Cyclic Nigerosyl-Nigerose as Oxygen Nanocarrier to Protect Cellular Models from Hypoxia/Reoxygenation Injury: Implications from an In Vitro Model

Heart failure (HF) prevalence is increasing among the aging population, and the mortality rate remains unacceptably high despite improvements in therapy. Myocardial ischemia (MI) and, consequently, ischemia/reperfusion injury (IRI), are frequently the basis of HF development. Therefore, cardioprotective strategies to limit IRI are mandatory. Nanocarriers have been proposed as alternative therapy for cardiovascular disease. Controlled reoxygenation may be a promising strategy. Novel nanocarriers, such as cyclic nigerosyl-nigerose (CNN), can be innovative tools for oxygen delivery in a controlled manner. In this study we analyzed new CNN-based formulations as oxygen nanocarriers (O₂-CNN), and compared them with nitrogen CNN (N₂-CNN). These different CNN-based formulations were tested using two cellular models, namely, cardiomyoblasts (H9c2), and endothelial (HMEC) cell lines, at different concentrations. The effects on the growth curve during normoxia (21% O₂, 5% CO₂ and 74% N₂) and their protective effects during hypoxia (1% O₂, 5% CO₂ and 94% N₂) and reoxygenation (21% O₂, 5% CO₂ and 74% N₂) were studied. Neither O₂-CNN nor N₂-CNN has any effect on the growth curve during normoxia. However, O₂-CNN applied before hypoxia induces a 15–30% reduction in cell mortality after hypoxia/re-oxygenation when compared to N₂-CNN. O₂-CNN showed a marked efficacy in controlled oxygenation, which suggests an interesting potential for the future medical application of soluble nanocarrier systems for MI treatment.     

Process optimization via confidence region: a case study from micro-injection molding

Journal of Intelligent Manufacturing - In industrial research, experiments are designed to determine the optimal factor levels of the process parameters. Typically, experimental data are used to...     

Nitro derivatives of PEEK‐WC

Nitrated poly(oxa‐p‐phenylene‐3,3‐phthalido‐p‐phenylene‐oxa‐p‐phenylene‐ oxy‐phenylene) (PEEK‐WC) with various average degrees of substitution was obtained by reaction with several nitrating agents. By working under controlled reaction conditions, little degradation of the parent polymer is observed. The nitro derivatives of PEEK‐WC show a high thermal stability, and are able to form membranes by means of phase inversion technique. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1037–1045, 2001     

Proton conducting membranes based on sulfonated PEEK-WC polymer for PEMFCs

Proton conducting membranes have been prepared from chloro-sulfonated polyetheretherketone with cardo group polymers at various sulfonation degree via casting solutions using dimethylformamide as a solvent. The proton conductivity of sulfonated polyetheretherketone with cardo group membranes has been evaluated in the temperature range between 80 and 120 °C and the best result of this work has been achieved at 120 °C and sulfonation degree equal to 60% with a value equal to 6.7·10⁻² S/cm. Furthermore, this sample shows an open circuit voltage varying from 0.881 V at 80 °C to 0.867 V at 120 °C, pointing out that the membrane performance is not greatly affected by a temperature variation. Nevertheless, an increase of temperature from 80 to 120 °C makes possible an increase of the cell resistance varying from 0.17 to 0.24 Ω cm². Thus, the present study investigates the performance of sulfonated polyetheretherketone with cardo group membranes in terms of polarization curves, open circuit voltage, cell resistance and proton conductivity in order to propose them for proton exchange membrane fuel cell applications, particularly at T > 100 °C.     

TLS/FUS, a pro-oncogene involved in multiple chromosomal translocations, is a novel regulator of BCR/ABL-mediated leukemogenesis

The leukemogenic potential of BCR/ABL oncoproteins depends on their tyrosine kinase activity and involves the activation of several downstream effectors, some of which are essential for cell transformation. Using electrophoretic mobility shift assays and Southwestern blot analyses with a double-stranded oligonucleotide containing a zinc finger consensus sequence, we identified a 68 kDa DNA-binding protein specifically induced by BCR/ABL. The peptide sequence of the affinity-purified protein was identical to that of the RNA-binding protein FUS (also called TLS). Binding activity of FUS required a functional BCR/ABL tyrosine kinase necessary to induce PKCbetaII-dependent FUS phosphorylation. Moreover, suppression of PKCbetaII activity in BCR/ABL-expressing cells by treatment with the PKCbetaII inhibitor CGP53353, or by expression of a dominant-negative PKCbetaII, markedly impaired the ability of FUS to bind DNA. Suppression of FUS expression in myeloid precursor 32Dcl3 cells transfected with a FUS antisense construct was associated with upregulation of the granulocyte-colony stimulating factor receptor (G-CSFR) and downregulation of interleukin-3 receptor (IL-3R) beta-chain expression, and accelerated G-CSF-stimulated differentiation. Downregulation of FUS expression in BCR/ABL-expressing 32Dcl3 cells was associated with suppression of growth factor-independent colony formation, restoration of G-CSF-induced granulocytic differentiation and reduced tumorigenic potential in vivo. Together, these results suggest that FUS might function as a regulator of BCR/ABL leukemogenesis, promoting growth factor independence and preventing differentiation via modulation of cytokine receptor expression.     

