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Dominant chemical compound of chicken bile extract

Tuty S.a, Fidrianny I.a, Sukrasnoa

a Department of Pharmaceutical Biology, School of Pharmacy, Bandung Institute of Technology, Bandung, 40132, Indonesia

[vc_row][vc_column][vc_row_inner][vc_column_inner][vc_separator css=”.vc_custom_1624529070653{padding-top: 30px !important;padding-bottom: 30px !important;}”][/vc_column_inner][/vc_row_inner][vc_row_inner layout=”boxed”][vc_column_inner width=”3/4″ css=”.vc_custom_1624695412187{border-right-width: 1px !important;border-right-color: #dddddd !important;border-right-style: solid !important;border-radius: 1px !important;}”][vc_empty_space][megatron_heading title=”Abstract” size=”size-sm” text_align=”text-left”][vc_column_text]© 2020 J. K. Welfare and Pharmascope Foundation All rights reserved.The purpose of this research is to study the dominant chemical compounds of chicken bile extract. Chicken bile, which is usually disposed of as useless waste, is made a choice. The study began with material collection from native chicken farmers, Kluwut Village, Bulakambah sub-district, Brebes Regency, Central Java. The determination was carried out at Bandungense Herbar-ium School of Biological Science and Technology-ITB. The choice of animals were native chickens. They belonged to the family Phylum: Chordata, Class: Aves, Nation: Galliformes, Tribe: Phasianidae, Surname: Gallus, Type: Gallus gallus Linn, The common name: native chicken (Indonesia), and domes-tic fowl in English.The bile portion was cut into small pieces and dried using a freeze dryer. The reflux method was then extracted using solvents with a different polarity, which are n-hexane, ethyl acetate, and ethanol. It gave out n-hexane extract, ethyl acetate extract, and ethanol extract.The extracts were evaporated using a rotary evaporator.The percentage of the obtained yield was n-hexane extract 7.63%, ethyl acetate extract 8.61%, and ethanol extract 34.91%. Selected extract ethyl acetate extract was fractionated by Vacuum Liquid Chromatography (VLCI) and was monitored by a thin layer of Chromatography (TLC). Then fraction 5-6 was continued to sub fractionation by Classical Column Chromatography (CCC). Nuclear Magnetic Reso-nance (NMR) investigated isolate X and found that isolate X appeared to be cholesterol. From the second fractionation (VLCII), fraction 2-7 proceeded to the VLCIII, and then subfraction 7 was evaluated using GC-MS. The dominant chemical compounds of subfraction 7 were oleic acid 38.72%, n-hexadecanoic acid (35.6%), octadecanoic acid (17.94%), palmitoleic acid (1.53%).[/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”Author keywords” size=”size-sm” text_align=”text-left”][vc_column_text][/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”Indexed keywords” size=”size-sm” text_align=”text-left”][vc_column_text]Chemical compound,Chicken bile,Dominant[/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”Funding details” size=”size-sm” text_align=”text-left”][vc_column_text][/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”DOI” size=”size-sm” text_align=”text-left”][vc_column_text]https://doi.org/10.26452/ijrps.v11i2.2274[/vc_column_text][/vc_column_inner][vc_column_inner width=”1/4″][vc_column_text]Widget Plumx[/vc_column_text][/vc_column_inner][/vc_row_inner][/vc_column][/vc_row][vc_row][vc_column][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][/vc_column][/vc_row]