Alejandro Baeza

Dr. Alejandro Baeza

Materials and Aeroespatial Production Department, Polymer Materials Research Group, Madrid, 28040, Spain
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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20 January 2011 in ACS Nano
Verified
Journal Article
Closed access
EREduardo Ruiz-Hernández
Eduardo Ruiz-Hernández
Alejandro BaezaAlejandro Baeza
Alejandro Baeza
MVMaría Vallet-Regí
María Vallet-Regí

11 January 2012 in Chemistry of Materials
Verified
Journal Article
Closed access
Alejandro BaezaAlejandro Baeza
Alejandro Baeza
EGEduardo Guisasola
Eduardo Guisasola
EREduardo Ruiz-Hernández
Eduardo Ruiz-Hernández
MVMaría Vallet-Regí
María Vallet-Regí

25 October 2014 in Expert Opinion on Drug Delivery
Verified
Journal Article
Closed access
Alejandro BaezaAlejandro Baeza
Alejandro Baeza
Montserrat ColillaMontserrat Colilla
Montserrat Colilla
María Vallet-RegíMaría Vallet-Regí
María Vallet-Regí
Mesoporous silica nanoparticles (MSNPs) are one of the most promising inorganic drug delivery systems (DDSs). The design and development of tumour-targeted MSNPs with stimuli-responsive drug release capability aim at enhancing the efficiency and minimising the side effects of anti-tumour drugs for cancer therapy. This review provides an overview of the scientific advances in MSNPs for tumour-targeted stimuli-responsive drug delivery. The key factors that govern the passive accumulation of MSNPs within solid tumours such as size, shape and surface functionalisation are roughly described. The different active targeting strategies for the specific retention and uptake of MSNPs by tumour cells are also outlined. The approaches developed so far for the synthesis of smart MSNPs capable of releasing the trapped drugs in response to internal or external stimuli and their applications are reviewed. Critical considerations in the use of MSNPs for the treatment of cancer treatment are discussed. The future prospects and key factors concerning the clinical application of MSNPs are considered throughout the manuscript. MSNPs are promising nanocarriers to efficiently transport and site-specifically deliver highly toxic drugs, such as chemotherapeutic agents for cancer treatment. However, there are certain issues that should be overcome to improve the suitability of MSNPs for clinical applications. Increasing the penetration capability of MSNPs within tumour tissues, providing them of appropriate colloidal stability in physiological fluids and ensuring that their active targeting capability and stimuli-responsive performance are preserved in complex biological media are of foremost significance. Few in vivo evaluation tests of MSNPs have been reported and much research effort into this field is mandatory to be able to move from bench to bedside.

9 September 2016 in Expert Opinion on Drug Delivery
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Journal Article
Closed access
Alejandro BaezaAlejandro Baeza
Alejandro Baeza
DRDaniel Ruiz-Molina
Daniel Ruiz-Molina
MVMaría Vallet-Regí
María Vallet-Regí
Introduction: Nanotechnology has provided new tools for addressing unmet clinical situations, especially in the oncology field. The development of smart nanocarriers able to deliver chemotherapeutic agents specifically to the diseased cells and to release them in a controlled way has offered a paramount advantage over conventional therapy. Areas covered: Among the different types of nanoparticle that can be employed for this purpose, inorganic porous materials have received significant attention in the last decade due to their unique properties such as high loading capacity, chemical and physical robustness, low toxicity and easy and cheap production in the laboratory. This review discuss the recent advances performed in the application of porous inorganic and metal-organic materials for antitumoral therapy, paying special attention to the application of mesoporous silica, porous silicon and metal-organic nanoparticles. Expert opinion: The use of porous inorganic nanoparticles as drug carriers for cancer therapy has the potential to improve the life expectancy of the patients affected by this disease. However, much work is needed to overcome their drawbacks, which are aggravated by their hard nature, exploiting the advantages offered by highly the ordered pore network of these materials.

17 June 2009 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
BWBarbara Weiner
Barbara Weiner
Alejandro BaezaAlejandro Baeza
Alejandro Baeza
TJThomas Jerphagnon
Thomas Jerphagnon
BFBen L. Feringa
Ben L. Feringa

21 March 2018 in ACS Applied Materials & Interfaces
Verified
Journal Article
Closed access
EGEduardo Guisasola
Eduardo Guisasola
LALaura Asín
Laura Asín
LBLillianne Beola
Lillianne Beola
Jesus M De La FuenteJesus M De La Fuente
Jesus M De La Fuente
Alejandro BaezaAlejandro Baeza
Alejandro Baeza
María Vallet-RegíMaría Vallet-Regí
María Vallet-Regí