Institute of Chemical Technology and Engineering, Poznań University of Technology, Berdychowo 4, 60-965 Poznań, Poland.
Institute of Chemical Technology and Engineering, Poznań University of Technology, Berdychowo 4, 60-965 Poznań, Poland.
Int J Pharm. 2020 Mar 30;578:119117. doi: 10.1016/j.ijpharm.2020.119117. Epub 2020 Feb 5.
This work describes the synthesis of calcium zeolites (type A and X) and their use as drug carriers. This is the first example of using calcium zeolites as intelligent carriers that release drugs under the influence of body fluids. Both zeolites and zeolite/drug systems have been extensively characterized. It has been proven that calcium zeolites can be used as carriers of bisphosphonates (drugs against skeletal system diseases). This is due to the fact that phosphonate groups have strong interactions with calcium ions. The sorption of risedronate on zeolites in the sodium form was also carried out, but it was ineffective. The lack of effectiveness of sorption on the sodium zeolites confirms the theoretical assumptions presented in this work. Sorption occurred faster on type A zeolites while the release is faster for type X zeolites. Loading capacity (LC%) were at least 10% for both zeolite forms. The release may take over 100 h depending on the form of zeolite which will be used. The obtained materials have great potential as a drug carrier in enteric-coated tablets as well as an element of implants allowing for controlled drug release.
本工作描述了钙沸石(A型和 X 型)的合成及其作为药物载体的应用。这是首次将钙沸石用作在体液影响下释放药物的智能载体的例子。沸石和沸石/药物系统都经过了广泛的表征。已经证明钙沸石可用作双膦酸盐(针对骨骼系统疾病的药物)的载体。这是因为膦酸根基团与钙离子之间具有很强的相互作用。还进行了在钠离子形式下将利塞膦酸盐吸附在沸石上的实验,但没有效果。在钠沸石上吸附无效证实了本工作中提出的理论假设。吸附在 A 型沸石上更快,而 X 型沸石的释放更快。两种沸石形式的负载能力(LC%)至少为 10%。根据将要使用的沸石形式,释放可能需要 100 小时以上。所得材料具有作为肠溶包衣片剂中的药物载体以及允许控制药物释放的植入物元件的巨大潜力。