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Highly penetrable nanoparticles co-loading doxorubicin and IDO1 siRNA enhance tumor immunotherapy
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Meng-hao SHI, Yu WANG, Yan-yan HAN, Jiu-long ZHANG, Shi-yang WU, Da-wei CHEN*
Acta Pharmaceutica Sinica | 2022, 57(1) : 242 - 250
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Acta Pharmaceutica Sinica | 2022, 57(1): 242-250
Original Articles
Highly penetrable nanoparticles co-loading doxorubicin and IDO1 siRNA enhance tumor immunotherapy
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Meng-hao SHI, Yu WANG, Yan-yan HAN, Jiu-long ZHANG, Shi-yang WU, Da-wei CHEN*
Affiliations
  • School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China
Published: 2022-01-12 doi: 10.16438/j.0513-4870.2021-1352
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There are two serious obstacles to tumor immunotherapy. Firstly, the immune response of the tumor is seriously reduced due to immunosuppressive tumor microenvironment (ITM) and low immunogenicity of tumor. The second obstacle is the dense and complex heterogeneous structures, which seriously prevent the nanoparticles (NPs) from penetrating deeper into tumor tissue. Immunogenic cell death (ICD) induced by doxorubicin (DOX) is an effective method to enhance tumor immune activity. However, interferon-γ (IFN-γ) secreted by cytotoxic T lymphocytes (CTL) after ICD induction would increase the expression of indoleamine 2, 3-dioxygenase 1 (IDO1) and enhance ITM. IDO1 siRNA would reduce the expression of IDO1 protein, regulate the tumor immunosuppressive microenvironment and regulate ITM, so as to enhance the ICD effect of DOX. In this paper, a novel charge conversional, particle size reduction and highly penetrable NPs based on a pH sensitive copolymer poly(ethylene glycol)-poly-L-lysine-2, 3-dimethylmaleic anhydride (mPEG-PLL-DMA, PLD) and polyamidoamine (PAMAM) dendrimers to achieve deep delivery of tumor tissue. DOX and IDO1 siRNA were encapsulated to achieve efficient tumor immunotherapy. Preparation and cell level experiments showed that PLD material had significant pH sensitivity. Results of 3D tumor penetrable experiment in vitro showed that adding the pH sensitive material PLD significantly improved the permeability of the preparation. In addition, 4T1 tumor model was established for BALB/c mice and all animal experiments were displayed in according with the requirements of the Animal Experiment Ethics Committee of Shenyang Pharmaceutical University. The results of in vivo efficacy experiments and tissue experiments evaluated that IDO1 siRNA significantly improved the ICD effect owing to DOX, so as to significantly inhibit tumor growth.

doxorubicin  /  siRNA  /  immunogenic cell death  /  tumor microenvironment  /  indoleamine 2, 3-dioxygenase 1
Meng-hao SHI, Yu WANG, Yan-yan HAN, Jiu-long ZHANG, Shi-yang WU, Da-wei CHEN. Highly penetrable nanoparticles co-loading doxorubicin and IDO1 siRNA enhance tumor immunotherapy[J]. Acta Pharmaceutica Sinica, 2022 , 57 (1) : 242 -250 . DOI: 10.16438/j.0513-4870.2021-1352
Year 2022 volume 57 Issue 1
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Article Info
doi: 10.16438/j.0513-4870.2021-1352
  • Receive Date:2021-09-15
  • Online Date:2025-12-22
  • Published:2022-01-12
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  • Received:2021-09-15
  • Revised:2021-09-30
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    School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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