http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Kyung Min Park,손종근,Ying Li,Bora Kim,Haiyan Zhang,Kyong Hwangbo,Dong Gen Piao,Mei Juan Chi,우미희,최재수,이제현,문동철,장현욱,김재룡 대한약학회 2012 Archives of Pharmacal Research Vol.35 No.12
Two stable high-performance liquid chromatography (HPLC) methods were developed that could quantitatively analyze 10 major marker compounds of Artemisia capillaris Thunb and could also distinguish among ‘Injinho’ and ‘Myeon-injin’ and ‘Haninjin’ – A. capillaris collected in autumn,A. capillaris collected in spring and A. iwayomogi, which can be misused as ‘Injinho’ in Korean herbal drug markets. The first HPLC method was a reversed-phase chromatography using a C18 column with an isocratic solvent system of phosphoric acid (0.05%) and acetonitrile at the flow rate of 1.0 mL/min, ultraviolet (UV) detection wavelength at 254 nm and column temperature at 40oC. Calibration and quantitation were made by using acetaminophen as an internal standard (I.S-A) and chlorogenic acid (1) was determined within 20 min. The second HPLC method was a reversed-phase chromatography using a C18 column with a gradient solvent system of phosphate buffer (0.015 M, pH 6) and acetonitrile at the flow rate of 1.0 mL/min, UV detection wavelength at 254 nm and column temperature at 40oC. Calibration and quantitation were made by using ethylparaben as an internal standard (I.S-B) and 3,5-di-O-caffeoylquinic acid (2), 3,4-di-O-caffeoylquinic acid (3), 4,5-di-O-caffeoylquinic acid (4), hyperoside (5), isoquercitrin (6), isorhamnetin 3-O-robinobioside (7), isorhamnetin-3-O-galactoside (8), isorhamnetin-3-O-glucoside (9) and scoparone (10) were determined within 60 min. Pattern recognition analysis of data from the 60 samples classified them clearly into three groups. These assay methods could be applied for QA/QC of A. capillaris and Artemisia iwayomogi.
( Kyung Min Park ),( Ying Li ),( Bora Kim ),( Haiyan Zhang ),( Kyong Hwangbo ),( Dong Gen Piao ),( Mei Juan Chi ),( Mi Hee Woo ),( Jae Sue Choi ),( Je Hyun Lee ),( Dong Cheul Moon ),( Hyeun Wook Chang 영남대학교 약품개발연구소 2013 영남대학교 약품개발연구소 연구업적집 Vol.23 No.0
Two stable high-performance liquid chromatography (HPLC) methods were developed that could quantitatively analyze 10 major marker compounds of Artemisia capillaris Thunb and could also distinguish among `Injinho` and `Myeon-injin` and `Haninjin`--A. capillaris collected in autumn, A. capillaris collected in spring and A. iwayomogi, which can be misused as `Injinho` in Korean herbal drug markets. The first HPLC method was a reversed-phase chromatography using a C18 column with an isocratic solvent system of phosphoric acid (0.05%) and acetonitrile at the flow rate of 1.0 mL/min, ultraviolet (UV) detection wavelength at 254 nm and column temperature at 40°C. Calibration andquantitation were made by using acetaminophen as an internal standard (I.S-A) and chlorogenic acid (1) was determined within 20 min. The second HPLC method was a reversed-phase chromatography using a C18 column with a gradient solvent system of phosphate buffer (0.015 M, pH 6) and acetonitrile at the flow rate of 1.0 mL/min, UV detection wavelength at 254 nm and column temperature at 40°C. Calibration and quantitation were made by using ethylparaben as an internal standard (I.S-B) and 3,5-di-O-caffeoylquinic acid (2), 3,4-di-O-caffeoylquinic acid (3), 4,5-di-O-caffeoylquinic acid (4), hyperoside (5), isoquercitrin (6), isorhamnetin 3-O-robinobioside (7), isorhamnetin-3-O-galactoside (8), isorhamnetin-3-O-glucoside (9) and scoparone (10) were determined within 60 min. Pattern recognitionanalysis of data from the 60 samples classified them clearly into three groups. These assay methods could be applied for QA/QC of A. capillaris and Artemisia iwayomogi.
