• 한국식품과학회지
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• 제27권2호
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• pp.210-215
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• 1995

발효주를 제조하고 증류하여 알코올 농도가 25, 35 및 45%로 조절된 침출액을 만들고 여기에 사삼, 길경, 작약, 당귀, 황기, 천궁 등의 약초를 넣어 75일 동안 침출시키면서 침출기간에 따른 알코올 농도, pH, 흡광도 그리고 작약의 peoniflorin과 당귀의 decursin을 분석하였으며, 최종 침출주의 품질을 관능검사로 평가하였다. 알코올 농도는 침출 15일째 빠르게 감소하였지만 pH는 증가하였으며, 그 이후에는 모두 완만한 감소를 보였다. 알코올 농도는 약초의 종류와 침출액의 알코올 농도에 따라 많은 영향을 받았는데 당귀와 침출액의 알코올 농도가 낮을 때 그 영향이 크게 나타났다. 작약과 당귀의 지표성분인 peoniflorin과 decursin은 최고 농도까지 증가하였다가 감소하였다. 관능검사 결과 전체적인 품질은 알코올 농도 45%로 침출시킨 침출주가 가장 좋았으며, 사삼, 작약, 천궁, 황기 순이었다.

• 한국식품조리과학회지
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• 제16권5호
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• pp.445-452
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• 2000

우리나라 야산에서 손쉽게 구할 수 있는 구황식물인 백작약을 건조시켜 분쇄한 후 methanol과 여러용매로 추출하여 식품 부패 미생물의 증식 억제 효과를 검색하고 그 향균물질을 분석하여 다음과 같은 결과를 얻었다. 백작약의 methanol 추출물은 1500$\mu\textrm{g}$/ml 농도에서 B. subtilis, S. aureus, V parahaemolyticus의 증식을 100% 억제하였으며 L. monocytogenes와 E. coli도 같은 농도에서 각각 65.93%와 83.27%의 억제 효과를 보였다. 백작약의 ethylacetate 분획 추출물은 낮은 농도인 1000$\mu\textrm{g}$/disc의 농도에서 식품 부패 미생물 5종 모두에 대하여 clear zone을 형성하여 항균력을 나타내었다. 특히 S. aureus, B. subtilis, V. parahaemolyticus, E. coli균에 대해서는 낮은 농도인 500$\mu\textrm{g}$/disc에서 clear zone을 나타내었으며 또한 2,000$\mu\textrm{g}$/disc 농도에서 L. monocytogenes, E. coli 및 V. parahaemolyticus는 각각 13, 15, 13m의 clear zone을 형성하였다. 백작약의 Ethylacetate 추출물을 silica gel colum chromatograhpy (7cm$\times$1.2cm한 후 thin layer chromatography(TLC)를 실시하여 항균성 실험을 한 결과 B. subtilis의 경우 1000$\mu\textrm{g}$/disc 농도에서 2nd fra. 3이 17mm, L. monocytogenes는 250$\mu\textrm{g}$/disc 농도에서 21mm를, S. aureus는 13mm의 clear zone을 형성하여 백작약의 methanol 추출물로부터 간 용매별로 계통 분획하여 분리한 ethylacetate 분획으로부터silica gel column chromatograpy와 TLC를 하여 항균성을 보인 2rd fra. 3의 성분을 알아보기 위히여 HPLC로 단일분리하여 얻은 peak III에 대한 compound를 GC-MS로 분석한 결과 peak III에서는 Cetyl alcohol이 있는 것으로 추정되었다.

