TY - JOUR
T1 - Development of a pediatric oral solution of ONC201 using nicotinamide to enhance solubility and stability
AU - Annereau, Maxime
AU - Secretan, Philippe Henri
AU - Vignes, Marina
AU - Ramos, Stéphanie
AU - Grill, Jacques
AU - Bizien, Thomas
AU - Sizun, Christina
AU - Michelet, Alexandre
AU - Rieutord, André
AU - Legrand, François Xavier
AU - Do, Bernard
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/12/25
Y1 - 2024/12/25
N2 - Diffuse intrinsic pontine glioma (DIPG) poses a significant treatment challenge in pediatric patients due to its aggressive nature and difficulty in crossing the blood–brain barrier with effective therapies. ONC201 (dordaviprone) shows promises in inducing apoptosis in cancer cells but suffers from poor water solubility and stability issues. Moreover, conventional solubilizing agents acceptable in formulations intended for adult patients are not suitable for pediatric use. So, this study aims to develop a stable, concentrated oral solution of ONC201 suitable for pediatric dosing without harmful excipients and efficient taste masking. Based on Molecular Dynamics simulations, a first screening among a selection of hydrotropes was carried out and, from the results obtained, nicotinamide was selected for experimental study. Given ONC201′s challenges of poor solubility and stability, the formulation's physical and chemical properties were meticulously optimized. Extensive analyses, including differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), powder X-ray diffraction (PXRD), and nuclear magnetic resonance (NMR) spectroscopy, confirmed the solution's stability across various storage conditions, with no evidence of precipitation or significant degradation. This newly formulated solution is now used inside daily practice in the French compassionate Use Program to give access to ONC201 allowing treating patients who suffer from swallowing disorders.
AB - Diffuse intrinsic pontine glioma (DIPG) poses a significant treatment challenge in pediatric patients due to its aggressive nature and difficulty in crossing the blood–brain barrier with effective therapies. ONC201 (dordaviprone) shows promises in inducing apoptosis in cancer cells but suffers from poor water solubility and stability issues. Moreover, conventional solubilizing agents acceptable in formulations intended for adult patients are not suitable for pediatric use. So, this study aims to develop a stable, concentrated oral solution of ONC201 suitable for pediatric dosing without harmful excipients and efficient taste masking. Based on Molecular Dynamics simulations, a first screening among a selection of hydrotropes was carried out and, from the results obtained, nicotinamide was selected for experimental study. Given ONC201′s challenges of poor solubility and stability, the formulation's physical and chemical properties were meticulously optimized. Extensive analyses, including differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), powder X-ray diffraction (PXRD), and nuclear magnetic resonance (NMR) spectroscopy, confirmed the solution's stability across various storage conditions, with no evidence of precipitation or significant degradation. This newly formulated solution is now used inside daily practice in the French compassionate Use Program to give access to ONC201 allowing treating patients who suffer from swallowing disorders.
KW - Benzoic acid
KW - Citric acid
KW - Dordaviprone
KW - Drug formulation
KW - Drug solubility
KW - Hydrotropes
KW - Hydroxypropyl-β-cyclodextrin
KW - Nicotinamide
KW - ONC201
KW - Pediatric formulation
UR - http://www.scopus.com/inward/record.url?scp=85210136718&partnerID=8YFLogxK
U2 - 10.1016/j.ijpharm.2024.124965
DO - 10.1016/j.ijpharm.2024.124965
M3 - Article
AN - SCOPUS:85210136718
SN - 0378-5173
VL - 667
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
M1 - 124965
ER -