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Métodos Terapéuticos y Terapias MTCI
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1.
Med Princ Pract ; 28(2): 167-177, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30517949

RESUMEN

OBJECTIVES: Nutraceuticals are advertised and sold with the label claim of being natural and safe herbal products. Due to the absence of clear regulations and guidelines for safety assessments of these products, nutraceuticals are commonly adulterated in order to increase sales. The objective of the current study was to design a comprehensive evaluation system to assess the safety, efficacy, authenticity according to label claim, and pharmaceutical quality of herbal slimming products in between 2015 and 2017. METHODS: We designed a comprehensive assessment system to evaluate the safety, authenticity according to label claim, and pharmaceutical quality of slimming nutraceuticals. Six different popular products were evaluated (Zotreem Plus®, Zotreem Extra®, Malaysian Super Slim®, AB Slim®, Chinese Super Slim®, and Metabolites®). The pharmaceutical evaluation included analyzing the samples via high-performance liquid chromatography to determine any possible adulterants. Additionally, the products' physical properties were assessed via pharmacopeial tests. Finally, a microbial evaluation and a cross-sectional observational retrospective prevalence study were conducted to assess the products' safety and efficacy. -Results: The tested products were found to be adulterated with unreported active pharmaceutical ingredients such as sibutramine, sildenafil, phenolphthalein, and orlistat. Furthermore, they contained heterogeneous amounts of adulterants and exhibited an unsatisfactory pharmaceutical and microbial quality. Finally, the observational survey conducted on users showed that high percentages of participants suffered from common side effects such as depression, diarrhea, and hypertension. CONCLUSIONS: These products threaten the health of consumers. There is a need to raise awareness of the lethal consequences of illegal nutraceuticals.


Asunto(s)
Fármacos Antiobesidad/análisis , Depresores del Apetito/análisis , Suplementos Dietéticos/análisis , Medicamentos Herbarios Chinos/análisis , Medicamentos sin Prescripción/análisis , Fármacos Antiobesidad/efectos adversos , Depresores del Apetito/efectos adversos , Estudios Transversales , Suplementos Dietéticos/efectos adversos , Medicamentos Herbarios Chinos/efectos adversos , Egipto , Humanos , Medicamentos sin Prescripción/efectos adversos , Pérdida de Peso
2.
Microb Drug Resist ; 23(1): 8-17, 2017 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-27228193

RESUMEN

Methicillin resistance among staphylococci isolated from patients in northern Egypt has escalated alarmingly in the past decade. Data about the prevalence of fusidic acid (FA) resistance in Egyptian clinical isolates are limited. This work investigates the prevalence and mechanism of FA resistance among 81 methicillin-resistant staphylococcal isolates from major hospitals of Alexandria, Egypt. Some combinations for treating infections due to resistant isolates were studied. Twenty-six isolates (32.1%) were FA resistant (minimum inhibitory concentrations [MICs] = 2-1,024 µg/ml), and fusB and fusC genes coding for FA resistance were detected in 30.77% and 34.62% of the FA-resistant strains, respectively. One highly resistant isolate, S502 (MIC = 1,024 µg/ml), possessed both genes. Plasmid curing resulted in fusB loss and MIC decrease by 16-64 folds. Conjugation caused acquisition of FA resistance among susceptible isolates. Serial passages in subinhibitory FA concentrations produced mutants with increased MIC by 4-32 folds. The combination of FA with rifampin, gentamicin, or ampicillin/sulbactam, in a subinhibitory concentration, was synergistic against the isolates, including serial passage mutants, decreasing number of survivors by an average of 2-4 logs. A relatively moderate rate of FA resistance was detected in Alexandria hospitals. Combination therapy with gentamicin, rifampin, or ampicillin/sulbactam is crucial to preserve the effectiveness of FA.


Asunto(s)
Antibacterianos/farmacología , Proteínas Bacterianas/genética , Ácido Fusídico/farmacología , Regulación Bacteriana de la Expresión Génica , Resistencia a la Meticilina/genética , Staphylococcus aureus Resistente a Meticilina/efectos de los fármacos , Meticilina/farmacología , Ampicilina/farmacología , Proteínas Bacterianas/metabolismo , Conjugación Genética , Combinación de Medicamentos , Farmacorresistencia Bacteriana Múltiple/genética , Sinergismo Farmacológico , Egipto/epidemiología , Gentamicinas/farmacología , Humanos , Staphylococcus aureus Resistente a Meticilina/genética , Staphylococcus aureus Resistente a Meticilina/crecimiento & desarrollo , Staphylococcus aureus Resistente a Meticilina/metabolismo , Pruebas de Sensibilidad Microbiana , Plásmidos/química , Plásmidos/metabolismo , Rifampin/farmacología , Infecciones Estafilocócicas/tratamiento farmacológico , Infecciones Estafilocócicas/epidemiología , Infecciones Estafilocócicas/microbiología , Sulbactam/farmacología
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