• 한국의류학회지
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• 제24권3호
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• pp.385-392
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• 2000

The adsorption ability of dyes on chitin, a natural polymer was investigated for decolorization of dye wastewater. Chitin was manufactured in lab by decalcification in dilute aqueous HCI solution and deproteination in dilute aqueous NaOH solution with shrimp shells. Absorbance of residue solution of dyebaths after dye adsorptions of chitin were measured in varieties of dye concentration and dipping periods. Four kinds of dyestuffs were used, C.I.Acid Blue 29. C.I.Direct Blue 6, C.I.Reactive Orange 12 and C.I.Basic Red 18. When chtin 1g was dipped in 0.05% of dyebath with stirring, maximum adsorption ratio of each kind of dyes was exhibited as 91.6% for C.I.Acid Blue 29, 95% for C.I.Direct Blue 6, 58.2% for C.I.Reactive Orange 13 and 75.8% for C.I.Basic Red 19. It shows that chitin has better adsorption abilities of ionic dyes of acid, direct and basic dye than non-ionic reactive dye. And chitin has better adsorption abilities of anionic acid direct dyes than cationic basic dye because of the presence of nitrogen atoms. All kinds of dyestuffs used showed speedy absorption effects by chitin, so chitin can absorb much amount of dyes in 5 mimutes reach to equilibrium of adsorption in 2 hours after dipping. Basic dye was absorbed the most speedily in 5 minutes, although maximum adsorption ratio is not high. That reason can be thought that chitin surface is essentially negatively charged due to polar funtional groups.

• 한국염색가공학회지
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• 제6권4호
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• pp.9-16
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• 1994

알칼리 수용액 중에서의 Vinylsulfone(VS)계 반응성염료의 혼합상태의 가수분해 반응을 정량적으로 조사하였다. 혼합이량체의 생성 및 분해반응 속도상수를 각각의 염료의 가수분해반응에서 구한 속도상수를 이용하여 계산하였다. 단독이량체를 생성하는 염료들을 조합하였을 경우에는 혼합이량체가 생성되었다. C.I.Reactive Blue 19가 다른 VS계 염료들과 혼합되었을 경우에는 일반적으로 혼합이량체가 생성되었다. Blue 19와 Orange 16의 조합의 경우에는 낮은 염료농도에서만 혼합이량체가 생성되었으며, Red 22의 경우에는 단독 및 혼합이량체가 생성되지 않았다. 단독이량체가 생성되지않는 Orange 7는 다른 VS계 염료들과의 조합에서 혼합이량체를 생성함을 확인하였다. Yellow 17의 혼합이량체의 분해속도 상수값이 가장 큼을 알 수 있었다.

• KSBB Journal
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• 제17권2호
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• pp.189-194
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• 2002

Trametes sp.에서 생산되는 laccase는 CNBr-activated Sepharose-4B(CAS4B)에 고정화 되었고, 염료의 연속적인 분해를 위하여 테스트되었다. Laccase는 CAS4B에 효율적으로 고정화되었고, CAS4B에 고정화 된 laccase는 pH, 열, 단백질 구조적인 안정성 면에서 상당히 증가하였다. CAS4B에 고정화 된 accase의 최적 pH는 5, 온도는 4$0^{\circ}C$로서 free laccase와 비교하여 변화가 없었다 기질로서 Reactive Blue 19를 사용하였을 때 free laccase와 고정화 laccase의 $K_{m}$ ($\mu$mol/mL) 값은 각각 0.34와 2.0이었고,V$_{max}$($\mu$mol/mL.min) 값은 각각 0.12, 0.1이었다. Repeated-batch 반응에서 효소의 안정성과 높은 분해 효율 만족하는 조건은 pH 5, 3$0^{\circ}C$이였다. 또한 HBT에 의한 효소의 불활성은 크게 나타나지 않았다. Packed-bed reactor에서 최적으로 운전되었을 때 100 $\mu$M Reactive Blue 19과 0.1 mM HBT가 존재하는 50 $\mu$M Acid Red 57의 연속적인 분해에서 30시간 후에도 분해 효율이 70%로 유지되었다. 고정화 laccase는 Packed-bed reactor에서 azo 염료의 연속적인 분해를 매우 안정적으로 수행하였다.다.

• KSBB Journal
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• 제15권1호
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• pp.66-71
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• 2000

Geotrichum candidum (KCTC 6195)를 이용하여 색도제거를 위한 최적조건은 초기 pH 6, $30^{\circ}C$, glucose 농도 30 g/L이었으며 빛은 세포성장과 색도제거에 영향을 주지 않았다. 한편, 세포성장과 색도제거를 위해서는 세포의 성장원(glucose)이 필수적이었다. 염료의 종류에 따라 색도제거량과 속도는 차이가 있지만 분산염료, 산성염료, 반응염료에 대해 색도제거가 고체배치와 액체배치에서 가능했으며 Acid goange 10 염료의 경우 배양 후 120 시간 후에는 초기 100 ppm에서 91%로, 초기 500ppm에서 84%까지 색도제거되는 것을 알 수 있었다. 색도제거에서 Acid red 1: 19.8%, Acid red 88, 73%, Acid orange 10; 12.1%, Reactive blue 19; 14.6%가 흡착으로 제거되었다. 이로서 효소에 의한 색도제거뿐만 아니라 흡착에 의해 색도제거됨을 알 수 있었다. 2일간 배양하고 glucose를 첨가하여 1일간 추가 배양한 경우 97%까지 색도제거 되었다.

