食品安全质量检测学报
食品安全質量檢測學報
식품안전질량검측학보
FOOD SAFETY AND QUALITY DETECTION TECHNOLOGY
2015年
2期
633-638
,共6页
许丽珠%李秀英%黄金凤%陈晓丹%邓伟恒%黄伟乾%冼燕萍%曾庆祝%郭新东
許麗珠%李秀英%黃金鳳%陳曉丹%鄧偉恆%黃偉乾%冼燕萍%曾慶祝%郭新東
허려주%리수영%황금봉%진효단%산위항%황위건%승연평%증경축%곽신동
超滤离心%高效液相色谱法%单糖%双糖%低聚果糖%配方乳粉
超濾離心%高效液相色譜法%單糖%雙糖%低聚果糖%配方乳粉
초려리심%고효액상색보법%단당%쌍당%저취과당%배방유분
ultra-filtration%high performance liquid chromatography%monosaccharides%disaccharides%fructooligosaccharides%milk powder
目的:采用超滤离心截留技术快速除杂,结合高效液相色谱仪,建立一种同时检测配方乳粉中7种糖类化合物(果糖、葡萄糖、蔗糖、乳糖、蔗果三糖、蔗果四糖、蔗果五糖)的分析方法。方法经实验优化,选用截留分子量3000的超滤离心管高速离心去除样品溶液中的蛋白质、核酸和多糖等大分子物质,以乙腈-水为流动相(75:25,v:v)等度洗脱, Luna氨基色谱柱分离,示差折光检测器检测。结果7种目标分析物在0.15~10.0 mg/mL范围内线性关系良好,相关系数大于0.999,方法检出限在0.039~0.087 g/100 g之间;当添加水平为0.50~2.0 g/100 g时,回收率在81.2%~105%之间,相对标准偏差(RSD,n=6)为1.1%~6.2%。结论该方法与国标方法的检测结果一致,且前处理简单、结果准确、回收率高,适合配方乳粉中7种单糖、双糖和低聚果糖的测定。
目的:採用超濾離心截留技術快速除雜,結閤高效液相色譜儀,建立一種同時檢測配方乳粉中7種糖類化閤物(果糖、葡萄糖、蔗糖、乳糖、蔗果三糖、蔗果四糖、蔗果五糖)的分析方法。方法經實驗優化,選用截留分子量3000的超濾離心管高速離心去除樣品溶液中的蛋白質、覈痠和多糖等大分子物質,以乙腈-水為流動相(75:25,v:v)等度洗脫, Luna氨基色譜柱分離,示差摺光檢測器檢測。結果7種目標分析物在0.15~10.0 mg/mL範圍內線性關繫良好,相關繫數大于0.999,方法檢齣限在0.039~0.087 g/100 g之間;噹添加水平為0.50~2.0 g/100 g時,迴收率在81.2%~105%之間,相對標準偏差(RSD,n=6)為1.1%~6.2%。結論該方法與國標方法的檢測結果一緻,且前處理簡單、結果準確、迴收率高,適閤配方乳粉中7種單糖、雙糖和低聚果糖的測定。
목적:채용초려리심절류기술쾌속제잡,결합고효액상색보의,건립일충동시검측배방유분중7충당류화합물(과당、포도당、자당、유당、자과삼당、자과사당、자과오당)적분석방법。방법경실험우화,선용절류분자량3000적초려리심관고속리심거제양품용액중적단백질、핵산화다당등대분자물질,이을정-수위류동상(75:25,v:v)등도세탈, Luna안기색보주분리,시차절광검측기검측。결과7충목표분석물재0.15~10.0 mg/mL범위내선성관계량호,상관계수대우0.999,방법검출한재0.039~0.087 g/100 g지간;당첨가수평위0.50~2.0 g/100 g시,회수솔재81.2%~105%지간,상대표준편차(RSD,n=6)위1.1%~6.2%。결론해방법여국표방법적검측결과일치,차전처리간단、결과준학、회수솔고,괄합배방유분중7충단당、쌍당화저취과당적측정。
ABSTRACT:Objective To establish a simple and rapid method based on ultra-filtration clean up method and high performance liquid chromatography (HPLC) to determine 7 kinds of carbohydrate compounds (fructose, glucose, sucrose, lactose, kestose, nystose and 1F-fructofuranosylnystose) in milk powder.Methods Milk powder sample was dissolved by water, and then treated with ultra-filtration centrifugal molecular weight cut-off 3000 tube to remove protein, nucleic acid and polysaccharide macromolecular substances by high-speed centrifugation. The separation was performed on a Luna NH2 column with isocratic elution of acetonitrile: water (75:25,v:v)as the mobile phase. The analytes were determined by a refractive index detector (RID). Results Under the optimal conditions, the calibration curves were linear in the range of 0.15 to 10.0 mg/mL with correlation coefficients larger than 0.999. The limits of detection (LODs) were from 0.039 to 0.087 g/100 g. The mean recoveries for milk powder sample at three spiked concentration levels of 0.50~2.0 g/100 g were in the range of 81.2% to 105%, and the relative standard deviations (RSD) ranged from 1.1% to 6.2% (n=6). Conclusion This method is simple, rapid, and it is suitable for the identification and quantification of monosaccharides, disaccharides and fructo-oligosaccharides in milk powder.