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Transferrin-Modified Doxorubicin-Loaded Biodegradable Nanoparticles Exhibit Enhanced Efficacy in Treating Brain Glioma-Bearing Rats

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机构: [1]Neurosurgery Department, The Second Affiliated Hospital of Soochow University, Suzhou, China. [2]Cardiovascular Department, The Second Affiliated Hospital of Soochow University, Suzhou, China. [3]Changyi People’s Hospital, Changyi, China. [4]Department of Biological Sciences, Xi’an Jiaotong-Liverpool University, Suzhou, China. [5]South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, China. [6]Radiology Department, The Second Affiliated Hospital of Soochow University, Suzhou, China.
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关键词: chemotherapy doxorubicin glioma nanoparticle transferrin

摘要:
Doxorubicin (Dox) is widely used for the treatment of solid tumors but its clinical utility on glioma is limited. In this study, we developed a novel nano-scale drug delivery system employing biodegradable nanoparticle (NP) as carriers to load Dox. Transferrin (Tf) was conjugated to the surface of NP to specifically target the NP to glioma. Tf-NP-Dox was prepared via emulsification-solvent evaporation method, and characterized for the size, Drug loading capacity (DLC), entrapment efficiency, and Tf number on the surface. The antitumor efficiency in vitro was evaluated via CCK-8 assay. The transmembrane transportation was evaluated via HPLC assay. The antitumor efficiency in vivo was assessed in C6 glioma intracranial implant rat model. The average diameter of Tf-NP-Dox was 100nm with approximate to 32 Tf molecules on the surface. DLC was 4.4%. CCK-8 assay demonstrated much stronger cytotoxicity of Tf-NP-Dox to C6 glioma cells compared to NP-Dox or Dox. HPLC assay showed that Tf-NP-Dox transported Dox into C6 cells with high efficiency. In vivo, Tf-NP-Dox could transport Dox into tumors compare to contralateral part, with tumor inhibitory ratio and survival higher than NP-Dox or Dox. Taken together, our results suggest that Tf-NP-Dox exhibits better therapeutic effects against glioma both in vitro and in vivo, and is a potential nano-scale drug delivery system for glioma chemotherapy.

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出版当年[2012]版:
大类 | 4 区 医学
小类 | 4 区 医学:研究与实验 4 区 肿瘤学 4 区 药学 4 区 核医学
最新[2023]版:
大类 | 4 区 医学
小类 | 4 区 医学:研究与实验 4 区 肿瘤学 4 区 药学 4 区 核医学
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出版当年[2011]版:
Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Q3 PHARMACOLOGY & PHARMACY Q3 ONCOLOGY Q3 MEDICINE, RESEARCH & EXPERIMENTAL
最新[2023]版:
Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Q3 MEDICINE, RESEARCH & EXPERIMENTAL Q3 ONCOLOGY Q3 PHARMACOLOGY & PHARMACY

影响因子: 最新[2023版] 最新五年平均 出版当年[2011版] 出版当年五年平均 出版前一年[2010版] 出版后一年[2012版]

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第一作者机构: [1]Neurosurgery Department, The Second Affiliated Hospital of Soochow University, Suzhou, China.
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通讯机构: [*]Neurosurgery Department, The Second Affiliated Hospital of Soochow University, 1055 Sanxiang Road, Suzhou 215004, China
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