• 제목/요약/키워드: TLC analysis

검색결과 439건 처리시간 0.03초

사향의 크로마토그램 패턴 분석을 통한 품질비교 연구 (Quality comparison of musk products using a chromatographic pattern analysis)

  • 조종운;가오단;강종성;정효원;박용기
    • 대한본초학회지
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    • 제36권4호
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    • pp.41-50
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    • 2021
  • Objectives : This study is to check the quality of Moschus products in Korean markets using a chromatographic analysis. Methods : We collected musk products, two genuine products from Russia (A, B), two authentic products from Hong Kong (C) and Korea (D), the Ministry of Food and Drug Safety (MFDS) standard (E), and two fire ants products (E, F). Results : For identification, TLC analysis of 60% ethanol extracts of each product showed that A, B, C, and E have the suitable patterns before color development at 365 nm UV light for the MFDS regulation in Korea. A clear red spot was observed from the E at Rf 0.6 with 365 nm UV light after color development, but this spot was not found in A and B. For the purity test, a distinct violet spot with Rf 0.87 was observed from the A and B in TLC analysis of methanol extracts of each product at white light, however, this spot was not matched with the impurities of E and F. In HPLC-UV pattern analysis, a similar peak pattern was shown in A, B and E, and similar peaks were observed C, although the similarity was weaker than that of A, B, and E. The F and G showed different peak patterns compared with the peak patterns of other samples. Conclusions : Hence, it is considered that the test methods need flexibility in application for identification and purity test depending on the type of sample.

On-line Screening HPLC-ABTS+ Assay을 이용한 산청목으로부터 Salidroside의 분리 및 생물활성 분석 (Isolation and Bioactivity Analysis of Salidroside from Acer tegmentosum using On-line Screening HPLC-ABTS+ Assay)

  • 이광진;송나영;마진열
    • KSBB Journal
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    • 제29권2호
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    • pp.124-130
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    • 2014
  • Acer tegmentosum was a traditional Korean herbal medicine showing various pharmacological activities. In this work, A. tegmentosum were extracted with boiling water and then successively partitioned with dichloromethane, ethyl acetate, n-butyl alcohol (n-BuOH), and water. Salidoside, the target compound, was purified in n-BuOH phase using a chromatography method. For the analysis of salidoside, TLC and LC-MS were used as well as on-line screening $HPLC-ABTS^+$ assay with three different wavelength of 254, 280, and 320 nm. An amount of 1.34 g of salidoside were obtained in n-BuOH phase fromAcer tegmentosum was a traditional Korean herbal medicine showing various pharmacological activities. In this work, A. tegmentosum were extracted with boiling water and then successively partitioned with dichloromethane, ethyl acetate, n-butyl alcohol (n-BuOH), and water. Salidoside, the target compound, was purified in n-BuOH phase using a chromatography method. For the analysis of salidoside, TLC and LC-MS were used as well as online screening $HPLC-ABTS^+$ assay with three different wavelength of 254, 280, and 320 nm. An amount of 1.34 g of salidoside were obtained in n-BuOH phase from 3 kg of dry biomass. The on-line screening $HPLC-ABTS^+$ assay is rapid and efficient tool to search bioactivity from A. tegmentosum. 3 kg of dry biomass. The on-line screening $HPLC-ABTS^+$ assay is rapid and efficient tool to search bioactivity from A. tegmentosum.

Bioconversion of Ginsenosides from Red Ginseng Extract Using Candida allociferrii JNO301 Isolated from Meju

  • Lee, Sulhee;Lee, Yong-Hun;Park, Jung-Min;Bai, Dong-Hoon;Jang, Jae Kweon;Park, Young-Seo
    • Mycobiology
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    • 제42권4호
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    • pp.368-375
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    • 2014
  • Red ginseng (Panax ginseng), a Korean traditional medicinal plant, contains a variety of ginsenosides as major functional components. It is necessary to remove sugar moieties from the major ginsenosides, which have a lower absorption rate into the intestine, to obtain the aglycone form. To screen for microorganisms showing bioconversion activity for ginsenosides from red ginseng, 50 yeast strains were isolated from Korean traditional meju (a starter culture made with soybean and wheat flour for the fermentation of soybean paste). Twenty strains in which a black zone formed around the colony on esculin-yeast malt agar plates were screened first, and among them 5 strains having high ${\beta}$-glucosidase activity on p-nitrophenyl-${\beta}$-D-glucopyranoside as a substrate were then selected. Strain JNO301 was finally chosen as a bioconverting strain in this study on the basis of its high bioconversion activity for red ginseng extract as determined by thin-layer chromatography (TLC) analysis. The selected bioconversion strain was identified as Candida allociferrii JNO301 based on the nucleotide sequence analysis of the 18S rRNA gene. The optimum temperature and pH for the cell growth were $20{\sim}30^{\circ}C$ and pH 5~8, respectively. TLC analysis confirmed that C. allociferrii JNO301 converted ginsenoside Rb1 into Rd and then into F2, Rb2 into compound O, Rc into compound Mc1, and Rf into Rh1. Quantitative analysis using high-performance liquid chromatography showed that bioconversion of red ginseng extract resulted in an increase of 2.73, 3.32, 33.87, 16, and 5.48 fold in the concentration of Rd, F2, compound O, compound Mc1, and Rh1, respectively.

