MBE growth and characterization of in situ arsenic doped HgCdTe

We report the results of in situ arsenic doping by molecular beam epitaxy using an elemental arsenic source. Single Hg_1−xCd_xTe layers of x ∼0.3 were grown at a lower growth temperature of 175°C to increase the arsenic incorporation into the layers. Layers grown at 175°C have shown typical etch pit densities of 2E6 with achievable densities as low as 7E4cm⁻². Void defect densities can routinely be achieved at levels below 1000 cm⁻². Double crystal x-ray diffraction rocking curves exhibit typical full width at half-maximum values of 23 arcsec indicating high structural quality. Arsenic incorporation into the HgCdTe layers was confirmed using secondary ion mass spectrometry. Isothermal annealing of HgCdTe:As layers at temperatures of either 436 or 300°C results in activation of the arsenic at concentrations ranging from 2E16 to 2E18 cm⁻³. Theoretical fits to variable temperature Hall measurements indicate that layers are not compensated, with near 100% activation after isothermal anneals at 436 or 300°C. Arsenic activation energies and 77K minority carrier lifetime measurements are consistent with published literature values. SIMS analyses of annealed arsenic doping profiles confirm a low arsenic diffusion coefficient.     

Intracellularly Degradable Hydrogen‐Bonded Polymer Capsules

The assembly of low‐fouling polymer capsules with redox‐responsive behavior and intracellular degradability is reported. Thiol‐containing poly(2‐ethyl‐2‐oxazoline) (PEtOxMA_SH) brushes are synthesized by atom transfer radical polymerization (ATRP) of oligo(2‐ethyl‐2‐oxazoline)methacrylate and glycidyl methacrylate (GMA) and subsequent ring‐opening reaction of the GMA. Sequential deposition of PEtOxMA_SH/poly(methacrylic acid) (PMA) multilayers onto silica (SiO₂) particle templates and crosslinking through disulfide formation yield stable capsules after the removal of the SiO₂ templates by buffered hydrofluoric acid (HF). The redox‐responsive nature of the disulfide crosslinking groups enables the degradation of these capsules under simulated intracellular conditions at pH 5.9 and 5 mm glutathione (GSH). Furthermore, capsule degradation is observed after incubation with dendritic (JAWS II) cells. Even at high capsule‐to‐cell ratios, PEtOxMA_SH capsules show only negligible cytotoxicity. Quartz crystal microgravimetry (QCM) studies, using 100% human serum, reveal that films prepared from PEtOxMA_SH exhibit low‐fouling properties. The degradation and low‐fouling properties are promising for application of PEtOxMA_SH films/capsules for the delivery and triggered release of therapeutics.     

The temporal interaction of corticosterone and prolactin in affecting liver lipid metabolism of the chick

Experiments were conducted to determine if Brown Leghorn chickens (Gallus domesticus) showed a daily differential responsiveness to the phased injections of corticosterone and prolactin. In experiment 1, 28 day old chicks, maintained on continuous lighting and a standard diet, were treated daily for 6 days with corticosterone (300 mug. in 0.2 cc. saline) and with prolactin (150 mug. in 0.2 cc. saline) for 4 days. The prolactin injections began 2 days after the first corticosterone injection. The interval between daily corticosterone injections at 1800 hours followed by prolactin injections 6, 12 or 18 hours later resulted in a significant increase in the liver lipidcontent in the chicks. However, when corticosterone and prolactin were given at the same time (1800 hours), no increase in liver lipid content was observed. Corticosterone admininstered at 6oo hours and followed by prolactin injections had no effect on liver lipid content regardless of the time of prolactin prolactin injections. Experiment 2 was designed to test the effect of the administration of corticosterone or prolactin alone at either 600 hours or 1800 hours on liver lipid metabolism. Two groups of Brown Leghorn chicks received prolactin alone (for 2 days) at either 600 hours or 1800 hours. None of these treatment groups were significantly different from the uninjected controls. It is concluded that the chick has a diurnal sensitivity to the effects of coritcosterone and that once the liver is affected by corticosterone, a temporal interaction between this steroid and prolactin can affect the liver lipid content of the Brown Leghorn chick.