Ezequiel Dias Foundation, Conde Pereira Carneiro, Belo Horizonte, Brazil.
Faculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, Brazil.
J Biomater Appl. 2021 Mar;35(8):1019-1033. doi: 10.1177/0885328220977605. Epub 2020 Dec 8.
Tacrolimus (TAC), a potent immunosuppressive macrolide, has been investigated for ocular diseases due to promising results in the treatment of anterior and posterior segments eye diseases. Mesoporous and functionalized silica nanoparticles show potential as TAC delivery platforms owing to their interesting characteristic as large surface area, uniform pore size distribution, high pore volume, and excellent biocompatibility. The purpose of this study was to incorporate TAC in functionalized silica nanoparticles with 3-aminopropyltriethoxysilane (MSNAPTES) and investigate the safety and biocompatibility of the systems. The MSNAPTES and MSNAPTES TAC nanoparticles were characterized. The cytotoxicity of MSNAPTES and MSNAPTES load with TAC (MSNAPTES-TAC) in retinal pigment epithelial cells (ARPE-19) was determined, chorioallantoic membrane (CAM) assay model was used to investigate the biocompatibility, and safety of intravitreal injection was evaluated using clinical examination (assessment of intraocular pressure and indirect fundus ophthalmoscopy), electroretinographic (ERG) and histologic studies in rats' eyes. The elemental analysis (CHN), thermogravimetric (TGA), photon correlation spectroscopy and Fourier transform infrared (FTIR) analysis confirmed the presence of functionalized agent and TAC in the MSNAPTES nanoparticles. TAC loading was estimated at 7% for the MSNAPTES TAC nanoparticles. MSNAPTES and MSNAPTES TAC did not present cytotoxicity. The drug delivery systems showed good biocompatibility on CAM. No retinal abnormalities, vitreous hemorrhage, neovascularization, retinal detachment, and optic nerve atrophy were observed during the study. Follow-up ERGs showed no changes in the function of the retina cells after 15 days of intravitreal injection, and histopathologic observations support these findings. In conclusion, MSNAPTES TAC was successfully synthesized, and physicochemical analyses confirmed the presence of TAC in the nanoparticles. and studies indicated that MSNAPTES TAC was safe to intravitreal administration. Taking into account the enormous potential of MSNAPTES to carry TAC, this platform could be a promising strategy for TAC ocular drug delivery in the treatment of eye diseases.
他克莫司(TAC)是一种强效免疫抑制剂大环内酯类药物,因其在前节和后节眼病治疗中具有良好的效果而被广泛用于眼部疾病的治疗。介孔和功能化的硅纳米粒子由于其具有大的表面积、均匀的孔径分布、高的孔体积和优异的生物相容性等特点,因此具有作为 TAC 递送平台的潜力。本研究的目的是将 TAC 包封在 3-氨丙基三乙氧基硅烷(MSNAPTES)功能化的硅纳米粒子中,并研究这些系统的安全性和生物相容性。对 MSNAPTES 和负载 TAC 的 MSNAPTES 纳米粒子(MSNAPTES-TAC)进行了表征。通过视网膜色素上皮细胞(ARPE-19)细胞毒性实验、鸡胚尿囊膜(CAM)实验模型来评估其生物相容性和安全性,通过临床检查(眼压和间接眼底镜检查)、视网膜电图(ERG)和大鼠眼组织学研究来评估玻璃体内注射的安全性。元素分析(CHN)、热重分析(TGA)、光子相关光谱和傅里叶变换红外(FTIR)分析证实了功能化试剂和 TAC 存在于 MSNAPTES 纳米粒子中。MSNAPTES-TAC 纳米粒子的 TAC 载药量估计为 7%。MSNAPTES 和 MSNAPTES-TAC 均无细胞毒性。药物递送系统在 CAM 上表现出良好的生物相容性。在研究过程中,没有观察到视网膜异常、玻璃体积血、新生血管形成、视网膜脱离和视神经萎缩。后续的 ERG 检查显示,玻璃体内注射 15 天后,视网膜细胞功能没有变化,组织病理学观察结果支持这一发现。综上所述,MSNAPTES-TAC 成功合成,理化分析证实了纳米粒子中 TAC 的存在。细胞毒性和生物相容性研究表明,MSNAPTES-TAC 经玻璃体内给药是安全的。考虑到 MSNAPTES 携带 TAC 的巨大潜力,该平台可能成为眼部疾病治疗中 TAC 眼用药物递送的一种有前途的策略。