Juliano R
Department of Pharmacology, University of North Carolina, Chapel Hill NC 27599, USA.
Biochem Soc Trans. 2007 Feb;35(Pt 1):41-3. doi: 10.1042/BST0350041.
The use of macromolecules, particularly monoclonal antibodies, as therapeutic agents has come to the forefront in recent years. The biodistribution and delivery issues for protein drugs are shared to a substantial degree with other emerging therapeutic approaches including pharmacologically active nucleic acids and nanoparticles. A generalized approach to these issues involves consideration of the multiple biological barriers that stand between the macromolecular drug or nanoparticle at its site of administration and its ultimate biological target. Considerations of size, stability, non-specific versus specific associations and potency versus toxicity all play a role. The creation of delivery approaches that combine high specificity for the target cell or tissue, high therapeutic payload and modest toxicity remains a challenge, although some very promising examples have emerged recently. A variety of sophisticated targeting strategies, based primarily on combinatorial library methods, when used in combination with new technologies to identify cell-surface receptor 'signatures' of specific tissues, will facilitate advances in targeted delivery of macromolecules and nanoparticles. The challenges to contemporary macromolecule drug delivery are complex, thus new research paradigms are emerging that combine the talents of physical and biological scientists to address this key issue for modern pharmacology and therapeutics.
近年来,使用大分子,特别是单克隆抗体作为治疗剂已成为前沿领域。蛋白质药物的生物分布和递送问题在很大程度上与其他新兴治疗方法相同,包括药理活性核酸和纳米颗粒。解决这些问题的一般方法涉及考虑大分子药物或纳米颗粒在给药部位与其最终生物靶点之间存在的多种生物屏障。尺寸、稳定性、非特异性与特异性结合以及效力与毒性等因素都发挥着作用。尽管最近出现了一些非常有前景的例子,但创建兼具对靶细胞或组织的高特异性、高治疗载荷和适度毒性的递送方法仍然是一项挑战。主要基于组合文库方法的各种复杂靶向策略,与识别特定组织的细胞表面受体“特征”的新技术相结合,将推动大分子和纳米颗粒靶向递送的进展。当代大分子药物递送面临的挑战很复杂,因此正在出现新的研究范式,将物理和生物科学家的才能结合起来,以解决现代药理学和治疗学中的这一关键问题。