52 research outputs found

    Cooperative Brønsted Acid-Type Organocatalysis for the Stereoselective Synthesis of Deoxyglycosides

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    A practical approach for the α-stereoselective synthesis of deoxyglycosides using cooperative Brønsted acid-type organocatalysis has been developed. The method is tolerant of a wide range of glycoside donors and acceptors, and its versatility is exemplified in the one-pot synthesis of a trisaccharide. Mechanistic studies suggest that thiourea-induced acid amplification of the chiral acid via H-bonding is key for the enhancement in reaction rate and yield, while stereocontrol is dependent on the chirality of the acid

    Síntesis estereoselectiva a partir de carbohidratos y catalizadores quirales. Obtención de compuestos de interés con actividad citotóxica

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    Tesis descargada desde TESEOHasta hace poco tiempo los fármacos con un solo enantiómero eran derivados de compuestos naturales y las mezclas racémicas predominaban en los fármacos sintéticos. Actualmente existe una clara tendencia de la industria farmacéutica hacia el desarrollo de fármacos quirales. Esto deriva directamente de la necesidad de no exponer el organismo humano a la acción de un agente, el distómero, que, en el mejor de los casos, y en principio, no es beneficioso para el organismo. Entre los aspectos más excitantes de la Química Orgánica en las últimas décadas está la interrelación entre subdisciplinas especializadas de la química de hidratos de carbono y la síntesis total, reforzándose unas a otras y avanzando en conjunto en nuevas direcciones y hacia mayores retos. Efectivamente, ricos en funcionalidad y estereoquímica, los carbohidratos son excelentes materiales de partida para la síntesis total estereoselectiva, el llamado en la literatura anglosajona el carbohydrate chiral pool, como valiosa fuente de diversos y valiosos building blocks para la síntesis orgánica. En esta Tesis hemos extendido el uso de carbohidratos al estudio de nuevas reacciones estereoselectivas, como la formación de dioles y aziridinas quirales. Además, nuestro grupo, ubicado en la Facultad de Farmacia de la Universidad de Sevilla, ha dedicado gran parte de su esfuerzo investigador en utilizar los hidratos de carbono como fuente de sustancias con potencial actividad biológica. En este sentido, en la tesis que aquí se presenta se han sintetizado derivados de glicolípidos y derivados aziridínicos con alto potencial biológico. La idea subyacente es minimizar los efectos secundarios propios de la quimioterapia usada en el tratamiento del cáncer uniendo la fracción activa a un metabolito primario como es un hidrato de carbono por el que las células cancerosas, en rápido crecimiento, tienen una gran demanda. Así, intentaremos conseguir una alta selectividad de nuestros nuevos compuestos sintetizados con alto potencial biológico frente a las células cancerígenas. Por otro lado, y en la misma línea de la búsqueda de compuestos estereoquimicamente puros y coincidiendo con mi estancia en la Universidad de Estocolmo en esta Tesis se presenta la puesta a punto de una nueva metodología de catálisis heterogénea usando partículas de Paladio y una amina quiral derivada de prolina como co-catalizador, dando lugar a una catálisis altamente enantioselectiva. El uso de metales de transición como catalizadores ha impulsado el desarrollo de la catálisis asimétrica en reacciones en cascada en estos últimos años. La Tesis que se presenta supone una profundización en dos líneas generales básicas, síntesis estereoselectiva usando derivados de carbohidratos como inductores quirales o catálisis asimétrica, y en segundo lugar la búsqueda de nuevos compuestos con potencial actividad farmacológica

    In Vitro Investigation of Thiol-Functionalized Cellulose Nanofibrils as a Chronic Wound Environment Modulator

