298 research outputs found
N1-Benzylidene-N2-(2-((2-((2-(benzylideneamino)ethyl)amino)ethyl)amino)ethyl)ethane-1,2-diamine
Supercritical CO2-assisted spray drying of strawberry-like gold-coated magnetite nanocomposites in chitosan powders for inhalation
Associate Laboratory Research Unit for Green Chemistry Clean Processes and Technologies-LAQV - (UID/QUI/50006/2013) ; UCIBIO from FCT/MEC - UID/Multi/04378/2013 ; ERDF - POCI-01-0145-FEDER-007265; FCT/MEC - SFRH/BD/51584/2011; SFRH/BPD/93982/2013 ; FCT-Lisbon - IF/00915/2014Lung cancer is one of the leading causes of death worldwide. Therefore, it is of extreme importance to develop new systems that can deliver anticancer drugs into the site of action when initiating a treatment. Recently, the use of nanotechnology and particle engineering has enabled the development of new drug delivery platforms for pulmonary delivery. In this work, POXylated strawberry-like gold-coated magnetite nanocomposites and ibuprofen (IBP) were encapsulated into a chitosan matrix using Supercritical Assisted Spray Drying (SASD). The dry powder formulations showed adequate morphology and aerodynamic performances (fine particle fraction 48%-55% and aerodynamic diameter of 2.6-2.8 μm) for deep lung deposition through the pulmonary route. Moreover, the release kinetics of IBP was also investigated showing a faster release of the drug at pH 6.8, the pH of lung cancer. POXylated strawberry-like gold-coated magnetite nanocomposites proved to have suitable sizes for cellular internalization and their fluorescent capabilities enable their future use in in vitro cell based assays. As a proof-of-concept, the reported results show that these nano-in-micro formulations could be potential drug vehicles for pulmonary administration. © 2017 by the authors.publishersversionpublishe
Synthesis of gold functionalised nanoparticles with the eranthis hyemalis lectin and preliminary toxicological studies on caenorhabditis elegans
The lectin found in the tubers of the Winter Aconite (Eranthis hyemalis) plant (EHL) is a Type II Ribosome Inactivating Protein (RIP). Type II RIPs have shown anti-cancer properties and have great potential as therapeutic agents. Similarly, colloidal gold nanoparticles are successfully used in biomedical applications as they can be functionalised with ligands with high affinity and specificity for target cells to create therapeutic and imaging agents. Here we present the synthesis and characterization of gold nanoparticles conjugated with EHL and the results of a set of initial assays to establish whether the biological effect of EHL is altered by the conjugation. Gold nanoparticles functionalised with EHL (AuNPs@EHL) were successfully synthesised by bioconjugation with citrate gold nanoparticles (AuNPs@Citrate). The conjugates were analysed by UV-Vis spectroscopy, Dynamic Light Scattering (DLS), Zeta Potential analysis, and Transmission Electron Microscopy (TEM).
Results indicate that an optimal functionalisation was achieved with the addition of 100 µL of EHL (concentration 1090 ± 40 µg/mL) over 5 mL of AuNPs (concentration [Au0] = 0.8 mM). Biological assays on the effect of AuNPs@EHL were undertaken on Caenorhabditis elegans, a free-living nematode commonly used for toxicological studies, that has previously been shown to be strongly affected by EHL. Citrate gold nanoparticles did not have any obvious effect on the nematodes. For first larval stage (L1) nematodes, AuNPs@EHL showed a lower biological effect than EHL. For L4 stage, pre-adult nematodes, both EHL alone and AuNPs@EHL delayed the onset of reproduction and reduced fecundity. These assays indicate that EHL can be conjugated to gold nanoparticles and retain elements of biocidal activity
Enhancing the teaching-research nexus in the undergraduate curriculum through assessment
Successful linkages between teaching and research in the undergraduate curriculum are strongly dependent on academics’ ability to encourage and facilitate an inquiry based approach to learning. An assessment strategy in which students become active participants in the assessment process is crucial to facilitate the development of this inquiry based approach. Developing this so-called research-mindedness is central to helping students' to become independent learners and to be more effective professionals in their future careers. This paper describes a distributed systems approach to assessment implemented in the undergraduate module Molecular Biology. The assessment comprised a series of sequence identification, database use and analysis steps, with each student being given a different starting gene. In combination, the students analysed an entire genetic pathway. This approach allows the assignments generated to be combined and used to address a single larger question, which can be either teaching or research based. This is then fed back into the teaching. This direct link between the assessment outcomes and the learning process increases student engagement with the subject and sense of ownership of the work carried out. This approach to assessment, in which students undertake a small part of a larger task, is ideal for various technical, skills-based, assignments, such as those central to the many types of bioinformatics analyses. However, it can be adapted to various types of meta-review. The paper discusses the details for the implementation, as well as the benefits and potential pitfalls of the approach
