Department of Dermatology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu 221002, P.R. China.
Department of Dermatology, The Affiliated Huai'an Hospital of Xuzhou Medical University, The Second People's Hospital of Huai'an, Huai'an, Jiangsu 223002, P.R. China.
Oncol Rep. 2019 Dec;42(6):2512-2520. doi: 10.3892/or.2019.7329. Epub 2019 Sep 20.
A novel core‑shell type thermo‑nanoparticle (CSTNP) co‑loaded with temozolomide (TMZ) and the fluorescein new indocyanine green dye IR820 (termed IT‑CSTNPs) was designed and combined with a near‑infrared (NIR) laser to realize its photothermal conversion. The IT‑CSTNPs were prepared using a two‑step synthesis method and comprised a thermosensitive shell and a biodegradable core. IR820 and TMZ were entrapped in the shell and the core, respectively. Dynamic light scattering results demonstrated that the average hydrodynamic size of the IT‑CSTNPs was 196.4±3.1 nm with a ζ potential of ‑24.9±1.3 mV. The encapsulation efficiencies of TMZ and IR820 were 6.1 and 16.6%, respectively. Temperature increase curves under NIR laser irradiation indicated that the IT‑CSTNPs exhibited the desired photothermal conversion efficiency. The in vitro drug release curves revealed a suitable release capability of IT‑CSTNP under physiological conditions, whereas NIR laser irradiation accelerated the drug release. Inverted fluorescence microscopy and flow cytometry results revealed that the uptake of IT‑CSTNPs by A375 melanoma cells occurred in a concentration‑dependent manner. Confocal laser scanning microscopy results indicated that IT‑CSTNPs entered tumour cells via endocytosis and were located in intercellular lysosomes. In summary, the present study explored the photothermal conversion capability, cellular uptake, and intracellular localization of IT‑CSTNPs.
一种新型核壳型热敏纳米粒子(CSTNP),共载有替莫唑胺(TMZ)和新型荧光吲哚菁绿染料 IR820(称为 IT-CSTNPs),被设计并结合近红外(NIR)激光实现其光热转换。IT-CSTNPs 采用两步合成法制备,由热敏外壳和可生物降解内核组成。IR820 和 TMZ 分别包封在壳和核中。动态光散射结果表明,IT-CSTNPs 的平均水动力粒径为 196.4±3.1nm,ζ 电位为-24.9±1.3mV。TMZ 和 IR820 的包封效率分别为 6.1%和 16.6%。NIR 激光照射下的温度升高曲线表明,IT-CSTNPs 表现出所需的光热转换效率。体外药物释放曲线表明,在生理条件下,IT-CSTNP 具有合适的药物释放能力,而 NIR 激光照射加速了药物释放。倒置荧光显微镜和流式细胞术结果表明,A375 黑色素瘤细胞对 IT-CSTNPs 的摄取呈浓度依赖性。共聚焦激光扫描显微镜结果表明,IT-CSTNPs 通过内吞作用进入肿瘤细胞,并位于细胞间溶酶体中。总之,本研究探讨了 IT-CSTNPs 的光热转换能力、细胞摄取和细胞内定位。