Therapeutic effect of orally administered microencapsulated oxaliplatin for colorectal cancer

被引:46
作者
Urbanska, Aleksandra M. [1 ,3 ]
Karagiannis, Emmanouil D. [1 ,3 ]
Guajardo, Gonzalo [1 ]
Langer, Robert S. [1 ,2 ,3 ,4 ]
Anderson, Daniel G. [1 ,2 ,3 ,4 ]
机构
[1] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
[2] Childrens Hosp Boston, Dept Anesthesiol, Boston, MA 02115 USA
[3] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[4] MIT, Harvard MIT Div Hlth Sci Technol, Cambridge, MA 02142 USA
基金
加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词
Oxaliplatin; Intestinal tumorigenesis; Colon cancer; Oral delivery; Alginate; C-REACTIVE PROTEIN; MULTIPLE INTESTINAL NEOPLASIA; CHRONIC INFLAMMATION; SERUM INTERLEUKIN-6; FECAL LACTOFERRIN; DISEASE-ACTIVITY; ANIMAL-MODELS; GROWTH-FACTOR; COLON-CANCER; ALGINATE;
D O I
10.1016/j.biomaterials.2012.03.023
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Colorectal cancer is a significant source of morbidity and mortality in the United States and other Western countries. Oral delivery of therapeutics remains the most patient accepted form of medication. The development of an oral delivery formulation for local delivery of chemotherapeutics in the gastrointestinal tract can potentially alleviate the adverse side effects including systemic cytotoxicity, as well as focus therapy to the lesions. Here we develop an oral formulation of the chemotherapeutic drug oxaliplatin for the treatment of colorectal cancer. Oxaliplatin was encapsulated in pH sensitive, mucoadhesive chitosan-coated alginate microspheres. The microparticles were formulated to release the chemotherapeutics after passing through the acidic gastric environment thus targeting the intestinal tract. In vivo, these particles substantially reduced the tumor burden in an orthotopic mouse model of colorectal cancer, and reduced mortality. (C) 2012 Published by Elsevier Ltd.
引用
收藏
页码:4752 / 4761
页数:10
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