A kind of anthocyanin liposome freeze-dried powder and preparation method thereof
A technology of freeze-dried powder and glycosides, which is applied in the biological field, can solve the problems of unstable liposome properties, single type of wall material, and low bioavailability, and achieves simple methods, high bioavailability, and good stability Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0034] Preparation of mannose erythritol lipid MEL-A:
[0035] MELs are fermented and synthesized by bacteria of the genus Ustligo maydis or Pseudazyma, and then separated and purified to obtain mannose erythritol lipid MEL-A with a purity of more than 95%. Specifically include the following steps:
[0036] The strain Pseudozyma aphidis DSMZ70725 was purchased from Deutsche Sammlung von Mikroorganismen und Zellkulturen; Ustligo maydis (No. 5.203) was purchased from China General Microbiological Culture Collection Center (CGMCC). Transfer one of the above purchased strains to slant medium (3.0g / L yeast extract, 3.0g / L malt extract, 5.0g / L peptone, 10.0g / L glucose, 15.0g / L agar, distilled water) , activated at 28°C for 2 days, and then transferred to liquid medium (4.0g / L glucose, 3.0g / L NaNO 3 , 0.3g / L MgSO4 ·7H 2 O, 0.3g / L KH 2 PO 4 , 1.0g / L yeast extract, distilled water, pH 6.0), cultured at 28°C and 220rpm for 3d. Insert the cultured seed liquid into the fermentation ...
Embodiment 1
[0047] A preparation method of anthocyanin liposome freeze-dried powder, comprising the following steps:
[0048] (1) Dissolving the prepared mannose erythritol lipid MEL-A in n-hexane to obtain a solution with a concentration of 15.0 mg / L;
[0049] (2) dissolving anthocyanins in distilled water to obtain a solution B with a concentration of 100.0 mg / L;
[0050] (3) Mix the A solution obtained in step (1) and the B solution obtained in step (2) according to a volume ratio of 1:1, ultrasonically treat it for 5 minutes at 30°C with a power of 100W, and let it stand for 15 minutes; then place Evaporate under reduced pressure in a rotary evaporator (vacuum degree is 0.1MPa, rotation speed is 120rpm, temperature is 55°C) to obtain lipid film;
[0051] (4) adding pH 5.0 to 7.0 and phosphate buffer solution with an ion concentration of 0.05 to 0.1M to the lipid film obtained in step (3), stirring and dissolving and passing through a 0.22 μm filter membrane to obtain a liposome suspe...
Embodiment 2
[0055] A preparation method of anthocyanin liposome freeze-dried powder, comprising the following steps:
[0056] (1) Dissolving the prepared mannose erythritol lipid MEL-A in chloroform to obtain a solution A with a concentration of 20.0 mg / L;
[0057] (2) dissolving anthocyanins in distilled water to obtain a solution B with a concentration of 300.0 mg / L;
[0058] (3) Mix the A solution obtained in step (1) and the B solution obtained in step (2) according to a volume ratio of 3:1, ultrasonically treat it at 40°C with a power of 300W for 10 minutes, and let it stand for 20 minutes; then place Evaporate under reduced pressure in a rotary evaporator (vacuum degree is 0.1MPa, rotation speed is 100rpm, temperature is 45°C) to obtain lipid film;
[0059] (4) adding pH 5.0 to 7.0 and phosphate buffer solution with an ion concentration of 0.05 to 0.1M to the lipid film obtained in step (3), stirring and dissolving and passing through a 0.45 μm filter membrane to obtain a liposome ...
PUM
Property | Measurement | Unit |
---|---|---|
concentration | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com