Wang Shi-Bo, Zhang Cheng, Ye Jing-Jie, Zou Mei-Zhen, Liu Chuan-Jun, Zhang Xian-Zheng
Key Laboratory of Biomedical Polymers of Ministry of Education & Department of Chemistry, Wuhan University, Wuhan 430072, P. R. China.
Institute for Advanced Studies (IAS), Wuhan University, Wuhan 430072, P. R. China.
ACS Cent Sci. 2020 Apr 22;6(4):555-565. doi: 10.1021/acscentsci.9b01342. Epub 2020 Mar 23.
Photothermal therapy (PTT) is an effective treatment modality with high selectivity for tumor suppression. However, the inflammatory responses caused by PTT may lead to adverse reactions including tumor recurrence and therapeutic resistance, which are regarded as major problems for PTT. Here, a near-infrared (NIR) light-responsive nanoreactor (P@DW/BC) is fabricated to simultaneously realize tumor PTT and carbon monoxide (CO)-mediated anti-inflammatory therapy. Defective tungsten oxide (WO) nanosheets (DW NSs) are decorated with bicarbonate (BC) via ferric ion-mediated coordination and then modified with polyethylene glycol (PEG) on the surface to fabricate PEG@DW/BC or P@DW/BC nanosheets. Upon 808 nm NIR laser irradiation, the DW content in P@DW/BC can serve as not only a photothermal agent to realize photothermal conversion but also a photocatalyst to convert carbon dioxide (CO) to CO. In particular, the generated heat can also trigger the decomposition of BC to produce CO near the NSs, thus enhancing the photocatalytic CO generation. Benefiting from the efficient hyperthermia and CO generation under single NIR laser irradiation, P@DW/BC can realize effective thermal ablation of tumor and simultaneous inhibition of PTT-induced inflammation.
光热疗法(PTT)是一种对肿瘤抑制具有高选择性的有效治疗方式。然而,PTT引起的炎症反应可能导致包括肿瘤复发和治疗抗性在内的不良反应,这些被视为PTT的主要问题。在此,制备了一种近红外(NIR)光响应纳米反应器(P@DW/BC),以同时实现肿瘤PTT和一氧化碳(CO)介导的抗炎治疗。通过铁离子介导的配位作用,用碳酸氢盐(BC)修饰有缺陷的氧化钨(WO)纳米片(DW NSs),然后在表面用聚乙二醇(PEG)进行改性,制备PEG@DW/BC或P@DW/BC纳米片。在808 nm近红外激光照射下,P@DW/BC中的DW含量不仅可以作为光热剂实现光热转换,还可以作为光催化剂将二氧化碳(CO₂)转化为CO。特别地,产生的热量还可以触发BC的分解,在纳米片附近产生CO,从而增强光催化CO的生成。受益于在单近红外激光照射下的高效热疗和CO生成,P@DW/BC可以实现肿瘤的有效热消融并同时抑制PTT诱导的炎症。