Biodegradable Thin Metal Foils and Spin‐On Glass Materials for Transient Electronics

Biodegradable substrates and encapsulating materials play critical roles in the development of an emerging class of semiconductor technology, generally referred as “transient electronics”, whose key characteristic is an ability to dissolve completely, in a controlled manner, upon immersion in ground water or biofluids. The results presented here introduce the use of thin foils of Mo, Fe, W, or Zn as biodegradable substrates and silicate spin‐on‐glass (SOG) materials as insulating and encapsulating layers, with demonstrations of transient active (diode and transistor) and passive (capacitor and inductor) electronic components. Complete measurements of electrical characteristics demonstrate that the device performance can reach levels comparable to those possible with conventional, nontransient materials. Dissolution kinetics of the foils and cytotoxicity tests of the SOG yield information relevant to use in transient electronics for temporary biomedical implants, resorbable environmental monitors, and reduced waste consumer electronics.     

Software Assisted Digital RF Processor (DRP™) for Single-Chip GSM Radio in 90 nm CMOS

This paper proposes and describes a new software and application programming interface view of an RF transceiver. It demonstrates benefits of using highly programmable digital control logic in an RF wireless system realized in a digital nanoscale CMOS process technology. It also describes a microprocessor architecture design in Digital RF Processor (DRP™) and how it controls calibration and compensation for process, temperature and voltage variations of the analog and RF circuits to meet the required RF performance. A few calibration examples to reduce a DCO bias current and improve device reliability, as well as to optimize transmit modulation and receive performance, are given. The presented circuits and techniques have enabled successful implementation of a commercial single-chip GSM radio in 90 nm CMOS.      

An application of univariate marginal distribution algorithm in MIMO communication systems

The paper discusses a sequence detector based on univariate marginal distribution algorithm (UMDA) that jointly estimates the symbols transmitted in a multiple input multiple output (MIMO) communication system. While an optimal maximum likelihood detection using an exhaustive search method is prohibitively complex, it has been shown that sphere decoder (SD) achieves the optimal bit error rate (BER) performance with polynomial time complexity for smaller array sizes. However, the worst‐case complexity of SD is exponential in the problem dimensions, this brings in question its practical implementation for larger number of spatial layers and for higher‐order signal constellation. The proposed detector shows promising results for this overly difficult and complicated operating environment, confirmed through simulation results. A performance comparison of the UMDA detector with SD is presented for higher‐order complex MIMO architectures with limited average transmit power. The proposed detector achieves substantial performance gain for higher‐order systems attaining a near optimal BER performance with reduced computational complexity as compared with SD. Copyright © 2009 John Wiley & Sons, Ltd.     

Towards a classification of energy aware MAC protocols for wireless sensor networks

Power management is an important issue in wireless sensor networks (WSNs) because wireless sensor nodes are usually battery powered, and an efficient use of the available battery power becomes an important concern specially for those applications where the system is expected to operate for long durations. This necessity for energy efficient operation of a WSN has prompted the development of new protocols in all layers of the communication stack. Provided that, the radio transceiver is the most power consuming component of a typical sensor node, large gains can be achieved at the link layer where the medium access control (MAC) protocol controls the usage of the radio transceiver unit. MAC protocols for sensor networks differ greatly from typical wireless networks access protocols in many issues. MAC protocols for sensor networks must have built‐in power conservation, mobility management, and failure recovery strategies. Furthermore, sensor MAC protocols should make performance trade‐off between latency and throughput for a reduction in energy consumption to maximize the lifetime of the network. This is in general achieved through duty cycling the radio transceiver. Many MAC protocols with different objectives were proposed for wireless sensor networks in the literature. Most of these protocols take into account the energy efficiency as a main objective. There is much more innovative work should be done at the MAC layer to address the hard unsolved problems. In this paper, we first outline and discuss the specific requirements and design trade‐offs of a typical wireless sensor MAC protocol by describing the properties of WSN that affect the design of MAC layer protocols. Then, a typical collection of wireless sensor MAC protocols presented in the literature are surveyed, classified, and described emphasizing their advantages and disadvantages whenever possible. Finally, we present research directions and identify open issues for future medium access research. Copyright © 2009 John Wiley & Sons, Ltd.     

Time to clinical stability in patients hospitalized with community-acquired pneumonia: implications for practice guidelines

CONTEXT: Many groups have developed guidelines to shorten hospital length of stay in pneumonia in order to decrease costs, but the length of time until a patient hospitalized with pneumonia becomes clinically stable has not been established. OBJECTIVE: To describe the time to resolution of abnormalities in vital signs, ability to eat, and mental status in patients with community-acquired pneumonia and assess clinical outcomes after achieving stability. DESIGN: Prospective, multicenter, observational cohort study. SETTING: Three university and 1 community teaching hospital in Boston, Mass, Pittsburgh, Pa, and Halifax, Nova Scotia. PATIENTS: Six hundred eighty-six adults hospitalized with community-acquired pneumonia. MAIN OUTCOME MEASURES: Time to resolution of vital signs, ability to eat, mental status, hospital length of stay, and admission to an intensive care, coronary care, or telemetry unit. RESULTS: The median time to stability was 2 days for heart rate (< or =100 beats/min) and systolic blood pressure (> or =90 mm Hg), and 3 days for respiratory rate (< or =24 breaths/min), oxygen saturation (> or =90%), and temperature (< or =37.2 degrees C [99 degrees F]). The median time to overall clinical stability was 3 days for the most lenient definition of stability and 7 days for the most conservative definition. Patients with more severe cases of pneumonia at presentation took longer to reach stability. Once stability was achieved, clinical deterioration requiring intensive care, coronary care, or telemetry monitoring occurred in 1% of cases or fewer. Between 65% to 86% of patients stayed in the hospital more than 1 day after reaching stability, and fewer than 29% to 46% were converted to oral antibiotics within 1 day of stability, depending on the definition of stability. CONCLUSIONS: Our estimates of time to stability in pneumonia and explicit criteria for defining stability can provide an evidence-based estimate of optimal length of stay, and outline a clinically sensible approach to improving the efficiency of inpatient management.     

