• 제목/요약/키워드: In-vivo Test.

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염증세포주를 이용한 생체재료 용출물의 체외 생체적합성 평가 (In vitro Biocompatibility Evaluation of Biomaterial-elution Using Inflammatory Cell Lines)

  • 신연호;송계용;서민지;김성민;박정극;김동섭;박기정;허찬희;차지훈;서영권
    • KSBB Journal
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    • 제26권3호
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    • pp.248-254
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    • 2011
  • Various biometerials have been researched and have been developed for treatment of some disease through transplantation to body. They have been evaluated by in vitro cytotoxicity test using some skin-derived cell lines for prediction of their biocompatibility in vivo. However, the results of experiments using mesenchymal or epithelial cells could not be considered in vivo immune reaction. In this study, we evaluated the biomaterial-elution (elute from high density polyethylene film) using some cell lines (L929, Jurkat, U937) in vitro, and then that results were compared with in vivo results from guinea pig sensitization test. In sensitization test, saline and elution of syringe could not induce erythema, but only DNCB (hypersensitive chemical) induce erythema at guinea pig sensitization test. In cell experiment, the cytotoxicity results of inflammatory cells (Jurkat; T lymphocyte, U937; monocyte) was no difference with L929 (fibroblast) in the overall trend. However, inflammatory cell lines were only secreted inflammatory cytokine (TNF-${\alpha}$, INF-${\gamma}$) in some materials (biomateriallution, FAC, DNCB). And the biomaterial-elution did not have toxicity to the cells, but it induced the inflammatory cytokines in inflammatory cell lines only. So, we were predicted inflammatory reaction through the cytokine resultes of inflammatory cell lines, and it was more correlated with in vivo results than cytotoxicity test. Therefore, we suggested that the inflammatory cytokine assay using inflammatory cell lines are more effective method in vitro for evaluation of biocompatibility of biomaterials or chemicals.

Immunological significance of recombinant VP2 and VP3 proteins of aquabirnavirus in olive flounder, Paralichthys olivaceus

  • Kim, Hyoung Jun;Kim, Ki Hong;Park, Jeong Su;Lee, Haeng Lim;Kwon, Hyuk Chu;Kwon, Se Ryun
    • 한국어병학회지
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    • 제28권2호
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    • pp.93-98
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    • 2015
  • Full-length recombinant VP2 and VP3 proteins of aquabirnavirus isolated from olive flounder were expressed successfully in E. coli expression system. After rats were immunized with these proteins, antisera were used for in vitro and in vivo neutralization test. In in vitro test, VP2 antibody titers were higher than that of VP3. In in vivo assays, fish challenged with aquabirnavirus neutralized with VP2 antibody survived longer than other fish.

점박이응애의 독성 시험방법과 유기인계 살비제 AChE 활성저해에 관한 연구 (Toxicological Test Methods and AChE Inhibition of Organophosphorus Acaricides of Twospotted Spider Mite, Tetranychus urticae)

  • 김도익;이승찬
    • 한국응용곤충학회지
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    • 제31권1호
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    • pp.1-6
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    • 1992
  • 점박이응애(Tetranychus urticae Koch)에 대한 독성시험방법을 비교하고, 감수성계통을 누대도태하여 in vivo에서 저항성 발달수준과 in vitro에서의 AChE insensitivity의 관계를 실험한 결과는 다음과 같다. 점박이응애의 살비제 저항성 수준결정의 독성시험방법중 slide dip법 (CV=8.7%)은 leaf dip법(CV=12.2%) 이나 leaf disc법(CV=13.6%)보다 변이가 적고 정확도가 높을 뿐만 아니라 처리방법이 간편하고 한가지 농도에 대하여 여러 계통을 동시에 처리할 수 있고 처리 후의 조건을 균일하게 유지시킬 수 있으며 기주식물 없이 시험이 가능하였다. topical application법(CV=8.1%) 역시 정확도는 높았으나 시험 조작이 어렵고 필요한 장비의 구입 비용이 더 들며 시간이 많이 소요되는 단점이 있었다. 두 유기인제에 의한 누대도태결과 22세대 carbophenothion 도태개체군은 동일약제에 156배의 저항성이 발달하였으며, ethion에 대하여 128배의 저항성 반응을 보였다. 24세대 ethion 도태개체군은 동일약제에 64.1배의 저항성 발달이 되었으며, carbophenothion에 대하여도 65배의 저항성 반응을 보였다. 도태개체군의 AChE 활성저해도를 보면 감수성계통에 비하여 carbophenotion 누대계통은 carbohenothion은 3.3배, ethion은 2.7배의 활성저해도를 보였다. 또한 ethion 도태개체군에 대해서는 ethion은 2.6배 carbophenothion은 3.0배의 활성저해도를 나타냈다. 위와 같이 in vivo에서의 저항성 발달 수준과 in vitro에서의 AChE 저해도와는 밀접한 관계가 있는 것으로 보아 유기인계 살비제에 대한 점박이응애의 저항성 발현에는 AChE의 insensitivity가 주요인으로 작용하는 것으로 생각된다.

