海峡药学
海峽藥學
해협약학
STRAIT PHARMACEUTICAL JOURNAL
2014年
9期
72-74
,共3页
唐何%罗艳%钟庆元%王伟姣
唐何%囉豔%鐘慶元%王偉姣
당하%라염%종경원%왕위교
腐竹%甲醛次硫酸氢钠%高效液相色谱法%含量测定
腐竹%甲醛次硫痠氫鈉%高效液相色譜法%含量測定
부죽%갑철차류산경납%고효액상색보법%함량측정
Dried beancurd sticks%Sodium formaldehyde sulfoxylate%HPLC%Determination
目的:建立高效液相色谱法测定腐竹中甲醛次硫酸氢钠的含量。方法样品中甲醛次硫酸氢钠分解释放的甲醛与2,4-二硝基苯肼反应生成的衍生物经HPLC检测;色谱柱:Agilent TC-C18(250mm ×4.6mm,5μm),流动相:乙腈-水(70∶30);流速1.0mL· min 1;检测波长355nm;柱温30℃。结果甲醛浓度在0~40μg 范围内与其衍生物峰面积线性关系良好( r=0.9997),平均回收率为98.2%,方法最低检出浓度为0.62μg· g1。结论本法简单、准确,可用于腐竹中甲醛次硫酸氢钠的检测。
目的:建立高效液相色譜法測定腐竹中甲醛次硫痠氫鈉的含量。方法樣品中甲醛次硫痠氫鈉分解釋放的甲醛與2,4-二硝基苯肼反應生成的衍生物經HPLC檢測;色譜柱:Agilent TC-C18(250mm ×4.6mm,5μm),流動相:乙腈-水(70∶30);流速1.0mL· min 1;檢測波長355nm;柱溫30℃。結果甲醛濃度在0~40μg 範圍內與其衍生物峰麵積線性關繫良好( r=0.9997),平均迴收率為98.2%,方法最低檢齣濃度為0.62μg· g1。結論本法簡單、準確,可用于腐竹中甲醛次硫痠氫鈉的檢測。
목적:건립고효액상색보법측정부죽중갑철차류산경납적함량。방법양품중갑철차류산경납분해석방적갑철여2,4-이초기분정반응생성적연생물경HPLC검측;색보주:Agilent TC-C18(250mm ×4.6mm,5μm),류동상:을정-수(70∶30);류속1.0mL· min 1;검측파장355nm;주온30℃。결과갑철농도재0~40μg 범위내여기연생물봉면적선성관계량호( r=0.9997),평균회수솔위98.2%,방법최저검출농도위0.62μg· g1。결론본법간단、준학,가용우부죽중갑철차류산경납적검측。
OBJECTIVE To establish a HPLC method for quantitation of sodium formaldehyde sulfoxylate in dried beancurd sticks.METHODS The formaldehyde released from the decomposition of sodium bisulfoxylate form-aldehyde in the sample reacted with 2,4-dinitrophenylhydrazine (DNPH) and was determined by HPLC.Agilent TC-C18 column (250mm ×4.6mm,5μm) was used with temperature at 30℃.The mobile phase consisted of acetonitril-water(70∶30)and the flow rate was 1.0mL· min -1,The detective wavelength was 355nm.RESULTS The calibra-tion curve of formaldehyde was linear within the range of 0 ~40μg ( r =0.999 7 ) , the average recovery rate was 98.2%.The minimum detectable limit was 0.62μg · g -1.CONCLUSION The method is simple and accurate , which can be used for the detecting of sodium for maldehyde sulfoxylate in dried beancurd sticks .