Sacchi Angelina, Gasparri Anna Maria, Monieri Matteo, Anderluzzi Giulia, Colombo Barbara, Gori Alessandro, Corti Angelo, Curnis Flavio
Tumor Biology and Vascular Targeting Unit, Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Università Vita-Salute San Raffaele, Milan, Italy.
Front Chem. 2021 May 28;9:690357. doi: 10.3389/fchem.2021.690357. eCollection 2021.
Gold nanoparticles functionalized with DGR, a tripeptide motif that recognizes αvβ3 integrin overexpressed in tumor vessels, have been used as nano-vectors for the delivery of cytokines to tumors. Functionalization of nanogold with this peptide has been achieved by coating nanoparticles with a peptide-albumin conjugate consisting of heterogeneous molecules with a variable number of linkers and peptides. To reduce nanodrug heterogeneity we have designed, produced and preclinically evaluated a homogeneous and well-defined reagent for nanogold functionalization, consisting of a head-to-tail cyclized CGDGRG peptide () coupled its thiol group to maleimide-PEG-lipoamide (LPA). The resulting -PEG-LPA compound can react with nanogold lipoamide to form a stable bond. studies have shown that , after coupling to nanogold, maintains its capability to bind purified αvβ3 and αvβ3-expressing cells. Nanogold functionalized with this peptide can also be loaded with bioactive tumor necrosis factor-α (TNF) to form a bi-functional nanodrug that can be stored for three days at 37°C or >1 year at low temperatures with no loss αvβ3-binding properties and TNF-cytolytic activity. Nanoparticles functionalized with both and TNF induced tumor eradication in WEHI-164 fibrosarcoma-bearing mice more efficiently than nanoparticles lacking the targeting moiety. These results suggest that -PEG-LPA is an efficient and well-defined reagent that can be used to produce robust and more homogeneous nano-vectors for the delivery of TNF and other cytokines to αvβ3 positive cells.
用DGR(一种能识别在肿瘤血管中过表达的αvβ3整合素的三肽基序)功能化的金纳米颗粒已被用作将细胞因子递送至肿瘤的纳米载体。通过用由具有可变数量连接子和肽的异质分子组成的肽 - 白蛋白缀合物包被纳米颗粒,实现了用该肽对纳米金的功能化。为了减少纳米药物的异质性,我们设计、制备并在临床前评估了一种用于纳米金功能化的均匀且定义明确的试剂,它由一个头尾环化的CGDGRG肽()组成,其硫醇基团与马来酰亚胺 - 聚乙二醇 - 硫代酰胺(LPA)偶联。所得的 - 聚乙二醇 - LPA化合物可与纳米金硫代酰胺反应形成稳定的键。研究表明,与纳米金偶联后,仍保持其结合纯化的αvβ3和表达αvβ3的细胞的能力。用该肽功能化的纳米金还可以负载生物活性肿瘤坏死因子 - α(TNF),形成一种双功能纳米药物,该药物可以在37°C下储存三天或在低温下储存>1年,而不会丧失αvβ3结合特性和TNF细胞溶解活性。用 和TNF功能化的纳米颗粒在携带WEHI - 164纤维肉瘤的小鼠中诱导肿瘤根除的效率比缺乏 靶向部分的纳米颗粒更高。这些结果表明, - 聚乙二醇 - LPA是一种有效且定义明确的试剂,可用于生产强大且更均匀的纳米载体,用于将TNF和其他细胞因子递送至αvβ3阳性细胞。