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Preparation of Modified Composite Nanofiltration Membrane Synergistically Using Carboxylic Multi- walled Carbon Nanotube and β-cyclodextrin
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作者 LIU Peng MAO Junpeng +7 位作者 FANG Yanfeng YU Yunwu CHEN Changxiu TANG Ning WAN Ye GU Yaxin LIU Yunxue WANG Lihua 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2025年第1期232-239,共8页
A new modified blend ultrafiltration(UF)membrane with good hydrophilicity,high porosity and excellent anti-fouling performance was developed by using carboxylic multi-walled carbon nanotube(CMWCNT)as casting solution ... A new modified blend ultrafiltration(UF)membrane with good hydrophilicity,high porosity and excellent anti-fouling performance was developed by using carboxylic multi-walled carbon nanotube(CMWCNT)as casting solution additive.Furthermore,a composite nanofiltration(NF)membrane with large water flux and good retention rate was fabricated by using the PVDF/CMWCNT blend UF membrane as the substrate,and polyvinyl alcohol(PVA),β-cyclodextrin(β-CD)and polyethylenimine(PEI)as the coating solution.The results show that with the appropriate addition of CMWCNT in the casting solution,the surface roughness,porosity and recovery rate of the PVDF/CMWCNT blend UF membrane is obviously increased.The water flux of blend UF membrane is significantly improved when the CMWCNT content increases from 0 wt%to 0.2 wt%.The water flux of blend UF membrane with 0.2 wt%CMWCNT is 162.7 L/(m^(2)·h),which is 44.3%higher than that of the pure PVDF membrane.Whenβ-CD content is 0.8 wt%,the retention rate of Congo red by PVDF/CMWCNT/β-CD composite NF membrane reaches 98.7%,which is 28.3%higher than that of single PVA/PEI modified membrane.This research will provide a new idea and simple method for developing novel high-performance composite NF membranes. 展开更多
关键词 CMWCNT cyclodextrin NANOFILTRATION MEMBRANE
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Cyclodextrin host-vip complex to facilitate sinomenine-based osteoporosis therapy
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作者 Meng-Qin Guo Ping Hu Zheng-Wei Huang 《World Journal of Stem Cells》 2025年第3期139-143,共5页
Xiao et al reported on the natural product sinomenine(SIN),which is a traditional Chinese medicine for treating osteoporosis via its modulation of autophagy;however,SIN was dissolved in dimethyl sulfoxide prior to adm... Xiao et al reported on the natural product sinomenine(SIN),which is a traditional Chinese medicine for treating osteoporosis via its modulation of autophagy;however,SIN was dissolved in dimethyl sulfoxide prior to administration,which is not conducive to the development of clinical injectables.By comparing solubilization techniques,including amorphisation,emulsification,micellisation,nanocrystallisation and host-vip inclusion,we found that the solubilization of SIN by host-vip inclusion can enhance solubility and improve stability and has an increased release rate and enhanced bioavailability.Therefore,we conclude that host-vip inclusion holds promise for SIN solubilization.To solubilise SIN,we selectedβ-cyclodextrin as the host agent considering its excellent biocompatibility,efficient encapsulation ability,mature preparation process and adequate drug stability.If the prerequisites of SIN-β-cyclodextrin complexes in terms of safety,efficacy,stability and the relevant laws and regulations are met,its clinical application for the treatment of osteoporosis may be achieved. 展开更多
