| Subject | Pharmacology, Toxicology and Pharmaceutical Science |
| Specific subject area | Pharmaceutical Science |
| Type of data | Table, Figure, Text |
| How data were acquired | High-pressure liquid chromatography (HPLC) |
| Data format | Raw and analyzed |
| Parameters for data collection | Data on lopinavir/ritonavir stability in suspension through two-weeks days from the preparation after storage at 4° and room temperature |
| Description of data collection | The pH 4.2-buffered suspension was prepared in a hospital pharmacy by manipulating the lopinavir/ritonavir tablet. It was characterized in terms of particle size distribution, osmolarity and 15-day chemical stability. The drug stability in suspensions was tested at different storage conditions (4 °C, RT) for two weeks. |
| Data source location | Milan, Italy |
| Data accessibility | Analyzed data with the article. Raw data and chromatograms and preparation procedure with supplementary materials. |
Official websites use .gov
A
.gov website belongs to an official
government organization in the United States.
Secure .gov websites use HTTPS
A lock (
) or https:// means you've safely
connected to the .gov website. Share sensitive
information only on official, secure websites.