光谱实验室
光譜實驗室
광보실험실
CHINESE JOURNAL OF SPECTROSCOPY LABORATORY
2010年
1期
300-304
,共5页
中蒙药苏斯-12(利胆胶囊)%分光光度法}微量铁
中矇藥囌斯-12(利膽膠囊)%分光光度法}微量鐵
중몽약소사-12(리담효낭)%분광광도법}미량철
Susi-12 of Mongolian(Cholagogic Capsule)%Spectrophotometry%Trace Iron
采用浓硝酸和高氯酸的混合消解法处理苏斯-12(利胆胶囊)样品.盐酸羟胺将铁(Ⅲ)还原成铁(Ⅱ),在pH为5的条件下,用联吡啶分光光度法测定铁含量,校准曲线回归方程为:y=0.1552x-0.0014(r=0.9999).方法的加标回收率在98.4%-101.6%之间,相对标准偏差为0.29%,苏斯-12(利胆胶囊)中铁含量为3457.76μg·g~(-1),该方法具有操作简单、重现性好的特点,可以运用于利胆胶囊中微量铁的测定.
採用濃硝痠和高氯痠的混閤消解法處理囌斯-12(利膽膠囊)樣品.鹽痠羥胺將鐵(Ⅲ)還原成鐵(Ⅱ),在pH為5的條件下,用聯吡啶分光光度法測定鐵含量,校準麯線迴歸方程為:y=0.1552x-0.0014(r=0.9999).方法的加標迴收率在98.4%-101.6%之間,相對標準偏差為0.29%,囌斯-12(利膽膠囊)中鐵含量為3457.76μg·g~(-1),該方法具有操作簡單、重現性好的特點,可以運用于利膽膠囊中微量鐵的測定.
채용농초산화고록산적혼합소해법처리소사-12(리담효낭)양품.염산간알장철(Ⅲ)환원성철(Ⅱ),재pH위5적조건하,용련필정분광광도법측정철함량,교준곡선회귀방정위:y=0.1552x-0.0014(r=0.9999).방법적가표회수솔재98.4%-101.6%지간,상대표준편차위0.29%,소사-12(리담효낭)중철함량위3457.76μg·g~(-1),해방법구유조작간단、중현성호적특점,가이운용우리담효낭중미량철적측정.
Susi-12 of Mongolian(cholagogic capsule)was digested with concentrated nitric acid and perchloric acid.Fe(Ⅲ)was reduced to Fe(Ⅱ)by hydroxylammonium chloride at pH 5.0,and determined by the spectrophotometry.The regression equation of calibration curve is y=0.1552x-0.0014,and its correlation coefficient r=0.9999.The standard addition method was used and good recovery(98.4%-101.6%)and RSD(0.29%)were obtained.The result showed that iton content in sample is 3457.76μg·g~(-1).The proposed method was simple and successfully applied to the determination of trace iron in cholagogic capsule.