• 제목/요약/키워드: capillary electrophoresis

검색결과 174건 처리시간 0.024초

Enhanced UV-Visible Absorbance Detection in Capillary Electrophoresis Using Modified T-Shaped Post-Column Flow Cell

  • Lim, Kwan-Seop;Kim, Su-Hyeon;Hahn, Jong-Hoon
    • Bulletin of the Korean Chemical Society
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    • 제23권2호
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    • pp.295-300
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    • 2002
  • The construction of the T-shaped post-column flow cell has been changed to enhance the practicability as a UV-visible absorbance detector for capillary electrophoresis. In this new design, a rectangular cube-shaped inner structure is employed, which completely fits the outer rectangular tubing. This arrangement has greatly facilitated the fabrication of the T-cells. In addition, the volume for the auxiliary flow has been dramatically reduced down to 300 ${\mu}L$, and its volume flow rate is optimized at 4.2 ${\mu}L$/min. The short optical path length in the sheath flows (500 ${\mu}m$ on each side) minimizes background absorption, and thus enhances its performance in low-UV wavelengths. We have optimized the auxiliary flow rate at 50 ${\mu}m$/s, so that migration times are insensitive to the flow rate. This optimization has improved repeatabilities in migration times and peak heights. A double-beam detection scheme using a pair of photodiodes is employed to increase the signal-to-noise ratio.

모세관 전기영동 장치용 Photodiode Array 다채널 검출기의 개발에 관한 연구 (Development of a Multi - channel Detector for Capillary Electrophoresis System)

  • 홍승국;김해동
    • 분석과학
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    • 제11권2호
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    • pp.96-104
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    • 1998
  • 수 많은 광검출기들이 직선으로 집적된 광다이오드 어레이를 이용한 모세관 전기영동장치용 다채널 검출기를 개발하였다. 본 연구에서 사용된 광다이오드 어레이는 1024개의 광검출소자를 가지고 있으며 275~675 nm 파장범위에서 시료의 흡수분광스펙트럼을 검출할 수 있다. 이 장치는 30 ms내에 전 파장영역의 스펙트럼을 얻을 수 있으며, PC에 의하여 시료분석에 필요한 여러 가지 조건들을 제어할 수 있도록 설계하였다. 개발된 검출기의 성능을 L-ascorbic acid와 alizarin yellow GG를 사용하여 시험하였다. 본 연구에서 개발한 모세관 전기영동장치용 다채널 검출기의 재현성 실험결과 상대 표준편차는 5.6%이었다.

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DNA Concentration Effect of Various Hydroxide Compounds on Stacking in Capillary Electrophoresis

  • Shin, Ah-Ram;Kang, Seong-Ho
    • Bulletin of the Korean Chemical Society
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    • 제32권12호
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    • pp.4316-4320
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    • 2011
  • The effects of various hydroxide compounds on base stacking (BS) were investigated for pre-concentration of DNA molecules in capillary electrophoresis (CE). In BS, hydroxide ions ($OH^-$) were electrokinetically introduced after DNA sample injection. A neutralization reaction occurred between the $OH^-$ and $Tris^+$ of the running buffer, which resulted in a zone of lower conductivity. Within the low conductivity zone of the high electric field, the DNA molecules moved more rapidly and were concentrated in front of the low conductivity zone. At the same BS conditions of CE, the enhanced sensitivity of the DNA samples was dependent on the kind of multivalent cations in the hydroxide compounds. Except for LiOH, the hydroxide compounds with monovalent cations showed more effective BS than those with divalent cations because of solubility, ionic strength and electronegativity. The order of hydroxide compounds that enhance the detection sensitivity of DNA molecules was as follows: NaOH > $NH_4OH$ > KOH > $Ba(OH)_2$ > $Sr(OH)_2$ > LiOH > $Ca(OH)_2$ > $Mg(OH)_2$. $NH_4OH$, KOH and $Ba(OH)_2$ proved to be efficient hydroxide compounds to use as effective BS reagents in CE instead of NaOH.

