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1.
ACS Sustain Chem Eng ; 12(32): 12236-12248, 2024 Aug 12.
Artigo em Inglês | MEDLINE | ID: mdl-39148517

RESUMO

The combination of CO2-selective ionic liquids (ILs) with block copolymers, such as Pebax 1657, has demonstrated an enhancement of the gas separation capabilities of polymeric membranes. In the current work, the development of composite membranes by applying a thin, concentrated selective layer made of Pebax/imidazolium-based ionic liquids (ILs) is presented. The objective of the experiments was to determine the optimized IL loading and investigate how the alteration of the anion impacts the properties of the membranes. Two membrane configurations have been studied: coated flat sheet membranes, supported on a porous poly(ether sulfone) (PES) layer, as well as composite hollow fiber membranes, supported on commercial polypropylene (PP) hollow fibers. Coated hollow fiber composites were fabricated using a continuous coating method, offering a straightforward scalability in the manufacturing process. The determined mechanical pressure stability of hollow fiber composites reached up to 5 bar, indicating their potential for various industrial gas separation applications. It was found that the Pebax 1657-based coating containing 40 wt % [C6mim][NTf2] yielded membranes with the best gas separation properties, for both the coated flat sheet and the hollow fiber configurations. The CO2 permeance of hollow fibers reached 23.29 GPU, whereas the CO2/N2 ideal selectivity stood at 8.7, suggesting the necessity of the further enhancement of the coating technique, which can be achieved, for example, through application of multiple coatings. Nonetheless, the superior ideal selectivity of the CO2/CO separation, reaching 12.44, gave a promising outlook for further novel membrane applications, which involve the separation of the aforementioned gases.

2.
Mult Scler Relat Disord ; 4(5): 406-408, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-26346788

RESUMO

UNLABELLED: Fingolimod is a potent drug in relapsing forms of multiple sclerosis. Visual impairment due to fingolimod-associated macular edema (FAME) usually leads to discontinuation of fingolimod therapy. METHODS: We report on a 24-year old woman with bilateral FAME. RESULTS: We continued fingolimod and added oral acetazolamide, which led to recovery of visual acuity and regression of macular edema. However, fingolimod had to be discontinued when fluorescein angiography revealed an enlarged foveal avascular zone. DISCUSSION AND CONCLUSION: Oral acetazolamide might be a treatment option for FAME, while ischemic conversion may be limiting. Ophthalmologic assessments are mandatory for follow-up when fingolimod therapy is continued after onset of FAME.


Assuntos
Acetazolamida/administração & dosagem , Cloridrato de Fingolimode/efeitos adversos , Imunossupressores/efeitos adversos , Edema Macular/induzido quimicamente , Edema Macular/tratamento farmacológico , Administração Oral , Feminino , Cloridrato de Fingolimode/uso terapêutico , Angiofluoresceinografia , Seguimentos , Fundo de Olho , Humanos , Imunossupressores/uso terapêutico , Edema Macular/patologia , Edema Macular/fisiopatologia , Esclerose Múltipla Recidivante-Remitente/tratamento farmacológico , Esclerose Múltipla Recidivante-Remitente/patologia , Esclerose Múltipla Recidivante-Remitente/fisiopatologia , Neurite Óptica/tratamento farmacológico , Neurite Óptica/patologia , Neurite Óptica/fisiopatologia , Acuidade Visual , Adulto Jovem
3.
Reprod Fertil Dev ; 25(6): 866-78, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-22953725

RESUMO

The European brown hare (Lepus europaeus) is the only species with superconception, whereby the maternal reproductive tract hosts two sets of conceptuses at different developmental stages. The embryonic development of the hare has not yet been described. To understand the mechanism of superconception, we studied oviduct transport and implantation stages by embryo flushing and live high-resolution ultrasound. Ultrasound data of implantation stages is correlated with histology. In the oviduct, a mucin coat is deposited on the zona pellucida. The blastocysts enter the uterine horns on Day 5, 1 day later than in the rabbit, and directly expand approximately threefold. Spacing is accompanied by peristaltic movement of the endometrium. The mucin coat disappears and the conceptuses attach. The yolk-sac expands in the blastocoel and syncytial knobs invade the antimesometrial endometrium. Maternal blood lacunae appear in the mesometrial endometrial folds, which are subsequently invaded by the syncytiotrophoblast. The haemochorial chorioallantoic placenta forms. The yolk-sac cavity is gradually replaced by the allantois and finally by the exocoel. The different reproductive strategies of the precocial hare and the altricial rabbit are discussed. We assume that the lagomorph-specific mucin coat and the hare-specific delay of the oviduct-uterine transition are prerequisites for superconception.


