Priya, BhanuBhanuPriyaJohnson, DelnaDelnaJohnsonDubey, GuruduttGuruduttDubeySuthar, DivitaDivitaSutharKumar, Indracanti PremIndracanti PremKumarThiruvenkatam, VijayVijayThiruvenkatamKirubakaran, SivapriyaSivapriyaKirubakaran2025-08-312025-08-312024-10-0510.1016/j.molstruc.2024.1387512-s2.0-85194549104http://repository.iitgn.ac.in/handle/IITG2025/28704Temozolomide (TMZ), the first-line anti-glioblastoma prodrug, hydrolyses at physiological pH (pH>7) in the aqueous medium. With a short elimination half-life (T1/2) of ∼1.8 h, TMZ hydrolytically metabolizes to its metabolites 5-(3-monomethyl-1-triazeno)imidazole-4-carboxamide (MTIC) and then further into 5-aminoimidazole-4-carboxamide (AIC). The objective of current work is to develop novel stable cocrystals of TMZ with safe coformers such as isonicotinic acid (INA), 4-nitrobenzoic acid (4NO<inf>2</inf>BA), 3-aminobenzoic acid (3ABA), salicylic acid (2-hydroxybenzoic acid, 2HBA) and aromatic amide 4-hydroxybenzamide (4HBz) to stabilize the drug in a cocrystal form. All the cocrystals were characterized by single crystal X-ray diffraction (SCXRD), powder XRD (PXRD), and thermogravimetry-differential scanning calorimetry (TG-DSC) analyses. Dissolution profiling in phosphate buffer saline pH 6.8 revealed that the drug release rate from TMZ–2HBA Form II cocrystals and TMZ–4NO<inf>2</inf>BA⋅H<inf>2</inf>O cocrystal hydrate were significantly higher than pure TMZ. The hydrolytic stability of all the cocrystals and hydrates in pH 6.8 buffer was longer than that of TMZ while showing three-fold hydrolytic stability in case of TMZ–4NO<inf>2</inf>BA⋅H<inf>2</inf>O and TMZ-2HBA cocrystals. Their lattice arrangements in SCXRD explain the improved hydrolytic stability in these two cases. In vitro studies on human glioblastoma cell lines showed a significant improvement in the cytotoxicity and possibly improved bioavailability of TMZ–4NO<inf>2</inf>BA⋅H<inf>2</inf>O cocrystal hydrate.falseAntitumor drug | Bioavailability | Cocrystals | Glioblastoma | Temozolomide | X-ray diffractionArticle5 October 20243138751arJournal4WOS:001249680700001