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1.
Transfusion ; 59(7): 2361-2367, 2019 07.
Article in English | MEDLINE | ID: mdl-30985961

ABSTRACT

BACKGROUND: China has not yet incorporated routine human T-lymphotropic virus (HTLV)-1/2 blood donor screening, even though HTLV has been reported in the southeastern coastal region. This study was conducted to investigate the prevalence of HTLV in five major regions across of China. METHODS: From January 2016 to December 2017, blood samples were collected in 20 blood centers located in different regions of China. These samples were screened for HTLV-1/2 antibodies using enzyme-linked immunosorbent assay (ELISA). If the test samples were reactive, the samples were confirmed with a western blot (WB) assay. If the results of WB were indeterminate, the donor was interviewed after a minimum lapse of 8 weeks. All follow-up samples from donors were tested for anti-HTLV-1/2 with ELISA and WB. RESULTS: There were 875,453 donor samples tested for anti-HTLV-1/2 by ELISA. In all, 365 samples tested negative, 22 samples tested positive by WB, and 14 samples with HTLV status undetermined due to being lost to follow-up. The prevalences were 11.09, 5.96, 3.16, 2.88 and 0.98 per 100,000 in Xiamen, Changsha, Beijing, Shenzhen, and Nanjing blood center, respectively. The prevalences were 0 per 100,000 for all 15 other blood centers. There was significant differences in the prevalence of HTLV in different regions of China (p = 0.0011). CONCLUSION: In China, HTLV-1 confirmed positive donors are mainly from southeastern coastal areas. It may be necessary to conduct HTLV screening in these areas to reduce the risk of transfusion-transmitted HTLV.


Subject(s)
Blood Donors , Donor Selection , HTLV-I Antibodies/blood , HTLV-I Infections , HTLV-II Antibodies/blood , HTLV-II Infections , Human T-lymphotropic virus 1/metabolism , Human T-lymphotropic virus 2/metabolism , Adult , China/epidemiology , Female , HTLV-I Infections/blood , HTLV-I Infections/epidemiology , HTLV-II Infections/blood , HTLV-II Infections/epidemiology , Humans , Male , Middle Aged , Prevalence
2.
Diabetologia ; 57(4): 801-8, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24370975

ABSTRACT

AIMS/HYPOTHESIS: Given the importance of glucagon in the development of type 2 diabetes and as a potential therapeutic agent, the aim of this study was to characterise glucagon kinetics in mice and its regulation by the nutritional state. METHODS: Anaesthetised C57BL/6 mice fed normal or high-fat diets, or fasted, were injected intravenously with glucagon (0.1, 0.3, 1.0, 10.0 or 20 µg/kg); blood samples were withdrawn before injection and 1, 3, 5, 10, 20 min thereafter for glucagon assay by RIA. Glucagon kinetics were described by two-compartment models using a population analysis. RESULTS: The population mean and between-animal SD of glucagon clearance in the fed mice was 6.03 ± 2.58 ml/min, with a rapid elimination half-life of 2.92 ± 1.21 min. Fasted mice showed a slower glucagon clearance. The kinetics of glucagon in the fed and fasted group was linear across this large dose range. The mice fed a high-fat diet, however, showed non-linear kinetics with a faster terminal clearance of 20.4 ± 5.45 ml/min (p < 0.001) and a shorter elimination half-life of 1.59 ± 0.606 (p < 0.001) min relative to normal mice. CONCLUSIONS/INTERPRETATION: This first systematic dose-ranging study of glucagon kinetics produced several findings: (1) a linear two-compartment model describes glucagon in normal C57BL/6 mice; (2) fasting reduces the clearance of glucagon and (3) high-fat diet enhances the clearance of glucagon. These results may direct future studies on glucagon physiology and indicate that there are other mechanisms, not included in the current model, needed to fully explain glucagon's kinetics.


