Determination of Fatty Acids Profiles and Volatile Compounds of Cows’ and Goats’ Butters
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Effect of Parity on Fatty Acids of Saudi Camels Milk and Colostrum
International Journal of Research in Agricultural Sciences Volume 4, Issue 6, ISSN (Online): 2348 – 3997 Effect of Parity on Fatty Acids of Saudi Camels Milk and Colostrum Magdy Abdelsalam1,2*, Mohamed Ali1 and Khalid Al-Sobayil1 1Department of Animal Production and Breeding, College of Agriculture and Veterinary Medicine, Qassim University, Al-Qassim 51452, Saudi Arabia. 2Department of Animal Production, Faculty of Agriculture, Alexandria University, El-Shatby, Alexandria 21545, Egypt. Date of publication (dd/mm/yyyy): 29/11/2017 Abstract – Fourteen Saudi she-camels were machine milked locations and different feeding regimes, but there is a scare twice daily and fatty acids of colostrum (1-7 days post partum) on the effect of parity of lactating camels on the fatty acids. and milk (10-150 days post partum) were analyzed. Short Therefore, the objective of this experiment was to study the chain fatty acids were found in small percentage in colostrums changes in the fatty acids profile of colostrums and milk of and milk at different parities without insignificant differences she-camel during the first three parities. and the C4:0 and C6:0 don't appear in the analysis. Colostrums has higher unsaturated fatty acids percentage than that of saturated fatty acids while the opposite was found II. MATERIALS AND METHODS in milk of camels. Myiristic acid (C14:0), palmitic (C16:0), stearic (C18:0) and oleic (C18:1) showed the highest A. Animals and Management percentage in either colostrums or milk of she-camels. Parity The present study was carried out on fourteen Saudi she had significant effect on atherogenicity index (AI) which is camels raised at the experimental Farm, College of considered an important factor associated the healthy quality of camel milk. -
Retention Indices for Frequently Reported Compounds of Plant Essential Oils
Retention Indices for Frequently Reported Compounds of Plant Essential Oils V. I. Babushok,a) P. J. Linstrom, and I. G. Zenkevichb) National Institute of Standards and Technology, Gaithersburg, Maryland 20899, USA (Received 1 August 2011; accepted 27 September 2011; published online 29 November 2011) Gas chromatographic retention indices were evaluated for 505 frequently reported plant essential oil components using a large retention index database. Retention data are presented for three types of commonly used stationary phases: dimethyl silicone (nonpolar), dimethyl sili- cone with 5% phenyl groups (slightly polar), and polyethylene glycol (polar) stationary phases. The evaluations are based on the treatment of multiple measurements with the number of data records ranging from about 5 to 800 per compound. Data analysis was limited to temperature programmed conditions. The data reported include the average and median values of retention index with standard deviations and confidence intervals. VC 2011 by the U.S. Secretary of Commerce on behalf of the United States. All rights reserved. [doi:10.1063/1.3653552] Key words: essential oils; gas chromatography; Kova´ts indices; linear indices; retention indices; identification; flavor; olfaction. CONTENTS 1. Introduction The practical applications of plant essential oils are very 1. Introduction................................ 1 diverse. They are used for the production of food, drugs, per- fumes, aromatherapy, and many other applications.1–4 The 2. Retention Indices ........................... 2 need for identification of essential oil components ranges 3. Retention Data Presentation and Discussion . 2 from product quality control to basic research. The identifi- 4. Summary.................................. 45 cation of unknown compounds remains a complex problem, in spite of great progress made in analytical techniques over 5. -
