Engineered dual-responsive mucoadhesive hydrogel co-delivering fullerenol against radiation-induced vaginal injury and microbiota dysbiosis.

IF 11 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Materials Today Bio Pub Date : 2026-07-16 eCollection Date: 2026-08-01 DOI:10.1016/j.mtbio.2026.103470
Maoru Zhao, Chengyan Wang, Yi Huang, Liangdi Wang, Jiangwei Xiao, Zhanjun Gu
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引用次数: 0

Abstract

Radiation-induced vaginal injury (RIVI) is a prevalent complication following pelvic radiotherapy for gynecological cancers, which is mainly caused by severe mucosal oxidative stress triggered by highly destructive reactive oxygen species (ROS), such as hydroxyl radicals (·OH). Conventional prophylactic agents struggle due to instability, inadequate radical targeting, and short residence time in the vaginal lumen. To overcome the existing challenges, we develop a biomaterial-based prophylactic strategy that enables effective neutralization of toxic radicals and smart mucosal adhesion. Taking advantage of carbon-based nano-antioxidant fullerenol (FOH) as a reliable "radical sponge" for ·OH clearance, we engineer pH- and temperature-responsive amino-terminated Pluronic F127 (AF127) in situ hydrogel as the carrier of FOH. The AF127@FOH system is suitable for facile vaginal administration and can achieve in situ gelation. More importantly, AF127 can be protonated in the acidic vaginal environment, thereby enhancing mucoadhesion with vaginal mucins through electrostatic interactions and prolonging local residence. This design enables a locally sustained release of FOH, which inhibits the initial burst of ROS, mitigating oxidative damage, early tissue damage, and subsequent vaginal microbial dysbiosis. Our work provides an advanced topical treatment approach for RIVI and expands the application of smart biomaterials in mucosal radiation protection.

工程双响应黏附水凝胶共同递送富勒烯醇对抗辐射引起的阴道损伤和微生物群失调。
放射性阴道损伤(RIVI)是妇科癌症盆腔放疗后常见的并发症,主要是由高破坏性活性氧(ROS)如羟基自由基(·OH)引发的严重粘膜氧化应激所致。传统的预防药物由于不稳定、不充分的根治靶向和在阴道腔内停留时间短而挣扎。为了克服现有的挑战,我们开发了一种基于生物材料的预防策略,能够有效中和有毒自由基和智能粘膜粘附。利用碳基纳米抗氧化剂富勒烯醇(FOH)作为清除·OH的可靠“自由基海绵”,我们设计了pH和温度响应的氨基端Pluronic F127 (AF127)原位水凝胶作为FOH的载体。AF127@FOH系统适合于阴道给药,可以实现原位凝胶。更重要的是,AF127可以在阴道酸性环境中质子化,从而通过静电相互作用增强与阴道粘蛋白的黏附,延长局部停留时间。这种设计能够局部持续释放FOH,从而抑制ROS的初始爆发,减轻氧化损伤、早期组织损伤和随后的阴道微生物生态失调。我们的工作为RIVI提供了一种先进的局部治疗方法,并扩展了智能生物材料在粘膜辐射防护中的应用。
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来源期刊
CiteScore
8.30
自引率
4.90%
发文量
303
审稿时长
30 days
期刊介绍: Materials Today Bio is a multidisciplinary journal that specializes in the intersection between biology and materials science, chemistry, physics, engineering, and medicine. It covers various aspects such as the design and assembly of new structures, their interaction with biological systems, functionalization, bioimaging, therapies, and diagnostics in healthcare. The journal aims to showcase the most significant advancements and discoveries in this field. As part of the Materials Today family, Materials Today Bio provides rigorous peer review, quick decision-making, and high visibility for authors. It is indexed in Scopus, PubMed Central, Emerging Sources, Citation Index (ESCI), and Directory of Open Access Journals (DOAJ).
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N,N'-Carbonyldiimidazole
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microplate reader
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2,2-diphenyl-1-picrohydrazine
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rheometer MCR92
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Triton X-100
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3,3',5,5'-tetramethylbenzidine
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Alexa Fluor 488-labeled Goat Anti-Mouse IgG (H+L)
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Caspase-3 activity assay kit
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Cy3-labeled Goat Anti-Rabbit IgG (H+L)
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cytochrome C Mouse mAb
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DCFH-DA probe
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JC-1 staining working solution
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nitroblue tetrazolium chloride
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reduced nicotinamide adenine dinucleotide
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Omni system
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ANCE IIITM 500 MHz NMR spectrometer
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Mito-Tracker Red CMXRos
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Phospho-Histone H2A.X (Ser139) Rabbit mAb
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fullerene C60
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Annexin V-FITC/PI Apoptosis detection kit
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Hoechst 33342
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X-ray irradiator
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transmission electron microscope
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simulated vaginal fluid
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Transwell insert
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laser scanning confocal microscope
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inverted fluorescence microscope
31
IVIS spectrum
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Pluronic F127
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2,2-azinobis (3-ethylbenzthiazoline-6-sulfonate) diammonium salt
35
Pluronic F-127
36
Fourier transform infrared spectrometer
37
microplate reader
38
X-ray photoelectron spectrometer
39
phenazine methosulfate
40
superoxide dismutase
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