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Combination therapy using siRNA nanocompelex and PD-L1 inhibitor for alcoholic liver fibrosis

Combination therapy using siRNA nanocompelex and PD-L1 inhibitor for alcoholic liver fibrosis
siRNA纳米复合物与PD-L1抑制剂联合治疗酒精性肝纤维化
批准号:
10451030
负责人:
Kun Cheng
金额:
$4.67万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-15 至 2023-06-30

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英文摘要
Project Summary The purpose of this administrative supplement application is to purchase a SpectraMax iD5 Multi- Mode Microplate Reader with bottom luminescence read mode. The SpectraMax iD5 Multi-Mode Microplate Reader is a five-mode reader that measures absorbance, fluorescence, luminescence, time- resolved fluorescence (TRF), and tunable fluorescence polarization (FP) for a broad range of applications. We currently have a 15-year-old plate reader (SpectraMax Gemini XPS), which is not working properly. In addition, our plate reader is an old model, which cannot be used for protein binding assay using HTRF. We have completed all the work in Aim 1 and most of the work in Aim 2 of the parent grant. For the rest studies in Aims 2 and 3, we will heavily depend on the use of a multi-mode microplate reader to frequently conduct protein binding assay, cellular uptake study, immunoassay, cell viability assay, ELISA, BCA assay, ALT/AST assay, western blot, and cell proliferation assay. Therefore, there is an urgent need to purchase the new SpectraMax iD5 plate reader for our research. The acquisition of the Multi-Mode Microplate Reader will significantly enhance our capability to make good progress in the research. This is essential for the success of the proposed animal studies to evaluate the stability, biodistribution, and activity of the PCBP2 siRNA nanocomplex in combination with the anti-PD-L1 inhibitor in a rat model of liver fibrosis.
期刊论文(29)
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会议论文
DOI: 10.1021/acs.jmedchem.2c00539
发表时间: 2022-09-22
期刊: JOURNAL OF MEDICINAL CHEMISTRY
影响因子: 7.3
作者: [Cheng, Kun, Fetse, John, Zhao, Zhen, Liu, Hao, Mamani, Umar-Farouk, Mustafa, Bahaa, Adhikary, Pratik, Ibrahim, Mohammed, Liu, Yanli, Patel, Pratikkumar, Nakhjiri, Maryam, Alahmari, Mohammed, Li, Guangfu]
通讯作者: Li, Guangfu
DOI: 10.1021/mp500426r
发表时间: 2014-10-06
期刊: Molecular pharmaceutics
影响因子: 4.9
作者: [Shukla RS, Qin B, Cheng K]
通讯作者: Cheng K
DOI: 10.1021/acs.molpharmaceut.6b00933
发表时间: 2017-05-01
期刊: Molecular pharmaceutics
影响因子: 4.9
作者: [Jain A, Barve A, Zhao Z, Jin W, Cheng K]
通讯作者: Cheng K
DOI: 10.1021/acs.molpharmaceut.5b00177
发表时间: 2015-06-01
期刊: Molecular pharmaceutics
影响因子: 4.9
作者: [Chen Z, Jin W, Liu H, Zhao Z, Cheng K]
通讯作者: Cheng K
21
    Normalizing PDAC stroma with PCBP2 siRNA nanoparticles to improve the antitumor activity of chemotherapy and immunotherapy
    Development of a targeted delivery platform for checkpoint inhibitors
    Development of a targeted delivery platform for checkpoint inhibitors
    Development of a targeted delivery platform for checkpoint inhibitors
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