Article(id=1304406833012167186, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.01.011, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1759939200000, receivedDateStr=2025-10-09, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788924423696, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788924423696, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788924423696, creator=13701087609, updateTime=1788924423696, updator=13701087609, issue=Issue{id=1304406818550206926, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='1', pageStart='1', pageEnd='389', issueExtLink='null', onlineDate='null', pubDate='1768147200000', pubDateStr='2026-01-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788924420249, creator='13701087609', updateTime=1788924674802, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304407886289986387, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304407886289986388, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=95, endPage=108, ext={EN=ArticleExt(id=1304406834945741332, articleId=1304406833012167186, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Preparation and in vitro anti-inflammatory evaluation of sinomenine nanoemulsion co-stabilized by Bletilla striata polysaccharide and glycyrrhizic acid, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To prepare sinomenine nanoemulsion (Sin-NE) co-stabilized by Bletilla striata polysaccharide and glycyrrhizic acid, systematically characterize its properties, investigate its stability and drug release behavior, and further evaluate its anti-inflammatory effects through in vitro experiments. Methods The Sin-NE was prepared using the ultrasonic emulsification method. Its morphology, particle size, polydispersity index (PDI), and ζ potential were observed and determined. Optimal formulation parameters were screened via single-factor and orthogonal experiments, followed by formulation validation. pH value, turbidity, viscosity, encapsulation efficiency, and drug loading capacity were measured. Stability was investigated under centrifugation, storage, dilution, and heating conditions was evaluated, and in vitro drug release behavior was investigated. A RAW264.7 cell inflammation model was established to validate the effects of the Sin-NE on nitric oxide (NO), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α). Results The optimized formulation comprised 3% Coicis Semen oil, 0.5% combined emulsifiers, a 1∶9 mass ratio of Bletilla striata polysaccharide to glycyrrhizic acid, 10 min of ultrasonic treatment, and 325 W ultrasonic power. The resulting Sin-NE exhibited an average particle size of (145.30 ±2.35) nm, ζ potential of (-39.51 ±0.43) mV, PDI of 0.095 ±0.022, and pH value of 3.990 ±0.033. Encapsulation efficiency and drug loading capacity reached 88.78% and 26.14 mg/g, respectively. The nanoemulsion demonstrated excellent stability under centrifugation, storage, dilution, and heating conditions and displayed sustained-release characteristics. In vitro , it significantly inhibited NO release and effectively reduced IL-6 and TNF-α levels in inflamed cells. Conclusion The Sin-NE significantly enhances sinomenine’s bioavailability and anti-inflammatory activity, providing experimental evidence for developing novel traditional Chinese medicine nanoemulsion formulations., authors=DAN Wulong, YANG Jing, CHEN Zhiyong, CHEN Teng, FENG