Zhao Ya-Nan, Gu Jianjun, Jia Siyu, Guan Ying, Zhang Yongjun
State Key Laboratory of Medicinal Chemical Biology and Key Laboratory of Functional Polymer Materials, Institute of Polymer Chemistry, College of Chemistry, Nankai University, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071, China.
Soft Matter. 2016 Jan 28;12(4):1085-92. doi: 10.1039/c5sm02186c.
Drug carriers capable of releasing drugs at a constant rate, or following zero-order kinetics, can lead to the best control of plasma drug concentration. Here we demonstrated that zero-order release of polyphenolic drugs, including tannic acid, epigallocatechin gallate, proanthocyanidins, and theaflavin-3'-gallate, could be achieved using hydrogen-bonded layer-by-layer films as the drug carrier. The films were fabricated using the polyphenolic drugs as hydrogen donors and polyethylene glycol (PEG) as the hydrogen acceptor. Because the drugs and PEG are bonded with reversible, dynamic hydrogen bonds, the films disintegrate gradually in aqueous solutions, and thus release the drugs into the media. Furthermore, because the PEG polymers have a narrow molecular weight distribution, the films disintegrate and release the polyphenolic drugs at a constant rate. Besides allowing for zero-order release, the drug carrier developed here also provides various ways to tune the drug release rate. The drug release rate increases with decreasing molecular weight of PEG. More importantly, the release rate could be tuned using external stimuli. Increasing the pH or temperature results in accelerated drug release, while the addition of salt retards the drug release.
能够以恒定速率释放药物或遵循零级动力学的药物载体,可以实现对血浆药物浓度的最佳控制。在这里,我们证明了使用氢键层层膜作为药物载体,可以实现包括单宁酸、表没食子儿茶素没食子酸酯、原花青素和茶黄素-3'-没食子酸酯在内的多酚类药物的零级释放。这些膜是使用多酚类药物作为氢供体和聚乙二醇(PEG)作为氢受体制备的。由于药物和PEG通过可逆的动态氢键结合,膜在水溶液中逐渐分解,从而将药物释放到介质中。此外,由于PEG聚合物的分子量分布较窄,膜以恒定速率分解并释放多酚类药物。除了实现零级释放外,这里开发的药物载体还提供了多种调节药物释放速率的方法。药物释放速率随PEG分子量的降低而增加。更重要的是,可以使用外部刺激来调节释放速率。提高pH值或温度会导致药物释放加速,而添加盐会阻碍药物释放。