• 한국염색가공학회지
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• 제19권3호
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• pp.18-25
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• 2007

The fixing behaviors of anthraquinone disperse dyes containing dimethylamino substituent, such as C. I. Disperse Violet 26(D.V.26) and C. I. Disperse Blue 14(D.V.14), or containing diamino substituent, such as C. I. Disperse Blue 73(D.B.73), and monochlorotriazinyl azo reactive dyes, such as C. I. Reactive Orange 13(R.O.13), C. I. Reactive Red 3(R.R.3). C. I. Reactive Yellow 2(R.Y.2) on polyester/cotton blend(P/C) fabrics were examined for the one-step printing of P/C fabrics. The high temperature steaming of $175^{\circ}C$ is the most satisfactory fixing method for P/C one-step printing with above disperse and reactive dyes among the four different fixing methods: $175^{\circ}C$ steaming, $102^{\circ}C$ steaming${\rightarrow}175^{\circ}C$ steaming, $190^{\circ}C$ thermosol, $102^{\circ}C$ steaming${\rightarrow}190^{\circ}C$ thermosol. $190^{\circ}C$ thermosol is unfit to fix R.R.3 and R.Y.2 whose heat stability is poor. It was found that D.V.26 and D.B.14 containing dimethylamino substituent are unstable for heat and alkali, but D.B.73 is stable for them to print P/C blend fabrics with R.O.13 which is also stable for heat. Therefore we found that D.B.73, R.O.13 and a pair of D.B.73 and R.O.13 were very suitable for one-step printing of P/C blend fabrics.

• 한국염색가공학회지
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• 제3권1호
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• pp.1-7
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• 1991

The influences, that various mercerization conditions had on the dying property of cotton fiber, were studied. Crystallization degrees accompained by lattice transformation of slack-mercerized cotton by IR spectroscopic analysis and morphology of the slack-merceized cotton by SEM were observed in this research. The above results were as follows; 1. Equilibrium dye adsorption rates of slack-mercerized cotton with C. I. Reactive Blue 19 were gained in the case of 8M NaOH, $10^{\circ}C$, 20 min., about 2 times as large as the rates of untreated cotton and gained about 2.5 times in the case of 8M $NH_3$, $10^{\circ}C$, , 20 min. 2. Equilibrium dye adsorption rates of slack-mercerized cotton with C. I. Reactive Blue 2 were gained in the case of 2M NaOH, $10^{\circ}C$, 20 min., about 1.7 times as large as the rates of untreated cotton and gained about 2.4 times in the case of 8M $NH_3$, $10^{\circ}C$, 20 min. 3. It was confirmed by SEM that untreated cotton fibrils are formed in the shape of screw and treated cotton is rearranged in the direction of fiber axis.

• 한국염색가공학회지
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• 제8권1호
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• pp.1-7
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• 1996

In discharge printing of cotton fabrics dyed with C.I. Reactive Orange 16(O-16), C.I. Reactive Blue 19(B-19) and C.I. Reactive Black 5(Bl-5), when the dyes were discharged by some chemicals, such as $K_{2}CO_{3}$, BASB, DSR, sarcosine and GSB, the single use of those chemicals made a very poor discharge, but mixing them with $K_{2}CO_{3}$ resulted to the outstanding improvement of discharge. Especially the dischargeability of $K_{2}CO_{3}$ BASB or $K_{2}CO_{3}$+DSR was very gratifying. For O―16, $K_{2}CO_{3}$+ DSR was slightly more effective than $K_{2}$CO$_{3}$+BASB, but for B―19 and Bl―5 $K_{2}CO_{3}$+BASB and $K_{2}CO_{3}$+DSR showed similar good results. In discharging of O―16 and B―19 by $K_{2}CO_{3}$+BASB or $K_{2}CO_{3}$ +DSR, the dischargeabilities of them increased as the time of 102$^{\circ}C$ steaming increased under the condition of 102$^{\circ}C$ steaming and no baking, but not under the condition of 102$^{\circ}C$ steaming and 16$0^{\circ}C$ baking. However for Bl-5, without regard to baking, the 102$^{\circ}C$ steaming of more than 15 minutes caused the discharge to be much more remarkable than that of 8 minutes did. Generally baking elevated the dischargeability, and this was sure in discharging by $K_{2}CO_{3}$+BASB or $K_{2}CO_{3}$+DSR. And it was confirmed that the structure of vinylsulfonyl reactive dyes could effect on the dischargeability because the three dyes, though little, showed different discharge behaviors.

