Preparation and release of curcumin/silk fibroin/sodium alginate film

The aim of this study was to prepare silk fibroin/sodium alginate composite film containing curcumin by casting method.Orthogonal test was used to optimize the formulation according to the values of tensile strength and elongation at break.The release of curcumin in the optimal film was studied in order to explore its application as wound dressing.The results showed that the optimum composition of curcumin/silk fibroin/sodium alginate composite film was as follows:Silk fibroin(70 mg/mL)2.7 g,sodium alginate(24 mg/mL)0.84 g,span 40(5.0 mg/mL)0.4 g,glycerol(3.75%,V/V)3 mL,curcumin(0.2 mg/mL)0.016 g.The optimum film showed the tensile strength and the elongation at break was(0.628±0.032)MPa and(0.794±0.046)%,respectively.

Relationship between tea pigments and health: A bibliometric and visual analysis

Tea pigments have significant effects on human health.However,more attention have been paid to their physiological functions.The aim of this study was to analyze the quantitative and qualitative impact of tea pigments on human health,together with their current and potential future research directions.The study searched and screened 520 publications on WOS from January 2002 to December 2022.The article collected and collated literature published in the last 20 years and analyzed it bibliometrically for years,journals,countries,authors,topics,keywords and strongest citation bursts.The findings of keywords and strongest citation bursts revealed that the most discussed research topics were anticancer,black tea polyphenol,antioxidant,activator inhibitor,in vivo,gut microbiota,and summarize the relevant literature.As a reference for future research,the literature pointed out current shortcomings and speculated future development trend of tea pigments.

A review on anti-inflammation activity of phenol compound paeonol

Paeonol is a bioactive phenol present in Dioscorea japonica,Paeonia suff ruticosa and Paeonia lactiflora.It is the main active ingredient in the traditional Chinese medicines Mudanpi and Xu Changqing.Clinical applications of paeonol are mainly focused on anti-inflammatory effects due to its ability to act as an antioxidant,a regulator of inflammatory enzyme activities,a modulator of inflammatory signaling pathways and a regulator of adhesion molecules to modulate inflammation through molecular mechanisms of action.In addition,paeonol also regulates inflammation by regulating the metabolism of gut microbes.In this review,we searched PubMed,Web of Science,ESI and other websites using“paeonol”“inflammation”“oxidative stress”“signaling pathways”and“gut microbiota”as keywords.We mainly referred to the relevant literature in the last decade and systematically summarized the studies on the anti-inflammatory effects of paeonol to provide a reference for new drug development and clinical application of paeonol.

基于“虚实结合”的医用有机化学实验混合教学模式的应用与探索

针对现有医用有机化学实验课程教学内容单一、教学模式传统、实验学时不足、学生重视程度不够等问题,构建了基于“虚实结合”的医用有机化学实验混合教学模式,主要包括教学方法变更、教学内容丰富、虚拟仿真实验引入、课程考核体系完善。实践发现,混合教学模式的应用更好地培养了学生自主创新的实践能力,为实践课程教育改革提供了有效依据,同时,让实践教学以时时、处处、人人皆可学的“新形态”展现在学生面前。

基础化学实验室安全运行管理探索与实践

基础化学实验室主要开设基础类、大面积通识课程,开课对象以非化学专业、低年级本科生为主。基础化学实验室在实践教学活动过程中往往涉及危险化学试剂以及高温、高压等危险操作,加之新形势下大类招生不断扩大,基础类课程教学任务与日俱增,基础化学实验室的安全运行管理面临的挑战更加严峻。以西安交通大学基础化学实验室为例,介绍了我校基础化学实验室现状及在安全运行与管理方面存在的问题和解决对策,为同类型化学实验室的安全运行与管理提供借鉴与参考。

A developed HPLC method for the determination of Alogliptin Benzoate and its potential impurities in bulk drug and tablets

Alogliptin(AGLT),active ingredient of Alogliptin Benzoate(AGLT-BZ),is a new dipeptidyl peptidase-4(DPP-4)inhibitor for the treatment of type 2 diabetes.This study aimed to build a suitable method to determine the potential related substances in AGLT-BZ bulk drug and tablets.Seven related substances in Alogliptin Benzoate substances were synthetized and identified by ^(1)H-NMR and ESI-MS.In addition,the impurities were detected by a gradient reverse-phase high performance liquid chromatography(RP-HPLC)with UV detection.The chromatographic system consisted of an Angilent Zobax SB-CN column(250×4.6 mm;5 μm).The mobile phase consisted of water/acetonitrile/trifluoroacetic acid 1900:100:1 v/v/v(solution A)and acetonitrile/water/trifluoroacetic acid 1900:100:1 v/v/v(solution B)using a gradient program at a flow rate of 1.0 ml/min with 278 nm detection and an injection volume of 20 ml.Additionally,selectivity,the limit of quantitation(LOQ)and limit of detection(LOD),linearity,accuracy,precision and robustness were determined.Linearity was good over the concentration range 50-1000 ng/ml and the coefficient of determination(R^(2))were 0.9991-0.9998.RSD% of the determination of precision were <2%(n=6).The method of RP-HPLC for the determination of impurities in AGLT-BZ was proved to be precise,accurate,robust and reliable.Three batches of self-made bulk drug and three dosages of commercial tablets were detected with this method.

