• Journal of Pharmaceutical Investigation
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• v.27 no.1
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• pp.1-10
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• 1997

For the purpose of improving the chemotherapeutic index of acyclovir(ACV), it was conjugated with asialofetuin(AF), which has been reported to enter into hepatocytes. When $[H^3]$ acyclovir in itself or its conjugate were administered to rats, the latter was taken up more selectively by the liver than any other tissues. The stability of ACVMP-AF conjugate in phosphate buffer (pH 5.0) and rat liver homogenate showed a pseudo-first order profile. ACVMP-AF, however, was relatively stable in pH7.4 phosphate buffer and rat plasma. The conjugate was added to the isolated rat hepatocyte and cellular uptake was monitored by scintillation counting for up to 6 hours at $37^{\circ}C$. Hepatocytes incubated with the conjugate exhibited radioactivities significantly enhanced over control levels dose-dependently, i.e., a 3-40 fold increase in radioactivities was observed over controls at the conjugate concentrations of $0.1-10\;{\mu}g/ml$. The AUQ in the liver, kidney, spleen, intestine and lung was higher in treatment with ACVMP-AF than that in treatment with ACV. In treatment with ACVMP-AF, the weighted-average overall drug targeting efficiency(Te) for the liver was higher than in treatment with ACV(57.00 vs 13.31 %), and the weighted-average tissue exposure(Re) was 5.03 for the liver. These results indicated that ACVMP-AF conjugate was rapidly taken up by hepatocytes and could be an efficient and selective hepatic targeting system.

• Journal of Korean Society of Environmental Engineers
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• v.30 no.11
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• pp.1123-1131
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• 2008

In this study, measurement uncertainty of instrumental neutron activation analysis was evaluated for ambient As concentration in PM2.5. Expanded uncertainties of the measurements were calculated by applying both ISO-GUM approximation and Monte Carlo Simulation(MCS). The estimate of As concentration on a specific day by the Monte Carlo Simulation differed from that of ISO-GUM approximation by less than 4%. Relative expanded uncertainties of As concentrations from a total number of 60 PM2.5 samples were also estimated to be more or less than 10% with 95% confidence level using the Monte Carlo Simulation. Sensitivity test of the measurement uncertainties showed that $\gamma$-ray counting error(62.3%), efficiency(18.5%), air volume(12.3%), neutron flux(2.3%), and absolute gamma-intensity(1.8%) are major factors of uncertainty variations.

• Korean Journal of Animal Reproduction
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• v.20 no.2
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• pp.143-153
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• 1996

To improve the efficiency of nuclear transplantation in the rabbit, this study were evaluated the influence of celly cycle of donor nuclei on the in vitro developmental potential in the nuclear transplant embryos. The embryos of 16-cell stage were collected from the mated does at 48h post-hCG injection and they were synchronized to G1 phase of 32-cell stage. Synchronization of the cell cylce of blastomeres were induced, first, using an microtubules polymerization inhibitor, 0.5$\mu\textrm{g}$/ml colcemid for 10h to arrest blastomeres in metaphase, and secondly, using a DNA synthesis inhibitor, 0.1$\mu\textrm{g}$/ml aphidicolin for 1.5 to 2h to cleave to 32-cell stage and arrest them in G1 phase. The separated G1 phase blastomeres of 32-cell stage were injectied into enucleated recipient cytoplasms by micromanipulation. After culture until 20h post-hCG injection, the nuclear transplant oocytes were electrofused and activated by electrical stimulation. The nuclear transplant embryos were co-cultured for 120h. In vitro cultured embryos were monitored every 24h to assess for development rate. After in vitro cultue for 120h, the nuclear transplant embryos developed to blastocyst stage were stained with Hoechst 33342 dye for counting the number of blastomeres under a fluorescence microscopy. The cleavage rate of blastomeres from 16-cell stage stage rabbit embryos treated with colcemid for 10h or aphidicolin for 6h following colcemid for 10h were not significantly different. The electrofusion rate was similar by high in S and G1 phase donor nuclei as 80.6 and 79.1%, respectively. However, the nuclear transplant embryos using G1 phase donor nuclei were developed to blastocyst at high rate(60.3%) than those using S phase donor nuclei(26.0%). Moreover, the mean blastocyst stage were increased significantly(P<0.05) with the G1 phase donor nuclei(176.6 cells and 1.50 cycles), as compared with the S phase donor nuclei(136.6 cells and 1.42 cycles). These results show that the blastomeres of G1 phase were more successful as donor nuclei in the nuclear transplant procedure, compared with S phase.

