Helena Ferreira

Dr. Helena Ferreira

University of Minho, I3B's - Research Institute on Biomaterials, Biodegradables and Biomimetics, Guimarães, Portugal
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Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

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30 May 2018 in Nature Microbiology
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Journal Article
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IKIrene Kyrmizi
Irene Kyrmizi
Helena FerreiraHelena Ferreira
Helena Ferreira
ACAgostinho Carvalho
Agostinho Carvalho
JFJulio Alberto Landero Figueroa
Julio Alberto Landero Figueroa
PZPavlos Zarmpas
Pavlos Zarmpas
GCGeorgios Chamilos
Georgios Chamilos

1 March 2010 in Ultrasonics Sonochemistry
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Journal Article
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RSRaquel Silva
Raquel Silva
Helena FerreiraHelena Ferreira
Helena Ferreira
CLCollin Little
Collin Little
Artur Cavaco-PauloArtur Cavaco-Paulo
Artur Cavaco-Paulo

27 August 2009 in Food Biophysics
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Marlene LúcioMarlene Lúcio
Marlene Lúcio
Cláudia NunesCláudia Nunes
Cláudia Nunes
DGDiana Gaspar
Diana Gaspar
Helena FerreiraHelena Ferreira
Helena Ferreira
JLJosé L. F. C. Lima
José L. F. C. Lima
Salette ReisSalette Reis
Salette Reis

16 April 2024 in Phytochemistry Reviews
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SVSara Vieira
Sara Vieira
RRRui M. Reis
Rui M. Reis
Helena FerreiraHelena Ferreira
Helena Ferreira
Nuno M. NevesNuno M. Neves
Nuno M. Neves
The immune system is a complex and fundamental network for organism protection. A minimal unbalance in the host defense system homeostasis can originate severe repercussions in human health. Fundamentally, immune-related diseases can arise from its compromise (immunodeficiency diseases), overactivation against itself (autoimmune diseases) or harmless substances (allergies), and failure of eliminating the harmful agent (chronic inflammation). The notable advances and achievements in the immune system diseases pathophysiology have been allowing for a dramatic improvement of the available treatments. Nevertheless, they present some drawbacks, including the inappropriate benefit/risk ratio. Therefore, there is a strong and urgent need to develop effective therapeutic strategies. Nature is a valuable source of bioactive compounds that can be explored for the development of new drugs. Particularly, plants produce a broad spectrum of secondary metabolites that can be potential prototypes for innovative therapeutic agents. This review describes the immune system and the inflammatory response and examines the current knowledge of eight plants traditionally used as immunomodulatory medicines (Boswellia serrata, Echinacea purpurea, Laurus nobilis, Lavandula angustifolia, Olea europaea, Salvia officinalis, Salvia rosmarinus, and Taraxacum officinale). Moreover, the issues responsible for possible biologic readout inconsistencies (plant species, age, selected organ, developmental stage, growth conditions, geographical location, drying methods, storage conditions, solvent of extraction, and extraction method) will also be discussed. Furthermore, a detailed list of the chemical composition and the immunomodulatory mechanism of action of the bioactive compounds of the selected plant extracts are presented. This review also includes future perspectives and proposes potential new avenues for further investigation.

20 November 2020 in Antioxidants
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SVSara Vieira
Sara Vieira
Helena FerreiraHelena Ferreira
Helena Ferreira
Nuno M. NevesNuno M. Neves
Nuno M. Neves
Chronic inflammation is characterized by an overproduction of several inflammatory mediators (e.g., reactive species and interleukins -IL) that play a central role in numerous diseases. The available therapies are often associated with serious side effects and, consequently, the need for safer drugs is of utmost importance. A plant traditionally used in the treatment of inflammatory conditions is Salvia officinalis. Therefore, conventional maceration and infusion of its leaves were performed to obtain hydroethanolic (HE-T) and aqueous extracts (AE-T), respectively. Their efficacy was compared to soxhlet extracts, namely aqueous (AE-S), hydroethanolic (HE-S), and ethanolic extracts (EE-S). Thin-layer chromatography demonstrated the presence of rosmarinic acid, carnosol, and/or carnosic acid in the different extracts. Generally, soxhlet provided extracts with higher antioxidant activities than traditional extraction. Moreover, under an inflammatory scenario, EE-S were the most effective, followed by HE-S, HE-T, AE-T, and AE-S, in the reduction of IL-6 and TNF-α production. Interestingly, the extracts presented higher or similar anti-inflammatory activity than diclofenac, salicylic acid, and celecoxib. In conclusion, the extraction method and the solvents of extraction influenced the antioxidant activity, but mainly the anti-inflammatory activity of the extracts. Therefore, this natural resource can enable the development of effective treatments for oxidative stress and inflammatory diseases.

31 July 2019 in Expert Opinion on Drug Delivery
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ALAna Cláudia Lima
Ana Cláudia Lima
Helena FerreiraHelena Ferreira
Helena Ferreira
RRRui M. Reis
Rui M. Reis
Nuno M. NevesNuno M. Neves
Nuno M. Neves
Introduction: The unique structure of bone and cartilage makes the systemic delivery of free drugs to those connective tissues very challenging. Consequently, effective and targeted delivery for bone and cartilage is of utmost importance. Engineered biodegradable polymers enable designing carriers for a targeted and temporal controlled release of one or more drugs in concentrations within the therapeutic range. Also, tissue engineering strategies can allow drug delivery to advantageously promote the in situ tissue repair. Areas covered: This review article highlights various drug delivery systems (DDS) based on biodegradable biomaterials to treat bone and/or cartilage diseases. We will review their applications in osteoporosis, inflammatory arthritis (namely osteoarthritis and rheumatoid arthritis), cancer and bone and cartilage tissue engineering. Expert opinion: The increased knowledge about biomaterials science and of the pathophysiology of diseases, biomarkers, and targets as well as the development of innovative tools has led to the design of high value-added DDS. However, some challenges persist and are mainly related to an appropriate residence time and a controlled and sustained release over a prolonged period of time of the therapeutic agents. Additionally, the poor prediction value of some preclinical animal models hinders the translation of many formulations into the clinical practice.