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作为超分子水凝胶交联剂的阿霉素纳米球。

Nanospheres of doxorubicin as cross-linkers for a supramolecular hydrogelation.

作者信息

Xue Qiang, Ren He, Xu Chao, Wang Gang, Ren Chunhua, Hao Jihui, Ding Dan

机构信息

National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Department of Pancreatic Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin, P. R. China.

State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, Nankai University, Tianjin. 300071, P. R. China.

出版信息

Sci Rep. 2015 Mar 5;5:8764. doi: 10.1038/srep08764.

Abstract

In this study, we synthesized a peptide of Nap-GFFYGRGD, which could self-assemble into supramolecular nanofibers. The peptide itself could only form nanofibers but not hydrogels due to the relative weak inter-fiber interactions. The resulting nanofibers were then utilized as the vehicles for anticancer drug doxorubicin. It was found that the nanofibers of Nap-GFFYGRGD could not encapsulate doxorubicin, whereas the drug formed nanospheres, which were located at the surface of the nanofibers. Due to the electrostatic interactions between the negatively charged nanofibers and the positively charged doxorubicin nanospheres, the doxorubicin nanospheres were able to serve as a cross-linker to increase the inter-fiber interactions, leading to the formation of stable three-dimentional fiber networks and hydrogels. The resulting doxorubicin-peptide hydrogels were capable of releasing the drug in a sustained manner, which also showed comparable cytotoxicity as compared to free doxorubicin against a variety of cancer cell lines including HeLa and MCF-7 cancer cells. Therefore, this successful example using drug as the peptide nanofiber cross-linkers provided a new strategy for fabricating supramolecular hydrogelation for controlled delivery of anticancer drugs.

摘要

在本研究中,我们合成了一种Nap-GFFYGRGD肽,它能够自组装成超分子纳米纤维。由于纤维间相互作用相对较弱,该肽本身只能形成纳米纤维而不能形成水凝胶。然后将所得纳米纤维用作抗癌药物阿霉素的载体。结果发现,Nap-GFFYGRGD纳米纤维不能包裹阿霉素,而药物形成纳米球,位于纳米纤维表面。由于带负电荷的纳米纤维与带正电荷的阿霉素纳米球之间的静电相互作用,阿霉素纳米球能够作为交联剂增加纤维间相互作用,导致形成稳定的三维纤维网络和水凝胶。所得的阿霉素-肽水凝胶能够持续释放药物,与游离阿霉素相比,对包括HeLa和MCF-7癌细胞在内的多种癌细胞系也显示出相当的细胞毒性。因此,这个将药物用作肽纳米纤维交联剂的成功例子为制备用于抗癌药物控释的超分子水凝胶提供了一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee5e/4350081/6f586ef92982/srep08764-f1.jpg

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