Article(id=1319291671439848130, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291472856338924, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2026.07.035, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1792473245724, onlineDateStr=2026-10-20, pubDate=1783612800000, pubDateStr=2026-07-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792473245724, onlineIssueDateStr=2026-10-20, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792473245724, creator=13701087609, updateTime=1792473245724, updator=13701087609, issue=Issue{id=1319291472856338924, tenantId=1146029695717560320, journalId=1255847919539208197, year='2026', volume='44', issue='7', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1783612800000', pubDateStr='2026-07-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1792473198379, creator='13701087609', updateTime=1792473406504, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1319292345858773669, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291472856338924, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1319292345858773670, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1319291472856338924, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=204, endPage=209, ext={EN=ArticleExt(id=1319291671624397507, articleId=1319291671439848130, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Preparation and Biological Evaluation of Isoliquiritigenin-Loadedγ-Cyclodextrin Metal-Organic Framework Complex, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective

In order to improve the physicochemical properties of isoliquiritigenin (ISO) and its anti-inflammatory activity, ISO-loaded γ-cyclodextrin metal-organic framework complex (γ-CD-MOF/ISO) was prepared.

Methods

①γ-CD-MOF was synthesized by hydrothermal synthesis method, and ISO was loaded to form γ-CD-MOF/ISO by agitating heater.γ-CD-MOF/ISO was characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectrometer (FR-IR). The drug loading of γ-CD-MOF/ISO was evaluated.②The anti-inflammatory activity of γ-CD-MOF/ISO was investigated in LPS-induced RAW 264.7 cell model in vitro. The effect of γ-CD-MOF/ISO on cell viability was detected by CCK-8 assay. NO content in the supernatant was detected by Griess assay and the levels of pro-inflammatory cytokines IL-6 and TNF-α were measured by ELISA kit. The expressions of COX-2 and iNOS in protein level were detected by Western blot (WB).

Results

The morphology of γ-CD-MOF/ISO was cubic crystals with uniform size. Drug loading efficiency ofγ-CD-MOF/ISO was 5.01%±0.21%.γ-CD-MOF/ISO at 2.5 μg/mL had no toxin in RAW 264.7 cells.γ-CD-MOF/ISO (0.1, 0.5, 2.5 μg/mL) concentration-dependently inhibited the NO production, the secretion of pro-inflammatory cytokines IL-6 and TNF-α, and COX-2 and iNOS in LPS-induced RAW 264.7 cells.

Conclusion

γ-CD-MOF/ISO exhibits high biocompability and improves the anti-inflammatory activity, which provides a new formulation in the treatment of acute lung injury.

, authors=Cuiping FAN1, Xin SHANG2, Xuyang LIU1, Mengya LIU1, Yanyan LU1, Bangrong CAI1, Gaizhi LIU1, authorsList=Cuiping FAN, Xin SHANG, Xuyang LIU, Mengya LIU, Yanyan LU, Bangrong CAI, Gaizhi LIU, authorCompany=null, correspAuthors=Gaizhi LIU, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1319291672018662084, articleId=1319291671439848130, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=γ-环糊精金属有机骨架负载异甘草素复合物的制备及其抗炎活性研究, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的

γ-环糊精金属有机骨架(γ-CD-MOF)为载体负载异甘草素(ISO)形成γ-环糊精金属有机骨架复合物(γ-CD-MOF/ISO)以改善ISO的物理化学性质及其抗炎活性。

方法

①运用水热合成法制备γ-CD-MOF,通过加热搅拌法负载ISO形成γ-CD-MOF/ISO。利用扫描电镜和红外光谱分析对其形态结构进行表征,并对其载药量进行评价。②以脂多糖(LPS)诱导的小鼠单核巨噬细胞(RAW 264.7)为炎症模型,考察γ-CD-MOF/ISO的体外抗炎活性。采用CCK-8法检测γ-CD-MOF/ISO的细胞毒性;Griess法检测细胞上清液一氧化氮(NO)水平;酶联免疫吸附测定(ELISA)法检测细胞上清液白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)水平;蛋白免疫印迹技术(WB)检测环氧化酶(COX-2)、诱导型一氧化氮合酶(iNOS)蛋白表达量。

