Xie Yizhuo, Ren Zhihui, Chen Hongyu, Tang Huan, Zhu Ming, Lv Zhe, Bao Han, Zhang Yan, Liu Rui, Shen Yujia, Zheng Yucui, Miao Dongfanghui, Guo Xin, Chen Hongli, Wang Shanshan, Pei Jin
Department of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Department of Biopharmacy, School of Pharmaceutical Sciences, Jilin University, Changchun, China.
Biomed Pharmacother. 2023 Apr;160:114304. doi: 10.1016/j.biopha.2023.114304. Epub 2023 Jan 30.
Ovarian cancer is the second cause of death among gynecological malignancies. In this study, we designed a novel estrogen-targeted PEGylated liposome loaded with oxaliplatin and paclitaxel (ES-SSL-OXA/PTX) which could target estrogen receptor (ER) highly expressed on the surface of SKOV-3 cells to enhance therapeutic efficacy and reduce the side effects for SKOV-3 tumor therapy. ES-SSL-OXA/PTX was prepared by thin film hydration method and exhibited a uniform spherical morphology. Encapsulation efficiency (EE) were determined by HPLC method with the results of 44.10% for OXA and 65.85% for PTX. The mean particle size and polydispersity index (PDI) were 168.46 nm and 0.145, respectively. In vivo and in vitro targeting study confirmed that ES-SSL-OXA/PTX has optimum specific targeting ability. Meanwhile, In vitro and in vivo antitumor results of ES-SSL-OXA/PTX exhibited a superior antiproliferative effect on SKOV-3 cells and a stronger anti-tumor efficacy with the tumor inhibition rate of 85.24%. The pharmacokinetics results of ES-SSL-OXA/PTX showed a prolonged half-life time and a slowed clearance rate. The preliminary safety study of acute toxicity and long-term toxicity demonstrated ES-SSL-OXA/PTX exhibited a reduced toxicity profile. Based on the above results, ES-SSL-OXA/PTX could be a promising novel formulation for the treatment of ovarian cancer in future clinic.
卵巢癌是妇科恶性肿瘤中第二大致死原因。在本研究中,我们设计了一种新型的、靶向雌激素的聚乙二醇化脂质体,其负载有奥沙利铂和紫杉醇(ES-SSL-OXA/PTX),该脂质体可靶向SKOV-3细胞表面高表达的雌激素受体(ER),以提高治疗效果并降低SKOV-3肿瘤治疗的副作用。ES-SSL-OXA/PTX采用薄膜水化法制备,呈现出均匀的球形形态。通过高效液相色谱法测定包封率(EE),结果显示奥沙利铂的包封率为44.10%,紫杉醇的包封率为65.85%。平均粒径和多分散指数(PDI)分别为168.46 nm和0.145。体内和体外靶向研究证实ES-SSL-OXA/PTX具有最佳的特异性靶向能力。同时,ES-SSL-OXA/PTX的体外和体内抗肿瘤结果显示,其对SKOV-3细胞具有优异的抗增殖作用,抗肿瘤效果更强,肿瘤抑制率为85.24%。ES-SSL-OXA/PTX的药代动力学结果显示半衰期延长,清除率减慢。急性毒性和长期毒性初步安全性研究表明ES-SSL-OXA/PTX的毒性特征降低。基于上述结果,ES-SSL-OXA/PTX可能是未来临床上一种有前景的治疗卵巢癌的新型制剂。