Pharmacokinetics of oxiracetam and its degraded substance (HOPAA) after oral and intravenous administration in rats

The pharmacokinetics of oxiracetam and its degraded substance(4-hydroxy-2-oxo-1-pyrrolidine acetic acid,HOPAA)after oral and intravenous administration in rats were studied using an established UPLC-MS/MS method.Three groups of rats after an overnight fasted received 10 g/kg(n=6)oxiracetam suspensions orally,and 2 g/kg(n=6)normal or degraded oxiracetam injections intravenously via a caudal tail vein,respectively.Before the pharmacokinetic experiment,a simple safety evaluation testwas conducted on the degraded oxiracetam injections containing 16.16% HOPAA in mice.There was no mortality by a single intravenous dose of 2 g/kg of degraded oxiracetam injections within twoweeks,demonstrating that HOPAA was non-toxic in mice.Following intravenous administration of the normal injections,the plasma concentration-time curves of oxiracetam and HOPAA both showed a rapid elimination phase.The values of t_(1/2)were 3.1±1.5 h for oxiracetamand 0.8±0.2 h for HOPAA,andthemean residencetimes(MRT)were 1.2±0.1h and 0.8±0.1h,respectively.Oxiracetam and HOPAA after intravenous administration of the degraded oxiracetam injections presented elimination patterns similar to those observed in the normal injections.Oral pharmacokinetic results showed that the Tmax was less than 1.5 h for the two analytes,and both had a longer t_(1/2) and MRT than those of intravenous administration.Contents of HOPAA in three groupswere calculated based on AUC_(0-t) values of the two analytes.The quantitative change of HOPAA in vivo was also evaluated by comparing the plasma concentrations of HOPAA and oxiracetamat the same time for every group.Additionally,the values of absolute bioavailability of oxiracetam were about 8.0%and 7.4%calculated by the normal or degraded oxiracetam injections,whichwere far less than the value of 75%reported in literature,indicating the necessity of further study.

Preparation and evaluation of taste masked oral suspension of arbidol hydrochloride

The purpose of this study was to cover the bitter taste of arbidol hydrochloride(ARB)and develop dry suspension with combination of solid dispersion and flavors.Taste masking was successfully done by solid dispersion using octadecanol as the carrier by fusion method.Suspending agents,carriers and other excipients were selected.Differential scanning calorimetry(DSC)and Fourier transform infrared spectroscopy(FTIR)were performed to identify the physicochemical interaction between drug and carrier,DSC analysis indicated that ARB was amorphous in the solid dispersion,FTIR spectroscopy showed no interaction between drug and carrier.Taste masking was evaluated on six volunteers with a score of 4.9.The results demonstrated successful taste masking.Water was used to study the in vitro dissolution performance of the three formulations of commercial tablet,capsule and self-made suspension.The self-made suspension showed a lower and slower release,the insoluble carrier octadecanol blocked the drug dissolving from the solid dispersion.It was indicated from the primary stability study,the self-made suspensions were sensitive to high temperature,high humidity and strong light conditions,they should be stored in sealed containers away from heat,light and humidity.

A promising choice in hypertension treatment:Fixed-dose combinations

Obtaining the target blood pressure level by monotherapy can be challenging currently,especially for the patients who are suffering from other diseases meanwhile.It is demonstrated that a majority of hypertensive patients need two or more antihypertensive drugs to lower their blood pressure effectively.Consequently,fixed-dose which can be defined as that several active agents were combined in single pharmaceutical formulations appears to be a novel and underlying power in overcoming the cardiovascular disease.Based on the analysis of some literature and relative data from FDA,the advantages of fixed-dose combination are elucidated and formulations of common dual,triple-combinations were summarized.Clinical practices proved that fixed-dose combinations had many benefits comparing with single drug and separate agents in terms of effects,convenience,compliance,and costs to a certain extent.From the patients’perspective,the fixed-dose combination therapy will be increasingly utilized in blood pressure control in the future.

