School of Pharmacy, Wannan Medical College, Wuhu, 241002, People's Republic of China.
School of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, People's Republic of China.
Int J Nanomedicine. 2024 Sep 18;19:9689-9705. doi: 10.2147/IJN.S473473. eCollection 2024.
Epidermal growth factor receptor (EGFR) is a major target for the treatment of colorectal cancer. Thus, anti-EGFR antibody conjugated lipid-polymer hybrid nanoparticles can offer a potential means of enhancing the efficacy of chemotherapeutics in EGFR overexpressing cancers. In addition, the combination of chemotherapy and photothermal therapy is a promising strategy for cancer treatment. Hence, it is highly desirable to develop a safe and effective delivery system for colorectal tumor therapy.
In this study, EGFR-targeted and NIR-triggered lipid-polymer hybrid nanoparticles (abbreviated as Cet-Iri-NPs) were prepared with copolymer PPG-PEG, lipids DSPE-PEG-Mal and lecithin as carriers, CPT-11 as an anticancer chemotherapeutic agent, indocyanine green (ICG) as a photothermal agent, and cetuximab as a surface-targeting ligand.
In vitro analyses revealed that Cet-Iri-NPs were spherical with size of 99.88 nm, charge of 29.17 mV, drug entrapment efficiency of 51.72%, and antibody conjugation efficiency of 41.70%. Meanwhile, Cet-Iri-NPs exhibited a remarkable photothermal effect, and pH/NIR-triggered faster release of CPT-11 with near infrared (NIR) laser irradiation, which induced enhanced cytotoxicity against SW480 cells. Furthermore, the promoted tumor-growth suppression effect of Cet-Iri-NPs on SW480 tumor xenograft nude mice was achieved under NIR laser irradiation.
These results indicate that the well-defined Cet-Iri-NPs are a promising platform for targeted colorectal cancer treatment with chemo-photothermal therapy.
表皮生长因子受体(EGFR)是治疗结直肠癌的主要靶点。因此,抗 EGFR 抗体偶联的脂质-聚合物杂化纳米粒可以提供一种增强 EGFR 过表达癌症中化疗药物疗效的潜在手段。此外,化疗和光热治疗的联合是癌症治疗的一种有前途的策略。因此,开发用于结直肠肿瘤治疗的安全有效的递送系统是非常理想的。
在这项研究中,制备了 EGFR 靶向和近红外触发的脂质-聚合物杂化纳米粒(简称 Cet-Iri-NPs),以共聚物 PPG-PEG、脂质 DSPE-PEG-Mal 和卵磷脂为载体,以伊立替康(CPT-11)作为抗癌化疗药物,以吲哚菁绿(ICG)作为光热剂,并用西妥昔单抗作为表面靶向配体。
体外分析表明,Cet-Iri-NPs 呈球形,粒径为 99.88nm,表面电荷为 29.17mV,药物包封率为 51.72%,抗体偶联率为 41.70%。同时,Cet-Iri-NPs 表现出显著的光热效应,在近红外(NIR)激光照射下,pH/NIR 触发更快地释放 CPT-11,从而对 SW480 细胞产生更强的细胞毒性。此外,在 NIR 激光照射下,Cet-Iri-NPs 对 SW480 肿瘤异种移植裸鼠的肿瘤生长抑制作用得到了增强。
这些结果表明,这种具有明确结构的 Cet-Iri-NPs 是一种有前途的用于结直肠癌靶向治疗的平台,具有化学-光热治疗作用。