[1]朱庆,曹燕丽,徐云燕,等.酸变性法构建转铁蛋白?姜黄素纳米粒子及其肿瘤靶向性[J].医学研究与战创伤救治(原医学研究生学报),2019,21(3):262-266.[doi:10.3969/j.issn.1672-271X.2019.03.009]
ZHU Qing,CAO Yan-li,XU Yun-yan,et al.Construction of transferrin curcumin nanoparticles by acid denaturation and its tumor targeting[J].JOURNAL OF MEDICALRESEARCH —COMBAT TRAUMA CARE,2019,21(3):262-266.[doi:10.3969/j.issn.1672-271X.2019.03.009]
点击复制
酸变性法构建转铁蛋白?姜黄素纳米粒子及其肿瘤靶向性(
)
ZHU Qing,CAO Yan-li,XU Yun-yan,et al.Construction of transferrin curcumin nanoparticles by acid denaturation and its tumor targeting[J].JOURNAL OF MEDICALRESEARCH —COMBAT TRAUMA CARE,2019,21(3):262-266.[doi:10.3969/j.issn.1672-271X.2019.03.009]
)《医学研究与战创伤救治》（原医学研究生学报）[ISSN:1672-271X/CN:32-1713/R]
- 卷:
- 第21卷
- 期数:
- 2019年3期
- 页码:
- 262-266
- 栏目:
- 出版日期:
- 2019-05-10
文章信息/Info
- Title:
- Construction of transferrin curcumin nanoparticles by acid denaturation and its tumor targeting
- 文章编号:
- 1672-271X（2019）03-0262-05
- Keywords:
- curcumin; transferrin; nanoparticles; self-assembly; tumor target
- 分类号:
- R285
- 文献标志码:
- A
- 摘要:
- 目的 提高姜黄素溶解度，改善姜黄素对肿瘤的靶向性。 方法 以盐酸为变性剂，打开转铁蛋白(Tf)疏水性空腔，转铁蛋白的输水区域与姜黄素结合，制备转铁蛋白-姜黄素(CCM)纳米粒子(NPs-CCM)。通过透视电镜观察纳米粒子的粒径和形貌；通过转铁蛋白及其相关制剂荧光光谱的变化，推测纳米粒子的形成过程中转铁蛋白某些基团极性的变化；通过转铁蛋白水溶液加入盐酸和姜黄素后8-苯氨基-1-萘磺酸(ANS)荧光光谱的变化，观察纳米粒子形成过程中转铁蛋白表面疏水区域的变化，推测纳米粒子的自组装的过程；通过激光共聚焦检测纳米粒子在细胞中的蓄积情况，考察纳米粒子在体外的靶向性；通过近红外活体成像实验，观察纳米粒子在小鼠肿瘤部位及其他器官的蓄积，考察纳米粒子在体内的靶向性。 结果 NPs-CCM为直径40～150 nm的球形颗粒。姜黄素的溶解度提高了200倍以上。在纳米粒子的形成过程中，转铁蛋白溶液加入盐酸后，酸使转铁蛋白变性，疏水区域暴露，姜黄素与酸变性的转铁蛋白结合后，疏水区域逐渐减少，通过酸对蛋白变性的作用形成转铁蛋白的自组装纳米粒子。在体内和体外的靶向实验中，NPs-CCM表现出较强的靶向性。 结论 纳米粒NPs-CCM是优良的CCM肿瘤靶向药物载体。
- Abstract:
- Objective To improve the solubility and targeting of curcumin to tumors. Methods Hydrochloric acid was used as a denaturing agent to open the hydrophobic cavity of transferrin (Tf). The hydrophobic region of transferrin was combined with curcumin to prepare transferrin-curcumin (CCM) nanoparticles (Nanoparticles, NPs-CCM). The particle size and morphology of the nanoparticles were observed by electron microscopy. The changes of the fluorescence spectra of transferrin and its related preparations were used to predict the polarity of certain groups of transferrin during the formation of nanoparticles. To predict the self-assembly process of nanoparticles, the changes of fluorescence spectra of ANS were used to speculate the hydrophobic region of transferrin. To speculate the targeting of nanoparticles in vitro, the accumulation of nanoparticles in cells was detected by laser confocal, and the nanoparticles were detected by near-infrared imaging including accumulation of NIR-797 and NIR-797 labelled nanoparticles at tumor sites and other organs in tumor loaded mice in vivo test. Results The NPs-CCM were about 40 to 150 nm with spherical shape. The solubility of nanoparticles is increased by more than 200 times. During the formation of the NPs-CCM, the hydrophobic region of Tf was exposed after the Tf solution being added with hydrochloric acid. Curcumin was combined with the acid-denatured transferrin after the acid denatures the transferrin. The hydrophobic region of Tf gradually reduced after the addition of CCM to the acid-denatured Tf solution. Self-assembled NPs-CCM is formed by denaturation of transferrin by hydrochloric acid. In tumor targeted experiments in vivo and in vitro, NPs-CCM showed targeting capability. Conclusion NPs-CCM are superior tumor-targeted nanocarrier system for CCM.