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    There is currently a huge need for new, improved therapeutic approaches for the treatment of chronic wounds. One promising strategy is to develop wound dressings capable of modulating the chronic wound environment (e.g., by controlling the high levels of reactive oxygen species (ROS) and proteases). Here, we selected the thiol-containing amino acid cysteine to endow wood-derived cellulose nanofibrils (CNF) with bioactivity toward the modulation of ROS levels and protease activity. Cysteine was covalently incorporated into CNF and the functionalized material, herein referred as cys-CNF, was characterized in terms of chemical structure, degree of substitution, radical scavenging capacity, and inhibition of protease activity. The stability of the thiol groups was evaluated over time, and an in vitro cytotoxicity study with human dermal fibroblasts was performed to evaluate the safety profile of cys-CNF. Results showed that cys-CNF was able to efficiently control the activity of the metalloprotease collagenase and to inhibit the free radical DPPH (1,1-Diphenyl-2-picrylhydrazyl radical), activities that were correlated with the presence of free thiol groups on the nanofibers. The stability study showed that the reactivity of the thiol groups challenged the bioactivity over time. Nevertheless, preparing the material as an aerogel and storing it in an inert atmosphere were shown to be valid approaches to increase the stability of the thiol groups in cys-CNF. No signs of toxicity were observed on the dermal fibroblasts when exposed to cys-CNF (concentration range 0.1-0.5 mg/mL). The present work highlights cys-CNF as a promising novel material for the development of bioactive wound dressings for the treatment of chronic wounds

    Prevalence, associated factors and outcomes of pressure injuries in adult intensive care unit patients: the DecubICUs study

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    Funder: European Society of Intensive Care Medicine; doi: http://dx.doi.org/10.13039/501100013347Funder: Flemish Society for Critical Care NursesAbstract: Purpose: Intensive care unit (ICU) patients are particularly susceptible to developing pressure injuries. Epidemiologic data is however unavailable. We aimed to provide an international picture of the extent of pressure injuries and factors associated with ICU-acquired pressure injuries in adult ICU patients. Methods: International 1-day point-prevalence study; follow-up for outcome assessment until hospital discharge (maximum 12 weeks). Factors associated with ICU-acquired pressure injury and hospital mortality were assessed by generalised linear mixed-effects regression analysis. Results: Data from 13,254 patients in 1117 ICUs (90 countries) revealed 6747 pressure injuries; 3997 (59.2%) were ICU-acquired. Overall prevalence was 26.6% (95% confidence interval [CI] 25.9–27.3). ICU-acquired prevalence was 16.2% (95% CI 15.6–16.8). Sacrum (37%) and heels (19.5%) were most affected. Factors independently associated with ICU-acquired pressure injuries were older age, male sex, being underweight, emergency surgery, higher Simplified Acute Physiology Score II, Braden score 3 days, comorbidities (chronic obstructive pulmonary disease, immunodeficiency), organ support (renal replacement, mechanical ventilation on ICU admission), and being in a low or lower-middle income-economy. Gradually increasing associations with mortality were identified for increasing severity of pressure injury: stage I (odds ratio [OR] 1.5; 95% CI 1.2–1.8), stage II (OR 1.6; 95% CI 1.4–1.9), and stage III or worse (OR 2.8; 95% CI 2.3–3.3). Conclusion: Pressure injuries are common in adult ICU patients. ICU-acquired pressure injuries are associated with mainly intrinsic factors and mortality. Optimal care standards, increased awareness, appropriate resource allocation, and further research into optimal prevention are pivotal to tackle this important patient safety threat

    Substrate-Controlled Direct α-Stereoselective Synthesis of Deoxyglycosides from Glycals Using B(C6F5)3 as Catalyst

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    B(C6F5)3 enables the metal-free unprecedented substrate-controlled direct α-stereoselective synthesis of deoxyglycosides from glycals. 2,3-Unsaturated α-O-glycoside products are obtained with deactivated glycals at 75 °C in the presence of the catalyst, while 2-deoxyglycosides are formed using activated glycals that bear no leaving group at C-3 at lower temperatures. The reaction proceeds in good to excellent yields via concomitant borane activation of glycal donor and nucleophile acceptor. The method is exemplified with the synthesis of a series of rare and biologically relevant glycoside analogues.Title in Web of Science: Substrate-Controlled Direct alpha-Stereoselective Synthesis of Deoxyglycosides from Glycals Using B(C6F5)(3) as Catalyst</p
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