• The Journal of Korean Institute of Communications and Information Sciences
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• v.33 no.11A
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• pp.1105-1116
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• 2008

Cognitive radio is one of the most effective techniques to improve the spectrum utilization efficiency. To implement the cognitive radio, spectrum sensing is considered as the key functionality because only counting on it, can the secondary users identify the spectrum holes and utilize them efficiently without causing interference to primary users. Generally, there are several spectrum sensing methods; the most common and simplest method is energy detection. However, the conventional energy detection has some disadvantages, which are caused by noise, especially, uncertain noise power leads to degradation of energy detector. In this paper, to solve this problem, we proposed sliding window-based energy detection method which can devide the frequency band of primary signal and noise using sliding window to estimate the power of primary user without the noise effect and achieve the better performance. It can calculate the energy of primary user only and can detect the primary signal. The simulation result shows that our proposed method outperforms conventional one.

• Journal of the Institute of Electronics and Information Engineers
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• v.52 no.2
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• pp.173-181
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• 2015

We developed a wireless gamma-ray probe based on radiation photon counting method to diagnose and detect remaining lesions after surgery, and its effectiveness was evaluated using calibration sources and a phantom. The probe was designed and miniaturized using a semi-conductor-based radiation sensor, and a Bluetooth remote communication module was used to implement the wireless diagnosis and detection system. Moreover, a remote monitoring system was implemented to monitor affected areas during diagnosis and surgery. To assess the effectiveness of the developed probe in this study, calibration sources $^{57}Co$, $^{133}Ba$, $^{22}Na$ and $^{137}Cs$ and a chicken breast phantom were used. Furthermore, the probe's detection response to gamma ray was confirmed through evaluation. Its clinical applicability was verified by assessing the response linearity and detection direction according to gamma-ray intensity, as well as the detection efficiency according to the depth of the gamma source in the phantom.

• Particle and aerosol research
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• v.9 no.3
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• pp.133-137
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• 2013

Measuring particle size distribution is one of the primary concerns in aerosol studies. For a nano-particle size distribution measurement, many scientists use a combination of a differential mobility analyzer (DMA) and a condensation particle counter (CPC) system, which is a called scanning mobility particle sizer (SMPS). Although it has a very high particle size resolution, some issues still remain. These problems include residence time between a DMA and a CPC, discontinuity of a CPC, and disturbance due to long scanning time during the precise measurement of particles. In particular, long scanning time is not adequate for measuring particle size distribution since the particle concentration is changing during the measurement. In this study, we developed radial exhaust multi-port system (REM-system) with no scanning time and high resolution to measure real-time particle size distribution. As a result of the REM-system performed using mono-disperse particle, it is expected that this system will be suitable for measuring continuously changing aerosol. If the counting efficiency of multi-condensation particle counter (M-CPC) and data inversion matrix are completed, REM-system will be a very adequate system for unsteady aerosol, which changes for SMPS scanning time.

• Proceedings of the Korean Society of Medical Physics Conference
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• 2002.09a
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• pp.411-414
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• 2002

The CdTe semiconductor detector has a higher detection efficiency for x-rays and $\square$amma rays and a wider energy band gap compared with Si and Ge semiconductor detectors. Therefore, the size of the detector element can be made small, and can be operated at room temperature. The interaction between a CdTe detector and incident x-rays is mainly photoelectric absorption in the photon energy range of up to 100 keV. In this energy range, Compton effects are almost negligible. We have developed a 256 channel CdTe array detector system for monochromatic x-ray CT using synchrotron radiation. The CdTe array detector system, the element size of which is 1.98 mm (h) x 1.98 mm (w) x 0.5 mm (t), was operated in photon counting mode. In order to improve the spatial resolution, we tilted the CdTe array detector against the incident parallel monochromatic x-ray beam. The experiments were performed at the BL20B2 experimental hutch in SPring-8. The energy of incident monochromatic x-rays was set at 55 keV. Phantom measurements were performed at the detector angle of 0, 30 and 45 degrees against the incident parallel monochromatic x-rays. The linear attenuation coefficients were calculated from the reconstructed CT images. By increasing the detector angle, the spatial resolutions were improved. There was no significant difference between the linear attenuation coefficients which were corrected by the detector angle. It was found that this method was useful for improving the spatial resolution in a parallel monochromatic x-ray CT system.