미강의 약리성분 감마-오리자놀의 정량 (Quantitative Analysis of ${\gamma}-oryzanol$ in Rice Bran)

  • 곽태순;박희준
    • 한국약용작물학회지
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    • 제5권2호
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    • pp.113-118
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    • 1997
  • 미강에 함유된 약리성분인 ${\gamma}-oryzanol$ 함량을 검정하여 용도 다양화 연구의 기초 자료를 제공코자 시험을 수행한 바 다음과 같은 결과를 얻었다. Soxhlet 추출장치에서 얻은 미강유에서 유리 sterol과 ferulic acid ester가 분리되었다. 유리 sterol은 GC-MS에 의하여 campesterol, ${\beta}-sitosterol$ 및 stigmasterol로 구성되어 있음을 알 수 있었다. ferulic acid ester는 알칼리 가수분해에 의하여 얻어지는 검화분해물을 분리용 TLC로 분리하여 triterpene과 sterol을 얻었다. sterol은 GC-MS 측정으로 유리 sterol과 같은 조성임을 알았으며 triterpene은 cycloartanol, cycloartenol, 24-methylenecycloartanol 및 미지의 triterpene로 구성되었다. 미강유나 pitch 중 ferulic acid ester의 흡광도를 기준으로 ${\gamma}-oryzanol$의 함량을 평가한다면 큰 오차는 없으리라 생각된다.

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항생제 대체 천연물질을 위한 아로니아 주정 추출물 개발에 있어 다양한 Leuconostoc mesenteroides 균주를 이용한 발효가 페놀계 화합물 및 항산화활성 변화에 미치는 영향 (Alteration in Phenolic Compounds and Antioxidant Activities of Aronia melanocarpa Ethanol Extracts following Fermentation Using Different Strains of Leuconostoc mesenteroides to Develop Natural Antibiotic Alternative)

  • 황주환;강주희;이기환;이재훈;이상무;김남형;김주영;김은중
    • 한국유기농업학회지
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    • 제22권4호
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    • pp.825-839
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    • 2014
  • Antioxidant activity is important for reducing oxidative stress that causes various metabolic disorders. Metabolic disorders are highly related to loss of productivity in livestock. Therefore, development of effective antioxidant compounds originating from plants is important for organic agriculture. Phenolic compounds in edible plants are regarded as major components relevant to antioxidant activity. The present study investigated the changes in antioxidant activity and phenolic compound profiles of Aronia (Aronia meloncarpa) by fermentation using different strains of Leuconostoc mesenteroides. A total of 5 strains of L. mesenteroides were used as starter cultures and their ${\beta}$-glucosidase activities were measured. A total of 6 experiment runs were prepared, one for control (uninoculated) and the others (inoculated) for treatments. For biological activity, antioxidant and antibacterial activities were measured. For phenolic compound profiling, TLC and HPLC analysis were performed. The strains of KACC12313 and KACC12315 showed greater enzyme activity than others. Treatment with KCCM35046 showed strong and broad antibacterial activity against to Listeria monocytogenes. Treatments with KCCM35046 and KACC12315 showed the highest total polyphenol content. The highest antioxidant activity was found in KACC12315 treatment. No remarkable alteration was found in thin layer chromatography (TLC) analysis. In phenolic compound profiling analysis, KCCM35046 showed notable alteration in compound area ratio compared to others and also showed the highest caffeic acid content. In chlorogenic acid, treatments with KCCM35046 and KACC12315 showed great content than others. Treatment with KACC12315 showed the greatest content of trans-ferulic acid. As a result of relative performance indexing analysis, L. mesenteroides KCCM35046 and KACC12315 were selected as the best strain for the fermentation of Aronia.

