• Bulletin of the Korean Chemical Society
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• 제31권5호
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• pp.1159-1164
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• 2010

Several triterpenoid saponins from root of Pulsatilla koreana Nakai (Ranunculaceae) were studied and their biological activities were reported. It is difficult to analyze triterpenoid saponins using HPLC-UV due to the lack of chromophores. So, evaporative light scattering detection (ELSD) is used as a valuable alternative to UV detection. More recently, a charged aerosol detection (CAD) has been developed to improve the sensitivity and reproducibility of ELSD. In this study, we developed and validated a novel method of high performance liquid chromatography coupled with a charged aerosol detector for the simultaneous determination of four triterpenoid saponins: pulsatilloside E, pulsatilla saponin H, anemoside B4 and cussosaponin C. Analytes were separated by the Supelco Ascentis$^{(R)}$ Express C18 column (4.6 mm ${\times}$ 150 mm, 2.7 ${\mu}m$) with gradient elution of methanol and water at a flow rate of 0.8 mL/min at $30^{\circ}C$. We examined various factors that could affect the sensitivity of the detectors, including various concentrations of additives, the pH of the mobile phase, and the CAD range. Linear calibration curves were obtained within the concentration ranges of 2 - 200 ${\mu}g$/mL for pulsatilloside E, anemoside $B_4$ and cussosaponin C, and 5 - 500 ${\mu}g$/mL for pulsatilla saponin H with correlation coefficient ($R^2$) greater than 0.995. The limit of detection (LOD) and quantification (LOQ) were 0.04 - 0.2 and 2 - 5 ${\mu}g$/mL, respectively. The validity of the developed HPLC-CAD method was confirmed by satisfactory values of linearity, intra- and inter-day accuracy and precision. This method could be successfully applied to quality evaluation, quality control and monitoring of Pulsatilla koreana.

• 한국약용작물학회지
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• 제9권1호
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• pp.21-25
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• 2001

인삼의 주종 사포닌인 7종 사포닌($Rb_1,\;Rb_2,\;Rc,\;Rd,\;Re,\;Rf\;and\;Rg_1$)을 고속액체크로마토그라피로 분석하는 일반적인 방법인 순상 column에서 $Rg_1$, Re 및 Rf가 명확히 분리되지 않는 문제점을 개선하기위하여 본 연구를 수행하였다. 고속액체크로마토그라피를 이웅하여 역상 ${\mu}{\beta}ondapak$ ODS컬럼으로 인삼중 주종 사포닌인 7종 ginsenosides $Rg_{1},\;Re,\;Rf,\;Rb_{1},\;RC,\;Rb_{2}$ 및 Rd를 양호하게 분리하였다. 이때 분석 조건으로 이동상 용매 조성은 (A) $H_{2}O$, (B) methyl cyanaide을 (A) 90/(B) 10에서 (A) 0/(B) 100으로 기울기 용리를 이용하였으며, 기울기 용리 제어장치를 사용하여 용리시켰다. 용매 흐름속도는 1.5ml/min, 검출기는 UV detector(203nm)이었다. 이 방법은 분리능과 재현성 및 회수율이 양호하므로, 앞으로 인삼중 ginsenosides 분석에 응용될 수 있을 것으로 사료된다.

• 분석과학
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• 제11권6호
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• pp.436-439
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• 1998

인삼 사포닌을 역상 고속 액체크로마토그래피 방법을 이용하여 여러 종류의 컬럼으로 분석하였다. 최적 조건은 Novapak $C_{18}$ ODS 역상 칼럼($3.9mm{\times}150mm$, $5{\mu}m$), $CH_3CN/H_2O$ 이성분 이동상 용액과 기울기 제어장치, 그리고 1.5 mL/min의 용매 흐름속도였으며, UV 검출기(203 nm)를 사용하였다. 인삼의 주성분인 ginsenoside $Rb_1$, $Rb_2$, Rc, Rd, Re, Rf 그리고 $Rg_1$ 7종을 50분 안에 양호하게 분리하였다. 각 성분에 대한 검량선은 직선성이 좋았으며, 회귀계수는 0.98~0.99이었다.

• Journal of Applied Biological Chemistry
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• 제66권
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• pp.320-327
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• 2023

Capsicum annuum belongs to the Solanaceae family, crops of which are extensively cultivated worldwide. It is a food source containing various nutrients and vitamins and also serves as a medicine for treating ailments. The burning feeling experienced while consuming Capsicum fruits is due to the presence of capsaicinoids, particularly capsaicin and dihydrocapsaicin. This study aimed to assess the content of these two compounds in 34 varieties of capsicum and paprika. High-performance liquid chromatography with a gradient elution system and a reverse-phase YMC Pack-Pro column with UV detection at 280 nm was employed. The results revealed that, among the 34 samples, only six samples (samples 1, 15, 20, 29, 32, and 34) contained capsaicin and dihydrocapsaicin, and their highest contents were found in sample 1 - variety name: Sungil-c (capsaicin: 3.42 mg/g extract, dihydrocapsaicin: 1.20 mg/g extract). These findings suggest that the content of these two compounds is attributed to the variety and is influenced by geographical location and environmental factors. Additionally, this study provides a basis for establishing a C. annuum variety with high capsaicin and dihydrocapsaicin contents.

