Kalász Huba, Antal István
Department of Pharmacology & Therapeutics, United Arab Emirates University, P.O. Box 17666, Al Ain, UAE.
Curr Med Chem. 2006;13(21):2535-63. doi: 10.2174/092986706778201648.
The therapeutical use of drugs involves the application of dosage forms, serving as carrier systems together with several excipients to deliver the active ingredient to the site of action. Drug delivery technology combines an understanding of medicinal chemistry and pharmacology with the skill of formulation, aiming the preparation of improved pharmaceuticals. The recently introduced Biopharmaceutical Classification System provides guidance for dosage form design, taking the molecular and physico-chemical properties of drugs into consideration through their solubility and permeability characteristics. Pharmaceutical excipients used for oral dosage form have been traditionally assumed as being inert. However, recent experience and new results have shown that they can interact with the active drug ingredient, affecting its dissolution, absorption and bioavailability. Classification of the excipients is based on their role in the pharmaceutical formulation and on their interactions influencing drug delivery, based on their chemical and physico-chemical properties. The main classes are the antioxidants, coating materials, emulgents, taste- and smell-improvers, ointment bases, conserving agents, consistency-improvers and disintegrating materials. Some of the excipients may serve multiple purposes; for example, methylcellulose is a coating material, is applied in the preparation of suspensions, to increase viscosity, as a disintegrating agent or binder in tablets. The aim of this paper is to review the drug-excipients with respect to their chemistry, importance and interactions altering the pharmacokinetics of the drug substances. Emphasis will be given to two major classes of excipients: the antioxidants and disintegrants (substances facilitating disintegration of the drug tablets in the gastro-intestinal tract). Details will be given on the mechanisms through which they can alter drug effectiveness and tolerance, and control their application. Examples and references will be given for their analysis.
药物的治疗用途涉及剂型的应用,剂型与多种辅料一起作为载体系统,将活性成分输送到作用部位。药物递送技术将药物化学和药理学知识与制剂技术相结合,旨在制备改良药物。最近引入的生物药剂学分类系统为剂型设计提供了指导,通过药物的溶解度和渗透性特征考虑其分子和物理化学性质。传统上认为用于口服剂型的药用辅料是惰性的。然而,最近的经验和新的研究结果表明,它们可以与活性药物成分相互作用,影响其溶解、吸收和生物利用度。辅料的分类基于它们在药物制剂中的作用以及基于其化学和物理化学性质对药物递送产生影响的相互作用。主要类别包括抗氧化剂、包衣材料、乳化剂、增味剂和除臭剂、软膏基质、防腐剂、增稠剂和崩解材料。一些辅料可能有多种用途;例如,甲基纤维素是一种包衣材料,用于制备混悬剂以增加粘度,也可作为片剂中的崩解剂或粘合剂。本文的目的是综述药物辅料的化学性质、重要性以及改变药物物质药代动力学的相互作用。重点将放在两类主要辅料上:抗氧化剂和崩解剂(促进药物片剂在胃肠道中崩解的物质)。将详细介绍它们改变药物有效性和耐受性的机制以及控制其应用的方法。将给出分析的实例和参考文献。