Polymeric Nanoparticle Technologies for Oral Drug Delivery

被引:110
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 USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Lab Nanomed & Biomat,Dept Anesthesiol, 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
Polymeric Nanoparticles; Oral Delivery; Intestinal Absorption; M cell; Mucoadhesives; FcRn; NEONATAL FC-RECEPTOR; TNF-ALPHA-SIRNA; COLORECTAL-CANCER; M-CELLS; TIGHT JUNCTIONS; INSULIN; TRANSPORT; CAPECITABINE; SYSTEMS; PROTEIN;
D O I
10.1016/j.cgh.2014.06.018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Biologics increasingly are being used for the treatment of many diseases. These treatments typically require repeated doses administered by injection. Alternate routes of administration, particularly oral, are considered favorable because of improved convenience and compliance by patients, but physiological barriers such as extreme pH level, enzyme degradation, and poor intestinal epithelium permeability limit absorption. Encapsulating biologics in drug delivery systems such as polymeric nanoparticles prevents inactivation and degradation caused by low pH and enzymes of the gastrointestinal tract. However, transport across the intestinal epithelium remains the most critical barrier to overcome for efficient oral delivery. This review focuses on recent advances in polymeric nanoparticles being developed to overcome transport barriers and their potential for translation into clinical use.
引用
收藏
页码:1605 / 1610
页数:6
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