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作 者:张胜男 周玲[2] 叶勒丹·马汉 张晓玲[2] 补娟[2] ZHANG Shengnan;ZHOU ling;MAHAN Yeledan;ZHANG Xiaoling;BU Juan(College of Life Science and Technology,Xinjiang University,Urumqi 830000,China;Medical Research and Transformation Center,People's Hospital of Xinjiang Uygur Autonomous Region,Urumqi 830000,China)
机构地区:[1]新疆大学生命科学与技术学院,新疆乌鲁木齐830000 [2]新疆维吾尔自治区人民医院医学研究与转化中心,新疆乌鲁木齐830000
出 处:《海南医科大学学报》2025年第4期241-247,253,共8页Journal of Hainan Medical University
基 金:新疆维吾尔自治区人民医院干细胞生物治疗基础和临床研究专项(GXBZX-2023007);新疆维吾尔自治区自然科学基金(2020D01C095)。
摘 要:目的:构建刺槐素(Acacetin)的外泌体(Exosomes,EXOs)递药系统。方法:以人脐带间充质干细胞(human umbilical cord mesenchymal stem cells,hUMSCs)来源外泌体为药物载体,采用共孵育法、超声法和反复冻融法3种方式包载刺槐素,制备负载刺槐素的外泌体(EX-Aca)。采用高效液相色谱法(High Performance Liquid Chromatography,HPLC)测定EX-Aca包封率和载药率。透射电镜(TEM)、粒径分析和Western Blot对EXOs和EX-Aca的表征进行检测,通过体外毒性实验检测Ex-Aca的安全性,同时考察其细胞摄取能力。结果:通过高效液相色谱计算得出共孵育法包封率及载药率均高于超声法和反复冻融法。当刺槐素浓度为80μg/mL时,包封率和载药量最高,分别为91.90%和19.68%。透射电镜(TEM)下EXOs和EX-Aca均呈杯碟状,平均粒径分别为(102.35696±0.65623)nm和(117.30038±0.74783)nm,呈现典型外泌体特性。Western Blot均检测到EXOs和EX-Aca表面标志物CD9、ALIX和TSG101的蛋白表达。因此,EX-Aca的最优制备方法参数为:刺槐素浓度为80μg/mL,与hUMSCs来源外泌体4℃共孵育48 h。体外实验验证了EX-Aca对细胞低毒性,细胞存活率>94%且EX-Aca可被BV2细胞摄取。结论:成功构建刺槐素的外泌体递药系统,制备的EX-Aca对细胞具有低毒性,具有一定靶向性。Objective:To construct exosomes(EXOs)drug delivery system of acacetin.Methods:Using exosomes derived from human umbilical cord mesenchymal stem cells(hUMSCs)as drug carriers,The exosomes loaded with acacetin(EX-Aca)were prepared by co-incubation,ultrasound and repeated freeze-thaw methods.The encapsulation rate and loading rate of EX-Aca were determined by high performance liquid chromatography.Transmission electron microscopy(TEM),particle size analysis and Western Blot were used to detect the characterization of EXOs and EX-Aca.The safety of Ex-Aca was tested by in vitro toxicity test,and its cellular uptake capacity was also investigated.Result:The results of high performance liquid chromatography showed that the encapsulation rate and drug loading rate of co-incubation method were higher than that of ultrasonic method and re‑peated freeze-thaw method.When the concentration of acacetin was 80μg/mL,the encapsulation rate and drug loading were the highest,which were 91.90%and 19.68%,respectively.Under transmission electron microscopy(TEM),EXOs and EX-Aca were cup-and-saucer-shaped,with average particle sizes of(102.35696±0.65623)nm and(117.30038±0.74783)nm,respectively,showing typical exosome characteristics.Western Blot detection of EXOs and EX-Aca surface markers CD9,ALIX and TSG101 protein expression.Therefore,the optimal preparation parameters of EX-Aca were as follows:The concentration of acacetin was 80μg/mL,and hUMSCs-derived exosomes were incubated at 4℃for 48 h.In vitro experiments confirmed that EX-Aca had low cytotoxicity,cell survival rate was>94%,and EX-Aca could be taken up by BV2 cells.Conclusion:The exosomes drug delivery system of acacetin was successfully constructed,and the prepared EX-Aca had low toxicity to cells and certain targeting.
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