关键词 SINOMENINE cyclodextrin OSTEOPOROSIS AUTOPHAGY SOLUBILIZATION
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Double response reversible phosphorescence based on cyclodextrin supramolecular flexible elastic achieved multicolor delayed fluorescence
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作者 Linnan Jiang Zhenkai Qian +7 位作者 Yong Chen Xiaoyong Yu Yugui Qiu Wen-Wen Xu Yonghui Sun Xiufang Xu Lihua Wang Yu Liu 《Chinese Chemical Letters》 2025年第8期315-321,共7页
Purely organic room-temperature phosphorescence(RTP)is current hotspot in the research fields of chemistry,biology,materials etc.Herein,we report that photo-thermal double response reversible ultralong RTP flexible el... Purely organic room-temperature phosphorescence(RTP)is current hotspot in the research fields of chemistry,biology,materials etc.Herein,we report that photo-thermal double response reversible ultralong RTP flexible elastic material with multicolor delayed fluorescence,which is constructed by 4-biphenylboronic acid(BOH),polyethylene glycol,2,2-bis(hydroxymethyl)propionic acid,isophorone diamine and isophorone diisocyanate copolymer.Importantly,the supramolecular phosphorescent elastomer not only exhibits extending RTP emission with a lifetime up to 1.21 s,but also gives a visible afterglow of 20 s via encapsulation of BOH unities by the deep cavities of hydroxypropyl-β-cyclodextrin(β-CD-HP)and in situ polymerization.Especially,after doping organic dyes(Fluorescein isothiocyanate,Sulforhodamine 101,Rhodamine B),supramolecular phosphorescent elastomer achieves multicolor delayed fluorescence realized by RTP energy transfer from phosphorescent donor to dye acceptors,which possesses reversible photo-thermal responsiveness and maintains high efficiency in delayed emission even after dozens of cycles.Present research provides a new approach for constructing multicolor delayed fluorescent supramolecular elastomers. 展开更多
关键词 Double response reversible cyclodextrin RTP Host-vipinteraction Flexibleelastic
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Research Progress on Trimethoprim Cyclodextrin Inclusion Complexes
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作者 Jiedan Liao Jiawei Weng +1 位作者 Zhuoran Deng Lanyi Zhang 《Journal of Clinical and Nursing Research》 2025年第8期359-367,共9页
