• Journal of Communications and Networks
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• 제14권6호
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• pp.692-702
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• 2012

Supporting quality of service (QoS) guarantees for diverse multimedia services are the primary concerns for WiMAX (IEEE 802.16) networks. A scheduling scheme that satisfies QoS requirements has become more important for wireless communications. We propose a downlink scheduling scheme called adaptive priority-based downlink scheduling (APDS) for providing QoS guarantees in IEEE 802.16 networks. APDS comprises two major components: Priority assignment and resource allocation. Different service-type connections primarily depend on their QoS requirements to adjust priority assignments and dispatch bandwidth resources dynamically. We consider both starvation avoidance and resource management. Simulation results show that our APDS methodology outperforms the representative scheduling approaches in QoS satisfaction and maintains fairness in starvation prevention.

• 소성∙가공
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• 제10권1호
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• pp.30-34
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• 2001

The magnetic and metallurgical characteristics of Mischmetal(MM) -Ferroboron (FeB) Permanent magnets have been investigated by X-ray diffractometer, scanning and transmission electron microscope and vibrating sample magnetometer under hot-pressing and die-upsetting process. The best magnetic properties obtained in these studies were $H_c$=5.8 kOe, $B_r$=5.0 kG with $(BH)_{max}=7.6 MGOe for melt-spun ribbons, $H_c$=3.0 kOe, $B_r$=4.6 kG with $(BH)_{max}$=2.9 MGOe for hot-pressed magnets and $H_c$=1.8 kOe, $B_r$=5.5 kG with $(BH)_{max}$=4.1 MGOe for die-upset magnets. The higher magnetic properties in die-upset magnets were resulted from alignment of the c-axis along the die-upsetting direction.

• 한국초전도학회:학술대회논문집
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• 한국초전도학회 2009년도 Korea Superconductivity Society Meeting 2009
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• pp.8-8
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• 2009

• Journal of Pharmaceutical Investigation
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• 제38권5호
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• pp.343-348
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• 2008

The bioequivalence of two cyclosporine A (CyA) 100 mg soft capsules (Chong Kun Dang's $Cipol-N^{(R)}$ as the test drug; Korea Novartis' Sandimmun $Neoral^{(R)}$ as the reference drug) was assessed in healthy male Korean volunteers after oral administration of 200 mg CyA according to a randomized crossover design. The whole blood samples were analyzed for the determination of parent CyA in the blood by using a validated HPLC/diode array detector method. The mean $AUC_t$ values for reference and test products were $4095.3{\pm}1397.2$ and $3958.3{\pm}1138.2\;ng{\cdot}hr/mL$, respectively. The mean $C_{max}$ values were $1135.9{\pm}293.2\;ng/mL$ for the reference product, and $985.0{\pm}207.9\;ng/mL$ for the test product. $T_{max}$ was $1.6{\pm}0.4\;hr$ for the reference and $1.8{\pm}0.5\;hr$ for the test product. The differences of $AUC_t$, $C_{max}$ and $T_{max}$ were -3.35, -13.28 and +10.63%, respectively. The point estimates and 90% confidence intervals for $AUC_t$ and $C_{max}$ were 0.981 (0.9171 to 1.0514) and 0.876 (0.8229 to 0.9336), respectively. Based on the pharmacokinetic and statistical data, we conclude that these two products are bioequivalent and can be considered interchangeable in the medical practice.

• Journal of Pharmaceutical Investigation
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• 제41권5호
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• pp.309-315
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• 2011

