A multifunctional drug nanocarrier for efficient anticancer therapy

被引:28
|
作者
Teijeiro-Valino, Carmen [1 ]
Novoa-Carballal, Ramon [2 ]
Borrajo, Erea [3 ]
Vidal, Anxo [3 ]
Alonso-Nocelo, Marta [4 ]
de la Fuente Freire, Maria [4 ]
Lopez-Casas, Pedro P. [5 ]
Hidalgo, Manuel [5 ]
Csaba, Noemi [1 ]
Jose Alonso, Maria [1 ]
机构
[1] Univ Santiago Compostela, Ctr Res Mol Med & Chron Dis CIMUS, Dept Pharm & Pharmaceut Technol, Santiago De Compostela, Spain
[2] Univ Minho, 3Bs Res Grp Biomat Biodegradables & Biomimet, Headquarters European Inst Excellence Tissue Engn, AvePk, Barco, Guimaraes, Portugal
[3] Univ Santiago Compostela, Ctr Res Mol Med & Chron Dis CIMUS, Dept Physiol, Santiago De Compostela, Spain
[4] Hlth Res Inst Santiago Compostela IDIS, Translat Med Oncol Grp, Nanooncol Unit, SERGAS,CIBERONC, Santiago De Compostela, Spain
[5] Spanish Natl Canc Res Ctr CNIO, Melchor Fernandez Almagro 3, Madrid 328029, Spain
关键词
Tumor homing peptide; Nanocapsules; Lymphatic targeting; Tumor targeting; Metastasis; Anti-cancer drug delivery; HYALURONIC-ACID NANOPARTICLES; ANTITUMOR EFFICACY; EMERGING PLATFORM; PACLITAXEL; DELIVERY; NANOMEDICINE; NANOCAPSULES; DOCETAXEL; TUMORS; TISSUE;
D O I
10.1016/j.jconrel.2018.12.002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
So far, the success of anticancer nanomedicines has been moderate due to their lack of adequate targeting properties and/or to their difficulties for penetrating tumors. Here we report a multifunctional drug nanocarrier consisting of hyaluronic acid nanocapsules conjugated with the tumor homing peptide tLyp1, which exhibits both, dual targeting properties (to the tumor and to the lymphatics), and enhanced tumor penetration. Data from a 3D co-culture in vitro model showed the capacity of these nanocapsules to interact with the NRP1 receptors over-expressed in cancer cells. The targeting capacity of the nanocapsules was evidenced in orthotopic lung cancer-bearing mice, using docetaxel as a standard drug. The results showed a dramatic accumulation of docetaxel in the tumor (37-fold the one achieved with Taxotere (R)). This biodistribution profile correlated with the high efficacy shown in terms of tumor growth regression and drastic reduction of metastasis in the lymphatics. When efficacy was validated in a pancreatic patient-derived tumor, the nanocapsule's activity was comparable to that of a dose ten times higher of Abraxane (R). Multi-functionality was found to be the key to the success of this new therapy.
引用
收藏
页码:154 / 164
页数:11
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