• 대한약침학회지
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• 제17권4호
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• pp.61-65
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• 2014

Objectives: In this study, we investigated the oral toxicity of Gami-Jakyak Gamcho buja Decoction (Mecasin) to develop safe treatments. Methods: All experiments were conducted at the Medvill, an institution authorized to perform non-clinical studies, under the Good Laboratory Practice (GLP) regulations. In order to investigate the oral toxicity of Mecasin, we administered Mecasin orally to rats. Sprague-Dawley rats were divided into four groups of five male and five female animals per group: group 1 being the control group and groups 2, 3, and 4 being the experimental groups. Doses of Mecasin, 500 mg/kg, 1,000 mg/kg and 2,000 mg/kg, were administered to the experimental groups, and a dose of normal saline solution, 10 mL/kg, was administered to the control group. We examined the survival rate, weight, clinical signs, and gross findings. This study was conducted under the approval of the Institutional Animal Ethics Committee. Results: No deaths or abnormalities occurred in any of the four groups. Although slight decreases in the weights of some female rats were noted on the third day, no significant changes in weights or gross findings between the control group and the experimental groups were observed. To check for abnormalities in organs, we used microscopy to examine representative histological sections of each specified organ; the results showed no significant differences in any of the organs. Conclusion: The results showed that administration of 500 - 2,000 mg/kg of Mecasin did not cause any changes in weight or in the results of necropsy examinations. It also did not result in any mortalities. The above findings suggest that treatment with Mecasin is relatively safe. Further studies on this subject are needed to yield more concrete evidence.

• Applied Biological Chemistry
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• 제39권5호
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• pp.368-373
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• 1996

6종의 약재(사삼, 길경, 작약, 당귀, 황기, 천궁)를 첨가하여 발호시킨 발효액을 증류하여 얻은 발효약용 증류주와 증류장치에 약재를 충전하고 약재를 첨가하지 않은 발효주(대조구)를 증류하여 얻은 약재충전 증류주의 증류 및 품질특성을 조사하였다. 발효약용 증류주와 대조구의 pH는 증류가 진행되면서 감소하였으며, 약재충전 증류주는 증류초기($1{\sim}4$분액)에 $0.05{\sim}0.97$의 완만한 증가를 보이다가 그 이후 부터 $0.92{\sim}0.98$의 많은 감소를 보였다. 평균 pH는 작약이 5.70으로 가장 높았으며, 길경이 4.37로 가장 낮았다. 약재충전 증류주의 흡광도는 $1{\sim}4$분액에서 $0.60{\sim}1.59$의 많은 감소를 보였고 그 이후 부터는 $0.19{\sim}0.54$의 완만한 감소를 보였다. 분액별 알코올농도와 증류속도는 증류가 진행되면서 감소하였으며, 대조구 보다 낮고 느렸다. 증류속도는 약재의 종류와 원주의 알코올 농도에 따라 다르게 나타났으며, 평균 증류속도는 당귀 및 대조구가 $0.102\;m{\ell}/sec$로 가장 빨랐고 길경이 $0.073\;m{\ell}/sec$로 가장 느렸다. 약재충전 증류주의 지표성분중 작약의 peaoniflorin은 5분약에서 293 mg%로 가장 많이 추출되었으며, 당귀의 decrusin은 1분액에서 3514 mg%로 가장 많이 추출되었다. 약재충전 증류주의 경우 약재의 지표성분중 작약은 41.3% 그리고 당귀는 20.5%가 추출되었다. 관능검사 펄과 품질은 황기주가 가장 좋았으며, 그 다음으로는 당귀, 길경주 순이었다.

• 약학회지
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• 제17권1호
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• pp.1-8
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• 1973

The pharmacological activities of paeoniflorin abtained from paeony roots, F$_M$100 from glycyrrhiza roots, crude saikosides from bupleurum roots, crude platycodin from platycodon roots, and bothj of ginsenoside Rb and ginsenoside Rg series from ginseng roots were investigated. Paeoniflorin, F$_M$ 100, crude saikosides, and crude platycodin exhibited sedative antipyretic, anlagesic and anti-ulcerative actions. In addition, crude saidosides and crude platycodin showed antitusaive and the potent anti-inflammatory action. An expectorant action was also observed with crude platycodin. These results coincided with the clinical applications of the aforementioned oriental medicinals. It also should be noted that crude saikosides nad crude platycodin are preferable to the other steroidal nad nonsteroidal drugs as an anti-inflammatory agent, because the drugs aggravate the digestive ulcer. In ginseng, G No3. and GNS frctions out of ginsenoside Rb series hsowed stimulant and antifatigue actions. The synergistic effects identified between paeoniflorin and F$_M$ 100 on the various pharmacological activities, have verified the reasonability of combined uses of two oriental drugs as Jakyak Gaqmcho-Tang.

