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药物递送中的生物共轭:实践观点与未来展望。

Bioconjugation in Drug Delivery: Practical Perspectives and Future Perceptions.

作者信息

Elzahhar Perihan, Belal Ahmed S F, Elamrawy Fatema, Helal Nada A, Nounou Mohamed Ismail

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.

Department of Pharmaceutics, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.

出版信息

Methods Mol Biol. 2019;2000:125-182. doi: 10.1007/978-1-4939-9516-5_11.

Abstract

For the past three decades, pharmaceutical research has been mainly converging to novel carrier systems and nanoparticulate colloidal technologies for drug delivery, such as nanoparticles, nanospheres, vesicular systems, liposomes, or nanocapsules to impart novel functions and targeting abilities. Such technologies opened the gate towards more sophisticated and effective multi-acting platform(s) which can offer site-targeting, imaging, and treatment using a single multifunctional system. Unfortunately, such technologies faced major intrinsic hurdles including high cost, low stability profile, short shelf-life, and poor reproducibility across and within production batches leading to harsh bench-to-bedside transformation.Currently, pharmaceutical industry along with academic research is investing heavily in bioconjugate structures as an appealing and advantageous alternative to nanoparticulate delivery systems with all its flexible benefits when it comes to custom design and tailor grafting along with avoiding most of its shortcomings. Bioconjugation is a ubiquitous technique that finds a multitude of applications in different branches of life sciences, including drug and gene delivery applications, biological assays, imaging, and biosensing.Bioconjugation is simple, easy, and generally a one-step drug (active pharmaceutical ingredient) conjugation, using various smart biocompatible, bioreducible, or biodegradable linkers, to targeting agents, PEG layer, or another drug. In this chapter, the different types of bioconjugates, the techniques used throughout the course of their synthesis and characterization, as well as the well-established synthetic approaches used for their formulation are presented. In addition, some exemplary representatives are outlined with greater emphasis on the practical tips and tricks of the most prominent techniques such as click chemistry, carbodiimide coupling, and avidin-biotin system.

摘要

在过去三十年里,药物研究主要集中于新型载体系统和用于药物递送的纳米颗粒胶体技术,如纳米颗粒、纳米球、囊泡系统、脂质体或纳米胶囊,以赋予其新功能和靶向能力。这些技术为更复杂、有效的多作用平台打开了大门,该平台可以使用单一多功能系统实现位点靶向、成像和治疗。不幸的是,这些技术面临着重大的内在障碍,包括成本高、稳定性差、保质期短以及生产批次间和批次内的重现性差,导致从实验室到临床的转化困难重重。目前,制药行业和学术研究正在大力投资生物共轭结构,将其作为纳米颗粒递送系统的一种有吸引力且具有优势的替代方案,因为在定制设计和量身嫁接方面它具有诸多灵活的优点,同时还能避免其大部分缺点。生物共轭是一种普遍存在的技术,在生命科学的不同分支中有大量应用,包括药物和基因递送应用、生物测定、成像和生物传感。生物共轭简单易行,通常是一步将药物(活性药物成分)与各种智能生物相容性、生物可还原或生物可降解的连接子、靶向剂、聚乙二醇层或另一种药物进行共轭。在本章中,介绍了不同类型的生物共轭物、其合成和表征过程中使用的技术,以及用于其制剂的成熟合成方法。此外,还概述了一些示例性代表物,更着重介绍了最突出技术(如点击化学、碳二亚胺偶联和抗生物素蛋白-生物素系统)的实用技巧。

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