HwangBo, Kwon,Son, Su-Hyun,Lee, Jong-Suk,Min, Sung-Ran,Ko, Suk-Min,Liu, Jang-R.,Choi, Dong-Su,Jeong, Won-Joong The Korean Society of Plant Biotechnology 2010 Plant biotechnology reports Vol.4 No.1
A DNA extraction method using Chelex 100 is widely used for bacteria, Chlamydomonas, and animal cell lines, but only rarely for plant materials due to the need for additional time-consuming and tedious steps. We have modified the Chelex 100 protocol and successfully developed a rapid and simple method of DNA extraction for efficient PCR-based detection of transgenes from a variety of transgenic plant and algal species. Our protocol consists of homogenizing plant tissue with a pestle, boiling the homogenized tissue in a microfuge tube with 5% Chelex 100 for 5 min, and centrifuging the boiled mixture. The supernatant, which is used for PCR analysis, was able to successfully amplify transgenes in transgenic tobacco, tomato, potato, Arabidopsis, rice, strawberry, Spirodela polyrhiza, Chlamydomonas, and Porphyra tenera. The entire DNA extraction procedure requires <15 min and is therefore comparable to that used for bacteria, Chlamydomonas, and animal cell lines.
Hwangbo, Min,Jung, Ji Yun,Ki, Sung Hwan,Park, Sang Mi,Jegal, Kyung Hwan,Cho, Il Je,Lee, Ju-Hee,Kang, Seung Ho,Park, Sun-Dong,Ku, Sae Kwang,Kim, Sang Chan,Zhao, Rong Jie,Jee, Seon Young,Kim, Young Woo Hindawi Publishing Corporation 2014 Evidence-based Complementary and Alternative Medic Vol.2014 No.-
<P>Since antiquity, medical herbs have been prescribed for both treatment and preventative purposes. Herbal formulas are used to reduce toxicity as well as increase efficacy in traditional Korean medicine. <I>U-bang-haequi tang</I> (UBT) is a herbal prescription containing <I>Arctii fructus</I> and <I>Forsythia suspensa</I> as its main components and has treated many human diseases in traditional Korean medicine. This research investigated the effects of UBT against an acute phase of inflammation. For this, we measured induction of nitric oxide (NO) and related proteins in macrophage cell line stimulated by lipopolysaccharide (LPS). Further, paw swelling was measured in carrageenan-treated rats. Carrageenan significantly induced activation of inflammatory cells and increases in paw volume, whereas oral administration of 0.3 or 1 g/kg/day of UBT inhibited the acute inflammatory response. In RAW264.7 cells, UBT inhibited mRNA and protein expression levels of iNOS. UBT treatment also blocked elevation of NO production, nuclear translocation of NF-<I>κ</I>B, phosphorylation of I<I>κ</I>-B<I>α</I> induced by LPS. Moreover, UBT treatment significantly blocked the phosphorylation of p38 and c-Jun NH2-terminal kinases by LPS. In conclusion, UBT prevented both acute inflammation in rats as well as LPS-induced NO and iNOS gene expression through inhibition of NF-<I>κ</I>B in RAW264.7 cells.</P>
Polymerization Shrinkage and Mass Change of Dental Restorative Materials
Min Hwangbo(황보민),Ri-Mo Ku(구이모),Tae-Sung Jeong(정태성),Shin Kim(김신),Hyung-Il Kim(김형일),Yong-Hoon Kwon(권용훈) 대한치과재료학회 2012 대한치과재료학회지 Vol.39 No.2
본 연구는 치과용 수복재료인 복합레진의 중합수축과 수분흡수 및 용해에 따른 무게변화를 평가한 것이다. 이를 위하여 각기 다르게 분류되는 11종의 복합레진을 택하였다. 이들 제품들의 광조사 중과 후의 중합수축을 130초 동안 측정하였다. ISO 4049 규정에 따라 시료를 제작하고 시료를 증류수에 7일간 보관하면서 수분흡수와 용해도를 각각 측정하였다. 그 결과 2 ㎜ 두께의 시료에서 12.2-38.8 ㎛의 중합수축이 발생하였다. 특히 제품 중에서 flowable 레진 (Admira flow와 Grandio flow)들이 가장 큰 수축값을 보였다. 수분흡수는 9.8-36.4 ㎍/㎣를 보였는데 이들 값은 ISO 4049가 규정하는 최고 수분흡수 값인 40 ㎍/mm3 보다는 낮았다. 용해도는 -1.4-7.7 ㎍/㎣을 기록하였다. Filtek P60의 경우 다른 제품들과 달리 용해도가 증가 (-)하는 즉 수분흡수를 통하여 시료의 무게가 증가하는 특성을 보였다.