• 혜화의학회지
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• 제10권1호
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• pp.201-220
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• 2001

1. The frequency of source of prescriptions is dangyesimbub(丹溪心法), euihakibmun(醫學入門), dongwonsibseo(東垣十書), goguemeuibang(古今醫方) in sequence. 2. The classification of prescriptions by efficacy is chungyeulsahoayak(淸熱瀉火藥), boumyak(補陰藥), hoalhyulguayak(活血祛瘀藥), igiyak(理氣藥), chunghwayuldamyak(淸化熱痰藥), bogiyak(補氣藥), balsanpunghanyak(發散風寒藥), balsanpungyeolak(發散風熱藥), etc. in sequence. 3. The frequency of used medicines is hoangum(黃芩), danguy(當歸), jakyak(芍藥), insam(人蔘), saengjihoang(生地黃), bokryung(茯笭), hoangbaek(黃柏), jimo(知母), makmundong(麥門冬), chija(梔子) etc. in sequence. 4. The sung of used medicines is mainly hangsung(寒性), onsung(溫性), the mi(味) is gomi(苦味), sinmi(辛味), gammi(甘味) in sequence. the gwigyung(歸經) is bigyung(脾經), wigyung(胃經), simgyung(心經), etc, in sequence.

• 대한약침학회지
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• 제18권4호
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• pp.45-50
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• 2015

Objectives: In this study, we investigated the 4-week repeated-dose oral toxicity of gami-jakyak gamcho buja decoction (Mecasin) to develop safe treatments. Methods: In order to investigate the 4-week oral toxicity of Mecasin, we administered Mecasin orally to rats. Sprague-Dawley (SD) rats were divided into four groups of five male and five female animals per group: group 1 being the control group and groups 2, 3, and 4 being the experimental groups. Doses of Mecasin of 500, 1,000, and 2,000 mg/kg of body weight were administered to the experimental groups, and a dose of normal saline solution of 10 mL/kg was administered to the control group. We examined the survival rate, weight, clinical signs, and gross findings for four weeks. This study was conducted under the approval of the Institutional Animal Ethics Committee. Results: No deaths occurred in any of the four groups. No significant changes in weights or food consumption between the control group and the experimental groups were observed. Serum biochemistry revealed that some groups showed significant decrease in inorganic phosphorus (IP) (P < 0.05). During necropsy on the rats, one abnormal macroscopic feature, a slight loss of fur, was observed in the mid dosage (1,000 mg/kg) male group. No abnormalities were observed in any other rats. In histopathological findings, the tubular basophilia and cast of the kidney and extramedullary hematopoiesis of the spleen were found. However, those changes were minimal and had occurred naturally or sporadically. No other organ abnormalities were observed. Conclusion: During this 4-week, repeated, oral toxicity test of Mecasin in SD rats, no toxicity changes due to Mecasin were observed in any of the male or the female rats in the high dosage group. Thus, we suggest that the doses in a 13-week, repeated test should be 0, 500, 1,000, and 2,000 mg/kg respectively.

• Journal of Acupuncture Research
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• 제31권4호
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• pp.29-32
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• 2014

Objectives : Jakyakgamcho decoction is a traditional prescription known to be an effective pain control medication and muscle relaxant. For more localized treatment outcomes achieved in a shorter period of time, Jakyakgamcho decoction was reprocessed into a form of pharmacopuncture. An analysis of Jakyakgamcho decoction pharmacopuncture showed that there was a significant loss of paeoniflorin(Jakyak's index component). This study was designed to investigate ways to minimize this loss. Methods : After making changes to the processing methods of Jakyakgamcho decoction pharmacopuncture, we measured the quantity of paeoniflorin using high performance liquid chromatography(HPLC) for a before-and-after analysis Results : Paeoniflorin loss was observed 15 minutes after sterilization with $Na_2HPO_4$ at $121^{\circ}C$ Conclusions : It was found that paeoniflorin loss did not occur when pH was not controlled for during processing.

