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LC/MS/MS를 이용한 식용란 중 fluoroquinolone계 항균물질의 분석법에 관한 연구 (Study on analytical method of fluoroquinolone residues in eggs by LC/MS/MS)

  • 최유정;윤이란;남상윤;박영호;김병훈;손성기
    • 한국동물위생학회지
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    • 제30권1호
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    • pp.13-21
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    • 2007
  • An atmospheric pressure chemical ionization (APcI) LC/MS/MS method was developed for the simultaneous analysis of fluoroquinolones (norfloxacin, ciprofloxacin, enrofloxacin, danofloxacin) residues in eggs. The spiked and blank samples were extracted from whole eggs using 50mM phosphate buffer (pH 7.4). The extract was cleaned up by passage though $Oasis^{(R)}$ MAX extraction cartridge for solid-phase extraction followed by elution with 4% formic acid in methanol. The extract of sample was separated on a Waters $Atlantis^{TM}$ $dC_{18}$ reversed-phase column ($4.6{\times}150mm,\;5{\mu}m$) and analyzed by APcI positive mode mass spectrometry. The mobile phase consists of aqueous 0.2% nonafluoropentanoic acid (NFPA) and methanol. Multiple reaction monitoring (MRM) using the precursor to product ion combinations of m/z $320\;{\dashrightarrow}\;302,\;332\;{\dashrightarrow}\;314,\;360\;{\dashrightarrow}\;342$ and m/z $358\;{\dashrightarrow}\;340$ were used to quantify norfloxacin (NOR), ciprofloxacin (CIP), enrofloxacin (ENR) and danofloxacin (DAN), respectively. The limits of quantification (LOQ) were 7.8ppb for NOR, 8.5ppb for CIP, 8.9ppb for ENR, and 4.8ppb for DAN. Average recoveries of fortified sample at levels of 0.025 to 0.1 ppm were estimated 71.29% for NOR, 75.27% for CIP, 85.51% for ENR and 81.22% for DAN. These results could be applied for the confirmation and quantification in eggs.

해수오염원추적자로서의 플루오르화물이온 및 진해만의 플루오르화물이온농도분포 (Eligibility of Fluoride Ion as A Tracer of Wastewaters and Distribution of Fluoride in Jinhae Bay)

  • 원종훈;박길순
    • 한국해양학회지
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    • 제8권1호
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    • pp.9-21
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    • 1973
  • 1. 플루오르를 함유하는 배수가 바다에 유입되었을 때 플루오르화물이온을 그 추적자로 이용할 수 있다. 2. "Dotite"시약 "알풋손"에 의한 해수중의 플루오르 정량법을 검토하였다. 3. 진해만의 플루오르화물이온 농도분포를 조사하여 진해만에 플루오르를 함유하는 배수가 평균 최소한 0.13% 혼입되어 있으며 그것은 진해 모화학공장의 폐수에 기인한다. 그리고 그것이 혼입되어가는 경로를 밝혔다. 그것이 혼입되어가는 경로를 밝혔다.

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시료고체상분산(matrix solid phase dispersion)전처리법과 액체크로마토그라피를 이용한 돈육중 enrofloxacin 및 ciprofloxacin 분석 (Matrix solid phase dispersion(MSPD) extraction and HPLC determination of enrofloxacin and ciprofloxacin in pork muscle tissue)

