• 한국식품과학회지
• /
• 제10권1호
• /
• pp.1-7
• /
• 1978

식품으로의 이용가치가 충분한 것으로 알려진 두유(豆乳) 제조시 부산물로 얻어지는 비지를 보존하기 위한 방법의 하나로 열풍건조를 실시하였다. 비지의 고형성분은 단백질 26.55%, 지방 12.50%, 회분 4.04%, 탄수화물 48.71%이었다. 건물중량비로 593%의 수분함량을 갖고 있는 비지를 기계적으로 압착하여 378%까지 수분함량을 감소시켰다. 이 때의 적합한 압착조건은 압착하중 $0.5\frac{M}{T}$, 압착시간 5분 이었다. 압착에 의하여 수분함량이 감소된 비지를 지름이 3mm, 길이가 10mm정도 크기의 과립모양으로 만들었다. 이러한 과립상 비지를 얇은층으로 쌓아 10%의 수분함량까지 열풍건조를 실시하였다. 그 결과 건조조건(열풍속도 160fpm, 건조온도 $120^{\circ}C$)에서 95분간 건조시킨 건조비지의 외관상의 품질변화가 거의 문제가 되지 않음이 밝혀졌다.

• 멤브레인
• /
• 제26권5호
• /
• pp.365-371
• /
• 2016

메탄을 순도 95% 이상으로 분리, 회수하기 위하여 메탄에 대한 분리특성이 우수한 폴리설폰 중공사 분리막 모듈을 2단으로 연결하고 재순환 흐름을 이용하여 회수율을 90% 이상으로 유지할 수 있도록 공정을 설계하였다. 이렇게 설계된 2단 공정을 통한 메탄 분리 거동 특성을 이론적으로 예측하기 위하여 Compaq Visual Fortran 6.6 소프트웨어를 이용하여 수치 해석하였다. 개발한 프로그램을 사용하여 수치 해석을 수행한 결과 공정 변수에 따라 최종 메탄의 농도 변화에 미치는 영향을 고찰할 수 있었다. 공급 기체 압력과 분리막 길이와 공급측 메탄 농도 증가, 유량이 감소함에 따라 최종 생산물 내 메탄 농도 증가를 관찰할 수 있었으며, 메탄의 회수율은 감소함을 알 수 있었다.

• Applied Biological Chemistry
• /
• 제28권4호
• /
• pp.233-238
• /
• 1985

Glucoamylase를 $ZrO_2$로 피복된 96% porous glass에 azo-linkage를 형성시켜 결합하게 한후, 2.5% glutaraldehyde로 처리하여 효소를 고정화시켰다. 효소기질로는 용해도가 높고 점도가 낮은 30% enzyme thinned cornstarch (dextrose equivalent 값 : 24)를 사용하여 plug flow-column reactor에서 연속반응시켰다. 반응 최적 pH는 수용성효소의 5.0보다 alkaline 쪽으로 기울어져 7.0으로 나타났고, 고정화반응에 따라 열안정성이 높아지고 $40{\sim}60^{\circ}C$에서 최적 온도범위를 가리키며, Km값은 수용성 효소의 1.25mM보다 낮은 1.04mM값을 보여 주었다. 따라서, pH 7.0, $45^{\circ}C$에서 160시간 동안 corn starch를 기질로 효소반응을 시켜 glucose 90.3%, maltose 8.0%인 DE값 94.0인 전분당분해산물을 획득할 수 있었다.

• Natural Product Sciences
• /
• 제22권2호
• /
• pp.93-101
• /
• 2016

For efficient quality control of the Samryeongbaekchul-san decoction, a powerful and accurate an ultra-performance liquid chromatography (UPLC) coupled with electrospray ionization (ESI) tandem mass spectrometry (MS) method was developed for quantitative analysis of the thirteen constituents: allantoin (1), spinosin (2), liquiritin (3), ginsenoside Rg1 (4), liquiritigenin (5), platycodin D2 (6), platycodin D (7), ginsenoside Rb1 (8), glycyrrhizin (9), 6-gingerol (10), atractylenolide III (11), atractylenolide II (12), and atractylenolide I (13). Separation of the compounds 1 - 13 was performed on a UPLC BEH $C_{18}$ column ($2.1{\times}100mm$, $1.7{\mu}m$) at a column temperature of $40^{\circ}C$ with a gradient solvent system of 0.1% (v/v) formic acid aqueous-acetonitrile. The flow rate and injection volume were 0.3 mL/min and $2.0{\mu}L$. Calibration curves of all compounds were showed good linearity with values of the correlation coefficient ${\geq}0.9920$ within the test ranges. The values of limits of detection and quantification for all analytes were 0.04 - 4.53 ng/mL and 0.13 - 13.60 ng/mL. The result of an experiment, compounds 2, 6, 12, and 13 were not detected while compounds 1, 3 - 5, and 7 - 11 were detected with 1,570.42, 5,239.85, 299.35, 318.88, 562.27, 340.87, 12,253.69, 73.80, and $115.01{\mu}g/g$, respectively.