A sensitive and specific liquid chromatographic method coupled with tandem mass spectrometry (LC-MS/MS) was developed for the analysis of ambroxol (active moiety of acebrophylline). After acetonitrile precipitation of proteins from plasma samples, ambroxol and the domperidone (internal standard, IS) were eluted on a C18 column. The isocratic mobile phase was consisted of 10 mM ammonium acetate and methanol (10 : 90, v/v), with flow rate at 0.2 mL/min. A tandem mass spectrometer, as detector, was used for quantitative analysis in positive mode by a multiple reaction monitoring mode to monitor the m/z 379.2${\rightarrow}$264.0 and the m/z 426.2${\rightarrow}$175.1 transitions for ambroxol and the IS, respectively. Twenty four healthy Korean male subjects received two capsules (100 mg ${\times}$ 2) of either the test or the reference formulation of acebrophylline HCl in a 2 ${\times}$ 2 crossover study, this was followed by a 1week washout period between either formulation. $AUC_{0-t}$ (the area under the plasma concentration-time curve) was calculated by the linear trapezoidal rule. $C_{max}$ (maximum plasma drug concentration) and $T_{max}$ (time to reach $C_{max}$) were compiled from the plasma concentration-time data. The 90% confidence intervals for the log transformed data were acceptable range of log 0.8 to log 1.25 (e.g., log 0.8964 - log 0.9910 for $AUC_{0-t}$ log 0.8690 - log 1.0750 for $C_{max}$). The major parameters, $AUC_{0-t}$ and $C_{max}$ met the criteria of Korea Food and Drug Administration for bioequivalence indicating that Acephyll$^{(R)}$ capsule (test) is bioequivalent to Surfolase$^{(R)}$ capsule (reference).

• Journal of Gastric Cancer
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• 제17권4호
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• pp.384-393
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• 2017

Purpose: The tumor microenvironment is known to be associated with the metabolic activity of cancer cells and local immune reactions. We hypothesized that glucose metabolism measured by 2-deoxy-2-($^{18}F$)fluoro-D-glucose ($^{18}F-FDG$) positron emission tomography (PET)-computed tomography (CT) ($^{18}F-FDG$ PET-CT) would be associated with local immune responses evaluated according to the presence of tumor infiltrating lymphocytes (TILs). Materials and Methods: We retrospectively reviewed 56 patients who underwent $^{18}F-FDG$ PET-CT prior to gastrectomy. In resected tumor specimens, TIL subsets, including cluster of differentiation (CD) 3, CD4, CD8, Forkhead box P3 (Foxp3), and granzyme B, were subjected to immunohistochemical analysis. The prognostic nutritional index (PNI) was calculated as: ($10{\times}serum$ albumin value)+($0.005{\times}peripheral$ lymphocyte counts). Additionally, the maximum standard uptake value ($SUV_{max}$) was calculated to evaluate the metabolic activity of cancer cells. Results: The $SUV_{max}$ was positively correlated with larger tumor size (R=0.293; P=0.029) and negatively correlated with PNI (R=-0.407; P=0.002). A higher $SUV_{max}$ showed a marginal association with higher CD3 (+) T lymphocyte counts (R=0.227; P=0.092) and a significant association with higher Foxp3 (+) T lymphocyte counts (R=0.431; P=0.009). No other clinicopathological characteristics were associated with $SUV_{max}$ or TILs. Survival analysis, however, indicated that neither $SUV_{max}$ nor Foxp3 held prognostic significance. Conclusions: FDG uptake on PET-CT could be associated with TILs, especially regulatory T cells, in gastric cancer. This finding may suggest that PET-CT could be of use as a non-invasive tool for monitoring the tumor microenvironment in patients with gastric cancer.

• 대한핵의학회지
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• 제39권4호
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• pp.224-230
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• 2005