WO 2017/074902 Al 4 May 20 17 (04.05.2017) W P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2017/074902 Al 4 May 20 17 (04.05.2017) W P O P C T (51) International Patent Classification: AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, A61K 8/37 (2006.01) A61Q 19/00 (2006.01) BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, A61K 31/215 (2006.01) DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, (21) International Application Number: KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, PCT/US2016/058591 MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, (22) International Filing Date: OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, 25 October 2016 (25.10.201 6) SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, (25) Filing Language: English ZW. (26) Publication Language: English (84) Designated States (unless otherwise indicated, for every (30) Priority Data: kind of regional protection available): ARIPO (BW, GH, 62/247,803 29 October 20 15 (29. 10.20 15) US GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, (71) Applicant: GLAXOSMITHKLINE CONSUMER TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, HEALTHCARE HOLDINGS (US) LLC [US/US]; 271 1 DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, Centerville Road, Suite 400, Wilmington, DE 19808 (US). -
Essential Oils and Oil from Seeds of Syagrus Coronata
Vol. 10(23), pp. 310-317, 17 June, 2016 DOI: 10.5897/JMPR2016.6098 Article Number: 89CD55858997 ISSN 1996-0875 Journal of Medicinal Plants Research Copyright © 2016 Author(s) retain the copyright of this article http://www.academicjournals.org/JMPR Full Length Research Paper Syagrus coronata seed oils have antimicrobial action against multidrug-resistant Staphylococcus aureus Cibele Maria Alves da Silva Bessa1, Rodrigo Santana do Nascimento1, Renata Carla Corrêa Alves1*, José Matias Anselmo2, Ana Paula Sant'Anna da Silva1, Alexandre Gomes da Silva1, Vera Lúcia de Menezes Lima1, Josean Fechine Tavares3, Luís Cláudio Nascimento da Silva1,2, Márcia Vanusa da Silva1 and Maria Tereza dos Santos Correia1 1Departamento de Bioquímica, Centro de Ciências Biológicas, Universidade Federal de Pernambuco, Av. Professor Moraes Rego, Cidade Universitária, 1235, 50670-901, Recife, Pernambuco, Brazil. 2Faculdade Pernambucana de Saúde, Av. Jean Emile Favre, 420, Imbiribeira, 51200-060, Recife, Pernambuco, Brazil. 3Departamento de Ciências Farmacêuticas, Universidade Federal da Paraíba, Campus I, Castelo Branco, 58051-970, Joao Pessoa, Paraíba, Brazil. Received 15 March, 2016; Accepted 20 May, 2016 Syagrus coronata (Mart.) Becc. (Arecaceae) is a native Brazilian palm (ouricuri) and despite the use of its derived products by traditional communities, few scientific reports have been published regarding its biomedical activity. This study investigates the chemical composition and anti-Staphylococcus aureus effects of both manufactured oil (SCO) and essential oil (SCEO) from S. coronata seeds. SCO was provided by rural inhabitants, while SCEO was obtained by hydrodistillation. Chemical characterization was performed by gas chromatography-mass spectrometry (GC/MS). In vitro antimicrobial activity was determined against 17 S. aureus strains, including multidrug-resistant strains. -