A powerful GABA(B) receptor-mediated inhibition of GABAergic neurons in the arcuate nucleus

We combined histofluorescence with in situ hybridization to identify GABAergic neurons in the arcuate nucleus (ARC) following electrophysiological recordings, using GAD65 as a marker. Intracellular recordings were made in hypothalamic slices prepared from ovariectomized guinea pigs. Over 90% of ARC neurons tested with the GABA(B) receptor agonist baclofen responded with a membrane hyperpolarization or an outward current. The hyperpolarization was dose-dependent, and the GABA(B) receptor antagonist CGP 35,348 produced a rightward shift in the agonist dose-response curve. Agonist potency was lower, and the efficacy greater, in GAD-positive neurons. The use of this novel technique for identifying GABAergic neurons thus reveals differences in the pharmacodynamics of GABA(B) receptor activation GABAergic and non-GABAergic ARC neurons.     

Comparative study of chronic aluminum-induced neurofilamentous aggregates with intracytoplasmic inclusions of amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis (ALS) is characterized neuropathologically by chromatolysis, Bunina bodies, hyaline inclusions, skein-like inclusions and axonal spheroids. Aluminum, a known neurotoxin, is the cause of dialysis encephalopathy and is considered to be a causative agent in high incidence foci of ALS in the western Pacific. We have developed an experimental model of motor neuron degeneration in New Zealand white rabbits using chronic low-dose intracisternal administration of aluminum and compared the clinical and neuropathological changes to those of human ALS. Aluminum-inoculated rabbits developed progressive hyperreflexia, hypertonia, limb splaying, gait impairment, muscle wasting, hindlimb paralysis and impaired tonic immobility responses without overt encephalopathic features over a 14-month period. Examination of spinal cords from these animals demonstrated the frequent occurrence and progressive development of anterior horn cell lesions that included small, round, argentophilic perikaryal inclusions similar to hyaline inclusions seen in human ALS. Other inclusions were more condensed and eosinophilic, while still others had neurofibrillary tangle-like morphologies. Axonal spheroids and neuritic thickenings were also prominent and were identical to those seen in human ALS. We believe that the similar and progressive development of neuropathological changes observed in the chronic aluminum-intoxication model, compared to human ALS, warrants further study to aid in understanding the cellular and molecular mechanisms of human motor neuron disease.     

Synthesis of the four isomers of 4-aminopyrrolidine-2,4-dicarboxylate: identification of a potent, highly selective, and systemically-active agonist for metabotropic glutamate receptors negatively coupled to adenylate cyclase

The four isomers of 4-aminopyrrolidine-2,4-dicarboxylate (APDC) were prepared and evaluated for their effects at glutamate receptors in vitro. (2R,4R)-APDC (2a), an aza analog of the nonselective mGluR agonist (1S,3R)-1-aminocyclopentane-1,3-dicarboxylate (1S,3R)-ACPD, 1), was found to possess relatively high affinity for metabotropic glutamate receptors (mGluRs) (ACPD-sensitive [3H]glutamate binding IC50 = 6.49 +/- 1.21 microM) with no effects on radioligand binding to NMDA, AMPA, or kainate receptors up to 100 microM. None of the other APDC isomers showed significant mGluR binding affinity, indicating that this interaction is highly stereospecific. Both 1 and 2a were effective in decreasing forskolin-stimulated cAMP formation in the adult rat cerebral cortex (EC50 = 8.17 +/- 2.21 microM for 1; EC50 = 14.51 +/- 5.54 microM for 2a); however, while 1 was also effective in stimulating basal tritiated inositol monophosphate production in the neonatal rat cerebral cortex (EC50 = 27.7 +/- 5.2 microM), 2a (up to 100 microM) was ineffective in stimulating phosphoinositide hydrolysis in this tissue preparation, further supporting our previous observations that 2a is a highly selective agonist for mGluRs negatively coupled to adenylate cyclase. Microelectrophoretic application of either 1 or 2a to intact rat spinal neurons produced an augmentation of AMPA-induced excitation (95 +/- 10% increase for 1, 52 +/- 6% increase for 2a). Intracerebral injection of 1 (400 nmol) produced characteristic limbic seizures in mice which are not mimicked by 2a (200-1600 nmol, ic). However, the limbic seizures induced by 1 were blocked by systemically administered 2a in a dose-dependent manner (EC50 = 271 mg/kg, ip). It is concluded that (2R,4R)-APDC (2a) is a highly selective, systemically-active agonist of mGluRs negatively coupled to adenylate cyclase and that selective activation of these receptors in vivo can result in anticonvulsant effects.