| Literature DB >> 31944768 |
Irfan Ullah1,2, Kunho Chung1, Sumin Bae1, Yan Li1,3, Chunggu Kim1, Boyoung Choi1,4, Hye Yeong Nam4, Sun Hwa Kim5, Chae-Ok Yun1, Kuen Yong Lee1, Priti Kumar2, Sang-Kyung Lee1.
Abstract
Glioblastoma multiforme (GBM) is an aggressive tumor with no curative treatment. The tumor recurrence after resection often requires chemotherapy or radiation to delay the infiltration of tumor remnants. Intracerebral chemotherapies are preferentially being used to prevent tumor regrowth, but treatments remain unsuccessful because of the poor drug distribution in the brain. In this study, we investigated the therapeutic efficacy of cancer-targeting arginyl-glycyl-aspartic tripeptide (RGD) conjugated paclitaxel (PTX)-loaded nanoparticles (NPs) against GBM by nose-to-brain delivery. Our results demonstrated that RGD-modified PTX-loaded NPs showed cancer-specific delivery and enhanced anticancer effects in vivo. The intranasal (IN) inoculation of RGD-PTX-loaded NPs effectively controls the tumor burden (75 ± 12% reduction) by inducing apoptosis and/or inhibiting cancer cell proliferation without affecting the G0 stage of normal brain cells. Our data provide therapeutic evidence supporting the use of intranasally delivered cancer-targeted PTX-loaded NPs for GBM therapy.Entities:
Keywords: PLGA; RGD; antitumor effect; glioblastoma; intranasal; paclitaxel
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Year: 2020 PMID: 31944768 DOI: 10.1021/acs.molpharmaceut.9b01215
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939