Related Experiment Video
Updated: Aug 7, 2025

Synthesis of High Purity Nonsymmetric Dialkylphosphinic Acid Extractants
Published on: October 19, 2017
Ultrasonication-mediated formation of V-type lotus seed starch for subsequent complexation with butyric acid
Huifang Liu1, Yingning Yao1, Yi Zhang2
1College of Food Science, Fujian Agriculture and Forestry University, Fuzhou 350002, China; Fujian Provincial Key Laboratory of Quality Science and Processing Technology in Special Starch, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Abstract:
V-type starches comprise single helical structures that can be complexed with other small hydrophobic molecules. The development of the subtypes of these assembled V-conformations is dependent on the helical state of the amylose chains during complexation, which is influenced by the pretreatment employed. In this work, the effect of preultrasonication on the structure and in vitro digestibility of preformed V-type lotus seed starch (VLS) and its potential for complexing with butyric acid (BA), was investigated. The results showed that ultrasound pretreatment did not affect the crystallographic pattern of the V6-type VLS. The optimal ultrasonic intensities increased the crystallinity and molecular ordering of the VLSs. With an increase in the preultrasonication power, the pores on the VLS gel surface decreased in size and were more densely distributed. The VLSs formed at 360 W were less vulnerable to digestive enzymes than their untreated counterparts. Additionally, their highly porous structures could accommodate numerous BA molecules, and thus generated inclusion complexes via hydrophobic interactions. These findings would provide valuable insights into the ultrasonication-mediated formation of VLSs and suggest their potential application as carriers for the delivery of BA molecules to the gut.
More Related Videos
Related Concept Videos
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Esters to Carboxylic Acids: Saponification
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview

