Previous Page  12 / 35 Next Page
Information
Show Menu
Previous Page 12 / 35 Next Page
Page Background

Page 63

Notes:

conferenceseries

.com

Volume 8, Issue 5 (Suppl)

J Chromatogr Sep Tech, an open access journal

ISSN: 2157-7064

Chromatography 2017

August 07-09, 2017

August 07-09, 2017 | Rome, Italy

4

th

World Congress on

Chromatography

Goat milk polyunsaturated fatty acids determination by gas chromatography

Mariana Ropota

1

, Margareta Olteanu

1

, Ilie Voicu

1

and

Angela Sava

1,2

1

INCDBNA-IBNA, Romania

2

USAMV-Bucharest, Romania

T

he differences in the fatty acids content of the goat milk were determined by gas chromatography in two groups of

Carpatina×Saanen (F3) goats (n=30), in the same physiological state (second lactation), fed fromApril to August according

to the intensive system (E1 indoor) or extensive system (E2 indoor + pasture). Group 1 received briquettes made of hays and

concentrates, alfalfa hay and barley straws. Group 2 received a supplement of alfalfa hay plus concentrates (corn and barley).

Ten milk samples from each group were collected monthly. The method involved the chemical processing of the samples by

transformation in fatty acids methyl esters (FAME), followed by separation of the components in the chromatographic column,

fatty acids identification by comparison with standard chromatograms and quantitative determination of FAME (g FAME of

% g Total FAME). Reference materials (CRM) were: Standard solution of methyl fatty acids SUPELCO 37 Component FAME

Mix; 10mg/mL and; infant/adult nutritional formula- standard reference material 1849. The method was validated “in house”,

determining the following parameters: accuracy, fidelity, reproducibility, sensitivity, detection limit, quantification limit and

tracing in agreement with SR EN ISO/CEI 17025:2005. The experimental determinations showed that Ω6/Ω3 ratio ranged

from 7.93 to 12.44 in E1, and from 3.62 to 8.32 in E2. CLA (conjugated linoleic acid) level increased in the middle period

of sampling (months 2, 3 and 4), from 0.52% to 0.68% in group 1, and from 0.35% to 0.80% in group 2. In the first and last

months, CLA level decreased from 0.57% to 0.53% in group 1, and from 0.63% to 0.52% in group 2, but the average CLA value

for the whole experimental period was 6.02% in group 2, compared to just 5.7% in group 1.

Biography

Mariana Ropota completed her PhD at Bucharest University. She is coordinating the compartment of gas chromatographic analyses within the laboratory of

chemistry and nutrition physiology of the National Research-Development Institute for Animal Biology and Nutrition-IBNA-Balotesti. She is a Researcher in

Analytical Chemistry. She has published more than 20 papers in national and international scientific journals, rated by ISI or by other databases.

m.ropota@yahoo.com

Mariana Ropota et al., J Chromatogr Sep Tech 2017, 8:5(Suppl)

DOI: 10.4172/2157-7064-C1-032