Novel Approach of Using Near-Infrared Responsive PEGylated Gold Nanorod Coated Poly(L-lactide) Microneedles to Enhance the Antitumor Efficiency of Docetaxel-Loaded MPEG-PDLLA Micelles for Treating an A431 Tumor

被引:125
|
作者
Hao, Ying [1 ]
Dong, MingLing [1 ]
Zhang, TaoYe [2 ]
Peng, JinRong [1 ]
Jia, YanPeng [1 ]
Cao, YiPing [2 ]
Qian, ZhiYong [1 ]
机构
[1] Sichuan Univ, West China Hosp, West China Med Sch, Collaborat Innovat Ctr Biotherapy,State Key Lab B, Chengdu 610041, Peoples R China
[2] Jianghan Univ, Key Lab Optoelect Chem Mat & Devices, Minist Educ, Wuhan 430056, Peoples R China
关键词
photothermal therapy (PTT); GNR-PEG@NINs; MPEG-PDLLA-DTX micelles; A431; tumor; synergetic effect; TRANSDERMAL DELIVERY; PHOTOTHERMAL THERAPY; CANCER-THERAPY; IN-VIVO; NANOPARTICLES; DRUG; COMBINATION; CHEMOTHERAPY; INSULIN; IMMUNOTHERAPY;
D O I
10.1021/acsami.7b03604
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The combination of chemotherapy and photothermal therapy (PTT) plays a significant role in synergistic tumor therapy. However, a high dosage of chemotherapy drugs or photothermal agents may cause series side effects. To overcome these challenges, we designed a near-infrared (NIR) responsive PEGylated gold nanorod (GNR-PEG) coated poly(L-lactide) microneedle (PLLA MN) system (GNR-PEG@MN) to enhance antitumor efficiency of docetaxel-loaded MPEG-PDLLA (MPEG-PDLLA-DTX) micelles for treating an A431 tumor. The as-made GNR-PEG@MINs contained only 31.8 +/- 31.22 mu g of GNR-PEG per patch and exhibited excellent heating efficacy both in vitro and in vivo. Meanwhile, GNR-PEG@MN with the height of 480,mu m had good skin insertion ability and was harmless to the skin. On the other hand, GNR-PEG@MN had good heating transfer ability in vivo, and the tumor sites could reach 50 C-circle within 5 min. In comparison with chemotherapy and PTT alone, the combination of low dosage MPEG-PDLLA-DTX micelles (5 mg/kg) and GNR-PEG@MNs completely eradicated the A431 tumor without recurrence in vivo, demonstrating a remarkable synergetic effect. Hence, GNR-PEG@MN could be a promising carrier to enhance the antitumor effect of MPEG-PDLLA-DTX micelles for treating superficial tumors and is expected to have a great potential in clinical translation for human epidermoid cancer therapy.
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页码:15317 / 15327
页数:11
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