쑥의 잎과 기내 배양세포로부터 약용물질의 탐색 (Investigation of Medicinal Substances from in vitro Cultured Cells and Leaves of Artemisia princeps var. Orientalis)

  • 신동호;인준교;유상렬;최관삼
    • 한국약용작물학회지
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    • 제13권3호
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    • pp.69-76
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    • 2005
  • 쑥의 어린 잎은 민간요법에서 복통이나 구토, 월경불순 등의 치료에 사용되어 온 귀중한 약재로 최근에는 항 말라리아 효과를 나타내는 artemisinin 성분이 주목을 받고 있다. 국내에 자생하는 야생 쑥에 대한 자원식물로써의 가능성을 제시하기 위하여 야생쑥과 이로부터 유도한 기내배양세포로부터 artemisinin의 생합성 여부를 조사하였다 그 결과 그 동안 개똥쑥에서만 존재하는 것으로 알려진 artemisinin이 국내 야생 쑥에서도 생합성되는 것을 확인하였다. Artemisinin 및 유용한 이차대사산물의 기내 배양을 통한 대량생산의 가능성을 조사하기 위해 쑥의 어린 식물체로부터 조직 및 현탁 세포배양계를 확립하였다. Callus와 현탁배양 세포의 유도 및 성장은 $0,2\;mg/{\ell}$ 2,4-Df와 $0.1\;mg/{\ell}$ BAP가 처리되고 2% sucrose를 첨가한 MS배지에서 가장 좋게 나타났다. 이들 callus와 현탁배양세포 그리고 식물체에 존재하는 다양한 대사물질들을 비교하기 위해 TLC분석을 실시한 결과, 기내배양세포에서 특이적인 페놀 화합물, 터펜화합물, 아미노산 등이 존재하고 있는 것을 확인하였다. 이러한 결과는 쪽의 기내 배양계를 통해 다양한 유용물질의 대량생산에 대한 가능성을 제시하고 있다.

Fomitopsis pinicola 균사체배양액의 Helicobacter pylori에 대한 저해물질의 분리 및 특성 (Isolation and Characterization of Inhibition Helicobacter pylori from Culture Media of Fomitopsis pinicola)

  • 이재경;최성우;황유현;박희국;윤정원
    • KSBB Journal
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    • 제21권6호
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    • pp.422-427
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    • 2006
  • Helicobacter pylori에 대하여 항균효과가 가장 높은 Fomitopsis pinicola를 동정하고 저해물질의 성질에 관한 연구를 수행한 결과 다음과 같은 결론이 얻어졌다. H. pylori에 대한 항균력이 가장크게 나타난 네팔에서 채취한 F. pinicola의 동정결과는 F. pinicola AY854083로 밝혀졌다. F. pinicola의 균사체는 액상배양을 시작한 후 5일이 경과하면서 H. pylori에 대한 항균력이 나타났으며 8일 이후부터 가장 높았다. 그러나 균사체 추출물에서는 항균력이 나타나지 않았다. F. pinicola 균사체 8일 배양액의 H. pylori에 대한 최소억제 농도는 $0.25\;mg/m{\ell}$ 이었고, 배양액의 낮은 pH (pH 2.0)가 H. pylori의 생육억제에 영향을 주지만 중화를 하여도 H. pylori에 대한 항균력은 유지되었다. F. pinicola 균사체 8일 배양액을 DEAE-sephadex A-25 LC로 분리하여 Fp-P1, Fp-P2 및 Fp-P3를 얻었으며 H. pylori에 대한 항균력은 Fp-P1에서만 나타났다. Fp-P1을 thin layer chromatography로 분리하였으며 H. pylori에 대한 항균력은 $R_{f}$ 값이 0.67인 Fp-T3에서만 나타났다. F. pinicola 균사체 8일 배양액, Fp-P1, Fp-T3를 HPLC의 Waters symmetry $300\;C_{18}\;5\;{\mu}m$ column ($3.9{\times}150\;mm$)으로 분리한 결과 Fp-T3에서 단일 peak만 남았으며 이것이 H. pylori에 대한 항균력을 확인하였다. H. pylori에 대한 항균력을 나타내는 F. pinicola 균사체 배양액에서 분리 정제한 물질은 BioLC 분석과 TLC 발색결과로써 아미노기를 포함한 당으로 사료된다.

Bacillus licheniformis로부터 생산된 ${\alpha}-Galactosidase$의 가수분해 활성 (Hydrolysis Activity of ${\alpha}-Galactosidase$ from Bacillus licheniformis)

