maria grazia rimoli

Prof. Dr. maria grazia rimoli

Department of Pharmacy, University of Naples Federico II, Via D. Montesano 49, 80131 Naples, Italy
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Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 June 2009 in Pharmaceutical Research
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ANAlessandro Nasti
Alessandro Nasti
NZNoha M. Zaki
Noha M. Zaki
PLPiero de Leonardis
Piero de Leonardis
SUSuwipa Ungphaiboon
Suwipa Ungphaiboon
PSProramate Sansongsak
Proramate Sansongsak
NTNicola Tirelli
Nicola Tirelli

17 December 2007 in Journal of Biomedical Materials Research Part A
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MRmaria grazia rimoli
maria grazia rimoli
MRMaria R. Rabaioli
Maria R. Rabaioli
DMDaniela Melisi
Daniela Melisi
Annalisa CurcioAnnalisa Curcio
Annalisa Curcio
SMSandro Mondello
Sandro Mondello
EAEnrico Abignente
Enrico Abignente

1 September 2001 in European Journal of Pharmaceutical Sciences
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Journal Article
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FBFrancesco Paolo Bonina
Francesco Paolo Bonina
Carmelo PugliaCarmelo Puglia
Carmelo Puglia
TBTony Barbuzzi
Tony Barbuzzi
PCPaolo de Caprariis
Paolo de Caprariis
FPFrancesco Palagiano
Francesco Palagiano
Antonina SaijaAntonina Saija
Antonina Saija

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Francesco FrecenteseFrancesco Frecentese
Francesco Frecentese
Federica SodanoFederica Sodano
Federica Sodano
Angela CorvinoAngela Corvino
Angela Corvino
MSMarica Erminia Schiano
Marica Erminia Schiano
EMElisa Magli
Elisa Magli
MRmaria grazia rimoli
maria grazia rimoli
The use of alternative energy sources, such as microwaves (MW) or ultrasounds (US), and their mutual cross-combination have been widely described in the literature in the development of new synthetic methodologies in organic and medicinal chemistry. In this review, our attention is focused on representative examples, reported in the literature in the year range 2013–2023 of selected N-containing bicyclic heterocycles, with the aim to highlight the advantages of microwave- and ultrasound-assisted organic synthesis.

11 November 2005 in Journal of Medicinal Chemistry
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ENEttore Novellino
Ettore Novellino
BCBarbara Cosimelli
Barbara Cosimelli
MEMarina Ehlardo
Marina Ehlardo
GGGiovanni Greco
Giovanni Greco
MIManuela Iadanza
Manuela Iadanza
Claudia MartiniClaudia Martini
Claudia Martini

28 October 2011 in Nanoscale
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MMMaria Ada Malvindi
Maria Ada Malvindi
RCRiccardo Di Corato
Riccardo Di Corato
Annalisa CurcioAnnalisa Curcio
Annalisa Curcio
DMDaniela Melisi
Daniela Melisi
MRmaria grazia rimoli
maria grazia rimoli
Andrea RagusaAndrea Ragusa
Andrea Ragusa
The development of fluorescent biolabels for specific targeting and controlled drug release is of paramount importance in biological applications due to their potential in the generation of novel tools for simultaneous diagnosis and treatment of diseases. Dopamine is a neurotransmitter involved in several neurological diseases, such as Parkinson's disease and attention deficit hyperactivity disorder (ADHD), and the controlled delivery of its agonists already proved to have beneficial effects both in vitro and in vivo. Here, we report the synthesis and multiple functionalization of highly fluorescent CdSe/CdS quantum rods for specific biolabeling and controlled drug release. After being transferred into aqueous media, the nanocrystals were made highly biocompatible through PEG conjugation and covered by a carbohydrate shell, which allowed specific GLUT-1 recognition. Controlled attachment of dopamine through an ester bond also allowed hydrolysis by esterases, yielding a smart nanotool for specific biolabeling and controlled drug release.