Lennernäs H, Aarons L, Augustijns P, Beato S, Bolger M, Box K, Brewster M, Butler J, Dressman J, Holm R, Julia Frank K, Kendall R, Langguth P, Sydor J, Lindahl A, McAllister M, Muenster U, Müllertz A, Ojala K, Pepin X, Reppas C, Rostami-Hodjegan A, Verwei M, Weitschies W, Wilson C, Karlsson C, Abrahamsson B
Uppsala University, Sweden.
University of Manchester, United Kingdom.
Eur J Pharm Sci. 2014 Jun 16;57:292-9. doi: 10.1016/j.ejps.2013.10.012. Epub 2013 Nov 1.
OrBiTo is a new European project within the IMI programme in the area of oral biopharmaceutics tools that includes world leading scientists from nine European universities, one regulatory agency, one non-profit research organization, four SMEs together with scientists from twelve pharmaceutical companies. The OrBiTo project will address key gaps in our knowledge of gastrointestinal (GI) drug absorption and deliver a framework for rational application of predictive biopharmaceutics tools for oral drug delivery. This will be achieved through novel prospective investigations to define new methodologies as well as refinement of existing tools. Extensive validation of novel and existing biopharmaceutics tools will be performed using active pharmaceutical ingredient (API), formulations and supporting datasets from industry partners. A combination of high quality in vitro or in silico characterizations of API and formulations will be integrated into physiologically based in silico biopharmaceutics models capturing the full complexity of GI drug absorption. This approach gives an unparalleled opportunity to initiate a transformational change in industrial research and development to achieve model-based pharmaceutical product development in accordance with the Quality by Design concept. Benefits include an accelerated and more efficient drug candidate selection, formulation development process, particularly for challenging projects such as low solubility molecules (BCS II and IV), enhanced and modified-release formulations, as well as allowing optimization of clinical product performance for patient benefit. In addition, the tools emerging from OrBiTo are expected to significantly reduce demand for animal experiments in the future as well as reducing the number of human bioequivalence studies required to bridge formulations after manufacturing or composition changes.
OrBiTo是欧洲创新药物计划(IMI)在口服生物药剂学工具领域的一个新项目,汇集了来自九所欧洲大学的顶尖科学家、一个监管机构、一个非营利性研究组织、四家中小企业,以及来自十二家制药公司的科学家。OrBiTo项目将填补我们在胃肠道(GI)药物吸收知识方面的关键空白,并提供一个合理应用口服药物递送预测性生物药剂学工具的框架。这将通过新颖的前瞻性研究来定义新方法以及完善现有工具来实现。将使用来自行业合作伙伴的活性药物成分(API)、制剂和支持数据集,对新型和现有生物药剂学工具进行广泛验证。API和制剂的高质量体外或计算机模拟表征相结合,将被整合到基于生理学的计算机模拟生物药剂学模型中,以捕捉胃肠道药物吸收的全部复杂性。这种方法为启动工业研发的变革性变化提供了无与伦比的机会,从而根据设计质量概念实现基于模型的药品开发。其好处包括加速和更高效地筛选候选药物、开发制剂过程,特别是对于低溶解度分子(BCS II类和IV类)等具有挑战性的项目、缓释和控释制剂,以及优化临床产品性能以造福患者。此外,预计OrBiTo项目所产生的工具未来将大幅减少对动物实验的需求,并减少在生产或成分变化后进行制剂桥接所需的人体生物等效性研究数量。