UPLCeMS/MS for the determination of azilsartan in beagle dog plasma and its application in a pharmacokinetics study

The purpose of the study is to develop an ultra performance liquid chromatographytandem mass spectrometry(UPLCeMS/MS)to determinate the concentration of azilsartan in the dog plasma.After precipitated by methanol,the plasma sample containing azilsartan and diazepam(internal standard,IS)was determined by UPLCeMS/MS.The mobile phase consisted of acetonitrile-water was pumped at a flow rate of 0.3 ml/min in gradient elution.Kinetex 2.6 m XB-C18 column(50
2.1 mm,100Å;Phenomenex,USA)were used for LC separations.The column temperature was 30℃ and the injection volume was 5 ml.The electrospray ionization(ESI)and multiple reaction monitoring(MRM)were applied at the transitions of m/z 457/279(azilsartan)and m/z 285/193(diazepam),respectively.The developed method was identified a good linearity over a concentration range of 2.5e5000 ng/ml.The lower limit of quantitation(LLOQ)was 2.5 ng/ml.The intraday and inter-day precision(relative standard deviation,RSD%)were less than 10%and accuracy(relative error,RE%)was less than 5%at three quality control levels.The extraction recovery of azilsartan at three quality control levels were 82.41±0.68%,98.66±11.00%,102.43±0.82%.And the recovery for IS(100 ng/ml)was 91.75±0.54%.A validated UPLCeMS/MS method was firstly developed for the quantification of azilsartan in dog plasma and it was applied to the pharmacokinetics study.

Research and Practice of theoretical framework of College Basketball sports education curriculum system

Education is the combination of basketball education and basketball activity. It is a kind of activity that basketball is as the core form, it is in order to enhance the skills of participants, technology, physical fitness, and promote a comprehensive development of their physical and mental activity, meanwhile basketball is not only a comprehensive gaming activity, but also an integral part of modern competitive sports, in some way, basketball culture is belonging to a particular social and cultural patterns. The quality of the basketball culture can cultivate people＇ s sentiments in the teaching process, and develop human wisdom, so that people grasp different spatial abilities and skills with the laws and govern the movement of the body under the time, the paper analyzes Practice mode theoretical framework of the construction of the basketball sports college education curriculum system.

Reflection on College Physical Education Reform Issues

College Physical Education is a teaching model which helps university students masters the basic knowledge, basic theory, basic skills and technology further so as to enhance their integrated abilities and levels of physical education. In recent years, under the joint efforts of government departments, schools and society, the reform of college physical education comes to show effects. China＇ s sports undertaking has become increasingly important in the social life and higher education. However, because of the effects of objective and subjective factors, there are some problems yet to be solved in the process of reform. This paper aims to analysis the problems existing in the work of University Physical Education Reform and proposes some targeted solutions to it.

Optimization of extraction of polyphenols from pomegranate peel by orthogonal experiment design and antioxidant activity

The aim of this study was to investigate the extraction process and antioxidant activity of polyphenols from Yunnan Mengzi pomegranate peel.Single factor and orthogonal test were used as optimize the extract rate(ER)of polyphenols from pomegranate peel(PGP).The polyphenols antioxidant activity was evaluated by DPPH·,·OH and total reducing ability,and compared with that of Vc.The optimum extraction conditions of polyphenols were as follows:ethanol concentration of 50%,liquid-solid ratio of 50:1,extraction temperature of 90°C,extraction for 4 h.Under these conditions,the ER of polyphenols from GPG was 8.15%.The results showed that the scavenging effects of polyphenols and Vc on DPPH·,·OH increased with increasing concentration,and the scavenging effect of polyphenols on DPPH·was higher than Vc in rang of 0.1-1.6µg/mL.When the concentration is greater than 0.6µg/mL,the scavenging effects of plyphenols on·OH is higher than Vc.The total reducing ability of polyphenols from PGP improved with the increase of concentration,and when the concentration was 8µg/mL,the total reducing ability was 114 U/mL.

Polyphenol content and antioxidant activity in mulberry powder treated at high temperature

The aim of this study was to investigate changes of polyphenols content and the antioxidant activity of mulberry fruit powder after heating at high temperature.The mulberry fruit powder was heated by baking method at different temperature and time.The DPPH scavenging ability,the OH^(•-) scavenging ability and the O_(2)^(•-) scavenging ability were used to evaluate the changes in the antioxidant activity of the mulberry fruit powder after the heat treatment.The results showed that 74.87%of the polyphenols in the mulberry powder were lost after heating at 150℃for 5 min,and almost all the polyphenols were lost with the increase of the heating time and temperature.The antioxidant experiment showed that the DPPH scavenging rate,OH^(•-) scavenging rate and O_(2)^(•-) scavenging rate of mulberry fruit powder were 68.90%,39.15%and 14.09%,respectively after treatment at 150℃ for 5 min.Mulberry fruit powder still has some potential to be added to baked goods as a functional ingredient.

