• 한국임상수의학회지
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• 제13권2호
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• pp.153-157
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• 1996

Ketosis can exist in both clinicla and subclinical forms. Detection of the subclinical form of ketosis by the use of a nitroprusside based test powder gas been shown to be a relatively simple and reliable procedure. Howere, very liffle is known about the indcidence or prevalence of the subclinical ketosis in Korea. In the present study, samples of urine taken from 288 dairy cows in Chonnam area were examined to demonstrate the presence of ketone bodies, using ross test. All the cows were within 4 weeks either before or after parturition. The gerd size was from 10 to more than 100 cows, and the cows did not show any clinical signs of ketosis. Of the 288 cows, 85 (29.5%) were positive to Ross test; of the positive cases 42.4% were +, 44.7% were ++, and the remaining 12.9% were +++. The prevalence increased from 3rd parity, peaked at 6th parity and thereafter decreased. The prevalence was higher after parturition than before parturition, with the highest occurrence during the 2nd week after calving. The prevalence was higher during winter. Also cows kept indoor throughout the year showed higher occurrence of the subclinical ketosis. The subclinical ketosis did not affect the specific gravity of the urine; however, increasing amount of ketone bodies in the urine decreased the pH of urine.

• Archives of Pharmacal Research
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• 제26권2호
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• pp.120-123
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• 2003

A method for the determination of terbutaline enantiomers in human urine by capillary elctrophoresis has been developed. Optimum resolution was achieved using 50 mM phosphate buffer, pH 2.5, containing 15 mM of hydroxypropyl-$\beta$-cyclodextrin as a chiral selector. Urine samples were prepared by solid-phase extraction with Sep-pak silica, followed by CE. The assay was linear between 2-250 ng/mL (R = 0.9998 for (S)-(+)-terbutaline and R = 0.9999 for (R)-(-)-terbutaline) and detection limit was 0.8 ng/mL. The intra-day variation ranged between 6.3 and 14.5% in relation to the measured concentration and the inter-day variation was 8.2-20.1%. It has been applied to the determination of (S)-(+)-terbutaline and (R)-(-)-terbutaline in urine from healthy volunteer dosed with racemic terbutaline sulfate.

• 대한화학회지
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• 제47권4호
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• pp.339-344
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• 2003

Paraquat는 가장 효과적이고 널리 사용되는 제초제이지만 인간에게 매우 유독한 물질이다. 중독환자에 있어 뇨중 농도는 가장 중요한 인자중의 하나로 알려져 있으나 일반 검사실에서 이를 위한 정량검사는 거의 시행되지 않고 있다. 본 연구에서는 sodium dithionite를 이용하여 뇨중의 paraquat의 농도를 측정하는 새로운 방법의 진단 시험지를 개발하였다. 이 이차유도성 방식을 사용하여 paraquat의 농도를 측정한 결과 $0.5{\%}$ borate 완충용액(pH 8.0), 유도체 0.25 M $Na_2S_2O_4,\0.1~0.8{\%}$ PolyVinyl Pyrrolidone(PVP) 안정제, $1{\%}$ decanol의 구성비로 만들어진 진단시험지의 반응 색상이 안정하며 표준 비색표에 의한 육안적인 감별은 물론 화학 자동분석기에서의 응용성이 좋았다.

• 대한한의학회지
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• 제16권1호통권29호
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• pp.319-338
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• 1995

This article is to investigate the effects of Euphorbia Pekinensis RUPR. on rats with acute renal failure induced by gentamicin sulfate. So this experimental research was focused on measuring (1)the levels of creatinine, blood urea nitrogen, glutamic oxaloacetic transaminase, glutamic pyruvic transaminase, total protein, sodium, potassium, chloride in the serum and (2)the levels of protein, blood, sodium, potassium, chloride, pH, specific gravity and volume in the urine and (3)intake water. The results were summarized as follows. 1. While the levels of creatinine and glutamic oxaloacetic transaminase, glutamic pyruvic transaminase in the serum were significantly increased, the level of BUN in the serum were partially increased and the levels of sodium and potassium in the serum were partially decreased on the Euphorbia Pekinensis $R_{UPR}$. group. 2. While the urine volume was significantly increased, the levels of protein, blood, sodium and chloride in the urine were partially increased and the specific gravity, pH in the urine were partially decreased. According to the above results, it is shown that Euphorbia Pekinensis $R_{UPR}$. without refinning had a diuretic effect on rats with acute renal failure induced by gentamicin sulfate, but aggravated the glomerular filtration rate and tubular reabsorption. So, it is supposed that Euphorbia Pekinensis $R_{UPR}$. without refinning needs to be used carefully on renal disease and futhermore research about the kinds of extracts form is necessary.

