Summary of a research project funded by the National Honey Board and
conducted at the University of Nebraska-Lincoln. Investigator: M.B. Preston
Ergogenic, organic, “all-natural”, nutraceutical–these buzzwords often bring success to products whose labels display them. In this age of ever-growing awareness of functional, natural foods, both honey and herbs are favorites among consumers interested in health. Teas, herbal drinks, fruit-based drinks and sodas sweetened with honey are growing in popularity. In these non-alcoholic beverages, honey serves as a carbohydrate/high energy source and provides flavor, sweetness, color and mouthfeel. However, the market for combining honey with botanical ingredients remains relatively untapped.
The goal of this project was to develop two fruit juice beverages containing
honey
and botanicals. Juice beverages containing ginseng or chamomile and sweetened
with honey would have great appeal to today’s consumers. The two
main objectives of this project were 1) to formulate two different types
of non-alcoholic beverages utilizing honey as the sole sweetener source
and 2) to
characterize the effects of the addition of liquid clover honey on non-alcoholic
juice beverages. Specific objectives were as follows:
Cranberry juice and lemonade-type beverages were developed. Both
beverages were formulated with fruit juice as a base. Each juice drink
contained
vitamin C and the tart flavors were a pleasant complement to the sweetness
of honey. The botanicals used in the cranberry juice-based beverage were guarana and
ginseng. Guarana has a high caffeine content, providing a “boost” to
the central nervous system, while ginseng provides a counter effect and
produces an adaptogenic effect. The lemon juice beverage contained chamomile,
which produces a calming effect.
The juice-based beverages were diluted to a lower percent soluble
solids content (oBrix) with distilled water. Concentrated, unsweetened
cranberry juice (oBrix: 50 ±0.1) was diluted to standard strength
(oBrix: 7.5). Unsweetened, single-strength lemon juice was used. Both beverages
were sweetened with liquid, grade A, white clover honey and combined with
botanical extracts. Extensive flavor development in both beverages was
necessary. Several flavors were evaluated before finalizing the finished
prototypes (Tables 1 and 2).
The colors of the guarana and ginseng extracts were very dark and did not present a problem in the dark-colored cranberry juice. However, in the lighter-colored lemon juice beverage, the chamomile extract turned the beverage a dark, gray-brown color. A fluid extract of chamomile (a much lighter-colored extract) was obtained and the color problem was resolved. The standard extracts of guarana and ginseng were extremely concentrated, requiring preparation of stock solutions to facilitate handling and weighing. Concentration of standard ginseng extract is 5:1 or 5x. According to recommendations from the botanical manufacturer, the target level for ginseng is 3000 milligrams per 10 ounce serving of juice beverage. Therefore, a 1x concentration stock solution was developed (four parts water were added to one part extract).
Standard guarana extract contains 10% caffeine. The target level for guarana is 250 to 500 milligrams per serving, or 2.5 milligrams to 10milligrams of caffeine per serving. Therefore, the guarana was diluted to !% caffeine (1 part standard extract to 9 parts water). The amount of stock solution used was based upon the dilution and desired target levels.
During the formulation phase, the beverages were mixed cold and held
refrigerated until evaluation. However, for shelf life studies the beverages
were
mixed and pasteurized. Prior to mixing with water, flavors and botanicals,
the honey was heated to facilitate blending. The blended beverages were
pumped through a coil pasteurizer, using a Masterflex pump, and heated
to 165 °F. The processing temperature of 165 °F was determined
in relation to the pH of the prototypes and was sufficient for pasteurizing
both beverages. The pasteurized product was filled hot into clean,
eight-ounce glass jars. The jars were capped using a plastisol-lined cap, inverted and allowed
to cool. The processed samples were stored upright in the dark at 70 ºF.
Shelf-life studies were conducted to evaluate color, pH, percent soluble
solids, clarity, sedimentation and microbial stability. The two honey-sweetened
juice-based products were processed and stored for 6 months at 70 ?F in
the dark.
Samples were evaluated and analyzed in triplicate at day 0, 3 months (90
days) and 6 months (180 days).
Beverage color was evaluated using a Minolta Chroma Meter CR-300 programmed
for the Hunter Lab Color System (Minolta Corporation, Instrument Systems,
Ramsey, NJ). The Hunter Lab Color system determines values for
perceived color. Lightness is expressed as a “L” value, while “a” and “b” values indicate
chromaticity coordinates. Lightness was expressed as dark to light with 0=black
and 100=white. Green to red was expressed by the “a” value.
A more positive value represented red, while a more negative value represented
green (-80=green, 100=red). Blue to yellow was expressed by the “b” value.
A more positive value represented yellow and a more negative value represented
blue (Tables 3 and 4).
An Orion ionAnalyzer, model EA 920, with a Ross Sure-flow combination
glass body electrode, was used for pH studies (Table 5). The Ross
Sure-flow electrode provided a free-flowing sleeve junction designed for
measurements
of viscous or colloidal samples. The pH meter was calibrated utilizing
standard solutions of pH 7.0 and 4.01. As expected, pH of the beverage
systems did not change during storage.

