阿霉素
胰腺癌
药物输送
细胞毒性
药理学
胶体金
癌细胞
蒽环类
癌症研究
酪氨酸激酶抑制剂
化学
靶向给药
癌症
药品
医学
化疗
纳米技术
体外
材料科学
纳米颗粒
内科学
生物化学
乳腺癌
作者
Sílvia Castro Coelho,Daniel Pires Reis,Maria do Carmo Pereira,Manuel A. N. Coelho
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2019-10-24
卷期号:11 (11): 551-551
被引量:25
标识
DOI:10.3390/pharmaceutics11110551
摘要
The aim of this study was to develop drug delivery nanosystems based on pegylated gold nanoparticles (PEGAuNPs) for a combination against pancreatic cancer cells. Doxorubicin and varlitinib, an anthracycline and a tyrosine kinase inhibitor respectively, were conjugated with gold nanoparticles. The systems were characterized, after synthesis, regarding their size, stability and morphology. An efficient conjugation of doxorubicin and varlitinib with PEGAuNPs was revealed. The cytotoxicity effect induced by the combination of the nanoconjugates was investigated in pancreatic cancer cell lines. Doxorubicin and varlitinib conjugated with PEGAuNPs revealed a combined effect to decrease the cell survival of the cancer line S2-013s, while reducing the drugs' toxicity for the healthy pancreatic cells hTERT-HPNE. This study highlights the promising potential of PEGAuNPs for targeted delivery of therapeutic drugs into human cells, enhancing the antitumor growth-inhibition effect on cancer cells, and decreasing the toxicity against normal cells. In cancer therapy, the present approach based on PEGAuNP functionalization can be further explored to increase drug targeting efficiency and to reduce side effects.
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