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开发双重交联的 Pluronic F127/壳聚糖注射水凝胶,其中包含石墨烯纳米系统,用于乳腺癌光热治疗和抗菌应用。

Development of dual-crosslinked Pluronic F127/Chitosan injectable hydrogels incorporating graphene nanosystems for breast cancer photothermal therapy and antibacterial applications.

机构信息

CICS-UBI - Centro de Investigação Em Ciências Da Saúde, Universidade Da Beira Interior, Covilhã, Portugal.

CICS-UBI - Centro de Investigação Em Ciências Da Saúde, Universidade Da Beira Interior, Covilhã, Portugal; AEROG-LAETA, Aerospace Sciences Department, Universidade Da Beira Interior, Covilhã, Portugal.

出版信息

Eur J Pharm Biopharm. 2024 Oct;203:114476. doi: 10.1016/j.ejpb.2024.114476. Epub 2024 Aug 28.

Abstract

Nanomaterials with responsiveness to near-infrared light can mediate the photoablation of cancer cells with an exceptional spatio-temporal resolution. However, the therapeutic outcome of this modality is limited by the nanostructures' poor tumor uptake. To address this bottleneck, it is appealing to develop injectable in situ forming hydrogels due to their capacity to perform a tumor-confined delivery of the nanomaterials with minimal off-target leakage. In particular, injectable in situ forming hydrogels based on Pluronic F127 have been emerging due to their FDA-approval status, biocompatibility, and thermosensitive sol-gel transition. Nevertheless, the application of Pluronic F127 hydrogels has been limited due to their fast dissociation in aqueous media. Such limitation may be addressed by combining the thermoresponsive sol-gel transition of Pluronic F127 with other polymers with crosslinking capabilities. In this work, a novel dual-crosslinked injectable in situ forming hydrogel based on Pluronic F127 (thermosensitive gelation) and Chitosan (ionotropic gelation in the presence of NaHCO), loaded with Dopamine-reduced graphene oxide (DOPA-rGO; photothermal nanoagent), was developed for application in breast cancer photothermal therapy. The dual-crosslinked hydrogel incorporating DOPA-rGO showed a good injectability (through 21 G needles), in situ gelation capacity and cytocompatibility (viability > 73 %). As importantly, the dual-crosslinking improved the hydrogel's porosity and prevented its premature degradation. After irradiation with near-infrared light, the dual-crosslinked hydrogel incorporating DOPA-rGO produced a photothermal heating (ΔT ≈ 22 °C) that reduced the breast cancer cells' viability to just 32 %. In addition, this formulation also demonstrated a good antibacterial activity by reducing the viability of S. aureus and E. coli to 24 and 33 %, respectively. Overall, the dual-crosslinked hydrogel incorporating DOPA-rGO is a promising macroscale technology for breast cancer photothermal therapy and antimicrobial applications.

摘要

具有近红外光响应性的纳米材料可以以出色的时空分辨率介导癌细胞的光烧蚀。然而,这种模式的治疗效果受到纳米结构在肿瘤中摄取不良的限制。为了解决这个瓶颈问题,开发可注射原位形成水凝胶是很有吸引力的,因为它们能够以最小的脱靶泄漏对纳米材料进行肿瘤限制的输送。特别是,基于 Pluronic F127 的可注射原位形成水凝胶由于其 FDA 批准的地位、生物相容性和热敏溶胶-凝胶转变而崭露头角。然而,Pluronic F127 水凝胶的应用受到其在水性介质中快速解离的限制。这种限制可以通过将 Pluronic F127 的热响应溶胶-凝胶转变与具有交联能力的其他聚合物结合来解决。在这项工作中,开发了一种基于 Pluronic F127(热敏凝胶化)和壳聚糖(在存在 NaHCO 的情况下离子凝胶化)的新型双重交联可注射原位形成水凝胶,负载多巴胺还原氧化石墨烯(DOPA-rGO;光热纳米剂),用于乳腺癌光热治疗。负载 DOPA-rGO 的双重交联水凝胶表现出良好的可注射性(通过 21 G 针头)、原位凝胶化能力和细胞相容性(存活率>73%)。同样重要的是,双重交联提高了水凝胶的多孔性并防止了其过早降解。近红外光照射后,负载 DOPA-rGO 的双重交联水凝胶产生光热加热(ΔT≈22°C),将乳腺癌细胞的存活率降低至仅 32%。此外,该制剂还通过将金黄色葡萄球菌和大肠杆菌的存活率分别降低到 24%和 33%,表现出良好的抗菌活性。总体而言,负载 DOPA-rGO 的双重交联水凝胶是一种有前途的用于乳腺癌光热治疗和抗菌应用的宏观技术。

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