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Cr 400 410

Manufactured by Konica Minolta
Sourced in Japan, China, United States

The CR-400/410 is a color and gloss measurement device developed by Konica Minolta. It is designed to measure the color and gloss of a wide range of materials and surfaces. The device uses advanced optical technology to capture accurate color and gloss data.

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15 protocols using cr 400 410

1

Color Measurement of Food Samples

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The color of the samples was expressed using the CIELAB system: L* (lightness, whiteness or brightness), a* (redness or greenness), and b* (yellowness or blueness) [16 (link)]. The measurements were performed using an automatic color chroma meter (CR-400/410, Konica Minolta Sensing Inc., Tokyo, Japan). A fixed amount, about 15 mL, of samples was poured into the measurement cell. Three replicates of each sample were measured.
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2

Colorimetric Analysis of CIElab Parameters

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The CIElab (L*, a*, and b*) color space was monitored using a colorimeter (CR-400/410, Konica Minolta, Japan). The L* represents brightness, the a* denotes redness (+)/greenness (−), and the b* displays yellowness (+)/ blueness (−). The chroma means color saturation, which varies from dull to vivid colors (low to high value), and is calculated by ((a*)2 + (b*)2) 1/2. The formula of the hue angle used is tan−1 (b*/a*), and ranged from red–purple to blue (0–270°).
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3

Instrumental Measurement of Banana Flour Color

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The banana flour color was measured by the instrumental measurement in triplicate using a Chroma Meter (CR-400/410, KONICA MINOLTA, Japan). Before getting the reading, the chroma meter was accurately calibrated using a standard white reference tile. The samples were collected and placed on top of a Glass Light-Projection tube (CR-A33f, Konica Minolta, Japan) while the reading was obtained. According to the Chroma meter, the L axis represented lightness (If, L* = 0; black and L* = 100; white). The redness to greenness was displayed on the a-axis as (if, a*-value = +a*; redder and a*-value = -a*; greener). However, the b*-value showed a change in color from yellow to blue (if b*-value = +b*, yellower, and b*-value = - b*, bluer).
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4

Quantitative Colour Analysis of Apples

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Colour changes on each apple fruit was measured based on Commission International del’ Eclairage (CIE) colour system using a digital Chroma-meter (CR 400/410 Konica Minolta Sensing Inc., Japan). Colour calibration of the chroma-meter was performed against a white and black tile background prior to each measurement. Colour measurements were taken using individual fruit (n = 3) and data obtained were average of individual colour parameters To describe the measured colour attributes hue angle (), which describes the qualitative attribute of colour shades (0° = red-purple and 180° = bluish-green), and Chroma (C∗), which denotes the quantitative attribute of colour intensity were calculated (Caleb et al., 2016 ) using Eqs. (2) and (3): h0=tan1(ba) C=(a)2+(b)2 where, L∗ denotes the lightness, a∗ describes red (+)/green (-) and b∗ for yellow (+)/blue (-).
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5

Chicken Wingette Color Analysis

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For the color analysis, a separate batch of chicken wingettes not inoculated with C. jejuni was allocated and coated with treatments as mentioned above. Following air-drying of wingette samples, color of the samples was measured using a chroma meter (CR 400/410, Konica Minolta Sensing Americas, Inc., Ramsey, NJ) as described previously (Wagle et al., 2017a (link)). The chroma meter provides information about 3 different colors (L, a, and b indicating relative lightness, redness, and yellowness, respectively). The instrument was calibrated against a tile, and average color values were recorded from 3 different locations on each sample. The samples were then vacuum-sealed to store at 4°C.
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6

Measuring Color Changes in Apple Slices

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The color of the apple slices was measured using a colorimeter (CR400/410, Konica Minolta, Shanghai, China). The colorimeter was first calibrated and then used to determine the color value of fresh and dried apple slices. All color measurements for each apple slice sample were performed in triplicate and averaged for calculation. Equation (1) was used to compute the overall color difference of the apple slices [26 (link)].
ΔEapple=(Lapple0*Lapple1*)2+(aapple0*aapple1*)2+(bapple0*bapple1*)2
where ΔEapple is the overall color difference value; Lapple0* , aapple0* , and bapple0* are the brightness, redness/greenness, and yellowness/blueness values of fresh apple slices, respectively; and Lapple1* , aapple1* , and bapple1* are the brightness, redness/greenness, and yellowness/blueness values of dried apple slices, respectively.
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7

Colorimetric Analysis of Apple Fruit

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Colour changes on each apple fruit exposed to VUV and control were measured based on Commission International del’ Eclairage (CIE) colour system using a digital Chroma-meter (CR 400/410 Konica Minolta Sensing Inc., Japan). Colour calibration of the chroma-meter was performed against a white and black tile background before each measurement. Colour measurements were taken using individual fruit n=6 and data obtained were average of individual colour parameters. To describe the measured colour attributes hue angle h0 , which describes the qualitative attribute of colour shades (0° red–purple and 180° bluish-green), and Chroma (C*), which denotes the quantitative attribute of colour intensity were calculated using Eqs. (4) and (5): h0=tan-1ba C=a2+b2 where, L* denotes the lightness, a describes red ( +)/green (−) and b describes yellow ( +)/blue (−).
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8

Color Analysis of Films

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The color of the films was determined on the CieLab scale by means of a colorimeter, model CR-400/410 (Konica Minolta, Foster City, USA). The parameters L* a* and b* were evaluated. The L* component corresponds to the luminosity. It ranges from 0 to 100 to describe the black and white color, respectively. The a* parameter describes the red (positive value) and green (negative value) colors. For the b* parameter, the positive values represent the yellow color, while negative values correspond to the blue color.
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9

Colorimetric Analysis of Polysaccharide Samples

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A colourimeter (CR-400/410 Konica Minolta Investment Co., Ltd., China) was utilised to measure the colour of the polysaccharide sample. Prior to conducting the measurements, the colourimeter was calibrated using a white standard plate. To ensure the accuracy of the experiment, three samples were randomly chosen from each group, with 5 points selected from each sample for further analysis. A colorimetric measurement based on the study by Yang et al. (2023) (link) assessed the brightness (L*), red/green (a*) and yellow/blue (b*) colour values.
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10

Non-Destructive Fruit Firmness Evaluation

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The firmness of the entire fruit was non-destructively measured using a method adapted from Tijskens [45 ]. A fruit hardness tester (FHM-1, Takemura, Japan) calibrated with a 1 kg weight and equipped with a 12 mm diameter probe was used. Seven readings were obtained for each fruit at two pared surfaces on the equator and recorded in units of N/cm2 after a controlled deformation. The SSC and the rind color were determined based on a method adapted from Liu [25 ]. The SSC of each melon was also measured by dropping the extracted juice from the equatorial region of flesh tissue onto a digital refractometer (DBR45, Huixia, Fujian, China). The rind color was detected using a chromatic color difference meter (CR—400/410, Konica Minolta, Japan); corresponding points on the fruit rind equator were detected, and seven values were recorded. Among these values, L* represents the brightness of the rind, which directly correlates with the fruit luster; a* represents the red/green ratio: higher positive values indicate red fruit, whereas negative values indicate green fruit; and b* represents the yellow/blue ratio: higher positive values indicate yellow fruit, whereas negative values indicate blue fruit. Each experiment was performed in triplicate.
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