A novel suprachoroidal microinvasive glaucoma implant: in vivo biocompatibility and biointegration.

BMC biomedical engineering Pub Date : 2020-10-14 eCollection Date: 2020-01-01 DOI:10.1186/s42490-020-00045-1
Ian Grierson, Don Minckler, Marian K Rippy, Andrew J Marshall, Nathalie Collignon, Jessica Bianco, Benoit Detry, Murray A Johnstone
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引用次数: 10

Abstract

Background: A major challenge for any glaucoma implant is their ability to provide long-term intraocular pressure lowering efficacy. The formation of a low-permeability fibrous capsule around the device often leads to obstructed drainage channels, which may impair the drainage function of devices. These foreign body-related limitations point to the need to develop biologically inert biomaterials to improve performance in reaching long-term intraocular pressure reduction. The aim of this study was to evaluate in vivo (in rabbits) the ocular biocompatibility and tissue integration of a novel suprachoroidal microinvasive glaucoma implant, MINIject™ (iSTAR Medical, Wavre, Belgium).

Results: In two rabbit studies, no biocompatibility issue was induced by the suprachoroidal, ab-externo implantation of the MINIject™ device. Clinical evaluation throughout the 6 post-operative months between the sham and test groups were similar, suggesting most reactions were related to the ab-externo surgical technique used for rabbits, rather than the implant material itself. Histological analysis of ocular tissues at post-operative months 1, 3 and 6 revealed that the implant was well-tolerated and induced only minimal fibroplasia and thus minimal encapsulation around the implant. The microporous structure of the device became rapidly colonized by cells, mostly by macrophages through cell migration, which do not, by their nature, impede the flow of aqueous humor through the device. Time-course analysis showed that once established, pore colonization was stable over time. No fibrosis nor dense connective tissue development were observed within any implant at any time point. The presence of pore colonization may be the process by which encapsulation around the implant is minimized, thus preserving the permeability of the surrounding tissues. No degradation nor structural changes of the implant occurred during the course of both studies.

Conclusions: The novel MINIject™ microinvasive glaucoma implant was well-tolerated in ocular tissues of rabbits, with observance of biointegration, and no biocompatibility issues. Minimal fibrous encapsulation and stable cellular pore colonization provided evidence of preserved drainage properties over time, suggesting that the implant may produce a long-term ability to enhance aqueous outflow.

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一种新型脉络膜上微创青光眼植入物:体内生物相容性和生物整合。
背景:任何青光眼植入物的一个主要挑战是它们能否提供长期的眼压降低效果。在器械周围形成低渗透性纤维囊,往往导致引流通道堵塞,影响器械的引流功能。这些与异物相关的限制表明需要开发生物惰性生物材料来提高长期降低眼压的性能。本研究的目的是评估一种新型脉光膜上微创青光眼植入物MINIject™(iSTAR Medical, Wavre, Belgium)的眼生物相容性和组织整合性。结果:在两项家兔研究中,MINIject™装置在脉络膜上ab-外植入未引起生物相容性问题。假手术组和试验组术后6个月的临床评价相似,表明大多数反应与兔使用的ab-externo手术技术有关,而与植入材料本身无关。术后1、3和6个月的眼组织组织学分析显示,植入物耐受性良好,仅诱导少量纤维增生,因此植入物周围极少有包封。该装置的微孔结构迅速被细胞定植,主要是通过细胞迁移的巨噬细胞,它们的性质不会阻碍房水通过装置的流动。时间过程分析表明,孔定殖一旦建立,随着时间的推移是稳定的。在任何时间点,均未观察到任何植入物内的纤维化或致密结缔组织发育。孔定殖的存在可能是将种植体周围的包封最小化的过程,从而保持了周围组织的渗透性。在两项研究过程中,植入物均未发生降解或结构变化。结论:新型MINIject™微创青光眼植入物在兔眼组织中耐受性良好,具有良好的生物整合性,无生物相容性问题。最小的纤维包封和稳定的细胞孔定植提供了长期保持引流特性的证据,表明植入物可能产生长期增强水流出的能力。
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