• 대한중풍순환신경학회지
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• 제21권1호
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• pp.21-32
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• 2020

■ Objectives 당귀작약산 단회 복용으로 정상인의 총경동맥 탄력도에 미치는 영향을 평가하고자 하였다. ■ Methods 본 연구는 정상인 남성을 대상으로 한 전향적 무작위 대조군 교차시험연구다. 모든 대상자들은 임의로 당귀작약산 복용군과 비복용군인 대조군으로 나누어졌다. 1주일 간격으로 총 2회 방문하며, 첫 번째 방문 시에 당귀작약산 복용군은 당귀작약산 1포(2.5g)과 물을 제공받고, 대조군은 물만 제공받아 복용하였다. 두 번째 방문 시 첫 번째 방문과 반대로 당귀작약산을 복용했던 복용군은 물만 제공받고, 물만 복용했던 피험자들은 당귀작약산 1포와 물을 제공받았다. 물은 100 cc로 매번 동일하게 제공되었다. 모든 대상자들은 복용 직전과 복용 2시간, 4시간 후에 총경동맥 탄력도, 혈압, 총경동맥 내막-중막 두께와 맥박수를 측정하였다. ■ Results 총 20명의 정상인 남성이 모집되었으며, 시간에 따라 당귀작약산 복용 후의 총경동맥 탄력도가 대조군에 비하여 유의하게 상승한 것이 확인되었다. 내막-중막 두께, 혈압 및 맥압, 맥박은 유의한 변화가 나타나지 않았다. ■ Conclusion 당귀작약산의 단회 복용으로 총경동맥 탄력도가 즉시 개선되는 것을 확인하였고, 이로써 당귀작약산이 동맥 경직도 완화 및 탄성의 개선에 영향을 미친다는 것을 알 수 있었다.

• 생약학회지
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• 제54권2호
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• pp.72-79
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• 2023

MRSA is Staphylococcus aureus resistant to β-lactam antibiotics, and is a worldwide infectious disease. Even with the discovery of new antibiotics, resistance develops rapidly, so new alternatives are needed. Jakyakgamcho-tang (JGT) is a combination of Jakyak and Gamcho, and has been mainly used as an antispasmodic and analgesic in oriental medicine. This study was conducted to find out whether there is an effect on MRSA in relation to the anti-inflammatory effect of JGT and the antibacterial effect of Jakyak and Gamcho found in previous studies. In this study, in order to investigate the antibacterial activity of JGT and the combined effect of existing antibiotics, after extracting JGT with 70% EtoH, the disc diffusion method, minimum inhibitory concentration (MIC), drug combination effect (FICI), and time-kill analysis (Time-kill assay), metabolic inhibition, Western blot and qRT-PCR analysis were used to confirm the antibacterial activity mechanism of MRSA of JGT. As a result of the experiment, all of MRSA showed antibacterial activity in JGT's disc diffusion method, and the MIC was 250-1000 ㎍/mL. When existing antibiotics and JGT were combined with drugs, most had synergy or partial synergy. In addition, it was confirmed that the degree of bacterial growth was suppressed over time when simultaneous administration for 24 hours. JGT showed a synergistic effect when administered together with the ATPase-inhibitor DCCD, suggesting that it affected the inhibition of ATPase. As a result of observing the expression of PBP2a, and hla protein in the JGT-treated group and the untreated control group through wstern blot, it was confirmed that the protein expression of the JGT-treated group was significantly suppressed, and the expression levels of mecA, mecR1 and hla genes were also suppressed during JGT treatment. was observed by qRT-PCR. Combining the results of the experiment, it can be seen that JGT has antibacterial activity in MRSA, and when combined with existing antibiotics, the effect was increased compared to treatment with the drug alone. This suggests that JGT can be an alternative to treatment for antibiotic resistance of MRSA.