Improvement of Lipid Production from an Oil-Producing Filamentous Fungus, Penicillium Brevicompactum NRC 829, Through Central Composite Statistical Design
Ann Microbiol (2017) 67:601–613 DOI 10.1007/s13213-017-1287-x ORIGINAL ARTICLE Improvement of lipid production from an oil-producing filamentous fungus, Penicillium brevicompactum NRC 829, through central composite statistical design Thanaa H. Ali1 & Mamdouh S. El-Gamal2 & Dina H. El-Ghonemy1 & Ghada E. Awad3 & Amir E. Tantawy1 Received: 12 March 2017 /Accepted: 13 July 2017 /Published online: 7 August 2017 # Springer-Verlag GmbH Germany and the University of Milan 2017 Abstract In the present study, 13 filamentous fungi were commercial development for the production of LA by fer- screened for their lipid production and an oleaginous fun- mentation using cheap raw material. gus, Penicillium brevicompactum NRC 829, was found to be the highest lipid producer. Screening of various agro- Keywords Linoleic acid . Penicillium brevicompactum NRC industrial residues was performed and sunflower oil cake 829 . Response surface methodology . Unsaturated fatty acids proved to be the best substrate for lipid production. A central composite design was employed to investigate the optimum concentrations of the most significant medi- Introduction um components required to improve the lipid production by P. brevicompactum. The results clearly revealed that Polyunsaturated fatty acids (PUFAs) are long-chain fatty − the maximal lipid production of 8.014 ± 0.06 gL 1 acids containing two or more double bonds in their acyl (representing 57.6% lipid/dry biomass) was achieved by chains. Biosynthesis of PUFAs involves both methyl- the fungus when grown for 6 days at 30 °C under static directed and carboxyl-directed desaturases. The primary condition in a medium containing sunflower oil cake, product of fatty acid biosynthesis in oilseed crops is the NaNO3 and KCl at final concentrations of 8, 0.75 and 18-carbon monounsaturated oleic acid (C18:1–9). -
National Food Safety Standard Determination of Fatty Acids in Foods
National Standard of the People’s Republic of China GB 5413.27 – 2010 National food safety standard Determination of fatty acids in foods for infants and young children, milk and milk products Issued on: 2010-03-26 Implemented on: 2010-06-01 Issued by the Ministry of Health of People’s Republic of China GB 5413.27–2010 Preface This standard replaces GB/T 21676 - 2008 Determination of Fatty Acids in Formula Foods and Milk Powder for Infants and Young Children, GB/T 5413.27 – 1997 Determination of DHA and EPA in Formula Foods and Milk Powder for Infants and Young Children and GB/T 5413.4 - 1997 Determination of Linoleic Acid in Formula Foods and Milk Powder for Infants and Young Children. Comparing with the original standards, the following main changes have been made to the Standard: the first method is Acetyl Chloride - Methanol Esterification; Integrate GB/T 21676 - 2008, GB/T 5413.27 – 1997 and GB/T 5413.4 – 1997 to the second method of this standard, Ammonia Water - Ethanol Extraction Method. Appendix A of this standard is informative. The versions replaced by this standard are: - GB/T 5413.4 – 1997, GB/T 5413.27 - 1997; - GB/T 21676 - 2008. 1 GB 5413.27–2010 National food safety standard Determination of fatty acids in foods for infants and young children, milk and milk products 1 Scope This standard provides the determination of fatty acids in infant foods and dairy. This standard applies to determination of fatty acids in infant foods and dairy; the second method doesn’t apply to determination of embedded fatty acid. -
