Iaso Biodelivery Fabricação de Dispositivos com Liberação de Fármacos LTDA, Florianópolis, Santa Catarina, Brazil.
Biomechanical Engineering Laboratory, University Hospital & Department of Mechanical Engineering, Federal University of Santa Catarina (UFSC), Florianópolis, Santa Catarina, Brazil.
Drug Dev Ind Pharm. 2024 Apr;50(4):285-296. doi: 10.1080/03639045.2024.2311177. Epub 2024 Mar 14.
The overactive bladder is a condition characterized by a sudden urge to urinate, even with small volumes of urine present in the bladder. The current treatments available for this pathology consist on conservative approaches and the continuous administration of drugs, which when made by conventional methods has limitations related to the first pass metabolism, bioavailability, severe side effects, and low patient adherence to treatments, ultimately leading to low effectiveness. Within this context, the present work proposes the design, manufacture, and characterization of an intravesical implant for the treatment of overactive bladder pathology, using EVA copolymer as a matrix and oxybutynin as a drug. The fabrication of devices through two manufacturing techniques (extrusion and additive manufacturing by fused filament fabrication, FFF) and the evaluation of the implants through characterization tests was proposed. The usability and functionality were evaluated through simulated insertion of the device/prototype in a bladder model through catheter insertion tests. The safety and effectiveness of the devices was investigated from mechanical testing as well as drug release assays. Drug release assays presented a burst release in the first 24 h, followed by a release of 1.8 and 2.8 mg/d, totalizing 32 d. Mechanical tests demonstrated an increase in the stiffness of the specimens due to the addition of the drug, showing a change in maximum stress and strain at break. The released dose was higher than that usually presented when considering the oral administration route, showing the optimization of the development of this implant has the potential to improve the quality of life of patients with overactive bladder.
膀胱过度活动症是一种以突然尿急为特征的病症,即使膀胱中只有少量尿液。目前,这种病理的治疗方法包括保守治疗和持续药物治疗,但常规方法存在与首过代谢、生物利用度、严重副作用和患者对治疗的低依从性相关的限制,最终导致治疗效果不佳。在这种情况下,本工作提出了使用 EVA 共聚物作为基质和奥昔布宁作为药物,设计、制造和表征用于治疗膀胱过度活动症病理的膀胱内植入物。通过两种制造技术(挤出和熔融沉积成型的添加剂制造,FFF)制造设备,并通过特性测试评估植入物。通过导管插入测试模拟将设备/原型插入膀胱模型中的插入测试来评估可用性和功能性。通过机械测试和药物释放试验研究了设备的安全性和有效性。药物释放试验在最初的 24 小时内呈现出突释,随后分别释放 1.8 和 2.8mg/d,总计 32 天。机械测试表明,由于药物的加入,样品的刚度增加,最大应力和断裂应变发生变化。释放的剂量高于口服给药途径通常呈现的剂量,表明这种植入物的开发优化有可能提高膀胱过度活动症患者的生活质量。