| Literature DB >> 27939904 |
Si Chen1, Qi Lei2, Wen-Xiu Qiu2, Li-Han Liu2, Di-Wei Zheng2, Jin-Xuan Fan2, Lei Rong2, Yun-Xia Sun3, Xian-Zheng Zhang4.
Abstract
In this work, mitochondria-targeting gold nanostar (AuNS) and anticarcinogen DOX were co-encapsulated in hyaluronic acid (HA) protective shell for tumor-targeting synergistic photothermal/chemo-therapy. Cationic peptide R8 and mitochondria-targeting pro-apoptotic peptide TPP-KLA were co-decorated on AuNS to form AuNS-pep via Au-S bonds. Then, electronegative HA was further coated on the surface via electrostatic interaction for cancer cell targeting. During the coating process, DOX was also introduced via electrostatic interaction to obtain a versatile nanoplatform AuNS-pep/DOX@HA. It was found that the nanoplatform could be internalized into tumor cells via CD44 receptor-mediated recognition. Followed digestion by hyaluronidase (HAase), the therapeutic nanoplatform was able to release DOX for chemotherapy and mitochondria-targeting nanoheater AuNS-pep for near infrared (NIR) light triggered subcellular photothermal therapy (PTT). This tumor-targeting nanoplatform AuNS-pep/DOX@HA displayed prominent non-resistant or resistant tumor inhibition both in vitro and in vivo.Entities:
Keywords: Combination therapy; Gold nanostar; Mitochondria-targeting; Photothermal therapy; Pro-apoptotic peptide
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Year: 2016 PMID: 27939904 DOI: 10.1016/j.biomaterials.2016.11.056
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479