Amparo Nacher

Prof. Amparo Nacher

orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

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

Representative Publications

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1 December 2015 in Biomaterials
Verified
Journal Article
Closed access
Maria Letizia MancaMaria Letizia Manca
Maria Letizia Manca
ICI. Castangia
I. Castangia
MZM. Zaru
M. Zaru
ANAmparo Nacher
Amparo Nacher
DVD. Valenti
D. Valenti
Maria ManconiMaria Manconi
Maria Manconi

1 November 2016 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
CCCarla Caddeo
Carla Caddeo
ANAmparo Nacher
Amparo Nacher
AVAntonio Vassallo
Antonio Vassallo
Maria Francesca ArmentanoMaria Francesca Armentano
Maria Francesca Armentano
RPRamon Pons
Ramon Pons
MMMaria Manconi
Maria Manconi

1 March 2014 in Acta Biomaterialia
Verified
Journal Article
Closed access
ICInes Castangia
Ines Castangia
ANAmparo Nacher
Amparo Nacher
CCCarla Caddeo
Carla Caddeo
DVDonatella Valenti
Donatella Valenti
Anna Maria FaddaAnna Maria Fadda
Anna Maria Fadda
Maria ManconiMaria Manconi
Maria Manconi

Verified
Journal Article
Open access
RTRaquel Taléns-Visconti
Raquel Taléns-Visconti
ODOctavio Díez-Sales
Octavio Díez-Sales
Jesus Vicente de Julián-OrtizJesus Vicente de Julián-Ortiz
Jesus Vicente de Julián-Ortiz
ANAmparo Nacher
Amparo Nacher
The drugs used for cancer treatment have many drawbacks, as they damage both tumor and healthy cells and, in addition, they tend to be poorly soluble drugs. Their transport in nanoparticles can solve these problems as these can release the drug into tumor tissues, as well as improve their solubility, bioavailability, and efficacy, reducing their adverse effects. This article focuses on the advantages that nanotechnology can bring to medicine, with special emphasis on nanoliposomes. For this, a review has been made of the nanoliposomal systems marketed for the treatment of cancer, as well as those that are in the research phase, highlighting the clinical trials being carried out. All marketed liposomes studied are intravenously administered, showing a reduced intensity of side-effects compared with the nonliposomal form. Doxorubicin is the active ingredient most frequently employed. Ongoing clinical trials expand the availability of liposomal medicines with new clinical indications. In conclusion, the introduction of drugs in nanoliposomes means an improvement in their efficacy and the quality of life of patients. The future focus of research could be directed to develop multifunctional targeted nanoliposomes using new anticancer drugs, different types of existing drugs, or new standardized methodologies easily translated into industrial scale.

1 June 2018 in European Journal of Pharmaceutics and Biopharmaceutics
Verified
Journal Article
Closed access
MMMaria Manconi
Maria Manconi
Maria Letizia MancaMaria Letizia Manca
Maria Letizia Manca
CCCarla Caddeo
Carla Caddeo
CCClaudia Cencetti
Claudia Cencetti
CMChiara Di Meo
Chiara Di Meo
Pietro MatricardiPietro Matricardi
Pietro Matricardi

1 September 2016 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
Maria Letizia MancaMaria Letizia Manca
Maria Letizia Manca
CCClaudia Cencetti
Claudia Cencetti
Pietro MatricardiPietro Matricardi
Pietro Matricardi
ICInes Castangia
Ines Castangia
MZMarco Zaru
Marco Zaru
MMMaria Manconi
Maria Manconi