오미자와 산수유 추출물이 dihydrotestosterone가 처리된 LNCaP 인간 전립선 암세포의 증식 및 전립선 비대 유발 인자 발현에 미치는 영향
김민영(Min Yeung Kim),지선영(Seon Yeong Ji),황보현(Hyun Hwangbo),이혜숙(Hyesook Lee),김태희(Tae Hee Kim),윤선혜(Seonhye Yoon),김현진(Hyun Jin Kim),김성연(Sung Yeon Kim),김태중(Tae Jung Kim),김민지(Min Ji Kim),정하은(Ha Eun Jung),최영현( 한국생명과학회 2021 생명과학회지 Vol.31 No.10
오미자와 산수유는 한국을 포함한 동아시아 지역에서 다양한 질병의 예방 및 치료에 오랫동안 사용되어 왔다. 최근에 이들 추출물에 의한 양성 전립선 비대증(BPH)의 발병 및 진행을 억제할 수 있다는 가능성에 대한 보고가 있었지만 관련 기전에 대한 연구는 여전히 부족한 실정이다. 본 연구에서는 LNCaP 전립선 세포를 사용하여 DHT 처리에 의한 in vitro BPH 모델에서 오미자 및 산수유 추출물에 의한 BPH의 개선 가능성을 조사하였다. 본 연구의 결과에 의하면, 오미자와 산수유의 열수 및 에탄올 추출물은 DHT 처리에 의해 LNCaP 세포의 증식을 유의적으로 억제하였으며, DHT로 유도된 BPH 바이오 마커와 성장인자의 발현을 현저히 감소시켰다. 그들은 또한 세포사멸 관련 인자의 발현을 조절하였고, DHT 매개 산화적 스트레스를 유의적으로 감소시켰으며, BPH 발병에 관여하는 주요 인자에 대한 보호 효과는 열수 추출물보다 에탄올 추출물 처리군에서 더 효과적이었다. 또한, BPH에 대한 보호 효과는 오미자와 산수유의 에탄올 추출물 단독 처리군보다 1:1 복합 혼합물 처리군에서 더 높았으며, 60% 에탄올 추출물이 40% 에탄올 추출물보다 더 높은 개선 효과를 보였다. 따라서 본 연구 결과는 오미자와 산수유 추출물이 항산화 활성과 연관된 androgen 신호 전달 경로의 억제를 통해 전립선 세포의 과다 증식을 방지함으로써 BPH 개선에 관여할 수 있음을 의미한다. 따라서 오미자와 산수유 추출물은 BPH의 임상 치료에 유용할 수 있으며, 이 두 추출물의 조합은 BPH 개선에 상승 효과를 낼 수 있을 것이다. Schisandrae Fructus (SF) and Corni Fructus (CF) have been used for a long time for the prevention and treatment of various diseases. Although reports have highlighted the possibility of inhibiting the onset and progression of benign prostatic hyperplasia (BPH), studies on related mechanisms are still lacking. In this study, we investigated the potential of SF and CF in improving BPH by using a dihydrotestosterone (DHT)-induced in vitro BPH model using LNCaP prostate carcinoma cells. According to our results, water and ethanol extracts of SF and CF significantly inhibited the proliferation of LNCaP cells by DHT treatment and markedly downregulated the expression of DHT-induced BPH biomarkers and growth factors. They also regulated the expression of apoptosis regulatory factors and significantly reduced DHT-mediated oxidative stress. In addition, the protective effect on major factors involved in the pathogenesis of BPH was more effective in the ethanol extract treatment group than in the water extract group. Furthermore, the improvement effect on BPH was higher in the 1:1 combined treatment group than in the ethanol extract alone treatment group of SF and CF, and 60% ethanol extracts showed a better effect than 40% ethanol extracts. Therefore, our findings demonstrate that SF and CF can protect against BPH by preventing the hyperproliferation of prostate cells through the inhibition of the androgen signaling pathway, which was correlated with their antioxidant activities. Therefore, SF and CF extracts may be useful in the clinical treatment of BPH, and the combination of these two extracts can be synergistic.