Assuntos
Blastocisto/fisiologia , Implantação do Embrião , Embrião de Mamíferos/fisiologia , Desenvolvimento Embrionário , Lebres/embriologia , Alantoide/diagnóstico por imagem , Alantoide/fisiologia , Animais , Animais Selvagens , Animais de Zoológico , Blastocisto/citologia , Blastocisto/diagnóstico por imagem , Embrião de Mamíferos/citologia , Embrião de Mamíferos/diagnóstico por imagem , Endométrio/citologia , Endométrio/diagnóstico por imagem , Endométrio/fisiologia , Tubas Uterinas/diagnóstico por imagem , Tubas Uterinas/fisiologia , Feminino , Alemanha , Mucinas/metabolismo , Placenta/diagnóstico por imagem , Placenta/fisiologia , Gravidez , Especificidade da Espécie , Trofoblastos/citologia , Trofoblastos/diagnóstico por imagem , Trofoblastos/fisiologia , Ultrassonografia , Saco Vitelino/citologia , Saco Vitelino/diagnóstico por imagem , Saco Vitelino/fisiologia , Zona Pelúcida/diagnóstico por imagem , Zona Pelúcida/metabolismo
4.
Oncogene ; 21(18): 2829-39, 2002 Apr 25.
Artigo em Inglês | MEDLINE | ID: mdl-11973642

RESUMO

H-rev107-1 is a growth inhibitory RAS target gene capable of suppressing anchorage independent growth in vitro and in vivo. Using a tumour tissue array with 241 matched tumour and normal tissue cDNA pools, we found down-regulation of H-REV107-1 in 7 out of 14 ovary-derived cDNAs. RT-PCR analysis and immunohistochemical investigation confirmed expression of H-REV107-1 in normal ovarian epithelial cells but down-regulation in high grade ovarian carcinomas. H-REV107-1 is also strongly expressed in immortalized rat and human ovarian epithelial cells in vitro, but suppressed in transformed cells by two different mechanisms. KRAS-transformed rat ovarian cells and PA1 teratocarcinoma cells, reversibly repress H-REV107-1 via MAP/ERK signaling. In contrast, treatment of A27/80 and OVCAR-3 epithelial ovarian cancer cells with IFNgamma stimulated H-REV107-1 expression. In NIH3T3 cells harbouring an estrogen-inducible IRF-1, H-rev107-1 is directly induced after activation of IRF-1, indicating that H-rev107-1 is a target of IRF-1. Stimulation of H-REV107-1 expression was also observed in ovarian epithelial cells suggesting that IRF-1 is involved in H-REV107-1 regulation in human ovarian epithelium. In the IFNgamma-sensitive cell line A27/80, H-REV107-1 suppresses colony formation. A27/80 and OVCAR-3 cells overexpressing H-REV107-1 protein underwent apoptosis. These results demonstrate down-regulation of the class II tumour suppressor H-REV107-1 in human ovarian carcinomas and suggest an involvement of H-REV107-1 in interferon-dependent cell death.


Assuntos
Proteínas de Ligação a DNA/metabolismo , Genes Supressores de Tumor/fisiologia , Interferon gama/metabolismo , Fosfoproteínas/metabolismo , Proteínas/genética , Proteínas Supressoras de Tumor/genética , Células 3T3 , Animais , Morte Celular , Proteínas de Ligação a DNA/genética , Regulação para Baixo , Feminino , Regulação Neoplásica da Expressão Gênica , Humanos , Fator Regulador 1 de Interferon , Interferon gama/farmacologia , Peptídeos e Proteínas de Sinalização Intracelular , Camundongos , Neoplasias Ovarianas , Fosfolipases A2 Independentes de Cálcio , Fosfoproteínas/genética , Ratos , Células Tumorais Cultivadas
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