山东大学教师主页李银萍 Paper Publications Home

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李银萍

Lab Master

Name (Simplified Chinese):李银萍

Name (Pinyin):liyinping

Date of Employment:2019-07-15

School/Department:国家糖工程技术研究中心

Education Level:With Certificate of Graduation for Study as Master's Candidates

Business Address:山东大学青岛校区淦昌苑F座237室

Gender:Female

Degree:硕士

Status:Employed

Alma Mater:山东大学

College:National Glycoengineering Research Center

Current position: Home >> Scientific Research >> Paper Publications

[1] 崔錾. In Silico-Guided Discovery of Polysaccharide Derivatives as Adjuvants in Nanoparticle Vaccines for Cancer Immunotherapy. ACS nano, 2025.
[2] 安苒. Chitosan/rutin multifunctional hydrogel with tunable adhesion, anti-inflammatory and antibacterial properties for skin wound healing. Carbohydrate Polymers, 2024.
[3] 徐莉. Enzymatic rhamnosylation of anticancer drugs by an alpha-l-rhamnosidase from Alternaria sp. L1 for cancer-targeting and enzyme-activated prodrug therapy. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY Journal, 103, 7997, 2019.
[4] 张甜甜. Glucose oxidase and polydopamine functionalized iron oxide nanoparticles: combination of the photothermal effect and reactive oxygen species generation for dual- modality selective cancer therapy. Journal of Materials Chemistry B, 7, 2190, 2019.
[5] 彭鹏. Photothermally triggered cytosolic drug delivery of glucose functionalized polydopamine nanoparticles in response to tumor microenvironment for the GLUT1-targeting chemo-phototherapy. Journal of Controlled Release, 2019.
[6] 李银萍 , 苑世领 , 彭鹏 , 徐莉 and 肖敏. Photothermally triggered cytosolic drug delivery of glucose functionalized polydopamine nanoparticles in response to tumor microenvironment for the GLUT1-targeting chemo-phototherapy. Journal of Controlled Release, 2020.
[7] 李银萍 , 靳岚 , 曲径遥 , 徐莉 , 肖敏 and 徐莉. Enzymatic rhamnosylation of anticancer drugs by an α-L-rhamnosidase from Alternaria sp. L1 for cancer-targeting and enzyme-activated prodrug therapy. Applied Microbiology and Biotechnology, 2019.
[8] 李银萍 , 靳岚 , 曲径遥 , 肖敏 and 徐莉. Enzymatic rhamnosylation of anticancer drugs by an α-L-rhamnosidase from Alternaria sp. L1 for cancer-targeting and enzyme-activated prodrug therapy. Applied microbiology and biotechnology, 2019.

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