Zhao Shuxian, Cao Weiwei, Xing Shanshan, Li Lei, He Yaqian, Hao Zining, Wang Shuai, He Hongyu, Li Chunhui, Zhao Qianqian, Gao Dawei
Applying Chemistry Key Lab of Hebei Province, Department of Bioengineering, Yanshan University, No. 438 Hebei Street, Qinhuangdao 066004, P. R. China.
State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, P. R. China.
ACS Biomater Sci Eng. 2019 Jul 8;5(7):3373-3379. doi: 10.1021/acsbiomaterials.9b00317. Epub 2019 Jun 24.
Chemotherapy is one of the most effective methods of treating tumors in clinical study currently, but drug side effects usually are unbearable to the patient, which also makes it difficult to continue chemotherapy. Enhanced drug efficacy and reduced drug side effects are the main strategies for tumor therapy. Herein, based on biochemical regulation, theanine liposomes were designed to adjuvant doxorubicin (DOX) therapy, which can reduce the adverse reactions and enhance the effect of DOX. Stigmasterol was applied instead of traditional cholesterol for reducing the risk of cardiovascular disease. The as-prepared theanine liposomes by two methods had optimal sizes (154.8 and 169.0 nm), which can effectively accumulate in tumor tissues. experiments demonstrated that the theanine liposomes had a good effect of sustaining drug release. Cell uptake indicated that the presence of theanine can effectively inhibit glutathione (GSH) levels in cells and increase the uptake of DOX. In tumor bearing mice experiments, the combination of the theanine liposomes and DOX showed a better tumor inhibitory effect with a smaller tumor volume (2.7 fold) compared with that of the free DOX group. Meanwhile, under the mediation of theanine, the amount of doxorubicin was greatly reduced to achieve the same therapeutic effect, and the side effects of the drug were largely inhibited. Therefore, theanine liposomes have great application potential in tumor chemotherapy.
化疗是目前临床研究中治疗肿瘤最有效的方法之一,但药物副作用通常让患者难以忍受,这也使得化疗难以持续进行。提高药物疗效和降低药物副作用是肿瘤治疗的主要策略。在此,基于生化调控,设计了茶氨酸脂质体用于辅助阿霉素(DOX)治疗,其可减少不良反应并增强DOX的效果。使用豆甾醇代替传统胆固醇以降低心血管疾病风险。通过两种方法制备的茶氨酸脂质体具有最佳尺寸(154.8和169.0 nm),可有效在肿瘤组织中蓄积。实验表明茶氨酸脂质体具有良好的药物缓释效果。细胞摄取表明茶氨酸的存在可有效抑制细胞内谷胱甘肽(GSH)水平并增加DOX的摄取。在荷瘤小鼠实验中,茶氨酸脂质体与DOX联合使用显示出比游离DOX组更好的肿瘤抑制效果,肿瘤体积更小(2.7倍)。同时,在茶氨酸的介导下,阿霉素用量大幅减少以达到相同治疗效果,且药物副作用得到很大程度抑制。因此,茶氨酸脂质体在肿瘤化疗中具有巨大的应用潜力。