Department of Oral Anatomy, School of Dentistry, Seoul National University and Dental Research Institute, 101 Daehak-ro, Jongno-gu, Seoul, 03080, South Korea.
Drug Deliv Transl Res. 2018 Jun;8(3):702-707. doi: 10.1007/s13346-018-0516-6.
The implant-mediated drug delivery system (IMDDS) is a novel, innovative device that allows drug delivery through bone marrow. The purpose of this study was to investigate the effect of an active plunger component made of super absorbent polymer (SAP) on the plasma concentration of dexamethasone released from the IMDDS. The IMDDSs were installed in a total of 18 rabbits. After complete healing, dexamethasone was loaded with the SAP active plunger and with water to cause expansion in the test group (n = 9), while only the drug was loaded in the control group, as per the original protocol (n = 9). The release patterns of each group were monitored for 2 weeks by measuring the plasma concentration of the drug. Both groups showed sustained release of drug. However, the test groups showed more rapid increase in plasma concentration and higher area under the curve (AUC) throughout the observation period. The incorporation of a SAP active plunger component in the IMDDS resulted in an increase in initial release of drug and higher bioavailability within the observation period of 2 weeks after dexamethasone administration.
植入介导的药物输送系统(IMDDS)是一种新颖的创新装置,可通过骨髓输送药物。本研究旨在探讨由超吸水性聚合物(SAP)制成的主动柱塞部件对从 IMDDS 释放的地塞米松的血浆浓度的影响。总共在 18 只兔子中安装了 IMDDS。完全愈合后,用 SAP 主动柱塞和水加载地塞米松以在实验组(n = 9)中引起膨胀,而仅按原始方案在对照组(n = 9)中加载药物。通过测量药物的血浆浓度,监测每组的释放模式 2 周。两组均表现出药物的持续释放。然而,实验组在整个观察期内显示出更快的血浆浓度增加和更高的曲线下面积(AUC)。在 IMDDS 中加入 SAP 主动柱塞部件会导致药物的初始释放增加,并且在给予地塞米松后的 2 周观察期内生物利用度更高。