• 분석과학
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• 제19권3호
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• pp.239-243
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• 2006

본 연구는 LLE(liquid-liquid extraction) 전처리 방법과 HPLC/UV를 이용하여 혈장에서 이트라코나졸을 정량 분석하는 방법을 연구하였다. 이트라코나졸과 내부표준물질(펠로디핀)을 디에틸에테르로 추출하고 C18 컬럼을 이용하여 분리한 후 UV 검출기를 통하여 254 nm에서 검출하였다. 이동상은 10 mM 아세트산 암모늄 완충액(pH 7) :아세토나이트릴(35:65, v/v) 혼합용액을 사용하였으며, 유속은 0.2 mL/min.으로 하였다. 정량범위는 2~1,000 ng/mL 이며, 상관관계($R^2$)는 0.9991로 좋은 직선성을 보였다. 정량한계는 2 ng/mL, 재현성은 변동계수가 10.8 이하, 정확도는 97.2~108.2% 였다. 이 분석방법은 혈장 중의 약물 정량 및 약물의 약동력학에 유용함을 보여주었다.

• Food Science and Biotechnology
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• 제18권6호
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• pp.1430-1434
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• 2009

The present study used the liquid extraction pretreatment method and developed a liquid chromatographyultraviolet detector (LC-UV) for the simultaneous determination of 14 sulfonamides (SAs) residues in porcine and chicken muscle. Linearity within a range of $50-150\;{\mu}g/kg$ was obtained with the correlation coefficient ($r^2$) of 0.9673-0.9997. The mean recovery of SAs was 55.9-109.7% (relative standard deviations; RSDs 1.7-17.3%) in porcine muscle and 52.8-112.4% (RSDs 2.3-16.9%) in chicken muscle. The limits of detection (LODs) and limits of quantification (LOQs) were 2-32 and $7-96\;{\mu}g/kg$ in porcine muscle, and 4-32 and $13-97\;{\mu}g/kg$ in chicken muscle, respectively. These values were lower than the maximum residue limits (MRLs) established by the European Union. The sum of all SAs residues present should be less than $100\;{\mu}g/kg$.

• 한국환경농학회지
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• 제4권1호
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• pp.43-51
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• 1985

식물체중의 IAA-아미노산 복합체를 확인하기 위하여 23종의 IAA-아미노산 복합체를 합성하여 이들의 UV와 IR spectra, TLC, HPLC 그리고 가수분해등 화학적 증거를 토대로, 암실재배한 완두 유묘의 줄기에서 IAA-Asp와 IAA-Glu를 잠정적으로 동정하였다. IAA-Asp는 식물체에서 IAA의 대사산물로 이미 확인된 화합물(化合物)이지만 IAA-Glu는 아직 확인되지 않고 있다.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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• pp.304.2-305
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• 2003

A simple and rapid method for the determination of theophylline (THP) in human serum was developed by a high performance liquid chromatography/UV detector and applied to pharmacokinetic study of THP in human volunteers. ${\beta}$-Hydroxyethyltheophylline as internal standard was added to 200 ${\mu}\ell$ of human serum and the mixture was centrifuged at 13000 rpm for 10 min. (omitted)

• 한국동물위생학회지
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• 제23권1호
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• pp.1-8
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• 2000

This study was carried out to simultaneous determination of penicillin G and chloramphenicol in livestock products by HPLC. The results obstained were as follows; 1. Penicillin G and chloramphenicol were analyzed by HPLC on symmetry $C_{18}$ column with acetonitrile-0.1 M phosphate buffer containing 0.0157 M thiosulfate (25 : 75) as mobile phase at UV 325nm and 280nm, respectively. 2. Samples were applied to a SeP-Pak $C_{18}$ cartridge, from which eluted penicillin derivatized with 2 M 1,2,4-triazole containing 0.001 M mercuric chloride. 3. The average recovery rates of penicillin G and chloramphenicol were 81.8% and 80.3%, respectively, and the detection limits were 5 ppb (5$\mu\textrm{g}$/kg: 7.9IU/kg) for penicillin G and chloramphenicol in porcine and bovine muscle.

• Journal of Applied Biological Chemistry
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• 제64권2호
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• pp.153-158
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• 2021

Cordyceps militaris (CM) is one of the most important medicinal mushrooms known to possess various biological activities. Cordycepin (CP) is a bioactive compound present in the fruiting bodies of CM and is known to have anti-tumor, anti-metastatic immunomodulatory and anti-inflammatory activities. In this study, we aim to analyze CP quantitatively under various CM extraction conditions. CP was measured using high-performance liquid chromatography, quantified using a reversed phase column using a gradient elution system of water and acetonitrile, and detected with a UV absorbance wavelength of 260 nm. The CP content of CM was the highest in 100% ethanol extract of the fruiting bodies and 60% ethanol extract of the mycelium. This study provides an efficient analysis method to determine the optimal extraction conditions for CP that can be used as a basis for developing functional foods and pharmaceutical products derived from CM.