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纳米抗体-葡聚糖聚合物偶联物对肿瘤球体的穿透作用。

Penetration of Nanobody-Dextran Polymer Conjugates through Tumor Spheroids.

作者信息

Bitsch Peter, Baum Eva S, Beltrán Hernández Irati, Bitsch Sebastian, Harwood Jakob, Oliveira Sabrina, Kolmar Harald

机构信息

Institute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, Peter-Grünberg-Str. 4, 64287 Darmstadt, Germany.

Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands.

出版信息

Pharmaceutics. 2023 Sep 22;15(10):2374. doi: 10.3390/pharmaceutics15102374.

Abstract

Here we report the generation of nanobody dextran polymer conjugates (dextraknobs) that are loaded with small molecules, i.e., fluorophores or photosensitizers, for potential applications in cancer diagnostics and therapy. To this end, the molecules are conjugated to the dextran polymer which is coupled to the C-terminus of an EGFR-specific nanobody using chemoenzymatic approaches. A monovalent EGFR-targeted nanobody and biparatopic version modified with different dextran average molecular weights (1000, 5000, and 10,000) were probed for their ability to penetrate tumor spheroids. For monovalent Cy5-labeled dextraknobs, the utilization of smaller sized dextran (MW 5000 vs. 10,000) was found to be beneficial for more homogeneous penetration into A431 tumor spheroids over time. For the biparatopic dual nanobody comprising MW 1000, 5000, and 10,000 dextran labeled with photosensitizer IRDye700DX, penetration behavior was comparable to that of a direct nanobody-photosensitizer conjugate lacking a dextran scaffold. Additionally, dextraknobs labeled with IRDye700DX incubated with cells in 2D and 3D showed potent cell killing upon illumination, thus inducing photodynamic therapy (PDT). In line with previous results, monovalent nanobody conjugates displayed deeper and more homogenous penetration through spheroids than the bivalent conjugates. Importantly, the smaller size dextrans did not affect the distribution of the conjugates, thus encouraging further development of dextraknobs.

摘要

在此,我们报告了纳米抗体-葡聚糖聚合物偶联物(dextraknobs)的生成,这些偶联物负载有小分子,即荧光团或光敏剂,可用于癌症诊断和治疗的潜在应用。为此,使用化学酶法将这些分子与葡聚糖聚合物偶联,该葡聚糖聚合物与表皮生长因子受体(EGFR)特异性纳米抗体的C末端相连。对单价EGFR靶向纳米抗体和用不同平均分子量(1000、5000和10000)的葡聚糖修饰的双特异性版本进行了穿透肿瘤球体能力的检测。对于单价Cy5标记的dextraknobs,发现使用较小尺寸的葡聚糖(分子量5000与10000相比)随着时间的推移更有利于更均匀地穿透A431肿瘤球体。对于包含用光敏剂IRDye700DX标记的分子量为1000、5000和10000的葡聚糖的双特异性双纳米抗体,其穿透行为与缺乏葡聚糖支架的直接纳米抗体-光敏剂偶联物相当。此外,用IRDye700DX标记的dextraknobs在二维和三维条件下与细胞孵育,光照后显示出强大的细胞杀伤作用,从而诱导光动力疗法(PDT)。与先前的结果一致,单价纳米抗体偶联物比二价偶联物在球体中表现出更深且更均匀的穿透。重要的是,较小尺寸的葡聚糖不会影响偶联物的分布,因此鼓励对dextraknobs进行进一步开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7676/10609859/65114a0039ce/pharmaceutics-15-02374-g001.jpg

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