Yao Mattisson Ingrid, Bäckström Sania, Ekengard Erik, Lekmeechai Sujinna, Liu Yi-Chi, Paris Juraj, Petoral Rodrigo, Sydoff Marie, Hansen Mats, Axelsson Oskar
Spago Nanomedical, Scheelevägen 22, 223 63 Lund, Sweden.
Lund University Bioimaging Centre, Klinikgatan 32, 221 84 Lund, Sweden.
ACS Omega. 2023 Jan 4;8(2):2357-2366. doi: 10.1021/acsomega.2c06755. eCollection 2023 Jan 17.
Although much progress has been made over the last decades, there is still a significant clinical need for novel therapies to manage cancer. Typical problems are that solid tumors are frequently inaccessible, aggressive, and metastatic. To contribute to solving some of these issues, we have developed a novel radioisotope-labeled 27 nm nanoparticle, Lu-SN201, to selectively target solid tumors via the enhanced permeability and retention effect, allowing irradiation intratumorally. We show that Lu-SN201 has robust stealth properties in vitro and anti-tumor efficacy in mouse mammary gland and colon carcinoma models. The possible clinical application is also addressed with single photon emission computed tomography imaging, which confirms uptake in the tumor, with an average activity of 19.4% injected dose per gram (ID/g). The properties of Lu-SN201 make it a promising new agent for radionuclide therapy with the potential to target several solid tumor types.
尽管在过去几十年里已经取得了很大进展,但临床上仍然非常需要新的癌症治疗方法。典型的问题是实体瘤常常难以触及、具有侵袭性且会发生转移。为了有助于解决其中一些问题,我们开发了一种新型的放射性同位素标记的27纳米纳米颗粒Lu-SN201,它通过增强的渗透和滞留效应选择性地靶向实体瘤,从而实现肿瘤内照射。我们表明,Lu-SN201在体外具有强大的隐身特性,并且在小鼠乳腺癌和结肠癌模型中具有抗肿瘤功效。还通过单光子发射计算机断层扫描成像探讨了其可能的临床应用,该成像证实了肿瘤对其的摄取,平均摄取活性为每克注射剂量的19.4%(ID/g)。Lu-SN201的特性使其成为一种有前景的放射性核素治疗新药物,有可能靶向多种实体瘤类型。