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Smart Nanofiber Mesh with Locally Sustained Drug Release Enabled Synergistic Combination Therapy for Glioblastoma
被引:5
|作者:
Li, Yinuo
[1
]
Matsumoto, Yoshitaka
[2
,3
]
Chen, Lili
[4
]
Sugawara, Yu
[3
]
Oe, Emiho
[4
,5
]
Fujisawa, Nanami
[4
,5
]
Ebara, Mitsuhiro
[4
]
Sakurai, Hideyuki
[2
,3
]
机构:
[1] Univ Tsukuba, Grad Sch Comprehens Human Sci, Dept Radiat Oncol, Tsukuba 3058575, Japan
[2] Univ Tsukuba, Fac Med, Dept Radiat Oncol, Clin Med, Tsukuba 3058575, Japan
[3] Univ Tsukuba Hosp, Proton Med Res Ctr, Tsukuba 3058576, Japan
[4] Natl Inst Mat Sci NIMS, Res Ctr Funct Mat, 1-1 Namiki, Tsukuba 3050044, Japan
[5] Univ Tsukuba, Grad Sch Pure & Appl Sci, Tsukuba 3050006, Japan
关键词:
glioblastoma;
combination therapy;
synergistic effect;
TMZ;
17AAG;
radiation therapy;
radiosensitization;
nanofiber;
GLIADEL WAFERS;
CELLS;
TEMOZOLOMIDE;
17-AAG;
HEAT-SHOCK-PROTEIN-90;
POLYCAPROLACTONE;
REPAIR;
HSP90;
D O I:
10.3390/nano13030414
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
This study aims to propose a new treatment model for glioblastoma (GBM). The combination of chemotherapy, molecular targeted therapy and radiotherapy has been achieved in a highly simultaneous manner through the application of a safe, non-toxic, locally sustained drug-releasing composite Nanofiber mesh (NFM). The NFM consisted of biodegradable poly(epsilon-caprolactone) with temozolomide (TMZ) and 17-allylamino-17-demethoxygeldanamycin (17AAG), which was used in radiation treatment. TMZ and 17AAG combination showed a synergistic cytotoxicity effect in the T98G cell model. TMZ and 17AAG induced a radiation-sensitization effect, respectively. The NFM containing 17AAG or TMZ, known as 17AAG-NFM and TMZ-NFM, enabled cumulative drug release of 34.1% and 39.7% within 35 days. Moreover, 17AAG+TMZ-NFM containing both drugs revealed a synergistic effect in relation to the NFM of a single agent. When combined with radiation, 17AAG+TMZ-NFM induced in an extremely powerful cytotoxic effect. These results confirmed the application of NFM can simultaneously allow multiple treatments to T98G cells. Each modality achieved a significant synergistic effect with the other, leading to a cascading amplification of the therapeutic effect. Due to the superior advantage of sustained drug release over a long period of time, NFM has the promise of clinically addressing the challenge of high recurrence of GBM post-operatively.
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页数:13
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