Intramolecular excimer formation and sensing behavior of new fluorimetric probes and their interactions with metal cations and barbituric acids
A new family of compounds able to promote host-guest interactions with specific molecules (e.g., cyanuric and parabanic acids) and to coordinate metal ions, namely Zn(II) and Cu(II), has been synthesized and fully characterized. The new probes derive from the attachment of two methylaminopyrene units to the carbonyl precursor 2,6-bis(2-formylphenoxymethyl)pyridine.http://www.sciencedirect.com/science/article/B6THH-4HF5KD3-1/1/ef66847d1e019d05e2068bef93cfbd9
Long Range Electron Transfer Quenching in Polyamine Chains Bearing a Terminal Naphthalene Unit
The fluorescence emission of a naphthalene unit attached to a polyamine chain is quenched by intramolecular electron transfer from the deprotonated amines to the excited fluorophore. Measurements of the respective quenching rate constants as a function of the distance, reveal an exponential dependence with β = 0.45 Å-1. Identical measurements carried out in deuterated water have shown a similar dependence with the distance β = 0.49 Å-1 but an average reduction of the absolute values of the rate constants of ca. 1.2. The polyamine chains seem to constitute a bridge through which the electron can find a route to its movement, more efficiently than through space
Atomic scale model and electronic structure of CuO/CHNHPbI interfaces in perovskite solar cells
Cuprous oxide has been conceived as a potential alternative to traditional
organic hole transport layers in hybrid halide perovskite-based solar cells.
Device simulations predict record efficiencies using this semiconductor, but
experimental results do not yet show this trend. More detailed knowledge about
the CuO/perovskite interface is mandatory to improve the photoconversion
efficiency. Using density functional theory calculations, here we study the
interfaces of CHNHPbI with CuO to assess their influence on
device performance. Several atomistic models of these interfaces are provided
for the first time, considering different compositions of the interface atomic
planes. The interface electronic properties are discussed on the basis of the
optimal theoretical situation, but in connection with the experimental
realizations and device simulations. It is shown that the formation of
vacancies in the CuO terminating planes is essential to eliminate dangling
bonds and trap states. The four interface models that fulfill this condition
present a band alignment favorable for photovoltaic conversion. Energy of
adhesion, and charge transfer across the interfaces are also studied. The
termination of CHNHPbI in PbI atomic planes seems optimal to
maximize the photoconversion efficiency.Comment: 16 pages; 8 figures. Submitted to ACS Applied Materials & Interfaces.
Published after changes not included her
Interaction of strontium chloride solution with calcium aluminate phosphate (CAP) system
Processing of contaminated water in Fukushima Daiichi Power Plant results in various aqueous secondary wastes. A significant strontium ( 90 Sr) contamination represents one of the key challenges for their management, and we have been developing a new cementing matrix based on calcium aluminate phosphate (CAP) system with reduced water content for such aqueous secondary wastes. In the present study, the interaction of CAP with SrCl2 was investigated to gain insight into the capability of CAP system in Sr immobilisation. It was found that the immobilisation is possible, and the incorporation of Sr appears to be associated with the formation of insoluble phosphate salts. The obtained results also suggest that 1 kg of CAP powders can incorporate 200 g of Sr under tested condition
Synthesis and H+, Cu2+, and Zn2+ Coordination Behavior of a Bis(fluorophoric) Bibrachial Lariat Aza-Crown
The synthesis, protonation behavior, and Cu2+ and Zn2+ coordination chemistry of the novel bibrachial aza lariat ether (naphthalen-1-ylmethyl)[2-(20-{2-[(naphthalen-1-ylmethyl)amino]ethyl}-3,6,9,17,20,23,29,30-octaazatricyclo[23.3.1.1*11,15*]triaconta-1(29),11(30),12,14,25,27-hexaen-6-yl)ethyl]amine (L) are discussed. The macrocycle, which has two aminoethyl naphthyl moieties symmetrically appended to a 2:2 azapyridinophane structure, displays, in the pH range 2−11, six protonation steps that correspond to the protonation of the secondary amino groups. Steady-state fluorescence measurements show emissions due to the monomer and to the excimer formed between the two naphthalene fragments of the macrocycle. The time-resolved fluorescence data, obtained by the time-correlated single photon counting technique, show that a significant percentage of excimer is preformed as ground-state dimers. The ligand L forms with the metal ions Cu2+ and Zn2+ mono- and dinuclear complexes in aqueous solution. The influence of metal coordination in the fluorescence emission of L is analyzed. The acid−base, coordination capabilities, and emissive behavior of L are compared with those presented by its synthetic precursor L1, which has a tripodal tris(2-aminoethyl)amine structure functionalized at one of its terminal amino groups with a naphthyl moiet
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