A Combination of the Frozen Raindrop Collection Method and a High-performance Capillary Electrophoresis Technique for the Size-resolved Raindrops Study

  • Ma, Chang-Jin
    • Journal of Korean Society for Atmospheric Environment
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    • 제22권E1호
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    • pp.27-34
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    • 2006
  • Although the importance of size-resolved raindrops study has been known, it has not been popularized up to the present. In the present study, an attempt was made to generalize the size-resolved raindrops study by a combination of the frozen raindrop collection method and a commercially available high-performance capillary electrophoresis (HPCE). Samplings were carried out at Kyoto, Japan in October 2002. The inorganic ions (chloride, nitrate, sulphate, calcium, ammonium, sodium, magnesium, potassium) in size classified raindrop samples were successfully analyzed by HPCE with good repeatability. To assure the accuracy and precision of HPCE data, t-test was conducted with paired analytical data, which were experimentally constructed by analyzing standard solutions with HPCE and IC, respectively. T-test showed that there is no notable difference between the concentrations determined by the two analytical methods. Every ionic concentration in both cation and anion was found to be strong raindrop size dependence. Though there was slight increase of sodium and sulphate concentrations between 0.85 mm and 1.15 mm raindrop radius, it showed a strong decrease for every ionic component with increasing droplet radius. The combination of the frozen raindrop collection method and a commercially available HPCE can meet the need of size-resolved raindrops study.

Chiral Separation of Arylalcohols by Capillary Electrophoresis Using Sulfonated β-Cyclodextrin and Ag Colloids as Additives

  • Choi, Seong-Ho;Noh, Hyen-Ju;Lee, Kwang-Pill
    • Bulletin of the Korean Chemical Society
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    • 제26권10호
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    • pp.1549-1554
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    • 2005
  • Chiral separation of arylalcohols such as 1-phenyl-1-propanol, 1-phenyl-2-propanol, and 2-phenyl-1-propanol by capillary electrophoresis was studied using sulfonated $\beta$-cyclodextrin (CD) as a chiral selector and Ag colloids as an additive. The optimum separation condition of arylalcohols was found to be the chiral selector concentration of 6.5 mM, applied voltage of 15 kV, and pH of 7.0. In order to improve chiral separation, an Ag colloid was mixed with a running buffer. The resolution in the Ag colloid-mixed running buffer was considerably superior to that obtained with the sulfonated $\beta$-CD alone. The molar ratio of sulfonated $\beta$-CD to Ag colloid, which is one of critical parameters affecting resolution, was found to be optimum at 65 : 1. In order to elucidate the resolution mechanism, an inclusion-complex of the arylalcohols with sulfonated $\beta$-CD was prepared by mixing and shaking in solution, and then characterized by cyclic voltammetry (CV). The inclusion mechanism was also discussed using experimental results.

Chiral Separation of ${\beta}_2$-Agonists by Capillary Electrophoresis Using Hydroxypropyl-${\alpha}$-Cyclodextrin as a Chiral Selector

  • Kim, Kyeon-Ho;Kim, Hyu-Ju;Jeun, Eu-Young;Seo, San-Hun;Hong, Seon-Pyo;Kang, Jong-Seong;Youm, Jeong-Rok;Lee, Sang-Cheal
    • Archives of Pharmacal Research
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    • 제24권4호
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    • pp.281-285
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    • 2001
  • Enantiomers of five racemic ${\beta}_2$-agonists were investigated by capillary electrophoresis employing a hydroxypropyl-${\beta}$-cyclodextrin (HP-${\beta}$-CD). The effects of the concentration of HP-${\beta}$-CD added to the background electrolyte and of the pH of the buffer on the effective mobility and resolution of the studied compounds were examined. Very good resolution was achieved for terbutaline and clenbuterol; salbutamol and bambuterol was able to be partially resolved. Enantioselectivity and resolution were influenced by the concentration of the HP-7-CD, buffer composition and pH.