Trimethoprim(TMP),as a broad-spectrum bacteriostatic antibiotic,is widely used in clinical anti-infection therapy and livestock breeding.However,its low water solubility leads to insufficient bioavailability,which has... Trimethoprim(TMP),as a broad-spectrum bacteriostatic antibiotic,is widely used in clinical anti-infection therapy and livestock breeding.However,its low water solubility leads to insufficient bioavailability,which has become a key problem restricting its development.Cyclodextrins and their derivatives,with their unique cyclic structures,can form inclusion complexes with TMP to improve its properties.This article reviews the pharmacological characteristics of TMP,the types and properties of common cyclodextrins,focusing on introducing various preparation methods of trimethoprim cyclodextrin inclusion complexes and multiple characterization methods for identifying the inclusion complexes,aiming to provide a reference for further research and development of trimethoprim cyclodextrin inclusion complexes. 展开更多
关键词 TRIMETHOPRIM cyclodextrin Inclusion technology Characterization method Research progress
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Cyclodextrins as versatile supramolecular building block in nanoscale drug delivery systems for precise tumor chemotherapy
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作者 Peng Liu 《Chinese Chemical Letters》 2025年第11期101-109,共9页
Nanoscale drug delivery systems(nano-DDSs)have attracted intense interest in tumor chemotherapy in the last decades,to improve antitumor efficacy and minimize toxic and side effects.As a versatile supramolecular build... Nanoscale drug delivery systems(nano-DDSs)have attracted intense interest in tumor chemotherapy in the last decades,to improve antitumor efficacy and minimize toxic and side effects.As a versatile supramolecular building block,cyclodextrins(CDs)have been widely used in the fabrication of the smart nano-DDSs.Besides their multifunctionality,which makes them versatile core in the star(co)polymers for micellar nanomedicines,specific host-vip inclusion complexation via their hydrophobic cavities endows them diversified functions:(i)design of amphiphilic copolymers for micellar nanomedicines,(ii)supramolecular hydrogels and poly(pseudo)rotaxane nano-hydrogels as drug carriers,and(iii)recipient for direct and indirect drug-loading.In the present work,the recent progress of CDs in nano-DDSs for tumor chemotherapy was reviewed,classified by the crucial roles of CD units.Based on the structureperformance relationship,the future perspective was also proposed. 展开更多
关键词 Nanoscale drug delivery system cyclodextrins Supramolecular building block Tumor chemotherapy Structural design
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One-pot in situ doping synthesis of phenylboronic acid-functionalized magnetic-cyclodextrin microporous organic network for specific enrichment and detection of sulfonylurea herbicides
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作者 Chun-Ying Xu Xiao-Lin Luan +1 位作者 Yuan-Yuan Cui Cheng-Xiong Yang 《Chinese Chemical Letters》 2025年第9期524-528,共5页
