Improving Dissolution of Artesunate from Immediate Release Tablet by Inclusion with Beta Β-Cyclodextrin: In Vitro Characterization

This study aimed to use an inclusion complex to increase the solubility of the medication artesunate. The kneading process prepared inclusion complexes of beta cyclodextrins and artesunate. In vitro dissolution tests and saturation solubility analysis were used to assess how the creation of inclusion complexes affected the drug solubility and dissolution. The infrared spectroscopy (IR) method was used to evaluate the complexes. The equimolar quantities of β-cyclodextrin and artesunate in the inclusion complex were then directly compressed into tablets and tested for several in-process quality control parameters. According to saturation solubility experiments, the drug solubility was enhanced by the beta cyclodextrin-PVP-K30 inclusion complex at a molar ratio of 1:2:1. FT-IR demonstrated that inclusion complexes were formed. In contrast to the pure medication, the produced inclusion complex tablets dissolved more quickly. To increase the solubility and dissolution of the poorly soluble medication, Artesunate can be complexed with β-cyclodextrin and PVP-K30.

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-06-28
DOI
https://doi.org/10.5281/zenodo.15762574
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Improving Dissolution of Artesunate from Immediate Release Tablet by Inclusion with Beta Β-Cyclodextrin: In Vitro Characterization

Zenodo (CERN European Organization for Nuclear Research)
Drug Solubulity and Delivery Systems
article

Improving Dissolution of Artesunate from Immediate Release Tablet by Inclusion with Beta Β-Cyclodextrin: In Vitro Characterization

article en

Abstract

This study aimed to use an inclusion complex to increase the solubility of the medication artesunate. The kneading process prepared inclusion complexes of beta cyclodextrins and artesunate. In vitro dissolution tests and saturation solubility analysis were used to assess how the creation of inclusion complexes affected the drug solubility and dissolution. The infrared spectroscopy (IR) method was used to evaluate the complexes. The equimolar quantities of β-cyclodextrin and artesunate in the inclusion complex were then directly compressed into tablets and tested for several in-process quality control parameters. According to saturation solubility experiments, the drug solubility was enhanced by the beta cyclodextrin-PVP-K30 inclusion complex at a molar ratio of 1:2:1. FT-IR demonstrated that inclusion complexes were formed. In contrast to the pure medication, the produced inclusion complex tablets dissolved more quickly. To increase the solubility and dissolution of the poorly soluble medication, Artesunate can be complexed with β-cyclodextrin and PVP-K30.

Zenodo (CERN European Organization for Nuclear Research)
Openalex Percentile: Top 60%
Drug Solubulity and Delivery Systems
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Improving Dissolution of Artesunate from Immediate Release Tablet by Inclusion with Beta Β-Cyclodextrin: In Vitro Characterization · Zenodo (CERN European Organization for Nuclear Research) (2025) | TGRS Research Map | TGRS