국내에서 유통되는 한약재 오공(蜈蚣)의 정·위품 유통 현황 파악과 유전자 감별법 개발을 위해 서로 다른 6개 유통사에서 오공으로 판매중인 전형약재를 구매하여 각 약재 포장 단위별 크기, 색깔, 무늬 등 형태적으로 차이가 있는 개체를 분류하여 국내에서 채집된 왕지네 표본 2개체를 포함 총 30개 시료를 대상으로 DNA 바코드 분석을 실시하였다. 확보한 미토콘드리아 COI 염기서열 정보와 기 등재된 NCBI GenBank 염기서열 정보를 이용하여 계통 분석을 실시한 결과, 28개 약재 시료 중 국산 및 중국산 전형약재 유통품 13 개체는 모두 대한민국약전외한약 (생약)규격집에 정품 기원종으로 수재된 Scolopendra subspinipes mutilans로 확인되었으며, 이들은 국내 채집 왕지네 개체들과 함께 하나의 단계통군을 형성하였다. 하지만 인도네시아산 전형약재 유통품 15 개체의 경우 4개의 그룹으로 구분되었는데, 그 중 3개 그룹은 S. dehaani, S. subspinipes, 그리고 명확한 종을 알 수 없는 Scolopendra sp.로 Scolopendra 속으로 확인되었고 나머지 그룹을 형성하는 한 개체는 Scolopendra 속에 속하지 않고 Rhysida singaporiensis와 89%의 유사도를 보였다. COI 바코드 분석을 통해 국내 유통되는 오공은 원산지가 한국 또는 중국인 경우 모두 정품 기원종으로 확인되었으며, 원산지가 인도네시아인 경우에는 모두 위품인 것으 로 확인되었다. 또한 위품으로 확인된 유통약재는 총 4개의 종으로 분류되었고, 대부분은 정품인 Scolopendra속 의 분류군이었으며 Rhysida속과 가까운 분류군도 오공으로 수입되어 유통되고 있는 것으로 확인되었다.

This study was carried out to investigate the residual sulfur dioxide residues (SO2) in commercial medicinal herbs in Korea in 2013. Among a total of 116 samples of 11 different kinds of herbs, 71 samples (11 Kinds) were domestic, and 45 samples (10 Kinds) were imported. The residual contents of SO2 in the samples were determinated by a modified Monier-Williams method. Of the 116 samples, 6 samples (5.2%, 4 Kinds) failed to meet the regulations for sulfur dioxide residues of KFDA in medicinal herbs. Among 6 unsuitable samples, 1 samples (1.4%) were domestic, and 5 samples (11.1%, 3 Kinds) were imported. The highest amount of sulfur dioxide residues was 1546.3 mg/kg (Lycii Fructus) in the domestic samples. Regardless of region, SO2 contents were not found at Anemarrhenae Rhizoma, Citri Unshius Pericarpium, Eucommiae Cortex, Forsythiae Fructus, Gardeniae Fructus, Leonuri Herba and Lonicerae Folium et caulis. These data will be used as a basic data for the future legislation on the regulation and control of sulfur dioxide of herbal medicines.

Molecular phylogenetic analysis was conducted to evaluate the taxonomic relationships of genus Arisaema L. distributed in Korea and the molecular phylogenetic characteristics of three authentic Arisaema species for the herbal medicine Arisaematis Rhizoma (the rhizomes of A. amurense, A. heterophyllum, and A. erubescens). The sequences of three DNA barcodes (rDNA-ITS, matK, and rbcL) were analyzed using 50 samples of nine taxa consisted of eight Korean and one Chinese Arisaema with one outgroup (Dracunculus vulgaris). Both individual and combined phylogenetic analyses of three DNA barcode sequences revealed that the treated nine taxa are independently classified into six distinct clades (Clade I, A. amurense f. amurense and A. amurense f. serratum; Clade II, A. serratum and A. takesimense; Clade III, A. ringens; Clade IV, A. erubescens; Clade V, A. heterophyllum; Clade VI, A. thunbergii subsp. thunbergii and A. thunbergii subsp. geomundoense). These six clades were reasonably divided into three individual sections, Pedatisecta, Sinarisaema, and Tortuosa. Futhermore, the results of comparative DNA barcode sequences analyses provided a significant information for the taxonomic reconsideration of Arisaema L. at the specific and intraspecific level. However, we could not confirm the taxonomic characteristics or identity among the three authentic medicinal species through the molecular phylogenetic analyses of genus Arisaema L. for Arisaematis Rhizoma.

The Ponciri fructus immaturus (Poncirus trifoliata Rafinesque) has been used in oriental medicine for uterinecontraction, stomachache, abdominal distension and cardiovascular diseases. Two main compounds, poncirin and naringinwere successfully analyzed by high performance liquid chromatography (HPLC) and carried out method validation accordingto ICH guideline. A successful resolution and retention times were obtained with a C18 reversed phase column, at an 1㎖min−¹ flow rate, with a gradient elution of a mixture of methanol, water and acetonitrile. Poncirin and naringin showed goodlinearity (R²>0.999) in relatively wide concentration ranged. The recovery of each compound was 95.81~101.48% withR.S.D. values less than 1.0%. The application of ultrasound-assisted extraction was shown to be more efficient in extractingponcirin and naringin from Ponciri fructus immaturus. The predicted optimal poncirin and naringin yield were poncirin2.15%, naringin 1.65% under an extraction temperature of 40℃, an extraction time of 10 min in a solvent of 70% methanol.