목적: 심근의 최대탄성도는 전부하 후부하에 독립적인 지표로서 SPECT를 이용하여 좌심실의 국소탄성도($rE_{max}$)를 비침습적으로 측정하였다. 게이트 심근 SPECT 영상에서 국소부피변화를 얻고, 요골동맥 긴장도를 측정하여 중심동맥의 압력 곡선을 얻어 측정한 최대탄성도를 관상동맥우회로 수술 전후 환자를 대상으로 수술전후 관류 및 기능지표와 비교하여보았다. 대상 및 방법: 관상동맥우회로 수술이 결정되어 시행한 환자 21명(남:여=17:4, $58{\pm}12$세)을 대상으로 $^{201}TI$ 휴식기 영상과 디피리다몰 부하 $^{99m}Tc$-sestamibi 게이트 SPECT를 수술전과 수술 후 3개월째 시행하였다. 동시에 요골동맥으로부터 압력곡선을 얻었다. 기능과의 관계를 보기 위해서 관류와 심벽두꺼워짐을 탄성도와 비교하였으며, 심벽두꺼워짐이 20%미만일 때 수술 후 10%이상 호전되지 않는 기능이상 분절에 대해 수술 전후의 탄성도를 비교하였다. 결과: 수술 전 탄성도가 $2.41{\pm}1.64$ mmHg/mL에서 $2.78{\pm}1.83$ mmHg/mL 으로 수술 후에 증가하였으나, 관류와 심벽두꺼워짐과는 낮은 상관성을 보였다. (r=0.35, p<0.001). 관류 60% 이상의 분절에서는 $2.65{\pm}1.67$ mmHg/mL 이었으나, 관류나 낮은 분절의 탄성도는 $1.30{\pm}1.24$ mmHg/mL 였다. 심벽두꺼워짐이 40% 이상 되는 분절의 수술 전 탄성도는 $3.01{\pm}1.92$ mmHg/mL 였고, 기능이 조금 약한 부분인 40%에서 20% 사이의 심벽두꺼워짐 값을 가진 분절에서는 $2.40{\pm}1.19$ mmHg/mL로 심각한 기능이상을 반영하는 20%미만 분절의 탄성도는 $1.13{\pm}0.89$ mmHg/mL의 분포를 보였다. 수술 전 심벽두꺼워짐이 20% 미만일 때 수술 후 10%이상 회복을 보인 생존심근와 그렇지 않은 비생존심근사이의 수술 전후 탄성도는 $1.27{\pm}1.07$ mmHg/mL에서 $1.79{\pm}1.48$ mmHg/mL, $0.97{\pm}0.59$ mmHg/mL에서 $1.22{\pm}0.71$ mmHg/mL로 생존심근의 수술 후 값의 향상이 조금 더 높았다. 그러나, 심벽두꺼워짐의 정도가 탄성도 높아짐의 정도 사이에는 상관성이 없었다(r=0.007). 결론: 수술 전 $rE_{max}$는 관류와 심벽두꺼워짐과 상관성이 약하게 있었다. 기능이상이면서 생존능이 있는 심근의 탄성도는 수술 후 증가하였지만 심벽두꺼워짐의 향상과는 상관성이 없었다. 심근기능의 전부하 후부하에 독립적인 지표인 탄성도는 실제 부피의 증가와 연관되지 않으면서도 생존능이 있는 심근의 기준과 일치하는 양상을 보였으므로 독립적인 매개변수로 사용될 수 있을 것으로 기대한다.

• Journal of Microbiology and Biotechnology
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• 제32권9호
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• pp.1146-1153
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• 2022

Many probiotic species have been used as a fermentation starter for manufacturing functional food materials. We have isolated Bifidobacterium animalis subsp. lactis LDTM 8102 from the feces of infants as a novel strain for fermentation. While Glycine max has been known to display various bioactivities including anti-oxidant, anti-skin aging, and anti-cancer effects, the immune-modulatory effect of Glycine max has not been reported. In the current study, we have discovered that the extract of Glycine max fermented with B. animalis subsp. lactis LDTM 8102 (GFB 8102), could exert immuno-modulatory properties. GFB 8102 treatment increased the production of immune-stimulatory cytokines in RAW264.7 macrophages without any noticeable cytotoxicity. Analysis of the molecular mechanism revealed that GFB 8102 could upregulate MAPK2K and MAPK signaling pathways including ERK, p38, and JNK. GFB 8102 also increased the proliferation rate of splenocytes isolated from mice. In an animal study, administration of GFB 8102 partially recovered cyclophosphamide-mediated reduction in thymus and spleen weight. Moreover, splenocytes from the GFB 8102-treated group exhibited increased TNF-α, IL-6, and IL-1β production. Based on these findings, GFB 8102 could be a promising functional food material for enhancing immune function.

