Systemic Targeting of Lymph Node Metastasis through the Blood Vascular System by Using Size-Controlled Nano carriers

被引:134
作者
Cabral, Horacio [1 ]
Makino, Jun [2 ]
Matsumoto, Yu [2 ]
Mi, Peng [3 ]
Wu, Hailiang [1 ]
Nomoto, Takahiro [3 ]
Toh, Kazuko [2 ]
Yamada, Naoki [4 ]
Higuchi, Yuriko [5 ]
Konishi, Satoshi [6 ]
Kano, Mitsunobu R. [7 ]
Nishihara, Hiroshi [8 ]
Miura, Yutaka [2 ]
Nishiyama, Nobuhiro [3 ]
Kataoka, Kazunori [1 ,2 ,4 ,9 ]
机构
[1] Univ Tokyo, Grad Sch Engn, Dept Bioengn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Univ Tokyo, Grad Sch Med, Ctr Dis Biol & Integrat Med, Bunkyo Ku, Tokyo 1130033, Japan
[3] Tokyo Inst Technol, Chem Resources Lab, Polymer Chem Div, Midori Ku, Yokohama, Kanagawa 2268503, Japan
[4] Univ Tokyo, Grad Sch Engn, Dept Mat Engn, Bunkyo Ku, Tokyo 1138656, Japan
[5] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
[6] Ritsumeikan Univ, Dept Mech Engn, Kusatsu, Shiga 5258577, Japan
[7] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pharmaceut Biomed, Kita Ku, Okayama 7008530, Japan
[8] Hokkaido Univ, Sch Med, Lab Translat Pathol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
[9] Innovat Ctr NanoMed, Kawasaki Ku, Kawasaki, Kanagawa 2100821, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
polymeric micelles; lymph node metastasis; melanoma; Doxil; oxaliplatin; intravital microscopy; POLYMERIC MICELLES; SOLID TUMORS; BREAST-CANCER; PHASE-I; NEOADJUVANT CHEMOTHERAPY; MELANOMA PATIENTS; DRUG-DELIVERY; NANOPARTICLE; NANOCARRIERS; DRAINAGE;
D O I
10.1021/nn5070259
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Occult nodal metastases increase the risk of cancer recurrence, demoting prognosis and quality of life of patients. While targeted drug delivery by using systemically administered nanocarriers can potentially control metastatic disease, lymph node metastases have been mainly dealt by locally injecting nanocarriers, which may not always be applicable. Herein, we demonstrated that sub-50 nm polymeric micelles incorporating platinum anticancer drugs could target lymph node metastases in a syngeneic melanoma model after systemic injection, even after removing the primary tumors, limiting the growth of the metastases. By comparing these micelles with clinically used doxorubicin-loaded liposomes (Doxil) having 80 nm, as well as a 70 nm version of the micelles, we found that the targeting efficiency of the nanocarriers against lymph node metastases was associated with their size-regulated abilities to extravasate from the blood vasculature in metastases and to penetrate within the metastatic mass. These findings indicate the potential of sub-50 nm polymeric micelles for developing effective conservative treatments against lymph node metastasis capable of reducing relapse and improving survival.
引用
收藏
页码:4957 / 4967
页数:11
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