Dissolution and pharmacokinetic properties of two paliperidone cocrystals with 4-hydroxybenzoic and 4-aminobenzoic acid

T Zhang, Y Yang, X Zhao, J Jia, H Su, H He, J Gu… - …, 2014 - pubs.rsc.org
The pharmaceutical cocrystal approach can be used to modify the properties of
paliperidone. We report here two novel cocrystals, paliperidone 4-hydroxybenzoic acid …

Improving the solubility of dexlansoprazole by cocrystallization with isonicotinamide

J Li, L Wang, YQ Ye, X Fu, Q Ren, H Zhang… - European Journal of …, 2016 - Elsevier
Cocrystallization of an active pharmaceutical ingredient (API) with a cocrystal former (co-
former) is widely used to tailor the physicochemical properties of parent APIs. For proton …

Comparison of nanomilling and coprecipitation on the enhancement of in vitro dissolution rate of poorly water-soluble model drug aripiprazole

AA Abdelbary, X Li, M El-Nabarawi… - Pharmaceutical …, 2014 - Taylor & Francis
The aim of this study was to evaluate the effect of coprecipitation and nanomilling on the
crystallinity of a model drug, aripiprazole and evaluate the in vitro dissolution rate (IDR) …

Using dissolution and pharmacokinetics studies of crystal form to optimize the original iloperidone

T Zhang, Y Yang, H Wang, F Sun, X Zhao… - Crystal growth & …, 2013 - ACS Publications
The crystal engineering strategy was used to facilitate the supramolecular synthesis of a
new crystalline phase of iloperidone, an atypical psychotropic drug with known problems …

Synthesis and structural characterization of two novel olanzapine cocrystals with decreased or enhanced dissolution rate

F Liang, X Tan, S Hao, W Liu, C Duan, G Zhang… - Journal of Molecular …, 2022 - Elsevier
Olanzapine (OLZ) is a second-generation atypical anti-schizophrenia drug, and it had been
developed into various formulations, including immediate release and long-acting …

Salts of amoxapine with improved solubility for enhanced pharmaceutical applicability

M Joshi, A Roy Choudhury - ACS omega, 2018 - ACS Publications
The objective of pharmaceutical cocrystallization is to create crystalline analogues that have
vastly different properties, such as solubility, melting point, stability, and bioavailability from …

Hydration Mechanism and Its Effect on the Solubility of Aripiprazole

Z Zheng, X Huang, N Wang, T Wang, L Zhou… - Pharmaceutical …, 2024 - Springer
Propose The propose is to investigate the reasons for the insolubility of Form III in water and
to explore the mechanism of the hydration process of Form III. Methods The conformational …

Computational and Experimental Screening Approaches to Aripiprazole Salt Crystallization

HS Shah, C Michelle, T Xie, K Chaturvedi… - Pharmaceutical …, 2023 - Springer
Introduction The screening of multicomponent crystal system (MCC) is a key method for
improving physicochemical properties of active pharmaceutical ingredients (APIs). The …

Salt engineering of aripiprazole with polycarboxylic acids to improve physicochemical properties

H Afrooz, EM Mohamed, SF Barakh Ali, S Dharani… - AAPS …, 2021 - Springer
Aripiprazole (APZ) has poor physicochemical properties and bitter taste. The current study
aimed to prepare salts of APZ with polycarboxylic acids (citric, malic, and tartaric acids) to …

Structural diversity of brexpiprazole and related analogues: impact on solubility and drug delivery

TA Zeidan, PA Tilak, JT Trotta, E Curran… - Crystal Growth & …, 2018 - ACS Publications
Brexpiprazole (BPZ) is an atypical antipsychotic drug indicated for the treatment of
schizophrenia and depression. Crystal form screening of BPZ resulted in the formation of …