Zu Guangyue, Cao Yi, Dong Jingjin, Zhou Qihui, van Rijn Patrick, Liu Min, Pei Renjun
CAS Key Laboratory of Nano-Bio Interface, Division of Nanobiomedicine, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123, China.
Department of Biomedical Engineering, W. J. Kolff Institute for Biomedical Engineering and Materials Science, University of Groningen, University Medical Center Groningen, A. Deusinglaan 1, Groningen 9713 AV, The Netherlands.
ACS Appl Bio Mater. 2019 Jan 22;2(1):406-416. doi: 10.1021/acsabm.8b00639. Epub 2019 Jan 8.
Gadolinium-based magnetic resonance imaging (MRI) contrast agents with biodegradability, biosafety, and high efficiency are highly desirable for tumor diagnosis. Herein, a biodegradable, AS1411-conjugated, α-cyclodextrin polyrotaxane-based MRI contrast agent (AS1411-G2(DTPA-Gd)-SS-PR) was developed for targeted imaging of cancer. The polyrotaxane-based contrast agent was achieved by the complexation of α-cyclodextrin (α-CD) and a linear poly(ethylene glycol) (PEG) chain containing disulfide linkages at two terminals. The disulfides enable the dethreading of the polyrotaxane into excretable small units due to cleavage of the disulfide linkages by reducing agents such as intracellular glutathione (GSH). Furthermore, the second-generation lysine dendron conjugated with gadolinium chelates and AS1411, a G-quadruplex oligonucleotide that has high binding affinity to nucleolin generally presenting a high level on the surface of tumor cells, coupled to the α-CD via click chemistry. The longitudinal relaxivity of AS1411-G2(DTPA-Gd)-SS-PR (11.7 mM s) was two times higher than the clinically used Gd-DTPA (4.16 mM s) at 0.5 T. The in vitro degradability was confirmed by incubating with 10 mM 1,4-dithiothreitol (DTT). Additionally, the cytotoxicity, histological assessment, and gadolinium retention studies showed that the prepared polyrotaxane-based contrast agent had a superior biocompatibility and was predominantly cleared renally without long-term accumulation toxicity. Importantly, AS1411-G2(DTPA-Gd)-SS-PR displayed the enhanced performance in MRI of breast cancer cells in vitro as well as a subcutaneous breast tumor in vivo due to the targeting ability of the AS1411 aptamer. The enhanced performance was due to efficient multivalent interactions with tumor cells, producing faster accumulation and longer contrast imaging time at the tumor site. This work clearly confirms that the specially designed and fabricated α-CD-based polyrotaxane is a promising contrast agent with an excellent contrast imaging performance and biosafety for tumor MR imaging.
具有生物可降解性、生物安全性和高效性的基于钆的磁共振成像(MRI)造影剂对于肿瘤诊断非常理想。在此,开发了一种可生物降解的、与AS1411偶联的、基于α-环糊精聚轮烷的MRI造影剂(AS1411-G2(DTPA-Gd)-SS-PR)用于癌症的靶向成像。基于聚轮烷的造影剂是通过α-环糊精(α-CD)与在两个末端含有二硫键的线性聚乙二醇(PEG)链络合而成。由于细胞内谷胱甘肽(GSH)等还原剂可使二硫键断裂,二硫键能使聚轮烷解绕成可排泄的小单元。此外,第二代赖氨酸树枝状分子与钆螯合物和AS1411偶联,AS1411是一种与核仁素具有高结合亲和力的G-四链体寡核苷酸,通常在肿瘤细胞表面呈现高水平,通过点击化学与α-CD偶联。在0.5 T时,AS1411-G2(DTPA-Gd)-SS-PR的纵向弛豫率(11.7 mM-1 s-1)比临床使用的钆喷酸葡胺(4.16 mM-1 s-1)高两倍。通过与10 mM 1,4-二硫苏糖醇(DTT)孵育证实了其体外可降解性。此外,细胞毒性、组织学评估和钆保留研究表明,所制备的基于聚轮烷的造影剂具有优异的生物相容性,主要通过肾脏清除,无长期蓄积毒性。重要的是,由于AS1411适配体的靶向能力,AS1411-G2(DTPA-Gd)-SS-PR在体外乳腺癌细胞的MRI以及体内皮下乳腺肿瘤中表现出增强的性能。增强的性能归因于与肿瘤细胞的有效多价相互作用,在肿瘤部位产生更快的积累和更长的对比成像时间。这项工作清楚地证实,特别设计和制造的基于α-CD的聚轮烷是一种有前途的造影剂,在肿瘤MR成像中具有优异的对比成像性能和生物安全性。