Effect of carboxylic acids on permeation of chlorpromazine through dimethyl polysiloxane membrane

The effect of carboxylic acids on the permeation of chlorpromazine was investigated through a dimethyl polysiloxane nonpolar membrane. The permeability of the diffusate, at pH 5.8, increases considerably in the presence of carboxylic acids or phosphate, probably due to an ion-pair formation between the relative anions and chlorpromazine.     

Minimization of combined sewer overflows by large-scale mathematical programming

There is a critical need for the development and implementation of control strategies for minimizing receiving water pollution caused by overflows from urban combined sewer systems. Automation and control of such systems has risen as a viable approach to this problem. Control is carried out through regulation of ambient and/or auxiliary storage in the system. The goal is to detain storm flows in the system long enough to prevent flows of a magnitude that exceeds treatment plant capacity, thereby reducing overflow into receiving waters. The problem is first attacked by dividing the large combined sewer system into several mildly interconnected subsystems for which control logic can be developed from application of mathematical programming algorithms consistent with the special characteristics of each subsystem. A flow-projection technique is developed for subsystems not amenable to direct solution by standard optimization techniques.     

New Technology for Preventing Residential Electrical Fires: Arc-Fault Circuit Interrupters (AFCIs)

A new generation of residential electrical branch circuit breakers that incorporates technology to detect and mitigate the effects of arcing faults is described. Fire loss estimates attributed to electrical wiring and the development of the arc-fault circuit interrupter for the prevention of residential electrical fires are discussed. The industry voluntary standard for arc-fault circuit interrupters as well as the 1999 National Electrical Code requirement are reviewed.     

Electrochemical characterization of sulfonated PEEK-WC membranes for PEM fuel cells

Sulfonated PEEK-WC polymer was obtained according to chloro-sulfonic acid procedure making possible the preparation of different membrane samples with a sulfonation degree from 48 to 90%. Dense membranes were prepared from casting solutions of S-PEEK-WC dissolved in DMF. Proton conductivity measurements were performed on such S-PEEK-WC membranes in a range of temperature from 30 to 120 °C and 100% of relative humidity, reaching 2.5 × 10⁻² S cm⁻¹ as the best value at 100 °C and with a sulfonation degree of 90%. In the meanwhile, the open circuit voltage of this S-PEEK-WC membrane (DS = 90%) varied from 0.963 V at 60 °C to 0.802 V at 100 °C, demonstrating that an increase of temperature negatively affects the membrane performance due to the mechanical properties degradation. In this work, a wide experimental campaign was carried out to investigate the electrochemical performances in terms of polarization curves, open circuit voltage and proton conductivity of S-PEEK-WC membranes as well as the fuel crossover and water uptake.     

Vitamin A palmitate photostability and stability over time

Vitamin A palmitate photostability in relation to ultravoilet A (UVA) and ultravoilet B (UVB) was tested in hydroxy ethyl cellulose hydrogels at pH 4.0, 5.6, 7.0, and 8.0, alone and with the addition of sunscreens (3,4‐methylbenzilidencamphor or butyl methoxy dibenzoylmethane) or an antioxidant (butylated hydroxy toluene). The photostability of vitamin A palmitate was also tested in encapsulated systems (Tagravit_A1 microcapsules, Lipotec_liposomes, phosphatidylcholine liposomes, and Lipotec_nanocapsules) dispersed in gels at pH 5.6 and 7.0. The stability of retinyl palmitate over time in hydroxy ethyl cellulose hydrogels at pH 5.6 and 7.0 (stored 1 month at 25 or 40 °C), alone or with butylated hydroxy toluene, was also tested. The stability of retinyl palmitate over time in encapsulated systems, dispersed in gels at pH 5.6 and 7.0, was also studied. O/W emulsions were also prepared to compare the stability of vitamin A palmitate introduced in a lipophilic/hydrophilic medium (O/W emulsions) and a hydrophilic medium (hydrogels). HPLC analysis showed that encapsulated systems such as Lipotec_nanocapsules, Tagravit_A1 microcapsules, phosphatidylcholine liposomes, and Lipotec_liposomes protect the vitamin A ester over time from hydrolysis and from oxidation to retinaldeide and retinoic acid, and that Lipotec_nanocapsules and phosphatidylcholine liposomes also improve the vitamin's photostability. A change in pH (5.6–7.0) of the gels did not influence the vitamin ester's stability. pH levels of 4.0 and 8.0 determined a decrease in the stability of retinyl palmitate in the gels. A high concentration of sunscreens improved the photostability of retinyl palmitate in the gels at pH 5.6 and 7.0. Butylated hydroxy toluene protected retinyl palmitate from degradation induced by light at all the pH levels studied and by heat at pH 5.6 and 7.0, as can be seen from the study of the photostability of vitamin A palmitate under UVB and UVA and of stability over time. Rheological studies showed a slight decrease in the viscosity of the gels after UVB–UVA irradiation and a higher decrease in the viscosity of the gels and the emulsions after storage at 25 and 40°C. This decrease can be attributed to a partial degradation of hydroxy ethyl cellulose and of emulsifier, as can be seen from the decrease in shear stress versus shear rate values under these conditions of storage, denoting a depolymerization of the rheological modifier.