开发含有石墨烯纳米系统的双交联 Pluronic F127/Chitosan 可注射水凝胶,用于乳腺癌光热疗法和抗菌应用。

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Manuel R. Pouso , Bruna L. Melo , Joaquim J. Gonçalves , António G. Mendonça , Ilídio J. Correia , Duarte de Melo-Diogo
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引用次数: 0

摘要

对近红外光有反应能力的纳米材料能以极高的时空分辨率对癌细胞进行光消融。然而,由于纳米结构对肿瘤的吸收率较低,这种方式的治疗效果受到限制。为了解决这一瓶颈问题,开发可注射的原位成型水凝胶很有吸引力,因为这种水凝胶能够在肿瘤范围内输送纳米材料,同时将脱靶泄漏降至最低。其中,基于 Pluronic F127 的可注射原位成型水凝胶因其获得美国食品及药物管理局(FDA)批准、具有生物相容性和热敏性溶胶-凝胶转变而崭露头角。然而,Pluronic F127 水凝胶在水介质中的快速解离限制了其应用。将 Pluronic F127 的热粘弹性溶胶-凝胶转变与其他具有交联能力的聚合物相结合,可以解决这种限制。本研究以 Pluronic F127(热敏凝胶化)和壳聚糖(在 NaHCO3 存在下呈离子凝胶化)为基础,开发了一种新型双交联可注射原位成型水凝胶,载入多巴胺还原氧化石墨烯(DOPA-rGO;光热纳米试剂),用于乳腺癌光热治疗。含有 DOPA-rGO 的双交联水凝胶显示出良好的可注射性(通过 21 G 针头)、原位凝胶能力和细胞相容性(存活率大于 73%)。更重要的是,双重交联改善了水凝胶的孔隙率,防止了其过早降解。用近红外光照射后,含有 DOPA-rGO 的双交联水凝胶会产生光热(ΔT ≈ 22 °C),使乳腺癌细胞的存活率降至 32%。此外,这种配方还具有良好的抗菌活性,可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%。总之,含有 DOPA-rGO 的双交联水凝胶是一种很有前景的宏观技术,可用于乳腺癌光热疗法和抗菌应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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 NaHCO3), 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.

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来源期刊
CiteScore
8.80
自引率
4.10%
发文量
211
审稿时长
36 days
期刊介绍: The European Journal of Pharmaceutics and Biopharmaceutics provides a medium for the publication of novel, innovative and hypothesis-driven research from the areas of Pharmaceutics and Biopharmaceutics. Topics covered include for example: Design and development of drug delivery systems for pharmaceuticals and biopharmaceuticals (small molecules, proteins, nucleic acids) Aspects of manufacturing process design Biomedical aspects of drug product design Strategies and formulations for controlled drug transport across biological barriers Physicochemical aspects of drug product development Novel excipients for drug product design Drug delivery and controlled release systems for systemic and local applications Nanomaterials for therapeutic and diagnostic purposes Advanced therapy medicinal products Medical devices supporting a distinct pharmacological effect.
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