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Freeze dryer

Manufactured by Labogene
Sourced in Denmark

A freeze dryer is a laboratory instrument used to remove water from samples through the process of lyophilization. It operates by freezing the material and then reducing the surrounding pressure to allow the frozen water in the sample to sublimate directly from the solid phase to the gas phase.

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4 protocols using freeze dryer

1

Evaluating Weight Loss and pH Changes of Biomembranes in SBF

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The membranes were immersed in SBF to assess their weight loss (%) and pH change (n = 5/group/time point). The pH change from the baseline pH of the SBF was measured using the pH meter (SevenCompact, Mettler Toledo GmbH, Greifensee, Switzerland). Then, the 10 mm × 10 mm membrane specimens were immersed in 4 mL of SBF/tube in 50 mL centrifuge tubes (Corning, Merck KgaA, Darmstadt, Germany). The tubes were incubated at 37 °C, and the pH of the solution of each membrane was measured on days 1, 3, 7, 14, and 21. The control group consisted of a solution without membranes. To measure the weight loss, each membrane was weighed (Wd0) using an analytical balance (Satorius, Goettingen, Germany) before immersion in 4 mL of SBF/well in 12-well plates (Corning, Merck KgaA, Darmstadt, Germany). The membranes were incubated at 37 °C, and the SBF was added every 10 days to maintain a constant volume. To measure the weight loss on days 15, 30, 60, 90, and 120, the membranes were collected, rinsed with distilled water, and freeze-dried in a freeze dryer (LaboGene, Lillerød, Denmark) for 3 h. Their dry weights (Wdt) were measured, and their weight loss was calculated as:
The morphology of the membranes during the test was evaluated via SEM (n = 2/time point).
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2

Novel Plant-Based Meat Formulation

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Duckweed (DW) (echoherb, Chungcheongnam-do, Republic of Korea) protein was extracted using hot distilled water (90°C) for 1 h and diluted 20 times with distilled water (w/v) concentrated in a vacuum concentrator (EYELA, Buenos Aires, Argentina) and dried in a freeze dryer (LABOGENE, Allerød, Denmark) and evenly ground. Powdered DW was added to the PBM.
Spirulina (SPI) (INGREDIENTS BY NATURE, New Brunswick, NJ, USA), yellow chlorella (YC) (Daesang, Seoul, Republic of Korea), and DW were added to the PBM. YC replaced TVP amount by 1.0, 2.0, and 3.0%, and SPI and DW by 0.5, 0.7, and 1.0%, respectively. The new material mix was formulated using TVP, shiitake mushrooms, Isolate soy protein, tapioca starch, isolate wheat protein, smoked flavor, emulsion, garlic, emulsifiers, oils, color, seasoning, salt, and binders. The pre-mix ratios are listed in Table 1. The control group of the current experiment is red meat (round beef steak). The control samples were obtained from the local supermarket in Seoul Korea. The quality characteristics of novel PBM patties measured in the present experiment were compared with the beef patty control.
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3

Extraction and Characterization of White Pitaya

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Fresh white pitaya fruits were obtained from the garden of Shenzhen Talent Training Institute in Shenzhen. The fruits were collected under relevant guidelines, and the minimum number of fruits required for the completion of the study was collected after permission was obtained from the Institute. Dr. Wang Jun from the Department of Food and Drug, Shenzhen Polytechnic University, authenticated the fruit with voucher No. SZPUH: 1261 and was deposited at the herbarium. The peel, flesh, and seeds were initially carefully separated from the fruit, properly cleaned with distilled water, and then dried using a freeze-dryer (LaboGene, Brigachtal, Germany). The freeze-dried materials were ground into a fine powder utilizing an electric grinder.
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4

Comprehensive Meat Quality Assessment

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All of the measurements below were performed on the -20°C stored muscle samples. The perimeter of the rib eye area was traced on a sheet of sulfuric paper, followed by calculation with a planimeter (Jilin University, China). The marbling grade was determined according to the Japanese Marbling scores (5-Excellent; 4-Good; 3-Average; 2-Below average; 1-Poor). Immediately after this, the meat sample was boiled and cooled, and the shear force was measured using a Warner-Bratzler shear force machine (Bodine Electric Co., Chicago, IL, USA) according to the manufacturer’s instructions. According to the AOAC official methods, the meat samples were dried in a freeze dryer (LaboGene, Allerod, Denmark) to determine the contents of H2O, crude protein and IMF. The Kjeldahl method was then applied to analyze the crude protein content using a Kjeltec 8400 Analyzer Unit (Foss Analytical, Höganäs, Sweden). Finally, the total IMF percentage was determined by the Soxhlet extraction method.
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