Eudragit S100 Coated Citrus Pectin Nanoparticles for Colon Targeting of 5-Fluorouracil

被引:110
|
作者
Subudhi, M. Biswaranjan [1 ]
Jain, Ankit [1 ]
Jain, Ashish [1 ]
Hurkat, Pooja [1 ]
Shilpi, Satish [1 ]
Gulbake, Arvind [1 ]
Jain, Sanjay K. [1 ]
机构
[1] Dr Hari Singh Gour Cent Univ, Dept Pharmaceut Sci, Sagar 470003, MP, India
来源
MATERIALS | 2015年 / 8卷 / 03期
关键词
DRUG-DELIVERY SYSTEM; IN-VITRO; PLGA NANOPARTICLES; MICROSPHERES; CHITOSAN; RELEASE; CANCER; ASSAY; VIVO; POLYSACCHARIDES;
D O I
10.3390/ma8030832
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In the present study, Eudragit S100 coated Citrus Pectin Nanoparticles (E-CPNs) were prepared for the colon targeting of 5-Fluorouracil (5-FU). Citrus pectin also acts as a ligand for galectin-3 receptors that are over expressed on colorectal cancer cells. Nanoparticles (CPNs and E-CPNs) were characterized for various physical parameters such as particle size, size distribution, and shape etc. In vitro drug release studies revealed selective drug release in the colonic region in the case of E-CPNs of more than 70% after 24 h. In vitro cytoxicity assay (Sulphorhodamine B assay) was performed against HT-29 cancer cells and exhibited 1.5 fold greater cytotoxicity potential of nanoparticles compared to 5-FU solution. In vivo data clearly depicted that Eudragit S100 successfully guarded nanoparticles to reach the colonic region wherein nanoparticles were taken up and showed drug release for an extended period of time. Therefore, a multifaceted strategy is introduced here in terms of receptor mediated uptake and pH-dependent release using E-CPNs for effective chemotherapy of colorectal cancer with uncompromised safety and efficacy.
引用
收藏
页码:832 / 849
页数:18
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