Cyclodextrin-mediated Enhancement of Haloperidol Solubility: Physicochemical Studies and In Vivo Investigation Using Planaria Worms

Cyclodextrins, particularly α-CD, methyl-β-CD, and hydroxypropyl-β-CD, effectively enhance the solubility of haloperidol by forming 1:1 inclusion complexes. The reduction in haloperidol-induced behavioral changes in planaria by CDs suggests a potential impact on drug bioavailability and supports the use of planaria as a simple in vivo model for screening neuroactive compounds and formulations.

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Publication Details

Journal
Pharmaceutical Research
Published
2025-08-01
DOI
https://doi.org/10.1007/s11095-025-03909-0
Primary Topic
Chemical synthesis and alkaloids
Type
article
Field-Weighted Citation Impact
0.00

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article

Cyclodextrin-mediated Enhancement of Haloperidol Solubility: Physicochemical Studies and In Vivo Investigation Using Planaria Worms

Vitaliy V. Khutoryanskiy, Yong Xiong, Kenneth Shankland
Pharmaceutical Research
Chemical synthesis and alkaloids
article

Cyclodextrin-mediated Enhancement of Haloperidol Solubility: Physicochemical Studies and In Vivo Investigation Using Planaria Worms

Vitaliy V. Khutoryanskiy, Yong Xiong, Kenneth Shankland
article en

Abstract

Cyclodextrins, particularly α-CD, methyl-β-CD, and hydroxypropyl-β-CD, effectively enhance the solubility of haloperidol by forming 1:1 inclusion complexes. The reduction in haloperidol-induced behavioral changes in planaria by CDs suggests a potential impact on drug bioavailability and supports the use of planaria as a simple in vivo model for screening neuroactive compounds and formulations.

Pharmaceutical ResearchVol. 42(8)
University of Reading (GB)
Royal Society, University of Reading
Openalex Percentile: Top 85%
Chemical synthesis and alkaloids
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