Nutrition enriched edible coating on baby carrots . . .
which exhibits vitamin E activity and in vivo antioxidant ef- scribed by Lawless and Heymann (1999). Sensory quality at-
fects as the result of enzymatic cleavage of the acetate ester tributes applied in this study include white surface discolora-
(Gregory III, 1996).
tion, orange color intensity, fresh aroma, fresh flavor, bitter-
ness, sweetness, crispness, and slipperiness. An unstructured
10 points scale was used with 0 = none, and 10 = intense. Car-
rots from each treatment were coded with different 3-digit ran-
dom numbers and placed at room temperature under fluores-
cent light for evaluation. Panelists were served with 8 carrots at
each session, 2 from each treatment. Panelists were asked to
rinse their mouths with distilled water and use crackers be-
tween tasting different samples. Four replicates were per-
formed for sensory quality evaluation.
Preparation of coating solutions
Xanthan gum coating was prepared by dissolving 0.3% xan-
than gum into distilled water. Xanthan gum/vitamin E coating
was manufactured by the following steps: 1) heating 1 liter of
0.3% xanthan gum solution to 60 °C; 2) dissolving 0.2% ␣–toco-
pherol acetate into 0.8% of acetylated monoglyceride based on
the weight of xanthan gum solution prepared as above; and 3)
integrating dissolved ␣–tocopheral acetate into xanthan gum so-
lution, and homogenizing the mixture using a homogenizer
(Brinkman Model PT10/35, Westbury, N.Y., U.S.A.) for 1 min with
the speed setting of 5. Xanthan gum/calcium coating was pre-
–carotene and –tocopheral acetate analysis
The analyses of –carotene and ␣–tocopheral acetate were
pared by dissolving 5% Gluconal Cal into the xanthan gum solu- conducted using a modified method from Howard and Dewi
tion prepared in step 1). All ratios in this study were on the (1996). Fifty g of the carrot tissue from each treatment was
weight basis.
ground in a Handy chopper (Black & Decker, Shelton, Conn.,
U.S.A.). A 10-g sample was then homogenized in 70 mL acetone
containing 0.04 g BHT and 1 g MgCO3. After filtering through
Na2SO4 on Whatman #4 filter paper, the residue was re-homog-
enized and re-filtered until the remaining residue was colorless.
Filtrates were concentrated using hexane on a rotary vacuum
evaporator (Dietz and others 1988) where the temperature was
set to be 40 °C to speed the concentration. The filtrates were
then pooled and adjusted to 100 mL with hexane. Twenty-five
mL of the filtrate was injected into a HPLC system for analysis.
–carotene and ␣–tocopheral acetate were simultaneously
measured using external standards by reversed-phase HPLC
utilizing isocratic elution with 2 detectors. The HPLC system
used in this study included a Waters model 510 pump and an
automated injection system (Model 717, Waters Associates, Mil-
ford, Mass., U.S.A.), connected in series to 2 absorbance detec-
tors, 1 detector set at 450 nm for –carotene and the other set at
285 nm for ␣–tocopheral acetate measurement. A C–18 5mm
Varian column (Varian Analytical Instruments, Walnut Creek,
Calif., U.S.A.) was used, and the mobile phase for chromatogra-
phy was acetonitrile/dichloromethane/methanol/1–octanol
(90:15:10:0.1, v/v/v/v), which was filtered through a 0.45mm
nylon filter before use (Barua and others 1993). The flow rate
was adjusted to 1.5 mL/min. For carotene analysis, only –caro-
tene was quantified since it is the predominant carotenoid
present in the carrots.
Sample preparation
Peeled baby carrots (unknown cultivar) packaged in polyeth-
ylene bags were purchased from a local supermarket when it ar-
rived immediately from the supplier. It was confirmed from the
supplier that no prior treatments had been applied on the car-
rots except washing. Carrot samples were carefully selected for
uniformity and randomly assigned for 4 dipping treatments: dis-
tilled water used as control, 0.3% xanthan gum solution, 0.3%
xanthan gum carrying 0.2% ␣–tocopheral acetate, and 0.3% xan-
than gum carrying 5% Gluconal Cal. Carrot samples were dipped
in above solutions for 30 s, drained on a stainless steel grill for 1 h
at ambient condition, and then packaged in perforated low den-
sity polyethylene bags (S.C.Johnson and Sons, Inc.) Racine, Wis.,
U.S.A.). All samples were stored on racks of a cooler at 2 °C and
85% RH without light. Samples were removed at the end of 7, 14,
and 21 d for color measurement and sensory evaluation, and also
were removed on 1, 7, 14, and 21 d for –carotene and ␣–toco-
pheral acetate analyses. As calcium is a stable mineral, calcium
determination was only conducted on 1 and 21 d. Four replica-
tions for each measurement were conducted where each replica-
tion used 2 to 10 carrot subsamples based on specific measure-
ment described below.
Color measurement
A Minolta Spectrophotometer (model CM-508d, Minolta Co.,
Ltd., Ramsey, N.J., U.S.A.) was used for color evaluation on L
(lightness), a (redness), and b (yellowness) values. Two readings
on different sites of each carrot were averaged for color measure-
ment of 1 carrot. Ten carrots from each treatment were used for 1
replication. The severity of surface white coloration was estimat-
ed by Whiteness Index (WI, in the range of 0 to 100), which is ex-
pressed as (Bolin and Huxsoll, 1991):
Calcium determination
A representative sample of up to 0.5 g from each treatment
was put in a fluorocarbon microwave vessel with 10 mL of con-
centrated nitric acid. The digestion was performed with the ves-
sel capped and heated using microwave heating in a discreet
flow automated microwave digestion unit (Qprep 5000, Ques-
Tron Technologies Corporation, Mississauga, Ontario, Canada)
for 30 min. After cooling, the vessel contents were filtered and
adjusted to 100 mL for analysis by Inductively Coupled Plasma
Optical Emission Spectrometer (Perkin Elmer Optima 3300XL,
Shelton, Conn., U.S.A.), which measured characteristic emission
spectra by optical spectrometry according to Method 6010B in
SW-846 (EPA 2000)
WI = 100 – ((100 – L)2 + a2 + b2)0.5
The numerical scale of WI is from 0 to 100, where higher WI
values represent more severe white surface discoloration.
Sensory evaluation
Statistical analysis
Sensory quality of carrots was conducted at 1, 2, and 3 wk of
storage. The sensory panel utilized was composed of 10 trained
panelists from the faculty, staff, and graduate students of the
Nutritional Science Department, University of Connecticut.
Panelists were selected and trained by a procedure as de-
Data were analyzed by analysis of variance (ANOVA) using
SAS (SAS 1988). General linear model (GLM) procedures were
performed (p<0.05) for all the treatments at different sampling
times.
Vol. 67, Nr. 5, 2002—JOURNAL OF FOOD SCIENCE 1965