Nitric Oxide-Loaded Bioinspired Lipoprotein Normalizes Tumor Vessels To Improve Intratumor Delivery and Chemotherapy of Albumin-Bound Paclitaxel Nanoparticles

被引:21
作者
Wu, Yao [1 ,2 ]
Xie, Honglei [3 ]
Li, Yongping [4 ]
Bao, Xinyue [1 ]
Lu, Guo-Liang [5 ]
Wen, Jingyuan [5 ]
Gao, Yuan [1 ]
Li, Yaping [2 ]
Zhang, Zhiwen [1 ,3 ]
机构
[1] Fudan Univ, Sch Pharm, Shanghai 201203, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[3] Yantai Inst Mat Med, Yantai Key Lab Nanomed & Adv Preparat, Yantai 264000, Shandong, Peoples R China
[4] Fudan Univ, Shanghai Pudong Hosp, Pudong Med Ctr, Dept Breast Surg, Shanghai 201399, Peoples R China
[5] Univ Auckland, Auckland 1142, New Zealand
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Nitric oxide (NO); bioinspired lipoprotein; albumin-bound paclitaxel nanoparticles; tumor penetration; vascular normalization; VASCULAR NORMALIZATION; DRUG-DELIVERY; BLOOD-VESSELS; CANCER; NANOMEDICINES; PROGRESS;
D O I
10.1021/acs.nanolett.2c04312
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The disorganized vasculatures in tumors represent a substantial challenge of intratumor nanomedicine delivery to exert the anticancer effects. Herein, we rationally designed a glutathione (GSH)-activated nitric oxide (NO) donor loaded bioinspired lipoprotein system (NO-BLP) to normalize tumor vessels and then promote the delivery efficiency of sequential albumin-bound paclitaxel nanoparticles (PAN) in tumors. NO-BLP exhibited higher tumor accumulation and deeper penetration versus the counterpart liposomal formulation (NO-Lipo) in 4T1 breast cancer tumors, thus producing notable vascular normalization efficacy and causing a 2.33-fold increase of PAN accumulation. The sequential strategy of NO-BLP plus PAN resulted in an 81.03% inhibition of tumor growth in 4T1 tumors, which was better than the NO-BLP monotherapy, PAN monotherapy, and the counterpart NO-Lipo plus PAN treatment. Therefore, the bioinspired lipoprotein of NO-BLP provides an encouraging platform to normalize tumor vessels and promote intratumor delivery of nanomedicines for effective cancer treatment.
引用
收藏
页码:939 / 947
页数:9
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