Determination of total and A1-Type β-casein in milk and milk-derivedingredients by liquid chromatography – mass spectrometry using characteristic tryptic peptides

Author(s):  
Stefan Ehling ◽  
Meibo Wang ◽  
Luke Weber

Abstract Background Gastrointestinal digestion of A1-type β-casein is conducive to β-casomorphin-7 with potential adverse digestive health effects. Monitoring of A1-type β-casein concentration in milk and milk-derived ingredients used in the formulation of A2-type nutritional products with associated health claims is important from a quality standpoint. Objective New analytical methods were developed and validated for total and A1-type β-casein in milk and milk-derived ingredients. Data on total and A1-type β-casein concentrations in milk, nonfat dry milk, and whey protein concentrate was generated. Methods The methods are based on a bottom-up proteomic approach using tryptic marker peptides and stable isotope dilution liquid chromatography – mass spectrometry. The measurement includes all protein sequences (intact, modified, partial) which are potential sources of β-casomorphin-7. Results Total β-casein was quantified using a neat calibration curve. Recovery and between-day precision RSD were 98% and 5.8%, respectively. A1-type β-casein was quantified by the method of standard additions. Between-day precision RSD was 7.2% and limit of quantitation was 0.01% in nonfat dry milk. The mass fraction of A1-type β-casein in β-casein standard was 0.444. Samples manufactured from A2-type milk contained 0.26–5.0% A1-type β-casein relative to total β-casein. Conclusions The methods described enable the monitoring of the A1-type β-casein concentration in milk and milk-derived ingredients destined for the manufacture of A2-type products with associated health claims. Highlights New methods are presented for the analysis of total and A1-type β-casein in milk and milk-derived ingredients. Mass fraction of A1-type β-casein in commercial β-casein standard was determined to enable its use as calibrant.

2009 ◽  
Vol 92 (1) ◽  
pp. 302-306 ◽  
Author(s):  
Xiao-Jing Yan ◽  
Xiao-Mei Liang ◽  
Yan-Jun Xu ◽  
Shu-Hui Jin ◽  
Dao-Quan Wang

Abstract A method was developed for the determination of 7B3 (12-propyloxyimino-1,15-pentadecanlactam), a novel macrolactam fungicide, by liquid chromatography/mass spectrometry (LC/MS) with positive electrospray ionization (ESI+). The method used a reversed-phase C18 column and acetonitrilewater (60 + 40, v/v) mobile phase. The quick, easy, cheap, effective, rugged, and safe method was used for extraction of 7B3 from cotton plants, which involved the extraction of 10 g homogenized sample with 10 mL acetonitrile, followed by the addition of 4 g anhydrous MgSO4 and 1.0 g NaCl. After centrifugation, 1 mL of the buffered acetonitrile extract was transferred into a tube containing 50 mg primary secondary amine sorbent and 100 mg anhydrous MgSO4. After shaking and centrifugation, the final extract was transferred to an autosampler vial for concurrent analysis by LC/MS. The results of 7B3 determined by LC/MS in the selective ion monitoring mode were linear, and the matrix effect of the method was evaluated. The average recoveries of 7B3 fortified at different levels were within 84.1100.2, and the relative standard deviations were <7.5 for all samples analyzed. The method limit of detection and the limit of quantitation values were 0.03 and 0.1 mg/kg, respectively. The proposed method was successfully applied to determine 7B3 residues in practical samples. This method is sensitive, accurate, reliable, simple, and safe.


1997 ◽  
Vol 80 (2) ◽  
pp. 392-400 ◽  
Author(s):  
Alexander J Krymtsky

Abstract A capillary electrophoresis (CE) method and an electrospray ionization (ESI) liquid chromatography/mass spectrometry (LC/MS) confirmatory method were developed to analyze 12 sulfonylurea herbicides and one sulfonamide (Flumetsulam) in runoff water. The water used for fortification was collected from a local marsh that contained high levels of potentially interfering compounds. Good recoveries and adequate sensitivity at the 0.2 ppb level (limit of quantitation) were obtained. A portion of the water was acidified and extracted with reversed- phase solid-phase extraction (SPE). Extracts were cleaned up with a tandem system consisting of a strong-anion exchange SPE cartridge stacked on an alumina SPE cartridge. CE/ultraviolet quantitation was achieved by capillary zone electrophoresis at pH 4.75 with 50 mM ammonium acetate buffer and an acetonitrile modifier. ESI LC/MS quantitation was achieved by using a time-scheduled selective-ion monitoring (positive mode) of the M+H ions for each compound. The extraction/cleanup procedure provided extracts such that in-source collision-induced dissociation gave product ions for confirmation at the 0.2 ppb fortification level.


2007 ◽  
Vol 90 (5) ◽  
pp. 1340-1345 ◽  
Author(s):  
Gianluca Dimartino

Abstract A convenient method is presented for determination of vitamin D in natural cheese, processed cheese, milk, cereals, noncarbonated soft drinks, and juice by liquid chromatography/mass spectrometry (LC/MS). Samples were saponified, extracted, evaporated, redissolved in acetonitrile, and injected into an LC-atmospheric pressure chemical ionization-MS system with no preparative chromatographic steps. Vitamin D was determined by selected ion monitoring. MS response was linear for vitamin D3 and its internal standard vitamin D2, and overall average recoveries ranged from 98 to 105. A blending experiment in which shredded vitamin D3-fortified cheddar was mixed with control nonfortified cheddar showed linearity. The limit of detection for vitamin D was 1.3 ng and the limit of quantitation was 3 ng. The method gave good accuracy and precision, with a standard deviation of 9.5 and relative standard deviation of 6.7. Results for vitamin D3 obtained with this method for different food matrixes, at different levels, were in agreement with those obtained with the reference LC/UV method currently used by many laboratories and derived from AOAC Official Method 982.29.


2010 ◽  
Vol 2 (2) ◽  
pp. 182-189 ◽  
Author(s):  
Ashok Marwah ◽  
Xu Nianzu ◽  
Padma Marwah ◽  
Terence P. Barry

17a-Methyltestosterone is used as feed additive to manipulate the gender of fish for aquaculture. Earlier a simple, yet specific and robust validated high performance liquid chromatographic method has been developed for the determination of 17a-methyltestosterone in fish feed. The present work describes a highly sensitive and robust Liquid Chromatography-Mass Spectrometry method for the quantitation of 17a-methyltestosterone in aquatic water systems using 17â-hydroxy-3â-methoxyandrost-5-en-7-one as internal standard. The method was validated in the concentration range of 0.2 to 25 ng of 17a-methyltestosterone on column leading to a limit of quantitation of 0.08 ppb or 0.08 mg/L in water, and has potential to increase the limit of detection and quantitation by an order of magnitude, if required.


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