Local delivery of macromolecules to treat diseases associated with the colon

被引:76
作者
Bak, A. [1 ]
Ashford, M. [2 ]
Brayden, D. J. [3 ,4 ]
机构
[1] AstraZeneca, IMED Biotech Unit, Pharmaceut Sci, Adv Drug Delivery, Gothenburg, Sweden
[2] AstraZeneca, IMED Biotech Unit, Pharmaceut Sci, Adv Drug Delivery, Macclesfield, Cheshire, England
[3] Univ Coll Dublin, UCD Sch Vet Med, Dublin 4, Ireland
[4] Univ Coll Dublin, UCD Conway Inst, Dublin 4, Ireland
基金
爱尔兰科学基金会;
关键词
Colonic drug delivery; Oral macromolecule delivery; Large intestine; Inflammatory bowel disease; Colorectal cancer; Enteric infections; INFLAMMATORY-BOWEL-DISEASE; TARGETED DRUG-DELIVERY; VASOACTIVE-INTESTINAL-PEPTIDE; SMALL INTERFERING RNA; GASTROINTESTINAL PH PROFILES; NECROSIS FACTOR ANTIBODY; FILM-COATED TABLETS; PROOF-OF-CONCEPT; IN-VIVO; ULCERATIVE-COLITIS;
D O I
10.1016/j.addr.2018.10.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Current treatments for intestinal diseases including inflammatory bowel diseases, irritable bowel syndrome, and colonic bacterial infections are typically small molecule oral dosage forms designed for systemic delivery. The intestinal permeability hurdle to achieve systemic delivery from oral formulations of macromolecules is challenging, but this drawback can be advantageous if an intestinal region is associated with the disease. There are some promising formulation approaches to release peptides, proteins, antibodies, antisense oligonucleotides, RNA, and probiotics in the colon to enable local delivery and efficacy. We briefly review colonic physiology in relation to the main colon-associated diseases (inflammatory bowel disease, irritable bowel syndrome, infection, and colorectal cancer), along with the impact of colon physiology on dosage form design of macromolecules. We then assess formulation strategies designed to achieve colonic delivery of small molecules and concluded that they can also be applied some extent to macromolecules. We describe examples of formulation strategies in preclinical research aimed at colonic delivery of macromolecules to achieve high local concentration in the lumen, epithelial-, or sub epithelial tissue, depending on the target, but with the benefit of reduced systemic exposure and toxicity. Finally, the industrial challenges in developing macromolecule formulations for colon-associated diseases are presented, along with a framework for selecting appropriate delivery technologies. Crown Copyright (C) 2018 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2 / 27
页数:26
相关论文
共 244 条
[1]   The use of scintigraphy to provide ''proof of concept'' for novel polysaccharide preparations designed for colonic drug delivery [J].
Adkin, DA ;
Kenyon, CJ ;
Lerner, EI ;
Landau, I ;
Strauss, E ;
Caron, D ;
Penhasi, A ;
Rubinstein, A ;
Wilding, IR .
PHARMACEUTICAL RESEARCH, 1997, 14 (01) :103-107
[2]   Alginate microparticles as oral colon drug delivery device: A review [J].
Aguero, Lissette ;
Zaldivar-Silva, Dionisio ;
Pena, Luis ;
Dias, Marcos L. .
CARBOHYDRATE POLYMERS, 2017, 168 :32-43
[3]   Current status of selected oral peptide technologies in advanced preclinical development and in clinical trials [J].
Aguirre, T. A. S. ;
Teijeiro-Osorio, D. ;
Rosa, M. ;
Coulter, I. S. ;
Alonso, M. J. ;
Brayden, D. J. .
ADVANCED DRUG DELIVERY REVIEWS, 2016, 106 :223-241
[4]   Coated minispheres of salmon calcitonin target rat intestinal regions to achieve systemic bioavailability: Comparison between intestinal instillation and oral gavage [J].
Aguirre, Tanira A. S. ;
Aversa, Vincenzo ;
Rosa, Monica ;
Guterres, Silvia S. ;
Pohlmann, Adriana R. ;
Coulter, Ivan ;
Brayden, David J. .
JOURNAL OF CONTROLLED RELEASE, 2016, 238 :242-252
[5]   Comparison of in vitro and in vivo performance of a colonic delivery system [J].
Ahmed, Iman S. ;
Ayres, James W. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 409 (1-2) :169-177
[6]   Budesonide loaded nanoparticles with pH-sensitive coating for improved mucosal targeting in mouse models of inflammatory bowel diseases [J].
Ali, H. ;
Weigmann, B. ;
Neurath, M. F. ;
Collnot, E. M. ;
Windbergs, M. ;
Lehr, C. -M. .
JOURNAL OF CONTROLLED RELEASE, 2014, 183 :167-177
[7]  
Allegretti JR, 2018, GASTROENTEROLOGY, V154, pS1049
[8]   Dual-coated lactic acid bacteria: an emerging innovative technology in the field of probiotics [J].
Alvarez-Calatayud, Guillermo ;
Margolles, Abelardo .
FUTURE MICROBIOLOGY, 2016, 11 (03) :467-475
[9]   Colon-Targeted Oral Drug Delivery Systems: Design Trends and Approaches [J].
Amidon, Seth ;
Brown, Jack E. ;
Dave, Vivek S. .
AAPS PHARMSCITECH, 2015, 16 (04) :731-741
[10]   AN INVITRO INVESTIGATION INTO THE SUITABILITY OF PH-DEPENDENT POLYMERS FOR COLONIC TARGETING [J].
ASHFORD, M ;
FELL, JT ;
ATTWOOD, D ;
WOODHEAD, PJ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 91 (2-3) :241-245