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In vivo and in vitro efficacy of florfenicol, terbinafine, and mometasone furoate topical otic solution for the treatment of canine otitis externa

  • Bae, Seulgi;Jin, Yunseok;Oh, Taeho
    • 대한수의학회지
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    • 제61권4호
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    • pp.37.1-37.6
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    • 2021
  • This study evaluated the efficacy of a new, single-dose otic solution combining florfenicol, terbinafine, and mometasone furoate for the treatment of canine otitis externa (OE) in vitro and in vivo. Forty-one client-owned dogs with OE were included in the study and divided into a treatment group that received the test solution and a negative control group that received a normal saline solution. On day 0, the dogs were treated either with the test or the control solution and evaluated over 30 days. Clinical efficacy was evaluated by clinical signs and cytological organism counts. In vitro antimicrobial susceptibility was evaluated by the minimum inhibitory concentration (MIC). After treatment with the test solution, clinical signs continuously decreased and cytological scores were significantly reduced. The results of MIC testing showed that the test solution was potent against the common pathogenic causes of canine OE. In this study, the most common causative pathogens were Staphylococcus pseudintermedius, Pseudomonas spp. and Malassezia pachydermatis. No issues related to safety were identified. Based on these results, this new ototopical drug can be used as first line treatment for canine OE.

In vitro cell recovery methoc as an altermative to human damaged skin recovery test

  • An, Su-Sun;Nam, Ki-Taek;Park, Jong-Ho;Koh, Jae-Sook
    • 대한화장품학회지
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    • 제23권3호
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    • pp.97-100
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    • 1997
  • These days, the raw materials that have the cell recovering effect are used commonly in cosmetics. In this study, six materials were rested for the characteristics of recovering effect both on vivo and in vitro. Tested raw materials were Soypol, 3-APPA, Apple extract, Polygonatum japonicum extract, Scutellarkd baicalensis extract, Aloe extract. Among these materials, Soypol and 3-APPA were synthesized and others were made by extraction at the Pacific R&D Center. Human forearm skin and cultured skin cell were damaged by sodium lauryl sulfare and then raw materials were applied for open treatment on SLS damaged human skin or cells. The recovering effects of raw materials in vivo were evaluated by measuring transepidermal water loss, skin hydration and erythema and in vitro effects of proliferationg cells were assessed by neutral red uptake assay. In the in vivo study, only the evaluation by TEWL showed correlation with the visual score. Our of six materials, 3-APPA had the most positive effect in both in vivo and in vitro studies and the correlation was r=0.8286 (p=0.042).

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재조합 인과립구 콜로니 자극인자 HM10411의 유전독성 연구 (Genotoxicity Study of HM10411, Recombinant Human Granulocyte Colony Stimulating Factor)

  • 권정;이미가엘;홍미영;조지희;정문구;권세창;이관순
    • Biomolecules & Therapeutics
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    • 제10권4호
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    • pp.268-273
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    • 2002
  • Mutagenic potential of HM10411 (recombinant human granulocyte colony stimulating factor) was evaluated by bacterial reverse mutation test, in vitro chromosome aberration test and in vivo micronucleus test. The bacterial reverse mutation test was performed using the histidine auxotroph strains of Salmonella typhimurium TA100, TA1535, TA98, TA1537 and tryptophan auxotroph strain of Escherichia coli WP2 uvrA. The negative results of the bacterial reverse mutation test suggest that HM10411 does not induce mutation, in the genome of Salmonella typhimurium and E. coli under the conditions used. In addition, it has little clastogenicity either in vitro chromosome aberration test or in vivo micronucleus test. For in vitro chromosomal aberration test, Chinese hamster lung(CHL) cells were exposed to HM10411 of 23, 46 or 92 $\mu\textrm{g}$/ml for 6 or 24 hours in the absence and for 6 hours in the presence of metabolic activation system. There was no significant increase in the number of aberrant metaphase in HM 10411-treated groups at any dose levels both in the presence and absence of metabolic activation system. The micronucleus test was carried out using specific pathogen free(SPF) 7-week old male ICR mice, The test item, HM10411 was intraperitoneally administered at 1150, 2300 or 4600 $\mu\textrm{g}$/kg once a day for 2 consecutive days. There was no significant increase in the frequencies of micronucleated polychromatic erythrocytes(PCEs) at any treated groups compared with negative control group. Therefore, these results demonstrate that the test item, HM10411, was not mutagenic under the condition of these studies.

