TY - JOUR
T1 - Reduction of curcuminoid extract from turmeric (Curcuma longa) rhizomes and its antibacterial activities
AU - Dewi, S. Q.
AU - Saepudin, E.
AU - Rahayu, D. U.C.
N1 - Publisher Copyright:
© Published under licence by IOP Publishing Ltd.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020
Y1 - 2020
N2 - Curcuminoid is an active compound of turmeric rhizomes commonly used as yellow pigment. In some cases, the presence of pigment in beauty product is not desirable due to its aesthetics effect. In this study, yellow color removal of curcuminoid was carried out by two steps hydrogenation, i.e. using LiAlH4 followed by Pd-C catalyst to form dihydrocurcuminol and hexahydrocurcuminol derivatives, respectively. Dihydrocurcuminol derivatives had successfully synthesized by observing a wavelength shift from 419 to 428 nm in UV-Vis spectra and FTIR spectra also showed a reduction intensity of the carbonyl groups at 1600 cm-1. Moreover, hexahydrocurcuminol derivatives were identified at 283 nm in UV-Vis spectra while in FTIR spectra showed an absorption band of C-H sp3 at 2942 cm-1. Curcuminoid and hexahydrocurcuminol derivatives were evaluated for their antibacterial activities against Staphyloccocus aureus with 2 and 2.5 mm and Fusobacterium nucleatum with 4 and 2.75 mm inhibitory zone diameter, respectively. It can be concluded that curcuminoid and hexahydrocurcuminol derivatives had a weak antibacterial activity against both bacteria tests.
AB - Curcuminoid is an active compound of turmeric rhizomes commonly used as yellow pigment. In some cases, the presence of pigment in beauty product is not desirable due to its aesthetics effect. In this study, yellow color removal of curcuminoid was carried out by two steps hydrogenation, i.e. using LiAlH4 followed by Pd-C catalyst to form dihydrocurcuminol and hexahydrocurcuminol derivatives, respectively. Dihydrocurcuminol derivatives had successfully synthesized by observing a wavelength shift from 419 to 428 nm in UV-Vis spectra and FTIR spectra also showed a reduction intensity of the carbonyl groups at 1600 cm-1. Moreover, hexahydrocurcuminol derivatives were identified at 283 nm in UV-Vis spectra while in FTIR spectra showed an absorption band of C-H sp3 at 2942 cm-1. Curcuminoid and hexahydrocurcuminol derivatives were evaluated for their antibacterial activities against Staphyloccocus aureus with 2 and 2.5 mm and Fusobacterium nucleatum with 4 and 2.75 mm inhibitory zone diameter, respectively. It can be concluded that curcuminoid and hexahydrocurcuminol derivatives had a weak antibacterial activity against both bacteria tests.
UR - http://www.scopus.com/inward/record.url?scp=85096504362&partnerID=8YFLogxK
U2 - 10.1088/1757-899X/902/1/012072
DO - 10.1088/1757-899X/902/1/012072
M3 - Conference article
AN - SCOPUS:85096504362
SN - 1757-8981
VL - 902
JO - IOP Conference Series: Materials Science and Engineering
JF - IOP Conference Series: Materials Science and Engineering
IS - 1
M1 - 012072
T2 - 4th International Symposium on Current Progress in Functional Materials, ISCPFM 2019
Y2 - 6 November 2019 through 7 November 2019
ER -