5-Fluorouracil crystal-incorporated, pH-responsive, and release-modulating PLGA/Eudragit FS hybrid microparticles for local colorectal cancer-targeted chemotherapy

被引:8
作者
Lee, Juho [1 ]
Bae, Junhwan [1 ]
Kwak, Dongmin [1 ]
Kim, Hyunwoo [1 ]
Kim, Jihyun [1 ]
Hlaing, Shwe Phyu [1 ]
Saparbayeva, Aruzhan [1 ]
Lee, Eun Hee [2 ]
Yoon, In-Soo [1 ]
Kim, Min-Soo [1 ]
Moon, Hyung Ryong [1 ]
Yoo, Jin-Wook [1 ]
机构
[1] Pusan Natl Univ, Coll Pharm, Pusan 46241, South Korea
[2] Korea Univ, Coll Pharm, Sejong 30019, South Korea
基金
新加坡国家研究基金会;
关键词
5-fluorouracil; pH-responsive; Release modulation; Colorectal cancer; Colon-targeted delivery; Local chemotherapy; MESOPOROUS SILICA NANOPARTICLES; COLON-CANCER; DRUG-DELIVERY; MURINE COLITIS; DESIGN; MICROSPHERES; BUDESONIDE;
D O I
10.1016/j.ijpharm.2022.122443
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
5-Fluorouracil (5-FU) is a widely used chemotherapeutic agent for colorectal cancer (CRC) owing to its potent anticancer effects. However, severe systemic side effects and poor drug accumulation in the CRC tissues limit its efficacy. This study aimed to develop 5-FU crystal-incorporated, pH-responsive, and release-modulating poly(D,L- lactide-co-glycolide)/Eudragit FS hybrid microparticles (5FU-EPMPs) for the local CRC-targeted chemotherapy. Approximately 150 mu m 5FU-EPMPs were fabricated via the S/O/W emulsion solvent evaporation method, with 7.93 +/- 0.24% and 87.23 +/- 2.64% 5-FU loading and encapsulation efficiencies, respectively. Drug release profiles in a simulated pH environment of the gastrointestinal tract revealed that premature 5-FU release in the stomach and small intestine was prevented, thereby minimizing systemic 5-FU absorption. After reaching the colon, 5-FU was continuously released for >15 h, allowing long-term exposure of CRC tissues to sufficient 5-FU concentra-tions. Furthermore, in a CRC mouse model, the 5FU-EPMPs showed potent inhibition of tumor growth without signs of systemic toxicity. Thus, the 5FU-EPMPs represent a promising drug delivery system for local CRC -targeted chemotherapy.
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页数:9
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