Stable Crystalline Salts of Haloperidol: A Highly Water-Soluble Mesylate Salt


Autoria(s): Rajput, Lalit
Data(s)

2014

Resumo

Haloperidol, an antipsychotic drug, was screened for new solid crystalline phases using high throughput crystallization in pursuit of solubility improvement. Due to the highly basic nature of the API, all the solid forms with acids were obtained in the form of salts. Eleven crystalline salts in the form of oxalate (1:1), benzoate (1:1), salicylate (1:1 and 1:2), 4-hydroxybenzoate (1:1), 4-hydroxybenzoate ethyl acetate solvate (1:1:1), 3,4-dihydroxybenzoate (1:1), 3,5-dihydroxybenzoate (1:1), mesylate (1:1), besylate (1:1), and tosylate (1:1) salt were achieved. There is an insertion of carboxylate or sulfonate anion into the hydrogen bonding pattern of haloperidol. The salts with the aliphatic carboxylic acids were found to be more prone to form salt hydrates compared with aromatic carboxylate salts. All the salts were subjected to solubility measurement in water at neutral pH. There was no direct correlation observed between the solubility of the salt and its coformer. All the salts are stable at room temperature as well as after 24 h slurry experiment except the oxalate salt, which showed an unusual phase transformation from its hydrated form to the anhydrous form. A structureproperty relationship was examined to analyze the solubility behavior of the solid forms.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/50259/1/cry_gro_des_14-10_5196_2014.pdf

Rajput, Lalit (2014) Stable Crystalline Salts of Haloperidol: A Highly Water-Soluble Mesylate Salt. In: CRYSTAL GROWTH & DESIGN, 14 (10). pp. 5196-5205.

Publicador

AMER CHEMICAL SOC

Relação

http://dx.doi.org/ 10.1021/cg500982u

http://eprints.iisc.ernet.in/50259/

Palavras-Chave #Solid State & Structural Chemistry Unit
Tipo

Journal Article

PeerReviewed