• 제목/요약/키워드: animal test

검색결과 2,425건 처리시간 0.027초

탄소나노튜브/아교 접착제를 이용한 돌침대용 목재 샌드위치 복합재의 계면, 열적 및 방수특성 증가 (Improvement on Interfacial, Thermal, and Water Resistance Properties of Wood Sandwich Composites for Stone Bed using CNT-Animal Glue Adhesive)

  • 김종현;권동준;신평수;백영민;박하승;문선옥;박종만
    • Composites Research
    • /
    • 제30권4호
    • /
    • pp.235-240
    • /
    • 2017
  • 아교는 수용성을 띄는 접착제로, 이 특징에 의해 물에 약하다는 단점에도 불구하고 전통적인 고가구에 많이 사용되어 왔다. 이러한 단점을 개선하기 위하여 많은 연구가 진행되고 있다. 본 연구에서는 탄소나노튜브를 도입에 따른 아교의 계면특성 및 열적특성 그리고 방수특성 개선에 대한 연구를 진행하였다. 탄소나노튜브의 비율이 증가함에 따라 아교를 이용하여 접착한 돌침대용 목재 샌드위치 판 상부의 실시간 온도측정을 진행하였다. 나무와 아교접착제 간의 계면특성의 변화를 알아보기 위하여 랩 전단 실험을 실시하였고, 습도가 높아짐에 따라 물성이 약해지는 아교의 단점을 개선하기 위하여 탄소나노튜브를 도입에 따른 아교의 방수특성이 개선되는지 대한 실험을 진행하였다. 랩 전단시편을 물에 담근 후 랩 전단 실험을 진행하여 기존의 결과와 비교하여 차이가 얼마나 나는지 비교하였다. 이를 증명하기 위하여 물과의 정적 접촉각을 이용해 탄소나노튜브의 함량에 따른 아교접착제의 소수성 정도를 비교하였다. 실험결과 아교 접착제에 탄소나노튜브를 도입으로 계면특성, 열적특성 및 방수특성이 개선되었다.

Determination and Prediction of Digestible and Metabolizable Energy from the Chemical Composition of Chinese Corn Gluten Feed Fed to Finishing Pigs

  • Wang, T.T.;Liu, D.W.;Huang, C.F.;Liu, L.;Piao, X.S.;Wang, F.L.
    • Asian-Australasian Journal of Animal Sciences
    • /
    • 제27권6호
    • /
    • pp.871-879
    • /
    • 2014
  • Two experiments were conducted to determine the digestible energy (DE) and metabolizable energy (ME) contents of corn gluten feed (CGF) for finishing pigs and to develop equations predicting the DE and ME content from the chemical composition of the CGF samples, as well as validate the accuracy of the prediction equations. In Exp. 1, ten CGF samples from seven provinces of China were collected and fed to 66 finishing barrows (Duroc${\times}$Landrace${\times}$Yorkshire) with an initial body weight (BW) of $51.9{\pm}5.5$ kg. The pigs were assigned to 11 diets comprising one basal diet and 10 CGF test diets with six pigs fed each diet. The basal diet contained corn (76%), dehulled soybean meal (21%) and premix (3%). The ten test diets were formulated by substituting 25% of the corn and dehulled soybean meal with CGF and contained corn (57%), dehulled soybean meal (15.75%), CGF (24.25%) and premix (3%). In Exp. 2, two additional CGF sources were collected as validation samples to test the accuracy of the prediction equations. In this experiment, 18 barrows (Duroc${\times}$Landrace${\times}$Yorkshire) with an initial BW of $61.1{\pm}4.0$ kg were randomly allotted to be fed either the basal diet or two CGF containing diets which had a similar composition as used in Exp. 1. The DE and ME of CGF ranged from 10.37 to 12.85 MJ/kg of dry matter (DM) and 9.53 to 12.49 MJ/kg of DM, respectively. Through stepwise regression analysis, several prediction equations of DE and ME were generated. The best fit equations were: DE, MJ/kg of DM = 18.30-0.13 neutral detergent fiber-0.22 ether extract, with $R^2$ = 0.95, residual standard deviation (RSD) = 0.21 and p<0.01; and ME, MJ/kg of DM = 12.82+0.11 Starch-0.26 acid detergent fiber, with $R^2$ = 0.94, RSD = 0.20 and p<0.01. These results indicate that the DE and ME content of CGF varied substantially but the DE and ME for finishing pigs can be accurately predicted from equations based on nutritional analysis.

