Drug Nanoparticles: Formulating Poorly Water-Soluble Compounds
By E. Merisko-Liversidge, G. Liversidge. Toxicologic pathology (Print), 2008
594 citations recorded by the source corpus.
Subfields: Biomaterials, Pharmaceutical Science
View Paper: https://www.semanticscholar.org/paper/806099c363d19939690a2d319f87799df78f66ad
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biomaterials
- W. Charman
- Colin W. Pouton
- Christopher J. H. Porter
- S. Charman
- H. Williams
- R. Shanker
- Natalie L. Trevaskis
In Pharmaceutical Science
- Christopher J. H. Porter
- W. Charman
- Natalie L. Trevaskis
- S. Charman
- H. Williams
- R. Shanker
- Colin W. Pouton
- D. McClements
Citations in the corpus
- Strategies to Address Low Drug Solubility in Discovery and Development (2013, background): “…incorporate readily into tablet and capsule formulations and to use the same technology to generate simple oral suspension formulations for preclinical pharmacokinetic, efficacy, and toxicity studies (Merisko-Liversidge et al., 1996; Langguth et al., 2005; Merisko-Liversidge and Liversidge, 2008).”
- Mesoporous silica nanoparticles in medicine--recent advances. (2013, background): “As more than 40% of substances discovered through combinatorial screening programs have poor solubility in water [49] it comes to no surprise that MSNs have attracted a high interest as drug carriers.”
- Sol-gel based materials for biomedical applications (2016, background): “As more than 40% of substances discovered through combinatorial screening programs have poor solubility in water [523] it comes as no surprise that MSNs based materials have attracted a high interest as drug carriers.”