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A natural protein based platform for the delivery of Temozolomide acid to glioma cells

Research output: Contribution to journalArticlepeer-review

Dina O. Helal, Nadia Rouatbi, Shunping Han, Julie Tzu-Wen Wang, Adam A. Walters, Mona M.A. Abdel-Mottaleb, Amany O. Kamel, Ahmed Shawky Geneidi, Gehanne A.S. Awad, Khuloud T. Al-Jamal

Original languageEnglish
Pages (from-to)297-308
Number of pages12
Early online date19 Oct 2021
E-pub ahead of print19 Oct 2021
PublishedDec 2021

Bibliographical note

Funding Information: D.H. is a recipient of Newton Musharafa Fellowship. Authors would like to acknowledge Professor Steven Pollard, University of Edinburgh for providing BL6 cell lines. Publisher Copyright: © 2021

King's Authors


Glioblastoma is one of the most difficult to treat cancers with poor prognosis and survival of around one year from diagnosis. Effective treatments are desperately needed. This work aims to prepare temozolomide acid (TMZA) loaded albumin nanoparticles, for the first time, to target glioblastoma (GL261) and brain cancer stem cells (BL6). TMZA was loaded into human serum albumin nanoparticles (HSA NPs) using the desolvation method. A response surface 3-level factorial design was used to study the effect of different formulation parameters on the drug loading and particle size of NPs. The optimum conditions were found to be: 4 mg TMZA with 0.05% sodium cholate. This yielded NPs with particle size and drug loading of 111.7 nm and 5.5% respectively. The selected formula was found to have good shelf life and serum stability but with a relatively fast drug release pattern. The optimized NPs showed excellent cellular uptake with ∼ 50 and 100% of cells were positive for NP uptake after 24 h incubation with both GL261 and BL6 glioblastoma cell lines, respectively. The selected formula showed high cytotoxicity with ̴ 20% cell viability at 1 mM TMZA after 72 h incubation time. Finally, the fluorescently labelled NPs showed co-localization with the bioluminescent syngeneic BL6 intra-cranial tumour mouse model after intravenous administration.

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