SciELO - Scientific Electronic Library Online

 
vol.56 número3SIMULTANEOUS DETERMINATION OF ENALAPRIL AND STATIN'S IN PHARMACEUTICAL FORMULATIONS BY RP-HPLCCHEMICAL STABILITY OF PREDNISONE ORAL SUSPENSION AND DRUG SUBSTANCE índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Journal of the Chilean Chemical Society

versión On-line ISSN 0717-9707

Resumen

MUNOZ, ORLANDO et al. DETERMINATION OF 10 - HYDROXY - 2 - DECENOIC ACID IN ROYAL JELLY BY CAPILLARY ELECTROPHORESIS. J. Chil. Chem. Soc. [online]. 2011, vol.56, n.3, pp. 738-740. ISSN 0717-9707.  http://dx.doi.org/10.4067/S0717-97072011000300004.

Two commercial samples of Royal Jelly sold in Chile, consisting of two imported sample and another sample of known origin obtained freshly harvested from beekeepers were analyzed. The application of capillary electrophoresis (CE) for the separation and determination of the active compound, 10 hydroxy -2 -decenoic acid, in Royal Jelly (RJ) in a capillary column with UV detection at 214 nm is described. In addition, the physicochemical composition of commercial samples was analyzed by determining moisture, ash, lipid and other properties. The importance of determining the 10-HDA acid lies in the fact that it is the main difference between Royal Jelly and the other bee products, i.e., it is what confers this product its unique characteristics, generating a marked difference. Therefore, a low 10-HDA content implies a low Royal Jelly activity, ascribed to decomposition, poor quality, or something else to the commercialization of a product other than Royal Jelly. This determination was conducted by comparison with a pure 10-HDA standard.

Palabras llave : Capillary electrophoresis; 10-hydroxy - 2 - decenoic acid; Royal Jelly.

        · texto en Inglés     · pdf en Inglés