Establishment of Validation Methods to Test the Biocompatibility of Titanium Dioxide

  • Kim, Mi-Ju;Lim, Hee-Joung;Lee, Byung Gun;Kim, Jong-Hoon;Choi, Jinsub;Kang, Hee-Gyoo
    • Bulletin of the Korean Chemical Society
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    • 제34권6호
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    • pp.1857-1863
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    • 2013
  • Most of biomaterials come in direct contact with the body, making standardized methods of evaluation and validation of biocompatibility an important aspect to biomaterial development. However, biomaterial validation guidelines have not been fully established, until now. This study was to compare the in vitro behavior of osteoblasts cultured on nanomaterial $TiO_2$ surfaces to osteoblast behavior on culture plates. Comparisons were also made to cells grown in conditioned media (CM) that creates an environment similar to the in vivo environment. Comparisons were made between the different growth conditions for osteoblast adhesion, proliferation, differentiation, and functionality. We found that the in vivo-like system of growing cells in concentrated CM provided a good validation method for biomaterial development and in vivo implant therapy. The $TiO_2$ materials were biocompatible, showing similar behavior to that observed in vivo. This study provided valuable information that would aid in the creation of guidelines into standardization and evaluation of biocompatibility in $TiO_2$ biomaterials.

구기자 가공품의 생리기능성 및 항고혈압 활성 검증 (Physiological Functionality of Gugija Products and an In Vivo Examination on Anti-hypertension Effects)

  • 이지수;박영춘;백승우;이석수;안용근;이종수
    • 한국식품영양학회지
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    • 제21권2호
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    • pp.115-120
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    • 2008
  • To develop a new Gugija(Lycium chinensis Mill) product having increased value, the physiological functionality of various commercial Gugija products were investigated. In addition, an in vivo study was performed using spontaneous hypertensive rats(SHR) to examine the anti-hypertension effects of products. The results showed that antioxidant activity was highest in the methanol extract of Gugija leaf pickle(97.7%), and anti-hypertensive angiotensin I -converting enzyme(ACE) inhibitory activity was 80.4% in Gugija doenjang(soybean paste) water extract. Anti-cholesterolemia HMG-CoA reductase inhibitory activity was highest in the methanol extract of Gugija rice cake(66.1 %). However, SOD-like activity was below 30% in most products; and fibrinolytic activity was not detected or was very weak. Ultimately, we selected Gugija tea and Gugija wine as superior anti-hypertensive Gugija products, and subsequent in vivo testing was performed using SHR, comparing the tea and wine to Gugija fruit. Among them, the Gugija fruit demonstrated the best anti-hypertension effects in SHR.

Comparative analysis of the energy values of oat hay, tall fescue, annual ryegrass, and barnyard millet using in vivo digestibility results and predicted values

  • Seul, Lee;Seoyoung, Jeon;Seongwon, Seo;Jungeun, Kim;Pilnam, Seong;Youl Chang, Baek
    • 농업과학연구
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    • 제48권4호
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    • pp.831-842
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    • 2021
  • Accurate measurements of feed energy values have a positive effect on the control of feed intake for animals, the formation of prices, and on economic profits. However, few studies have attempted to measure the energy values of domestic roughages and to validate an energy value prediction model. The purpose of this study is to build a database through measurements of the nutrient digestibility and digestible energy results of roughages used in Korea and to evaluate the domestic applicability of the National Research Council (NRC) estimation model. Oat hay, annual ryegrass, tall fescue, barnyard millet, and concentrates for beef cattle were used in the test. As a result of an in vivo digestibility trial, the total digestible nutrients (TDN) of oat hay, annual ryegrass, tall fescue, and barnyard millet were found to be 68.73, 55.02, 55.71, and 52.89%, respectively. As a result of comparing the estimated values using the NRC equation with the in vivo results, there was a difference of 3.55 to 6.84%P in the TDN. Inferred from this result, it is considered that TDN calculations using the NRC equation can be reasonable for the test feeds used in this study. These results can be utilized when revising the Korean Standard Tables of Feed Composition, which provides a comprehensive overview of Korean feed.

Studies on the anti-coagulant component of Loranthus yadoriki

  • Lee, Sun-Kyung;Song, Hee-Sun;Yoo, Eun-A;Yang, Hyun-Ok
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 2003년도 Annual Meeting of KSAP : International Symposium on Pharmaceutical and Biomedical Sciences on Obesity
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    • pp.71-71
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    • 2003
  • Methanol extract of Loranthus yadoriki showed the prolongation effect of bleeding time in vivo using mice in dose dependent manner. From the MeOH extract of Loranthus yadoriki, compound-A was isolated by the activity guided isolation method using silicagel column chromatography. The anti-coagulant activity was evaluated by the bleeding time test in vivo and plasma recalcification time test in vitro. Compound A showed moderate anti -coagulant activity on plasma recalcification time in vitro.

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