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  1. Article ; Online: Editorial: Highlights in nano-based drug delivery 2021/22.

    Kumar, Santosh / Florindo, Helena F / Pasut, Gianfranco

    Frontiers in medical technology

    2023  Volume 5, Page(s) 1130414

    Language English
    Publishing date 2023-02-24
    Publishing country Switzerland
    Document type Editorial
    ISSN 2673-3129
    ISSN (online) 2673-3129
    DOI 10.3389/fmedt.2023.1130414
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Clinically-relevant and predictive cancer models for nanomedicine evaluation.

    Satchi-Fainaro, Ronit / Florindo, Helena F / Vicent, María J

    Advanced drug delivery reviews

    2022  Volume 183, Page(s) 114140

    MeSH term(s) Drug Delivery Systems ; Humans ; Nanomedicine ; Neoplasms/diagnosis ; Neoplasms/drug therapy
    Language English
    Publishing date 2022-02-05
    Publishing country Netherlands
    Document type Editorial
    ZDB-ID 639113-8
    ISSN 1872-8294 ; 0169-409X
    ISSN (online) 1872-8294
    ISSN 0169-409X
    DOI 10.1016/j.addr.2022.114140
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Special Issue "A perspective of drug delivery and translational research in Europe".

    Blanco-Prieto, María J / Florindo, Helena F

    Drug delivery and translational research

    2021  Volume 11, Issue 2, Page(s) 343–344

    MeSH term(s) Drug Delivery Systems ; Europe ; Pharmaceutical Preparations
    Chemical Substances Pharmaceutical Preparations
    Language English
    Publishing date 2021-03-04
    Publishing country United States
    Document type Introductory Journal Article
    ZDB-ID 2590155-2
    ISSN 2190-3948 ; 2190-393X
    ISSN (online) 2190-3948
    ISSN 2190-393X
    DOI 10.1007/s13346-021-00950-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Selenium Nanoparticles for Biomedical Applications: From Development and Characterization to Therapeutics.

    Ferro, Cláudio / Florindo, Helena F / Santos, Hélder A

    Advanced healthcare materials

    2021  Volume 10, Issue 16, Page(s) e2100598

    Abstract: Selenium (Se) is an essential element to human health that can be obtained in nature through several sources. In the human body, it is incorporated into selenocysteine, an amino acid used to synthesize several selenoproteins, which have an active center ... ...

    Abstract Selenium (Se) is an essential element to human health that can be obtained in nature through several sources. In the human body, it is incorporated into selenocysteine, an amino acid used to synthesize several selenoproteins, which have an active center usually dependent on the presence of Se. Although Se shows several beneficial properties in human health, it has also a narrow therapeutic window, and therefore the excessive intake of inorganic and organic Se-based compounds often leads to toxicity. Nanoparticles based on Se (SeNPs) are less toxic than inorganic and organic Se. They are both biocompatible and capable of effectively delivering combinations of payloads to specific cells following their functionalization with active targeting ligands. Herein, the main origin of Se intake, its role on the human body, and its primary biomedical applications are revised. Particular focus will be given to the main therapeutic targets that are explored for SeNPs in cancer therapies, discussing the different functionalization methodologies used to improve SeNPs stability, while enabling the extensive delivery of drug-loaded SeNP to tumor sites, thus avoiding off-target effects.
    MeSH term(s) Humans ; Nanoparticles ; Pharmaceutical Preparations ; Selenium
    Chemical Substances Pharmaceutical Preparations ; Selenium (H6241UJ22B)
    Language English
    Publishing date 2021-06-13
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2649576-4
    ISSN 2192-2659 ; 2192-2640
    ISSN (online) 2192-2659
    ISSN 2192-2640
    DOI 10.1002/adhm.202100598
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Challenges in the implementation of MIRIBEL criteria on nanobiomed manuscripts.

    Florindo, Helena F / Madi, Asaf / Satchi-Fainaro, Ronit

    Nature nanotechnology

    2019  Volume 14, Issue 7, Page(s) 627–628

    MeSH term(s) Editorial Policies ; Humans ; Nanomedicine ; Nanotechnology ; Periodicals as Topic ; Reproducibility of Results ; Research
    Language English
    Publishing date 2019-07-03
    Publishing country England
    Document type Letter
    ZDB-ID 2254964-X
    ISSN 1748-3395 ; 1748-3387
    ISSN (online) 1748-3395
    ISSN 1748-3387
    DOI 10.1038/s41565-019-0498-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Development of Chitosan Particles Loaded with siRNA for Cystatin C to Control Intracellular Drug-Resistant

    Pires, David / Mandal, Manoj / Matos, Ana I / Peres, Carina / Catalão, Maria João / Azevedo-Pereira, José Miguel / Satchi-Fainaro, Ronit / Florindo, Helena F / Anes, Elsa

    Antibiotics (Basel, Switzerland)

    2023  Volume 12, Issue 4

    Abstract: The golden age of antibiotics for tuberculosis (TB) is marked by its success in the 1950s of the last century. However, TB is not under control, and the rise in antibiotic resistance worldwide is a major threat to global health care. Understanding the ... ...