• Natural Product Sciences
• /
• 제13권4호
• /
• pp.378-383
• /
• 2007

Phenathrene derivatives, such as batatasins, are well-known constituents in Dioscorea Rhizoma. Although phenanthrenes have been reported as representative compounds in this plant, standard markers for quality control have been focused on the polar constituents (saponins and purine derivatives). Herein, simple, rapid and reliable HPLC method was developed to determine 3,5-dimethoxyphenanthrene-2,7-diol (DMP) and batatasin-I (BA-I) as non-polar standard maker compounds of Dioscorea Rhizoma. DMP and BA-I were analyzed under optimized HPLC conditions [column: Columbus $5{\mu}$ C18 100A ($30{\times}4.6mm$ i.d., $5{\mu}m$; mobile phase: $H_2O$ with 0.025% $CH_3COOH$ (v/v) for solvent A and $CH_3CN$ with 0.025% $CH_3COOH$ (v/v) for solvent B, gradient elution; flow rate: 2 mL/min; detection: 260 nm), and each experiment was finished within 13 min. Good linearity was achieved in the range from 0.5 to $10.0{\mu}g/mL$ for each compound, and intra- and inter-day precision were in the acceptable levels. The recovery test were performed with three different Dioscorea Rhizoma samples (D. opposita, D. batatas and D. japonica), and showed its accuracy values in the range of 97.2 - 102.8% for three different concentrations of DMP and BA-I. The content levels of DMP and BA-I were ranged under 0.0020%. These results demonstrated that amounts of DMP and BA-I are easily determined with conventional HPLC-UV-DAD method although the content levels were lower than those of saponins and allantoin in Dioscorea Rhizoma. This HPLC method could be used for quality control of various Dioscorea preparations.

• Natural Product Sciences
• /
• 제16권2호
• /
• pp.116-122
• /
• 2010

A high-performance liquid chromatography (HPLC) with diode array detector (DAD) and electrospray ionization mass spectrometry (ESI-MS) was established for the simultaneous determination of five representative metabolites of the iridoid and phenolic classes from Rehmannia glutinosa. The optimal chromatographic conditions were obtained on an ODS column (5 mm, $4.6{\times}250\;mm$) with the column temperature at $25^{\circ}C$. The mobile phase was composed of water and acetonitrile using a gradient elution with the flow rate 0.3 mL/min. Detection wavelength was set at 205 nm. All calibration curves showed good linear regression ($r^2$ > 0.997) within test ranges. Limits of detection (LOD) and quantitation (LOQ) values were lower than 0.123 and $0.373\;{\mu}g/mL$, respectively. The developed method provided satisfactory precision and accuracy with overall intra-day and inter-day variations of 0.09 - 0.76% and 0.16 - 1.41%, respectively, and the overall recoveries of 99.03 - 102.67% for all of the compounds analyzed. In addition, effectiveness of diverse extraction methods was compared to each other for the development of standard analytic method. The verified method was successfully applied to the quantitative determination of five representative metabolites in twenty-one commercial Rehmannia glutinosa samples from different markets in Korea and China. The analytical results showed that the contents of the five analytes vary significantly with sources.

• Natural Product Sciences
• /
• 제18권3호
• /
• pp.158-165
• /
• 2012

A UPLC method for the simultaneous determination of seven compounds was established for the quality control in H. cordata. The UPLC was performed on a $C_{18}$ HSS T3 $2.1{\times}100$ mm, 1.8 ${\mu}m$ column during a 13 minute gradient elution of 0.2% aqueous acetic acid and acetonitrile with the flow rate of 0.2 mL/min at $30^{\circ}C$. The UPLC method was validated according to the ICH guideline of analytical procedures with respect to precision, accuracy, and linearity. The limit of determination and quantitation for the seven compounds were 0.01-0.09 and 0.03-0.28 ${\mu}g/mL$, respectively. The calibration curves of all seven compounds showed good linearity ($r^2$ > 0.999). The intra-day and inter-day the RSD values used to evaluate the precision of analysis were less than 0.9%. The recoveries of quantified compounds ranged from 98.63 to 103.85%. The developed UPLC method was found to be effective, convenient and sensitivity for quantitative analysis of seven compounds in H. cordata. This work could be provided a baseline source for quality control of H. cordata.

