• 한국환경보건학회지
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• 제41권5호
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• pp.289-298
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• 2015

Objectives: The method of analyzing urinary arsenic by flow injection hydride generation atomic absorption spectrometry (FI-HG-AAS) is generally used because it shows relatively greater sensitivity, low detection limits, low blocking action, and is simple to operate. In this study, the results of analysis according to three pre-reductants commonly used in the FI-HG-AAS method were compared with each other. Methods: To analyze urinary arsenic, nineteen urine samples were collected from adults aged 43-79 years old without occupational arsenic exposure. Analysis equipment was FI-HG-AAS (AAnalyst 800/FIAS 400, Perkin- Elmer Inc., USA). The three pre-reductants were potassium iodide (KI/AA), C3H7NO2S (L-cysteine), and a mixture of KI/AA and L-cysteine (KI/AA&L-cysteine). Results: In the results of the analysis, the recovery rate of the method using KI/AA was 82.3%, 95.7% for Lcysteine, and 123.5% for KI/AA and L-cysteine combined. When compared with the results by use of high performance liquid chromatography inductively-coupled plasma mass spectrometry (HPLC-ICP-MS), the method using L-cysteine was the closest to those using HPLC-ICP-MS ($98.57{\mu}g/L$ for HPLC-ICP-MS; $74.96{\mu}g/L$ for L-cysteine; $69.23{\mu}g/L$ for KI/AA and L-cysteine; $13.06{\mu}g/L$ for KI/AA) and were significantly correlated (R2=0.882). In addition, they showed the lowest coefficient of variation in the results between two laboratories that applied the same method. Conclusion: The efficiency of hydride generation is considered highly important to the analysis of urinary arsenic via FI-HG-AAS. This study suggests that using L-cysteine as a pre-reductant may be suitable and the most rational among the FI-Hg-AAS methods using pre-reductants.

• 한국임상약학회지
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• 제11권2호
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• pp.49-56
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• 2001

Acetyl-L-carnitine (ALC), an endogenous component of the L-carnitine family, is a naturally existing molecule synthesized from L-carnitine (LC) by carnitine acetyl transferase. ALC has been shown to improve the cognitive performance of patients suffering from dementia of the Alzheimer's type and proposed for treating Alzheimer's disease in pharmacological doses. The purpose of the present study was to evaluate the bioefuivalence of two ALC tablets, $Nicetile^{TM} (Dong-A Pharmaceutical Co.) and $L-Cartin^{TM}$ (Kuhn Il Pharmaceutical Co.), according to the guidelines of Korea Food and Drug Administration (KFDA). The ALC release from the two ALC tablets in vitro was tested using KP VII Apparatus II method in various dissolution media (pH 1.2, 6.0 and 6.8). Twenty six normal male volunteers, $24.46\pm3.67$ years in age and $64.45\pm5.54$ kg in body weight, were divided into two groups and a randomized $2\times2$cross-over study was employed. After one tablet containing 500 mg of ALC was orally administered, blood was taken at predetermined time intervals and the concentrations of ALC in serum were determined using HPLC with fluorescence detector. Because of the presence of endogenous ALC, the calibration was performed using dialyzed serum. The dissolution profiles of the two ALC tablets were similar in all the dissolution media. The pharmacokinetic parameters such as $AUC_t,\;C_{max}\;and\;T_{max}$ were calculated and ANOVA was utilized for the statistical analysis of the parameters. The results showed that the differences in $AUC_t,\;C_{max}\;and\;T_{max}$ between two tablets were $0.35\%,\;0.93\%\;and\;2.34\%$ respectively, when calculated against the $Nicetile^{TM} tablet. The powers $(1-\beta)\;for\;AUC_t$ , and Cmax were $98.72\%\;and\;85.48\%$, respectively. Minimum detectable differences $(\Delta)\;at\;\alpha=0.05\;and\;1-\beta=0.8$ were less than $20\%,\;(e.g.,\;13.21\%\;and\;18.42\%\;for\;AUC_t,\;and\;C_{max}$ respectively). The $90\%$ confidence intervals were within $\pm20\%\;(e.g.,\;-7.38\sim8.09\;and\;-9.86\sim11.72\;for\;AUC_t,\;and\;C_{max}$, respectively). These two parameters met the criteria of KFDA for bioequivalence, indicating that $L-Cartin^{TM}$ tablet is bioequivalent to $Nicetile^{TM} tablet.

