Yamakawa Ryuto, Onoe Hiroaki, Kurashina Yuta
Division of Advanced Mechanical Systems Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Nakacho, Koganei-shi, Tokyo 184-8588, Japan.
Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama 223-8522, Japan.
Ultrason Sonochem. 2025 Jan;112:107173. doi: 10.1016/j.ultsonch.2024.107173. Epub 2024 Nov 22.
Hydrogel-based drug carriers provide on-demand drug release via external stimuli. Ultrasound is a promising method because of the potential for remotely releasing the drug. However, intense ultrasound irradiation has been required in previous studies. This paper reports drug model release from hydrogel carriers encapsulating bubble vibration enhancers (BVEs) consisting of microbubbles coated with a lipid membrane. Vibration of BVEs induced by ultrasound stimulation promoted the release of drug models with ultrasound irradiation controlled to a biologically safe acoustic pressure based on spatial-peak temporal-average intensity (I). The release ratio increased significantly from 2.3 % without BVEs and ultrasound to 10.2 % with both. To evaluate the frequency response, the release ratio was measured at three different ultrasound frequencies (0.3, 1.8, and 2.5 MHz), showing increased efficiency as the frequency approached the resonance frequency of the BVEs. For in vivo applications, hydrogel microspherical carriers with BVEs achieved a 12 % release ratio. Poly-L-lysine coating successfully suppressed the drug release to 0.2 %. The carriers demonstrated repeated responsiveness when ultrasound was applied in three 5-minute intervals. The hydrogel carrier encapsulating BVEs we proposed is a promising in vivo device capable of releasing drugs on demand by ultrasound irradiation based on its high biosafety and acoustic responsiveness.
基于水凝胶的药物载体可通过外部刺激实现按需药物释放。超声是一种很有前景的方法,因为它具有远程释放药物的潜力。然而,以往的研究需要高强度的超声照射。本文报道了药物模型从包裹有气泡振动增强剂(BVE)的水凝胶载体中的释放情况,BVE由涂有脂质膜的微泡组成。超声刺激引起的BVE振动促进了药物模型的释放,在基于空间峰值时间平均强度(I)控制在生物安全声压的超声照射下。释放率从无BVE和超声时的2.3%显著增加到同时存在时的10.2%。为了评估频率响应,在三个不同的超声频率(0.3、1.8和2.5 MHz)下测量释放率,结果表明随着频率接近BVE的共振频率,效率提高。对于体内应用,含有BVE的水凝胶微球载体实现了12%的释放率。聚-L-赖氨酸包被成功地将药物释放抑制到0.2%。当以三个5分钟的间隔施加超声时,载体表现出重复的响应性。我们提出的包裹BVE的水凝胶载体是一种很有前景的体内装置,基于其高生物安全性和声响应性,能够通过超声照射按需释放药物。