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Programmed pH-responsive core-shell nanoparticles for precisely targeted therapy of ulcerative colitis
被引:20
|作者:
Zhang, Guangshuai
[1
]
Han, Wen
[1
]
Zhao, Peixu
[1
]
Wang, Zijun
[1
,2
]
Li, Mo
[3
]
Sui, Xiaofan
[3
]
Liu, Yanhua
[4
]
Tian, Baocheng
[5
]
He, Zhonggui
[1
]
Fu, Qiang
[1
]
机构:
[1] Shenyang Pharmaceut Univ, Wuya Coll Innovat, 103 Wenhua Rd, Shenyang 110016, Peoples R China
[2] Sichuan Univ, West China Sch Pharm, 17 Sect 3,Renmin South Rd, Chengdu 610041, Peoples R China
[3] Liaoning Inst Drug Control, 7 Chongshan West Rd, Shenyang 110016, Peoples R China
[4] Ningxia Med Univ, 1160 Shengli St, Yinchuan 750004, Peoples R China
[5] Binzhou Med Univ, Sch Pharm, 346 Guanhai Rd, Yantai 264003, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
DELIVERY;
EUDRAGIT(R);
D O I:
10.1039/d2nr04968f
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
pH-Responsive nanotherapeutics were recently developed for the treatment of ulcerative colitis (UC). However, they target the entire colon rather than the UC site, which leads to insufficient accumulation in inflamed colon lesions and causes side effects. Core-shell nanoparticles exhibit unique advantages in improving the precision of targeted delivery. In this study, Eudragit (R) EPO and L100, two pH-sensitive materials, were coated on nano-sized curcumin to fabricate core-shell nanoparticles. The developed CNs@EPO@L100 exhibited programmed pH-responsive drug release behavior, improved in vitro anti-inflammatory ability, and enhanced accumulation at the site of inflammation in the colon. Furthermore, after oral administration, CNs@EPO@L100 significantly ameliorated the inflammatory symptoms in mice. Taken together, this study provides insights into programmed release through the rational application of pH-sensitive materials and offers strategies for a precisely targeted therapy of UC using core-shell nanoparticles.
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页码:1937 / 1946
页数:10
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