Subject(s)
Glucagon/metabolism , Nutritional Status , Animals , Diet, High-Fat/adverse effects , Female , Mice , Mice, Inbred C57BL
3.
Annu Int Conf IEEE Eng Med Biol Soc ; 2020: 4506-4509, 2020 07.
Article in English | MEDLINE | ID: mdl-33018995

ABSTRACT

Smart devices are quickly becoming ubiquitous with the rise of portable biosensors and the internet of things. There exists particular interest in enhancing common objects to have smart capabilities and finding inexpensive solutions for diagnostic tools. One such example is transforming paper items into interactive devices and point-of-care analytic products. Due to the lightweight, flexible, and cost-efficient qualities of paper, unobtrusively powering these devices remains an outstanding problem. In this paper, we demonstrate an electrostatic human-touch powered energy harvesting system, integrated with flexible painted conductive electrodes on paper. This system harvests 8.5 nJ of energy and reaches a voltage of 1.3 V on a 10 nF energy storage capacitor. This technology not only provides a method of powering paper-based products with routine human gestures but can also detect human touch for input communication to sensors.


Subject(s)
Electronics , Electric Conductivity , Electrodes , Humans , Physical Phenomena , Static Electricity
4.
Annu Int Conf IEEE Eng Med Biol Soc ; 2017: 775-778, 2017 Jul.
Article in English | MEDLINE | ID: mdl-29059987

ABSTRACT

Sensors are becoming ubiquitous and increasingly integrated with and on the human body; powering such "body network" devices remains an outstanding problem. In this paper, we demonstrate a touch interrogation powered energy harvesting system. This system transforms the kinetic energy of a human finger to electric energy, with each tap producing approximately 1 nJ of energy at a storage capacitor. As is well known for touch display devices, the proximity of a finger can alter the effective value of small capacitances; we demonstrate that these capacitance changes can drive a current which is rectified to charge a capacitor. As a demonstration, an untethered circuit charged this way can deliver enough instantaneous power to light a red LED every ~ 10 seconds. This technology illustrates the ability to communicate with and operate low-power sensors with motions already used for interfacing to devices.


Subject(s)
Electric Capacitance , Electric Power Supplies , Electricity , Humans , Motion , Touch
5.
PLoS One ; 12(9): e0184994, 2017.
Article in English | MEDLINE | ID: mdl-28915277

ABSTRACT

Current technologies are lacking in the area of deployable, in situ monitoring of complex chemicals in environmental applications. Microorganisms metabolize various chemical compounds and can be engineered to be analyte-specific making them naturally suited for robust chemical sensing. However, current electrochemical microbial biosensors use large and expensive electrochemistry equipment not suitable for on-site, real-time environmental analysis. Here we demonstrate a miniaturized, autonomous bioelectronic sensing system (BESSY) suitable for deployment for instantaneous and continuous sensing applications. We developed a 2x2 cm footprint, low power, two-channel, three-electrode electrochemical potentiostat which wirelessly transmits data for on-site microbial sensing. Furthermore, we designed a new way of fabricating self-contained, submersible, miniaturized reactors (m-reactors) to encapsulate the bacteria, working, and counter electrodes. We have validated the BESSY's ability to specifically detect a chemical amongst environmental perturbations using differential current measurements. This work paves the way for in situ microbial sensing outside of a controlled laboratory environment.


Subject(s)
Bioreactors , Biosensing Techniques , Electrochemical Techniques , Environmental Monitoring , Shewanella/metabolism , Biosensing Techniques/instrumentation , Biosensing Techniques/methods , Electrochemical Techniques/instrumentation , Electrochemical Techniques/methods , Environmental Monitoring/instrumentation , Environmental Monitoring/methods
6.
Article in English | MEDLINE | ID: mdl-26738031

ABSTRACT

We present a miniaturized, free-floating monitoring system which makes use of electron transfer in Shewanella oneidensis sequestered behind a permeable membrane while maintaining diffusive contact with the environment, allowing for sensing environmental conditions. The system makes use of a commercial off-the-shelf (COTS) integrated circuit (IC) which sets a potential between a working electrode and a Ag/AgCl reference electrode while recording the resulting current from the electroactive cells. We successfully sensed both pyruvate and the environmental presence of E. coli via changes in the currents sensed. This work will enable the development of mobile aquatic sensing systems which make use of bacterial electron transfer as a transduction method. Further miniaturization of the recording mote, electrodes, packaging, and system is discussed.


Subject(s)
Biosensing Techniques , Electrochemical Techniques , Environmental Microbiology , Shewanella/physiology , Biosensing Techniques/instrumentation , Biosensing Techniques/methods , Electrochemical Techniques/instrumentation , Electrochemical Techniques/methods , Electrodes , Electron Transport , Escherichia coli/isolation & purification
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