  • 강환구;손성완;이혜숙;김재학;조명행
    • 대한수의학회지
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    • 제37권1호
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    • pp.195-202
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    • 1997
  • A method for the isolation by matrix solid phase dispersion method and liquid chromatographic determination of enrofloxacin and ciprofloxacin in pork muscle tissue is presented. Blank or enrofloxacin and ciprofloxacin spiked samples(0.5g) containing 0.05g oxalic acid were blended with $C_{18}$(octadecylsilyl derivatized silica) packing material. After homogenization, $C_{18}$/muscle tissue matrix was transferred to glass column made from 10ml glass syringe and filter paper, and compressed to 4~4.5ml volume. A column was washed with 8ml of hexane and dried under vacuum. Interfering materials were removed by ethylacetate 8ml and dried, following which enrofloxacin and ciprofloxacin were eluted with 8ml of methanal under gravity. The eluate containing enrofloxacin and ciprofloxacin wase free from interfering compound when analysed by HPLC with UV detection at 278nm. Enrofloxacin and ciprofloxacin showed linear response with UV detector at the range of $0.05{\sim}1.0{\mu}g/ml$ and eluted within 5ml elution volume of methanol from the matrix. Fortified sample containing 0.05g oxalic acid represented more good recoveries than that of control sample. Average percentages of enrofloxacin and ciprofloxacin were $93.30{\pm}4.56%$ and $91.84{\pm}4.17%$, respectively, for the concentration range(0.05, 0.1, 0.25, 0.5 and $0.75{\mu}g/g$). The interassay variability of enrofloxacin was $6.02{\pm}5.33%$ with an intra-assay variability of 4.89% and $6.75{\pm}2.68%$ with 4.54% for ciprofloxacin. Detection limit of enrofloxacin and ciprofloxacin was $0.030{\mu}g/g$ in the spiked sample.

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Modified Renshen Wumei Decoction Alleviates Intestinal Barrier Destruction in Rats with Diarrhea

  • Guan, Zhiwei;Zhao, Qiong;Huang, Qinwan;Zhao, Zhonghe;Zhou, Hongyun;He, Yuanyuan;Li, Shanshan;Wan, Shifang
    • Journal of Microbiology and Biotechnology
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    • 제31권9호
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    • pp.1295-1304
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    • 2021
  • Modified Renshen Wumei decoction (MRWD), a famous traditional Chinese medicine, is widely used for treating persistent diarrhea. However, as the mechanism by which MRWD regulates diarrhea remains unknown, we examined the protective effects of MRWD on intestinal barrier integrity in a diarrhea model. In total, 48 male rats were randomly distributed to four treatment groups: the blank group (CK group), model group (MC group), Medilac-Vita group (MV group) and Chinese herb group (MRWD group). After a 21-day experiment, serum and colon samples were assessed. The diarrhea index, pathological examination findings and change in ᴅ-lactate and diamine oxidase (DAO) contents illustrated that the induction of diarrhea caused intestinal injury, which was ameliorated by MV and MRWD infusion. Metabolomics analysis identified several metabolites in the serum. Some critical metabolites, such as phosphoric acid, taurine, cortisone, leukotriene B4 and calcitriol, were found to be significantly elevated by MRWD infusion. Importantly, these differences correlated with mineral absorption and metabolism and peroxisome proliferator-activated receptor (PPAR) pathways. Moreover, it significantly increased the expression levels of TLR4, MyD88 and p-NF-κB p65 proteins and the contents of IL-1 and TNF-α, while the expression levels of occludin, claudin-1 and ZO-1 proteins decreased. These deleterious effects were significantly alleviated by MV and MRWD infusion. Our findings indicate that MRWD infusion helps alleviate diarrhea, possibly by maintaining electrolyte homeostasis, improving the intestinal barrier integrity, and inhibiting the TLR4/NF-κB axis.

시료고체상분산처리와 액체크로마토그라피를 이용한 소의 근육, 간 및 천엽에서의 벤지미다졸계 구충제 잔류분석 (Matrix solid phase dispersion isolation and high performance liquid chromatographic determination of five benzimidazole anthelmintics in bovine muscle, liver and omasum)