  • 김현숙;이경섭;소재호;윤기홍
    • 미생물학회지
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    • 제40권4호
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    • pp.328-333
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    • 2004
  • [ ${\alpha}$ ]-갈락토올리고 당인 melibiose, raffinose와 stachyose의 ${\alpha}-1,6$으로 결합된 D-galactosyl 잔기를 완전히 가수분해하는 것으로 확인된 Bacillus licheniformis YB-42의 ${\alpha}-galactosidase$는 사멸기에 도달하였을 때 배양상등액에서 최대활성을 보였다. ${\alpha}$-갈락토올리고 당의 가수분해 정도를 TLC와 환원당 생성량으로 분석한 결과, ${\alpha}-galactosidase$는 melibiose, raffinose, stachyose 순서로 가수분해 활성이 높았다. 반응산물인 당을 첨가하여 반응하였을 때 첨가 된 반응산물에 따라 가수분해 활성의 저해정도가 다르게 나타났으며, galactose에 의한 저해도가 가장 높았다. 첨가된 당의 농도 (20 mM)가 기질과 동일할 때는 가수분해 활성의 저해도가 미미하였으며 5배 농도로 첨가하였을 때도 가수분해 활성의 저해정도가 높지 않았다. 한편 소량의 효소로melibiose를 가수분해 하였을 때 반응초기에 TLC 상에서 기질보다 이동도가 낮은 물질이 생성되었으며, 이로보아 B. licheniformis YB-42의 ${\alpha}-galactosidase$는 당 전이활성을 갖는 것으로 여겨진다. 또한 대두분 추출액을 ${\alpha}-galactosidase$로 처리한 후 최종 반응산물을 분석한 결과, 대두분에 존재하는 raffinose와 stachyose가 완전히 가수분해 되었다.

Bacillus sp. DYL130 균주의 Biosurfactant의 정제 및 특성 (Purification and Characterization of Biosurfactant from Bacillus sp. DYL130)

  • 박인혜;김선희;이상철;하순옥;이용석;유아름;김근기;최용락
    • 한국해양바이오학회지
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    • 제1권4호
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    • pp.268-274
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    • 2006
  • 해양 원유 오염원의 제거 및 항진균 활성을 가진 균주를 분리하기 위해 1% crude oil을 탄소원으로 이용하여 생육하는 수십 종의 균주를 분리하였다. 분리된 균주 중 biosurfactant를 생성하는 균주를 1% tributyrin에서 투명환 생성 유무를 통해 선별되었으며, 이를 Bacillus sp. DYL130으로 명명하였다. Bacillus sp. DYL130의 표면장력은 최저 28 mN/m까지 감소되었다. 이 균주로부터 biosurfactant를 정제하기 위해 배양 상등액을 친화성 크로마토그래피와 TLC를 이용하여 정제된 biosurfactant를 얻었다. TLC 결과 0.78정도의 Rf값을 확인하였다. 정제된 biosurfactant의 CMC 값은 35 mg/l인 것으로 나타났으며, 유화활성과 안정성은 soybean oil을 기질로 사용하였을 경우 최대인 것으로 나타났다. Botrytis cineria에 대한 길항작용도 우수한 것으로 보인다.

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Development of Standard Operating Procedures (SOPs), Standardization, TLC and HPTLC Fingerprinting of a Polyherbal Unani Formulation

  • Naaz, Arjumand;Viquar, Uzma;Naikodi, Mohammad Abdul Rasheed;Siddiqui, Javed Inam;Zakir, Mohammad;Kazmi, Munawwar Husain;Minhajuddin, Ahmed
    • 셀메드
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    • 제11권4호
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    • pp.21.1-21.9
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    • 2021
  • Background: Unani System of Medicine (USM) has its origin to Greece. To ensure and develop the quality, authenticity of Unani drugs, standardization on modern analytical parameter is essential requirement for drugs. Objectives: The aimed of the present study was to develop a standard profile of "Qurṣ-e-Mafasil" by systematic study through authenticated ingredients, pharmacognostic identification followed by physicochemical, TLC, HPTLC fingerprinting analysis as per standard protocol. Material and Methods: In this study three batches of "Qurṣ-e-Mafasil" QM were prepared by standard method as per UPI had been followed by organoleptic properties of formulation such as appearance, color, odor, taste. Powder Microscopy and physicochemical studies were carried out such as Uniformity of weight, Friability, Disintegration time, hardness, LOD, ash vales and extractive values in like aqueous, alcohol & hexane. Further qualitative tests such as Thin-Layer Chromatography (TLC), and High-Performance Thin Layer Chromatography (HPTLC) studies were also carried out to develop fingerprint pattern of the alcoholic solvent extract of QM. Phytochemical screening was carried out in different solvent extracts such as alcoholic, aqueous and chloroform extracts to detect the presence phytoconstituents in the formulation QM. Heavy metals, Microbial Load Contamination and pesticidal residues were also determined. Results: Qurṣ-e-Mafasil showed tablet-like appearance, light brown colour, mild pungent odour and acrid taste. Uniformity of weight (mg), friability (rpm), and hardness (kg/cm) and disintegration time was ranged between (500 to 503), (0.0340 to 0.038), (8.40 to 8.67) and (4-5 minutes) respectively for the three batches. Loss in weight on drying at 105℃ was ranged between (8.3425 to 8.7346). Extracted values were calculated in distilled water ranged between (30.9091 to 31.4358), hexane (1.1419 to 1.4281), and alcohol (3.3352 to 3.3962). The ash values recorded were ranged between (3.7336 to 3.8378), and acid insoluble ash (0.5859 to 0.6112).