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Dive into the research topics where Franco Francesco Vincieri is active.

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Featured researches published by Franco Francesco Vincieri.


Free Radical Research | 2004

Evaluation of Antioxidant Effect of Different Extracts of Myrtus communis L.

Annalisa Romani; Rita Coinu; Stefania Carta; Patrizia Pinelli; Carlotta Galardi; Franco Francesco Vincieri; Flavia Franconi

Oxidative stress is involved in the pathogenesis of numerous diseases. Nevertheless, no optimal natural antioxidant has been found for therapeutics, therefore polyphenol antioxidants have been looked for in myrtle leaves, a plant that in folk medicine has been used as anti-inflammatory drug. Antioxidant-rich fractions were prepared from myrtle (Myrtus communis L.) leaves liquid–liquid extraction (LLE) with different solvents. All myrtle extracts were very rich in polyphenols. In particular, hydroalcoholic extracts contain galloyl-glucosides, ellagitannins, galloyl-quinic acids and flavonol glycosides; ethylacetate extract and aqueous residues after LLE are enriched in flavonol glycosides and hydrolysable tannins (galloyl-glucosides, ellagitannins, galloyl-quinic acids), respectively. Qualitative and quantitative analysis for the single unidentified compound was also performed. Human LDL exposed to copper ions was used to evaluate the antioxidant activity of the myrtle extracts. Addition of these extracts did not affect the basal oxidation of LDL but dose-dependently decreased the oxidation induced by copper ions. Moreover, the myrtle extracts reduce the formation of conjugated dienes. The antioxidant effect of three myrtle extracts decreased in the following order: hydroalcoholic extracts, ethylacetate and aqueous residues after LLE. The extracts had the following IC50: 0.36, 2.27 and 2.88 μM, when the sum of total phenolic compounds was considered after the correction of molecular weight based on pure compounds. Statistical analysis showed a significant difference among hydroalcoholic extracts vs. the ethylacetate and aqueous residues after LLE. These results suggest that the myrtle extracts have a potent antioxidant activity mainly due to the presence of galloyl derivatives.


Life Sciences | 2002

Kava-kava and anxiety: Growing knowledge about the efficacy and safety

Anna Rita Bilia; Sandra Gallori; Franco Francesco Vincieri

Kava-kava (Piper methysticum G. Forster) has been used in social and ceremonial life in the Pacific islands from ancient times for the soporific and narcotic effects. Today several extracts standardized in the biologically active constituents kavalactones are marketed both as herbal medicinal products for anxiety disorders and as dietary supplements to improve stress disorders, nervous tension and restlessness. Unlike other substances used for these purposes, kava-kava has been shown to have minimal negative effects, and possibly positive effects, on reaction time and cognitive processing. Furthermore, it decreases anxiety without the loss of mental acuity. Although kava-kava has been found to be very effective, well tolerated, and non-addictive at therapeutic dosages, potential side effects can occur when very high doses are taken for extended periods. In addition, in the last two years unexpected high liver toxicity has been reported in two patients. Until now no studies support the liver toxicity of kavalactones and it is unknown which compound could have provoked the liver disease. On the other hand, it should be possible that unknown or unexpected constituents are the responsible or contributed to the liver toxicity.


International Journal of Pharmaceutics | 2001

Evaluation of chemical stability of St. John's wort commercial extract and some preparations

Anna Rita Bilia; Maria Camilla Bergonzi; Fabrizio Morgenni; Giovanni Mazzi; Franco Francesco Vincieri

Thermal and photostability of a commercial dried extract and capsules of St. Johns wort (Hypericum perforatum L.) were evaluated under the ICH test conditions. The extract was considered as drug substance and its preparations as drug products. In addition, capsules of different colours corresponding to different opaficient and pigment contents were also evaluated as primary package of drug product and the tests in the secondary pack were performed with amber containers, as well. A selective high-performance liquid chromatography (HPLC) for determination of stability of all the characteristic constituents, namely flavonols, hyperforins and hypericins, was carried out. Photostability testing showed all the constituents to be photosensitive in the tested conditions. However, different opaficients and pigments present in the capsules influenced the stability of the different classes of constituents. Amber containers suggested as secondary packages influenced only in part the photostability of the investigated constituents. Long-term thermal stability testing showed a very low (less than 4 months) hyperforins and hypericins t(90), even if ascorbic and citric acids were added to the formulation. From the results we have obtained it is clear that for St. Johns wort preparations, a mere translation of the ICH guidelines to the field of herbal products, as suggested by the WPHMP of the EMEA, cannot be accepted. A revision and adaptation of the storage conditions should be elaborated.


