Fresh preserving method of flatfish fillets
A fresh-keeping method and flounder technology are applied in the fields of preserving meat/fish with chemicals, preserving meat/fish by freezing/cooling, etc., which can solve the problem that the application of fresh-keeping is easily limited, the requirements for fresh-keeping equipment are high, and it is easy to lose water. Air-dried fat and other problems, to achieve the effect of easy promotion and application, low requirements for fresh-keeping equipment, and avoidance of juice loss
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[0032] The preparation of the antistaling agent: firstly dissolving jujube flavonoids and hawthorn flavonoids in hot water at 40°C to 50°C, then mixing them with the prepared jujube polysaccharide solution in proportion, dissolving with the aid of ultrasonic waves, and preparing jujube flavonoids A preservative with a concentration of 1 g / L to 7 g / L, a hawthorn flavonoid concentration of 1 g / L to 7 g / L, and a jujube polysaccharide concentration of 2 g / L to 12 g / L.
[0033] The preservation effect was evaluated by volatile base nitrogen (TVB-N value) and the total number of bacteria. Volatile basic nitrogen was determined by reference to SC / T2032-2007 method, and the total number of bacteria was determined by reference to GB / T4789.2-2008 plate count method. According to GB18406.4-2001 (Safety and Quality of Agricultural Products - Safety Requirements for Pollution-free Aquatic Products): TVB-N value (mg / 100 g) in pollution-free aquatic products≤30, total number of bacte...
Embodiment 1
[0035] (1) Extraction of Hawthorn Flavonoids
[0036] First, remove the core of the hawthorn and dry it at 60°C, crush it with a plant pulverizer, weigh 20 g of hawthorn fruit powder into a flask, add 400 mL of 80% ethanol solution, place the flask in an ultrasonic cleaner, and connect the condenser tube, under the conditions of ultrasonic power of 400 W and water temperature of 70 °C in the cleaning tank, reflux extraction for 50 min, vacuum filtration of the extract, and the filtrate was concentrated by a rotary evaporator, and the concentrated solution was taken out and vacuum freeze-dried to obtain crude flavonoids from hawthorn The crude extract was dissolved in 50 mL of absolute ethanol, passed through a D101 macroporous resin column (40 cm × 2.6 cm), and eluted with a 75% ethanol solution by volume fraction, and the eluate was collected and concentrated by a rotary evaporator Freeze-dry for 24 hours to obtain hawthorn flavonoids. The total amount of rutin, hyperin and ...
Embodiment 2
[0045] (1) Extraction of Hawthorn Flavonoids
[0046] First, remove the core of the hawthorn and dry it at 60°C, crush it with a plant pulverizer, weigh 20 g of hawthorn fruit powder into a flask, add 400 mL of 80% ethanol solution, place the flask in an ultrasonic cleaner, and connect the condenser tube, under the conditions of ultrasonic power of 400 W and water temperature of 70 °C in the cleaning tank, reflux extraction for 50 min, vacuum filtration of the extract, and the filtrate was concentrated by a rotary evaporator, and the concentrated solution was taken out and vacuum freeze-dried to obtain crude flavonoids from hawthorn The crude extract was dissolved in 50 mL of absolute ethanol, passed through a D101 macroporous resin column (40 cm × 2.6 cm), and eluted with a 75% ethanol solution by volume fraction, and the eluate was collected and concentrated by a rotary evaporator Then freeze-dry for 24 hours to obtain hawthorn flavonoids. The total amount of rutin, hyperin...
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