Biochemistry Prologue to Lipids
Paper : 05 Metabolism of Lipids Module: 01 Prologue to Lipids Principal Investigator Dr. Sunil Kumar Khare, Professor, Department of Chemistry, IIT-Delhi Paper Coordinator and Dr. Suaib Luqman, Scientist (CSIR-CIMAP) Content Writer & Assistant Professor (AcSIR) CSIRDr. Vijaya-CIMAP, Khader Lucknow Dr. MC Varadaraj Content Reviewer Prof. Prashant Mishra, Professor, Department of Biochemical Engineering and Biotechnology, IIT-Delhi 1 METABOLISM OF LIPIDS Biochemistry Prologue to Lipids DESCRIPTION OF MODULE Subject Name Biochemistry Paper Name 05 Metabolism of Lipids Module Name/Title 01 Prologue to Lipids 2 METABOLISM OF LIPIDS Biochemistry Prologue to Lipids 1. Objectives To understand what is lipid Why they are important How they occur in nature 2. Concept Map LIPIDS Fatty Acids Glycerol 3. Description 3.1 Prologue to Lipids In 1943, the term lipid was first used by BLOOR, a German biochemist. Lipids are heterogeneous group of compounds present in plants and animal tissues related either actually or potentially to the fatty acids. They are amphipathic molecules, hydrophobic in nature originated utterly or in part by thioesters (carbanion-based condensations of fatty acids and/or polyketides etc) or by isoprene units (carbocation-based condensations of prenols, sterols, etc). Lipids have the universal property of being: i. Quite insoluble in water (polar solvent) ii. Soluble in benzene, chloroform, ether (non-polar solvent) 3 METABOLISM OF LIPIDS Biochemistry Prologue to Lipids Thus, lipids include oils, fats, waxes, steroids, vitamins (A, D, E and K) and related compounds, such as phospholipids, triglycerides, diglycerides, monoglycerides and others, which are allied more by their physical properties than by their chemical assests. -
Fast and Simple Free Fatty Acids Analysis Using UPC2/MS Giorgis Isaac,1 Michael D
Fast and Simple Free Fatty Acids Analysis Using UPC2/MS Giorgis Isaac,1 Michael D. Jones,1 Besnik Bajrami,1 Wassim Obeid,2 James Langridge,3 Patrick Hatcher2 1Waters Corporation, Milford, MA, USA 2Old Dominion University, Norfolk, VA, USA 3Waters Corporation, Manchester, UK APPLICATION BENEFITS INTRODUCTION ■■ Demonstrates the separation of free fatty Fatty acids, both free and as part of complex lipids, play a number of key roles acid (FFA) species based on chain length in metabolism – as major metabolic fuel (storage and transport of energy), as and number of double bonds essential components of all membranes, and as gene regulators. In addition, dietary lipids provide polyunsaturated fatty acids that are precursors of powerful ■■ No derivatization is required, which results in easier and fast sample preparation and locally acting metabolites, e.g., eicosanoids. eliminates artifact formation The common fatty acids of animal and plant origin have even-numbered chains ■■ Organic phase lipid extract can be directly of 16 to 24 carbon atoms with 0 to 6 double bonds. Nature provides countless injected onto the system, saving time and exceptions, however, and odd- and even-numbered fatty acids with up to nearly reducing cost per analysis 100 carbon atoms exist. In addition, double bonds can be of the cis (Z) and trans (E) configuration and there can be innumerable other structural features, ■■ Less than three-minute chromatographic including branch points, rings, oxygenated functions, and many more. separation is up to 10X faster compared to GC/MS Fatty acid chains may contain one or more double bonds at specific positions (unsaturated and poly unsaturated with cis (Z) or trans (E) configuration) or they ■■ Unlike GC/MS, low volatile and very long chain fatty acids (>24 carbon atoms) can be may be fully saturated. -