  • 김충희;김곤섭;박정희;하대식;류재두;손성기;허정호;정명호;김종수
    • 대한수의학회지
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    • 제42권2호
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    • pp.171-181
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    • 2002
  • Simultaneous multiresidue analysis using liquid chromatography determination for five benzimidazole anthelmintics(thiabendazole, oxibendazole, albendazole, mebendazole and fenbendazole) in bovine muscle, liver and omasum has been described. Blank or benzimidazole-fortified samples(0.5g) were blended with bulk $C_{18}$($40{\mu}m$, 18% load, endcapped, 2g). A column made from the resultant $C_{18}$/animal tissue matrix was first washed with hexane($8m{\ell}$), following which the benzimidazoles were eluted with acetonitrile($8m{\ell}$). Analytes of extracted sample were determined by liquid chromatography with UV detector at 290nm. Correlation coefficients of standard curves for individual benzimidazole isolated from fortified samples, using internal standardization, were linear($0.991{\pm}0.007$ to $0.996{\pm}0.005$) with average relative percentage recoveries from $62.1{\pm}3.8(%)$ to $92.3{\pm}7.5(%)$ for the concentration range($0.2{\sim}6.4{\mu}g/g$), respectively. Recoveries rates of TBZ, MBZ in liver, OBZ, MBZ in muscle and TBZ, MBZ in omasium from fortified benzimidazole were 92.%, 87.3%, 74.5%, 82.7%, 75.2% and 83.5% at condition II, respectively. Condition II showed higher recoveries rates than condition I. These results indicated that the matrix solid phase dispersion(MSPD) methodology is acceptable for the determination of 5 benzimidazole anthelmintics and may also suitable for other matrixes of food animal origin.

우리나라 상토의 물리적 표준분석법 설정 연구 1. 입자밀도 및 용적밀도 (Development of Standard Analysis Methods for Physical Properties on Korean bedsoil 1. Particle density and Bulk density)

  • 김이열;조희기
    • 한국토양비료학회지
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    • 제35권6호
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    • pp.327-334
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    • 2002
  • 우리나라 유통상토에 대한 물리적 표준분석법을 설정하기 위한 연구를 실시하였다. 국내 시중에 유통되고 있는 53개 품목의 원예용 상토와 9개 품목의 수도용 상토를 대상으로 설정된 분석법을 적용하여 실험하였다. 입자밀도의 측정은 가스형 피크노메타 (Micromeritics Co. Model 1305)를 사용하면 속도와 정확성 면에서 매우 유리 하였다. 용적밀도는 구미에서 Sandbox법에 의한 용적밀도를 기본으로 하기 때문에 이와 유사한 성적을 얻을 수 있는 다양한 실험을 한 결과, 추다짐법 (Plunger compaction method)이 가장 유의성 있는 측정 방법으로 밝혀졌다. 한편 가스형 피크노메타법에 의한 우리나라 유통상토의 입자밀도는 원예용이 1.93, 수도용이 $2.43Mg\;m^{-3}$로 나타났으며, 추다짐법에 의한 용적밀도는 원예용이 0.22, 수도용이 $1.01Mg\;m^{-3}$로 각각 나타났다.

LC-MS/MS를 이용한 농산물 중 살균제 tridemorph의 시험법 개발 및 검증 (Development and Validation of an Analytical Method for Determination of Fungicide Tridemorph in Agricultural Commodities Using LC-MS/MS)

  • 박원민;도정아;임승희;박신민;윤지혜;이동석;장문익
    • 한국식품위생안전성학회지
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    • 제32권4호
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    • pp.290-297
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    • 2017
  • 본 연구는 2017년 수입식품 중 신규 기준설정 예정 농약인 tridemorph의 안전성 관리를 위한 공정시험법을 확립하기 위하여 수행하였다. Tridemorph의 잔류물의 정의는 모화합물로 규정하며, 확립된 시험법은 실험실내 및 실험실간 검증을 통해 공정시험법으로의 유효성을 확인하였다. 대표 농산물 5종(감귤, 감자, 고추, 대두, 현미)에 대하여 잔류분석이 가능하도록 선택성과 감도가 우수한 LC-MS/MS를 사용하여 수용성 유기용매인 ACN로 추출 후 $NH_2$ 카트리지에 가장 회수율이 우수한 용매인 MeOH/DCM (1/99, v/v)를 정제조건으로 확립하여 시험법을 개발하였다. 개발된 tridemorph의 직선성은 결정계수($r^2$)가 0.99 이상으로 우수하였으며, 검출한계 및 정량한계는 각각 0.001 및 0.005 mg/kg으로 높은 감도를 나타내었다. 개발된 시험법의 평균 회수율은 75.9~103.7%였으며, 분석오차는 8.5%이하로 정확성 및 재현성이 우수함을 확인할 수 있었다. 또한, 외부기관 검증 결과 평균 회수율은 87.0~109.2%이었으며, 상대표준편차는 모두 7.8% 이하로 조사되어 국제적 잔류농약 분석 가이드라인 및 식품의약품안전평가원 가이드라인에 적합한 수준임을 확인하였다. 따라서 본 시험법은 농산물 중 tridemorph의 잔류검사를 위한 공정시험법으로 활용할 수 있을 것으로 판단된다.

