Synthesis and characterization of poly(propylene terephthalate/2,6-naphthalate) random copolyesters

Poly(propylene terephthalate/2,6-naphthalate) random copolyesters (PPT-PPN) were synthesized and characterized from the molecular and thermal point of view. All the polymers showed a good thermal stability. The main effect of copolymerization was a lowering in the crystallinity and a decrease of T_m respect to homopolymers. WAXD measurements indicated that PPT-PPN copolymers are characterized by isodimorphic cocrystallization. The defect free energies, calculated on the basis of the inclusion model proposed by Wendling and Suter, indicated that the amount of PT units incorporated in the poly(propylene 2,6-naphthalate) (PPN) β crystals is higher than the amount of PN units which cocrystallizes in the poly(propylene terephthalate) (PPT) crystalline phase, probably due to the larger molar volume of PN units compared to PT ones. Amorphous samples showed a monotonic increment of T_g as the content of PN units is increased, due to the stiffening effect of naphthalene rings in the chain. Finally, the Fox equation described well the T_g-composition data.     

New catalysts for poly(butylene terephthalate) synthesis. Part 3: effect of phosphate co-catalysts

An exhaustive study of the co-catalytic activity of phosphates on titanium and titanium/hafnium based catalytic systems in poly(butylene terephthalate) synthesis was conducted in order to investigate any improvement in the process and/or in the properties of the final polymer with respect to the industrially used titanium based catalyst. Small scale polymerisation and subsequent scale up in higher capacity reactors showed a strong co-catalytic effect of phosphates. A screening on model compounds showed NaH₂PO₄ to be the most active co-catalyst. The co-catalysts had a stronger effect on titanium with respect to hafnium. Decreases in polymerisation time and tetrahydrofuran formation were observed, which in turn can improve the productivity of the whole process. Moreover, the use of phosphate improved the thermal stability of the final polymers.     

Endothelial-dependent dynamic and antithrombotic properties of porcine aortic and pulmonary valves

BACKGROUND: In the present study, the endothelium-dependent antithrombotic and dynamic properties of porcine aortic (AoV) and pulmonary valves (PuV) were investigated. METHODS: Fifteen fresh AoV and 15 fresh PuV were obtained from 25 9-month-old swines. The valves were examined for endothelial function by pharmacologic evaluation (with and without endothelium) of both the endothelial-releasing capacity of prostacyclin and the endothelial-dependent dynamic response to relaxing (acetylcholine from 10[-10] mol/L to 10[-4] mol/L in AoV and PuV segments precontracted with norepinephrine [3 x 10(-6) mol/L]) and contracting (endothelin-1, from 10[-11] mol/L to 10[-5] mol/L; and NG-monomethyl-L-arginine, 10[-4] mol/L) drugs. The ultrastructural integrity of the endothelial valve layer was also examined with transmission electron microscopy. RESULTS: Acetylcholine caused potent relaxation in both AoV and PuV specimens with, but not in those without, endothelium. Endothelin-1 produced a concentration-dependent tension increase in AoV and PuV with and without endothelium. However, the intrinsic activity of the peptide significantly increased in tissues without endothelium. NG-monomethyl-L-arginine evoked a progressive increase in resting tension of the preparations, but the AoV and PuV without endothelium were less sensitive to the inhibition of the nitric oxide generation. Aortic and pulmonary valves with an intact endothelium showed a spontaneous ability to release prostacyclin. The basal release of this lipidic autacoid significantly decreased in cardiac valves without endothelium. This phenomenon was observed in both basal conditions, and under stimulation with the aforementioned drugs. Transmission electron microscopy showed the perfect preservation of endothelial cells in all the preparations examined. CONCLUSIONS: Valvular endothelium of AoV and PuV seems to have similar antithrombotic and dynamic functions of vascular endothelium, actively participating in valvular homeostasis.     

The role of the V/III ratio in the growth and structural properties of metalorganic vapor phase epitaxy GaAs/Ge heterostructures

GaAs epitaxial layers have been grown on (001) 6† off-oriented toward (110) Ge substrates by metalorganic vapor phase epitaxy. In order to study the influence of V/III ratio on the growth mechanisms and the structural properties of the layers, the input flow of arsine was changed over a wide range of values, while keeping constant all other experimental settings. Optical microscopy in the Nomarski contrast mode, x-ray topography and high resolution diffractometry, transmission electron microscopy and Rutherford backscattering have been used to investigate the epilayers. It has been found that the growth rate increases and the surface morphology worsens with increasing V/III ratio. The abruptness of the layer-substrate interface has also been found to strongly depend on the V/III ratio, the best results being obtained under Ga-rich conditions. The main structural defects within the layers are stacking faults and misfit dislocations. Layers grown under As-rich conditions only contain stacking faults, probably originated by a growth island coalescence mechanism, whereas layers grown under Ga-rich conditions contain both misfit dislocations and stacking faults generated by dissociation of threading segments of interfacial dislocations. In spite of the different defects, the strain relaxation has been found to follow the same trend irrespective of the V/III ratio. Finally, the relaxation has been found to start at a thickness exceeding the theoretical critical value.     

