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用于乳腺肿瘤治疗的脂质包覆的 Ag@MnO₂ 核壳纳米颗粒协同递送 Survivin siRNA
Authors Zhang J, Zha M, Xiao S , Filipczak N , Yalamarty SSK, Wu X, Gong C, Li X
Received 5 December 2024
Accepted for publication 12 May 2025
Published 22 May 2025 Volume 2025:20 Pages 6515—6531
DOI http://doi.org/10.2147/IJN.S510514
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Sachin Mali
Jing Zhang,1,2 Min Zha,1 Shanghua Xiao,1 Nina Filipczak,3 Satya Siva Kishan Yalamarty,4 Xiangping Wu,1 Chenkai Gong,1 Xiang Li1
1Key Laboratory of Modern Preparation of TCM, Ministry of Education, National Key Laboratory for the Modernization of Classical and Famous Prescriptions of Chinese Medicine, National Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Chinese Medicine, Nanchang, Jiangxi, 330004, People’s Republic of China; 2Jiangzhong Pharmaceutical Co. Ltd, Nanchang, Jiangxi, 330049, People’s Republic of China; 3Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, 02115, USA; 4Department of Biomedical Engineering, Tufts University, Medford, MA, 02155, USA
Correspondence: Xiang Li, Key Laboratory of Modern Preparation of TCM, Ministry of Education, National Key Laboratory for the Modernization of Classical and Famous Prescriptions of Chinese Medicine, National Pharmaceutical Engineering Center for Solid Preparation in Chinese Herbal Medicine, Jiangxi University of Chinese Medicine, Meiling Road 1688, Xinjian District, Nanchang, Jiangxi, 330004, People’s Republic of China, Tel/Fax +86 79187119661, Email xiang.li@jxutcm.edu.cn
Objective: Nanoparticles constructed with silver/manganese dioxide (Ag@MnO2) as the core, in conjunction with survivin siRNA (sis) and cyclo(RGD-DPhe-K) (Ag@MnO2-sis-c-L), were prepared for integrated tumor diagnosis and therapy.
Methods: Ag@MnO2-sis-c-L particles were prepared and characterized. The silver and manganese content were determined by inductively coupled plasma optical emission spectroscopy (ICP-OES). The stability of sis in the system was evaluated by incubation with 50% FBS before the agarose gel electrophoresis experiment. The in vitro photothermal conversion ability, cytotoxicity to 4T1 cells, and cellular uptake of preparations were evaluated. The dialysis technique was employed to determine the in vitro release profile of Ag and Mn from Ag@MnO2-sis-c-L under various pH conditions. The pharmacokinetic behavior and tissue distribution of silver in vivo were detected by ICP-OES. Animal model experiments were conducted to further evaluate the anti-tumor efficacy of Ag@MnO2-sis-c-L against breast cancer in combination with infrared irradiation.
Results: Our newly synthesized Ag@MnO2-sis-c-L nanoparticles displayed superior physicochemical properties. The combined application of these nanoparticles with photothermal therapy (PTT) exerted the strongest synergistic inhibitory effects on tumor growth. Survivin protein expression in tumor tissues were markedly suppressed following delivery of nanoparticles loaded with sis. Additionally, magnetic resonance imaging revealed the high imaging capability of hybrid nanoparticles.
Conclusion: This study supports the potential utility of Ag@MnO2-sis-c-L coupled with PTT in therapeutic and diagnostic imaging applications.
Keywords: survivin siRNA, breast cancer, photothermal therapy, Ag@MnO2, combination therapy