Pharmaceutical hydrates analysis—overview of methods and recent advances

E Jurczak, AH Mazurek, Ł Szeleszczuk, DM Pisklak… - Pharmaceutics, 2020 - mdpi.com
This review discusses a set of instrumental and computational methods that are used to
characterize hydrated forms of APIs (active pharmaceutical ingredients). The focus has been …

An examination of water vapor sorption by multicomponent crystalline and amorphous solids and its effects on their solid-state properties

A Newman, G Zografi - Journal of pharmaceutical sciences, 2019 - Elsevier
This commentary critically evaluated the unique effects of water vapor sorption by
multicomponent solid forms of active pharmaceutical ingredients (APIs), and its effects on …

Mechanosynthesis of Stable Salt Hydrates of Allopurinol with Enhanced Dissolution, Diffusion, and Pharmacokinetics

RB Varsa S, N Pandey, A Ghosh, A Srivastava… - ACS …, 2023 - ACS Publications
Allopurinol (ALO) is a medication that treats gout and kidney stones by lowering uric acid
synthesis in the blood. The biopharmaceutics classification system (BCS) IV drug exhibits …

Toward an understanding of the propensity for crystalline hydrate formation by molecular compounds. Part 2

R Sanii, E Patyk-Kazmierczak, C Hua… - Crystal Growth & …, 2021 - ACS Publications
The propensity of molecular organic compounds to form stoichiometric or nonstoichiometric
crystalline hydrates remains a challenging aspect of crystal engineering and is of practical …

First crystal structures of pharmaceutical ibrutinib: systematic solvate screening and characterization

V Zvonicek, E Skorepova, M Dusek… - Crystal Growth & …, 2017 - ACS Publications
A search for new solid forms of an active pharmaceutical ingredient (API) is an integral part
of the drug product development process. The studied compound, Ibrutinib, is a recently …

Crystal engineering for enhanced solubility and bioavailability of poorly soluble drugs

J Varshosaz, E Ghassami… - Current pharmaceutical …, 2018 - ingentaconnect.com
Background: Crystal engineering is dealing with the creation of new structures and new
properties in drug molecules through inter-molecular interactions. Researchers of …

A data-driven and topological mapping approach for the a priori prediction of stable molecular crystalline hydrates

RS Hong, A Mattei, AY Sheikh… - Proceedings of the …, 2022 - National Acad Sciences
Predictions of the structures of stoichiometric, fractional, or nonstoichiometric hydrates of
organic molecular crystals are immensely challenging due to the extensive search space of …

Composing novel diclofenac potassium and l-proline salt cocrystal as a strategy to increase solubility and dissolution

I Nugrahani, SW Komara, A Horikawa… - Journal of Pharmaceutical …, 2020 - Elsevier
This research dealt with the multicomponent crystal developed from diclofenac potassium
and l-proline to improve the pharmaceutical performance of this anti-inflammatory drug …

Biowaiver monograph for immediate-release solid oral dosage forms: sitagliptin phosphate monohydrate

NA Charoo, DB Abdallah, AA Bakheit… - Journal of …, 2022 - Elsevier
Sitagliptin is an antihyperglycemic drug used in adults for the treatment of diabetes Type 2.
Literature data and in-house experiments were applied in this monograph to assess whether …

Explaining dissolution properties of rivaroxaban cocrystals

E Hriňová, E Skořepová, I Čerňa, J Královičová… - International Journal of …, 2022 - Elsevier
The aim of this study was to improve rivaroxaban water-solubility by cocrystal preparation
and to understand this process. The screening with water-soluble coformers was performed …