Preparation and Characterization Evaluation of Poly(L-Glutamic Acid)-g-Methoxy Poly(Ethylene Glycol)/Combretastatin A4/BLZ945 Nanoparticles for Cervical Cancer Therapy

被引:1
作者
Guo, Dongmei [1 ]
Huang, Yue [2 ]
Wang, Kun [2 ]
Yang, Chenguang [2 ]
Ma, Lili [2 ]
Zhang, Yu [2 ]
Yu, Haiyang [2 ]
Cui, Manhua [1 ,3 ]
Tang, Zhaohui [2 ]
机构
[1] Second Hosp Jilin Univ, Dept Gynecol & Obstet, Changchun 130041, Jilin, Peoples R China
[2] Chinese Acad Sci, Key Lab Polymer Ecomat, Changchun Inst Appl Chem, Changchun 130022, Peoples R China
[3] Second Hosp Jilin Univ, Dept Gynecol & Obstet, 218 Ziqiang Rd, Changchun 130041, Jilin, Peoples R China
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2023年 / 18卷
基金
中国国家自然科学基金;
关键词
combretastatin A4; BLZ945; glutamic acid; nano character; cervical cancer; DRUG-DELIVERY; TUMOR; CISPLATIN; CHEMOTHERAPY; AGENTS;
D O I
10.2147/IJN.S441131
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Purpose: Cervical cancer (CC) is a highly vascularized tumor with abundant abnormal blood vessel, which could be targeted by therapeutic strategies. Poly(L-glutamic acid)-g-methoxy poly(ethylene glycol)/combretastatin A4 (CA4)/BLZ945 nanoparticles (CB NPs) have shown great potential as nano vascular disrupting agents (VDAs) in the realm of synergistic cancer therapy.Methods: In this study, we investigated the nanocharacteristics of CB-NPs, focusing on active pharmaceutical ingredients (API), as well as lyophilized samples combining API with protective agents (PAs). The in vivo efficacy of final sample (API + PAs) was evaluated. Results: The assembled sphere of API with complex core and thin-shell structure was confirmed. PAs were found to significantly influence in vivo efficacy. Collaborative efforts between API and PAs, namely mannitol and lactose, resulted in the most promising lyophilized sample, ie, the final sample (FS2) for CC therapy. Impressively, FS2 demonstrated an exceptional 100% cure rate on the CC U14-bearing mice model.Conclusion: FS2 has provided significant insights for cervical cancer therapy. It is also crucial to develop a comprehensive evaluation strategy for the formulation of nanomedicine, which has the potential to serve as a guideline for future clinical trials.
引用
收藏
页码:6901 / 6914
页数:14
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