Pharmacy, Pharmacology and Therapeutics Section, School of Clinical and Experimental Medicine, College of Medical and Dental Sciences, Medical School Building, University of Birmingham, Edgbaston B15 2TT, United Kingdom.
Department of Pharmacy and Pharmacology, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom.
Adv Drug Deliv Rev. 2014 Jun;73:102-26. doi: 10.1016/j.addr.2013.10.006. Epub 2013 Nov 1.
The complex process of oral drug absorption is influenced by a host of drug and formulation properties as well as their interaction with the gastrointestinal environment in terms of drug solubility, dissolution, permeability and pre-systemic metabolism. For adult dosage forms the use of biopharmaceutical tools to aid in the design and development of medicinal products is well documented. This review considers current literature evidence to guide development of bespoke paediatric biopharmaceutics tools and reviews current understanding surrounding extrapolation of adult methodology into a paediatric population. Clinical testing and the use of in silico models were also reviewed. The results demonstrate that further work is required to adequately characterise the paediatric gastrointestinal tract to ensure that biopharmaceutics tools are appropriate to predict performance within this population. The most vulnerable group was found to be neonates and infants up to 6 months where differences from adults were greatest.
口服药物吸收的复杂过程受到许多药物和制剂特性的影响,以及它们与胃肠道环境在药物溶解度、溶解、渗透性和前体药物代谢方面的相互作用。对于成人剂型,生物制药工具的使用在药物设计和开发中得到了很好的记录。本综述考虑了当前的文献证据,以指导定制儿科生物药剂学工具的开发,并回顾了将成人方法外推到儿科人群的现有理解。还审查了临床测试和使用计算机模型。结果表明,需要进一步研究以充分描述儿科胃肠道,以确保生物药剂学工具适合预测该人群中的性能。最脆弱的群体被发现是新生儿和 6 个月以下的婴儿,他们与成年人的差异最大。