School of Life Science, Chongqing University, Chongqing, 400044, China.
Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing, 400044, China.
Biomaterials. 2021 Feb;269:120623. doi: 10.1016/j.biomaterials.2020.120623. Epub 2020 Dec 28.
Surgery is the mainstream treatment for melanoma, but its clinical implementation suffers from some major drawbacks including residual infiltrating melanoma cells at resection margins and severe tissue injury. In this study, a nanocomposite scaffold is developed for in-situ therapy after melanoma surgery as well as wound healing, which is fabricated by embedding photothermal-capable black phosphorus nanosheets (BPNSs) into bioresorbable Gelatin-PCL (GP) nanofibrous scaffold. GP scaffold is a clinically-tested biomaterial with temperature sensitivity and tissue-healing effect, while the BPNSs are loaded with the anticancer antibiotic of doxorubicin (DOX) and conjugated with NH-PEG-FA for tumor-targeted delivery. The GP scaffold could undergo a sol-gel transition upon NIR irritation and release the BPNSs in situ. During this process, most of the BP-based nanoformulations were selectively internalized by the melanoma cells for the cooperative photothermal therapy and heat-triggerable DOX therapy, while some of the loaded DOX was released into the wound tissue to create a tumor-suppressive microenvironment. Moreover, BPNSs could be gradually degraded to phosphates/phosphonates and thus enhance tissue repair by activating the ERK1/2 and PI3K/Akt pathway. Meanwhile, the detached DOX molecules would also enter the wound tissues for continuous melanoma inhibition. Considering the anti-melanoma and wound healing effect of this composite scaffold, it may offer a facile strategy for the wound treatment after melanoma surgery.
手术是治疗黑色素瘤的主流方法,但它在临床实施中存在一些主要缺陷,包括切除边缘残留浸润性黑色素瘤细胞和严重的组织损伤。在这项研究中,开发了一种用于黑色素瘤手术后原位治疗和伤口愈合的纳米复合材料支架,该支架是通过将光热能力的黑磷纳米片(BPNSs)嵌入可生物降解的明胶-聚己内酯(GP)纳米纤维支架中制成的。GP 支架是一种经过临床测试的具有温度敏感性和组织修复作用的生物材料,而 BPNSs 则负载了抗癌抗生素阿霉素(DOX),并与 NH-PEG-FA 缀合以实现肿瘤靶向递药。GP 支架在近红外刺激下会发生溶胶-凝胶转变,并原位释放 BPNSs。在此过程中,大多数基于 BP 的纳米制剂被黑色素瘤细胞选择性内化,用于协同光热治疗和热触发 DOX 治疗,而一些负载的 DOX 则释放到伤口组织中,以创造一个肿瘤抑制的微环境。此外,BPNSs 可以逐渐降解为磷酸盐/膦酸盐,从而通过激活 ERK1/2 和 PI3K/Akt 通路来增强组织修复。同时,分离的 DOX 分子也会进入伤口组织,持续抑制黑色素瘤。考虑到这种复合支架的抗黑色素瘤和伤口愈合作用,它可能为黑色素瘤手术后的伤口处理提供一种简便的策略。