• 한국체육학회지인문사회과학편
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• 제51권3호
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• pp.373-382
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• 2012

본 연구의 목적은 신체변인과 최대하 대사반응을 이용하여 최대산소섭취량(VO₂max)을 간편하고 정확하게 추정하는 데 있다. 18~34세 남성 250명을 대상으로 추정집단(n=179)과 타당도 검증집단(n=71)으로 나누어 최대 운동부하검사를 실시하였으며 3분인 1단계와 6분인 2단계 종료 시점의 대사반응을 측정하였다. 추정 집단을 대상으로 단계선택법(stepwise method)으로 다중회귀분석 (multiple regression analysis)을 실시하였다. 단계별분석법으로 분석한 모형 1의 추정변인은 체중, 6분HR, 6분VO₂이고 R은 0.64(p<.01)이었으며 SEE와 CV는 각각 4.74, 11.7%로 나타났고(p<.01), 추정식은 VO₂max(ml/kg/min)= 72.256-0.340(Weight)-0.220(6분HR)+0.013(6분VO₂)이며 다중공선성이 나타나지 않았다. 모형 2의 추정변인은 체중, 6분HR, 6분VO₂, 6분VCO₂이고 R은 0.66(p<.01)이었으며 SEE와 CV는 각각 4.59, 11.3%로 나타났고(p<.01), 추정식은 VO₂max(ml/kg/min)= 68.699-0.277(Weight) -0.206(6분HR)+0.020(6분VO₂)-0.009(6분VCO₂)이며, 역시 다중공선성이 나타나지 않았다. 모형 1과 비교했을 때 모형 2는 상관이 더 높지만 다중공선성 측면에서는 다소 불리하게 나타났다. 모형 1과 모형 2를 교차타당도 검증집단에 적용했을 때, 측정된 VO₂max와 추정된 VO₂Max 간에 유의한 상관관계가 나타났다(R=0.53, 0.56, P<.001). 타당도 검증을 통해 유용성과 간편성을 고려하면, 본 연구에서 얻은 신체변인 및 최대하 대사반응을 이용한 추정모형들이 모두 사용가능하나 모형 2가 정확도 측면에서 다소 유리하다.

• Journal of Pharmaceutical Investigation
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• 제28권4호
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• pp.283-288
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• 1998

Lovastatin, one of the potent cholesterol-lowering agents, is an inactive lactone prodrug which is metabolized to its active open acid, lovastatin acid (LVA). Bioequivalence study of two lovastatin preparations, the test drug ($Mevacor^{\circledR}$: Chungwae Pharmaceutical Co., Ltd.) and the reference drug ($Lovaload^{\circledR}$: Chong Kun Dang Pharmaceutical Co., Ltd.), was conducted according to the guidelines of Korea Food and Drug Administration (KFDA). Fourteen healthy male volunteers, $23.9{\pm}3.9$ years old and $67.6{\pm}8.0$ kg of body weight in average, were divided randomly into two groups and administered the drug orally at the dose of 160 mg as lovastatin in a $2{\times}2$ crossover study. Plasma concentrations of lovastatin acid were analysed by HPLC method for 12 hr after administration. The extent of bioavailability was obtained from the plasma concentration-time profiles of total lovastatin acid after alkaline hydrolysis of the plasma samples. By alkaline hydrolysis, trace amounts of unmetabolized lovastatin were converted to lovastatin acid. The $AUC_{0-12hr}$ was calculated by the linear trapezoidal rule method. The $C_{max}$ and $T_{max}$ were compiled directly from the plasma drug concentration-time data. Student's t-test indicated no significant differences between the formulations in these parameters. Analysis of variance (ANOVA) revealed that there were no differences in AUC, $C_{max}$, and $T_{max}$ between the formulations. The apparent differences between the formulations were far less than 20% (e.g., 7.07, 5.77 and 1.18% for AUC, $C_{max}$, and $T_{max}$, respectively). Minimum detectable differences(%) between the formulations at ${\alpha}=0.05$ and $1-{\beta}=0.8$ were less than 20% (e.g., 17.2, 15.1, and 15.9% for AUC, Cmax, and Tmax, respectively). The 90% confidence intervals for these parameters were also within ${\pm}20%$ (e.g.. $-5.20{\sim}19.3$, $-5.00{\sim}16.5$, and $-10.2{\sim}12.5%$ for AUC, $C_{max}$, and $T_{max}$, respectively). These results satisfied the bioequivalence criteria of KFDA guidelines, indicating that the two formulations of lovastatin were bioequivalent.