结果

γ-CD-MOF/ISO为立方晶体,形状规则,负载ISO前后其形态和粒径无明显变化。γ-CD-MOF/ISO的载药量为5.01%±0.21%。2.5 μg/mL的γ-CD-MOF/ISO对RAW 264.7细胞活力无影响。γ-CD-MOF/ISO(0.1、0.5、2.5 μg/mL)呈浓度依赖性抑制RAW 264.7细胞NO的生成、促炎因子IL-6、TNF-α的分泌,降低COX-2和iNOS蛋白表达水平。

结论

γ-CD-MOF/ISO生物安全性良好,具有较好的抗炎活性,为治疗急性肺损伤提供新剂型。

, authors=樊翠萍1, 尚鑫2, 刘旭洋1, 刘萌芽1, 鲁妍妍1, 蔡邦荣1, 刘改枝1, authorsList=樊翠萍, 尚鑫, 刘旭洋, 刘萌芽, 鲁妍妍, 蔡邦荣, 刘改枝, authorCompany=null, correspAuthors=刘改枝, authorNote=

樊翠萍(2002-),女,河南南阳人,硕士在读,研究方向:中药活性成分及天然产物修饰、新剂型研发。

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刘改枝(1981-),女,河南新乡人,教授,硕士研究生导师,博士,研究方向:中药活性成分与新药研发、药物新制剂与新技术。E-mail:。
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樊翠萍(2002-),女,河南南阳人,硕士在读,研究方向:中药活性成分及天然产物修饰、新剂型研发。

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樊翠萍(2002-),女,河南南阳人,硕士在读,研究方向:中药活性成分及天然产物修饰、新剂型研发。

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γ-环糊精金属有机骨架负载异甘草素复合物的制备及其抗炎活性研究
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樊翠萍 1 , 尚鑫 2 , 刘旭洋 1 , 刘萌芽 1 , 鲁妍妍 1 , 蔡邦荣 1 , 刘改枝 1
中华中医药学刊 | 国家项目点击 2026,44(7): 204-209
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中华中医药学刊 |国家项目点击 2026 , 44 (7) : 204 -209
γ-环糊精金属有机骨架负载异甘草素复合物的制备及其抗炎活性研究
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樊翠萍(2002-),女,河南南阳人,硕士在读,研究方向:中药活性成分及天然产物修饰、新剂型研发。

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樊翠萍(2002-),女,河南南阳人,硕士在读,研究方向:中药活性成分及天然产物修饰、新剂型研发。

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樊翠萍1, 尚鑫2, 刘旭洋1, 刘萌芽1, 鲁妍妍1, 蔡邦荣1, 刘改枝1
作者信息
  • 1.河南中医药大学药学院,河南 郑州 450046
  • 2.长春健康职业学院,吉林 长春 130012
通讯作者:
刘改枝(1981-),女,河南新乡人,教授,硕士研究生导师,博士,研究方向:中药活性成分与新药研发、药物新制剂与新技术。E-mail:。
作者简介:

樊翠萍(2002-),女,河南南阳人,硕士在读,研究方向:中药活性成分及天然产物修饰、新剂型研发。

Preparation and Biological Evaluation of Isoliquiritigenin-Loadedγ-Cyclodextrin Metal-Organic Framework Complex
Cuiping FAN1, Xin SHANG2, Xuyang LIU1, Mengya LIU1, Yanyan LU1, Bangrong CAI1, Gaizhi LIU1
Affiliations
  • 1.School of Pharmacy, Henan University of Chinese Medicine, Zhengzhou 450046, Henan, China
  • 2.Changchun Vocational College of Health, Changchun 130012, Jilin, China
出版时间: 2026-07-10 doi: 10.13193/j.issn.1673-7717.2026.07.035
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目的

γ-环糊精金属有机骨架(γ-CD-MOF)为载体负载异甘草素(ISO)形成γ-环糊精金属有机骨架复合物(γ-CD-MOF/ISO)以改善ISO的物理化学性质及其抗炎活性。

方法

①运用水热合成法制备γ-CD-MOF,通过加热搅拌法负载ISO形成γ-CD-MOF/ISO。利用扫描电镜和红外光谱分析对其形态结构进行表征,并对其载药量进行评价。②以脂多糖(LPS)诱导的小鼠单核巨噬细胞(RAW 264.7)为炎症模型,考察γ-CD-MOF/ISO的体外抗炎活性。采用CCK-8法检测γ-CD-MOF/ISO的细胞毒性;Griess法检测细胞上清液一氧化氮(NO)水平;酶联免疫吸附测定(ELISA)法检测细胞上清液白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)水平;蛋白免疫印迹技术(WB)检测环氧化酶(COX-2)、诱导型一氧化氮合酶(iNOS)蛋白表达量。