• 한국가금학회:학술대회논문집
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• 한국가금학회 2002년도 가을 학술발표논문집
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• pp.130-132
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• 2002

본 실험은 산란노계에서 강제환우 후에 단백질과 에너지수준이 다른 사료를 급여시에 생산성에 미치는 영향을 구명하고자 실행하였다. 76주령 이사브라운 노계를 강제환우후에 2수준의 단백질(15,17%)과 3수준의 대사에너지(2,750, 2,800, 2,850kca1/kg)를 2$\times$3요인 시험으로 처리구당 72수, 반복당 18수, 전체 432수를 배치하였다. 조사항목은 체중의 변화, 산란율, 난중, 사료섭취량, 사료요구율을 24주간 조사하였다. 체중은 2,800 kca1/kg ME 처리구에서 낮은 경향을 보였으며 이러한 처리구의 단백질 수준이 15%일 때 산란율이 가장 높게 나타났다. 사료섭취량은 사료의 대사에너지와 단백질 수준이 높아질수록 감소되었다. 본 실험의 결과 2,800 kca1/kg 대사에너지 급여구에서 15%의 단백질이 함유된 사료를 급여시에 체중의 변화가 적었으며, 산란율이 가장 높게 나타났다.

• Parasites, Hosts and Diseases
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• 제31권3호
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• pp.259-268
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• 1993

폐흡충의 분비배설물은 항원성이 높아 폐흡충증의 진단용 항원으로 가치가 있다고 보고되었다. 이 까닭은. 분비배설물에는 숙주내에서 여러 생물학적 반응을 일으키는 물질뿐 아니라 충체의 일부구성 성분 및 여러 효소 등이 포함되어 있기 때문이라 가정할 수 있다. 이 연구는 폐흡충 성충의 분비배설물에서 숙주의 산소라디칼을 분해시키는 효소인 catalase, superoxide dismutasr (SOD), peroxidase 등이 존재하는지를 확인하고 그 활성도를 측정하였으며 그 중 peroxidase를 정제하여 생화학적 특성의 일부 및 항원성을 관찰하였다. 폐흡충 성충 50마리를 $37^{\circ}C$ 부란기에 12시간 배양한 뒤 배양액을 원심분리하고 이를 분비배설 조효소로 사용하였다. 분비배설물에서 catalase, SOD와 peroxidase의 활성도를 측정할 수 있었고 그 비활성도(specific activity)는 각각 11.1, 3.4 및 48.5 이었다. 분비배설물의 peroxidase 비활성도는 충체추출액의 비활성도보다 1.5배 높았다 이 효소를 Sephacryl 5-300 Superfine gel filtration. DEAE-Tnsacryl M anion exchange chromatography로 정제하였다. 정제한 peroxidase의 분자량은 HPLC에서는 19 kDa이었고 SDS-전기영동에서는 16 kDa이었다. 정제한 효소를 전기영동한 후 diaminobenzidine으로 specific staining한 결과 이 효소는 충체추출액의 효소와 같은 영동이동거리를 나타내었다 즉 이 효소는 충체로부터 분비되는 것임을 알 수 있었다. 한편 폐흡충 감염 환자의 혈청과 반응시킨 immunoblot에서 분비배설물의 구성 단백질중 84, 64, 42, 32, 30, 28, 26, 24, 22, 11 및 8 kDa가 항원성을 보인 반면 정제한 peroxidase는 미약한 반응을 보였다 이상의 결과로 폐흡충 peroxidase는 분비배설되어 SOD, catalase와 함께 산소 독성을 제거하는데 작용하고 있으나 패흡충 감염 환자에서 특이 항체 반응을 일으키는데 에는 미약한 작용을 한다는 것을 알 수 있었다.