参考文献/References:
1 NaharPP，SlittAL，SeeramNP.Anti-Inflammatory Effects of Novel Standardized Solid Lipid Curcumin Formulations[J].J Med Food，2015，18(7):786.
2 VallianouNG，EvangelopoulosA，SchizasN，et al.Potential Anticancer Properties and Mechanisms of Action of Curcumin[J].Anticancer Res，2015，35(2):645.
3 朱国华,张琦,戴海萍,等.姜黄素抑制RPMI8226细胞增殖时丝裂原活化蛋白激酶及基质金属蛋白酶的表达[J].医学研究生学报,2014,27(10):1016-1019.
4 KuritaT，MakinoY.Novel curcumin oral delivery systems[J].Anticancer Res，2013，33(7):2807-2821.
5 PrasadS，TyagiAK，AggarwalBB.Recent Developments in Delivery，Bioavailability，Absorption and Metabolism of Curcumin:the Golden Pigment from Golden Spice[J].Cancer Res Treat，2014，46(1):2.
6 FangRH，HuCM，LukBT，et al.Cancer cell membrane-coated nanoparticles for anticancer vaccination and drug delivery[J].Nano Lett，2014，14(4):2181-2188.
7 章磊,流小舟,孙畅，等.多途径靶向给药系统在骨肉瘤治疗中的研究进展[J].东南国防医药,2016,18(6):632-635
8 LohcharoenkalW，WangL，ChenYC，et al.Protein nanoparticles as drug delivery carriers for cancer therapy[J].Biomed Res Int，2014，doi:10.1155/2014/180549
9 TortorellaS，KaragiannisTC.Transferrin Receptor-Mediated Endocytosis:A Useful Target for Cancer Therapy[J].J Membr Biol，2014，247(4):291-307.
10 KanoA，MoriyamaK，YamanoT，et al.A Grafting of poly(ethylene glycol) to poly-lysine augments its lifetime in blood circulation and accumulation in tumors without loss of the ability to as sociate with siRNA[J].J Control Release，2011，149(1):2-7.
11 TortorellaS，KaragiannisTC.Transferrin receptor-mediated endocytosis:a useful target for cancer therapy[J].J Membr Biol，2014，247(4):291-307.
12 刘苒.转铁蛋白修饰的新型多聚物载药纳米粒的研制及靶向逆转白血病多药耐药的体外研究[D].东南大学,2015.
13 WuD，GaoY，ChenL，et al.Anti-tumor effects of a novel chim-eric peptide on S180 and H22 xenografts bearing nude mice[J].Peptides，2010，31(5):850-864．
14 HorowitzPM，HuaS，GibbonsDL.Hydrophobic surfaces that are hidden in chaperonin Cpn60 can be exposed by formation of assembly-competent monomers or by ionic perturbation of the oligomer[J].J Biol Chem，1995，270(4):1535-1542.
15 龚光明,陈美惠,王曙东,等.人血浆蛋白多烯紫杉醇纳米粒子的自组装及对肿瘤的靶向性[J].东南国防医药，2016，18(5):468-471.
16 BezkorovainyA，GrohlichD.The behavior of native and reduced-alkylated human transferrin in urea and guanidine-HCl solutions[J].Biochim Biophys Acta，1967，147(3):497-510.
相似文献/References:
[1]赵志刚,曹燕丽,高茗,等.姜黄素诱导转铁蛋白纳米载体体系的组装及其抗肿瘤靶向作用[J].医学研究与战创伤救治(原医学研究生学报),2023,25(2):160.[doi:10.3969/j.issn.1672-271X.2023.02.010]
ZHAO Zhigang,CAO Yanli,GAO Ming,et al.Assembly of curcumin-induced transferrin nanocarrier system and its anti-tumor targeting[J].JOURNAL OF MEDICALRESEARCH —COMBAT TRAUMA CARE,2023,25(3):160.[doi:10.3969/j.issn.1672-271X.2023.02.010]
备注/Memo
- 备注/Memo:
- 收稿日期：2018-09-06
常用功能
统计/Statistics
- 摘要浏览/Viewed784
- 全文下载/Downloads404
- 评论/Comments