한국산 P.V.C.의 생물학적 안정도 및 적합성에 대한 실험적 고찰 (An experimental study on the biological safety and compatability of P.V.C. made in Korea)

  • 선경
    • Journal of Chest Surgery
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    • 제17권1호
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    • pp.157-166
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    • 1984
  • These biologic test procedures are designed to test the suitability of P.V.C. made in Korea intended for parenteral preparation, which were based on the U.S. Pharmacopeia XIX "Biologic Test-Plastic Container", Official from July 1, 1975. Healthy adult human blood and rabbits weighing 2\ulcorner.2Kg were used for test materials. Sample P.V.C. were sampled from the medical equipments made in Korea randomly and Control P.V.C. were sampled from the standardized Cobe and Polystan P.V.C. tubes. P.V.C. extract was prepared from a homogeneous P.V.C. samples by incubating 60 square centimeters of the sample per 20 millimeters of sterile pyrogen-free saline at 70\ulcorner for 72 hours or autoclaving at 120\ulcorner for 1 hour. The Implantation Test was designed to evaluate the reaction of living tissue to the plastic by the method of the implantation of the Sample itself into animal tissue. The Systemic Injection Test, the Intracutaneous Test, and the remainders were designed to determine the biological response of animals to plastics by the single-dose injection of specific extracts prepared from a Sample. The results are as follows; 1.Implantation Test - No significant difference for reactions was noted between the Sample treated animal and the Control after 72 hours of implantation. 2.Systemic Toxicity Injection Test - No sign of toxicity and/or death immediately after injection and at 4, 24, 48 hours respectfully after injection. 3.Intracutaneous Test - None of the animals treated with the Sample showed a significantly greater reaction than the observed in the animals treated with Blank. 4.Pyrogen Assay-Only one animal treated with the Sample showed the maximal rise of rectal temperature about 0.2\ulcorner after 3 hours of injection, but remainders showed no change. 5.Hemolytic Index - The positive Control tube of distilled water exhibited complete hemolysis while the negative Control tube and P.V.C. extract were negative demonstrating no hemolysis. 6.Cell Morphology of Erythrocytes and Leukocytes on Stored, Heparinized Human Blood -- There was no significant difference in the morphology of either the Control or Sample extract. 7.Clotting Mechanism of Human Blood in vitro - After allowing to the P.V.C. extract at room temperature for 5 Hours and at 10\ulcorner for 24 hours, there was no appreciable difference in Prothrombin Time under these conditions. 8.Clotting Mechanism of Rabbit in vivo - At the termination of 5 days after intraperitoneal injection of the P.V.C. extract, no significant changes in Clotting Time were observed. According to the above results, it could be concluded that the P.V.C. made in Korea was acceptable for parenteral preparation, especially treated with physiologic saline and/or human blood.man blood.