Mass Spectrometry of Astrobiologically Relevant Organic Material – Implications on Future Space Missions to Ocean Worlds in the Outer Solar System
Mass Spectrometry of Astrobiologically Relevant Organic Material – Implications on Future Space Missions to Ocean Worlds in the Outer Solar System Fabian Klenner1, Frank Postberg1, Ferdinand Stolz2, René Reviol1, and Nozair Khawaja1 1Institute of Earth Sciences, Heidelberg University, Germany 2Wilhelm-Ostwald-Institute, Leipzig University, Germany 51st ESLAB Symposium - Extreme Habitable Worlds ESA ESTEC, The Netherlands The Solar System‘s ocean worlds Steve Vance; NASA/JPL-Caltech December 6, 2017 2 The Solar System‘s ocean worlds Steve Vance; NASA/JPL-Caltech December 6, 2017 3 Sampling dust and ice particles in space E ring NASA/JPL December 6, 2017 4 The Cosmic Dust Analyzer (CDA) Chemical Analyzer subsystem (CA) § Sensitive to cations § Determines impact rates, mass, speed, electric charge, and composition § Mass resolution: ≤ 50 m/Dm § Maximum recorded mass: ca. 200 u Srama et al. 2004 December 6, 2017 5 Analog experiment: IR-FL-MALDI-ToF-MS IR Laser adapted from Beinsen 2011 § Liquid beam: r = 7.5 µm § Laser: l = 2480 nm; I ≤ 1152 MW/cm2 § Vaccum chamber: P = 5 x 10-5 mbar § ToF-MS: R = 700 – 800 m/Dm December 6, 2017 6 Comparison of the impact mechanisms of CDA and the analog experiment CDA Analog experiment Postberg et al. 2009 December 6, 2017 7 Comparison of the impact mechanisms of CDA and the analog experiment CDA Analog experiment Postberg et al. 2009 Khawaja 2016 December 6, 2017 8 Future missions and Enceladus Ice Analyzer (ENIA) § Sensitive to cations and anions § Mass resolution > 2000 m/Dm § Maximum recorded mass: 2000 -
Marine Oil Fatty Acids Named
Method MARINE1 Page 1 Method: MARINE1 MARINE OIL ANALYSIS Version: 1.02 Description: Marine Oil Fatty Acid Analysis Naming Table: Index Peak Name IUPAC / Systematic Name Other Names 1 10:0 Decanoic Acid Capric Acid 2 11:0 iso 9-Methyldecanoic Acid 9-Methylcapric Acid 3 11:0 anteiso 8-Methyldecanoic Acid 8-Methylcapric Acid 4 11:0 Undecanoic Acid Undecylic Acid 5 10:0 2OH 2-Hydroxydecanoic Acid 2-Hydroxycapric Acid 6 10:0 3OH 3-Hydroxydecanoic Acid 3-Hydroxycapric Acid 0 Phthalate 1 --- --- 7 12:0 iso 10-Methylundecanoic Acid Isolauric Acid 8 12:0 anteiso 9-Methylundecanoic Acid Anteisolauric Acid 9 12:3 w3c (3Z, 6Z, 9Z)-3,6,9-Dodectrienoic Acid --- 10 12:1 w5c (7Z)-7-Dodecenoic Acid --- 11 12:0 Dodecanoic Acid Lauric Acid 0 11:0 iso 3OH 3-Hydroxy-9-Methyldecanoic Acid --- 12 13:0 iso 11-Methyldodecanoic Acid Isotridecanoic Acid 13 13:0 anteiso 10-Methyldodecanoic Acid Anteisotridecanoic Acid 14 13:1 w5c (8Z)-8-Tridecenoic Acid --- 15 13:1 w4c (9Z)-9-Tridecenoic Acid --- 16 13:1 w3c (10Z)-10-Tridecenoic Acid --- 17 13:0 Tridecanoic Acid Tridecylic Acid 0 12:0 2OH 2-Hydroxydodecanoic Acid 2-Hydroxylauric Acid 18 14:1 iso w7c (6Z)-12-Methyl-6-Tridecenoic Acid --- Printed on 27-Feb-2018 Method MARINE1 Page 2 19 14:0 iso 12-Methyltridecanoic Acid Isomyristic Acid 20 14:0 anteiso 11-Methyltridecanoic Acid Anteisomyristic Acid 21 14:1 w9c (5Z)-5-Tetradecenoic Acid --- 22 14:3 w3c (5Z, 8Z, 11Z)-5,8,11-Tetradectrienoic Acid --- 23 14:1 w7c (7Z)-7-Tetradecenoic Acid --- 24 14:1 w5c (9Z)-9-Tetradecenoic Acid Myristoleic Acid 25 15:0 aldehyde Pentadecanal -
