Comparison of extraction processes, characterization and intestinal protection activity of Bletilla striata polysaccharides
View abstract on PubMed
Summary
This summary is machine-generated.Optimized Bletilla striata polysaccharide extraction using Box-Behnken design and genetic algorithm-back propagation improved yield and antioxidant activity. The purified polysaccharide demonstrated intestine protective effects in cell models.
Area Of Science
- Biochemistry
- Pharmacology
- Materials Science
Background
- Bletilla striata polysaccharides (BSP) are known for their bioactivities.
- Optimizing extraction methods is crucial for maximizing BSP yield and efficacy.
- Understanding the structural and functional properties of BSP is essential for its applications.
Purpose Of The Study
- To optimize the extraction of Bletilla striata polysaccharides (BSP) using orthogonal design, Box-Behnken design (BBD), and genetic algorithm-back propagation (GA-BP).
- To characterize the structure and properties of the purified BSP (pBSP1).
- To evaluate the protective effects of pBSP1 on intestinal cells.
Main Methods
- Extraction process optimization using orthogonal design, BBD, and GA-BP.
- Purification of BSP to obtain pBSP1.
- Structural characterization using SEM, UV, FTIR, HPLC, XRD, NMR, and periodate oxidation.
- Assessment of thermal stability and viscoelastic behavior.
- In vitro evaluation of protective effects on LPS-induced GES-1 and Caco2 cells.
Main Results
- The optimal extraction parameters (liquid-to-solid ratio 15 mL/g, power 450 W, time 34 min) yielded 8.29% BSP with high antioxidant activity.
- Purified pBSP1 (Mw 255.172 kDa) exhibited an amorphous structure with specific glucose and mannose compositions and good thermal/viscoelastic properties.
- pBSP1 reduced apoptosis, reactive oxygen species (ROS) production, and lowered transepithelial electrical resistance (TEER) synthesis in intestinal cells.
Conclusions
- The combination of BBD and GA-BP effectively optimized BSP extraction, enhancing yield and antioxidant activity.
- pBSP1 possesses a unique structure and favorable physicochemical properties.
- pBSP1 demonstrates potential as an intestine-protective agent by mitigating LPS-induced cellular damage.

