Proton exchange membranes by radiation grafting of styrene onto fep films. III. Structural investigation

Structural investigation on proton-exchange membranes, obtained by the radiation grafting of styrene onto FEP films and subsequent sulfonation, was carried out by differential scanning calorimetry. The membrane crystallinity was found to show a decreasing trend with increasing degree of grafting. The melting temperature of all the membranes also showed a slight decrease as compared to the ungrafted FEP. The results have been explained in terms of the cumulative effect of the decrease in the crystalline/amorphous ratio by the incorporation of amorphous polystyrene grafts and of disruption of spherulitic crystallites of the FEP component in the membranes. The glass transition temperature of the membranes with different water contents was also evaluated. A correlation of the glass transition temperature with the residual water in dried membranes was established. © 1994 John Wiley & Sons, Inc.     

Ein elektrisches Me\verfahren zur Integral- und Mittelwertbestimmung

Zusammenfassung Die beschriebene Me\anordnung gestattet, den Integralwert eines beliebigen. Kurvenverlaufes zu messen. Die für die jeweilige Ordinate der Kurven ma\gebenden Grö\en, z. B. Druck, Geschwindigkeit usw. werden vermittels eines verÄnderlichen Widerstandes in verhÄltnisgleiche Leitwerte umgesetzt. Der jeweilige Leitwert des Widerstandes ist bestimmend für die Geschwindigkeit der Teilentladung eines Kondensators. Die Summe der aufeinanderfolgenden Ladungs- bzw. Entladungsstö\e innerhalb einer gewissen Zeit gibt ein Ma\ für den Integralwert des Vorganges wÄhrend derselben Zeit. Die mittlere sekundliche Wechselzahl bestimmt den Mittelwert des Verlaufes. Die Anlegung einer zeitabhÄngigen Betriebsspannung an den Kondensatorkreis ermöglicht eine Kompensation des ursprünglich zeitbedingten Charakters der Ergebnisse und lÄ\t sonach auch die Integration zeitunabhÄngiger KurvenverlÄufe zu. Eine überlagung der resultierenden Frequenz bzw. Spannung mit anderen Einflu\grö\en bietet die Möglichkeit der Messung von VorgÄngen, die von mehreren Faktoren bestimmt sind.     

Overview of randomized trials of intravenous heparin in patients with acute myocardial infarction treated with thrombolytic therapy

Intravenous heparin is routinely given after thrombolytic therapy for patients with acute myocardial infarction in the United States and in some, but by no means all, other countries. Several trials have documented improved infarct-artery patency in patients treated with heparin; however, none was large enough individually to assess the effect of heparin on clinical outcomes. We performed a systematic overview of the 6 randomized controlled trials (1,735 patients) to summarize the available data concerning the risks and benefits of intravenous heparin versus no heparin after thrombolytic therapy. Mortality before hospital discharge was 5.1% for patients allocated to intravenous heparin compared with 5.6% for controls (relative risk reduction of 9%, odds ratio 0.91, 95% confidence interval 0.59 to 1.39). Similar rates of recurrent ischemia and reinfarction were observed among those allocated to heparin therapy or control. The rates of total stroke, intracranial hemorrhage, and severe bleeding were similar in patients allocated to heparin; however, the risk of any severity of bleeding was significantly higher (22.7% vs 16.2%; odds ratio 1.55, 95% confidence interval 1.21 to 1.98). There was no significant difference in the observed effects of heparin between patients receiving tissue-type plasminogen activator and those receiving streptokinase or anisoylated plasminogen streptokinase activator complex, or between patients who did and did not receive aspirin. The findings of this overview demonstrate that insufficient clinical outcome data are available to support or to refute the routine use of intravenous heparin therapy after thrombolysis. It is not known if these findings are due to lack of statistical power, inappropriate levels of anticoagulation, or lack of benefit of intravenous heparin. Large randomized studies of heparin (and of new antithrombotic regimens) are needed to establish the role of such therapy.     

Gelatinases in drug-induced toxic epidermal necrolysis

BACKGROUND: The matrix metalloproteinases (MMPs) MMP2 and MMP9 play a significant role in epidermal detachment, inflammation and re-epithelialization. We have evaluated their activity in toxic epidermal necrolysis (TEN). DESIGN: The level and pattern of activity of MMP2 and MMP9 were investigated by measuring the degradation of 3H-labelled gelatin and by zymography in blister fluid from six TEN patients and compared the results with three other blistering conditions: bullous pemphigoid (n = 6), second-degree burn (n = 13) or suction blister (n = 3). RESULTS: A higher amount of MMP2 was found in TEN blister fluid with the constant presence of a significantly larger proportion of the activated forms of MMP2, a particular feature of TEN, than the other blistering diseases studied. CONCLUSION: This study emphasizes the potential role of MMP2 in the specific inflammatory reaction and reparation process in TEN skin.     

Expression of 72-kDa gelatinase (matrix metalloproteinase-2) in the developing mouse craniofacial complex

Tissue remodelling is an important feature during embryogenesis. Although the matrix metalloproteinases are believed to participate in these processes, the relation between matrix metalloproteinases and tissue remodelling during craniofacial morphogenesis remains unclear. The purpose of the study was to look for the presence of enzymes involved in extracellular matrix degradation during craniofacial morphogenesis. Protein expression of the matrix metalloproteinase, 72-kDa gelatinase (matrix metalloproteinase-2, gelatinase A, 72-kDa type IV collagenase) was studied by gelatine zymography and by indirect immunofluorescence with conventional and confocal microscopy. In the anterior region of the developing mouse face, 72-kDa gelatinase was labelled mainly in the tips and peripheral regions of the nasal and facial prominences. Upon contact and fusion of the prominences, the staining was intensely localized to the zone of the fusion and the tips and peripheral regions of the nasal prominences and the maxilla. The labelling of 72-kDa gelatinase was also present in the peripheral regions of the mandible, second branchial arch, and the face around the developing eye. However, during lens vesicle formation, the staining of 72-kDa gelatinase was absent in the invaginated lens ectoderm. After the lens had completely detached from the surface ectoderm, the staining was resumed in the corneal epithelium and mesenchyme. Gelatine zymography was used to confirm the presence of active and latent 72-kDa gelatinase in the developing mouse craniofacial complex. Collectively, these data indicate that 72-kDa gelatinase may play a significant part in localized tissue remodelling during craniofacial morphogenesis and the aberrant expression or function of the enzyme could be involved in causing facial abnormalities.     

T cell response to two immunodominant proteolipid protein (PLP) peptides in multiple sclerosis patients and healthy controls

Despite the fact that the neuroleptic drugs have been widely used for more than 40 years, one of their most common side-effects, akathisia, has been relatively neglected. There are still no universally agreed diagnostic criteria for akathisia, particularly chronic akathisia, and in this review article, we discuss the controversies surrounding the voluntary nature of its motor features and the importance of the dysphoric component. We also review the published epidemiological studies to show the great variation in frequency of occurrence. Finally, we discuss the possible neurotransmitters involved in the pathophysiology and treatment of this condition.