Stable Porous Organic Cage Nanocapsules for pH-Responsive Anticancer Drug Delivery for Precise Tumor Therapy

被引:3
|
作者
Deng, Yanping [1 ]
Du, Zhenhong [1 ]
Du, Shunfu [2 ,3 ]
Li, Nan [1 ]
Wang, Wenjing [2 ,3 ]
Su, Kongzhao [2 ,3 ]
Yuan, Daqiang [2 ,3 ]
机构
[1] Fujian Med Univ, Sch Pharm, Fujian Key Lab Nat Med Pharmacol, Fuzhou 350122, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
来源
ACS APPLIED BIO MATERIALS | 2024年 / 7卷 / 11期
关键词
porous organic cages; pH-responsive delivery; paclitaxel; nanocarrier drug delivery; tumortherapy; STABILIZATION; FRAMEWORK; WATER;
D O I
10.1021/acsabm.4c01123
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The search for drug nanocarriers with stimuli-responsive properties and high payloads for targeted drug delivery and precision medicine is currently a focal point of biomedical research, but this endeavor still encounters various challenges. Herein, a porous organic cage (POC) is applied to paclitaxel (PTX) drug delivery for cancer therapy for the first time. Specifically, water-soluble, stable, and biocompatible POC-based nanocapsules (PTX@POC@RH40) with PTX encapsulation efficiency over 98% can be synthesized by simply grafting nonionic surfactant (Polyoxyl 40 hydrogenated castor oil, RH40) on the POC surface. These PTX@POC@RH40 nanocapsules demonstrate remarkable stability for more than a week without aggregation and exhibit pH-responsive behavior under acidic conditions (pH 5.5) and display sustained release behavior at both pH 7.4 and pH 5.5. Intravenous administration of PTX@POC@RH40 led to a 3.5-fold increase in PTX bioavailability compared with the free PTX group in rats. Moreover, in vivo mouse model experiments involving 4T1 subcutaneous breast cancer tumors revealed that PTX@POC@RH40 exhibited enhanced anticancer efficacy with minimal toxicity compared with free PTX. These findings underscore the potential of POCs as promising nanocarriers for stimuli-responsive drug delivery in therapeutic applications.
引用
收藏
页码:7535 / 7543
页数:9
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