    Abstract The golden age of antibiotics for tuberculosis (TB) is marked by its success in the 1950s of the last century. However, TB is not under control, and the rise in antibiotic resistance worldwide is a major threat to global health care. Understanding the complex interactions between TB bacilli and their host can inform the rational design of better TB therapeutics, including vaccines, new antibiotics, and host-directed therapies. We recently demonstrated that the modulation of cystatin C in human macrophages via RNA silencing improved the anti-mycobacterial immune responses to
    Language English
    Publishing date 2023-04-08
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2681345-2
    ISSN 2079-6382
    ISSN 2079-6382
    DOI 10.3390/antibiotics12040729
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Cisplatin-Membrane Interactions and Their Influence on Platinum Complexes Activity and Toxicity.

    Martinho, Nuno / Santos, Tânia C B / Florindo, Helena F / Silva, Liana C

    Frontiers in physiology

    2019  Volume 9, Page(s) 1898

    Abstract: Cisplatin and other platinum(II) analogs are widely used in clinical practice as anti-cancer drugs for a wide range of tumors. The primary mechanism by which they exert their action is through the formation of adducts with genomic DNA. However, multiple ... ...

    Abstract Cisplatin and other platinum(II) analogs are widely used in clinical practice as anti-cancer drugs for a wide range of tumors. The primary mechanism by which they exert their action is through the formation of adducts with genomic DNA. However, multiple cellular targets by platinum(II) complexes have been described. In particular, the early events occurring at the plasma membrane (PM), i.e., platinum-membrane interactions seem to be involved in the uptake, cytotoxicity and cell-resistance to cisplatin. In fact, PM influences signaling events, and cisplatin-induced changes on membrane organization and fluidity were shown to activate apoptotic pathways. This review critically discusses the sequence of events caused by lipid membrane-platinum interactions, with emphasis on the mechanisms that lead to changes in the biophysical properties of the membranes (e.g., fluidity and permeability), and how these correlate with sensitivity and resistance phenotypes of cells to platinum(II) complexes.
    Language English
    Publishing date 2019-01-11
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2564217-0
    ISSN 1664-042X
    ISSN 1664-042X
    DOI 10.3389/fphys.2018.01898
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Sulphur Amino Acids: How Important is it to Set Reference Ranges for Each Population?

    Araújo, Helena Caldeira / Florindo, Cristina / Gomes, Alexandra / Caio, João / Castro, Rita / Rivera, Isabel

    Endocrine, metabolic & immune disorders drug targets

    2024  

    Abstract: ... tγ-Glu-Cys), were analysed as SBD-F derivatives by HPLC with fluorescence detection.: Results ...

    Abstract Introduction: Metabolism of sulfur amino acids requires an optimal interplay between nutritional demand, enzymes, transporters, and adequate dietary intake of B vitamins. Insufficient intake and excess are detrimental, and concentrations depend on health status. However, plasma aminothiol concentrations, previously reported in healthy subjects using highly sensitive methods, vary considerably, and age- and gender differences were observed. Therefore, defining age- and gender-specific ranges for each population is crucial to evaluate the meaning of plasma thiol redox state in health and disease.
    Methods: A healthy Portuguese pediatric population (n=90), aged 9- (n=38) and 17-year-old (n=52), was evaluated. Plasma aminothiols, total homocysteine (tHcy), cysteine (tCys), glutathione (tGSH) and γ-glutamylcysteine (tγ-Glu-Cys), were analysed as SBD-F derivatives by HPLC with fluorescence detection.
    Results/case report: Mean plasma concentrations (SD) for the 9- and the 17-year-old groups, were as following: tHcy = 4.58 (0.98); 8.13 (3.27) µM, p <0.001; tCys = 207.34 (32.07); 198.59 (21.24) µM, p = 0.274; tGSH = 4.54 (1.08); 5.20 (1.84) µM, p = 0.123 and tγ-Glu-Cys = 1.47 (0.30); 1.06 (0.28) µM, p < 0.001, respectively. No statistically significant differences were found between males and females in the 9-year-old group. However, in the 17-year-old group, significant differences between genders were observed for tHcys (p < 0.001) and tγ-Glu-Cys (p = 0.039), with males presenting the highest concentrations. When correlating the four thiols' plasma concentrations, only the precursors of glutathione, tγ-Glu-Cys and tCys, were positively correlated (r = 0.450, p < 0.001).
    Conclusion: Our results showed significant differences in tHcy and tγ-Glu-Cys levels across both age groups, which increased and decreased with age, respectively. It is interesting to highlight that in the 17-year-old group, tHcy and tγ-Glu-Cys levels were higher in males than in females. These observations showed that age and gender influence plasma levels of thiols, which may impact cellular oxidative status. In conclusion, setting age and gender distinct ranges for each specific population is of utmost importance for understanding disease mechanisms and the effectiveness of therapeutic interventions.
    Language English
    Publishing date 2024-01-12
    Publishing country United Arab Emirates
    Document type Journal Article
    ZDB-ID 2228325-0
    ISSN 2212-3873 ; 1871-5303
    ISSN (online) 2212-3873
    ISSN 1871-5303
    DOI 10.2174/0118715303282774231128053723
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Design of Experiments to Achieve an Efficient Chitosan-Based DNA Vaccine Delivery System.