Microporous organic networks(MONs)are attractive adsorbents for use in sample pretreatment owning to their unique structure and properties.However,methods for constructing functional MONs are still limited because the... Microporous organic networks(MONs)are attractive adsorbents for use in sample pretreatment owning to their unique structure and properties.However,methods for constructing functional MONs are still limited because the lack of monomers via direct synthesis and their complex procedures via postmodification.To address this issue,a facile one-pot in situ doping strategy was proposed herein for synthesis a novel phenylboronic acid-functionalized magnetic cyclodextrin-based microporous organic network([PBA]_(3/4)-MCD-MON-0.04).[PBA]_(3/4)MCD-MON-0.04 was used for the selective and efficient extraction of sulfonylurea herbicides(SUHs)from complex food and environmental water samples via the synergistic hydrogen bonding,host-vip,hydrophobic andπ-πinteractions and the specific B-N coordination.[PBA]_(3/4)-MCD-MON-0.04 had a large surface area,high saturation magnetism,good reusability,and remarkable stability.A rapid,sensitive,and selective method was proposed for monitoring SUHs from diverse matrices.This study provides a new strategy for synthesizing novel and multifunctional magnetic CD-MONs-based adsorbents and reveals the considerable potential of CD-MONs in sample pretreatment. 展开更多
关键词 cyclodextrin microporous organic network Magnetic solid phase extraction In situ doping Sulfonylurea herbicide B-N coordination
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A promising strategy of brain targeted delivery for the treatment of Parkinson's disease:Cyclodextrin supramolecular inclusion complex based thermosensitive gel
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作者 Yan-Qiu Wang Li-Ming Wang +2 位作者 Li-Feng Han Yi-Bing Chen Yuan-Lu Cui 《Journal of Pharmaceutical Analysis》 2025年第5期1166-1169,共4页
Parkinson's disease(PD)is a debilitating and progressive neurodegenerative disorder with complex pathology and multiple membrane barriers that hinder drug delivery,resulting in the absence of ideal therapeutic dru... Parkinson's disease(PD)is a debilitating and progressive neurodegenerative disorder with complex pathology and multiple membrane barriers that hinder drug delivery,resulting in the absence of ideal therapeutic drugs with minimal side effects[1].Recently,natural medicine has garnered significant attention due to its remarkable efficacy and limited side effects.Icariin,a naturally occurring flavonoid,exhibits excellent potential as a therapeutic agent for neurodegenerative disease[2].However,its clinical application is limited by poor water solubility,low bioavailability,and high clearance rates.Here,an aqueous formulation of icariin/hydroxypropyl-β-cyclodextrin(HP-β-CD)supramolecular inclusion complex was obtained to optimize icariin properties.Furthermore,icariin cyclodextrin supramolecular inclusion complex based thermosensitive(icariin gels)was innovated.At lower temperatures,it remained in a liquid phase with high fluidity.Upon reaching the gelation temperature,it underwent a transition to a gel phase with significantly reduced fluidity,which may be suitable for the design of an intranasal delivery system for PD treatment.The innovative approach capitalizes on the exceptional characteristics of HP-β-CD,which was utilized to synergize with nasal delivery for targeted brain delivery and with icariin for PD treatment[3,4]. 展开更多
