"Drug Liberation" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Release of drugs from DOSAGE FORMS into solution.
Descriptor ID |
D065546
|
MeSH Number(s) |
G02.211 G03.787.321 G07.690.725.321
|
Concept/Terms |
Drug Liberation- Drug Liberation
- Liberation, Drug
- Drug Release
- Release, Drug
- Drug Dissolution
- Dissolution, Drug
|
Below are MeSH descriptors whose meaning is more general than "Drug Liberation".
Below are MeSH descriptors whose meaning is more specific than "Drug Liberation".
This graph shows the total number of publications written about "Drug Liberation" by people in this website by year, and whether "Drug Liberation" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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2015 | 0 | 1 | 1 |
2016 | 0 | 1 | 1 |
2017 | 0 | 1 | 1 |
2018 | 0 | 4 | 4 |
2019 | 2 | 2 | 4 |
2020 | 0 | 1 | 1 |
2021 | 0 | 1 | 1 |
2022 | 0 | 2 | 2 |
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Below are the most recent publications written about "Drug Liberation" by people in Profiles.
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Pharmacokinetic Evidence of Steady and Sustained Drug Release from Long-Acting Implantable Corticosteroid Matrices for Chronic Rhinosinusitis. Am J Rhinol Allergy. 2022 Nov; 36(6):733-740.
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Engineering in vitro immune-competent tissue models for testing and evaluation of therapeutics. Adv Drug Deliv Rev. 2022 03; 182:114111.
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Novel Salt-Cocrystals of Berberine Hydrochloride with Aliphatic Dicarboxylic Acids: Odd-Even Alternation in Physicochemical Properties. Mol Pharm. 2021 04 05; 18(4):1758-1767.
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The impact of solid-state form, water content and surface area of magnesium stearate on lubrication efficiency, tabletability, and dissolution. Pharm Dev Technol. 2021 Feb; 26(2):150-156.
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A systematic evaluation of poloxamers as tablet lubricants. Int J Pharm. 2020 Feb 25; 576:118994.
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Crystallographic and Energetic Insights into Reduced Dissolution and Physical Stability of a Drug-Surfactant Salt: The Case of Norfloxacin Lauryl Sulfate. Mol Pharm. 2020 02 03; 17(2):579-587.
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Expedited Tablet Formulation Development of a Highly Soluble Carbamazepine Cocrystal Enabled by Precipitation Inhibition in Diffusion Layer. Pharm Res. 2019 Apr 23; 36(6):90.
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Polymer Nanocoating of Amorphous Drugs for Improving Stability, Dissolution, Powder Flow, and Tabletability: The Case of Chitosan-Coated Indomethacin. Mol Pharm. 2019 03 04; 16(3):1305-1311.
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Improving solid-state properties of berberine chloride through forming a salt cocrystal with citric acid. Int J Pharm. 2019 Jan 10; 554:14-20.
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A novel strategy for in vivo angiogenesis and osteogenesis: magnetic micro-movement in a bone scaffold. Artif Cells Nanomed Biotechnol. 2018; 46(sup2):636-645.