Chromatographia | 1999

Identification and Quantitation of Polyphenols in Leaves of Myrtus communis L.

Annalisa Romani; Patrizia Pinelli; Nadia Mulinacci; Franco Francesco Vincieri; Massimiliano Tattini

SummaryA liquid-solid extraction and purification procedure (LSE) was developed to identify and quantify polyphenols in the leaf tissue ofMyrtus communis L. Identification and quantitation of individual compounds was performed using HPTLC, HPLC-DAD and HPLC-MS analysis. Leaves ofMyrtus communis L. contain small amounts of phenolic acids (caffeic, ellagic and gallic acids) and quercetin derivatives (quercetin 3-O-galactoside and quercetin 3-O-rhamnoside), whereas catechin derivatives (epigallocatechin, epigallocatechin 3-O-gallate, epicatechin 3-O-gallate) and myricetin derivatives (myricetin 3-O-galactoside, myricetin 3-O-rhamnoside) are present in large amounts. This is the first report on the occurrence of galloyl-derivatives of catechin and gallo-catechin inMyrtus communis L. leaves.


Phytochemistry | 1995

Flavonol glycosides from sedum telephium subspecies Maximum leaves

Nadia Mulinacci; Franco Francesco Vincieri; Alessandro Baldi; Massimo Bambagiotti-Alberti; A. Sendl; Hildebert Wagner

Abstract Two new flavonol glycosides, kaempferol 3- O - β -neohesperidoside-7- O - α -rhamnoside and quercetin 3- O - β -neohesperidoside-7- O - α -rhamnoside were identified in the fresh leaves of Sedum telephium ssp. maximum . The known compounds, quercetin, kaempferol and their 3-glucosides, 7-rhamnosides and 3,7-dirhamnosides were also identified. All compounds were characterized by means of chemical and spectroscopic methods. NOE experiments were performed to detect the glycosidic bond at the 7-hydroxyl of the aglycone molecules.


Journal of Pharmaceutical and Biomedical Analysis | 2002

Stability of the constituents of Calendula, Milk-thistle and Passionflower tinctures by LC-DAD and LC-MS

Anna Rita Bilia; Maria Camilla Bergonzi; Sandra Gallori; Giovanni Mazzi; Franco Francesco Vincieri

As a part of our investigations on the stability of tinctures, we evaluated 40 and 60% v/v tinctures of Calendula flower, Milk-thistle fruit and Passionflower. These preparations are widely employed in phytotherapy, thus Calendula is used externally for anti-inflammatory properties, Milk-thistle and Passionflower are employed for hepatic injuries and in tenseness with difficulty in falling asleep, respectively. Aim of this work was to assess the chemical stability of their active or marker constituents from accelerated and long-term testing by using HPLC. For Calendula flower and Passionflower active constituents are not known, however, flavonoids seem to have a crucial importance for the activity, and thus are considered the markers of Calendula and of Passionflower. Active constituents of Milk-thistle are represented by silymarin that is a phytocomplex mainly constituted by three flavolignans: silybin, silychristin and silydianin. Our investigation showed a very low thermal stability of the constituents from accelerated and long-term testing and determined by HPLC-DAD and -MS analyses and was related both to the class of flavonoids and water content of the investigated tinctures. Thus, shelf-lives at 25 degrees C of the most stable tincture (Passionflower 60% v/v) was about 6 months and only about 3 months the stability of Milk-thistle tinctures.


Food Chemistry | 2003

Minor polar compound and fatty acid analyses in monocultivar virgin olive oils from Tuscany

Patrizia Pinelli; Carlotta Galardi; Nadia Mulinacci; Franco Francesco Vincieri; Antonio Cimato; Annalisa Romani

Virgin olive oil is a typical component of the Mediterranean diet, consumed unrefined and rich in important molecules, such as minor polar compounds (hydroxytyrosol, tyrosol, secoiridoids and flavonoids) and fatty acids. These molecules not only influence the sensorial properties of both olives and virgin oil but they are also important markers for typicity, biodiversity and quality determination of this product. The aim of this study was to evaluate the minor polar compound and fatty acid contents of 10 monocultivar virgin olive oils, typical of Tuscany, in order to have better knowledge about the quali-quantitative profiles of these compounds in samples obtained from both the same collecting season and same processing technique. Quali-quantitative analysis (performed by HPLC/DAD, HPLC/MS and GC) could be a useful tool to better correlate the typicity of the virgin olive oil with its minor polar compound and fatty acid pattern. Further studies are in progress to isolate the unknown compounds and to further investigate the quality index of this food product.