• 분석과학
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• 제19권6호
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• pp.519-528
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• 2006

본 연구에서는 뇨시료를 고체상 추출법으로 추출한 후 HPLC/DAD/ESI-MS(high-performance liquid chromatograph/diode array detector/electro-spray ionitation mass spectrometry)를 사용하여 분석하였다. 7종의 thyroid hormones의 HPLC 분리조건은 Hypersil ODS(octadecylsilica) 컬럼(4.6mm I.D., 100 mm length, particle size $5{\mu}m$)을 사용하고 ammonium formate buffer와 acetonitrile을 이동상으로 하여 기울기 용리한 결과 완전 분리가 가능하였으며, UV spectra 및 질량스펙트럼을 확인할 수 있었다. 고체상 추출법에 의한 전처리 최적 조건을 조사한 결과 시료를 pH 3으로 한 후 C18 고체상을 사용하여 4 mL의 methanol/ammonium hydroxide(9:1) 혼합용액으로 용리할 경우 회수율이 89.0-113.1%로 나타났다. HPLC/DAD를 이용하여 10-1000 ng/mL범위에서 검량선을 작성한 결과 $r^2$값은 0.992-0.998 으로 나타났으며 검출한계는 2-4 ng/mL(3.8-13.0 pmol/mL)로 계산되었다.

• Toxicological Research
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• 제7권1호
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• pp.21-27
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• 1991

We developed a simple method to determine benzodiazepines in biological samples using electron capature detectors and nitrogen-phosphorous detectors. The extraction of 13 benezodiazepines in urine at pH 9.5 with toluene and its analysis in GC/NPD showed the peaks in 9-16 min. In this retention time range, the biological backaground was fairly low and the drugs could be identified in low concentrations. The benzodiazepines in urine samples were screened by the fluorescence polarization immunoassay and positive samples were confirmed by the GC/NPD method.

• 대한디지털의료영상학회논문지
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• 제16권2호
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• pp.1-7
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• 2014

This study is to increase the accuracy of the diagnosis of benign prostatic hyperplasia by presenting a method that can accurately measure the residual urine amount of the bladder by using an ultrasound image. Agar powder, Propanol and distilled water were used as materials for making a phantom. In order to measure the volume, a $10m{\ell}$ cylinder, syringe and beaker were used. The image was obtained by scanning phantoms produced into six shapes. Each constant value was obtained by using the expression designed to measure the residual urine amount of the bladder and was compared and analyzed. The measuring method of Bladder volume was presented and a constant value for each shape was obtained and five observers measured it five times. According to the results of clinical application, the errors of Ellipse-beanbag, Shield-shield were 11.0%, 18.2%, respectively. Constant values depending on the shape of each phantom were presented in order to accurately measure the volume of the bladder in measuring the amount of residual urine for the diagnosis of benign prostatic hyperplasia. The accuracy of the volume using this was verified statistically(p > 0.05). Therefore, it is considered to be useful in diagnosing benign prostatic hyperplasia by using the ultrasound imaging measuring method presented.

• 한국축산시설환경학회지
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• 제18권3호
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• pp.201-206
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• 2012

말의 성장단계별 분뇨의 시료를 채취하여 비료성분 및 오염물질 성분을 채취하여 분석하여 본 결과 다음과 같았다. 1. 말의 분뇨의 수분함량은 각각 76.1%, 96.0%로 조사되었다. 2. 또한 말의 분 중 유기물함량은 21.3%로 조사되었으며, 뇨는 약 2.0%로 조사되었다. 3. 또한 말의 분뇨 중 비료성분인 T-N, T-P, T-K의 성분이 각각 0.18%, 0.10% 및 0.23% 이며, 뇨는 각각 2.88%, 0.0015% 및 0.84%로 조사되었다. 4. 말 분뇨의 오염물질을 조사한 결과, 말의 분뇨의 pH는 각각 7.10, 8.48이며, BOD는 분이 26,906.2 $mg/{\ell}$, 뇨는 14,298.9 $mg/{\ell}$, COD는 분이 36,642.3 $mg/{\ell}$, 뇨는 7,484.3 $mg/{\ell}$, SS (Suspended Solid, 부유물질)은 분에서 89,375.0 $mg/{\ell}$, 뇨에서 6,987.0 $mg/{\ell}$로 조사되었다. 5. 말의 분과 뇨의 중금속함량 중 Cr은 각각 2.65 mg/kg, 1.52 mg/kg으로 조사되었으며, Cu 성분도 7.05 mg/kg, 1.62 mg/kg 으로 조사된 반면에 Ni 성분은 말의 분뇨에서 각각 1.24 mg/kg, 0.0 mg/kg으로 조사되었다. 6. 따라서 말의 분뇨는 퇴비원료물로 사용이 가능한 것으로 조사 분석되었으며, 향후 승마사업의 급격한 발전으로 말의 분뇨 발생량이 증가될 것으로 전망되며, 이를 적정 처리하기 위해서는 퇴비화 방법으로 자원화가 가능 할 것으로 조사되었다.