    Rodolfo, Carlos / Eusébio, Dalinda / Ventura, Cathy / Nunes, Renato / Florindo, Helena F / Costa, Diana / Sousa, Ângela

    Pharmaceutics

    2021  Volume 13, Issue 9

    Abstract: In current times, DNA vaccines are seen as a promising approach to treat and prevent diseases, such as virus infections and cancer. Aiming at the production of a functional and effective plasmid DNA (pDNA) delivery system, four chitosan polymers, ... ...

    Abstract In current times, DNA vaccines are seen as a promising approach to treat and prevent diseases, such as virus infections and cancer. Aiming at the production of a functional and effective plasmid DNA (pDNA) delivery system, four chitosan polymers, differing in the molecular weight, were studied using the design of experiments (DoE) tool. These gene delivery systems were formulated by ionotropic gelation and exploring the chitosan and TPP concentrations as DoE inputs to maximize the nanoparticle positive charge and minimize their size and polydispersity index (PDI) as DoE outputs. The obtained linear and quadratic models were statistically significant (
    Language English
    Publishing date 2021-08-31
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527217-2
    ISSN 1999-4923
    ISSN 1999-4923
    DOI 10.3390/pharmaceutics13091369
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Polyoxazoline-Based Nanovaccine Synergizes with Tumor-Associated Macrophage Targeting and Anti-PD-1 Immunotherapy against Solid Tumors.

    Matos, Ana I / Peres, Carina / Carreira, Barbara / Moura, Liane I F / Acúrcio, Rita C / Vogel, Theresa / Wegener, Erik / Ribeiro, Filipa / Afonso, Marta B / Santos, Fábio M F / Martínez-Barriocanal, Águeda / Arango, Diego / Viana, Ana S / Góis, Pedro M P / Silva, Liana C / Rodrigues, Cecília M P / Graca, Luis / Jordan, Rainer / Satchi-Fainaro, Ronit /
    Florindo, Helena F

    Advanced science (Weinheim, Baden-Wurttemberg, Germany)

    2023  Volume 10, Issue 25, Page(s) e2300299

    Abstract: Immune checkpoint blockade reaches remarkable clinical responses. However, even in the most favorable cases, half of these patients do not benefit from these therapies in the long term. It is hypothesized that the activation of host immunity by co- ... ...

    Abstract Immune checkpoint blockade reaches remarkable clinical responses. However, even in the most favorable cases, half of these patients do not benefit from these therapies in the long term. It is hypothesized that the activation of host immunity by co-delivering peptide antigens, adjuvants, and regulators of the transforming growth factor (TGF)-β expression using a polyoxazoline (POx)-poly(lactic-co-glycolic) acid (PLGA) nanovaccine, while modulating the tumor-associated macrophages (TAM) function within the tumor microenvironment (TME) and blocking the anti-programmed cell death protein 1 (PD-1) can constitute an alternative approach for cancer immunotherapy. POx-Mannose (Man) nanovaccines generate antigen-specific T-cell responses that control tumor growth to a higher extent than poly(ethylene glycol) (PEG)-Man nanovaccines. This anti-tumor effect induced by the POx-Man nanovaccines is mediated by a CD8
    MeSH term(s) Mice ; Animals ; Tumor-Associated Macrophages ; Cell Line, Tumor ; Immunotherapy ; CD8-Positive T-Lymphocytes ; Melanoma ; Tumor Microenvironment
    Language English
    Publishing date 2023-07-11
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2808093-2
    ISSN 2198-3844 ; 2198-3844
    ISSN (online) 2198-3844
    ISSN 2198-3844
    DOI 10.1002/advs.202300299
    Database MEDical Literature Analysis and Retrieval System OnLINE

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