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Self-assembly of photosensitive and chemotherapeutic drugs for combined photodynamic-chemo cancer therapy with real-time tracing property
Wang, Shengtao1,2; Li, Jingtao3; Ye, Zhou1; Li, Jieling2; Wang, Anhe2; Hu, Jing1; Bai, Shuo2; Yin, Jian1
刊名COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
2019-08-05
卷号574页码:44-51
关键词Nanoparticles Self-assembly Combined therapy Real-time tracing Cancer treatment
ISSN号0927-7757
DOI10.1016/j.colsurfa.2019.04.060
英文摘要Herein, an amphipathic polymeric photosensitizer, designated as PEGylated distyryl boron dipyrromethenes with real-time tracing property, is synthesized as a kind of multifunctional carrier to load drugs for combined photodynamic-chemo therapy. The hydrophilic PEG side chains on the carriers prolong its blood circulation time and the self-assembly capacity of PEGylated distyryl boron dipyrromethenes effectively solves the problem of low drug loading efficiency and difficulty in drug release. Meanwhile, with the assistance of the photochemical internalization effect more carriers are taken up and accumulate in the cancer cells. Moreover, the auto-fluorescence of BODIPY can trace and visualize the carriers in cells or tissues and the damage of reactive oxygen species (ROS) to the multidrug resistance (MDR) transporter proteins can overcome MDR in cancer chemotherapy. The IC50 of PEGylated BODIPY is 250 mu g/mL while the IC(50 )decreased to 100 mu g/mL for Dox@ PEGylated BODIPY. As shown in our experiment the self-carriers itself without loading other bioactive constituents can obviously inhibit the growth of cancer cells, and the therapeutic effect is improved after the loading of Dox, indicating the amphipathic polymeric photosensitizer with tracing and self-assembling properties a potential multifunctional cancer treatment platform.
资助项目National Natural Science Foundation of China[21703253] ; National Natural Science Foundation of China[21774132] ; National Natural Science Foundation of China[21877052] ; National Natural Science Foundation of China[31700706] ; Natural Science Foundation for Distinguished Young Scholars of Jiangsu Province[BK20180030] ; Fundamental Research Funds for the Central Universities[JUSRP51712B] ; State Key Laboratory of Biochemical Engineering[2019KF-02] ; Max Planck Society International Partner Group Program
WOS关键词MESOPOROUS SILICA NANOPARTICLES ; RESPONSIVE NANOCARRIERS ; MULTIDRUG-RESISTANCE ; HIGHLY EFFICIENT ; CARRIER-FREE ; CO-DELIVERY ; COMBINATION ; DOXORUBICIN ; CONJUGATE ; MICELLES
WOS研究方向Chemistry
语种英语
出版者ELSEVIER SCIENCE BV
WOS记录号WOS:000471654700006
资助机构National Natural Science Foundation of China ; Natural Science Foundation for Distinguished Young Scholars of Jiangsu Province ; Fundamental Research Funds for the Central Universities ; State Key Laboratory of Biochemical Engineering ; Max Planck Society International Partner Group Program
内容类型期刊论文
源URL[http://ir.ipe.ac.cn/handle/122111/29981]  
专题中国科学院过程工程研究所
通讯作者Bai, Shuo; Yin, Jian
作者单位1.Jiangnan Univ, Sch Biotechnol, Key Lab Carbohydrate Chem & Biotechnol, Minist Educ, Wuxi 214122, Jiangsu, Peoples R China
2.Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, Beijing 100190, Peoples R China
3.China Japan Friendship Hosp, Dept Gastroenterol, Beijing 100029, Peoples R China
推荐引用方式
GB/T 7714
Wang, Shengtao,Li, Jingtao,Ye, Zhou,et al. Self-assembly of photosensitive and chemotherapeutic drugs for combined photodynamic-chemo cancer therapy with real-time tracing property[J]. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,2019,574:44-51.
APA Wang, Shengtao.,Li, Jingtao.,Ye, Zhou.,Li, Jieling.,Wang, Anhe.,...&Yin, Jian.(2019).Self-assembly of photosensitive and chemotherapeutic drugs for combined photodynamic-chemo cancer therapy with real-time tracing property.COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,574,44-51.
MLA Wang, Shengtao,et al."Self-assembly of photosensitive and chemotherapeutic drugs for combined photodynamic-chemo cancer therapy with real-time tracing property".COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS 574(2019):44-51.
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