Comparative energy content and amino acid digestibility of barley obtained from diverse sources fed to growing pigs

  • Wang, Hong Liang;Shi, Meng;Xu, Xiao;Ma, Xiao Kang;Liu, Ling;Piao, Xiang Shu
    • Asian-Australasian Journal of Animal Sciences
    • /
    • 제30권7호
    • /
    • pp.999-1005
    • /
    • 2017
  • Objective: Two experiments were conducted to determine the content of digestible energy (DE) and metabolizable energy (ME) as well as the apparent ileal digestibility (AID) and standardized ileal digestibility (SID) of crude protein (CP) and amino acids (AA) in barley grains obtained from Australia, France or Canada. Methods: In Exp. 1, 18 growing barrows ($Duroc{\times}Landrace{\times}Yorkshire$; $31.5{\pm}3.2kg$) were individually placed in stainless-steel metabolism crates ($1.4{\times}0.7{\times}0.6m$) and randomly allotted to 1 of 3 test diets. In Exp. 2, eight crossbred pigs ($30.9{\pm}1.8kg$) were allotted to a replicate $3{\times}4$ Youden Square designed experiment with three periods and four diets. Two pigs received each diet during each test period. The diets included one nitrogen-free diet and three test diets. Results: The relative amounts of gross energy (GE), CP, and all AA in the Canadian barley were higher than those in Australian and French barley while higher concentrations of neutral detergent fiber, acid detergent fiber, total dietary fiber, insoluble dietary fiber and ${\beta}-glucan$ as well as lower concentrations of GE and ether extract were observed in the French barley compared with the other two barley sources. The DE and ME as well as the SID of histidine, isoleucine, leucine and phenylalanine in Canadian barley were higher (p<0.05) than those in French barley but did not differ from Australian barley. Conclusion: Differences in the chemical composition, energy content and the SID and AID of AA were observed among barley sources obtained from three countries. The feeding value of barley from Canada and Australia was superior to barley obtained from France which is important information in developing feeding systems for growing pigs where imported grains are used.

Serological responses and protection levels in chickens administered with Newcastle disease vaccines

  • Geumji Seung;Jiye Kim;Hyobi Kim;Ji-Yeon Kim;Yang-Ho Jang;Yeon-Hee Kim;Moon Her;Seong-Joon Yi;Keun-Woo Lee;Il Jang;Young Ju Lee
    • 대한수의학회지
    • /
    • 제62권4호
    • /
    • pp.29.1-29.7
    • /
    • 2022
  • Vaccination against Newcastle disease (ND) is the most effective means of controlling the disease, and these vaccines are commercialized only after their safety and effectiveness have been verified through tests that comply with Korean Standards of National Lot Release for Veterinary Biologics. This study investigated whether a relatively convenient and safe serological test can be used in place of the challenge test using highly virulent ND virus. Hemagglutination inhibition (HI) assay and enzyme-linked immunosorbent assay (ELISA) were considered positive of log2 2 or more and cutoff value of 200 or more, respectively, in both live and inactivated vaccines. However, when the antibody levels of the live and inactivated vaccines induced using the Ulster 2C, KBNP-C4152R2L, and K148/08 strains were compared, the antibody titers for inactivated vaccines were significantly higher than those for live vaccines in both the HI assay and ELISA. A strong positive correlation was observed between HI and ELISA antibody titers. The live vaccines corresponded to a survival rates of ≥ 80% and the inactivated vaccines corresponded to 100% survival rates. This study confirmed that standard efficacy tests can serve as serological tests, and can replace the challenge test and that the vaccine approval process can be improved.

A Web-based Alternative Non-animal Method Database for Safety Cosmetic Evaluations

  • Kim, Seung Won;Kim, Bae-Hwan
    • Toxicological Research
    • /
    • 제32권3호
    • /
    • pp.259-267
    • /
    • 2016
  • Animal testing was used traditionally in the cosmetics industry to confirm product safety, but has begun to be banned; alternative methods to replace animal experiments are either in development, or are being validated, worldwide. Research data related to test substances are critical for developing novel alternative tests. Moreover, safety information on cosmetic materials has neither been collected in a database nor shared among researchers. Therefore, it is imperative to build and share a database of safety information on toxicological mechanisms and pathways collected through in vivo, in vitro, and in silico methods. We developed the CAMSEC database (named after the research team; the Consortium of Alternative Methods for Safety Evaluation of Cosmetics) to fulfill this purpose. On the same website, our aim is to provide updates on current alternative research methods in Korea. The database will not be used directly to conduct safety evaluations, but researchers or regulatory individuals can use it to facilitate their work in formulating safety evaluations for cosmetic materials. We hope this database will help establish new alternative research methods to conduct efficient safety evaluations of cosmetic materials.