关键词 cyclodextrin brain targeted delivery ideal therapeutic drugs supramolecular inclusion complex parkinsons disease pd neurodegenerative disorder thermosensitive gel neurodegenerative disease howeverits
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糖原脱支酶和环糊精葡聚糖转移酶联用提高β-环糊精产量
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作者 黄靖佳 陶秀梅 +4 位作者 孔德明 陈星奕 吴敬 陈晟 王蕾 《食品与发酵工业》 北大核心 2026年第1期244-250,共7页
环糊精葡萄糖基转移酶(cyclodextrin glucosyltransferase,CGTase)制备环糊精(cyclodextrin,CD)时,部分淀粉底物无法被利用,导致淀粉原料利用率以及生产效率低,为解决上述问题,该研究用Escherichia coli BL21(DE3)克隆表达了一种新型淀... 环糊精葡萄糖基转移酶(cyclodextrin glucosyltransferase,CGTase)制备环糊精(cyclodextrin,CD)时,部分淀粉底物无法被利用,导致淀粉原料利用率以及生产效率低,为解决上述问题,该研究用Escherichia coli BL21(DE3)克隆表达了一种新型淀粉脱支酶,来源于光滑念珠菌(Candida glabrata)的糖原脱支酶(glycogen debranching enzyme,GDE)CgGDE,当摇瓶发酵温度为25℃,诱导剂IPTG终浓度为0.1 mmol/L,诱导时间为36 h时,CgGDE的酶活力达69.3 U/mL。酶学性质结果表明,CgGDE的最适pH值为6.0,最适温度为35℃。利用CgGDE与β-CGTase复配制备β-CD,结果表明,在非溶剂条件下,当马铃薯淀粉质量浓度为50 g/L,温度40℃,反应pH值为6.0,CgGDE添加量为750 U/g干淀粉,β-CGTase添加量为7 U/g干淀粉,转化周期24 h时,β-CD转化率为53.1%,比单独使用β-CGTase转化率提高了93.8%,与异淀粉酶β-CGTase联用相比,转化率提高了50.9%,为β-CD在非溶剂条件下的转化奠定了基础。 展开更多
关键词 糖原脱支酶 酶学性质 β-环糊精葡萄糖基转移酶 Β-环糊精 淀粉
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β-环糊精对蓝湿革中三氯苯酚的洗脱机理研究
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作者 曹艳妮 杨朝晖 +2 位作者 唐余玲 周建飞 石碧 《皮革科学与工程》 北大核心 2026年第2期1-8,共8页
【目的】开发高效、环保的氯酚脱除技术,提升皮革制品生态安全性,实现行业可持续发展。【方法】以β-环糊精(β-CD)为洗脱剂,含2,4,5-三氯苯酚(TCP)的蓝湿革为研究对象,系统考察表面活性剂的种类及浓度、NaCl浓度、β-CD用量、pH、时间... 【目的】开发高效、环保的氯酚脱除技术,提升皮革制品生态安全性,实现行业可持续发展。【方法】以β-环糊精(β-CD)为洗脱剂,含2,4,5-三氯苯酚(TCP)的蓝湿革为研究对象,系统考察表面活性剂的种类及浓度、NaCl浓度、β-CD用量、pH、时间、温度、次数等因素对蓝湿革中TCP去除效果的影响。【结果】研究结果表明,当非离子表面活性剂DW质量浓度为0.1 g/L、β-CD质量浓度为7 g/L、洗脱温度为298.15 K、洗脱时间为60 min、洗脱pH为5、蓝湿革中初始TCP含量为55.42 mg/kg时,经4次β-CD洗脱后蓝湿革中TCP含量可降低至4.83 mg/kg,去除率达到91.3%。【结论】最后对洗脱前后蓝湿革的性能进行检测,发现β-CD洗脱操作不仅可有效降低TCP含量,还有利于蓝湿革后续的制革工艺。 展开更多
关键词 蓝湿革 Β-环糊精 2 4 5-三氯苯酚 包合作用 洗脱效率
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β-环糊精强化过硫酸盐/Fe(Ⅱ)体系降解四氯乙烯的性能及机理
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作者 杨朝格 李博文 +2 位作者 李俊孟 刘方圆 董军 《中南大学学报(自然科学版)》 北大核心 2026年第1期15-24,共10页
在处理地下水四氯乙烯(PCE)污染过程中,传统过硫酸盐/Fe^(2+)氧化技术面临非水相污染物传质限制、Fe^(3+)/Fe^(2+)循环效率低和氧化剂利用率低等瓶颈。本研究引入β-环糊精(β-CD)作为强化剂,利用分子包合与金属络合双重机制强化PCE的... 在处理地下水四氯乙烯(PCE)污染过程中,传统过硫酸盐/Fe^(2+)氧化技术面临非水相污染物传质限制、Fe^(3+)/Fe^(2+)循环效率低和氧化剂利用率低等瓶颈。本研究引入β-环糊精(β-CD)作为强化剂,利用分子包合与金属络合双重机制强化PCE的降解效能。首先,构建β-CD与Fe^(2+)的络合体系,通过紫外可见光谱仪和循环伏安法表征β-CD对Fe^(2+)的螯合作用及其对Fe^(2+)/Fe^(3+)氧化还原行为的影响;其次,采用顶空平衡实验研究β-CD对PCE的增溶作用,结合吹扫-气相色谱质谱法定量分析PCE质量浓度,通过增溶平衡方程与增溶动力学阐明β-CD增溶PCE的机制;最后,动态监测PCE、Fe^(2+)/Fe^(3+)、PDS及Cl-质量浓度的变化,以评估β-CD对PCE降解动力学与脱氯矿化过程的促进作用。研究结果表明:β-CD独特的截锥状空腔结构可将PCE包合,形成水溶性复合物,相比于PCE在水中的溶解度(157.2 mg/L),β-CD使PCE的质量浓度(406.23 mg/L)提高了2.58倍;β-CD可以有效降低Fe^(2+)/Fe^(3+)的氧化还原电位,加速Fe^(3+)/Fe^(2+)的氧化还原反应;形成了β-CD与PCE物质的量比为1꞉1的增溶复合物,并且Fe^(2+)的存在并不影响复合物的比例与结构;β-CD对PCE的增溶动力学遵循伪二级动力学模型;增强PDS/Fe^(2+)反应体系的最佳β-CD质量浓度为1 g/L,与PDS/Fe^(2+)体系相比,加入β-CD使PCE的降解速率提高了14倍,同时实现了对PDS的高效利用(88.00%)和PCE的完全脱氯矿化。 展开更多
关键词 PCE污染 地下水修复 氧化降解 过硫酸盐/Fe^(2+)体系 Β-环糊精
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VOLTAMMETRIC BEHAVIOR OF ASCORBIC ACID AT α-CYCLODEXTRIN INCORPORATED CARBON NANOTUBES-COATED ELECTRODE 被引量:2
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作者 肖素芳 王宗花 +1 位作者 王义明 罗国安 《青岛大学学报(自然科学版)》 CAS 2002年第4期1-6,共6页
