湖北中医药大学学报
湖北中醫藥大學學報
호북중의약대학학보
JOURNAL OF HUBEI UNIVERSITY OF CHINESE MEDICINE
2015年
3期
36-39
,共4页
秦春华%武玲%汪鋆植%张盼%黄年玉%贺海波%姜从良
秦春華%武玲%汪鋆植%張盼%黃年玉%賀海波%薑從良
진춘화%무령%왕윤식%장반%황년옥%하해파%강종량
桑黄%hispolon%原儿茶酸%高效液相色谱法
桑黃%hispolon%原兒茶痠%高效液相色譜法
상황%hispolon%원인다산%고효액상색보법
Igniarius phellinus%Hispolon%Protocatechuic acid%HPLC
目的:通过活性成分的 HPLC 含量测定,为控制桑黄质量提供依据。方法收集市场上常见的桑黄品种样品,用高效液相色谱法测定 hispolon 和原儿茶酸含量。色谱柱为 UItimateAQ -C18(4.6mm ×250mm,5μm);(A)测定 hi-spolon 流动相为乙腈-水(38:62),检测波长363nm,(B)测定原儿茶酸流动相为乙腈-0.1%磷酸溶液(12:88),检测波长256nm;柱温为25℃;流速为1mL/min;进样量为10μL。结果 hispolon 及原儿茶酸分别在线性范围1.3-0.043mg/mL(r =0.9997),0.4-0.025mg/mL(r =0.9998)线性关系良好。鲍氏针层孔菌、裂蹄针层孔菌、火木针层孔菌、忍冬木层孔菌不同种、不同宿主的9个样品均含有原儿茶酸,含量42.8-96.8μg/g。松木上生长的不同种桑黄,均未检出 hispolon,其它样品含有 hispolon,含量90.9-223.3μg/g。结论不同桑黄样品均含有原儿茶酸,可作为桑黄的指示成分进行检测。受试样品 hispolon 含量差异大,表明品种、宿主和生长环境对桑黄成分具有明显影响,影响最大的是宿主,松木上生长的桑黄,均未检出 hispolon。监测 hispolon 含量,对控制桑黄质量,具有重要意义。
目的:通過活性成分的 HPLC 含量測定,為控製桑黃質量提供依據。方法收集市場上常見的桑黃品種樣品,用高效液相色譜法測定 hispolon 和原兒茶痠含量。色譜柱為 UItimateAQ -C18(4.6mm ×250mm,5μm);(A)測定 hi-spolon 流動相為乙腈-水(38:62),檢測波長363nm,(B)測定原兒茶痠流動相為乙腈-0.1%燐痠溶液(12:88),檢測波長256nm;柱溫為25℃;流速為1mL/min;進樣量為10μL。結果 hispolon 及原兒茶痠分彆在線性範圍1.3-0.043mg/mL(r =0.9997),0.4-0.025mg/mL(r =0.9998)線性關繫良好。鮑氏針層孔菌、裂蹄針層孔菌、火木針層孔菌、忍鼕木層孔菌不同種、不同宿主的9箇樣品均含有原兒茶痠,含量42.8-96.8μg/g。鬆木上生長的不同種桑黃,均未檢齣 hispolon,其它樣品含有 hispolon,含量90.9-223.3μg/g。結論不同桑黃樣品均含有原兒茶痠,可作為桑黃的指示成分進行檢測。受試樣品 hispolon 含量差異大,錶明品種、宿主和生長環境對桑黃成分具有明顯影響,影響最大的是宿主,鬆木上生長的桑黃,均未檢齣 hispolon。鑑測 hispolon 含量,對控製桑黃質量,具有重要意義。
목적:통과활성성분적 HPLC 함량측정,위공제상황질량제공의거。방법수집시장상상견적상황품충양품,용고효액상색보법측정 hispolon 화원인다산함량。색보주위 UItimateAQ -C18(4.6mm ×250mm,5μm);(A)측정 hi-spolon 류동상위을정-수(38:62),검측파장363nm,(B)측정원인다산류동상위을정-0.1%린산용액(12:88),검측파장256nm;주온위25℃;류속위1mL/min;진양량위10μL。결과 hispolon 급원인다산분별재선성범위1.3-0.043mg/mL(r =0.9997),0.4-0.025mg/mL(r =0.9998)선성관계량호。포씨침층공균、렬제침층공균、화목침층공균、인동목층공균불동충、불동숙주적9개양품균함유원인다산,함량42.8-96.8μg/g。송목상생장적불동충상황,균미검출 hispolon,기타양품함유 hispolon,함량90.9-223.3μg/g。결론불동상황양품균함유원인다산,가작위상황적지시성분진행검측。수시양품 hispolon 함량차이대,표명품충、숙주화생장배경대상황성분구유명현영향,영향최대적시숙주,송목상생장적상황,균미검출 hispolon。감측 hispolon 함량,대공제상황질량,구유중요의의。
s:Objective To provide the basis for controlling quality of igniarius phellinus , we determined the active constituent contents by HPLC.Method Collecting the common phellinus igniarius varities as the samples , we analyzed the contents of hispolon and protocate -chuic acid using the HPLC method with UItimateAQ -C18 column (4.6mm ×250mm, 5μm) in 25℃ (column temperature).Hispolon was detected with 38% acetonitrile in water under 363nm ( detecting wavelength ), and protocatechuic acid was 12% acetonitrile in 0.1%psophate solution at 256nm.The injection volum was 10μL with the flow rate of 1mL/min.Result The liner ranges of hispolon and proto -catechuic acid were 1.3 -0.043mg/mL(r =0.9997)and 0.4 -0.025mg/mL(r =0.9998), respectively.The contents of protocatechuic acid in the nine kinds of samples (Phellinus baumii, Phellinus linteus, Phellinus igniariusPhellinus lonicerinu ect .) were from 42.8μg/g to 96.8μg/g.Hisplon was not found in live phellinus igniarius on pine tree , but the contents of other verities were from 90.9μg/g to 223.3μg/g.Conclusion Protocatechuic acid was found in all kinds of phellinus igniarius , which could be determined as an indicating ingredient . The content of hispolon in igniarius phellinus was seriously influenced by the varities , parasitifers and growing environment .Determining the content of hispolon has an important implication for the control the quality of phellinus igniarius .