Helicobacter pylori에 대한 천련자 추출물의 in vitro와 in vivo 실험에서의 항균활성 (In vitro and in vivo antibacterial activity of Meliae fructus extract against Helicobacter pylori)

  • 이현아;김옥진
    • 대한수의학회지
    • /
    • 제52권2호
    • /
    • pp.105-113
    • /
    • 2012
  • In this study, a medicinal herbal plant, Meliae fructus, was examined and screened for anti-Helicobacter (H.) pylori activity. Seventy percent ethanol was used for herbal extraction. For anti-H. pylori activity screening, inhibitory zone tests as an in vitro assay and in vivo study using a Mongolian gerbil (Meriones unguiculatus) model were performed. Also, the safety of herbal compounds was evaluated by animal study. As a result of inhibitory zone test, Meliae fructus extract demonstrated strong anti-H. pylori activities. Also, as results of in vivo animal studies, Meliae fructus demonstrated strong therapeutic effects against H. pylori infection according to the criteria of histological examination and rapid urease test. As results of the safety study, after 28 days treatment of the Meliae fructus extract, the animals were not detected any grossly and histological changes. These results demonstrate that it can be successfully cured against H. pylori infection and protected from H. pylori-induced pathology with Meliae fructus. It could be a promising native herbal treatment for patients with gastric complaints including gastric ulcer caused by H. pylori.

A rapid and quantitative fluorescent microsphere immunochromatographic strip test for detection of antibodies to porcine reproductive and respiratory syndrome virus

  • Wei, Yanqiu;Yang, Baozhi;Li, Yunlong;Duan, Yongcheng;Tian, Deyu;He, Baoxiang;Chen, Chuangfu;Liu, Wenjun;Yang, Limin
    • Journal of Veterinary Science
    • /
    • 제21권4호
    • /
    • pp.68.1-68.8
    • /
    • 2020
  • A fluorescent microsphere-based immunochromatographic strip test (FICT) was developed for the rapid, sensitive, and quantitative detection of porcine reproductive and respiratory syndrome virus (PRRSV) antibodies at the pen-side. The assay was based on the formation of a sandwich immune-complex (anti-pig IgG-PRRSV antibodies-NSP7/N), which was validated by a comparison with IDEXX-ELISA using 3325 clinical specimens. The diagnostic specificity, sensitivity, and accuracy of FICT were 97.28, 93.41, and 94.95%, respectively. FICT showed a good correlation with the virus neutralization assay. Overall, a promising pen-side diagnostic tool was developed for the rapid and quantitative detection of PRRSV antibodies within 15 min.

Triladyl-난황 희석제가 한국 재래 흑염소의 정소상체 및 전기자극 유래 정자의 융해 후 생존성에 미치는 영향 (Effects of Triladyl-egg Yolk Diluents on the Viability of Frozen Korean Black-goat Spermatozoa from Cauda Epididymis and Electro-ejaculated Semen)