• Journal of Preventive Medicine and Public Health
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• 제17권1호
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• pp.269-279
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• 1984

The optimum conditions for measuring cadmium content of less than 0.2ppm by flame atomic absorption spectrophotometry were investigated. The cadmium in urine was extracted by APDC-MIBK for the analysis by atomic absorption spectrophotometry after ashing them by a wet method. 1. Optimum conditions by APDC-MIBK and DDTC-MIBK extractions. The acidic aqueous solution was prepared with appropriate amount of 0.IN nitric acid, 5ml of 25% (W/V) sodium potasstum tartarate, 10ml of saturated ammonium sulfate, and 2ml of 2% APDC(or 1 ml of 5% DDTC) chelating agent. The total volume of solution was adjusted to 55 ml and pH to $2{\sim}10$ (or$7{\sim}10$). The aqueous solution was extracted with 10ml MIBK. Concentration of Triton X-100 did not effect the absorbance for APDC-MIBK extraction of cadmium, but absorbance decreased as the concentration increased for DDTC-MIBK extraction. The sensitivity and detection limits for the cadmium determination from APDC-MIBK extraction were 0.0038ppm and 0.0102, 0.0022ppm and 0.0116 for DDTC-MIBK, and 0.0132ppm and 0.0034 for 0.1N nitric acid. APDC-MIBK and DDTC-MIBK extractions were 3 times higher than 0.1N nitric acid for the sensitivity. 2. Excretion of cadmium in 24-hour urine by APDC-MIBK extraction. Determination of cadmium in urine by atomic absorption spectrophotometry of A.A. (Cd=2 mA) mode and B.C. (Cd=4 mA) mode and B.C. (Cd=4mA, $D_2=20mA$) mode showed some difference (p<0.05). The difference of cadmium determination and recovery according to method of standard additions and standard calibration curve method in urine was not significant (p>0.05, $93.48{\pm}11.78%,\;94.83{\pm}22.00%$). Excretion of cadmium in 24-hour urine collection from normal person and variance analysis within measurement variation was not significant (p>0.05), but between interindividual was significant (0.05). Determination of cadmium content by two different methods of flame atomic absorption spectrophotometry and dithizone colorimetry showed that the results from the two methods can be described by a regression line with a good correlation (y=1.0153x-0.2927, x=Cd by D.C., y=Cd by A.A.S., $r=0.8651^*$, p<0.01).

• Journal of Veterinary Science
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• 제21권6호
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• pp.81.1-81.10
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• 2020

Background: Although previous in vivo studies explored urinary microRNA (miRNA), there is no agreement on nephrotoxicity-specific miRNA biomarkers. Objectives: In this study, we assessed whether urinary miRNAs could be employed as biomarkers for nephrotoxicity. Methods: For this, literature-based candidate miRNAs were identified by reviewing the previous studies. Female Sprague-Dawley rats received subcutaneous injections of a single dose or repeated doses (3 consecutive days) of gentamicin (GEN; 137 or 412 mg/kg). The expression of miRNAs was analyzed by real-time reverse transcription-polymerase chain reaction in 16 h pooled urine from GEN-treated rats. Results: GEN-induced acute kidney injury was confirmed by the presence of tubular necrosis. We identified let-7g-5p, miR-21-3p, 26b-3p, 192-5p, and 378a-3p significantly upregulated in the urine of GEN-treated rats with the appearance of the necrosis in proximal tubules. Specifically, miR-26-3p, 192-5p, and 378a-3p with highly expressed levels in urine of rats with GEN-induced acute tubular injury were considered to have sensitivities comparable to clinical biomarkers, such as blood urea nitrogen, serum creatinine, and urinary kidney injury molecule protein. Conclusions: These results indicated the potential involvement of urinary miRNAs in chemical-induced nephrotoxicity, suggesting that certain miRNAs could serve as biomarkers for acute nephrotoxicity.