| Literature DB >> 29162424 |
Pilar de la Puente1, Nicole Fettig2, Micah J Luderer1, Abbey Jin3, Shruti Shah1, Barbara Muz1, Vaishali Kapoor1, Sreekrishna M Goddu1, Noha Nabil Salama4, Christina Tsien5, Dinesh Thotala5, Kooresh Shoghi6, Buck Rogers5, Abdel Kareem Azab7.
Abstract
Overall survival of patients with newly diagnosed glioblastoma (GBM) remains dismal at 16 months with state-of-the-art treatment that includes surgical resection, radiation, and chemotherapy. GBM tumors are highly heterogeneous, and mechanisms for overcoming tumor resistance have not yet fully been elucidated. An injectable chitosan hydrogel capable of releasing chemotherapy (temozolomide [TMZ]) while retaining radioactive isotopes agents (iodine, [131I]) was used as a vehicle for localized radiation and chemotherapy, within the surgical cavity. Release from hydrogels loaded with TMZ or 131I was characterized in vitro and in vivo and their efficacy on tumor progression and survival on GBM tumors was also measured. The in vitro release of 131I was negligible over 42 days, whereas the TMZ was completely released over the first 48 h. 131I was completely retained in the tumor bed with negligible distribution in other tissues and that when delivered locally, the chemotherapy accumulated in the tumor at 10-fold higher concentrations than when delivered systemically. We found that the tumors were significantly decreased, and survival was improved in both treatment groups compared to the control group. Novel injectable chemo-radio-hydrogel implants may potentially improve the local control and overall outcome of aggressive, poor prognosis brain tumors.Entities:
Keywords: glioblastoma; hydrogels; injectable; localized chemotherapy; localized radiotherapy
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Year: 2017 PMID: 29162424 PMCID: PMC6093750 DOI: 10.1016/j.xphs.2017.10.042
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534