• 한국도로학회논문집
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• 제8권1호
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• pp.1-13
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• 2006

본 논문은 가열 재생아스팔트 흔합물의 성능을 향상시키기 위한 방법을 개발하기 위한 연구의 일부분이다. 새로이 개발된 혼합 방법은 회수 아스팔트 포장의 기존 바인더를 훨씬 많이 회생시켜 재생 혼합물에서 균일한 바인더의 정도를 갖게 한다. 본 연구의 목적은 새로이 개발된 혼합 방법으로 제조된 재생아스팔트 혼합물의 소성변형 저항 특성을 평가하는 것이다. 두 종류 골재(편마암 화강암), RAP의 두 가지 함량(15, 30%), LDPE의 두 가지 첨가량(0, 6%)를 이용하였으며, 혼합방법은 바인더의 불균등 상태를 개선하기 위한 두 가지 방법, 즉 일반적인 기존의 A 방법과 새롭게 개발한 F 방법을 이용하였다. 재생 혼합물 내의 바인더 산화 정도의 차를 조사하기 위하여 GPC분석을 실시하였고, 흔합 방법에 따른 소성변형 저항성을 평가하기 위하여 각 혼합 방법에 따라 제작한 재생 흔합물을 휠 트랙킹 시험과 변형강도를 측정하였다. 소성변형 저항 특성과 변형강도와의 상관관계는 기존의 A 방법보다 새롭게 개발된 F 방법이 더 높게 나타나, F 방법으로 제조된 혼합물의 품질이 보다 일관성 있는 소성변형 저항성을 나타내는 것을 알 수 있었다.

• The Journal of Korean Physical Therapy
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• 제17권4호
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• pp.537-557
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• 2005

The purpose of this study was to investigate the effect of pelvic traction and muscle energy technique(MET) for hemiplegic patients on static standing balance. The scale for static standing balance is measured by using mean balance(%), frequence(Hz), sway area($mm^2$), sway path(mm), max sway velocity(mm/s), ant/post sway angle($^{\circ}$), lateral sway angle($^{\circ}$), sway number, change of pelvic height is measured in relation to the height of ASIS and PSIS. The subjects of this study were thirty hemiplegic patients: 15men and 15 women, with an average ages of 50.80 years. The thirty subjects were divided into 3 group of 10 at random ; ten subjects had pelvic traction after bobath therapy (the pelvic traction group), ten subjects had muscle energy technique after bobath therapy (the MET group), and ten subjects had only bobath therapy (the control group). Static standing balance was measured using BPM (balance performance monitor; data print software version 5.3), pelvic height was measured using height measuring with an adjustable horizontal arm. In order to assure the statistical significant of the result, an one-way ANOVA, the paired t-test, and a person's correlation were applied at the.05 level of significance. The results of this study were as follows: 1) The change in pelvic height were statistically significant between the pelvic traction group, the MET group and the control group on pre-treatment and post-treatment(p<.05). 2) The change in affected and non-affected on weight bearing were not statistically significant between the pelvic traction group, the MET group and the control group on pre-treatment and post-treatment(p>.05). 3) The change in frequency were statistically significant between the MET group, the control group and the pelvic traction group on pre-treatment and post-treatment(p<.05). 4) The change in sway area were statistically significant between the MET group, the control group and the pelvic traction group on pre-treatment and post-treatment(p<.05). 5) The change in sway pa1h were statistically significant between the pelvic traction group, the MET group and the control group on pre-treatment and post-treatment(p<.05). 6) The change in max sway velocity were statistically significant between the pelvic traction group, the MET group and the control group on pre-treatment and post-treatment(p<.05). 7) The change in ant/post sway angle were statistically significant between the pelvic traction group, the MET group and the control group on pre-treatment and post-treatment(p<.05). 8) The change in lateral sway angle were statistically significant between the pelvic traction group, the MET group and the control group on pre-treatment and post-treatment(p<.05). 9) The change in sway number were statistically significant between the pelvic traction group, the MET group and the control group on pre-treatment and post-treatment(p<.05). In conclusion, there was a difference between the experimental group and the control group. In the future, we have to study continuously about pelvic traction and muscle energy technique in hemiplegic patients.

