光谱学与光谱分析
光譜學與光譜分析
광보학여광보분석
Spectroscopy and Spectral Analysis
2015年
10期
2773-2775
,共3页
韩斯琴高娃%哈斯乌力吉%林翔%林爽%杨芳%娄秀涛%吕志伟
韓斯琴高娃%哈斯烏力吉%林翔%林爽%楊芳%婁秀濤%呂誌偉
한사금고왜%합사오력길%림상%림상%양방%루수도%려지위
拉曼光谱%中药%蒙药%朱砂
拉曼光譜%中藥%矇藥%硃砂
랍만광보%중약%몽약%주사
Raman spectroscopy%Herb%Mongolian medicines%Cinnabars
朱砂有凉性、解热、收敛作用,一般以粉末状入药于中药或蒙药中。然而朱砂具有一定的毒性,因此有必要对药品中朱砂的含量进行检测分析。利用便携式拉曼光谱仪对朱砂进行了鉴别分析,获得了朱砂较为全面的分子结构振动信息。实验结果显示朱砂的拉曼光谱在253,290和343 cm-1等处出现了较强的拉曼特征峰,文中确定以此三处特征峰作为研究对象。同时,检测了蒙药八味止血红花散、朝伦‐雄胡‐5、外用溃疡散以及中药口腔溃疡散的拉曼光谱。结果在含有朱砂的几种蒙药八味止血红花散、朝伦‐雄胡‐5和外用溃疡散均检测到了朱砂的特征峰,而在不含有朱砂的中药口腔溃疡散中未检测到拉曼特征峰。此外,对口腔溃疡散中的朱砂进行半定量分析,检测极限可达到质量分数的10%左右。拟合得到了中药口腔溃疡散的拉曼光谱特征峰强度与其中朱砂的掺杂量之间的关系,获得曲线的相关系数 r=0.9959,验证了拟合结果的准确性。该拉曼光谱检测方法具有快速、简便、准确等优点,值得在中蒙药成分鉴定方面得到广泛的应用。
硃砂有涼性、解熱、收斂作用,一般以粉末狀入藥于中藥或矇藥中。然而硃砂具有一定的毒性,因此有必要對藥品中硃砂的含量進行檢測分析。利用便攜式拉曼光譜儀對硃砂進行瞭鑒彆分析,穫得瞭硃砂較為全麵的分子結構振動信息。實驗結果顯示硃砂的拉曼光譜在253,290和343 cm-1等處齣現瞭較彊的拉曼特徵峰,文中確定以此三處特徵峰作為研究對象。同時,檢測瞭矇藥八味止血紅花散、朝倫‐雄鬍‐5、外用潰瘍散以及中藥口腔潰瘍散的拉曼光譜。結果在含有硃砂的幾種矇藥八味止血紅花散、朝倫‐雄鬍‐5和外用潰瘍散均檢測到瞭硃砂的特徵峰,而在不含有硃砂的中藥口腔潰瘍散中未檢測到拉曼特徵峰。此外,對口腔潰瘍散中的硃砂進行半定量分析,檢測極限可達到質量分數的10%左右。擬閤得到瞭中藥口腔潰瘍散的拉曼光譜特徵峰彊度與其中硃砂的摻雜量之間的關繫,穫得麯線的相關繫數 r=0.9959,驗證瞭擬閤結果的準確性。該拉曼光譜檢測方法具有快速、簡便、準確等優點,值得在中矇藥成分鑒定方麵得到廣汎的應用。
주사유량성、해열、수렴작용,일반이분말상입약우중약혹몽약중。연이주사구유일정적독성,인차유필요대약품중주사적함량진행검측분석。이용편휴식랍만광보의대주사진행료감별분석,획득료주사교위전면적분자결구진동신식。실험결과현시주사적랍만광보재253,290화343 cm-1등처출현료교강적랍만특정봉,문중학정이차삼처특정봉작위연구대상。동시,검측료몽약팔미지혈홍화산、조륜‐웅호‐5、외용궤양산이급중약구강궤양산적랍만광보。결과재함유주사적궤충몽약팔미지혈홍화산、조륜‐웅호‐5화외용궤양산균검측도료주사적특정봉,이재불함유주사적중약구강궤양산중미검측도랍만특정봉。차외,대구강궤양산중적주사진행반정량분석,검측겁한가체도질량분수적10%좌우。의합득도료중약구강궤양산적랍만광보특정봉강도여기중주사적참잡량지간적관계,획득곡선적상관계수 r=0.9959,험증료의합결과적준학성。해랍만광보검측방법구유쾌속、간편、준학등우점,치득재중몽약성분감정방면득도엄범적응용。
Cinnabar could soothe the nerves and the powder of cinnabar is always added in traditional Chinese medicine or mongolian medicines .The surface‐enhanced Raman spectrum of cinnabar was identified using a portable Raman spectrometer and most structure vi‐bration information was obtained .The results show that the Raman peaks of cinnabars were located at 253 ,290 ,343 cm-1 and this three Raman characteristic peaks were selected for cinnabar identification .Meanwhile ,the Raman spectra of several mongolian medicines were collected .The results showed that Raman signal of cinnabar could be observed in several mongolian medicines which contain cinnabar and Raman signal of cinnabar couldn’t be detected in several mongolian medicines without cinnabar .In addition ,the cinnabar in the oral ulcer powder was semi‐quantitative analyzed and the limit of detection could reach to 10% of mass fraction .The relationship between the doped amount of cinnabar in the oral ulcer powder and the Raman intensity of characteristic peak was fitted and the correlation coefficient (r) was 0.995 9 ,which validated the accuracy of the result .This Raman analysis method for cinnabar detection is rapid ,simple and ac‐curate and it can be applied widely in mongolian medicines determination .