Lesbian families: Clinical issues and theoretical implications.

Examines the influence of lesbian family structure on parenting within the context of both psychodynamic and family systems theories by providing a review of the literature, as well as information based on the author's clinical work with lesbians and their families. The uniqueness of the lesbian family is considered, and the varieties of lesbian family structure are outlined (e.g., blended, single parent, couples having children together, donors, and noncustodial fathers). The impact of parenting is discussed in terms of common issues in lesbian distance and boundary regulation, power/equality, shared parenting, relationships with extended families, lesbian friendship networks, and issues unique to lesbian "divorce." (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

On the Nature and Location of Organic Template Molecules and Their Effect on the Stability and Redox Properties of Microporous CoAlPO-34 Catalyst

Small-pore CoAlPO-34 materials were synthesized with a variety of organic template molecules and were characterized in detail, employing microcrystal diffraction, powder diffraction and in situ combined XRD/XAS techniques. We found that, when two template molecules or two nitrogen atoms of a single template molecule are present inside the chabazitic cage, the concentration of cobalt present in the system is ca. 25?at%, which introduces instability in the framework structure during the removal of the organic template. In contrast, when only one template molecule is present, it is possible to control the concentration of Co(II) ions in the framework to ca. 10?at%; these systems show good structural integrity and redox chemistry that was exploited for the regio-selective conversion of linear alkane molecules.     

Benzene-induced hydro(solvo)thermal synthesis of Cu and Zn coordination polymers based on 1,3-benzenedicarboxylate

Hydro(solvo)thermal reactions of Cu(NO₃)₂·2.5H₂O or Zn(NO₃)₂·6H₂O with 1,3-H₂bdc provided two structurally different coordination polymers; a 2D network “metallacalixarene” based on the paddlewheel-type cluster with the formula [Cu(1,3-bdc)·H₂O]·H₂O (1) and a 3D framework [Zn(1,3-bdc)] (2), respectively. The use of a base was unnecessary in this synthesis; however, the presence of benzene played a crucial role in the crystallization of the desired products and could act as a template molecule in the synthesis of polymer (1). The unsaturated apical sites in the Cu₂ cluster of polymer (1) were occupied by water molecules, what consequently led to the structural decomposition of the framework after exposing the sample in air, which was not the case of the Zn-coordination polymer (2).     

Targeted luminescent near-infrared polymer-nanoprobes for in vivo imaging of tumor hypoxia

Polystyrene nanoparticles (PS-NPs) were doped with an oxygen-sensitive near-infrared (NIR)-emissive palladium meso-tetraphenylporphyrin and an inert reference dye which are both excitable at 635 nm. The nanosensors were characterized with special emphasis on fundamental parameters such as absolute photoluminescence quantum yield and fluorescence lifetime. The PS-NPs were employed for ratiometric dual-wavelength and lifetime-based photoluminescent oxygen sensing. They were efficiently taken up by cultured murine alveolar macrophages, yielding a characteristic and reversible change in ratiometric response with decreasing oxygen concentration. This correlated with the cellular hypoxic status verified by analysis of hypoxia inducible factor-1α (HIF-1α) accumulation. In addition, the surface of PS-NPs was functionalized with polyethylene glycol (PEG) and the monoclonal antibody herceptin, and their binding to HER2/neu-overexpressing tumor cells was confirmed in vitro. First experiments with tumor-bearing mouse revealed a distinctive ratiometric response within the tumor upon hypoxic condition induced by animal sacrifice. These results demonstrate the potential of these referenced NIR nanosensors for in vitro and in vivo imaging that present a new generation of optical probes for oncology.     

Dynamic analysis of drug-induced cytotoxicity using chip-based dielectrophoretic cell immobilization technology

Quantification of programmed and accidental cell death provides useful end-points for the anticancer drug efficacy assessment. Cell death is, however, a stochastic process. Therefore, the opportunity to dynamically quantify individual cellular states is advantageous over the commonly employed static, end-point assays. In this work, we describe the development and application of a microfabricated, dielectrophoretic (DEP) cell immobilization platform for the real-time analysis of cancer drug-induced cytotoxicity. Microelectrode arrays were designed to generate weak electro-thermal vortices that support efficient drug mixing and rapid cell immobilization at the delta-shape regions of strong electric field formed between the opposite microelectrodes. We applied this technology to the dynamic analysis of hematopoietic tumor cells that represent a particular challenge for real-time imaging due to their dislodgement during image acquisition. The present study was designed to provide a comprehensive mechanistic rationale for accelerated cell-based assays on DEP chips using real-time labeling with cell permeability markers. In this context, we provide data on the complex behavior of viable vs dying cells in the DEP fields and probe the effects of DEP fields upon cell responses to anticancer drugs and overall bioassay performance. Results indicate that simple DEP cell immobilization technology can be readily applied for the dynamic analysis of investigational drugs in hematopoietic cancer cells. This ability is of particular importance in studying the outcome of patient derived cancer cells, when exposed to therapeutic drugs, as these cells are often rare and difficult to collect, purify and immobilize.     