• 한국가금학회지
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• 제36권3호
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• pp.215-222
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• 2009

항생제 대체제 개발을 위한 용규와 감초 건조분말 복합제를 육계사료에 첨가 급여 하여 생산성과 혈액성상에 미치는 영향을 조사하기 위하여 수행하였다. 7일령 이후 육계 숫병아리(Ross)를 3단 케이지에 5처리 3반복, 반복당 10수씩, 총 150수를 공시하여 5주 동안 실험을 실시하였다. 시험 사료는 무첨가구, 항생제(avilamycin) 첨가구, 항생제 대체 용규 감초 건조 분말 0.5%(0.25+0.25), 1.0%(0.5+0.5%) 및 2.0%(1.0+1.0) 첨가구로 구분하여 사양 시험을 실시하였다. 증체량, 사료 섭취량 및 사료 요구율은 처리구간에 차이가 없었다. 도체중은 4주령에서 용규 감초 1.0% 첨가구에서 높았으며(P<0.05), 6주령시에는 용규 감초 1.0% 첨가구에서 약간 높았다. 도체율은 4주령과 6주령에서 처리구간에 비슷하게 측정되었다. 간장 중량은 4주령과 6주령에서 용규 감초 0.5% 첨가구에서 무거웠다(P<0.05). 비장중량은 4주령과 6주령에서 처리간 차이가 없었다. 4주령과 6주령시 혈중 protein, albumin, glucose, total bilirubin 농도와 GOT 및 GPT, TG, HDL-cholesterol, LDL-cholesterol, total cholesterol 농도에서 처리간에 차이가 없었다. 용규 감초 복합 첨가급여는 육계의 생산성 및 혈액성상에서 처리간의 차이가 없었음은 항생제 대체 물질로서의 사용가능이 있는 것으로 사료된다.

• Journal of Pharmaceutical Investigation
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• 제32권2호
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• pp.119-125
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• 2002

A rapid, selective and reproducible high-performance liquid chromatographic method has been developed for the determination of terazocin in human plasma. Terazocin plus the internal standard, prazocin hydrochloride, were extracted from alkalified plasma with tert-butylmethyl ether, back-extracted into 0.05% phosphoric acid. Fifty ${\mu}l-portions$ of extract were injected onto a octadecylsilane column and eluted with a mixture of acetonitrile, water and triethylamine (30 : 70 : 0.1 v/v, adjusted to pH 5.0 with dilute phosphoric acid) at a flow rate of 1.0 ml/min. The fluorescence intensity of column eluents was monitored at excitation wavelength of 250 nm and emission wavelength of 370 nm. No interference peaks were observed. The practical limit of quantitation was 5 ng/ml for terazocin. The average intraday and interday coefficients of variation were 4.15 and 3.54%, respectively. Also intraday and interday precisions over the range $5{\sim}60\;ng/ml$ were $0.49{\sim}2.92\;and\;0.38{\sim}5.12%$, respectively. The bioequivalence of two terazosin tablets, the $Hytrine^{\circledR}$ (Il Yang Pharmaceutical Co., Ltd.) and the $Teratonin^{\circledR}$ (Sam-A Pharmaceutical Co., Ltd.), was evaluated according to the guideline of Korea Food and Drug Administration (KFDA). Sixteen healthy male volunteers $(24.6{\pm}2.0\;years\;old)$ were divided into two groups and a randomized $2{\times}2$ cross-over study was employed. After one tablet containing 2 mg of terazosin was orally administered, blood was taken at predetermined time intervals and the concentration of terazosin in plasma was determined with a HPLC method using spectrofluorometric detector. AUC was calculated by the linear trapezoidal method. $C_{max}\;and\;T_{max}$ were compiled from the plasma drug concentration-time data. Analysis of variance (ANOVA) was utilized for the statistical analysis of the parameters. The results showed that the differences in $AUC_t,\;C_{max}\;and\;T_{max}$ between the two preparations were 0.21 %, 5.53% and 8.82%, respectively. The powers $(1-{\beta})\;for\;AUC_t,\;C_{max}\;and\;T_{max}$ were >99%, 97.49%, and 33.26%, respectively. Minimum detectable differences $({\Delta},\;%)\;at\;{\alpha}=0.1\;and\;1-{\beta}=0.8$ and the 90% confidence intervals were all less than ${\pm}20%$ except for $T_{max}.\;AUC_t\;and\;C_{max}$ met the criteria of KDFA for bioequivalence, indicating that $Teratonin^{circledR}$ tablets are bioequivalent to $Hytrine^{circledR}$ tablets.

