Mau Robert, Eickner Thomas, Jüttner Gábor, Gao Ziwen, Wei Chunjiang, Fiedler Nicklas, Senz Volkmar, Lenarz Thomas, Grabow Niels, Scheper Verena, Seitz Hermann
Microfluidics, Faculty of Mechanical Engineering and Marine Technology, University of Rostock, Justus-von-Liebig Weg 6, 18059 Rostock, Germany.
Institute for Biomedical Engineering, University Medical Center Rostock, Friedrich-Barnewitz-Straße 4, 18119 Rostock, Germany.
Pharmaceutics. 2023 May 24;15(6):1584. doi: 10.3390/pharmaceutics15061584.
A novel approach for the long-term medical treatment of the inner ear is the diffusion of drugs through the round window membrane from a patient-individualized, drug-eluting implant, which is inserted in the middle ear. In this study, drug-loaded (10 wt% Dexamethasone) guinea pig round window niche implants (GP-RNIs, 1.30 mm × 0.95 mm × 0.60 mm) were manufactured with high precision via micro injection molding (µIM, T = 160 °C, crosslinking time of 120 s). Each implant has a handle (3.00 mm × 1.00 mm × 0.30 mm) that can be used to hold the implant. A medical-grade silicone elastomer was used as implant material. Molds for µIM were 3D printed from a commercially available resin (T = 84 °C) via a high-resolution DLP process (xy resolution of 32 µm, z resolution of 10 µm, 3D printing time of about 6 h). Drug release, biocompatibility, and bioefficacy of the GP-RNIs were investigated in vitro. GP-RNIs could be successfully produced. The wear of the molds due to thermal stress was observed. However, the molds are suitable for single use in the µIM process. About 10% of the drug load (8.2 ± 0.6 µg) was released after 6 weeks (medium: isotonic saline). The implants showed high biocompatibility over 28 days (lowest cell viability ~80%). Moreover, we found anti-inflammatory effects over 28 days in a TNF-α-reduction test. These results are promising for the development of long-term drug-releasing implants for human inner ear therapy.
一种用于内耳长期医学治疗的新方法是通过圆窗膜从植入中耳的患者个体化药物洗脱植入物中扩散药物。在本研究中,通过微注射成型(µIM,温度160°C,交联时间120秒)高精度制造了载药(10重量%地塞米松)豚鼠圆窗龛植入物(GP-RNI,约1.30毫米×0.95毫米×0.60毫米)。每个植入物都有一个手柄(约3.00毫米×1.00毫米×0.30毫米),可用于握持植入物。使用医用级硅橡胶弹性体作为植入材料。µIM模具通过高分辨率DLP工艺(xy分辨率32微米,z分辨率10微米,3D打印时间约6小时)由市售树脂(温度84°C)3D打印而成。在体外研究了GP-RNI的药物释放、生物相容性和生物疗效。GP-RNI能够成功生产。观察到模具因热应力而磨损。然而,这些模具适用于µIM工艺中的一次性使用。6周后(介质:等渗盐水)释放了约10%的载药量(8.2±0.6微克)。植入物在28天内显示出高生物相容性(最低细胞活力约80%)。此外,在TNF-α降低试验中,我们发现其在28天内具有抗炎作用。这些结果对于开发用于人类内耳治疗的长期药物释放植入物很有前景。