Synthesis of a functionalized dipeptide for targeted delivery and pH-sensitive release of chemotherapeutics

被引:13
|
作者
Kiran, Sonia [1 ]
Dwivedi, Pankaj [2 ]
Khatik, Renuka [1 ]
Hameed, Sadaf [3 ]
Dwivedi, Monika [2 ]
Huang, Fangsheng [2 ]
Xu, Ronald X. [2 ,4 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Hefei Natl Lab Phys Sci Microscale, 96 Jinzhai Rd, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Sch Engn Sci, Dept Precis Machinery & Precis Instrumentat, Hefei 230026, Anhui, Peoples R China
[3] Peking Univ, Coll Engn, Dept Biomed Engn, Beijing 100871, Peoples R China
[4] Ohio State Univ, Dept Biomed Engn, Columbus, OH 43210 USA
关键词
IN-VITRO; DRUG; CANCER; SYSTEM; ANTICANCER; PEPTIDES;
D O I
10.1039/c9cc09131a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Targeted delivery of chemotherapeutics to tumor cells is one of the biggest challenges in cancer treatment. Herein, we synthesized smart dipeptide nanoparticles for cancer-specific targeting and intracellular pH-sensitive release of chemotherapeutics. Diphenylalanine peptide was synthesized and further developed as nanoparticles (NPs), which were functionalized with folic acid utilizing the carbodiimide reaction. Doxorubicin (Dox) was loaded to self-assembled non-functionalized (FF-Dox) and folate functionalized peptides NPs (FA-FF-Dox). Moreover, the experiments revealed the pH-sensitive release of Dox for both FA-FF-Dox and FF-Dox due to the protonation of the Schiff base and the amines present in the peptides at low pH, enhancing intracellular release subsequent to receptor-mediated endocytosis. Further, biodistribution and the pharmacokinetics study revealed enhanced targeting efficiency of FA-FF-Dox with high accumulation in tumor cells.
引用
收藏
页码:285 / 288
页数:4
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