• 제목/요약/키워드: $E_iC_{50}$

검색결과 566건 처리시간 0.035초

트리아세테이트/PET 혼방 직물의 분산염료 혼합염색 (Combination Dyeing of Triacetate/PET Blended Fabric with Disperse Dye)

  • 김명옥;이정순
    • 감성과학
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    • 제19권4호
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    • pp.3-12
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    • 2016
  • 본 연구의 목적은 트리아세테이트와 흡한속건성 PET 합연사로 구성된 복합직물의 염착량 증진 및 동일색상 염색(union dyeing)을 위한 최적 혼합염색 조건을 찾는 것이다. 이를 위하여 E-type 분산염료(C.I. Disperse red 50)와 S-type 분산염료(C.I. Disperse red 92)를 혼합하여 1욕 혼합염색으로 염색온도, 염색시간, 염료의 혼합비율에 따른 염색직물의 흡진율, 염착율, 색상 및 색차를 측정하였다. 혼합염색의 염착평형은 $100^{\circ}C$에서 일어났으나 염색된 직물의 K/S 값과 겉보기 색상을 비교해보았을 때 트리아세테이트와 흡한속건성 PET의 색이 동일한 색으로 발현되는 온도는 $120^{\circ}C$임을 확인하였다. 염색 시간 증가에 따른 혼합염료 흡진율과 염착량의 변화는 크게 나타나지 않았으나 염색시간이 길수록 그리고 혼합염료를 사용할 경우 균일한 색상을 얻을 수 있었다. E-type에 S-type염료의 혼합비율을 적절히 조절하여 혼합염색 하면 단독염색 보다 E-type 염료의 색상과 차이 없이 염착량을 증대시킬 수 있었다.

Scavenging Capacities of DPPH and ABTS Free Radicals and Anti-inflammatory Activities of Ethanol Extracts and their Fractions from Sophora tonkinensis

  • Eun Sun Moon;Ji Yoon Lee;Seongdae Kim;Chang Won Choi
    • 한국자원식물학회:학술대회논문집
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    • 한국자원식물학회 2021년도 춘계학술대회
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    • pp.46-46
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    • 2021
  • The first purpose of this study was to evaluate the scavenging capacity (SC) of DPPH and ABTS free radicals for ethanol extract (STR-E) and its active fractions from Sophora tonkinensis root (STR). Four different fractions from STR-E were prepared by using different types of solvents such as chloroform (STR-E-C), ethyl acetate (STR-E-EA), n-butanol (STR-E-B), and water (STR-E-W). STR-E-C showed the highest value of total phenolic content, while STR-E showed the highest value of total flavonoid and terpenoid content. In STR-E and its four fractions, STR-E-EA showed the strongest SC with the lowest SC50 values of the DPPH radicals and ABTS radicals. The second purpose of this study was to evaluate anti-inflammatory activity in the lipopolysaccharide (LPS)-induced RAW 264.7 macrophages treated with STR-E, STR-E-C, and STR-E-EA, respectively. No cytotoxic effect to RAW 264.7 cells was observed at 20 ~ 25 ㎍/ml of STR-E, 10 ㎍/ml of STR-E-C, and 5 ㎍/ml of the STR-E-EA, presenting cell viability values close to that of the untreated control (100%). STR-E, STR-E-C, and STR-E-EA significantly suppressed the LPS-induced nitric oxide (NO) in a dose-dependent manner. Results of reverse-transcription (RT)-qPCR analysis showed that the peak mRNA levels of IL-1β, TNF-α, iNOS, IL-6, and IL-10 were observed in the LPS-stimulated macrophages at 4 h, 2 h, 12 h, 12 h, and 12 h, respectively. The peak mRNA levels of IL-1β, TNF-α, iNOS, and IL-6 were significantly reduced in the LPS-stimulated macrophages co-treated with 20 ㎍/ml and 25 ㎍/ml of STR-E, respectively. In the case of IL-10, its peak mRNA level slightly increased without statistical significance. Compared with the LPS-stimulated macrophages, the peak mRNA levels of IL-1β, TNF-α, iNOS, and IL-6 reduced in the LPS-stimulated macrophages co-treated with 10 ㎍/ml and 20 ㎍/ml of STR-E-C, respectively. In contrast, the peak mRNA level of IL-10 significantly increased at 8 h. Compared with the LPS-stimulated macrophages, the peak mRNA levels of IL-1β, TNF-α, iNOS, and IL-6 reduced in the LPS-stimulated macrophages co-treated with 5 ㎍/ml and 10 ㎍/ml of STR-E-EA, respectively. In contrast, the peak mRNA level of IL-10 increased at 4 h. Taken together, our data indicated that STR-E, STR-E-C, and STR-E-EA activate macrophages to secrete both pro-inflammatory and anti-inflammatory cytokines.

