Nanoparticles for oral delivery: Design, evaluation and state-of-the-art

被引:346
作者
Date, Abhijit A. [1 ,2 ]
Hanes, Justin [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ]
Ensign, Laura M. [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Ctr Nanomed, Wilmer Eye Inst, 400 N Broadway, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Dept Ophthalmol, Wilmer Eye Inst, 400 N Broadway, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Dept Chem & Biomol Engn, 3400 N Charles St, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Dept Environm & Hlth Sci, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Dept Oncol, Baltimore, MD 21205 USA
[7] Johns Hopkins Univ, Dept Pharmacol, Baltimore, MD 21205 USA
[8] Johns Hopkins Univ, Dept Mol Sci, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
Inflammatory bowel disease; Colon targeting; Intestinal lymphatic system; Targeted delivery; In vitro-in vivo correlation; INFLAMMATORY-BOWEL-DISEASE; SOLID LIPID NANOPARTICLES; HELICOBACTER-PYLORI INFECTION; IN-VIVO EVALUATION; ON-A-CHIP; SENSITIVE POLYMERIC NANOPARTICLES; FOLLICLE-ASSOCIATED EPITHELIUM; CELL-TARGETING NANOPARTICLES; INFLAMED INTESTINAL-MUCOSA; ZINC-OXIDE NANOPARTICLES;
D O I
10.1016/j.jconrel.2016.06.016
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The oral route is a preferred method of drug administration, though achieving effective drug delivery and minimizing off-target side effects is often challenging. Formulation into nanoparticles can improve drug stability in the harsh gastrointestinal (GI) tract environment, providing opportunities for targeting specific sites in the GI tract, increasing drug solubility and bioavailability, and providing sustained release in the GI tract. However, the unique and diverse physiology throughout the GI tract, including wide variation in pH, mucus that varies in thickness and structure, numerous cell types, and various physiological functions are both a barrier to effective delivery and an opportunity for nanoparticle design. Here, nanoparticle design aspects to improve delivery to particular sites in the GI tract are discussed. We then review new methods for evaluating oral nanoparticle formulations, including a short commentary on data interpretation and translation. Finally, the state-of-the-art in preclinical targeted nanoparticle design is reviewed. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:504 / 526
页数:23
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