制备了α -环糊精掺杂纳米碳管涂层电极并应用于抗坏血酸的电催化氧化 ,结果表明 ,氧化电位降低了 2 80mV ,电流响应明显增加。我们首次结合两种物质的特性 :纳米碳管的导电性及催化性能、α -环糊精的分子认知能力 ,对电极表面进行修... 制备了α -环糊精掺杂纳米碳管涂层电极并应用于抗坏血酸的电催化氧化 ,结果表明 ,氧化电位降低了 2 80mV ,电流响应明显增加。我们首次结合两种物质的特性 :纳米碳管的导电性及催化性能、α -环糊精的分子认知能力 ,对电极表面进行修饰。实验了抗坏血酸与α -环糊精超分子络合物的特性。差示脉冲技术用于定量分析抗坏血酸 ,线性范围为 2 .5× 10 -6~ 1.0× 10 展开更多
关键词 伏安行为 Α-环糊精 纳米碳管涂层电级 超分子络 抗坏血酸 电催化氧化
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Separation Properties of a New Polysiloxane-Anchored β-Cyclodextrin Derivative as Gas Chromatography Stationary Phase 被引量:1
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作者 史雪岩 傅若农 顾峻岭 《Journal of Beijing Institute of Technology》 EI CAS 2002年第3期285-289,共5页
A new capillary gas chromatography stationary phase, monokis (2,6 di O benzyl 3 O propyl (3’)) hexakis(2,6 di O benzyl 3 O methyl) β CD bonded polysiloxane, was synthesized. It ex... A new capillary gas chromatography stationary phase, monokis (2,6 di O benzyl 3 O propyl (3’)) hexakis(2,6 di O benzyl 3 O methyl) β CD bonded polysiloxane, was synthesized. It exhibited separation abilities to disubstituted benzene isomers and some chiral solutes. It was also found that the polarity of CD derivatives can be lowered both by chemically bonding it to polysiloxane and by diluting it in polysiloxane. The separation abilities of the polysiloxane anchored CDs (SP CD) are higher than that of the unbonded CDs (S CD) and the diluted S CD at lower column temperature. Hydrosilylation reaction is one of the best methods to lower the operating temperature of CDs. 展开更多
关键词 capillary gas chromatography stationary phase polysiloxane anchored β cyclodextrin derivative di substituted benzene isomers separation enantiomers separation
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负载百里香酚的淀粉复合涂膜的制备及性能
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作者 丁天华 魏嘉彧 +3 位作者 张脂函 庄雨涵 苟韬 刘耀文 《塑料工业》 北大核心 2026年第1期34-41,55,共9页
针对百里香酚水溶性较差和挥发性较强的问题,本研究采用β-环糊精(β-CD)对百里香酚(THY)进行包埋,制备THY@β-CD微胶囊,并以淀粉为基材构建复合涂膜。借助扫描电子显微镜(SEM)探究微胶囊包含情况,并通过单因素与正交试验优化微胶囊制... 针对百里香酚水溶性较差和挥发性较强的问题,本研究采用β-环糊精(β-CD)对百里香酚(THY)进行包埋,制备THY@β-CD微胶囊,并以淀粉为基材构建复合涂膜。借助扫描电子显微镜(SEM)探究微胶囊包含情况,并通过单因素与正交试验优化微胶囊制备工艺。结果表明,THY成功被β-CD包埋,形成微胶囊结构;当反应温度50℃、时间2 h、芯壁比1∶13时,微胶囊包封率达73.24%,百里香酚热稳定性与水溶性提升效果显著,缓释性能较好。通过傅里叶变换红外光谱、水接触角测定仪等筛选最佳淀粉基材,探究复合涂膜的理化性能。结果表明,相较于其他淀粉,马铃薯淀粉拉伸强度2.85 MPa、断裂伸长率52.31%,具备更优异的力学性能和良好的成膜性,被选为最佳基材;添加10%微胶囊的复合涂膜对致腐败菌抑菌圈直径达1.53~1.97 cm,抑菌性能较好,负载百里香酚的淀粉复合涂膜综合性能最优,为制备天然可降解食品抑菌涂膜提供了一种可行技术方案。 展开更多
关键词 百里香酚 Β-环糊精 微胶囊 淀粉 涂膜保鲜
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羟丙基-β-环糊精对阿魏酸-烟酰胺共晶的包合作用及溶液性质研究
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作者 井艺霏 王小永 +3 位作者 宁德勇 马晓烨 宋轲薪 黄子昊 《华东理工大学学报(自然科学版)》 北大核心 2026年第1期83-89,共7页
为了研究环糊精类材料的包合作用对植物活性物性质的影响,制备了阿魏酸-烟酰胺(FA-NIC)共晶/羟丙基-β-环糊精(HP-β-CD)包合物,研究了HP-β-CD对FA-NIC共晶的包合作用及溶液性质。相溶解度曲线和Job's曲线表明,FA-NIC共晶与HP-β-C... 为了研究环糊精类材料的包合作用对植物活性物性质的影响,制备了阿魏酸-烟酰胺(FA-NIC)共晶/羟丙基-β-环糊精(HP-β-CD)包合物,研究了HP-β-CD对FA-NIC共晶的包合作用及溶液性质。相溶解度曲线和Job's曲线表明,FA-NIC共晶与HP-β-CD按照1:1的物质的量之比形成包合物。X射线衍射和傅里叶变换红外光谱结果说明,包合于HP-β-CD疏水内腔的FA-NIC共晶与HP-β-CD的羟基存在氢键作用。由于FA-NIC共晶与HP-β-CD疏水内腔的C—H和糖苷键存在疏水作用,这使得FA表现出更高的紫外吸收强度和荧光强度。相比于纯FA,FA-NIC/HP-β-CD包合物中的FA在水中的平衡溶解度、紫外光照稳定性和DPPH(1,1-二苯基-2-三硝基苯肼)自由基清除率分别提高了5.7倍、17.9个百分点和1倍左右。 展开更多
