AI Article Synopsis

  • Glioblastoma multiforme has a poor prognosis and is difficult to treat due to its resistance to chemotherapy.
  • In a study using C6 glioma-bearing rats, a new biodegradable drug delivery system with poly[(d,l)-lactide-co-glycolide] (BIC/PLGA) was tested, showing significantly higher drug concentrations in the brain compared to blood.
  • Results indicated that rats treated with BIC/PLGA nanofibers experienced slower tumor growth, longer survival times, and reduced malignancy of gliomas, making it a promising approach for cancer treatment.

Article Abstract

Glioblastoma multiforme has a poor prognosis and is highly chemoresistant. In this study, we implanted biodegradable 1,3-bis[2-chloroethyl]-1-nitroso-urea-, irinotecan-, and cisplatin-eluting poly[(d,l)-lactide-co-glycolide] (BIC/PLGA) and virgin nanofibrous membranes on the brain surface of C6 glioma-bearing rats in concurrent and virgin groups, respectively. The concentrations of all applied drugs were significantly higher in the brain than in the blood for more than 8 weeks in all studied rats. Tumor growth was more rapid in the vehicle-treated group, and tumor volumes were significantly higher in the vehicle-treated group. Moreover, the average survival time was significantly shorter in the vehicle-treated group (P = 0.026), and the BIC/PLGA nanofibrous membranes significantly reduced the risk of mortality (P < 0.001). Furthermore, the results suggested that the BIC/PLGA nanofibers reduced the malignancy of C6 glioma. The experimental findings indicate that the multianticancer drug (i.e., BIC)-eluting PLGA nanofibers are favorable candidates for treating malignant glioma.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965810PMC
http://dx.doi.org/10.1038/srep30630DOI Listing

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