• 한국유전체학회:학술대회논문집
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• 한국유전체학회 2005년도 The 14th Korea Genome Conference
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• pp.59-59
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• 2005

• 유전체소식지
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• 제6권1호
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• pp.7-8
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• 2006

• Archives of Pharmacal Research
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• 제26권2호
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• pp.120-123
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• 2003

A method for the determination of terbutaline enantiomers in human urine by capillary elctrophoresis has been developed. Optimum resolution was achieved using 50 mM phosphate buffer, pH 2.5, containing 15 mM of hydroxypropyl-$\beta$-cyclodextrin as a chiral selector. Urine samples were prepared by solid-phase extraction with Sep-pak silica, followed by CE. The assay was linear between 2-250 ng/mL (R = 0.9998 for (S)-(+)-terbutaline and R = 0.9999 for (R)-(-)-terbutaline) and detection limit was 0.8 ng/mL. The intra-day variation ranged between 6.3 and 14.5% in relation to the measured concentration and the inter-day variation was 8.2-20.1%. It has been applied to the determination of (S)-(+)-terbutaline and (R)-(-)-terbutaline in urine from healthy volunteer dosed with racemic terbutaline sulfate.

• Bulletin of the Korean Chemical Society
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• 제25권3호
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• pp.377-381
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• 2004

Chiral separation of aryalcohols such as 1-phenyl-propanol, 1-phenyl-2-proanol, and 2-phenyl-1-propanol by capillary electrophoresis has been optimized using the overlapping resolution mapping (ORM) scheme. Three critical parameters of the electrophoretic media, i.e. phosphate concentration, sulfated ${\beta}$-cyclodextrin (CD) concentration and pH, were chosen for optimization. The working ranges were initially presumed by 7 preexperiments. Further optimization was carried out by another seven experiments within the narrow working ranges. From the final overlapping resolution mapping all peak pairs, the area of maximum separations were located. Using the conditions of a point in this area, we found that the target compounds were a baseline separated within 30 min. The maximum separation conditions of arylalcohols were a chiral selector concentration of 5.4%, a phosphate concentration of 28 mM, and a pH of 5.0.

• Bulletin of the Korean Chemical Society
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• 제30권9호
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• pp.2141-2144
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• 2009

• 대한화학회지
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• 제52권6호
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• pp.630-636
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• 2008

• International Journal of Oral Biology
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• 제42권4호
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• pp.197-201
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• 2017

A novel method for the detection of hydrogen peroxide in aqueous solution was developed via reaction between $H_2O_2$, trivalent titanium ion ($Ti^{3+}$) and 4-(2-thiazolylazo) resorcinol (TAR), resulting in a ternary complex with a maximum UV absorbance at 530 nm. The CE detection of $H_2O_2$ was fast, sensitive and cost-effective without pretreatment procedures. $H_2O_2$ was detected within 15 min at 1 to $100{\mu}M$ range with the lowest detection limit at $1.0{\mu}M$. Under the optimized CE conditions, the concentration of $H_2O_2$ in coffee or tea extract was quantitatively determined. Our results show that CE detection of the ternary complex of $H_2O_2-Ti^{3+}$-TAR has potential applications for the detection of $H_2O_2$ in aqueous sources.

• 통합자연과학논문집
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• 제9권1호
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• pp.28-34
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• 2016

A number of chiral selectors have been developed and applied for enantiomer separation of a variety of chiral compounds. Among these chiral selectors are chiral crown ethers, a class of synthetic host polyether molecules that bind protonated chiral primary amines with high selectivity and affinity. In this paper, two important chiral crown ethers as chiral selectors of bis-(1,1'-binaphthyl)-22-crown-6 and (18-crown-6)-2,3,11,12-tetracarboxylic acid (18-C-6-TA) are focused. They have been widely used to resolve the enantiomers of chiral compounds containing a primary amino moiety using chiral stationary phases (CSPs) or chiral selectors by high-performance liquid chromatography (HPLC), capillary electrophoresis (CE) and so on in chirotechnology. Also, it was described that the commercially available covalent type HPLC CSPs derived from (+)- and (-)-18-C-6-TA have been developed and successfully applied for the resolution of various primary amino compounds including amino acids.

• Mass Spectrometry Letters
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• 제15권2호
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• pp.107-119
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• 2024

We aimed to develop a suitable quantification method for detecting asparagine deamidation and aspartic acid isomerization in peptide mapping using LC-MS. Our assessment of its validity and suitability involved comparing its quantitative findings with those obtained from cation-exchange chromatography and capillary electrophoresis methods. By subjecting trastuzumab to rigorous conditions to induce these modifications, we validated the efficacy of this new analytical method in peptide mapping via LC-MS, evaluating both qualitative and quantitative aspects of asparagine deamidation and aspartic acid isomerization. Our investigation underscored the significance of enzyme selection and the presence of miss-cleaved or non-specific peptides in achieving accurate quantitative results. The experimental results demonstrated a strong correlation with results from cation-exchange chromatography and capillary electrophoresis analyses, confirming the reliability of the LC-MS based peptide mapping approach.

• 한국식품과학회지
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• 제30권6호
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• pp.1252-1258
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• 1998

재배 면적이 비교적 넓은 국내산벼 10품종 백미의 알콜용해성단백질을 capillary elictrophoresis로 분석하고 품종간 단백질 pattern의 차이를 비교 분석하므로써 신속한 품종판별법으로서의 적용가능성을 검토하였다. P-ACN buffer를 이용한 분석조건에서 각 품종은 25분 이내에 분석완료 되었으며 peak pattern의 특징에 따라 동진벼 group, 추청벼 group 및 일품벼 group의 3group으로 분류할 수 있었다. 동진벼, 계화벼, 영남벼가 동진벼 group으로 분류되었으며 이 group에서는 다른 품종에서는 거의 나타나지 않은 peak h가 전체 peak area의 $6{\sim}8%$를 차지하며 뚜렷이 검출되었다. 추청벼 group은 peak h를 제외한 대부분의 peak가 동진벼 group과 비슷하게 나타났으며 추청벼, 오대벼, 만금벼 및 봉광벼 4품종이 해당되었다. 일품벼 group으로 분류된 일품벼, 화성벼 및 화영벼에서는 peak g가 전체 peak의 약 70%라는 압도적인 비율을 나타내었다. 주요 peak의 뚜렷한 차이에 따라 3 group으로 분류하기는 하였으나 일품벼, 오대벼 등의 일부 품종은 단독으로 구별이 가능하였으며 각 group 내에서도 미미하기는하나 구성 peak들을 면밀히 비교 분석하므로써 품종에 따른 특성을 도출할 수 있었다. 또한 다른 분석법과 비교할 때 우리 나라에서 재배면적이 50% 이상으로 가장 많은 동진벼와 추청벼는 각 현미의 윗면, 측면, 앞면의 화상을 이용한 품종판별법에서 서로 오판될 확률이 비교적 높았으나 CE로는 peak h에 의해 서로 쉽게 구분되었다.