Effect of draw ratio on fiber structure development of polyethylene terephthalate

Fiber properties are decided by its structure, and the structure are mainly formed in the fiber drawing process. In this study, the effects of the draw ratio on the fiber structure development of polyethylene terephthalate after continuous neck-drawing were investigated using simultaneous WAXD/SAXS measurements. Low-oriented amorphous as-spun fibers were drawn to a draw ratio of 3.0-4.5, at which the fiber can be stably neck drawn. WAXD and SAXS images were obtained up to 2.0 ms when the structure was mainly developed. The smectic (0010) diffraction intensity and long period increased with increasing draw ratio up to 4.2, and a larger (0010) diffraction d-spacing was observed at a draw ratio of 4.5. The results suggest that more fibrillar structures were formed with increasing draw ratio up to 4.2, and more constrained molecular bundles were formed at a draw ratio of 4.5. A larger amount of constrained fibrillar structures can bear a greater tensile force in tensile tests, therefore the drawn fibers have higher tensile strengths. (C) 2017 Elsevier Ltd. All rights reserved.ArticlePOLYMER.116:357-366(2017)journal articl

Effect of melt spinning conditions on the fiber structure development of polyethylene terephthalate

The effects of spinning conditions on fiber properties are not well explained by the fiber structures because the birefringence, crystallinity, and SAXS patterns are often similar. In this study, the effects on the fiber structure development of polyethylene terephthalate after necking was analyzed by simultaneous WAXD/SAXS measurements. An X-shaped SAXS pattern was observed for all fibers drawn at the minimum draw ratio. In contrast, by drawing under a drawing stress of 100 MPa, the strong diffraction of the smectic phase and an obviously larger long period less than 1 ms after necking were observed for fibers spun at 500-1500 m/min, while almost no smectic phase was observed for fibers spun at 2000 m/min. A higher crystallization rate and clear draw ratio dependence of crystallization rate were also observed for the fiber spun at 2000 m/min. The clear differences in structure development can explain their differences in tensile strength and thermal shrinkage. (C) 2017 Elsevier Ltd. All rights reserved.ArticlePOLYMER.116:367-377(2017)journal articl

Periodate-treated, non-anticoagulant heparin-carrying polystyrene (NAC-HCPS) affects angiogenesis and inhibits subcutaneous induced tumour growth and metastasis to the lung

Periodate-treated, non-anticoagulant heparin-carrying polystyrene consists of about ten periodate-oxidized, alkaline-degraded low molecular weight-heparin chains linked to a polystyrene core and has a markedly lower anti-coagulant activity than heparin. In this study, we evaluated the effect of non-anticoagulant heparin-carrying polystyrene on tumour growth and metastasis. Non-anticoagulant heparin-carrying polystyrene has a higher activity to inhibit vascular endothelial growth factor-165-, fibroblast growth factor-2- or hepatocyte growth factor-induced human microvascular endothelial cell growth than heparin, ten periodate-oxidized-heparin and ten periodate-oxidized-low molecular weight-heparin, which is probably due to the heparin-clustering effect of non-anticoagulant heparin-carrying polystyrene. Non-anticoagulant heparin-carrying polystyrene inhibited human microvascular endothelial cell, B16 melanoma and Lewis lung cancer cell adhesion to Matrigel-coated plates. Non-anticoagulant heparin-carrying polystyrene also showed strong inhibitory activities in the tubular formation of endothelial cells on Matrigel and B16-melanoma and Lewis lung cancer cell invasion in a Matrigel-coated chamber assay. In vivo studies showed that growth of subcutaneous induced tumours and lung metastasis of B16-melanoma and Lewis lung cancer cells were more effectively inhibited by non-anticoagulant heparin-carrying polystyrene than ten periodate-oxidized-heparin and ten periodate-oxidized-low molecular weight-heparin. Furthermore, non-anticoagulant heparin-carrying polystyrene markedly reduced the number of CD34-positive vessels in subcutaneous Lewis lung cancer tumours, indicating a strong inhibition of angiogenesis. These results suggest that non-anticoagulant heparin-carrying polystyrene has an inhibitory activity on angiogenesis and tumour invasion and may be very useful in cancer therapy

Identification of human renal cell carcinoma associated genes by suppression subtractive hybridization