Anthropogenic and natural radionuclides in caribou and muskoxen in the western Alaskan Arctic and marine fish in the Aleutian Islands in the first half of 2000s

A number of caribou and muskoxen samples from the western Alaskan Arctic and fish samples from the Aleutian Islands were collected between 1998 and 2006 and analyzed for anthropogenic (⁹⁰Sr and ¹³⁷Cs) and natural radionculides (⁴⁰ K, ²¹⁰Pb and ²²⁶Ra), as part of the radiological assessment for the regional subsistence hunting communities in the first half of 2000s. We examined the relationship between the activities of these nuclides with the size of the fish. In caribou samples, concentration of ⁹⁰Sr in muscle was below the detection limit of 0.14 Bq kg^− 1 and ¹³⁷Cs concentration in bones was below the detection limit of 0.15 Bq kg^− 1.¹³⁷Cs activity varied over an order of magnitude in caribou muscle samples with an average value of 2.5 Bq/kg wet wt. Average ¹³⁷Cs activity in muskoxen muscle was found to be 9.7 Bq/kg wet wt. However, there were a little variation (less than 60%) in ²¹⁰Pb, ⁴⁰ K, and ²²⁶Ra in both muscle and bone of both caribou and muskoxen. The activities of total ²¹⁰Pb in caribou and muskox bones were found to be 1-2 orders of magnitude higher than that of parent-supported ²¹⁰Pb indicating the potential for dating of bones of terrestrial mammals (time elapsed since the death of the animal) based on the excess ²¹⁰Pb method exists. In fish muscle samples, ¹³⁷Cs activity varied from below detection limit to 154 mBq/kg wet wt. and its content increased with the size of the fish due to its transfer through the food chain. Among the seven fish species investigated, ²¹⁰Pb activities varied almost an order of magnitude; however, ⁴⁰K and ²²⁶Ra activities varied less than a factor of two. Total annual effective dose due to ⁹⁰Sr and ¹³⁷Cs from the ingestion of those terrestrial and marine meats was estimated to be negligible (ca. 9 μSV/a) compared to the natural radionuclides present thus posing negligible radiological threat to humans.     

Bioinspired Scaffolds with Varying Pore Architectures and Mechanical Properties

Scaffolds with potential biological applications having a variety of microstructural and mechanical properties can be fabricated by freezing colloidal solutions into porous solids. In this work, the structural and mechanical properties of TiO₂ freeze cast with different soluble additives, including polyethylene glycol, NaOH or HCl, and isopropanol alcohol, are characterized to determine the effects of slurry viscosity, pH, and alcohol concentration on the freezing process. TiO₂ powders mixed with water and these different additives are directionally frozen in a mold, then sublimated and sintered to create the porous scaffolds. The different scaffolds are characterized to compare the compressive strength, modulus, porosity, and pore morphology. For all scaffolds, the overall porosity remains constant (80–85%). By changing the concentration of each additive, the lamellar thickness, pore area, and aspect ratio vary significantly, showing inverse relationships to both the compressive strength and modulus. The strength is predicted from the pore aspect ratio of the scaffolds when subjected to compressive loading with the primary failure mode identified as Euler buckling. TiO₂ scaffolds freeze cast with different soluble additives are suitable for biomedical applications, such as bone replacements, requiring high porosity and specific pore morphologies.     

Magnesium-Catalyzed Asymmetric Thia-Michael Addition to α,β-Unsaturated Ketones

We demonstrate the application of chiral magnesium complexes in an asymmetric carbon-sulfur bond-forming reaction. Enantioselective and cost-effective methodology under mild condition for the thia-Michael addition, utilizing an in situ generated chiral dinuclear magnesium-ProPhenol complex, has been developed. The versatility of this protocol is demonstrated with a broad range of thiol nucleophiles and a wide selection of enones. Enantioenriched β-ketosulfides are obtained in good to excellent yields and moderate to excellent enantioselectivity. The presented catalytic system exhibits excellent tolerance for structurally different substrates while maintaining high enantioselectivity. This observation aligns with proposed mechanism, wherein the sulfur atom coordinates to the catalyst in close proximity to the reaction center.     

The Size-Dependent Effects of Silver Nanoparticles on Germination,Early Seedling Development and Polar Metabolite Profile of Wheat (Triticum aestivum L.)

The phytotoxicity of silver nanoparticles (Ag NPs) to plant seeds germination and seedlings development depends on nanoparticles properties and concentration, as well as plant species and stress tolerance degrees. In the present study, the effect of citrate-stabilized spherical Ag NPs (20 mg/L) in sizes of 10, 20, 40, 60, and 100 nm, on wheat grain germination, early seedlings development, and polar metabolite profile in 3-day-old seedlings were analyzed. Ag NPs, regardless of their sizes, did not affect the germination of wheat grains. However, the smaller nanoparticles (10 and 20 nm in size) decreased the growth of seedling roots. Although the concentrations of total polar metabolites in roots, coleoptile, and endosperm of seedlings were not affected by Ag NPs, significant re-arrangements of carbohydrates profiles in seedlings were noted. In roots and coleoptile of 3-day-old seedlings, the concentration of sucrose increased, which was accompanied by a decrease in glucose and fructose. The concentrations of most other polar metabolites (amino acids, organic acids, and phosphate) were not affected by Ag NPs. Thus, an unknown signal is released by small-sized Ag NPs that triggers affection of sugars metabolism and/or distribution.