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Determination of Recombinant Human Epidermal Growth factor (rhEGF) in a Pharmaceutical Preparation by Capillary Electrophoresis

  • Hwang, Kyung-Hwa;Lee, Kang-Woo;Kim, Chang-Soo;Han, Kun;Chung, Youn-Bok;Moon, Dong-Cheul
    • Archives of Pharmacal Research
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    • 제24권6호
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    • pp.601-606
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    • 2001
  • A simple assay method of recombinant human epidermal growth factor (rhEGF) in a pharmaceutical preparation was studied and validated by capillary electrophoresis (CE) using micellar electrokinetic chromatography (MEKC) techniques. Factors affecting the migration behavior and separation performances of the peptide; type of buffers pH, butler concentration, and concentration of sodium dodecyl sulfates (SDS) were investigated to optimize the analytical performance. CE was performed using running buffers 50.0 mM borate (pH 8.5) containing 12.5 mM SDS at 20 $mutextrm{V}$ of the applied voltage. Calibration curves for the rhEGF showed good linearity (r>0.999) over the wide dynamic range from 1.25 to $100{\mu\textrm{g}}/ml$. Sample analysis was performed by using standard addition method to eliminate the matrix effects of dosage vehicle. This method is assumed to be useful for quality control (QC) of various forms of pharmaceutical products of the peptide.

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모세관전기영동장치 및 고속액체 크라마토그래피에 의한 황금의 성분 분석법 비교 (Studies on the Comparison of Scutellaria Radix Analyses by CE and HPLC)

  • 면노홍;김효진
    • 약학회지
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    • 제43권4호
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    • pp.429-436
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    • 1999
  • A simple, accurate and reproducible Capillary electrophoresis (CE) assay has been developed for the determination of baicalin, baicalein, wogonin and chrysin in Scutellaria baicalensis. Successful separation of these compounds has been obtained in 35 mM phosphate butter (pH 7.0) using a untreated fused silica capillary ($57{\;}cm{\times}75{\;}{\mutextrm{m}}$ i.d.) at $25^{\circ}C$ with the electric field of 19kV. Baicalin, baicalein wogonin and chrysin was separated and detected at 280 nm 13 min. The detection limits of CE were acceptable compared to HPLC. Reproducibilities of migration time and peak area were 0.66~1.11% (within-run), 2.18~3.38% (between-run) and 3.50~4.55% (within-run), 3.97~4.82%(between-run) at CE. The results indicate that CE could be a promising technique for quality and quantity control analysis of Scutellaria baicalensis as a validation method.

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제작된 모세관 전기영동 시스템의 유기물 분석에의 응용 (Application of Home-made Capillary Zone Electrophoresis System to the Separation of Organic Molecules)

  • 이공주;허귀석
    • 대한화학회지
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    • 제35권3호
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    • pp.219-225
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    • 1991
  • 고도로 효율적인 분석방법인 모세관 전기영동 시스템을 최적의 감도를 갖는 상태의 기기로 국내에서 제작하였다. 50 ${\mu}m$ 내경을 가진 모세관을 완충용액으로 채워준 후 모세관의 양끝에 20∼35 kV의 전압을 걸어주는 이 분석방법은 20분 이내에 10 nl 이하의 소량의 시료를 이론단수가 20∼50만 정도가 되도록 분리할 수 있는 매우 좋은 분리능으 가지고 있다. 모세관 전기영동법의 분리능과 분리도를 증가시키는데 영향을 주는 요소들을 알아보기 위하여 catecholamine과 adenine 유도체를 분석하였다.

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Nonaqueous Capillary Electrophoresis of Chlorinated Phenols

  • 김보정;전만석;신상무;정두수
    • Bulletin of the Korean Chemical Society
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    • 제20권12호
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    • pp.1483-1486
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    • 1999
  • The contents of pentachlorophenol (PCP) and 2,3,5,6-tetrachlorophenol (TeCP) in textile products are regulated for safety. Since an organic solvent such as 2-methoxyethanol is needed to extract chlorinated phenols from textile samples, nonaqueous capillary electrophoresis has been applied to achieve the separation of PCP and isomers of TeCP. The run buffer was 100 mM Tris/acetate in methanol whose pH was adjusted to 8.0. All of the analytes were negatively charged at pH 8.0 and their electrophoretic velocities were higher than the electroosmotic flow of the methanol buffer. A reverse voltage of -20 kV was applied along a 27-cm fused silica capillary with ID of 50 μm, and PCP and 3 TeCP isomers were separated based on the difference in $pK_a$ values in less than 4 min. The limits of detection (S/N = 3) were about 0.02 μM. By varying pH of the methanol run buffer, $pK_a$ values of the 4 chlorinated phenols were also estimated.