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카본 블랙/유기화 클레이로 보강된 SBR 나노 복합재료: 모폴로지와 기계적 물성 (Properties of SBR Nanocomposites Reinforced with Organoclay/Carbon Black Dual Phase Fillers)

  • 강병석;김원호
    • Elastomers and Composites
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    • 제42권1호
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    • pp.9-19
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    • 2007
  • 본 연구에서는 카본블랙과 유기화 클레이(C18-MMT) 로 보강된 SBR 나노 복합재료를 라텍스법(latex method)으로 제조하였다. 필러의 함량은 50 phr로 고정하였으며, 카본 블랙/C18-MMT의 함량비를 50/0, 49/1, 48/2, 47/3, 45/5, 44/6, 40/10 phr로 정하고 함량비에 따른 가황 특성 및 기계적 물성을 비교하였다. 각 컴파운드의 가황 특성 및 기계적 물성을 비교 평가한 결과 carbon black(49phr)/C18-MMT(1phr) 컴파운드가 ODR에서 가장 높은 최대 토크 값을 나타내었으며, 높은 인장 강도 및 모듈러스, 인열 에너지를 나타내었다. 이러한 기계적 물성 증가는 클레이의 박리 정도 및 분산도의 향상으로 인한 C18-MMT의 우수한 보강 효과 때문이라고 판단된다.

Variations in Karyotypic Characteristics of Different Breed Groups of Water Buffaloes (Bubalus bubalis)

  • Bondoc, O.L.;Flor, M.C.G.T.;Rebollos, S.D.N.;Albarace, A.G.
    • Asian-Australasian Journal of Animal Sciences
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    • 제15권3호
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    • pp.321-325
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    • 2002
  • Karyotype analysis was carried out on blood samples of 30 water buffaloes belonging to different breed groups (i.e. Philippine Carabao (PC), Indian Murrah (IM), Bulgarian Murrah (BM), "$F_1$ 50% IM-50% PC", "$F_1$ 50% BM-50% PC" and "75% IM-25% PC"), using the modified Leucocyte Culture Technique. The modal chromosome numbers of the PC, "$F_1$ 50% IM-50% PC", "$F_1$ 50% BM-50% PC", IM, BM and "75% IM-25% PC" were 2n=48, 49, 49, 50, 50 and 50, respectively. The water buffalo chromosomes are mostly acrocentric (79.67%) and the remainder submetacentric (20.33%). Results of the ordinary least square analysis showed significant breed effects (p<0.01) on other karyotypic characteristics (i.e. relative length, arm ratio and centromeric index). Significant correlation between karyotypic characteristics and some animal performance traits were also found. The significant correlation values imply that karyotypic characteristics can be used as important criteria to select potentially productive young water buffaloes. In the future, more production and reproduction traits from non-institutional herds should be included in the analysis to reveal meaningful correlations with various karyotypic characteristics.

산국 꽃의 항염 활성 연구 (Anti-inflammatory effects of Chrysanthemum boreale flower)

  • 유기선;방찬성;이경진;함인혜;최호영
    • 대한본초학회지
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    • 제26권4호
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    • pp.31-37
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    • 2011
  • Objectives : Chrysanthemum boreale flower is widely distributed in Korea, Japan, China, and Eastern countries. C. boreale flower is also one of the herbs used for the treatment of various inflammatory disease in Korean Medicine. So, this research was designed to study anti-inflammatory effect of C. boreale flower and its mechanism. Methods : We investigated nitro oxide (NO) and prostaglandin $E_2$ ($PGE_2$) production by ELISA. And expressions of inducible nitric oxide synthase (iNOS), Cyclooxygenase-2 (COX-2) and nuclear factor-${\kappa}B$ P50/65 (NF-${\kappa}B$ P50, NF-${\kappa}B$ P65) were measured in RAW 264.7 murine macrophage cells induced by LPS. Results : MeOH ex., EtOAc fr., $CHCl_3$ fr. and Water fr. of C. boreale flower showed anti-inflammatory effect through inhibition of NO and PGE expression respectively. Among them, EtOAc fr. and $CHCl_3$ fr. inhibited production of NO and $PGE_2$ through inhibition of iNOS and COX-2 expression. And MeOH ex., EtOAc fr. and $CHCl_3$ fr. inhibited translocation of NF-${\kappa}B$ P65, NF-${\kappa}B$ P50 by inhibiting phosphrylation of $I{\kappa}B$. Conclusions : MeOH ex. EtOAc fr, $CHCl_3$ fr., and Water fr. of the C. boreale flower have anti-inflammatory activity.