Alginate-chitosan conjugated nanoliposome for catechin:Preparation,characterization and stability

Catechin(CTC)is a phenolic active compound with multiple biological activities.However,CTC is relatively unstable,easily oxidized and poorly soluble in water,showing limited bioavailability,which is a challenge for its application in the pharmaceutical and food industry.The purpose of this study was to promote the controlled release of CTC in the simulated gastrointestinal(GI)tract by using biopolymer-coupled nanoliposomes(NL).The nanoliposome was characterized by multifunctional polycrystalline X-ray diffraction(XRD),and Fourier transform infrared spectroscopy(FTIR).The results exhibited that the size of the nanocarrier was in the range of 87-178 nm,the encapsulation efficiency of CTC was 93.5%,and the combination of chitosan(CS)and alginate(ALG)was better than that of monopolymer.In vitro digestion studies showed that ALG-CS-NL significantly controlled the release of CTC by the diffusion,dissolution,and slow release mechanism and retained about 33%-37%of CTC under the GI condition.These results demonstrated that ALG-CS-NL could increase the stability of CTC,which may be important for the development of nutraceutical-enriched functional foods.

Extraction and application of tannin in the medical,food and chemical industries

Tannins are kinds of polyphenols found in plants,which can be divided into hydrolyzed tannins and condensed tannins according to the structure.They are extracted using solid/liquid,supercritical,pressurized water,and microwave-assisted extraction approaches.Because of the excellent antioxidant and antibacterial properties,tannins are widely used in medicine and food process.Considering the above advantages,the present review focused on various techniques to extract tannins and their application in the medical,food and chemical industries.

Application and action mechanism of polyphenol delivery system

Polyphenols are a class of chemical components that are beneficial to human health.Polyphenol compounds provide advanced biomedical applications due to their antioxidant and anti-inflammatory activity.They can also play a role in reducing the risk of various chronic diseases.However,most polyphenols are unstable compounds with low absorption and poor bioavailability which greatly limited their applications.Therefore,the delivery of polyphenols to specific parts of the body has become a therapeutic necessity.In this study,the research of polyphenol delivery systems such as microspheres,nanoparticles,liposomes and gels were mainly summarized.The action mechanism of polyphenols to intestinal microbiota,tumor cells,the brain,pancreas,and liver was analyzed.

Pharmacological effects and mechanisms of polyphenols in Radix Puerariae on liver protection and anti-diabetes

In recent years,the incidence of liver diseases and diabetes is increasing year by year,and the patients are younger than before.Although the clinical medicine treatment is eff ective,but it would produce side eff ects.Radix Puerariae is the dried root of the Pueraria lobata(Willd.)Ohwi.Puerarin is an isofl avone compound with polyphenol structure.It is one of the main bioactive components of Radix Puerariae.Studies have found that the application of puerarin off ers beatifical act on liver protection,hypoglycemia,blood lipid,antioxidant,anti-osteoporosis,anti-cancer,anti-inflammatory and cardiovascular protection.Puerarin has been used in the treatment of liver disease and diabetes.In this study,the eff ect of puerarin on liver protection,diabetes treatment and the relationship between the two diseases were reviewed.The therapeutic mechanism and molecular targets of puerarin were explored in order to further improve the development of puerarin and increase its clinical application in protection against liver disease and diabetes.

Preparation,characterization and antioxidant activity of inclusion complex loaded with puerarin and corn peptide

Puerarin with antioxidant ability has been applied in the food industry as well as in medicine.However,Puerarin is poorly soluble in water and is unstable at high temperatures.A new delivery system of puerarin-corn peptide-β-cyclodextrin(PA-CP-βCD)ternary complexes was developed in this study.The Taguchi design method was applied to optimize the preparation of the inclusion complex.PA-CP-βCD with an inclusion rate of 95.52%was achieved under stirring at 50◦C for 4 h,molar ratio of host and guest molecules of 2:1 and corn peptides of 40%.PA-CP-βCD dissolves faster in different media of pH 1.2,4.5,6.8,7.4,and water than pure puerarin.Compared with free puerarin,the antioxidant activity and the stability of puerarin in PA-CP-βCD were significantly improved.In addition,the morphology of PA-CP-βCD was characterized by scanning electron microscopy(SEM).The X-ray diffractometry(XRD)and differential scanning calorimetry(DSC)results indicated that PA-CP-βCD was an amorphous form.Molecular docking analysis confirmed intermolecular hydrogen bonds between puerarin andβ-cyclodextrin.This study provides a formulation design to enhance the solubility,stability and antioxidant activity of puerarin.

Review on the pharmacological mechanisms and novel drug delivery system of vitexin

Vitexin is a natural phytofl avonoid glycoside extracted from the leaves of vitexin,a plant of the Verbenaceae family,which is an active ingredient in many traditional Chinese medicines and is present in a wide range of medicinal plants.In this review,pharmacological eff ects including anti-infl ammatory,diabetes mellitus are described.The novel formulation of vitexin of nano delivery and hybrid micelles are elucidated.