  • 김성우;이진욱;김관우;김찬란;전익수;이성수
    • 한국수정란이식학회지
    • /
    • 제32권3호
    • /
    • pp.235-241
    • /
    • 2017
  • 가축유전자원으로서 흑염소 정액은 가축의 증식 및 유전적 개량을 위하여 동결정액으로서 보존될 필요성이 높으나 아직까지 연구 결과가 많이 누적되어 있지 않은 것으로 판단된다. 국내의 흑염소 동결유전자원의 생산성과 효율성 분석을 위하여 가축유전자원센터에서 보유 중인 흑염소 3 계통을 이용하여 전기자극방법에 의하여 채취된 정자와 정소상체유래 정자를 동결 보존하였다. 동결 전 Triladyl 난황희석액을 이용하여 흑염소의 정액과 혼합하여 $17^{\circ}C$에서 2시간 보존하면 응고현상을 관찰할 수 있었으며 42.9%의 비율로 난황이 변화한다는 것을 육안으로 관찰할 수 있었다. 정장 제거용 배양액으로 전기자극 유래 정자를 세정 후 동결 보존하면 융해 후 정자 생존율이 정액 세정용 배양액 $53.8{\pm}5.2%$로 나타났으며 정소상체 정자는 $74.6{\pm}10.6%$로 유의적으로 높게 관찰되었다. 융해된 정자의 장수성을 $17^{\circ}C$에서 조사해 보면 정소상체 유래 정자가 전기자극 유래 정자보다 우수한 것으로 조사되었다. 그러므로, 염소 동결 유전자원을 보존하는 방법으로 정소상체 정자는 활용성이 인정되며, 염소의 개량과 선발을 위하여 농가에서 활용 가능한 동결정액의 생산과 융해 후 생존성 증진을 위하여 더 많은 동결 보존 연구가 필요하다고 판단된다.

체세포점수와 홀스타인 유방형질간의 관계 (Relationship of Somatic Cell Score and Udder Type Traits of Holstein Cattle)

  • 최태정;서강석;김시동;박병호;최재관;윤호백;나승환;손삼규;권오섭;조광현
    • Journal of Animal Science and Technology
    • /
    • 제50권3호
    • /
    • pp.285-292
    • /
    • 2008
  • 본 연구는 국제적인 경쟁력을 갖기 위한 젖소개량방법으로 체세포를 활용하는 방법을 모색하고자 선형심사 자료에서 유방염에 관련된 형질을 이용하여 새로운 선발지수를 개발하기 위한 단계로 국내 젖소집단의 체세포점수 분포와 변화추이를 분석해보고 연령, 분만계절, 비유단계의 환경효과를 구명하고 유방관련 형질과의 유전상관과 유전력을 구하여 기초자료로 활용하고자 본 연구를 진행하였다. 분석은 유우군 능력검정을 통하여 2000년부터 수집된 자료를 이용하였고 자료는 1산차 기록을 갖는 10,929개체의 290,144 검정일 기록과 37,723개의 유방형질 기록을 이용하였다. 분석에 이용된 유방형질은 전유방붙음성, 뒷유방높이, 뒷유방너비, 유방깊이, 앞유두길이의 형질이며 체세포 점수간의 표현형상관과 유전상관을 구하고 분산성분을 추정하였으며 개체모형을 이용하여 표현형상관과 유전상관을 분석하였다. 분석에 이용된 모형은 개체모형으로 DF-REML방식을 이용하여 추정하였고 유방깊이와 앞유두길이의 유전력은 0.23, 0.22로 체세포점수의 유전력은 0.08로 분석되었다. 유방형질과 체세포점수간의 표현형상관은 -0.03~-0.06으로 낮게 나타났으며 높은 유방붙음성을 갖을수록 낮은 체세포점수를 보였다. 체세포점수와 유방깊이, 체세포점수와 앞유두길이의 유전상관은 부의 상관을 보였다.

Single-Dose Intramuscular Toxicity Test Using No-Pain Pharmacopuncture in Sprague-Dawley Rats

  • Ji Hye Hwang;Chul Jung
    • 대한약침학회지
    • /
    • 제26권1호
    • /
    • pp.86-93
    • /
    • 2023
  • Objectives: This study aimed to evaluate the potential toxicity of a recently developed and clinically used No-Pain pharmacopuncture (NPP) solution. We also assessed the lethal dose of the NPP agent following a single intramuscular injection in Sprague-Dawley (SD) rats. Methods: Animals were divided into two groups: the NPP test material group and the normal saline control group. A single intramuscular injection of the NPP agent (1.0 mL/animal) was administered to rats of the NPP test material group. The control group rats received the same volume of normal saline. Both female and male rats were included in each group. All rats were monitored for clinical signs and body weight changes for 14 days after administration of the test substance or saline. At the end of the observation period, a gross necropsy was conducted and localized tolerance at the injection site was analyzed. Results: No mortality was observed in the NPP test material and control groups. Moreover, no test substance-related effects were observed on clinical signs, body weight, necropsy findings, and localized tolerance at the injection site. Conclusion: The approximate lethal dose of the NPP agent is greater than 1.0 mL/animal under the conditions used in this study. Additional toxicity evaluations and clinical studies are needed to confirm the safety of NPP use in clinical practice.