关键词 阿魏酸 共晶 环糊精 包合作用 溶液
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β-环糊精及其衍生物在兽用药物递送系统中的应用进展
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作者 李應英 徐飞 王桂琴 《中国畜牧兽医》 北大核心 2026年第3期1145-1154,共10页
在畜禽养殖中,传统兽用药物存在水溶性低、稳定性差、生物利用度低等问题,而β-环糊精(β-cyclodextrin,β-CD)作为一种环状低聚糖,具有“内疏水、外亲水”的独特空腔结构,可与不同种类的兽用药物形成包合物来提升药物性能以此减少用药... 在畜禽养殖中,传统兽用药物存在水溶性低、稳定性差、生物利用度低等问题,而β-环糊精(β-cyclodextrin,β-CD)作为一种环状低聚糖,具有“内疏水、外亲水”的独特空腔结构,可与不同种类的兽用药物形成包合物来提升药物性能以此减少用药剂量和给药次数。研究表明,β-CD与抗菌药物包合后可大幅提高药物水溶性、稳定性与生物利用度,减少用药剂量及耐药性;与抗寄生虫药包合后,能增加溶解度并保护药物免受胃肠道酶降解;与中兽药包合后,可提升药物稳定性、掩盖不良气味并降低胃肠道刺激性。同时,β-CD还可与纳米颗粒、金属有机骨架、凝胶等新型纳米药物递送系统结合,进而提升载药量与缓控释效果,实现药物长效抗菌作用并增强生物相容性,以此发挥双重作用。基于当前研究,笔者系统综述了β-CD及其衍生物的结构特性、包合工艺及其优化策略,阐述了β-CD及其衍生物与不同种类的兽用药物包合后的应用以及与新型纳米系统结合后的应用潜力,为推动高效、低残留的兽用药物技术研发提供参考。 展开更多
关键词 β-环糊精(β-CD) 衍生物 兽用药物 包合物 纳米系统
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表没食子儿茶素没食子酸酯与表没食子儿茶素没食子酸酯-β-环糊精抗破骨细胞生成作用对运动员骨质疏松的防治
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作者 刘楠 张泽正 《应用化学》 北大核心 2026年第1期108-115,共8页
本文旨在探讨表没食子儿茶素没食子酸酯(EGCG)及其与β-环糊精(β-CD)的复合物(EGCG-β-CD)在抗破骨细胞生成及防治运动员骨质疏松中的作用差异。通过高效液相色谱(HPLC)证实EGCG与β-CD成功包合,n(EGCG)∶n(β-CD)=1.89∶1。利用核因子... 本文旨在探讨表没食子儿茶素没食子酸酯(EGCG)及其与β-环糊精(β-CD)的复合物(EGCG-β-CD)在抗破骨细胞生成及防治运动员骨质疏松中的作用差异。通过高效液相色谱(HPLC)证实EGCG与β-CD成功包合,n(EGCG)∶n(β-CD)=1.89∶1。利用核因子κB受体活化因子配体(RANKL)诱导的RAW264.7破骨细胞分化模型,通过抗酒石酸酸性磷酸酶(TRAP)染色、实时荧光定量PCR(qRT-PCR)及蛋白免疫印迹分析评估发现,在相同浓度(10μmol/L)下,EGCG-β-CD复合物对破骨细胞分化的抑制效果显著强于EGCG,表现为成熟破骨细胞数量减少(P<0.05),破骨细胞标志基因NFATc1、CTSK、TRAP的mRNA及蛋白表达水平显著下调(P<0.001)。研究表明,β-CD通过与EGCG形成特定化学计量比的包合物,协同提升其抗破骨细胞活性,为运动员骨质疏松的防治提供了新型植物活性成分递送策略。 展开更多
关键词 骨质疏松 破骨细胞 表没食子儿茶素没食子酸酯(EGCG) Β-环糊精 EGCG-β-CD复合物
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巨噬细胞膜仿生纳米给药系统的制备及性能
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作者 陈晋 丁尧 肖新荣 《精细化工》 北大核心 2026年第3期524-531,共8页
首先,将β-环糊精(β-CD)修饰在具有乙二胺核的聚酰胺-胺(PAMAM)树枝状聚合物5.0代(PAMAM G5.0)表面,构筑了CD-G5载药腔;然后,将疏水性抗炎药姜黄素(CUR)作为模型药物负载于CD-G5内,得到了负载CUR的纳米粒子(CURNPs);最后,在CURNPs外包... 首先,将β-环糊精(β-CD)修饰在具有乙二胺核的聚酰胺-胺(PAMAM)树枝状聚合物5.0代(PAMAM G5.0)表面,构筑了CD-G5载药腔;然后,将疏水性抗炎药姜黄素(CUR)作为模型药物负载于CD-G5内,得到了负载CUR的纳米粒子(CURNPs);最后,在CURNPs外包裹具有免疫逃逸反应和药物缓释作用的巨噬细胞膜(MM),制备了仿生纳米给药系统(MM@CURNPs)。采用FTIR、^(1)HNMR对CD-G5进行了表征;通过TEM和纳米粒度分布仪对MM@CURNPs的微观形貌和粒径分布进行了测定,基于药物释放实验和体外细胞毒性、巨噬细胞摄取实验,进行了MM@CURNPs的缓释性能和体外活性评价。结果表明,CURNPs经MM包覆后,MM@CURNPs平均粒径(162.2 nm)增大13.9 nm;MM@CURNPs放置1 d时平均粒径为162.2 nm,10 d时平均粒径为238.6 nm;CURNPs载药率为9.60%,MM@CURNPs体外释药速率较CURNPs慢,72 h累积释放量达到约50%;MM@CURNPs比PAMAM G5.0和CURNPs的毒性小,即使在浓度1000 nmol/L下,小鼠单核巨噬细胞白血病细胞(Raw 264.7细胞)仍具有90%的活性;MM上保留有巨噬细胞固有膜蛋白和功能,可以帮助MM@CURNPs具备巨噬细胞免疫逃逸功能,4 h时,Raw 264.7细胞对荧光标记的MM@CURNPs粒子摄取的平均荧光强度为72,Raw 264.7细胞对荧光标记的CURNPs粒子摄取的平均荧光强度为80。 展开更多
关键词 仿生纳米给药系统 聚酰胺-胺树枝状聚合物 Β-环糊精 巨噬细胞膜 姜黄素 功能材料
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具有相变储能功能的环糊精超分子气凝胶纤维制备与热管理应用
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作者 孙欢 余财霞 +2 位作者 郝莹 刘玲 王锦 《纺织工程学报》 2026年第1期63-72,共10页
