Development of CD133 Targeting Multi-Drug Polymer Micellar Nanoparticles for Glioblastoma - In Vitro Evaluation in Glioblastoma Stem Cells

• Published in: Pharmaceutical research 2021-06, Vol.38 (6), p.1067-1079
• Main Authors: Smiley, Shelby B., Yun, Yeonhee, Ayyagari, Pranav, Shannon, Harlan E., Pollok, Karen E., Vannier, Michael W., Das, Sudip K., Veronesi, Michael C.
• Format: Article
• Language: English
• Subjects: Antigens; Aptamers; Biochemistry; Biomedical and Life Sciences; Biomedical Engineering and Bioengineering; Biomedicine; Brain cancer; Brain tumors; CD133 antigen; Cell viability; Drug therapy; Evaluation; Glioblastoma; MDM2 protein; Medical Law; Nanoparticles; Neuroimaging; Pharmacology/Toxicology; Pharmacy; Polylactide-co-glycolide; Polymer industry; Polymers; Prognosis; Research Paper; Stem cell transplantation; Stem cells; Styrene; Temozolomide; Zirconium
• ISSN: 0724-8741; 1573-904X
• DOI: 10.1007/s11095-021-03050-8

Purpose Glioblastoma (GBM) is a malignant brain tumor with a poor long-term prognosis due to recurrence from highly resistant GBM cancer stem cells (CSCs), for which the current standard of treatment with temozolomide (TMZ) alone will unlikely produce a viable cure. In addition, CSCs regenerate rapidly and overexpress methyl transferase which overrides the DNA-alkylating mechanism of TMZ, leading to resistance. The objective of this research was to apply the concepts of nanotechnology to develop a multi-drug therapy, TMZ and idasanutlin (RG7388, a potent mouse double minute 2 (MDM2) antagonist), loaded in functionalized nanoparticles (NPs) that target the GBM CSC subpopulation, reduce the cell viability and provide possibility of in vivo preclinical imaging. Methods Polymer-micellar NPs composed of poly(styrene- b -ethylene oxide) (PS- b -PEO) and poly(lactic- co -glycolic) acid (PLGA) were developed by a double emulsion technique loading TMZ and/or RG7388. The NPs were covalently bound to a 15-nucleotide base-pair CD133 aptamer to target the CD133 antigen expressed on the surfaces of GBM CSCs. For diagnostic functionality, the NPs were labelled with radiotracer Zirconium-89 ( 89 Zr). Results NPs maintained size range less than 100 nm, a low negative charge and exhibited the ability to target and kill the CSC subpopulation when TMZ and RG7388 were used in combination. The targeting function of CD133 aptamer promoted killing in GBM CSCs providing impetus for further development of targeted nanosystems for localized therapy in future in vivo models. Conclusions This work has provided a potential clinical application for targeting GBM CSCs with simultaneous diagnostic imaging.