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载姜黄素纳米金微球的制备及缓释性能研究

Preparation and Slow-release Property of Curcumin-loaded Gold Nanoparticles
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摘要 以HAuCl;和十六烷基三甲基溴化铵(CTAB)分别作为Au源和表面活性剂,采用晶种生长法制备Au纳米微球,经硅烷偶联剂表面修饰并进一步装载姜黄素,探究Au纳米微球负载Cur的载药及缓释性能,利用FTIR、XRD、SEM等分析技术对所制备材料的理化性质进行表征。结果表明,成功制备以Au为载体的姜黄素纳米金微球,与姜黄素作对比,姜黄素突释明显,在6 h完全释放,而Cur-Au在6 h释放率为17%,表明经修饰后的Au纳米微球作为载体具有药物缓释的作用。 Using HAuCl;as Au source and cetyltrimethylammonium bromide(CTAB)as surfactant, Au nanospheres were prepared by seed growth method. After surface modification with silane coupling agent and further loading with curcumin, the drug loading and slow-release properties of Cur supported by Au nanoparticles were investigated. The physical and chemical properties of the prepared materials were characterized by FTIR, XRD and SEM. The results showed that the curcumin nanomicrospheres with Au as the carrier were successfully prepared. The modified nanoparticles had good drug loading performance. Compared with curcumin, Cur-Au release rate was 17% at 6 h, while pure curcumin was completely released at 6 h, indicating that the modified gold nanoparticles as carriers had the effect of drug slow-release.
作者 冯建海 徐雪梅 黎姿 覃乙棉 罗雪玲 李胜英 FENG Jian-hai;XU Xue-mei;LI Zi;QIN Yi-mian;LUO Xue-ling;LI Sheng-ying(School of Chemical and Biological Engineering,Hechi University,Guangxi Yizhou 546300,China)
出处 《广州化工》 CAS 2022年第7期72-75,共4页 GuangZhou Chemical Industry
基金 广西高校中青年教师基础能力提升项目(2020KY15019) 河池学院2019校级科研课题(2019XJZD007) 2020年自治区级大学生创新创业计划项目(202010605015)。
关键词 姜黄素 金纳米 缓释 药物载体 curcumin gold nanoparticles release drug carrier
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  • 1马秀玲,黄丽梅,郑思宁,陈盛.磁性微球的制备及研究进展[J].广州化学,2003,28(3):58-64. 被引量:16
  • 2沈星灿,刘新艳,梁宏,卢昕.牛血红蛋白与银纳米粒子相互作用的光谱研究[J].化学学报,2006,64(6):469-474. 被引量:23
  • 3韩刚,霍文,李秋影,孙广利,段离潼.姜黄素的稳定性研究[J].中成药,2007,29(2):291-293. 被引量:43
  • 4HAAS JIMOH AKANBI M, POST E, METER-ARKEMA A, et al. Use of hydrophobins in formulation of water insoluble drugs for oral administration [J]. Colloids Surf B Biointerfaces, 2010, 75(2): 526-531.
  • 5MERISKO-LIVERSIDGE E, LIVERSIDGE G G. Nanosizing for oral and parenteral drug delivery: a perspective on formulating poorly-water soluble compounds using wet media milling technology [J]. Adv Drug Deliv Rev, 2011, 63(6): 427-440.
  • 6CHEN M C, SONAJE K, CHEN K J, et al. A review of the prospects for polymeric nanoparticle platforms in oral insulin delivery [J]. Biomaterials, 2011, 32(36): 9826-9838.
  • 7GAUCHER G, SATTURWAR P, JONES M C, et al. Polymeric micelles for oral drug delivery [J]. Eur J Pharm Biopharm, 2010, 76(2): 147-158.
  • 8ENSIGN L M, CONE R, HANES J. Oral drug delivery with polymeric nanoparticles: the gastrointestinal mucus barriers [J] Adv Drug Deliv Rev, 2012, 64(6): 557-570.
  • 9SINHA S, ALl M, BABOOTA S, et al. Solid dispersion as an approach for bioavailability enhancement of poorly water-soluble drug ritonavir [J]. AAPS PharmSciTech, 2010, 11(2): 518-527.
  • 10GOU M L, MEN K, SHI H S, et al. Curcumin-loaded biodegradable polymeric micelles for colon cancer therapy in vitro and in vivo [J]. Nanoscale, 2012, 3(4): 1558-1567.

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