• Asian-Australasian Journal of Animal Sciences
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• 제15권4호
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• pp.522-527
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• 2002

The experiment was conducted for a period of 56 days with twelve Bangladeshi bull calves of average body weight of $127.20{\pm}11.34$ kg. The calves were divided into 3 groups having 4 animals in each. The animals were fed urea-treated rice straw designated as A) 4% urea-treated rice straw, B) 4% urea+4% soybean-treated rice straw and C) 4% urea+6% soybean-treated rice straw. In addition, all the animals were supplied 2 kg green grass, 350 g Til-oil-cake and 100 g common salt per 100 kg body weight of animals. Straw was treated with 4% urea solution and soybean meal at 4 and 6% were added to treated straw and kept for 48 h in double layer polythene bags under anaerobic condition. Urea treatment improved crude protein (CP) content of rice straw from 2.68 to 8.70% and it was further increased by 10.74 and 12.12% with the addition of 4 and 6% soybean meal. Dry matter (DM) intake (kg) was higher (p<0.05) in C (4.2) followed by B (4.1) and A (4.0). Crude protein intake was significantly higher (p<0.05) in group B and C than group A. Total live weight gains were 20.2, 24.8 and 25.6 kg for calves of group A, B and C respectively (p<0.01). The addition of soybean meal to treated rice straw did not affect the coefficients of digestibility of DM, OM, EE and NFE. However, CP and CF digestibility were significantly higher in group B and C (p<0.05). The values for digestible crude protein (DCP), digestible ether extract (DEE), digestible nitrogen free extract (DNFE) and total digestible nutrients (TDN) were significantly (p<0.05) higher in diet C and B in comparison to diet A, but there were no significant difference in digestible organic matter (DOM) and digestible crude fibre (DCF) value among the groups. It may be concluded that 4% urea treated rice straw can be fed to growing bull calves with 2 kg green grass and a small quantity of concentrate without any adverse effect on feed intake and growth. Moreover, soybean meal at 4 and 6% can be added to urea treated rice straw at the time of treatment for rapid hydrolyzing of urea, which resulted an improvement in nutrient digestibility and better utilization of rice straw for growth of growing bull calves.

• Asian-Australasian Journal of Animal Sciences
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• 제19권10호
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• pp.1514-1518
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• 2006

English crossbred steers (n = 32) and heifers (n = 32) were fed a corn-based finishing diet and supplemented with 2% Ascophyllum nodosum on a DM basis to for various feeding stages of the 119 d feeding period determine the supplementation strategy that maximized intramuscular fat deposition as determined by quality grade. All cattle were implanted with Ralgro$^{(R)}$ on d 36 of the trial and re-implanted with Revalor-S$^{(R)}$ or Revalor-H$^{(R)}$ on d 92. Cattle were blocked by sex and divided into one control and three treatment groups receiving Ascophyllum nodosum. Treatment 1 (trt 1) received Ascophyllum nodosum from d 36 to 50 of the feeding period, trt 2 received Ascophyllum nodosum for the last 14 d of the feeding period, and trt 3 which received Ascophyllum nodosum for both d 36-50 and the last 14 d of the feeding period. Cattle were weighted initially ($385{\pm}4.53kg$) and every 28 d following until they reach an average BW of $554{\pm}7.46kg$. No effect for Ascophyllum nodosum supplementation was found on measured performance characteristics. All treatment groups supplemented with Ascophyllum nodosum had higher actual marbling scores (p<0.05) than controls. Trt 1 was found to have a highest marbling score (572.5; p<0.05), whereas the control group having the lowest marbling score (473.8). Trt 1 had a higher quality grade (5.25; p<0.05) than the control (3.94) group, but did not differ from trt 2 (4.56; p = 0.105) and trt 3 (4.75; p = 0.236) where high Select = 4, and low Choice = 5. Trt 2 did not differ from trt 3 (p = 0.655), or the control group (p = 0.140) for quality grade. However, trt 3 did tend to differ (p = 0.057) from the control group for quality grade. Control group animals graded 25% Choice, 62.5% Select; trt 1 graded 75% Choice, 18.8% Select; trt 2 graded 62.5% Choice, 25% Select and trt 3 graded 56.3% Choice and 31.2% Select. Overall, treatment groups had a 39.6% increase in Choice quality grade and a 37.5% decrease in Select quality grade when compared to the control animals.