一种基于 PDMS 的超软柔性球囊式植入装置,用于控制药物输送。

IF 8.1 Q1 ENGINEERING, BIOMEDICAL Biomaterials research Pub Date : 2024-03-28 eCollection Date: 2024-01-01 DOI:10.34133/bmr.0012
Tausif Muhammad, Byungwook Park, Aseer Intisar, Minseok S Kim, Jin-Kyu Park, Sohee Kim
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引用次数: 0

摘要

非生物降解植入物作为一种药物输送设备,在实现先进的医疗保健、迈向个性化医疗方面经历了广泛的研究。然而,成纤维细胞包裹是所有非生物降解植入物面临的主要挑战之一,此外还有其他挑战,如初始爆破率高、膜破裂风险大、起效时间长、与组织的非形式接触以及组织损伤等。针对这些挑战,我们提出了一种新型超软柔性球囊式给药装置,可实现单向和长期控制释放。这种超软球囊式给药装置(USBD)是通过在两片聚二甲基硅氧烷(PDMS)膜之间进行选择性粘合,并在两片膜之间的非粘合区域注入液体而制成的。气球充当了装有液体药物的容器,与此同时,气球膜本身充当了基于扩散的释放途径。通过调节 PDMS 膜的厚度和成分,可以调节药物的释放。无论厚度和成分如何,所有装置都表现出零阶释放行为。最长的零阶释放期为 30 天,接近零阶释放期为 58 天,释放率分别为 1.16 微克/天和 1.68 微克/天。对活体大鼠进行了为期 35 天的体内评估,USBD 在 28 天和 35 天内分别保持了零阶和接近零阶释放。由于采用了超软柔性膜和装置设计,USBD 可将组织损伤和异物反应降至最低。预计该装置可为长期给药提供一种新的治疗模式。
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An Ultrasoft and Flexible PDMS-Based Balloon-Type Implantable Device for Controlled Drug Delivery.

Non-biodegradable implants have undergone extensive investigation as drug delivery devices to enable advanced healthcare toward personalized medicine. However, fibroblast encapsulation is one of the major challenges in all non-biodegradable implants, besides other challenges such as high initial burst, risk of membrane rupture, high onset time, non-conformal contact with tissues, and tissue damage. To tackle such challenges, we propose a novel ultrasoft and flexible balloon-type drug delivery device for unidirectional and long-term controlled release. The ultrasoft balloon-type device (USBD) was fabricated by using selective bonding between 2 polydimethylsiloxane (PDMS) membranes and injecting a fluid into the non-bonded area between them. The balloon acted as a reservoir containing a liquid drug, and at the same time, the membrane of the balloon itself acted as the pathway for release based on diffusion. The release was modulated by tuning the thickness and composition of the PDMS membrane. Regardless of the thickness and composition, all devices exhibited zero-order release behavior. The longest zero-order release and nearly zero-order release were achieved for 30 days and 58 days at a release rate of 1.16 μg/day and 1.68 μg/day, respectively. In vivo evaluation was performed for 35 days in living rats, where the USBD maintained zero-order and nearly zero-order release for 28 days and 35 days, respectively. Thanks to the employment of ultrasoft and flexible membranes and device design, the USBD could achieve minimal tissue damage and foreign body responses. It is expected that the proposed device may provide a novel approach for long-term drug delivery with new therapeutic modalities.

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