47 research outputs found

    Cyclodextrins and ternary complexes: technology to improve solubility of poorly soluble drugs

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    Cyclodextrins (CDs) are cyclic oligosaccharides composed of D-glucopyranoside units linked by glycosidic bonds. Their main property is the ability to modify the physicochemical and biological characteristics of low-soluble drugs through the formation of drug:CD inclusion complexes. Inclusion complexation requires that host molecules fit completely or partially within the CD cavity. This adjustment is directly related to the physicochemical properties of the guest and host molecules, easy accommodation of guest molecules within the CD cavity, stoichiometry, therapeutic dose, and toxicity. However, dosage forms may achieve a high volume, depending on the amount of CD required. Thus, it is necessary to increase solubilization efficiency in order to use smaller amounts of CD. This can be achieved by adding small amounts of water-soluble polymers to the system. This review addresses aspects related to drug complexation with CDs using water-soluble polymers to optimize the amount of CD used in the formulation in order to increase drug solubility and reduce dosage form volume.Ciclodextrinas (CDs) sĂŁo oligossacarĂ­deos cĂ­clicos, compostos por unidades D-glicopiranosĂ­dicas ligadas entre si por meio de ligaçÔes glicosĂ­dicas e sua principal propriedade estĂĄ na capacidade de alterar as caracterĂ­sticas fĂ­sico-quĂ­micas e biolĂłgicas de fĂĄrmacos com baixa solubilidade por meio da formação de complexos de inclusĂŁo fĂĄrmaco:CD. Para a formação dos complexos de inclusĂŁo a molĂ©cula hospedeira necessita ajustar-se total ou parcialmente no interior da cavidade da CD, onde este ajuste estĂĄ diretamente ligado a propriedades fĂ­sico-quĂ­micas da molĂ©cula hĂłspede e hospedeira, facilidade de alojamento da molĂ©cula hĂłspede no interior da cavidade da CD, estequiometria, dose terapĂȘutica e toxicidade. No entanto, as formas farmacĂȘuticas podem atingir um elevado volume, em função da quantidade de CD requerida, sendo necessĂĄrio aumentar sua eficiĂȘncia de solubilização para que seja possĂ­vel utilizar menores quantidades das mesmas. Isso pode ser obtido com a inclusĂŁo de pequenas quantidades de polĂ­meros hidrossolĂșveis ao sistema. Nessa revisĂŁo, sĂŁo abordados aspectos relacionados Ă  complexação de fĂĄrmacos com ciclodextrinas empregando-se polĂ­meros hidrossolĂșveis para otimização da quantidade de CD utilizada na formulação, com a finalidade de aumentar a solubilidade do fĂĄrmaco e reduzir o volume das preparaçÔes

    Highly-parallelized simulation of a pixelated LArTPC on a GPU

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    The rapid development of general-purpose computing on graphics processing units (GPGPU) is allowing the implementation of highly-parallelized Monte Carlo simulation chains for particle physics experiments. This technique is particularly suitable for the simulation of a pixelated charge readout for time projection chambers, given the large number of channels that this technology employs. Here we present the first implementation of a full microphysical simulator of a liquid argon time projection chamber (LArTPC) equipped with light readout and pixelated charge readout, developed for the DUNE Near Detector. The software is implemented with an end-to-end set of GPU-optimized algorithms. The algorithms have been written in Python and translated into CUDA kernels using Numba, a just-in-time compiler for a subset of Python and NumPy instructions. The GPU implementation achieves a speed up of four orders of magnitude compared with the equivalent CPU version. The simulation of the current induced on 10^3 pixels takes around 1 ms on the GPU, compared with approximately 10 s on the CPU. The results of the simulation are compared against data from a pixel-readout LArTPC prototype

    Problems associated with the presence of cyanobacteria in recreational and drinking waters

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    Eutrophication of waters can lead to the development of blooms of cyanobacteria (blue-green algae) and consequent health and environmental problems. The presence of these organisms in recreational and drinking waters is generally undesirable or even hazardous, although nitrogen fixing blue-green algae can be beneficially used as biofertilisers for plantation crops. This paper reviews the characteristics of cyanobacteria and particularly their toxins. The mechanisms of toxic algal blooms are discussed, as are the factors influencing toxin production. The nuisance and health hazards associated with freshwater bluegreen algae are discussed and the options for public health control are evaluated. The problems associated with statutory control of toxic algae problems is also considered

    Liver regeneration after portal and hepatic vein embolization improves overall survival compared with portal vein embolization alone: mid-term survival analysis of the multicentre DRAGON 0 cohort

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    Background: the purpose of this study was to compare 3-year overall survival after simultaneous portal (PVE) and hepatic vein (HVE) embolization versus PVE alone in patients undergoing liver resection for primary and secondary cancers of the liver.Methods: in this multicentre retrospective study, all DRAGON 0 centres provided 3-year follow-up data for all patients who had PVE/HVE or PVE, and were included in DRAGON 0 between 2016 and 2019. Kaplan-Meier analysis was undertaken to assess 3-year overall and recurrence/progression-free survival. Factors affecting survival were evaluated using univariable and multivariable Cox regression analyses.Results: in total, 199 patients were included from 7 centres, of whom 39 underwent PVE/HVE and 160 PVE alone. Groups differed in median age (P = 0.008). As reported previously, PVE/HVE resulted in a significantly higher resection rate than PVE alone (92 versus 68%; P = 0.007). Three-year overall survival was significantly higher in the PVE/HVE group (median survival not reached after 36 months versus 20 months after PVE; P = 0.004). Univariable and multivariable analyses identified PVE/HVE as an independent predictor of survival (univariable HR 0.46, 95% c.i. 0.27 to 0.76; P = 0.003).Conclusion: overall survival after PVE/HVE is substantially longer than that after PVE alone in patients with primary and secondary liver tumours.</p
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