Su Yu-Lin, Chen Kuan-Ting, Sheu Yu-Chen, Sung Shuo-Yuan, Hsu Ru-Siou, Chiang Chi-Shiun, Hu Shang-Hsiu
Department of Biomedical Engineering and Environmental Sciences, National Tsing Hua University , Hsinchu 300, Taiwan.
ACS Nano. 2016 Oct 25;10(10):9420-9433. doi: 10.1021/acsnano.6b04414. Epub 2016 Oct 3.
Delivery of drug and energy within responsive carriers that effectively target and accumulate in cancer cells promises to mitigate side effects and to enhance the uniquely therapeutic efficacy demanded for personalized medicine. To achieve this goal, however, these carriers, which are usually piled up at the periphery of tumors near the blood vessel, must simultaneously overcome the challenges associated with low tumor penetration and the transport of sufficient cargos to deep tumors to eradicate whole cancer cells. Here, we report a sponge-like carbon material on graphene nanosheet (graphene nanosponge)-supported lipid bilayers (lipo-GNS) that doubles as a photothermal agent and a high cargo payload platform and releases a burst of drug/energy (docetaxel (DTX) and gasified perfluorohexane (PFH)) and intense heat upon near-infrared irradiation. Ultrasmall lipo-GNS (40 nm) modified with a tumor-targeting protein that penetrates tumor spheroids through transcytosis exhibited a 200-fold increase in accumulation relative to a 270 nm variant of the lipo-GNS. Furthermore, a combination of therapeutic agents (DTX and PFH) delivered by lipo-GNS into tumors was gasified and released into tumor spheroids and successfully ruptured and suppressed xenograft tumors in 16 days without distal harm when subjected to a single 10 min near-infrared laser treatment. Moreover, no tumor recurrence was observed over 60 days post-treatment. This sophisticated lipo-GNS is an excellent delivery platform for penetrated, photoresponsive, and combined gasification/chemo-thermotherapy to facilitate tumor treatment and for use in other biological applications.
在能够有效靶向并积聚于癌细胞的响应性载体中递送药物和能量,有望减轻副作用,并提高个性化医疗所需的独特治疗效果。然而,要实现这一目标,这些通常堆积在血管附近肿瘤周边的载体,必须同时克服与肿瘤低穿透性相关的挑战,以及将足够的货物运输到深部肿瘤以根除整个癌细胞的问题。在此,我们报道了一种基于石墨烯纳米片(石墨烯纳米海绵)支撑的脂质双层(脂质-GNS)的海绵状碳材料,它兼具光热剂和高载药量平台的双重功能,并在近红外照射下释放出一阵药物/能量(多西他赛(DTX)和气化全氟己烷(PFH))以及强烈的热量。用肿瘤靶向蛋白修饰的超小脂质-GNS(40纳米)通过转胞吞作用穿透肿瘤球体,其积累量相对于270纳米的脂质-GNS变体增加了200倍。此外,脂质-GNS递送至肿瘤中的治疗剂(DTX和PFH)组合被气化并释放到肿瘤球体中,在单次10分钟近红外激光治疗后16天内成功使异种移植肿瘤破裂并得到抑制,且无远端损伤。此外,治疗后60天内未观察到肿瘤复发。这种先进的脂质-GNS是一种出色的递送平台,可用于穿透性、光响应性以及联合气化/化学热疗法以促进肿瘤治疗,并用于其他生物应用。