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Sincere efforts entrapped data, regarding modified forms of RF values are determined by specified formula as per the
(Isomers and active site analogues) of both the bioactive method notified by [4].
components recorded positive impact on human health Distance travelled by spot
which is very close to pharmaceutical drugs obtained by Rf =
purification and characterization processes. The paucity of Distance travelled by solvent
cutting edge applications in formulation and development of F. Characterization of curcumin by high performance
functional foods remained deprived off health benefits liquid chromatography (HPLC)
confirmatory index dully associated with top to down
Review base sorted out unique salem curcumin sample
(Animal to human studies) roadmap model of clinical
along with standard curcumin (Sigma Aldrich) were
assessment.
analyzed by HPLC for molecular separation. The selectivity
In the present investigation sincere efforts are made to
of column C18 [14] based on characterization data of earlier
design the research projects based on molecular
scientists gave way to set up anticipated experimental process
transformation, characterization and food constituent
governed by 20µl sample injection followed by elution with
accessible technology development to justify need base
gradient solvent system (flow rate of 1.0ml/min,25 oC
anticipatory antioxidant efficacy. The isomerization of
temperature) and mobile phase developed with ethanol and
lycopene and demethoxylation of curcumin emerged out as a
methanol. The results are tabulated by wavelength (254nm)
paradigm to change the philosophy of nutraceutical base
generative data.
formulation of functional foods to justify futuristic
contributory share in rejuvenation of agro base industry G. Antioxidant activity determination
portfolio. Antioxidant activity of both the bioactive compounds is
determined by DPPH (Free radical) assay as a commercial
II. MATERIALS AND METHODS experimental asset to determine free radical scavenging
efficacy with requisite volume of antioxidant through
A. Preparation of processed tomato puree: Lycopene reduction process. DPPH as a free radical scavenger is
case study allowed to react with known volume of crude antioxidant
Tomato puree prepared by using deep red colored tomatoes extract (Lycopene and curcumin) for holding period of 30
(Local cultivar) through enforced tissue maceration process minutes. The relative changes in optical density (O.D.) are
in screw type extractor, strained (100 mesh sieve) and directly related to free radicals scavenging efficacy and
homogenized as per the method described by [9]. further represented as antioxidant activity facilitated by the
B. Thermal processing of tomato puree equation.
AbsorbanceControl- AbsorbanceSample
The homogenized tomato puree was further processed by
Inhibition (%) = X100
thermal treatment at 900C for 1hto assess effect of heat AbsorbanceControl
treatment on lycopene isomerization. Lycopene extraction Per cent inhibition was plotted against concentration and
was undertaken by standard extraction procedure using IC50 was calculated on relative volume basis. Ascorbic acid
petroleum ether [10]. was used as a standard to co-relate IC50 of lycopene enriched
C. Characterization of lycopene puree.
Lycopene characterization with respect to all trans and cis
isomers was assessed for unique type of lycopene extracts III. RESULTS AND DISCUSSION
(Raw tomato puree and thermal treated puree - 900C for 1h) Food science and technology research philosophy is
using High Performance Liquid Chromatography (HPLC) rightly coiling around targeted functional scenario of
system with non-polar C30 chromatographic column and specialty group of foods notified as functional foods.
peaks were eluted with gradient solvent system of methanol: Molecular characterization driven efficacy of lycopene and
methyl-tert-butyl ether using 472nm wavelength [11]. The curcumin has vibrant potential ingredient accessibility to
data and chromatograms were compiled, compared with modulate formulation mechanism of functional foods in
standard lycopene and quantitative analysis was carried out collaboration with advanced processing technology. The
on the basis of peak area measurements. strategic action plan of present investigation has also
absolutely focused on molecular reorientation of natural
D. Extraction of curcumin from turmeric
antioxidants to underline their functional efficacy.
Curcumin extraction is undertaken as per the standardized
process technology developed by earlier scientists from the A. Characterization of lycopene (All trans and cis
selected cultivars – Salem, Rajapuri and Local [12], [13]. isomers)
HPLC chromatogram profile generative data of reference
E. Thin layer chromatographic assessment for
separation of curcuminoids and tomato puree lycopene presented in following figures
(Fig. 1, 2 and 3) clearly
Thin layer chromatographic separation of curcuminoids,
leading to three components (Curcumin, Demethoxy
curcumin, Bisdemethoxy curcumin), quantified on the basis
processing parameters (time and temperature- 64o C) [18]. C DMC BDMC BDMC activity(%
Quotie Inhibition)
More over optimum efficacy governing index likely to be nt (DPPH)
presented as DMC/BDMC quotient has unique type of Salem 0.71 0.62 0.32 1.94 52.31
feature to justify potential antioxidant efficacy getting Standard 0.75 0.55 0.27 2.03 61.70
deviated during processing of food products as an active curcumin
ingredient because of application of heat. The data on *Each observation is an average of three determinations.
DMC/BDMC quotient from table no.2 is self- explanatory C= Curcumin
to notify the impact of processing technology. DMC = Demethoxycurcumin
DMC/BDMC quotient value (1.94) of salem cultivar BDMC= Bisdemethoxycurcumin
recorded to be very close to reference value of standard Table III: HPLC base curcumin characterization
curcumin (2.03). (Salem)
Commercial curcumin review base reported value of Curcumi
DMC/BDMC quotient admissible to calculate on n base Expect Identific Retenti Area Area Yield
ed No. ation of on time (mAU* (%) Curcu
fractionation of DMC and BDMC (18/5=3.6) [19] that of Peak Peak (Min) S) min
(%)
might have represented by quoting Sigma Aldrich as a Salem 02 peaks
reference curcumin. The requisite proportion of both the
1
analogues appeared to be at par with the standard that may Unknow 2.243 162.474 0.808
be expected in multiple times. Heat treatment being one of n 0 0
the prime parameter of processing may have direct impact
on demethoxylation causing deviation in antioxidant 2 Curcumi 3.615 1.9946 99.19 42.60
n 20
efficacy. Monitoring of antioxidant efficacy of curcumin Sigma 1
molecule to cutting edge bismethoxylation during Aldric Curcumi 3.601 4.5802 100.0
h std n 00
successive demethoxylation results in sustainability of curcu
DMC/BDMC quotient value responsible for optimum free min
The isomer base trans/cis quotient (25.84 and 33.40 for 18. B. T. Kurien, H. Matsumoto and R. H. Scofield, (2017). “Nutraceutical
value of pure curcumin”. Pharmacognasy Magazine. pp. 161-163.
raw and processed tomato puree) of lycopene and 19. P. Basnet, and N. S. Basnet (2011). “Curcumin: anti- inflammatory
demethoxylation base DMC/BDMC quotient (1.94 and 2.03 molecule from a curry spice on the path to cancer treatment”.
for salem cultivar and standard curcumin) emerged out from Molecules.16, pp. 4567-4598.