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dissolution rate
Description:
The amount of a solid substance that dissolves per unit time under specified physical and chemical conditions.
Primary topic:
Drug Solubulity and Delivery Systems (49%)
Related topics:
Drug Solubulity and Delivery Systems (49%),
Crystallization and Solubility Studies (7%)
OpenAlex ID:
keywords/dissolution-rate
Kinetic modeling on drug release from controlled drug delivery systems.
2010
·
Suvakanta Dash
, Padala Narasimha Murthy
, et al.
·
PubMed
·
2,734
The Rate of Solution of Solid Substances in Their Own Solutions.
1897
·
Arthur A. Noyes
, Willis R. Whitney
·
Journal of the American Chemical Society
·
1,886
Cyclodextrins as pharmaceutical solubilizers
2007
·
Marcus E. Brewster
, Thorsteinn Loftsson
·
Advanced Drug Delivery Reviews
·
1,883
Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates
2007
·
N. Blagden
, M. de Matas
, et al.
·
Advanced Drug Delivery Reviews
·
1,451
Salt formation to improve drug solubility
2007
·
Abu T.M. Serajuddin
·
Advanced Drug Delivery Reviews
·
1,431
Nanosuspensions as particulate drug formulations in therapy
2001
·
R.H Müller
, C Jacobs
, et al.
·
Advanced Drug Delivery Reviews
·
1,373
Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: Basic approaches and practical applications
2011
·
Yohei Kawabata
, Koichi Wada
, et al.
·
International Journal of Pharmaceutics
·
1,182
Nanosizing — Oral formulation development and biopharmaceutical evaluation
2007
·
Filippos Kesisoglou
, Santipharp Panmai
, et al.
·
Advanced Drug Delivery Reviews
·
1,056
Pharmaceutical applications of cyclodextrins: basic science and product development
2010
·
Thorsteinn Loftsson
, Marcus E Brewster
·
Journal of Pharmacy and Pharmacology
·
1,031
PDF
Pharmaceutical particle technologies: An approach to improve drug solubility, dissolution and bioavailability
2014
·
Prakash Khadka
, Jieun Ro
, et al.
·
Asian Journal of Pharmaceutical Sciences
·
999
PDF
Flow in porous media — pore-network models and multiphase flow
2001
·
Martin J. Blunt
·
Current Opinion in Colloid & Interface Science
·
974
The mechanisms of drug release from solid dispersions in water-soluble polymers
2002
·
Duncan Q.M Craig
·
International Journal of Pharmaceutics
·
936
Evaluation of Various Dissolution Media for Predicting In Vivo Performance of Class I and II Drugs
1998
·
E. Galia
, E. Nicolaides
, et al.
·
Pharmaceutical Research
·
927
The anodic dissolution of magnesium in chloride and sulphate solutions
1997
·
G. Song
, A. Atrens
, et al.
·
Corrosion Science
·
891
Advances in understanding cement hydration mechanisms
2019
·
Karen Scrivener
, Alexandre Ouzia
, et al.
·
Cement and Concrete Research
·
831
Solubility and dissolution of iron oxides
1991
·
U. Schwertmann
·
Plant and Soil
·
812
State of the art of nanocrystals – Special features, production, nanotoxicology aspects and intracellular delivery
2011
·
Rainer H. Müller
, Sven Gohla
, et al.
·
European Journal of Pharmaceutics and Biopharmaceutics
·
705
Crystal Engineering of Novel Cocrystals of a Triazole Drug with 1,4-Dicarboxylic Acids
2003
·
Julius F. Remenar
, Sherry L. Morissette
, et al.
·
Journal of the American Chemical Society
·
684
Crystalline solids
2001
·
Sudha R. Vippagunta
, Harry G. Brittain
, et al.
·
Advanced Drug Delivery Reviews
·
680
Solubility and Solubilization in Aqueous Media
1999
·
Samuel H. Yalkowsky
·
669
Crystal Engineering Approach To Forming Cocrystals of Amine Hydrochlorides with Organic Acids. Molecular Complexes of Fluoxetine Hydrochloride with Benzoic, Succinic, and Fumaric Acids
2004
·
Scott L. Childs
, Leonard J. Chyall
, et al.
·
Journal of the American Chemical Society
·
636
Pharmaceutical cocrystals and poorly soluble drugs
2012
·
Ranjit Thakuria
, Amit Delori
, et al.
·
International Journal of Pharmaceutics
·
615
Drug polymorphism and dosage form design: a practical perspective
2003
·
D Singhal
·
Advanced Drug Delivery Reviews
·
597
Crystal structures of drugs: advances in determination, prediction and engineering
2004
·
Sharmistha Datta
, David J. W. Grant
·
Nature Reviews Drug Discovery
·
584
The use of amorphous solid dispersions: A formulation strategy to overcome poor solubility and dissolution rate
2011
·
Guy Van den Mooter
·
Drug Discovery Today Technologies
·
580
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Works count:
17,100
Citation count:
294,100
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