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    請使用永久網址來引用或連結此文件: https://ir.lib.ncu.edu.tw/handle/987654321/103054


    題名: Synthesis, characterization, and biological evaluation of anti-her2 indocyanine green-encapsulated peg-coated plga nanoparticles for targeted phototherapy of breast cancer cells
    作者: 李宇翔;Lee, Yu-Hsiang;Lai, Yun-Han
    貢獻者: 生醫理工學院生醫科學與工程學系
    關鍵詞: Acids;Biomedical materials;Breast;Breast cancer;Breast Neoplasms - therapy;Cancer;Cancer therapies;Care and treatment;Degradation;Drug Delivery Systems - methods;Encapsulation;Engineering and Technology;Epidermal growth factor;Equivalence;ErbB-2 protein;FDA approval;Gene expression;Glycolic acid;HER2 receptor;Humans;Hyperthermia;Illumination;Indocyanine Green - administration & dosage;Indocyanine Green - chemistry;Indocyanine Green - therapeutic use;Irradiation;Lactic Acid - administration & dosage;Lactic Acid - chemistry;Light;Light therapy;MCF-7 Cells;Medical prognosis;Medicine and Health Sciences;Metastasis;Nanoparticles;Nanoparticles - administration & dosage;Nanoparticles - chemistry;Oxygen;Oxygen - metabolism;Photosensitizing Agents - administration & dosage;Photosensitizing Agents - chemistry;Photosensitizing Agents - therapeutic use;Phototherapy;Physical Sciences;Polyethylene;Polyethylene glycol;Polyglycolic Acid - administration & dosage;Polyglycolic Acid - chemistry;Polylactic Acid-Polyglycolic Acid Copolymer;Polylactide-co-glycolide;Polymers;Polyvinyl alcohol;Receptor, ErbB-2 - antagonists & inhibitors;Research and Analysis Methods;Signal transduction;Singlet oxygen;Tumors;Viability
    日期: 2016-12-01
    上傳時間: 2026-04-23 11:22:26 (UTC+8)
    出版者: Public Library of Science;United States: Public Library of Science (PLoS)
    摘要: 摘要: Human epidermal growth factor receptor 2 (HER2)-overexpressed breast cancer is known to be more aggressive and resistant to medicinal treatment and therefore to whom an alternative therapeutics is needed. Indocyanine green (ICG) has been widely exploited in breast cancer phototherapy. However, drawbacks of accelerated degradation and short half-life (2-4 min) in blood seriously hamper its use in the clinic. To overcome these challenges, an anti-HER2 ICG-encapsulated polyethylene glycol-coated poly(lactic-co-glycolic acid) nanoparticles (HIPPNPs) were developed in this study. Through the analyses of degradation rate coefficients of ICG with and without polymeric encapsulation, the photostability of HIPPNP-entrapped ICG significantly enhanced 4 folds (P < 0.05) while its thermal stabilities at 4 and 37°C significantly enhanced 5 and 3 (P < 0.05 for each) folds, respectively, under equal lighting and/or heating treatment for 48 h. The target specificity of HIPPNPs to HER2-positive cells was demonstrated based on a 6-fold (P < 0.05) enhancement of uptake efficiency of HIPPNPs in MDA-MB-453/HER2(+) cells within 4 h as compared with that in MCF7/HER2(-) cells. Moreover, the HIPPNPs with ≤ 25 μM ICG equivalent were nontoxic to cells in the absence of light illumination, and enabled to generate similar amount of singlet oxygen and hyperthermia effect as compared with that used by free ICG upon NIR irradiation. After 808 nm-laser irradiation with intensity of 6 W/cm2 for 5 min, the viability of MDA-MB-453 cells pre-treated by HIPPNPs with ≥ 5 μM ICG equivalent for 4 h significantly reduced as compared with that treated by equal concentration of free ICG (P < 0.05) and > 90% of the cells were eradicated while the dose of HIPPNPs was increased to 25 μM ICG equivalent. In summary, the developed HIPPNPs are anticipated as a feasible tool for use in phototherapy of breast cancer cells with HER2 expression.
    其他題名: PLoS One
    出版者: United States: Public Library of Science (PLoS)
    出版日期: 2016-12-12
    出處: PLOS ONE, 2016-12, Vol.11 (12), p.e0
    資源來源: Agricultural & Environmental Science Collection
    版權: COPYRIGHT 2016 Public Library of Science
    版權: 2016 Lee, Lai. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
    版權: 2016 Lee, Lai 2016 Lee, Lai
    識別號: ISSN: 1932-6203
    識別號: EISSN: 1932-6203
    識別號: DOI: 10.1371/journal.pone.0168192
    識別號: PMID: 27942034
    顯示於類別:[生醫科學與工程學系] 期刊論文

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