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Starch-lipid complex is a new type of resistant starch, which is of great significance for the prevention of chronic diseases such as diabetes. Most of starch-lipid complexes usually need to be treated by heating in order to make them ideal for a variety of application and starch based foods are generally not edible without heat treatment process. However, the digestion and structural properties of starch-lipid complex will be changed after heating. In this study, microwave and conventional heating were used to treat debranched quinoa starch-oleic acid complexes (DQS-OA) with different water addition, and the effects of the two methods on the physicochemical, digestive and structural properties of DQS-OA were compared.The results of in vitro digestibility showed that the resistant starch content (235.34-269.55 g kgThis study demonstrated that conventional water-bath heating was better than microwave heating in increasing the digestion resistance, improving the short-range and long-range molecular order and promoting the formation of DQS-OA. In addition, with the increase of water addition, the influence of microwave or water bath treatment on the properties of DQS-OA became greater. This article is protected by copyright. All rights reserved.

Background Ferula persica is one of the most important traditional medicinal plants that is used to treat various diseases such as diabetes, backache and rheumatism. The aim of the present study was to evaluate the anti‐inflammatory and wound healing potential of F. persica using stereological and molecular methods in experimental models. Methods In the present study, two wound models (circular excision and linear incision) were used. Male Wistar rats were divided into four groups (n = 16), including control, vehicle treated, treated with F. persica extract ointment (5% w/w) and treated with the reference drug (Madecassol). All the animals were treated topically once a day. The circular and linear wounds were treated for 9 and 17 days, respectively. At the end of the study, samples from wounds area were harvested for histology, stereology, immunohistochemistry and molecular assessments to determine the in vivo healing potential and anti‐inflammatory activity. Results We observed significant recovery in macroscopic evaluation of wound healing in the F. persica extract treated group compared with the control and vehicle treated groups (p 0.05, p, Stereological and molecular studies on the effects of Ferula persica extract on wound healing in rats.

Comparative plastomics approaches have been used to identify available molecular markers for different taxonomic level studies of orchid species. However, the adoption of such methods has been largely limited in phylogeographic studies. Therefore, in this study, Dendrobium huoshanense, an endangered species with extremely small populations, was used as a model system to test whether the comparative plastomic approaches could screen available molecular markers for the phylogeographic study. We sequenced two more plastomes of D. huoshanense and compared them with our previously published one. A total of 27 mutational hotspot regions and six polymorphic cpSSRs have been screened for the phylogeographic studies of D. huoshanense. The cpDNA haplotype data revealed that the existence of haplotype distribution center was located in Dabieshan Mts. (Huoshan). The genetic diversity and phylogenetic analyses showed that the populations of D. huoshanense have been isolated and evolved independently for long period. On the contrary, based on cpSSR data, the genetic structure analysis revealed a mixed structure among the populations in Anhui and Jiangxi province, which suggested that the hybridization or introgression events have occurred among the populations of D. huoshanense. These results indicated that human activities have played key roles in shaping the genetic diversity and distributional patterns of D. huoshanense. According to our results, both two markers showed a high resolution for the phylogeographic studies of D. huoshanense. Therefore, we put forth that comparative plastomic approaches could revealed available molecular markers for phylogeographic study, especially for the species with extremely small populations.

Introduction The Epimedium herb, Yinyanghuo in Chinese, is a famous Chinese herbal medicine. In this study, an efficient extraction method was developed for the extraction of major bioactive constituent epimedin A, epimedin B, epimedin C and icariin from E. pubescens Maxim. using deep eutectic solvents (DESs). Methodology A series of choline chloride-based DESs were synthesised for the extraction of four target compounds. DES composed of lactic acid and choline chloride with the ratio of 2:1 was selected as the most promising. Three vital factors affecting the extraction yields including water content, volume of DES aqueous solution and extraction time were optimised systematically by Box-Behnken experimental design in combination with response surface methodology. A high-performance liquid chromatography ultraviolet (HPLC-UV) method was developed for the sensitive and accurate quantification. Results The optimal extraction conditions were obtained as follows: water content of 17.5% (v/v), volume of DES aqueous solution 3.14 ml, and extraction time of 21 min. Under the optimal extraction conditions, the developed DES method could supply almost the same extraction yield as 50% ethanol, which were 98%, 99%, 97%, 96% for epimedin A, epimedin B, epimedin C and icariin, respectively. Conclusion The present study exhibited high efficiency in extraction of prenylflavonol glycosides in E. pubescens Maxim. Thus, DESs could be used as an alternative for efficient extraction and quantification of biologically active components from natural medical plants.

In this study, a covalent organic framework designated as TpPaNO2 was synthesized by a mechanochemical grinding method and then coated on stainless steel wire by a sol-gel technique to prepare a solid-phase microextraction fiber. The TpPaNO2 fiber based solid-phase microextraction coupled with gas chromatography-electron capture detection was applied to determine the residues of 11 pesticides (trlfuralln, dicofol, α-endosulfan, 1-chloro-4-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene, nitrofen, β-endosulfan, 1-chloro-4-[2,2-dichloro-1-(4-chlorophenyl)ethyl]benzene, 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane, bifenthrin, permethrin and fenvalerate) in vegetable and fruit samples. The effects of extraction time, extraction temperature, sample pH, stirring rate and desorption temperature on the extraction efficiency were investigated. Under the optimized conditions, the limits of detection for the eleven pesticides were in the range of 0.04-0.25 μg/kg. The recoveries of the eleven pesticides in the vegetable and fruit samples were 81.5-111% with the relative standard deviations less than 11.2%.