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J. Dairy Sci. 88:3095-3100
© American Dairy Science Association, 2005.

Influence of Storage and Preservation on Fossomatic Cell Count and Composition of Goat Milk

A. Sánchez1, D. Sierra2, C. Luengo2, J. C. Corrales1, C. T. Morales2, A. Contreras1 and C. Gonzalo3

1 Departamento de Sanidad Animal, Facultad de Veterinaria, Universidad de Murcia, 30071 Murcia, Spain
2 Laboratorio Agroalimentario y de Sanidad Animal, Consejería de Agricultura y Agua, Comunidad Autónoma de la Región de Murcia, El Palmar, 30120 Murcia, Spain
3 Departamento de Producción Animal, Facultad de Veterinaria, Universidad de León, 24071 León, Spain

Corresponding author: A. Contreras; e-mail: acontrer{at}um.es.

This study was designed to evaluate the effects of different test conditions on the somatic cell count (SCC) and composition of goat milk. To this end, 3600 tests were performed on 1800 aliquots taken from 40 goat milk samples using a combined instrument set-up based on flow cytometry for SCC and Fourier transform infrared analysis for fat, total protein, lactose, total solids, and freezing point determinations. The conditions tested were storage temperature (refrigeration and freezing), use of a preservative [no preservative (NP), azidiol (AZ), and bronopol (BR)], and age of the milk samples at each storage temperature (24 h to 42 d at refrigeration temperature and 21 to 105 d at freezing temperature). Significant effects on logSCC variation were shown by the storage temperature, the preservation treatment, the interaction of storage temperature x preservation treatment, and milk age within the interaction of storage temperature x preservative. Highest counts were recorded in the BR-preserved milk samples (logSCC = 5.877), and lowest counts were recorded in milk samples preserved using AZ (logSCC = 5.803). The use of frozen/thawed samples led to a significantly decreased logSCC for the treatments AZ and NP; the logSCC was not modified when BR-preserved frozen/thawed samples were analyzed. During storage, variations in the SCC observed for BR-preserved samples stored at refrigeration temperature for up to 25 d and at freezing temperature for all times tested were always <10%. The preservation treatment was the main factor affecting the milk composition variables examined. Highest values of most variables were obtained in the BR-preserved samples, and the lowest values were obtained in the AZ-preserved samples. The freezing point was lower in the preserved samples than in the NP samples. The levels of milk constituents recorded in the BR-preserved samples were independent of both the storage temperature and age of milk sample. Our findings indicate that the freezing point of goat milk must be interpreted according to the preservative used.

Key Words: goat milk • somatic cell count • milk composition • preservation

Abbreviation key: AZ = azidiol, BR = bronopol, FT = freezing temperature, NP = no preservative, RT = refrigeration temperature.




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