Animal models for evaluation of oral delivery of biopharmaceuticals

被引:33
作者
Harloff-Helleberg, Stine [1 ]
Nielsen, Line Hagner [2 ]
Nielsen, Hanne Morck [1 ]
机构
[1] Univ Copenhagen, Dept Pharm, Fac Hlth & Med Sci, Univ Pk 2, DK-2100 Copenhagen O, Denmark
[2] Tech Univ Denmark, Dept Micro & Nanotechnol, Orsteds Plads 345C, DK-2800 Lyngby, Denmark
关键词
Peptides; Proteins; Insulin; In situ perfusion; In vivo; Macromolecules; IN-VIVO EVALUATION; GLUCAGON-LIKE PEPTIDE-1; INTESTINAL DRUG ABSORPTION; SOLID LIPID NANOPARTICLES; CELL-PENETRATING PEPTIDE; SINGLE-PASS VS; INSULIN DELIVERY; SALMON-CALCITONIN; PERORAL DELIVERY; HYDROGEL MICROPARTICLES;
D O I
10.1016/j.jconrel.2017.09.025
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biopharmaceuticals are increasingly important for patients and the pharmaceutical industry due to their ability to treat and, in some cases, even cure chronic and potentially life-threatening diseases. Most biopharmaceuticals are administered by injection, but intensive focus on development of systems for oral delivery of biopharmaceuticals may result in new treatment modalities to increase the patient compliance and reduce product cost. In the preclinical development phase, use of experimental animal models is essential for evaluation of new formulation designs. In general, the limited oral bioavailability of biopharmaceuticals, of just a few percent, is expected, and therefore, the animal models and the experimental settings must be chosen with utmost care. More knowledge and focus on this topic is highly needed, despite experience from the numerous studies evaluating animal models for oral drug delivery of small molecule drugs. This review highlights and discusses pros and cons of the most currently used animal models and settings. Additionally, it also looks into the influence of anesthetics and sampling methods for evaluation of drug delivery systems for oral delivery of biopharmaceuticals primarily with examples on insulin.
引用
收藏
页码:57 / 71
页数:15
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