Tingting, ZHU Yue, ZHOU Ying, WANG Zuhua, authorsList=DAN Wulong, YANG Jing, CHEN Zhiyong, CHEN Teng, FENG Tingting, ZHU Yue, ZHOU Ying, WANG Zuhua, authorCompany=null, correspAuthors=null, 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=1304406834836689427, articleId=1304406833012167186, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=白及多糖和甘草酸共稳定的青藤碱纳米乳的制备及其体外抗炎评价, columnId=1304140189132149234, journalTitle=中草药, columnName=药剂与工艺, runingTitle=null, highlight=null, articleAbstract=目的 制备白及多糖/甘草酸共稳定的青藤碱纳米乳(sinomenine nanoemulsion,Sin-NE),并系统表征其性质,考察其稳定性与释药行为,进而通过体外实验评价其抗炎效果。方法 采用超声乳化法制备Sin-NE,观测其形貌、粒径、多分散指数(polydispersity index,PDI)、ζ电位,单因素实验和正交试验筛选最佳处方并进行处方验证,测量其pH值、浊度、黏度、包封率和载药量,进行稳定性考察,探究其体外释药行为。构建RAW264.7细胞炎症模型,验证Sin-NE对一氧化氮(nitric oxide,NO)、白细胞介素-6(interleukin-6,IL-6)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)的影响。结果 Sin-NE的最优处方为薏苡仁油用量3%,联合表面活性剂用量0.5%,白及多糖与甘草酸质量比1∶9,超声处理时间10 min,超声功率325 W。该处方所制备的Sin-NE平均粒径为(145.30±2.35)nm,ζ电位为(-39.51±0.43)mV,PDI为0.095±0.022,pH值为3.990±0.033。其包封率达到88.78%,载药量为26.14 mg/g。此外,Sin-NE在离心、储存、稀释及加热条件下均表现出良好的稳定性,并具备缓释特性,在体外能显著抑制炎症细胞中NO的释放,有效降低炎症因子IL-6和TNF-α的水平。结论 Sin-NE显著提高了青藤碱的生物利用度和抗炎活性,为新型中药纳米乳制剂的开发提供了实验依据。, authors=但武龙1,2 , 杨菁1 , 陈智勇1,2 , 陈滕1,2 , 俸婷婷1,2 , 朱月1,2 , 周英1,2 , 汪祖华1,2 , authorsList=但武龙, 杨菁, 陈智勇, 陈滕, 俸婷婷, 朱月, 周英, 汪祖华, authorCompany=1 贵州中医药大学药学院, 贵州 贵阳 550025; 2 贵州省现代中药创制全省重点实验室, 贵州 贵阳 550025, correspAuthors=汪祖华, authorNote=但武龙: 但武龙,男,硕士研究生,研究方向为纳米创新药物制剂开发。E-mail:ll2906291286@163.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=ejFCg/LAIE7z0Q8Xk1vfbA==, pdfFileSize=2160959, 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=国家自然科学基金项目 (82360852); 贵州省科技计划项目 (黔科合基础-ZK[2023]重点046); 贵州省现代中药创制全省重点实验室 (黔科合平台[2025]019); 贵州中医药大学纳米药物技术研究中心 (贵中医ZX合字[2024]070))}, authors=null, keywords=[Keyword(id=1304406835109319190, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304406833012167186, language=CN, orderNo=1, keyword=白及多糖), Keyword(id=1304406835214176791, tenantId=1146029695717560320, journalId=1302319053441957962, 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中草药
|药剂与工艺
2026
, 57
(1) :
95
-108
白及多糖和甘草酸共稳定的青藤碱纳米乳的制备及其体外抗炎评价
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但武龙1,2 , 杨菁1 , 陈智勇1,2 , 陈滕1,2 , 俸婷婷1,2 , 朱月1,2 , 周英1,2 , 汪祖华1,2
作者信息
1 贵州中医药大学药学院, 贵州 贵阳 550025; 2 贵州省现代中药创制全省重点实验室, 贵州 贵阳 550025
通讯作者:
汪祖华
作者简介:
但武龙: 但武龙,男,硕士研究生,研究方向为纳米创新药物制剂开发。E-mail:ll2906291286@163.com
Preparation and in vitro anti-inflammatory evaluation of sinomenine nanoemulsion co-stabilized by Bletilla striata polysaccharide and glycyrrhizic acid
DAN Wulong, YANG Jing, CHEN Zhiyong, CHEN Teng, FENG Tingting, ZHU Yue, ZHOU Ying, WANG Zuhua
Affiliations
doi: 10.7501/j.issn.0253-2670.2026.01.011
文章导航
目的 制备白及多糖/甘草酸共稳定的青藤碱纳米乳(sinomenine nanoemulsion,Sin-NE),并系统表征其性质,考察其稳定性与释药行为,进而通过体外实验评价其抗炎效果。方法 采用超声乳化法制备Sin-NE,观测其形貌、粒径、多分散指数(polydispersity index,PDI)、ζ电位,单因素实验和正交试验筛选最佳处方并进行处方验证,测量其pH值、浊度、黏度、包封率和载药量,进行稳定性考察,探究其体外释药行为。构建RAW264.7细胞炎症模型,验证Sin-NE对一氧化氮(nitric oxide,NO)、白细胞介素-6(interleukin-6,IL-6)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)的影响。结果 Sin-NE的最优处方为薏苡仁油用量3%,联合表面活性剂用量0.5%,白及多糖与甘草酸质量比1∶9,超声处理时间10 min,超声功率325 W。该处方所制备的Sin-NE平均粒径为(145.30±2.35)nm,ζ电位为(-39.51±0.43)mV,PDI为0.095±0.022,pH值为3.990±0.033。其包封率达到88.78%,载药量为26.14 mg/g。此外,Sin-NE在离心、储存、稀释及加热条件下均表现出良好的稳定性,并具备缓释特性,在体外能显著抑制炎症细胞中NO的释放,有效降低炎症因子IL-6和TNF-α的水平。结论 Sin-NE显著提高了青藤碱的生物利用度和抗炎活性,为新型中药纳米乳制剂的开发提供了实验依据。
白及多糖
/
青藤碱
/
甘草酸
/
纳米乳
/
抗炎活性
