Laboratório de Controle de Qualidade de Medicamentos e Cosméticos, Departamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.
Instituto de Física, Universidade Federal do Mato Grosso do Sul, 79074-460 Campo Grande, MS, Brazil.
Mol Pharm. 2024 Jul 1;21(7):3661-3673. doi: 10.1021/acs.molpharmaceut.4c00393. Epub 2024 Jun 10.
Dacarbazine (DTIC) is a widely prescribed oncolytic agent to treat advanced malignant melanomas. Nevertheless, the drug is known for exhibiting low and pH-dependent solubility, in addition to being photosensitive. These features imply the formation of the inactive photodegradation product 2-azahypoxanthine (2-AZA) during pharmaceutical manufacturing and even drug administration. We have focused on developing novel DTIC salt/cocrystal forms with enhanced solubility and dissolution behaviors to overcome or minimize this undesirable biopharmaceutical profile. By cocrystallization techniques, two salts, two cocrystals, and one salt-cocrystal have been successfully prepared through reactions with aliphatic carboxylic acids. A detailed structural study of these new multicomponent crystals was conducted using X-ray diffraction (SCXRD, PXRD), spectroscopic (FT-IR and H NMR), and thermal (TG and DSC) analyses. Most DTIC crystal forms reported display substantial enhancements in solubility (up to 19-fold), with faster intrinsic dissolution rates (from 1.3 to 22-fold), contributing positively to reducing the photodegradation of DTIC in solution. These findings reinforce the potential of these new solid forms to enhance the limited DTIC biopharmaceutical profile.
达卡巴嗪(DTIC)是一种广泛用于治疗晚期恶性黑色素瘤的处方抗肿瘤药物。然而,该药物的溶解度低且依赖于 pH 值,同时具有光敏感性。这些特性意味着在药物制造过程中甚至在药物给药过程中会形成无活性的光降解产物 2-氮杂次黄嘌呤(2-AZA)。我们专注于开发具有增强的溶解度和溶解行为的新型 DTIC 盐/共晶形式,以克服或最小化这种不理想的药物生物利用度特征。通过共晶技术,使用与脂肪族羧酸的反应成功制备了两种盐、两种共晶和一种盐-共晶。通过 X 射线衍射(SCXRD、PXRD)、光谱(FT-IR 和 H NMR)和热(TG 和 DSC)分析对这些新的多组分晶体进行了详细的结构研究。所报道的大多数 DTIC 晶体形式显示出溶解度的显著提高(高达 19 倍),固有溶解速率更快(提高 1.3 到 22 倍),这有助于减少 DTIC 在溶液中的光降解。这些发现强调了这些新的固体形式有潜力改善 DTIC 的有限药物生物利用度特征。