NM23 gene expression in human breast carcinomas: loss of correlation with cell proliferation in the advanced phase of tumor progression

NM23 is a protein associated with tumor progression, expressed in all tissues and in human tumors. Reduced expression of NM23.H1 is related to high incidence of lymph node and distant metastasis or to poor prognosis of the patient in several human malignant tumors. In this study we analyze NM23 expression in non-neoplastic mammary tissues surrounding the tumoral lesions, in human mammary carcinomas and in lymph node metastasis. Our analysis shows that NM23.H1 expression is lower in the mammary cells surrounding the tumor than in the tumor itself. In the primary tumors we observed a negative trend between degree of local invasion and level of NM23.H1 expression. A further decrease of NM23.H1 was detected in the invasive tumors that metastasized to axillary lymph nodes and in the metastasis. NM23.H2 was always more highly expressed than NM23.H1, and reduced expression of NM23.H1 but not NM23.H2 was concordant with the presence of lymph node metastasis or local invasiveness of the primary tumor. A positive correlation between NM23.H1 mRNA content and cell growth rate of breast tumor cells has been confirmed. However, this trend was not maintained in cancer cells from tumors that metastasized to axillary lymph nodes and in metastatic cells; in these 2 situations the NM23.H1 mRNA content varied without any relationship to the proliferative rate of the cells. In addition, in comparison with the initial tumor, the metastatic cell population showed a strong decrease of NM23.H1 expression and increased proliferative activity.     

Novel three-dimensional cocoon-like hydrogels for soft tissue regeneration

Large three-dimensional hydrogels (> 150 cm³) of bacterial cellulose (BC) were synthesized by using Gluconacetobacter hansenii ATCC 23769 under controlled agitated culture conditions. The macroscopic cocoon-like structures are gelatinous and translucent and may find applications in several areas, particularly in tissue and organ engineering. Internal microstructure was investigated by scanning electron microscopy (SEM) and field emission scanning electron microscopy (FESEM), which revealed that the cocoons are composed of cellulosic nanofibres randomly and three-dimensionally dispersed. The macroscopic bodies are delimited by a dense semi-permeable membrane with thickness between 0.2 and 2 mm, also composed of cellulosic nanofibres. Endothelial cells were seeded on the hydrogels and incubated for 7 days. HUVECs grew and migrated into the inner part of the structure. The three-dimensional BC hydrogel structures can be directly implanted in tissue deficient regions as scaffolds containing the appropriate cultured cells.     

Ultrastructure and distribution of superficial neuromasts of blind cavefish,Phreatichthys andruzzii,juveniles

Transmission and scanning electron microscopy (TEM, SEM) were used to study the ultrastructure of superficial neuromasts in 15 six-month old blind cavefish juveniles, Phreatichthys andruzzii (Cyprinidae). In five specimens examined with SEM, the number of superficial neuromasts over the fish body (480–538) was recorded. They were localized mainly on the head (362–410), including the dorsal surface, the mentomandibular region, and laterally from the mouth to the posterior edge of the operculum. Neuromasts were also present laterally on the trunk and near the caudal fin (116–140). A significantly higher number of neuromasts were present on the head compared to the trunk (t-test, P < 0.05). Superficial neuromasts of the head and those along the trunk were similar in ultrastructure. Each neuromast comprised sensory hair cells surrounded by nonsensory support cells (mantle cells and supporting basal cells) with the whole covered by a cupula. Each hair cell was pear-shaped, 15–21 μm high and 4–6 μm in diameter, with a single long kinocilium and several short stereocilia. Most support cells were elongated, with nuclei occupying a large portion of the cytoplasm. In the margin of the neuromast, mantle cells were particularly narrow. Both types of support cells had well-developed Golgi apparatus and rough endoplasmic reticulum. The number of hair cells and nonsensory support cells of the anterior lateral line (head) did not differ significantly from those of the posterior lateral line (trunk) (t-test, P > 0.05). Microsc. Res. Tech. 2009. © 2009 Wiley-Liss, Inc.     

Chromatographic determination of angiotensin-converting enzyme and angiotensinase activity

An analytical method utilizing an automatic amino acid analyzer is described for the separation, identification, and measurement of 5 to 50 nmol of angiotensin I, angiotensin II, [Des-Phe8]angiotensin II, Phe-His-Leu, His-Leu, isoleucine, leucine, tyrosine, and phenylalanine. Aminex A-5 cation-exchange resin (0.9 x 15 cm) is sequentially eluted with three sodium citrate buffers: pH 3.25, 0.2 N; pH 4.85, 0.54 N, and pH 6.5, 0.39 N at 60 and 80 degrees C. Reaction with ninhydrin is used for detection. This chromatographic system was used to determine angiotensin-converting enzyme activity and the angiotensinase activity of rabbit brain endopeptidase B. In each assay, the unhydrolyzed substrate and both products were measured simultaneously in one step without pretreatment of the hydrolysate. Products were recovered in 1:1 molar ratios and the overall recovery of an hydrolyzed substrate of products was quantitative.