감과실의 성숙과 추숙중의 Polygalacturonase활성 변화 및 특성 (Characteristics and Activity Changes of Polygalacturonase during Maturation and Postharvest of Persimmon Fruits)

  • 신승렬;김진구;김순동;김광수
    • 한국식품영양과학회지
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    • 제19권6호
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    • pp.596-604
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    • 1990
  • Polygalacturonase의 활성은 미숙감과실에서 나타나지 않았으나 완숙감과 연시에서 각각 55.01. 206.70unit/100g-fr. wt.로 연시에서 급격히 증가하였다. 연시에서 추출한 polygalacturonase의 isoenzyme은 2종이었고, 분자량은 다같이 55,000 dal-ton이었다. Polygalacturonase isoenzyme의 특성을 조사한 결과, polygalacturonase I의 Vmax는 0.195$\mu$ mole reducing-sugar/$m\ell$/30min., Km값은 3.50mg/$m\ell$이었고, 최적온도 4$0^{\circ}C$, 최적 pH 3.5이었으며, 열처리시 6$0^{\circ}C$까지 안정하였다. Polygalacturonase II 의 Vmax는 0.11$\mu$mole reducing-sugar /$m\ell$/30min., Km값은 2.50mg/$m\ell$이었고, 최적 온도와 pH는 35$^{\circ}C$와 4.0이었으며. 4$0^{\circ}C$까지 안정하였다. Polygalacturonase I 과 II는 K+, Cu++, Zn++, SDS, EDTA에 의해서 활성이 저해되었고 Ca++ 의해 다소 촉진되었다.

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새로운 섬유소분해 균주 Trichoderma sp. C-4에서 분리한 Endoglucanase (F-I-III)에 대한 연구 (Characterization of Endoglucanase (F-I-III) Purified from Trichoderma sp. C-4)

  • 설옥주;정대균;한인섭;정춘수
    • 미생물학회지
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    • 제41권1호
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    • pp.81-86
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    • 2005
  • 국내에서 분리된 우수섬유소분해 균주인 Trichodema sp. C-4가 생성하는 endoglucanase 중하나를 $(NH_4)_2SO_4$ 침전, Sephacryl S-200 gel filtration, DEAE-Sepharose A-50 ion exchange, Mono-P chromatofocusing (EPLC)의 단계로 정제하고 이를 F-I-III라 명명하였다. 분리된 효소 F-I-III는 분자량 56,000Da, 둥전점 4.9로 측정된 단일 단백질이었다. F-I-III는 $55^{\circ}C$에서 가장 높은 활성을 보였으며, pH 5.0이 반응 최적 조건이었다. $50^{\circ}C$에서 24시간 동안 안정하였으며, pH 4-7의 범위에서 안정하였다. CMC에 대한 비활성은 315.4U/mg 이었으며, PNPG2에 대한 Km 값은 2.69 mM이었다. 이 효소는 같은 균주에서 분리한 다른 endoglucanase와 exoglucanase를 섞었을 때 결정형 섬유소인 Avicel분해에 대한 상승효과를 보였다. $Mg^{2+},\;CO^{2+},\;Fe^{2+},\;Ca^{2+},\;CS^+,\;Li^+$ 등의 이온은 1 mM의 농도에서 효소의 활성에 큰 영향을 미치지 않았고, 1 mM의 환원제 (cystein, EDIA, \beta-mercaptoethanol, dithiothreitol(DTT), L-ascorbic acid)들은 효소의 활성을 증가시켰다. E-I-III의 N-말단 서열을 분석하여 QPGTSTPEVHPKKLTTYK의 서열을 얻었다. 이는 Trichodema reesei의 endoglucanase인 EGI과 $95\%$의 유사도를나타내었다. 분리된 효소 F-I-III는 높은 비활성을 가지고 있어서 활용가치가 높을 것으로 사료되었다.

