Chen Guojun, Wang Liwei, Cordie Travis, Vokoun Corinne, Eliceiri Kevin W, Gong Shaoqin
Materials Science Program, University of Wisconsin-Madison, Madison, WI 53715, USA; Wisconsin Institutes for Discovery, University of Wisconsin-Madison, Madison, WI 53715, USA.
Wisconsin Institutes for Discovery, University of Wisconsin-Madison, Madison, WI 53715, USA; Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI 53715, USA.
Biomaterials. 2015 Apr;47:41-50. doi: 10.1016/j.biomaterials.2015.01.006. Epub 2015 Feb 4.
A novel type of self-fluorescent unimolecular micelle nanoparticle (NP) formed by multi-arm star amphiphilic block copolymer, Boltron® H40 (H40, a 4th generation hyperbranched polymer)-biodegradable photo-luminescent polymer (BPLP)-poly(ethylene glycol) (PEG) conjugated with cRGD peptide (i.e., H40-BPLP-PEG-cRGD) was designed, synthesized, and characterized. The hydrophobic BPLP segment was self-fluorescent, thereby making the unimolecular micelle NP self-fluorescent. cRGD peptides, which can effectively target αvβ3 integrin-expressing tumor neovasculature and tumor cells, were selectively conjugated onto the surface of the micelles to offer active tumor-targeting ability. This unique self-fluorescent unimolecular micelle exhibited excellent photostability and low cytotoxicity, making it an attractive bioimaging probe for NP tracking for a variety of microscopy techniques including fluorescent microscopy, confocal laser scanning microscopy (CLSM), and two-photon microscopy. Moreover, this self-fluorescent unimolecular micelle NP also demonstrated excellent stability in aqueous solutions due to its covalent nature, high drug loading level, pH-controlled drug release, and passive and active tumor-targeting abilities, thereby making it a promising nanoplatform for targeted cancer theranostics.
设计、合成并表征了一种新型的自荧光单分子胶束纳米颗粒(NP),它由多臂星形两亲嵌段共聚物Boltron® H40(H40,第四代超支化聚合物)-可生物降解的光致发光聚合物(BPLP)-聚乙二醇(PEG)与cRGD肽共轭而成(即H40-BPLP-PEG-cRGD)。疏水性BPLP片段具有自荧光特性,从而使单分子胶束NP具有自荧光性。能够有效靶向表达αvβ3整合素的肿瘤新生血管和肿瘤细胞的cRGD肽被选择性地共轭到胶束表面,以提供主动肿瘤靶向能力。这种独特的自荧光单分子胶束表现出优异的光稳定性和低细胞毒性,使其成为用于包括荧光显微镜、共聚焦激光扫描显微镜(CLSM)和双光子显微镜在内的多种显微镜技术的NP追踪的有吸引力的生物成像探针。此外,这种自荧光单分子胶束NP由于其共价性质、高载药量、pH控制的药物释放以及被动和主动肿瘤靶向能力,在水溶液中也表现出优异的稳定性,从而使其成为用于靶向癌症诊疗的有前景的纳米平台。