Fatty Acids, Trivial and Systematic Names
FATTY ACIDS, TRIVIAL AND SYSTEMATIC NAMES Trivial Name Systematic Name Abbreviation Formic Acid Methanoic Acid Acetic Acid Ethanoic Acid Propionic Acid Propanoic Acid Butyric Acid Butanoic Acid 4:0 Valerianic Acid Pentanoic Acid 5:0 Caproic Acid Hexanoic Acid 6:0 Enanthic Acid Heptanoic Acid 7:0 Caprylic Acid Octanoic Acid 8:0 Pelargonic Acid Nonanoic Acid 9:0 Capric Acid Decanoic Acid 10:0 Obtusilic Acid 4-Decenoic Acid 10:1(n-6) Caproleic Acid 9-Decenoic Acid 10:1(n-1) Undecylic Acid Undecanoic Acid 11:0 Lauric Acid Dodecanoic Acid 12:0 Linderic Acid 4-Dodecenoic Acid 12:1(n-8) Denticetic Acid 5-Dodecenoic Acid 12:1(n-7) Lauroleic Acid 9-Dodecenoic Acid 12:1(n-3) Tridecylic Acid Tridecanoic Acid 13:0 Myristic Acid Tetradecanoic Acid 14:0 Tsuzuic Acid 4-Tetradecenoic Acid 14:1(n-10) Physeteric Acid 5-Tetradecenoic Acid 14:1(n-9) Myristoleic Acid 9-Tetradecenoic Acid 14:1(n-5) Pentadecylic Acid Pentadecanoic Acid 15:0 Palmitic Acid Hexadecanoic Acid 16:0 Gaidic acid 2-Hexadecenoic Acid 16:1(n-14) Sapienic Acid 6-Hexadecenoic Acid 16:1(n-10) Hypogeic Acid trans-7-Hexadecenoic Acid t16:1(n-9) cis-Hypogeic Acid 7-Hexadecenoic Acid 16:1(n-9) Palmitoleic Acid 9-Hexadecenoic Acid 16:1(n-7) Palmitelaidic Acid trans-9-Hexadecenoic Acid t16:1(n-7) Palmitvaccenic Acid 11-Hexadecenoic Acid 16:1(n-5) Margaric Acid Heptadecanoic Acid 17:0 Civetic Acid 8-Heptadecenoic Acid 17:1 Stearic Acid Octadecanoic Acid 18:0 Petroselinic Acid 6-Octadecenoic Acid 18:1(n-12) Oleic Acid 9-Octadecenoic Acid 18:1(n-9) Elaidic Acid trans-9-Octadecenoic acid t18:1(n-9) -
(12) United States Patent (10) Patent No.: US 9,655,847 B1 Halwani Et Al
US0096.55847B1 (12) United States Patent (10) Patent No.: US 9,655,847 B1 Halwani et al. (45) Date of Patent: May 23, 2017 (54) THERAPEUTIC LIPOSOME AND METHOD (56) References Cited OF TREATING ASUBJECT HAVING CANCER U.S. PATENT DOCUMENTS 5,731,346 A * 3/1998 Egberg................... A61K 31, 20 (71) Applicants:National Guard Health Affairs, 514,458 Riyadh (SA); King Saud bin 2002/0146448 A1* 10, 2002 KOZbor .................. A61K 9,127 Abdulaziz University for Health 424/450 2007/0116753 A1* 5/2007 Hong ................... A61K9/0019 Sciences, Riyadh (SA); King Abdullah 424/450 International Medical Research 2011/0274746 A1* 11/2011 Schmidt ................. A61K 9,127 Center, Riyadh (SA) 424/450 2012/0076795 A1 3/2012 Debs (72) Inventors: Majed Abdulaziz Saleh Halwani, 2012/0288558 A1* 11/2012 Gabizon .............. A61K 31,337 Riyadh (SA); Moayad Abdulaziz 424/450 Alhariri, Riyadh (SA) (Continued) (73) Assignees: National Guard Health Affairs, FOREIGN PATENT DOCUMENTS Riyadh (SA); King Saud bin EP O 198765 A2 10, 1986 Abdulaziz University for Health EP O 198765 A3 10, 1986 Sciences, Riyadh (SA); King Abdullah WO WO 2011 (143271 A2 11/2011 International Medical Research Center, Riyadh (SA) OTHER PUBLICATIONS (*) Notice: Subject to any disclaimer, the term of this PG Rose. “Pegylated Liposomal Doxorubicin: Optimizing the Dos patent is extended or adjusted under 35 ing Schedule in Ovarian Cancer.” The Oncologist, vol. 10, 2005, pp. U.S.C. 154(b) by 0 days. 205-214. (Continued) (21) Appl. No.: 15/212,389 Primary Examiner — Isaac Shomer (22) Filed: Jul. 18, 2016 (74) Attorney, Agent, or Firm — Oblon, McClelland, Maier & Neustadt, L.L.P.