紫杉醇
胶质瘤
药理学
细胞毒性
血脑屏障
药物输送
肽
化疗
药代动力学
医学
材料科学
癌症研究
化学
内科学
纳米技术
生物化学
体外
中枢神经系统
作者
Meinan Yu,Dunyan Su,Yuanyuan Yang,Lin Qin,Chuan Hu,Rui Liu,Yang Zhou,Chuanyao Yang,Xiaotong Yang,Guanlin Wang,Huile Gao
标识
DOI:10.1021/acsami.8b16219
摘要
The blood-brain tumor barrier (BTB) and blood-brain barrier (BBB) have always been the major barriers in glioma therapy. In this report, we proposed D-T7 peptide-modified nanoparticles actively targeted glioma by overcoming the BBB and BTB to improve the antiglioma efficacy. Glioma-targeting experiments showed that the penetration effect of the D-T7 peptide-modified nanoparticles was 7.89-fold higher than that of unmodified nanoparticles. Furthermore, cediranib (CD) and paclitaxel (PTX) were used for the combination of the antiangiogenesis and chemotherapy for glioma. PEGylated bilirubin nanoparticles (BRNPs) were selected as a suitable drug delivery system (CD&PTX@TBRBPs) owing to the antioxidant, anti-inflammatory, and reactive oxygen species-responsive ability. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and apoptosis assays showed that CD&PTX@TBRBPs had the highest cytotoxicity and the median survival time of the CD&PTX@TBRNP group was 3.31-fold and 1.23-fold longer than that of the saline and CD&PTX@BRNP groups, respectively. All the results showed that we constructed a novel and accessible peptide-modified dual drug carrier with an enhanced antiglioma effect.
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