Department of Radiotherapy Central Hospital, Affiliated Xuzhou Clinical College of Xuzhou Medical University, Xuzhou, 221009, People's Republic of China.
Key Laboratory for Biotechnology on Medicinal Plants of Jiangsu Province, School of Life Science, Jiangsu Normal University, Xuzhou, 221116, People's Republic of China.
Int J Nanomedicine. 2023 Feb 14;18:743-763. doi: 10.2147/IJN.S394377. eCollection 2023.
Realgar, as a kind of traditional mineral Chinese medicine, can inhibit multiple solid tumor growth and serve as an adjuvant drug in cancer therapy. However, the extremely low solubility and poor body absorptive capacity limit its application in clinical medicine. To overcome this therapeutic hurdle, realgar can here be fabricated into a nano-realgar hydrogel with enhanced chemotherapy and radiotherapy (RT) ability. Our objective is to evaluate the superior biocompatibility and anti-tumor activity of nano-realgar hydrogel.
We have successfully synthesized nano-realgar quantum dots (QDs) coupling with 6-AN molecules (NRA QDs) and further encapsulated with a pH-sensitive dextran hydrogel carrier with hyaluronic acid coating (DEX-HA gel) to promote bioavailability, eventually forming a multifunctional nano-realgar hydrogel (NRA@DH Gel). To better investigate the tumor therapy efficiency of the NRA@DH Gel, we have established the mice in situ bearing GL261 brain glioblastoma as animal models assigned to receive intratumor injection of NRA@DH Gel.
The designed NRA@DH Gel as an antitumor drug can not only exert the prominent chemotherapy effect but also as a "sustainable reactive oxygen species (ROS) generator" can inhibit in the pentose phosphate pathway (PPP) metabolism and reduce the production of nicotinamide adenine dinucleotide phosphate (NADPH), thereby inhibiting the conversion of glutathione disulfide (GSSG) to glutathione (GSH), reducing GSH concentrations in tumor cells, triggering the accumulation of ROS, and finally enhancing the effectiveness of RT.
Through the synergistic effect of chemotherapy and RT, NRA@DH Gel effectively inhibited the proliferation and migration of tumor cells, suppressed tumor growth, improved motor coordination, and prolonged survival in tumor-bearing mice. Our work aims to improve the NRA@DH Gel-mediated synergistic chemotherapy and RT will endow a "promising future" for the old drug in clinically comprehensive applications.
雄黄作为一种传统的矿物中药,能抑制多种实体瘤的生长,并可作为癌症治疗的辅助药物。然而,其极低的溶解度和较差的体吸收能力限制了其在临床医学中的应用。为了克服这一治疗障碍,可以将雄黄制成具有增强化疗和放疗(RT)能力的纳米雄黄水凝胶。我们的目的是评估纳米雄黄水凝胶的卓越生物相容性和抗肿瘤活性。
我们成功地合成了与 6-AN 分子偶联的纳米雄黄量子点(NRA QDs),并进一步用透明质酸涂层的 pH 敏感葡聚糖水凝胶载体(DEX-HA 凝胶)包封,以提高生物利用度,最终形成多功能纳米雄黄水凝胶(NRA@DH Gel)。为了更好地研究 NRA@DH Gel 的肿瘤治疗效率,我们建立了原位荷 GL261 脑胶质瘤的小鼠动物模型,接受 NRA@DH Gel 瘤内注射。
设计的 NRA@DH Gel 作为抗肿瘤药物不仅能发挥显著的化疗作用,而且还可以作为“持续的活性氧(ROS)发生器”,抑制磷酸戊糖途径(PPP)代谢,减少烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的产生,从而抑制谷胱甘肽二硫化物(GSSG)向谷胱甘肽(GSH)的转化,降低肿瘤细胞内 GSH 浓度,引发 ROS 积累,最终增强 RT 的效果。
通过化疗和 RT 的协同作用,NRA@DH Gel 有效抑制了肿瘤细胞的增殖和迁移,抑制了肿瘤生长,改善了运动协调能力,延长了荷瘤小鼠的生存时间。我们的工作旨在提高 NRA@DH Gel 介导的协同化疗和 RT 将为老药在临床综合应用中带来“光明的未来”。