• Nutrition Research and Practice
• /
• 제11권4호
• /
• pp.275-280
• /
• 2017

BACKGROUND/OBJECTIVES: Re-epithelialization has an important role in skin wound healing. Astaxanthin (ASX), a carotenoid found in crustaceans including shrimp, crab, and salmon, has been widely used for skin protection. Therefore, we investigated the effects of ASX on proliferation and migration of human skin keratinocyte cells and explored the mechanism associated with that migration. MATERIAL/METHOD: HaCaT keratinocyte cells were exposed to $0.25-1{\mu}g/mL$ of ASX. Proliferation of keratinocytes was analyzed by using MTT assays and flow cytometry. Keratinocyte migration was determined by using a scratch wound-healing assay. A mechanism for regulation of migration was explored via immunocytochemistry and western blot analysis. RESULTS: Our results suggest that ASX produces no significant toxicity in human keratinocyte cells. Cell-cycle analysis on ASX-treated keratinocytes demonstrated a significant increase in keratinocyte cell proliferation at the S phase. In addition, ASX increased keratinocyte motility across the wound space in a time-dependent manner. The mechanism by which ASX increased keratinocyte migration was associated with induction of filopodia and formation of lamellipodia, as well as with increased Cdc42 and Rac1 activation and decreased RhoA activation. CONCLUSIONS: ASX stimulates the migration of keratinocytes through Cdc42, Rac1 activation and RhoA inhibition. ASX has a positive role in the re-epithelialization of wounds. Our results may encourage further in vivo and clinical study into the development of ASX as a potential agent for wound repair.

• 한국정보통신학회논문지
• /
• 제11권9호
• /
• pp.1694-1701
• /
• 2007

현재 국내에서는 이동통신사마다 별도 무선인터넷 플랫폼을 사용하고 있어 콘텐츠 제공업 체와 단말기 제조사가 개발시간이나 비용이 많이 소요되고 있다. 이에 국내 이동통신 3사와 전자통신연구원 등을 주체로 무선인터넷 표준 플랫폼인 WIPI(Wireless Internet Platform for Interoperability)를 제정하고 표준화작업을 국내외로 추진하고 있다. 그러나 국내환경에서도 WIPI는 표준화 작업이 진행중이며 WIPI환경을 기반으로 한 콘텐츠가 미비한 현실이다. 특히 무선인터 넷 플랫폼이 하나로 통합되면서 기존의 여러 플랫폼이 공존하던 환경에 비해 해킹이나 악성코드의 집중적인 공격이 예상되며 이를 대비해 모바일 환경에서 데이터를 효과적으로 보호할 필요성이 대두하였다. 이에 본 논문에서는 모바일 환경에서 XML 문서로 데이터를 교환하는 상황을 고려하여 PC 환경에서 사용되던 여러 암호화 기법을 적용하여 WIPI 환경에서 XML문서 암호화 시스템을 설계 및 구현하였다.

• Bulletin of the Korean Chemical Society
• /
• 제19권6호
• /
• pp.671-676
• /
• 1998

The formation and dissociation rates of $Ce^{3+}$ Complexes of the 1,4,7,10-tetraaza-13,16-dioxacyclooctadecane-NN', N",N"'-tetraacetic acid (1), 1,4,7,10-tetraaza-13,16-dioxacyclooctadecane-N,N',N",N"'-tetramethylacetic acid (2), and 1,4,7,10-tetraaza-13,16-dioxacyclooctadecane-N,N',N",N"'-tetrapropionic acid (3) have been measured by the use of stopped-flow spectrophotometry. Observations were made at 25.0±0.1 ℃ and at an ionic strength of 0.10 M $NaClO_4$. The complexation of $Ce^{3+}$ ion with 1 and 2 proceeds through the formation of an intermediate complex $(CeH_3L^{2+})^*$ in which the $Ce^{3+}$ ion is incompletely coordinated. This may then lead to be a final product in the rate-determining step. Between pH 4.76 and 5.76, the diprotonated $(H_2L^{2-})$ from is revealed to be a kinetically active species despite of its low concentration. The stability constants $(logK(CeH_3L^{2+}))$ and specific water-assisted rate constants $(k_{OH})$ of intermediate complexes have been determined from the kinetic data. The dissociation reactions of $Ce^{3+}$ complexes of 1, 2, and 3 were investigated with $Cu^{2+}$, ions as a scavenger in acetate buffer. All complexes exhibit acid-independent and acid-catalyzed contributions. The effect of buffer and $Cu^{2+}$ concentration on the dissociation rate has also been investigated. The ligand effect on the dissociation rate of $Ce^{3+}$ complexes is discussed in terms of the side-pendant arms and the chelate ring sizes of the ligands.