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N Mulinacci

Publications and source records attributed to N Mulinacci.

20 records · Page 2Linked to original sources

Identification and quantification of galloyl derivatives, flavonoid glycosides and anthocyanins in leaves of Pistacia lentiscus L.

Separation, identification and quantification of polyphenols was carried out on leaves of Pistacia lentiscus L., an evergreen member of the family Anacardiaceae, using semi-preparative HPLC, HPLC-photodiode array detection and HPLC-MS analysis, together with 1H- and 13C NMR. Three major classes of secondary metabolites were detected: (i) gallic acid and galloyl derivatives of both glucose and quinic acid; (ii) flavonol glycosides, i.e. myricetin and quercetin glycosides; and (iii) anthocyanins, namely delphinidin 3-O-glucoside and cyanidin 3-O-glucoside. Low amounts of catechin were also detected. The concentration of galloyl derivatives was extremely high, representing 5.3% of the leaf dry weight, and appreciable amounts of myricetin derivatives were also detected (1.5% on a dry weight basis). These findings may be useful in establishing a relationship between the chemical composition of the leaf extract and the previously reported biological activity of P. lentiscus, and may also assign a new potential role of P. lentiscus tissue extracts in human health care.

Anthocyanins↗

Improvement of dissolution characteristics of psoralen by cyclodextrins complexation.

Psoralen was found to form an inclusion complex with beta-cyclodextrin (beta CD), heptakis(2,6-di-O-methyl)-beta-cyclodextrin (DM beta CD) and hepatakis(2,3,6-tri-O-methyl)-beta-cyclodextrin (TM beta CD). Phase solubility studies revealed the formation of a 1:1 molar complexes. The stability constant were 663 M-1 for beta CD, 603 M-1 for DM beta CD and 69.6 M-1 for TM beta CD. The formation of complexes in the solid state was confirmed by spectroscopic analyses, X-ray diffractometry and differential thermal data. The solubility and dissolution rate of the complexed forms were improved, particularly for the DM beta CD complex. The strength of binding of psoralen to DNA was not influenced by complexation with cyclodextrins.

Animals↗