacos e Medicamentos Faculdade de Ciências Farmacêuticas UNESP, Rodovia Araraquara-Jaú, km 1, Araraquara, SP, CEP 14801-902