Stability of milk fatty acid profile during simulated shipping for analysis by gas chromatography

被引:0
|
作者
Schmidt, A. J. [1 ,2 ]
Bomberger, R. [1 ]
Harvatine, K. J. [1 ]
机构
[1] Penn State Univ, Dept Anim Sci, University Pk, PA 16802 USA
[2] Univ Penn, Coll Vet Med, Philadelphia, PA 19104 USA
来源
JDS COMMUNICATIONS | 2021年 / 2卷 / 05期
基金
美国食品与农业研究所;
关键词
D O I
10.3168/jdsc.2020-0072
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Milk fat trans- 10 C18:1 can be used in diagnosing low milk fat production on dairy farms because it is a specific marker of biohydrogenation-induced milk fat depression. Individual fatty acids (FA), including the trans C18:1 isomer, can be determined only by gas-liquid chromatography. The analysis is currently available at a limited number of laboratories and often requires long-distance shipping. Expedited shipping with dry ice or ice packs is expensive. Therefore, the objective of this study was to determine the effect of heat treatment before shipping, shipping temperature, and shipping time on milk FA profile. Samples were collected from 3 farms on 2 occasions and stored in a polystyrene foam cooler with an ice pack, at room temperature, or at 37 degrees C for 1, 2, 3, and 7 d. Heating the sample before shipping, shipping temperature, and shipping time had very little effect on any FA analyzed. Differences observed were of small magnitude and not of practical importance, demonstrating that milk FA profile is expected to be very stable during shipping. Based on this, we propose that freezing samples and shipping in a sealed bag by second-day shipment is appropriate and demonstrated that this had little effect on FA profile of 48 milk samples. Importantly, these methods are recommended only for gas-liquid chromatography analysis of FA profile. Freezing is not appropriate for shipping for analysis by mid-infrared spectrometry-based methods or methods quantifying compounds per unit of milk because it is difficult to homogenize samples after freezing or extended shipping that results in denaturization of proteins and breaking of fat globules.
引用
收藏
页码:253 / 256
页数:5
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