主题:用高效液相色谱分析三聚氰胺困难吗

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hollior
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我们省里统一用这个方法,但是测定过程中三聚氰胺的特征吸收峰会发生变化,两个会成一个,辅助定性有点困难,另外,10ppm以下出峰比较难辨认
千雪子
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日出看日落
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个人认为首要的难点是样品的前处理
如果样品前处理能较完美的把蛋白质分离出来
用HPLC做的话 难度应该不大
niubeibei
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最近可是净听说三聚氰胺无法检测了,如果按照所给出的色谱条件检测的话,未尝不可检测出三聚氰胺的含量来,有没有那位兄台用此种方法测试过呢?可否请教一下!
wsy18
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【转帖】美国FDA 有关三聚氰胺的检测方法(HPLC-UV)

Updated FCC Developmental Melamine Quantitation (HPLC-UV)


Sample Preparation/Extraction:
Wheat gluten: Ground in a Retsch ZM 100 centrifugal rotor mill (ring sieve 0.5 mm).
Moist pet food: Moist chunks and gravy were blended to the consistency of a gritty pudding prior to sampling.

Samples weighed into glass scintillation vials. Extract using 50:50 acetonitrile:water.

Procedure: Add indicated volume of extraction solvent (see note below) 1. Cap and vortex thoroughly, get aggressive with this step (critical due to slow dissolution rate of melamine). Sonicate 30 minutes. Filter portion of extract through 2-stage GMF-nylon (0.45 m m) filters. Dilute filtered extract 250 ml extract + 750 ml solvent 2 to maintain solubility of matrix components.

1 Wheat gluten: Extract in proportion 0.1 g to 10 ml. For melamine contents above 2% w/w, extract in proportion 0.05 g to 15 ml.

1 Moist pet food: Extract in proportion 2.0 – 2.5 g to 10 ml.

2 Solvent for final dilution may be water or 0.1 N HCl. Final dilution is necessary for compatibility with ion-pairing chromatography. We have observed some differences in behavior between the wheat gluten and pet food samples with respect to maintaining solubility during final dilution (these are most likely matrix components which fall out). 0.1 N HCl seems to help maintain solubility for final dilution of the wheat glutens.

HPLC-UV Operating Parameters:
Column: Zorbax Rx C8 (retention is too high on C18 column)
Buffer: 10 mM citric acid, 10 mM sodium octane sulfonate, adjusted to pH 3.0
Mobile phase: 85:15 buffer:acetonitrile
Flow rate: 1.0 ml/min.
Injection volume: 10 ml
Column thermostat: 40 oC (column thermostatting is necessary for ion-pair separations)
Detection wavelength: 240 nm
Spectral collection: 200 – 400 nm (look for lmax near 236 nm)
Retention time: 4.2 - 4.3 min.
Run time: 10 min.

Standard Preparation:
Stock standard was prepared in 76:24 acetonitrile: water. A check stock standard was prepared in 60:40 acetonitrile: water. Dilutions were made in either water or 0.1N HCl giving equivalent calibration curves.

Figures of Merit:
Linear range: established from 1.0 – 400 mg/ml; calibration range 1.0 – 200 mg/ml used for most of work
Reproducibility: duplicate preparations agree within 0.1 - 5% relative basis
Spike/recovery (based on spiking solid melamine powder into test matrix prior to extraction): 90 -110%.

原稿由no.Escape所贴,连接:http://www.instrument.com.cn/bbs/shtml/20080916/1485202/
wsy18
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上海伍丰发布的一则新闻,供参考:

            上海伍丰开发出奶粉中三聚氰胺的液相色谱检测方法


        近期由于食用“三鹿奶粉”导致婴儿死亡的事件炒的沸沸扬扬,一时间成了大城小巷人们集中议论的话题,罪魁祸首就是奶粉中的三聚氰胺在作祟。这是一种对人体有害的化学物质,长期食用将会导致肾结石,严重的甚至危及生命,特别是对于丝毫没有抵抗力的婴儿来说,其危害更是致命的!但国内某些厂商利用其能够提高含氮量的特点,作为添加剂加入进奶粉流入市场,造成了极其严重的不良影响。
      本公司现针对这一现象,研制出了三聚氰胺的液相色谱检测方法,能够准确的检测出 奶粉中的三聚氰胺含量,严格控制了产品本身的质量,保证了广大消费者的利益,具体设备方法相关厂家可来电咨询!



wuyue-5
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ysyxy
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wdl158160
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10mM 柠檬酸, 10mM 庚烷磺酸钠,用1M NaOH调pH为3.0
请问各们,其中的"10mM"中的"mM"是什么单位啊,毫摩尔每升吗?
阿宝
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原文由 easyboy 发表:
如题,欢迎讨论,如果用液相分析较复杂和困难,难点在那里。什么手段分析较简单,准确,检测能力高。一定得用质谱吗?

主要是样品预处理比较麻烦
液相做的还可以
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