An injectable composite hydrogel containing polydopamine-coated curcumin nanoparticles and indoximod for the enhanced combinational chemo-photothermal-immunotherapy of breast tumors

IF 5.4 2区 医学 Q1 BIOPHYSICS
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Abstract

The complexity and compensatory evolution of tumors weaken the effectiveness of single antitumor therapies. Therefore, multimodal combination therapies hold great promise in defeating tumors. Herein, we constructed a multi-level regulatory co-delivery system based on chemotherapy, phototherapy, and immunotherapy. Briefly, curcumin (Cur) was prepared as nanoparticles and coated with polydopamine (PDA) to form PCur-NPs, which along with an immune checkpoint inhibitor (indoximod, IND) were then loaded into a thermosensitive Pluronic F127 (F127) hydrogel to form a multifunctional nanocomposite hydrogel (PCur/IND@Gel). The in situ-formed hydrogel exhibited excellent photothermal conversion efficiency and sustained drug release behavior both in vitro and in vivo. In addition, PCur-NPs showed enhanced cellular uptake and cytotoxicity under NIR laser irradiation and induced potent immunogenic cell death (ICD). After intratumoral injection of PCur/IND@Gel, significant apoptosis in 4T1 tumors was induced, dendritic cells in lymph nodes were highly activated, potent CD8+ and CD4+ antitumor immune responses were elicited and regulative T cells in tumors were significantly reduced, which notably inhibited the tumor growth and prolonged the survive time of 4T1 tumor-bearing mice. Therefore, this injectable nanocomposite hydrogel is a promising drug co-delivery platform for chemo-photothermal-immunotherapy of breast tumors.

一种含有聚多巴胺包裹的姜黄素纳米颗粒和吲哚西莫德的可注射复合水凝胶,用于增强乳腺肿瘤的化疗-光热-免疫联合疗法
肿瘤的复杂性和代偿性演变削弱了单一抗肿瘤疗法的有效性。因此,多模式联合疗法在战胜肿瘤方面大有可为。在此,我们构建了一种基于化疗、光疗和免疫疗法的多级调控联合给药系统。简而言之,将姜黄素(Cur)制备成纳米颗粒,并用聚多巴胺(PDA)包覆形成PCur-NPs,然后将其与免疫检查点抑制剂(indoximod,IND)一起载入热敏性Pluronic F127(F127)水凝胶中,形成多功能纳米复合水凝胶(PCur/IND@Gel)。这种原位形成的水凝胶在体外和体内均表现出优异的光热转换效率和持续的药物释放行为。此外,PCur-NPs 在近红外激光照射下显示出更强的细胞摄取和细胞毒性,并诱导强效免疫原性细胞死亡(ICD)。瘤内注射 PCur/IND@Gel 后,4T1 肿瘤细胞明显凋亡,淋巴结中的树突状细胞高度活化,CD8+和 CD4+ 抗肿瘤免疫应答被激发,肿瘤中的调节性 T 细胞显著减少,从而明显抑制了肿瘤的生长,延长了 4T1 肿瘤小鼠的存活时间。因此,这种可注射的纳米复合水凝胶是一种很有前景的乳腺肿瘤化疗-光热-免疫治疗联合给药平台。
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来源期刊
Colloids and Surfaces B: Biointerfaces
Colloids and Surfaces B: Biointerfaces 生物-材料科学:生物材料
CiteScore
11.10
自引率
3.40%
发文量
730
审稿时长
42 days
期刊介绍: Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields. Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication. The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.
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