Li Qi, Li Xiaosi, Zhao Chao
Department of Chemical and Biological Engineering, The University of Alabama, Tuscaloosa, AL, United States.
Front Bioeng Biotechnol. 2020 May 13;8:437. doi: 10.3389/fbioe.2020.00437. eCollection 2020.
The therapeutic effect of small hydrophilic molecules is limited by the rapid clearance from the systemic circulation or a local site of administration. The unsuitable pharmacokinetics and biodistribution can be improved by encapsulating them in drug delivery systems. However, the high-water solubility, very hydrophilic nature, and low molecular weight make it difficult to encapsulate small hydrophilic molecules in many drug delivery systems. In this mini-review, we highlight three strategies to efficiently encapsulate small hydrophilic molecules and achieve controlled release: physical encapsulation in micro/nanocapsules, physical adsorption via electronic interactions, and covalent conjugation. The principles, advantages, and disadvantages of each strategy are discussed. This review paper could be a guide for scientists, engineers, and medical doctors who want to improve the therapeutic efficacy of small hydrophilic drugs.
小的亲水性分子的治疗效果受到其从体循环或局部给药部位快速清除的限制。通过将它们封装在药物递送系统中,可以改善不合适的药代动力学和生物分布。然而,高水溶性、极强的亲水性和低分子量使得在许多药物递送系统中封装小的亲水性分子变得困难。在这篇小型综述中,我们重点介绍了三种有效封装小的亲水性分子并实现控释的策略:物理包封于微/纳米胶囊中、通过电子相互作用进行物理吸附以及共价缀合。讨论了每种策略的原理、优点和缺点。这篇综述论文可为希望提高小的亲水性药物治疗效果的科学家、工程师和医生提供指导。