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촉매반응을 이용한 수용액중 흔적량 셀렌의 분광광도법 정량 (Spectrophotometric Determination of Trace Selenium in Aqueous Solutions by Catalytic Reaction)

  • 이승화;최종문;최희선;김영상
    • 대한화학회지
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    • 제38권5호
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    • pp.351-358
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    • 1994
  • 셀렌이 촉매작용을 하는 반응을 이용한 수용액중 흔적량 셀렌의 분광광도법 정량에 관하여 검토하였다. 즉, 산성의 수용액 매질에서 셀렌에 의한 페닐히드라진의 촉매반응은 H-acid(8-아미노-1-나프톨-3,6-이슬폰산의 이나트륨염)과 반응하여 붉은 색의 아조 염료로 변하는 벤젠디아조뮴이온을 생성한다. 이 반응에 대해, 시약들의 가하는 양과 용액의 pH등과 같은 실험조건들을 최적화시켰다. 시료용액 15ml를 0.1 M EDTA용액으로 처리하여 철 등을 제거한 다음에 0.06 M 페닐히드라진 염산 1 ml, 0.02 M H-acid 1 ml, 및 0.3 M-$KClO_4$ 3 ml를 용액에 순서대로 가하였다. 염산으로 용액의 pH를 1.4로 조정하였다. 끓는 물중탕에서 30분간 가열한 다음, 식혀서 탈염수로 25.00ml되게 묽혔다. 흡광도 측정을 위한 바탕용액은 탈염수로 만들었다. 527nm에서 흡광도를 측정하였다. 위의 실험과정으로 표준검정곡선법에 의해 수도물, 강물, 및 저수지물 등의 물시료중 흔적량 셀렌을 정량하고, 시료들에 가해진 일정량의 셀렌을 정량하여 회수율을 구하였다. 이렇게 얻은 104 내지 111%의 회수율로부터 이 방법이 자연수중 ng/ml수준의 셀렌 분석에 정량적으로 응용될수 있음을 알 수 있었다.

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A Study on 10 Metabolites Separated from DNA Adduce of Blood Lymphocytes in Rats Exposed Orally with 3,3-dichlorobenzidine(DCB) by GC/MS-SIM

  • Shin, Ueon-Sang;Lee, Jin-Heon
    • 한국환경보건학회지
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    • 제28권4호
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    • pp.6-11
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    • 2002
  • 3.3'-Dichlorobenzidine(DCB) has be shown carcinogenic in several animals, and the development of non-invasive biomonitoring method in workers exposed with it is a very important subject. DNA adduct is a good biomarker for biomonitoring about carcinogens exposure, and lymphocytes is a good non-invasive samples. So we studied to analyze metabolites in blood lymphocytes of female Sprague-Dawley rats exposed orally with DCB(20, 30, and 40 mg/kg wt.) for 3 weeks. For analysis of them, we isolated DNA adducts from blood lymphocytes by using the enzymes method in /sup 32/P-postlabeling, and measured them by using gas chromatography/mass spectrometry-selected ion monitoring(GC/MS-SIM). 4-aminobiphenyl and phenanthrene-d/sub 10/ were added as internal standard for blank sample. Standard metabolites of DCB were synthesized with using pyridine and acetic acid which were promoter and controller in acetylation of DCB. And they were used for calibration curve. Our results showed two kinds of metabolites in DNA adducts of blood lymphocytes. They were N-acetyl 3,3'-dichlorobenzidine(acDCB) and N,N'-diacetyl 3,3'-dichiorobenzidine(di-acDCB ). They were combined with DNA at the same time as an acetyl of it was removed. So we measured DCB and acDCB for two kinds of metabolites in DNA adducts of blood lymphocytes. Our results showed the levels of DCB were 1.46∼2.26 times more than that of acDCB. And also the levels of metabolites in 20, 30 and 40 mg/kg wt. were gradually increased with going days from 1st to 3rd week. They are 1.66, 1.38 and 0.90 times in total metabolites, 1.76, 1.49 and 1.02 times in DCB, and 1.51, 1.22 and 1.28 times in acDCB. In conclusion, the results of this study showed DCB exposed to rats formed DNA adduct in blood lymphocytes after acetylated to N-acetyl 3.3'-dichloro benzidine(acDCB) and N,N'-diacetyl 3,3'-dichlorobenzidine(di-acDCB), and they could be analyzed by us ing gas chromatography/mass spectrometry-selected ion monitoring(GC/MS-SIM).