气凝胶纤维是近年来发展出来的具有超低密度、超低热导率、高孔隙率和高比表面积的新型纤维,在保温隔热、智能纺织等方面展现出独特的性能。然而气凝胶纤维的制备通常需要经过溶胶-凝胶纺丝过程,这一过程对凝固浴、前驱体以及纺丝速率... 气凝胶纤维是近年来发展出来的具有超低密度、超低热导率、高孔隙率和高比表面积的新型纤维,在保温隔热、智能纺织等方面展现出独特的性能。然而气凝胶纤维的制备通常需要经过溶胶-凝胶纺丝过程,这一过程对凝固浴、前驱体以及纺丝速率具有严格的要求。为此,提出了可注射水凝胶直接纺丝的策略。首先制备了基于α-环糊精-聚乙二醇主客体作用的超分子可注射水凝胶,该凝胶体系在水相中可快速形成凝胶网络结构,具备良好的流动性与剪切响应,可通过注射实现定向成型,为纤维化加工及挤出式3D打印提供可行途径。随后经叔丁醇置换和冷冻干燥处理后得到气凝胶纤维。该气凝胶纤维的密度为0.068 g/cm^(3)、孔隙率高达71.2%。此外,该气凝胶纤维骨架中具有聚乙二醇结晶,潜热到达57.09 J/g,具备本征的相变储能功能。综合而言,提出了气凝胶纤维制备的一种新思路,通过良好的可注射性简化了制备过程,制备的气凝胶纤维具有本征相变储能功能,在人体可穿戴热管理方面具有重要的应用潜力。 展开更多
关键词 气凝胶纤维 超分子水凝胶 可注射水凝胶 环糊精包合物 热管理材料
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Injectable Supramolecular Hydrogels via Inclusion Complexation of m PEG-grafted Copolyglutamate with α-Cyclodextrin 被引量:2
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作者 Lian-ying Wu Lei Yu +1 位作者 Xiao-hui Fu 李志波 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2015年第8期1140-1149,共10页
A series of monomethoxy poly(ethylene glycol) (mPEG) grafted copolyglutamates (PmPEGs) were synthesized through ring-opening polymerization (ROP) followed by click chemistry. Supramolecular hydrogels based on ... A series of monomethoxy poly(ethylene glycol) (mPEG) grafted copolyglutamates (PmPEGs) were synthesized through ring-opening polymerization (ROP) followed by click chemistry. Supramolecular hydrogels based on polymer inclusion complexes (ICs) between PmPEG and α-cyclodextriri (α-CD) were prepared in aqueous solution. The rheological measurements indicated their gelation properties were affected by several factors including the mPEG length, graft density and the sample concentration. These hydrogels displayed thermo-sensitive gel-sol transition under appropriate conditions due to the reversible mPEG and α-CD inclusion complexation. These hydrogels also showed pH-sensitive behavior due to the deprotonate of carboxylic acid side groups. The ICs formation of a channel-type crystalline structure induced gelation mechanism was verified by various techniques. In vitro cytotoxicity assays demonstrated that the supramolecular hydrogels are nontoxic and cytocompatible. 展开更多
关键词 Supramolecular hydrogel Inclusion complexation Copolyglutamate α-cyclodextrin.
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Enantioseparation of Aminoglutethimide by High-speed Countercurrent Chromatography Using Carboxymethly-β-cyclodextrin as Chiral Selector 被引量:3
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作者 Ping AI Jia Chuan LIU Min ZI Zhi Hua DENG Zhi Hong YAN Li Ming YUAN 《Chinese Chemical Letters》 SCIE CAS CSCD 2006年第6期787-790,共4页
Enantioseparation of aminoglutethimide was performed by high-speed counter-current chromatography with a two-phase system composed of ethyl acetate: methanol: water = 10: 1: 9. The lower phase contained 20 mmol/L ... Enantioseparation of aminoglutethimide was performed by high-speed counter-current chromatography with a two-phase system composed of ethyl acetate: methanol: water = 10: 1: 9. The lower phase contained 20 mmol/L of carboxymethly-β-cyclodextrin as chiral selector. The enantiomers were separated in 1.2 h and identified by chiral HPLC. This method was very efficient for the chiral preparative separation. 展开更多
关键词 High speed countercurrent chromatography ENANTIOSEPARATION aminoglutethimide carboxymethly-β-cyclodextrin.
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