A Protective Effect for Panax ginseng in the Rat Stomach

  • Omar M.E.Abdel Salam;Batran, Seham-El;Shenawy, Siham-El;Mahmoud S.Arbid
    • Journal of Ginseng Research
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    • 제25권4호
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    • pp.141-149
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    • 2001
  • The effect of ginseng on gastric ulcer and gastric acid secretion was investigated in pylorus-ligated rats. Methods: Sprague-Dawley strain rats were used after 24 hours fast. Pylorus-ligation was performed under light ether anaesthesia, then gastric mucosal damage was evoked in conscious pylorus-ligated rats by the administration of subcutaneous (s.c.) indomethancin (20mg/kg), s.c. histamine (150mg/kg) or by pylorus-ligation (Shay ulcer). Ginseng was given by intragastric (i.g.) or intraperitoneal (i.p.) route simultaneously with the ulcerogens. Rats were killed after 3h (indomethacin) and histamine models) or after 18h (Shay ulcer), when the gastric secretory responses, the number and severity of gastric mucosal lesions and mucosal mucus content deetermined. the effect of i.p. ginseng on basal gastric acid secretion and on gastric acide secretion in indomethacin (20mg/kg, s.c.)-treated rats was also investigated in urethane anesthetized rats. Gastric acid secretion was measured by flushing of the gastric lumen with saline every 15min through an oesophageal cannula. Results: In conscious pylorus-ligated rats, i.g. ginseng(12.5-50mg/$m\ell$; 50-200mg/kg) protected against gastric mucosal lesions evoked by s.c. indomethacin or s.c. histanmine in the d3-h pylorus-lighted rat, withoutmodifying gastric acid secretory responses. Ginseng given i.p. (150 or 200mg/kg) did not reduce the gastric lesions produced by histamine or by ligating the pylorus (Shay ulcer) Ginseng given orally in 50mg/$m\ell$ (200mg/kg) increased gastric mucus secretion in saline- and indomethacin-treated conscious pylorus-ligated rats. In anaesthetized rats ginseng (50 or 200mg/kg) did not modify basal gastric acid secretion or gastric acid secretion in the indomethacin-treated rats. Conclusions: ginseng given orally exerts gastroprotective effects in the rat stomach. Such anti-ulcer effect does not involve changes in gastric acid secretory responses. In addition, ginseng possesses stimulatory effect on gastric mucus secretion, which could be one mechanism by which the compound exerts its antiulcer effect. Our data are in favor for a beneficial effect for topically applied ginseng on the gastric mucosa.

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Functional characterization of naturally-occurring constitutively activating/inactivating mutations in equine follicle-stimulating hormone receptor

  • Byambaragchaa, Munkhzaya;Ahn, Tae-Young;Choi, Seung-Hee;Kang, Myung-Hwa;Min, Kwan-Sik
    • Animal Bioscience
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    • 제35권3호
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    • pp.399-409
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    • 2022
  • Objective: Follicle-stimulating hormone (FSH) is the central hormone involved in mammalian reproduction, maturation at puberty, and gamete production that mediates its function by control of follicle growth and function. The present study investigated the mutations involved in the regulation of FSH receptor (FSHR) activation. Methods: We analyzed seven naturally-occurring mutations that were previously reported in human FSHR (hFSHR), in the context of equine FSHR (eFSHR); these include one constitutively activation variant, one allelic variant, and five inactivating variants. These mutations were introduced into wild-type eFSHR (eFSHR-wt) sequence to generate mutants that were designated as eFSHR-D566G, -A306T, -A189V, -N191I, -R572C, -A574V, and -R633H. Mutants were transfected into PathHunter EA-parental CHO-K1 cells expressing β-arrestin. The biological function of mutants was analyzed by quantitating cAMP accumulation in cells incubated with increasing concentrations of FSH. Results: Cells expressing eFSHR-D566G exhibited an 8.6-fold increase in basal cAMP response, as compared to that in eFSHR-wt. The allelic variation mutant eFSHR-A306T was not found to affect the basal cAMP response or half maximal effective concentration (EC50) levels. On the other hand, eFSHR-D566G and eFSHR-A306T displayed a 1.5- and 1.4-fold increase in the maximal response, respectively. Signal transduction was found to be completely impaired in case of the inactivating mutants eFSHR-A189V, -R572C, and -A574V. When compared with eFSHR-wt, eFSHR-N191I displayed a 5.4-fold decrease in the EC50 levels (3,910 ng/mL) and a 2.3-fold decrease in the maximal response. In contrast, cells expressing eFSHR-R633H displayed in a similar manner to that of the cells expressing the eFSHR-wt on signal transduction and maximal response. Conclusion: The activating mutant eFSHR-D566G greatly enhanced the signal transduction in response to FSH, in the absence of agonist treatment. We suggest that the state of activation of the eFSHR can modulate its basal cAMP accumulation.

In vitro Evaluation of AraC Prodrugs for Their Antiviral Activity

  • Lee, Hee-Joo;Shin, Hae-Soon;Lee, Chong-Kyo
    • Biomolecules & Therapeutics
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    • 제1권2호
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    • pp.125-130
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    • 1993
  • The araC prodrugs (1~5) carrying a special acyl group at 5'-Ο-or $N^4$-position were evaluated for in vitro antiviral activity against various human viruses. When tested against HSV-1 and HSV-2 cultured in the verso cells, the prodrugs exhibited slightly higher $ED_{50}$ values compared with one of the parent araC but showed more increased $CC_{50}$ values in all cases. Consequently the overall selectivity indexes of prodrugs were higher than that of arab. The prodrugs, except compound 5, exhibited very potent activity similar to that of araC ($ED_{50}$ about $0.12{\mu}g/mι$) when evaluated against another human DNA virus, cytomegarovirus. However, theses araC prodrugs were completely inactive against RNA viruses i.e. poliovirus and coxackie B3 virus at the concentration of 4250{\mu}g/mι.$

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