 Solubility
"Solubility" 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.
The ability of a substance to be dissolved, i.e. to form a solution with another substance. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
| Descriptor ID |
D012995
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| MeSH Number(s) |
G02.842.800
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Solubility".
Below are MeSH descriptors whose meaning is more specific than "Solubility".
This graph shows the total number of publications written about "Solubility" by people in this website by year, and whether "Solubility" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1980 | 0 | 2 | 2 | | 1984 | 0 | 1 | 1 | | 1986 | 0 | 5 | 5 | | 1987 | 0 | 1 | 1 | | 1989 | 0 | 5 | 5 | | 1990 | 0 | 2 | 2 | | 1991 | 0 | 1 | 1 | | 1992 | 0 | 2 | 2 | | 1993 | 0 | 3 | 3 | | 1994 | 0 | 2 | 2 | | 1995 | 0 | 3 | 3 | | 1996 | 0 | 4 | 4 | | 1997 | 0 | 4 | 4 | | 1998 | 0 | 3 | 3 | | 1999 | 0 | 5 | 5 | | 2000 | 0 | 4 | 4 | | 2001 | 0 | 3 | 3 | | 2002 | 0 | 7 | 7 | | 2003 | 0 | 10 | 10 | | 2004 | 0 | 5 | 5 | | 2005 | 0 | 4 | 4 | | 2006 | 0 | 8 | 8 | | 2007 | 0 | 7 | 7 | | 2008 | 0 | 4 | 4 | | 2009 | 0 | 8 | 8 | | 2010 | 0 | 4 | 4 | | 2011 | 0 | 4 | 4 | | 2012 | 0 | 6 | 6 | | 2013 | 0 | 5 | 5 | | 2014 | 0 | 5 | 5 | | 2015 | 0 | 6 | 6 | | 2016 | 0 | 3 | 3 | | 2017 | 1 | 9 | 10 | | 2018 | 1 | 1 | 2 | | 2019 | 0 | 7 | 7 | | 2020 | 0 | 5 | 5 |
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Below are the most recent publications written about "Solubility" by people in Profiles.
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Yamashita H, Sun CC. Material-Sparing and Expedited Development of a Tablet Formulation of Carbamazepine Glutaric Acid Cocrystal- a QbD Approach. Pharm Res. 2020 Jul 23; 37(8):153.
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Sun WJ, Sun CC. A microcrystalline cellulose based drug-composite formulation strategy for developing low dose drug tablets. Int J Pharm. 2020 Jul 30; 585:119517.
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Fu C, Demir B, Alcantara S, Kumar V, Han F, Kelly HG, Tan X, Yu Y, Xu W, Zhao J, Zhang C, Peng H, Boyer C, Woodruff TM, Kent SJ, Searles DJ, Whittaker AK. Low-Fouling Fluoropolymers for Bioconjugation and In Vivo Tracking. Angew Chem Int Ed Engl. 2020 03 16; 59(12):4729-4735.
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Liu R, Boehlein SK, Tracy WF, Resende MFR, Hudalla GA. Characterizing the Physical Properties and Cell Compatibility of Phytoglycogen Extracted from Different Sweet Corn Varieties. Molecules. 2020 Feb 01; 25(3).
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Zhao X, Li Q, Wang C, Hu S, He X, Sun CC. Simultaneous taste-masking and oral bioavailability enhancement of Ligustrazine by forming sweet salts. Int J Pharm. 2020 Mar 15; 577:119089.
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Dun J, Osei-Yeboah F, Boulas P, Lin Y, Sun CC. A systematic evaluation of poloxamers as tablet lubricants. Int J Pharm. 2020 Feb 25; 576:118994.
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Guo Y, Mishra MK, Wang C, Sun CC. 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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Chen H, Wang C, Kang H, Zhi B, Haynes CL, Aburub A, Sun CC. Microstructures and pharmaceutical properties of ferulic acid agglomerates prepared by different spherical crystallization methods. Int J Pharm. 2020 Jan 25; 574:118914.
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Yamashita H, Sun CC. 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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Zerweck J, Venkata BS, Pittman JM, Srivastava AK, Moore PC, Sachleben JR, Thinakaran G, Meredith SC. A versatile method for producing labeled or unlabeled Aß55, Aß40, and other ß-amyloid family peptides. Protein Expr Purif. 2019 10; 162:72-82.
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