COMPARISON OF DRUG DELIVERY PROPERTIES OF PEG-b-PDHPC MICELLES WITH DIFFERENT COMPOSITIONS
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COMPARISON OF DRUG DELIVERY PROPERTIES OF PEG-b-PDHPC MICELLES WITH DIFFERENT COMPOSITIONS
COMPARISON OF DRUG DELIVERY PROPERTIES OF PEG-b-PDHPC MICELLES WITH DIFFERENT COMPOSITIONS
Chinese Journal of Polymer Science2012年30卷第3期 页码:387-396
Affiliations:
National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, China
Author bio:
**Zhong-wei Gu (顾忠伟), E-mail: zwgu@scu.edu.cn
Funds:
National Basic Research Program of China(2011CB606206);National Natural Science Foundation of China(50830105);International collaboration project of Ministry of Science & Technology(2010DFA51550);Program for New Century Excellent Talents in Universities, Ministry of Education(NCET-10-0564)
Chun-yan Long, Ming-ming Sheng, Bin He, 等. COMPARISON OF DRUG DELIVERY PROPERTIES OF PEG-b-PDHPC MICELLES WITH DIFFERENT COMPOSITIONS[J]. Chinese Journal of Polymer Science, 2012,30(3):387-396. DOI: 10.1007/s10118-012-1138-y.
Chun-yan Long, Ming-ming Sheng, Bin He, et al. COMPARISON OF DRUG DELIVERY PROPERTIES OF PEG-b-PDHPC MICELLES WITH DIFFERENT COMPOSITIONS[J]. Chinese Journal of Polymer Science, 2012, 30(3): 387-396. DOI: 10.1007/s10118-012-1138-y.
Chun-yan Long, Ming-ming Sheng, Bin He, 等. COMPARISON OF DRUG DELIVERY PROPERTIES OF PEG-b-PDHPC MICELLES WITH DIFFERENT COMPOSITIONS[J]. Chinese Journal of Polymer Science, 2012,30(3):387-396. DOI: 10.1007/s10118-012-1138-y.DOI:
Chun-yan Long, Ming-ming Sheng, Bin He, et al. COMPARISON OF DRUG DELIVERY PROPERTIES OF PEG-b-PDHPC MICELLES WITH DIFFERENT COMPOSITIONS[J]. Chinese Journal of Polymer Science, 2012, 30(3): 387-396. DOI: 10.1007/s10118-012-1138-y.DOI:
COMPARISON OF DRUG DELIVERY PROPERTIES OF PEG-b-PDHPC MICELLES WITH DIFFERENT COMPOSITIONS
An anti-tumor drug doxorubicin was encapsulated in micelles of poly(ethylene glycol)-
b
-poly(2
2-dihydroxylmethyl propylene carbonate) (PEG-
b
-PDHPC) diblock copolymers. The morphology of both blank micelles and drug loaded micelles was characterized by TEM. The
in vitro
drug release profiles of micelles were investigated. The cytotoxicity of the micelles was evaluated by incubating with Hela tumor cells and 3T3 fibroblasts. The drug loaded micelles were co-cultured with HepG2 cells to evaluate the
in vitro
anti-tumor efficacies. The results showed that the mean sizes of both micelles with different copolymer compositions increased after being loaded with drugs. The drug release rate of PEG
45
-
b
-PDHPC
34
micelles was faster than that of mPEG
114
-
b
-PDHPC
26
micelles. Both of the two block copolymers were non-toxic. The confocal laser scanning microscopy and flow cytometry results showed that both the drug loaded micelles could be internalized efficiently in HepG2 cells. The PEG
45
-
b
-PDHPC
34
micelles exhibited higher anti-tumor activity comparing to mPEG
114
-
b
-PDHPC
26
micelles.
关键词
Keywords
references
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Characterization of a Multi-responsive Magnetic Graphene Oxide Nanocomposite Hydrogel and Its Application for DOX Delivery
Resorcinarene-centered Amphiphilic Star-block Copolymers: Synthesis, Micellization and Controlled Drug Release
Microenvironment Responsive Polymeric Nitric Oxide Releasing Micelles for Enhancing Eradication of Methicillin-resistant Staphylococcus aureus Biofilm
pH/Glutathione (GSH) Co-triggered Degradable Polyprodrug as Drug Self-delivery System for Tumor-specific Doxorubicin Delivery: Effect of Aggregation States
Upgrading Commercially Available Polyethylene to High-value Materials with Strong Mechanical Performance and Hydrophilicity by Blending with Ethylene/meta-Methoxystyrene Copolymers
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相关机构
Department of Chemistry, Karaj Branch, Islamic Azad University, Karaj
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Henan Institute of Flexible Electronics (HIFE) and School of Flexible Electronics (SoFE), Henan University
State Key Laboratory of Molecular Engineering of Polymers, Fudan University