Paola Maria Manconi
University of Sassari
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Featured researches published by Paola Maria Manconi.
International Journal of Nanomedicine | 2014
Vanna Sanna; Nicolino Pala; Giuseppina Dessì; Paola Maria Manconi; Alberto Mariani; Sonia Dedola; Mauro Rassu; Claudia Crosio; Ciro Iaccarino; Mario Sechi
Background Gold nanoparticles (GNPs) are likely to provide an attractive platform for combining a variety of biophysicochemical properties into a unified nanodevice with great therapeutic potential. In this study we investigated the capabilities of three different natural polyphenols, epigallocatechin-3-gallate (EGCG), resveratrol (RSV), and fisetin (FS), to allow synergistic chemical reduction of gold salts to GNPs and stabilization in a single-step green process. Moreover, antioxidant properties of the nanosystems, as well as preliminary antiproliferative activity and apoptotic process investigation of model EGCG-GNPs on stable clones of neuroblastoma SH-SY5Y cells expressing CFP-DEVD-YFP reporter, were examined. Methods The GNPs were characterized by physicochemical techniques, polyphenol content, and in vitro stability. The antioxidant activity of the GNPs was also determined by 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) cation (ABTS) radical-scavenging assays. Stable clones of neuronal SH-SY5Y-CFP-DEVD-YFP were generated and characterized, and cell viability after treatment with EGCG-GNPs was assessed after 72 hours through a 3(4,5-dimethylthiazol-2yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium assay. Activation of the apoptotic pathways was also investigated by Western blot analysis. Results With a diameter in the size range of 10–25 nm, the obtained nanoparticles (NPs) were found to contain 2.71%, 3.23%, and 5.47% of EGCG, RSV, and FS, respectively. Nanoprototypes exhibited remarkable in vitro stability in various media, suggesting that NP surface coating with phytochemicals prevents aggregation in different simulated physiological conditions. The scavenging activities for DPPH and ABTS were highly correlated with EGCG, RSV, and FS content. Moreover, high correlation coefficients between the ABTS and DPPH values were found for the prepared nanosystems. EGCG-GNPs induce a dose-dependent reduction on SH-SY5Y-CFP-DEVD-YFP cell viability that is likely to involve the activation of the apoptotic pathways, similarly to free EGCG, as suggested by the processing of the CFP-DEVD-YFP reporter. Conclusion These results prompted us to propose the ecofriendly synthesized EGCG-, RSV-, and FS-based nanogold conjugates as suitable carriers for bioactive polyphenols to be used for the treatment of disorders associated with oxidative stress, including neurodegenerative disorders, cardiovascular disease, and cancer.
Contact Dermatitis | 1991
P. Ena; Riccardo Cerri; Giuseppina Dessì; Paola Maria Manconi; A. D. Atzei
After classification and identification of the plant, the alcoholic extract of Cachrys libanotis L. was analysed in order to identify the phototoxic agents. The substances responsible for photodermatitis were found to be 4 furocoumarins, of which 3 have been clearly identified, namely 5‐methoxy‐, 8‐methoxy‐and 5,8‐dmiethoxypsoralen. The structure of a 4th compound was not completely defined.
Phytomedicine | 2014
Giovanna Rassu; Maria Nieddu; Paolo Bosi; P. Trevisi; M. Colombo; D. Priori; Paola Maria Manconi; Paolo Giunchedi; Elisabetta Gavini; Gianpiero Boatto
The aim of this study was to encapsulate, thymol, in natural polymers in order to obtain (i) taste masking effect and, then, enhancing its palatability and (ii) two formulations for systemic and local delivery of herbal drug as adjuvants or substitutes to current medications to prevent and treat several human and animal diseases. Microspheres based on methylcellulose or hydroxypropyl methylcellulose phthalate (HPMCP) were prepared by spray drying technique. Microparticles were in vitro characterized in terms of yield of production, drug content and encapsulation efficiency, particle size, morphology and drug release. Both formulations were in vivo orally administered and pharmacokinetic analysis was carried out. The polymers used affect the release and, then, the pharmacokinetic profile of thymol. Encapsulation into methylcellulose microspheres leads to short half/life but bioavailability remarkably increases compared to the free thymol. In contrast, enteric formulation based on HPMCP shows very limited systemic absorption. These formulations could be proposed as alternative or adjuvants for controlling pathogen infections in human or animal. In particular, methylcellulose microspheres can be used for thymol systemic administration at low doses and HPMCP particles for local treatment of intestinal infections.
Natural Product Research | 2016
Claudia Clelia Assunta Juliano; Paola Maria Manconi; Massimo Cossu
Abstract Perna canaliculus is a nutritional supplement recently studied and highly recommended for its anti-inflammatory effects in both animals and humans. In this study, the physicochemical properties, the microbiological quality, the total lipid content and fatty acids composition of three commercial samples of Perna powder were determined. Subsequently, three simple formulations of extemporaneous oral pastes containing Perna were prepared and designed for veterinary use. Their microbiological stability was assessed after 1-month storage at either room temperature or 35 °C. The results demonstrated that commercial Perna samples lack homogeneity, in regard to some technological properties and fatty acid composition; therefore, a preliminary characterisation of commercial Perna samples is recommended to assure the quality of formulations containing this nutritional supplement. Oral paste formulations are easy and simple to prepare and show good physical and microbiological stability, suggesting their large-scale production. Graphical abstract
Journal of Chromatography A | 2007
Gianpiero Boatto; Maria Nieddu; Giuseppina Dessì; Paola Maria Manconi; Riccardo Cerri
Forensic Science International | 2004
Gianpiero Boatto; Maria Nieddu; Antonio Carta; Amedeo Pau; Salvatore Lorenzoni; Paola Maria Manconi; Domenico Serra
Pharmazie | 2000
Luciana Auzzas; Michele Francesco Luigi Palomba; Gianpiero Boatto; Paola Maria Manconi; Amedeo Pau; A. Becciu; Riccardo Cerri; Vivian Tullio; Janira Roana; Nicola Carlone
SARDINIACHEM2008. Giornata di studio dedicata alla chimica organica delle molecole biologicamente at | 2008
Giorgio Antonio Mario Pintore; Mario Chessa; Andrea Piana; Maria Dolores Masia; Stefania Pischedda; G. Piras; Paola Maria Manconi; N. Scanu
Archive | 2008
Mario Chessa; Paola Maria Manconi; Barbara Sechi; Mauro Marchetti; Paola Molicotti; Giorgio Antonio Mario Pintore
Archive | 2004
Fabrizio Carta; Luciano Sannia; Massimiliano Derudas; Paola Maria Manconi; Michele Francesco Luigi Palomba; Mario Sechi; Roberto Dallocchio; Alessandro Dessì; Tino Sanchez; Nouri Neamati