Polymeric nanoparticle drug delivery technologies for oral delivery applications

被引:193
作者
Pridgen, Eric M. [1 ]
Alexis, Frank [2 ]
Farokhzad, Omid C. [3 ,4 ]
机构
[1] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[2] Clemson Univ, Dept Bioengn, Clemson, SC 29634 USA
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Anesthesiol,Lab Nanomed & Biomat, Boston, MA 02115 USA
[4] King Abdulaziz Univ, Jeddah 21413, Saudi Arabia
基金
美国国家卫生研究院;
关键词
chemotherapy; inflammatory bowel disease; insulin; M cells; mucoadhesives; mucosal vaccinations; oral delivery; polymeric nanoparticles; transcytosis; WHEAT-GERM-AGGLUTININ; NEONATAL FC-RECEPTOR; M-CELLS; COLORECTAL-CANCER; IN-VITRO; BIODEGRADABLE MICROPARTICLES; INSULIN DELIVERY; TIGHT JUNCTIONS; CHITOSAN; SYSTEM;
D O I
10.1517/17425247.2015.1018175
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Many therapeutics are limited to parenteral administration. Oral administration is a desirable alternative because of the convenience and increased compliance by patients, especially for chronic diseases that require frequent administration. Polymeric nanoparticles (NPs) are one technology being developed to enable clinically feasible oral delivery. Areas covered: This review discusses the challenges associated with oral delivery. Strategies used to overcome gastrointestinal (GI) barriers using polymeric NPs will be considered, including mucoadhesive biomaterials and targeting of NPs to transcytosis pathways associated with M cells and enterocytes. Applications of oral delivery technologies will also be discussed, such as oral chemotherapies, oral insulin, treatment of inflammatory bowel disease, and mucosa! vaccinations. Expert opinion: There have been many approaches used to overcome the transport barriers presented by the GI tract, but most have been limited by low bioavailability. Recent strategies targeting NPs to transcytosis pathways present in the intestines have demonstrated that it is feasible to efficiently transport both therapeutics and NPs across the intestines and into systemic circulation after oral administration. Further understanding of the physiology and pathophysiology of the intestines could lead to additional improvements in oral polymeric NP technologies and enable the translation of these technologies to clinical practice.
引用
收藏
页码:1459 / 1473
页数:15
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