Renal cell carcinoma (RCC) are frequently chemo- and radiation resistant. Thus, there is a need for identifying biological features of these cells that could serve as alternative therapeutic targets. We performed suppression subtractive hybridization (SSH) on patient-matched normal renal and RCC tissue to identify variably regulated genes. 11 genes were strongly up-regulated or selectively expressed in more than one RCC tissue or cell line. Screening of filters containing cancer-related cDNAs confirmed overexpression of 3 of these genes and 3 additional genes were identified. These 14 differentially expressed genes, only 6 of which have previously been associated with RCC, are related to tumour growth/survival (EGFR, cyclin D1, insulin-like growth factor-binding protein-1 and a MLRQ sub-unit homologue of the NADH:ubiquinone oxidoreductase complex), angiogenesis (vascular endothelial growth factor, endothelial PAS domain protein-1, ceruloplasmin, angiopoietin-related protein 2) and cell adhesion/motility (protocadherin 2, cadherin 6, autotaxin, vimentin, lysyl oxidase and semaphorin G). Since some of these genes were overexpressed in 80–90% of RCC tissues, it is important to evaluate their suitability as therapeutic targets. © 2001 Cancer Research Campaig

Establishment of canine hemangiosarcoma xenograft models expressing endothelial growth factors, their receptors, and angiogenesis-associated homeobox genes

<p>Abstract</p> <p>Background</p> <p>Human hemangiosarcoma (HSA) tends to have a poor prognosis; its tumorigenesis has not been elucidated, as there is a dearth of HSA clinical specimens and no experimental model for HSA. However, the incidence of spontaneous HSA is relatively high in canines; therefore, canine HSA has been useful in the study of human HSA. Recently, the production of angiogenic growth factors and their receptors in human and canine HSA has been reported. Moreover, the growth-factor environment of HSA is very similar to that of pathophysiological angiogenesis, which some homeobox genes regulate in the transcription of angiogenic molecules. In the present study, we established 6 xenograft canine HSA tumors and detected the expression of growth factors, their receptors, and angiogenic homeobox genes.</p> <p>Methods</p> <p>Six primary canine HSAs were xenografted to nude mice subcutaneously and serially transplanted. Subsequently, the expressions of vascular endothelial growth factor (VEGF)-A, basic fibroblast growth factors (bFGF), flt-1 and flk-1 (receptors of VEGF-A), FGFR-1, and angiogenic homeobox genes HoxA9, HoxB3, HoxB7, HoxD3, Pbx1, and Meis1 were investigated in original and xenograft tumors by histopathology, immunostaining, and reverse transcription polymerase chain reaction (RT-PCR), using canine-specific primer sets.</p> <p>Results</p> <p>Histopathologically, xenograft tumors comprised a proliferation of neoplastic cells that were varied in shape, from spindle-shaped and polygonal to ovoid; some vascular-like structures and vascular clefts of channels were observed, similar to those in the original tumors. The expression of endothelial markers (CD31 and vWF) was detected in xenograft tumors by immunohistochemistry and RT-PCR. Moreover, the expression of VEGF-A, bFGF, flt-1, flk-1, FGFR-1, HoxA9, HoxB3, HoxB7, HoxD3, Pbx1, and Meis1 was detected in xenograft tumors. Interestingly, expressions of bFGF tended to be higher in 3 of the xenograft HSA tumors than in the other tumors.</p> <p>Conclusion</p> <p>We established 6 xenograft canine HSA tumors in nude mice and found that the expressions of angiogenic growth factors and their receptors in xenograft HSAs were similar to those in spontaneous HSA. Furthermore, we detected the expression of angiogenic homeobox genes; therefore, xenograft models may be useful in analyzing malignant growth in HSA.</p

Exploitation of uncertain weather forecast data in power network management

In power network management, the heat capacity of transmission lines originally arises from the line temperature constraint. The line temperatures are affected not only by the Joule heat but also by the thermal environment. This motivates us to exploit weather forecast data to improve the power management performance. The goal of this paper is to propose a stochastic model predictive control scheme for this purpose. In particular, we compensate for the probabilistic uncertainty by means of chance constraint optimization. The effectiveness of the proposed control scheme is examined through numerical simulation of power grids under the area dependent uncertainty and transmission line failure