Warren DB - Search Results

1

Using polymeric precipitation inhibitors to improve the absorption of poorly water-soluble drugs: A mechanistic basis for utility.

Warren DB, Benameur H, Porter CJ, Pouton CW. Warren DB, et al. J Drug Target. 2010 Dec;18(10):704-31. doi: 10.3109/1061186X.2010.525652. Epub 2010 Oct 26. J Drug Target. 2010. PMID: 20973755 Review.

2

Structure and dynamics of glyceride lipid formulations, with propylene glycol and water.

Warren DB, Chalmers DK, Pouton CW. Warren DB, et al. Mol Pharm. 2009 Mar-Apr;6(2):604-14. doi: 10.1021/mp8001667. Mol Pharm. 2009. PMID: 19260675

3

Using molecular dynamics to study liquid phase behavior: simulations of the ternary sodium laurate/sodium oleate/water system.

King DT, Warren DB, Pouton CW, Chalmers DK. King DT, et al. Among authors: warren db. Langmuir. 2011 Sep 20;27(18):11381-93. doi: 10.1021/la2022903. Epub 2011 Aug 26. Langmuir. 2011. PMID: 21838286

4

In vitro digestion testing of lipid-based delivery systems: calcium ions combine with fatty acids liberated from triglyceride rich lipid solutions to form soaps and reduce the solubilization capacity of colloidal digestion products.

Devraj R, Williams HD, Warren DB, Mullertz A, Porter CJ, Pouton CW. Devraj R, et al. Among authors: warren db. Int J Pharm. 2013 Jan 30;441(1-2):323-33. doi: 10.1016/j.ijpharm.2012.11.024. Epub 2012 Nov 23. Int J Pharm. 2013. PMID: 23178598

5

Evaluation of the structural determinants of polymeric precipitation inhibitors using solvent shift methods and principle component analysis.

Warren DB, Bergström CA, Benameur H, Porter CJ, Pouton CW. Warren DB, et al. Mol Pharm. 2013 Aug 5;10(8):2823-48. doi: 10.1021/mp300576u. Epub 2013 Jul 2. Mol Pharm. 2013. PMID: 23631696

6

In vitro assessment of drug-free and fenofibrate-containing lipid formulations using dispersion and digestion testing gives detailed insights into the likely fate of formulations in the intestine.

Devraj R, Williams HD, Warren DB, Mohsin K, Porter CJ, Pouton CW. Devraj R, et al. Among authors: warren db. Eur J Pharm Sci. 2013 Jul 16;49(4):748-60. doi: 10.1016/j.ejps.2013.04.036. Epub 2013 May 16. Eur J Pharm Sci. 2013. PMID: 23684915

7

Glyceride lipid formulations: molecular dynamics modeling of phase behavior during dispersion and molecular interactions between drugs and excipients.

Warren DB, King D, Benameur H, Pouton CW, Chalmers DK. Warren DB, et al. Pharm Res. 2013 Dec;30(12):3238-53. doi: 10.1007/s11095-013-1206-1. Epub 2013 Oct 3. Pharm Res. 2013. PMID: 24092054

8

Choice of nonionic surfactant used to formulate type IIIA self-emulsifying drug delivery systems and the physicochemical properties of the drug have a pronounced influence on the degree of drug supersaturation that develops during in vitro digestion.

Devraj R, Williams HD, Warren DB, Porter CJ, Pouton CW. Devraj R, et al. Among authors: warren db. J Pharm Sci. 2014 Apr;103(4):1050-63. doi: 10.1002/jps.23856. Epub 2014 Jan 27. J Pharm Sci. 2014. PMID: 24470073

9

Digestion of phospholipids after secretion of bile into the duodenum changes the phase behavior of bile components.

Birru WA, Warren DB, Ibrahim A, Williams HD, Benameur H, Porter CJ, Chalmers DK, Pouton CW. Birru WA, et al. Among authors: warren db. Mol Pharm. 2014 Aug 4;11(8):2825-34. doi: 10.1021/mp500193g. Epub 2014 Jul 16. Mol Pharm. 2014. PMID: 24987935

10

Computational Models of the Gastrointestinal Environment. 2. Phase Behavior and Drug Solubilization Capacity of a Type I Lipid-Based Drug Formulation after Digestion.

Birru WA, Warren DB, Han S, Benameur H, Porter CJ, Pouton CW, Chalmers DK. Birru WA, et al. Among authors: warren db. Mol Pharm. 2017 Mar 6;14(3):580-592. doi: 10.1021/acs.molpharmaceut.6b00887. Epub 2017 Feb 15. Mol Pharm. 2017. PMID: 27936778

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