Percent soluble solids (refractive index) of the beverages samples were
measured in °Brix using a ReicherJung hand-held refractometer (model
10431,
Cambridge Instruments, Buffalo, NY). Brix (range 0-50 degrees) was measured
in sucrose equivalents by placing a drop of sample on a prism. Refractometry
is when a ray of electromagnetic radiation strikes a flat surface at an
angle. The ray may be bent upward (reflected) or bent downward (refracted).
The amount of refraction defines the concentration of a solute in a solution.
The refractive index of the lemon and cranberry juices did not change
in both beverage systems during storage (Table 6).
Clarity of juice samples was evaluated with a Lambda 3 Double-Beam UV-Visible Spectrophotometer (a electoroptical mechanical instrument utilizing a reflecting Littrow monochromator, Perkin Elmer, Norwalk, CT). The spectrophotometer was set at 650 nm wavelength. Distilled water was used as a reference for zeroing. Samples were placed in cuvettes, inserted into the sample port and measurements were recorded. Clarity was not effected in the lemon and cranberry beverages during storage (Table 7).

Sedimentation was analyzed by measuring the thickness of sediment at the bottom of beverage containers (beverage samples were stored in eight-ounce clear glass containers). The amount of sedimentation increased for lemon and cranberry samples over time (Table 8). The greatest amount of sedimentation was observed on day 180 for both beverages. However, less sedimentation was found in the lemon-based beverage.
Beverage samples were analyzed for lactic acid content and yeast and
mold
growth during six-month storage. Microbial analysis provides valuable
information about the effectiveness of pasteurization in beverage production
and the effect of time on beverage stability. As expected, microbial
counts for all test dates were below detectable levels, indicating the
beverage
systems were stable during storage. Results revealed there was minimal
microbial load present in the fruit beverages (Tables 9 and 10).

*One of the triplicate samples resulted in an unusually high value. The other two samples resulted in zero yeast growth.
A modified hedonic scale was used to determine overall liking and acceptability of appearance, texture, flavor and overall acceptability in the lemon and cranberry beverages. Beverage samples were also evaluated for specific attributes such as lemon and chamomile flavors (lemon-chamomile beverage) or cranberry flavor (cranberry beverage). Two sensory panels analyzed 2 samples of each beverage on test days–giving a total of 4 replications. Significant differences (p?0.05) were found in the general flavor and the chamomile flavor for the honey, lemon-chamomile beverage. The flavor attribute was found to be more acceptable on day 90. On day 180 the flavor acceptability decreased to that found on day 0. The acceptability of the chamomile flavor increased (p?0.05) on day 90 and this level of acceptability was still present on day 180. All other attributes increased numerically on day 90 and then decreased on day 180. However, the values were not significantly different (Table 11). The data indicate optimum storage time at 70 ?F for the lemon-chamomile beverage was 90 days.
*Where 9=like extremely, 5=neither like nor dislike and 0=dislike extremely. Means with different number superscripts in a column are significantly different at p=0.05.
Appearance was the only attribute that indicated a significant loss (p>0.05)
of acceptability over storage time in the cranberry beverage. All other
attributes demonstrated the same trend as seen in the lemon-chamomile
beverage Acceptability was optimal on day 90 of storage. The differences
in the cranberry
beverage were all significant (p>0.05) over time (Table 12).
Honey-sweetened, nonalcoholic beverages combined with botanicals were
successfully produced. Shelf-life studies revealed very little change
in beverage color, pH, percent soluble solids and clarity during six month
storage. The amount of sedimentation increased in both beverages over
time. However the lemon-chamomile beverage had less sedimentation compared
to the cranberry beverage. Both beverages were microbiologically stable
during storage. Sensory analysis revealed the lemon-chamomile and cranberry juice drinks were
acceptable for 180 days, with the highest degree of acceptability at 90
days.
©2007 National Honey Board
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