• Journal of IKEEE
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• v.19 no.3
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• pp.282-287
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• 2015

In this study, an optical fiber detector was constructed by using a Ce:GAGG scintillator, optical fiber, and photomultiplier. The single crystal size of the scintillator was set to $3{\times}3{\times}20mm^3$ after simulating the counting efficiency of gamma rays in the scintillator by using the MCNPX code. The constructed detector used the standard gamma ray sources $^{137}Cs$ and $^{133}Ba$ to measure radiation and analyze the spectral characteristics of gamma rays. The resulting trend curve showed excellent linearity with an R-squared value of 0.99741, and the detector characteristics were found to vary 2% or less with distance based on comparison with the MCNPX value. Furthermore, the spectroscopic analysis of the gamma ray energy from the single-ray and mixed-ray sources showed that $^{137}Cs$ had its peak energy at 662 keV, and $^{133}Ba$ had at 356 keV. It seems that if the fiber-optics detector is used, working hours and exposure of worker can be reduced.

• Asian Pacific Journal of Cancer Prevention
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• v.16 no.4
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• pp.1343-1348
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• 2015

Human UHRF1 (ubiquitin-like PHD and RING finger domain-containing 1) has been reported to be over-expressed in many cancers, but its role in ovarian cancer remains elusive. Here, we determined whether knockdown of UHRF1 by lentivirus-mediated shRNA could inhibit ovarian cancer cell growth. Lentivirus-mediated short hairpin RNAs (lv-shRNAs-UHRF1) were designed to trigger the gene silencing RNA interference (RNAi) pathway. The efficiency of lentivirus-mediated shRNA infection into HO-8910 and HO-8910 PM cells was determined using fluorescence microscopy to observe lentivirus-mediated GFP expression and was confirmed to be over 80 percent. UHRF1 expression in infected HO-8910 and HO-8910 PM was evaluated by real-time PCR and Western blot analysis. The Cell Counting Kit-8 (CCK-8) assay was used to measure cell viability; flow cytometry and Hoechst 33342 assay was applied to measure cell cycle arrest and apoptosis. Cell invasion was assessed using transwell chambers. Our results demonstrated that the loss of UHRF1 promoted HO-8910 and HO-8910 PM cell apoptosis, while inhibiting cell proliferation. In addition, UHRF1 knockdown significantly inhibited the invasion of human ovarian cancer cells. In the present study, we also showed that depleting HO-8910 cells of UHRF1 caused activation of the DNA damage response pathway, with the cell cycle arrested in G2/M-phase. The DNA damage response in cells depleted of UHRF1 was illustrated by phosphorylation of CHK (checkpoint kinase) 2 on Thr68, phosphorylation of CDC25 (cell division control 25) on Ser 216 and phosphorylation of CDK1 (cyclin-dependent kinase 1) on Tyr 15.

• Fire Science and Engineering
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• v.33 no.5
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• pp.140-148
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• 2019

In line with the "mandatory seismic design of fire protection facilities," development of design automation software is indispensable for improving the reliability and efficiency of seismic design. The seismic design automation software developed in this study is an automated S/W for seismic design of fire-fighting facilities, and functions such as automatic arrangement of anti-shake braces according to Korea National Fire Agency's Seismic Design Standards for fire-fighting facilities, output of seismic bracing calculation bills and automatic quantities counting. In addition, the seismic design automation software not only reduces the work speed by three times compared to the manual design of the designer, but also improves the reliability of the design by reducing the human error related to the design quantity such as the brace. In addition, in the seismic design method of fire protection facilities that have been approached conservatively, it was possible to perform the optimal seismic design by using computer algorithms for at least in the use of braces.