/
超声乳化法
/
白细胞介素-6
/
肿瘤坏死因子-α
Objective To prepare sinomenine nanoemulsion (Sin-NE) co-stabilized by Bletilla striata polysaccharide and glycyrrhizic acid, systematically characterize its properties, investigate its stability and drug release behavior, and further evaluate its anti-inflammatory effects through in vitro experiments. Methods The Sin-NE was prepared using the ultrasonic emulsification method. Its morphology, particle size, polydispersity index (PDI), and ζ potential were observed and determined. Optimal formulation parameters were screened via single-factor and orthogonal experiments, followed by formulation validation. pH value, turbidity, viscosity, encapsulation efficiency, and drug loading capacity were measured. Stability was investigated under centrifugation, storage, dilution, and heating conditions was evaluated, and in vitro drug release behavior was investigated. A RAW264.7 cell inflammation model was established to validate the effects of the Sin-NE on nitric oxide (NO), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α). Results The optimized formulation comprised 3% Coicis Semen oil, 0.5% combined emulsifiers, a 1∶9 mass ratio of Bletilla striata polysaccharide to glycyrrhizic acid, 10 min of ultrasonic treatment, and 325 W ultrasonic power. The resulting Sin-NE exhibited an average particle size of (145.30 ±2.35) nm, ζ potential of (-39.51 ±0.43) mV, PDI of 0.095 ±0.022, and pH value of 3.990 ±0.033. Encapsulation efficiency and drug loading capacity reached 88.78% and 26.14 mg/g, respectively. The nanoemulsion demonstrated excellent stability under centrifugation, storage, dilution, and heating conditions and displayed sustained-release characteristics. In vitro , it significantly inhibited NO release and effectively reduced IL-6 and TNF-α levels in inflamed cells. Conclusion The Sin-NE significantly enhances sinomenine’s bioavailability and anti-inflammatory activity, providing experimental evidence for developing novel traditional Chinese medicine nanoemulsion formulations.
Bletilla striata polysaccharide
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sinomenine
/
glycyrrhizic acid
/
nanoemulsion
/
anti-inflammatory activity
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ultrasonic emulsification method
/
interleukin-6
/
tumor necrosis factor-α
但武龙, 杨菁, 陈智勇, 陈滕, 俸婷婷, 朱月, 周英, 汪祖华.
白及多糖和甘草酸共稳定的青藤碱纳米乳的制备及其体外抗炎评价.
中草药,
2026
, 57
(1)
: 95
-108
.
DOI: 10.7501/j.issn.0253-2670.2026.01.011
DAN Wulong, YANG Jing, CHEN Zhiyong, CHEN Teng, FENG Tingting, ZHU Yue, ZHOU Ying, WANG Zuhua.
Preparation and in vitro anti-inflammatory evaluation of sinomenine nanoemulsion co-stabilized by Bletilla striata polysaccharide and glycyrrhizic acid[J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(1)
: 95
-108
.
DOI: 10.7501/j.issn.0253-2670.2026.01.011
国家自然科学基金项目 (82360852); 贵州省科技计划项目 (黔科合基础-ZK[2023]重点046); 贵州省现代中药创制全省重点实验室 (黔科合平台[2025]019); 贵州中医药大学纳米药物技术研究中心 (贵中医ZX合字[2024]070)
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2026年第57卷第1期
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doi: 10.7501/j.issn.0253-2670.2026.01.011
接收时间:2025-10-09
首发时间:2026-09-09
https://castjournals.cast.org.cn/joweb/zcy/CN/10.7501/j.issn.0253-2670.2026.01.011
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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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