Drug Development and Industrial Pharmacy | 2001

Variability in the content of the constituents of Hypericum perforatum L. and some commercial extracts

Maria Camilla Bergonzi; Anna Rita Bilia; Sandra Gallori; D. Guerrini; Franco Francesco Vincieri

Seven samples of Hypericum perforatum L. (St. Johns wort) were collected throughout Tuscany; the dried extracts were assayed to determine the concentration of the constituents. Total flavonol content ranged from 4.58% to 15.90%; hypericins ranged from 0.05% to 0.11%; and hyperforins ranged from 1.37% to 20.80%. In addition, four commercially dried extracts were analyzed using the same high-performance liquid chromatographic (HPLC) method; their flavonol contents varied from 10.64% to 15.01%, hypericins varied from 0.03% to 0.20%, and hyperforins varied from 1.18% to 6.54%. The aim of this investigation was to evaluate the contents of the different constituents depending on environmental factors and drying and storage conditions of the wild samples. In addition, the contents of the constituents of the products available to the consumer that were related to quality and the relation of this to safety and efficacy were also evaluated.


Planta Medica | 2009

Oral Metabolism and Efficacy of Kalanchoe pinnata Flavonoids in a Murine Model of Cutaneous Leishmaniasis

Michelle Frazão Muzitano; Camila Alves Bandeira Falcão; Elaine A. Cruz; Maria Camilla Bergonzi; Anna Rita Bilia; Franco Francesco Vincieri; Bartira Rossi-Bergmann; Sônia Soares Costa

Leishmaniasis is a parasitic disease that threatens 350 million people worldwide. In a search for new antileishmanial drugs, the in vitro activity of flavonoids from Kalanchoe pinnata (Crassulaceae) was previously demonstrated in infected cells. In order to demonstrate the safety and oral activity of K. pinnata, flavonoids were evaluated in vivo in a murine model of cutaneous leishmaniasis. Daily oral doses of quercetin 3-O-alpha-L-arabinopyranosyl (1-->2)-alpha-L-rhamnopyranoside, quercetin 3-O-alpha-L-rhamnopyranoside, and free quercetin (16 mg/kg body weight) all were able to control the lesion growth caused by Leishmania amazonensis and to significantly reduce parasite load. These flavonoids were as effective as the crude K. pinnata aqueous extract given at 320 mg/kg body weight. HPLC-DAD-MS analysis of the plasma of extract-treated mice suggested that quercetin and quercetin glucuronides are the main metabolites of K. pinnata quercetin glycosides. Our results indicate that K. pinnata quercetin glycosides are important active components of the aqueous extract and that they possess potent oral efficacy against cutaneous leishmaniasis.


Talanta | 2005

An optical DNA-based biosensor for the analysis of bioactive constituents with application in drug and herbal drug screening

Maria Minunni; Sara Tombelli; Marco Mascini; Anna Rita Bilia; M.Camilla Bergonzi; Franco Francesco Vincieri

The efficient and rapid detection of bioactive compounds in complex matrices of different origins (natural or synthetic) is a key step in the discovery of molecules with potential application in therapy. Among them, molecules able to interact with nucleic acids can represent important targets. In this study, an optical DNA biosensor, based on surface plasmon resonance (SPR) transduction, has been studied in its potential application as new analytical device for drug screening. This device was applied to the analysis of pure synthetic or natural molecules and also to some fractions obtained by chromatographic separation of an extract of Chelidonium majus L. (great celandine), a plant containing benzo[c]phenanthridinium alkaloids having intercalating properties. The ability of these molecules to interact with the double stranded nucleic acid (dsDNA) immobilised on the sensor surface has been investigated. The optical sensing relies on the SPR-based bench instrument Biacore Xtrade mark and represents an example of multiuse sensor. The results obtained demonstrate the potential application of this device for the rapid screening of bioeffective compounds. The characteristics of the biosensor offer the possibility to be coupled to chemical analysis as in hyphenated technologies.

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