• Journal of Ginseng Research
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• 제47권1호
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• pp.65-73
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• 2023

Background: Age-related macular degeneration (AMD) is a significant visual disease that induces impaired vision and irreversible blindness in the elderly. However, the effects of ginseng berry extract (GBE) on the retina have not been studied. Therefore, this study aimed to investigate the protective effects of GBE on blue light (BL)-induced retinal damage and elucidate its underlying mechanisms in human retinal pigment epithelial cells (ARPE-19 cells) and Balb/c retina. Methods: To investigate the effects and underlying mechanisms of GBE on retinal damage in vitro, we performed cell viability assay, pre-and post-treatment of sample, reactive oxygen species (ROS) assay, quantitative real-time PCR (qRT-PCR), and western immunoblotting using A2E-laden ARPE-19 cells with BL exposure. In addition, Balb/c mice were irradiated with BL to induce retinal degeneration and orally administrated with GBE (50, 100, 200 mg/kg). Using the harvested retina, we performed histological analysis (thickness of retinal layers), qRT-PCR, and western immunoblotting to elucidate the effects and mechanisms of GBE against retinal damage in vivo. Results: GBE significantly inhibited BL-induced cell damage in ARPE-19 cells by activating the SIRT1/PGC-1α pathway, regulating NF-kB translocation, caspase 3 activation, PARP cleavage, expressions of apoptosis-related factors (BAX/BCL-2, LC3-II, and p62), and ROS production. Furthermore, GBE prevented BL-induced retinal degeneration by restoring the thickness of retinal layers and suppressed inflammation and apoptosis via regulation of NF-kB and SIRT1/PGC-1α pathway, cleavage of caspase 3 and PARP, and expressions of apoptosis-related factors in vivo. Conclusions: GBE could be a potential agent to prevent dry AMD and progression to wet AMD.

• 한국염색가공학회:학술대회논문집
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• 한국염색가공학회 2004년도 추계학술발표회 논문집
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• pp.167-171
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• 2004

• Reproductive and Developmental Biology
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• 제28권4호
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• pp.211-219
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• 2004

The effects of adenosine 5'-triphosphate (ATP) and ATP analogs, P/sub 2y/ purinoceptor agonists, on growth of normal mouse mammary epithelial cells (NMuMG) were examined. Cells were plated onto 24 well plates in DMEM supplemented with 10 % fetal calf serum. After serum starvation for 24 hours, ATP, P/sub 2y/ purinoceptor agonists (AdoPP[NH]P, ATP-α-S, ATP-γ-S, β, γ-me-ATP and 2me-S-ATP), P/sub 2u/ purinoceptor agonist (UTP) and P/sub 2y/ purinoceptor antagonists (Reactive Blue 2, more selective to P/sub 2y/ receptor than PPADS; PPADS) were added. DNA synthesis was estimated as incorporation of 3H-thymidine into DNA (1 hour pulse with 1 μ Ci/ml, 18～19 hours after treatment). ATP, Adopp[NH]P, ATP-α-S or ATP-γ-S, significantly increased DNA synthesis at 1, 10 and 100 μM concentrations with dose-dependency (P<0.05), and the maximum responses of ATP and ATP analogs were shown at 100 μM concentration (P<0.05). The potency order of DNA synthesis was ATP≥ATP- γ -S>Adopp [NH]P>ATP-α-S. β, γ -me-ATP, 2me-S-ATP and UTP did not increase DNA synthesis. In autoradiographic analysis of percentage of S-phase cells, similar results were observed to those of DNA synthesis. Addition of 1, 10 or 100 μM Reactive Blue 2 or PPADS significantly decreased ATP (100 μM)-induced DNA synthesis, however, PPADS was less effective than Reactive Blue 2. In Elvax 40P implant experiment, ATP directly stimulated mammary endbud growth in situ suggesting the physiological regulator of ATP in mammary growth. ATP 100 μM rapidly increased MAPK activity, reaching a maximum at 5 min and then gradually decreasing to the base level in 30 min. ATP analogs, Adopp[NH]P and ATP-γ-S also increased MAPK activity, however, β, γ-me-ATP and 2me-S-ATP did not. The inhibitor of the upstream MAPK kinase (MEK), PD 98059 (25 μM), effectively reduced ATP (100 μM) or EGF(10 ng/ml, as positive control)-induced MAPK activity and DNA synthesis (P<0.05). These results indicate that ATP-induced DNA synthesis was prevented from the direct inhibition of MAPK kinase pathway. Overall results support the hypothesis that the stimulatory effects of normal mouse mammary epithelial growth by addition of ATP or ATP analogs are mediated through mammary tissue specific P/sub 2y/ purinoceptor subtype, and MAPK activation is necessary for the ATP-induced cell growth.