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1.
Shokuhin Eiseigaku Zasshi ; 63(4): 141-150, 2022.
Artículo en Japonés | MEDLINE | ID: mdl-36047090

RESUMEN

In the pharmaceutical ingredients contamination testing of 702 commercial dietary supplement products, during fiscal years 2014-2021, 14 pharmaceutical ingredients, barrenwort, leaf axils of senna, and small leaf of senna were detected in 28 products. Screening and confirmation of the pharmaceutical ingredients in the products were performed by ultra-high performance liquid chromatography with photodiode array detector and ultra-high performance liquid chromatography-quadrupole-kingdon trap mass spectrometry, respectively. In particular, leaf axils and small leaf of senna were identified by stereomicroscopy and scanning electron microscopy. Furthermore, we found several pharmaceutical ingredients that exceeded the daily medicated dosage; therefore, it is important to prevent the distribution of such products to prevent the occurrence of health hazard. For that reason, it is necessary to continue the sample purchasing and testing systems to monitor the distribution of products containing pharmaceutical ingredients.


Asunto(s)
Suplementos Dietéticos , Contaminación de Medicamentos , Cromatografía Líquida de Alta Presión/métodos , Suplementos Dietéticos/análisis , Contaminación de Medicamentos/prevención & control , Espectrometría de Masas/métodos , Preparaciones Farmacéuticas
2.
Shokuhin Eiseigaku Zasshi ; 62(2): 65-72, 2021.
Artículo en Japonés | MEDLINE | ID: mdl-33883338

RESUMEN

This study determined the configuration of the isomers of tadalafil, nortadalafil, and homotadalafil in dietary supplements. The products purchased over the Internet studied included a honey product and a tablet, which contained tadalafil, and a candy, which contained nortadalafil and homotadalafil. Each of the pharmaceutical ingredients isolated from the products was measured with circular dichroism (CD).As a result, the CD spectrum of each isolated pharmaceutical ingredient was found to align with the standard CD spectrum of the 6R,12aR isomer, confirmed that each isolated tadalafil or tadalafil analogue included in a 6R,12aR isomer. According to a report, among the stereoisomers of tadalafil, the 6R,12aR isomers have the most potent inhibitory activities of phosphodiesterase-type-5. From the report, the potential strength of the inhibitory activity of the 6R,12aR isomers of nortadalafil and homotadalafil was suggested. Therefore, it seemed that the 6R,12aR isomer often used in the product.


Asunto(s)
Suplementos Dietéticos , Cromatografía Líquida de Alta Presión , Fosfodiesterasas de Nucleótidos Cíclicos Tipo 5 , Suplementos Dietéticos/análisis , Espectroscopía de Resonancia Magnética , Tadalafilo
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