结果

γ-CD-MOF/ISO为立方晶体,形状规则,负载ISO前后其形态和粒径无明显变化。γ-CD-MOF/ISO的载药量为5.01%±0.21%。2.5 μg/mL的γ-CD-MOF/ISO对RAW 264.7细胞活力无影响。γ-CD-MOF/ISO(0.1、0.5、2.5 μg/mL)呈浓度依赖性抑制RAW 264.7细胞NO的生成、促炎因子IL-6、TNF-α的分泌,降低COX-2和iNOS蛋白表达水平。

结论

γ-CD-MOF/ISO生物安全性良好,具有较好的抗炎活性,为治疗急性肺损伤提供新剂型。

异甘草素  /  环糊精金属有机骨架  /  急性肺损伤  /  抗炎活性
Objective

In order to improve the physicochemical properties of isoliquiritigenin (ISO) and its anti-inflammatory activity, ISO-loaded γ-cyclodextrin metal-organic framework complex (γ-CD-MOF/ISO) was prepared.

Methods

①γ-CD-MOF was synthesized by hydrothermal synthesis method, and ISO was loaded to form γ-CD-MOF/ISO by agitating heater.γ-CD-MOF/ISO was characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectrometer (FR-IR). The drug loading of γ-CD-MOF/ISO was evaluated.②The anti-inflammatory activity of γ-CD-MOF/ISO was investigated in LPS-induced RAW 264.7 cell model in vitro. The effect of γ-CD-MOF/ISO on cell viability was detected by CCK-8 assay. NO content in the supernatant was detected by Griess assay and the levels of pro-inflammatory cytokines IL-6 and TNF-α were measured by ELISA kit. The expressions of COX-2 and iNOS in protein level were detected by Western blot (WB).

Results

The morphology of γ-CD-MOF/ISO was cubic crystals with uniform size. Drug loading efficiency ofγ-CD-MOF/ISO was 5.01%±0.21%.γ-CD-MOF/ISO at 2.5 μg/mL had no toxin in RAW 264.7 cells.γ-CD-MOF/ISO (0.1, 0.5, 2.5 μg/mL) concentration-dependently inhibited the NO production, the secretion of pro-inflammatory cytokines IL-6 and TNF-α, and COX-2 and iNOS in LPS-induced RAW 264.7 cells.

Conclusion

γ-CD-MOF/ISO exhibits high biocompability and improves the anti-inflammatory activity, which provides a new formulation in the treatment of acute lung injury.

isoliquiritigenin  /  cyclodextrin metal-organic framework  /  acute lung injury  /  anti-inflammatory activity
樊翠萍, 尚鑫, 刘旭洋, 刘萌芽, 鲁妍妍, 蔡邦荣, 刘改枝. γ-环糊精金属有机骨架负载异甘草素复合物的制备及其抗炎活性研究. 中华中医药学刊, 2026 , 44 (7) : 204 -209 . DOI: 10.13193/j.issn.1673-7717.2026.07.035
Cuiping FAN, Xin SHANG, Xuyang LIU, Mengya LIU, Yanyan LU, Bangrong CAI, Gaizhi LIU. Preparation and Biological Evaluation of Isoliquiritigenin-Loadedγ-Cyclodextrin Metal-Organic Framework Complex[J]. Chinese Archives of Traditional Chinese Medicine, 2026 , 44 (7) : 204 -209 . DOI: 10.13193/j.issn.1673-7717.2026.07.035
  • 国家自然科学基金青年科学基金项目(82104561)
  • 中国博士后科学基金面上项目(2020M682311)
  • 河南省高等学校重点科研项目(25A350007)
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文章信息
doi: 10.13193/j.issn.1673-7717.2026.07.035
  • 首发时间:2026-10-20
  • 出版时间:2026-07-10
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基金
国家自然科学基金青年科学基金项目(82104561)
中国博士后科学基金面上项目(2020M682311)
河南省高等学校重点科研项目(25A350007)
作者信息
    1.河南中医药大学药学院,河南 郑州 450046
    2.长春健康职业学院,吉林 长春 130012

通讯作者:

刘改枝(1981-),女,河南新乡人,教授,硕士研究生导师,博士,研究方向:中药活性成分与新药研发、药物新制剂与新技术。E-mail:。
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https://castjournals.cast.org.cn/joweb/zhzyyxk/CN/10.13193/j.issn.1673-7717.2026.07.035
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2种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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