Rogério Gaspar

Rogério Gaspar

Auto-generated profile, based on publicly available information

Rogério Gaspar

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisbon, Portugal

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

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

Representative Publications

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5 October 2011 in Molecular Pharmaceutics
Verified
Journal Article
Closed access
RDRuth Duncan
Ruth Duncan
RGRogerio Gaspar
Rogerio Gaspar

1 October 2002 in Journal of Controlled Release
Verified
Journal Article
Closed access
CFCristina Fonseca
Cristina Fonseca
SSSérgio Simões
Sérgio Simões
RGRogério Gaspar
Rogério Gaspar

1 December 2015 in Biochemical and Biophysical Research Communications
Verified
Journal Article
Closed access
VSVanessa Sainz
Vanessa Sainz
JCJoão Conniot
João Conniot
AMAna I. Matos
Ana I. Matos
CPCarina Peres
Carina Peres
EZEva Zupanǒiǒ
Eva Zupanǒiǒ
RGRogério S. Gaspar
Rogério S. Gaspar

1 November 2009 in Advanced Drug Delivery Reviews
Verified
Journal Article
Closed access
RGRogério Gaspar
Rogério Gaspar
RDRuth Duncan
Ruth Duncan

1 June 2013 in Journal of Controlled Release
Verified
Journal Article
Closed access
JSJoana M. Silva
Joana M. Silva
MVMafalda Videira
Mafalda Videira
RGRogério Gaspar
Rogério Gaspar
VPVéronique Préat
Véronique Préat
HFHelena Florindo
Helena Florindo

26 November 2014 in Frontiers in Chemistry
Verified
Journal Article
Open access
PDF file
JCJoã£O Conniot
Joã£O Conniot
JSJoana M. Silva
Joana M. Silva
JFJoana G. Fernandes
Joana G. Fernandes
LSLiana Silva
Liana Silva
RGRogã©Rio Gaspar
Rogã©Rio Gaspar
TBTeresa Barata
Teresa Barata
Cancer is one of the most common diseases afflicting people globally. New therapeutic approaches are needed due to the complexity of cancer as a disease. Many current treatments are very toxic and have modest efficacy at best. Increased understanding of tumor biology and immunology has allowed the development of specific immunotherapies with minimal toxicity. It is important to highlight the performance of monoclonal antibodies, immune adjuvants, vaccines and cell-based treatments. Although these approaches have shown varying degrees of clinical efficacy, they illustrate the potential to develop new strategies. Targeted immunotherapy is being explored to overcome the heterogeneity of malignant cells and the immune suppression induced by both the tumor and its microenvironment. Nanodelivery strategies seek to minimize systemic exposure to target therapy to malignant tissue and cells. Intracellular penetration has been examined through the use of functionalized particulates. These nano-particulate associated medicines are being developed for use in imaging, diagnostics and cancer targeting. Although nano-particulates are inherently complex medicines, the ability to confer, at least in principle, different types of functionality allows for the plausible consideration these nanodelivery strategies can be exploited for use as combination medicines. The development of targeted nanodelivery systems in which therapeutic and imaging agents are merged into a single platform is an attractive strategy. Currently, several nanoplatform-based formulations, such as polymeric nanoparticles, micelles, liposomes and dendrimers are in preclinical and clinical stages of development. Herein, nanodelivery strategies presently investigated for cancer immunotherapy, cancer targeting mechanisms and nanocarrier functionalization methods will be described. We also intend to discuss the emerging nano-based approaches suitable to be used as imaging techniques and as cancer treatment options.