Henein Christin, Awwad Sahar, Ibeanu Nkiruka, Vlatakis Stavros, Brocchini Steve, Tee Khaw Peng, Bouremel Yann
Biomedical Research Centre at Moorfields Eye Hospital, NHS Foundation Trust and UCL Institute of Ophthalmology, National Institute for Health Research (NIHR), London EC1V 9EL, UK.
School of Pharmacy, University College London, London WC1N 1AX, UK.
Pharmaceutics. 2019 Aug 1;11(8):371. doi: 10.3390/pharmaceutics11080371.
Intravitreal injections have become the cornerstone of retinal care and one of the most commonly performed procedures across all medical specialties. The impact of hydrodynamic forces of intravitreal solutions when injected into vitreous or vitreous substitutes has not been well described. While computational models do exist, they tend to underestimate the starting surface area of an injected bolus of a drug. Here, we report the dispersion profile of a dye bolus (50 µL) injected into different vitreous substitutes of varying viscosities, surface tensions, and volumetric densities. A novel 3D printed in vitro model of the vitreous cavity of the eye was designed to visualize the dispersion profile of solutions when injected into the following vitreous substitutes-balanced salt solution (BSS), sodium hyaluronate (HA), and silicone oils (SO)-using a 30G needle with a Reynolds number () for injection ranging from approximately 189 to 677. Larger bolus surface areas were associated with faster injection speeds, lower viscosity of vitreous substitutes, and smaller difference in interfacial surface tensions. Boluses exhibited buoyancy when injected into standard S1000. The hydrodynamic properties of liquid vitreous substitutes influence the initial injected bolus dispersion profile and should be taken into account when simulating drug dispersion following intravitreal injection at a preclinical stage of development, to better inform formulations and performance.
玻璃体内注射已成为视网膜护理的基石,也是所有医学专业中最常进行的手术之一。当玻璃体内溶液注入玻璃体或玻璃体替代物时,其流体动力的影响尚未得到充分描述。虽然存在计算模型,但它们往往低估了注射药物团块的起始表面积。在此,我们报告了将50微升染料团块注入不同粘度、表面张力和体积密度的玻璃体替代物后的分散情况。设计了一种新型的3D打印眼玻璃体腔体外模型,以使用30G针头将溶液注入以下玻璃体替代物——平衡盐溶液(BSS)、透明质酸钠(HA)和硅油(SO)时可视化溶液的分散情况,注射时的雷诺数()范围约为189至677。较大的团块表面积与更快的注射速度、较低的玻璃体替代物粘度以及较小的界面表面张力差异相关。当注入标准S1000时,团块表现出浮力。液体玻璃体替代物的流体动力学特性会影响初始注射团块的分散情况,在临床前开发阶段模拟玻璃体内注射后的药物分散时应予以考虑,以便更好地指导配方和性能。