J. Mike Walker '66 Department of Mechanical Engineering, Texas A&M University, College Station, TX, USA.
Department of Chemistry, Texas A&M University, College Station, TX, USA.
Nanomedicine. 2021 Jul;35:102392. doi: 10.1016/j.nano.2021.102392. Epub 2021 Apr 16.
This paper reports a smart intracellular nanocarrier for sustainable and controlled drug release in non-invasive neuroregeneration. The nanocarrier is composed by superparamagnetic iron oxide-gold (SPIO-Au) core-shell nanoparticles (NPs) conjugated with porous coordination cages (PCCs) through the thiol-containing molecules as bridges. The negatively charged PCC-2 and positively charged PCC-3 are compared for intracellular targeting. Both types result in intracellular targeting via direct penetration across cellular membranes. However, the pyrene (Py)-PEG-SH bridge enabled functionalization of SPIO-Au NPs with PCC-3 exhibits higher interaction with PC-12 neuron-like cells, compared with the rhodamine B (RhB)-PEG-SH bridge enabled case and the stand-alone SPIO-Au NPs. With neglectable toxicities to PC-12 cells, the proposed SPIO-Au-RhB(Py)-PCC-2(3) nanocarriers exhibit effective drug loading capacity of retinoic acid (RA) at 13.505 μg/mg of RA/NPs within 24 h. A controlled release of RA is achieved by using a low-intensity 525 nm LED light (100% compared to 40% for control group within 96 h).
本文报道了一种用于非侵入性神经再生的智能细胞内纳米载体,可实现可持续和可控的药物释放。该纳米载体由超顺磁性氧化铁-金(SPIO-Au)核壳纳米粒子(NPs)通过含巯基分子作为桥梁与多孔配位笼(PCCs)偶联而成。比较了带负电荷的 PCC-2 和带正电荷的 PCC-3 用于细胞内靶向。这两种类型都通过直接穿透细胞膜实现细胞内靶向。然而,与罗丹明 B(RhB)-PEG-SH 桥功能化的 SPIO-Au NPs 相比,带芘基(Py)-PEG-SH 桥功能化的 SPIO-Au NPs 与 PC-12 神经元样细胞的相互作用更高。与 PC-12 细胞的可忽略毒性相比,所提出的 SPIO-Au-RhB(Py)-PCC-2(3)纳米载体在 24 小时内以 13.505μg/mg RA/NPs 的载药量有效负载维甲酸(RA)。通过使用低强度 525nm LED 光(96 小时内对照组为 40%,实验组为 100%)实现 RA 的控制释放。