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Journal of Controlled Release : Official Journal of the Controlled Release Society
|
April 19, 2011
Nanostructured liquid crystalline particles provide long duration sustained-release effect for a poorly water soluble drug after oral administration
Tri-Hung Nguyen, Tracey Hanley, Christopher J H Porter, et al.
The Journal of Pharmacy and Pharmacology
|
February 9, 2002
Evaluation of the in-vitro digestion profiles of long and medium chain glycerides and the phase behaviour of their lipolytic products
Leab Sek, Christopher J H Porter, Ann Marie Kaukonen, et al.
Journal of Pharmaceutical Sciences
|
April 18, 2014
Lipid-based formulations solidified via adsorption onto the mesoporous carrier Neusilin® US2: effect of drug type and formulation composition on in vitro pharmaceutical performance
Hywel D Williams, Michiel Van Speybroeck, Patrick Augustijns, et al.
Drug Delivery and Translational Research
|
March 20, 2015
Nanostructured reverse hexagonal liquid crystals sustain plasma concentrations for a poorly water-soluble drug after oral administration
Tri-Hung Nguyen, Tracey Hanley, Christopher J H Porter, et al.
Pharmaceutical Research
|
April 28, 2011
Fatty acid binding proteins: potential chaperones of cytosolic drug transport in the enterocyte?
Natalie L Trevaskis, Gary Nguyen, Martin J Scanlon, et al.
The Journal of Pharmacy and Pharmacology
|
June 1, 2006
Examination of the impact of a range of Pluronic surfactants on the in-vitro solubilisation behaviour and oral bioavailability of lipidic formulations of atovaquone
Leab Sek, Ben J Boyd, William N Charman, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society
|
February 26, 2004
Influence of physicochemical properties on the patterns of association of a series of aliphatic esters of halofantrine with plasma lipoproteins
Michelle P McIntosh, William N Charman, Michael Campbell, et al.
Molecular Pharmaceutics
|
March 17, 2021
Digestion of Lipid-Based Formulations Not Only Mediates Changes to Absorption of Poorly Soluble Drugs Due to Differences in Solubilization But Also Reflects Changes to Thermodynamic Activity and Permeability
Yusuke Tanaka, Tri-Hung Nguyen, Estelle J A Suys, et al.
Molecular Pharmaceutics
|
January 19, 2012
Association of chemotherapeutic drugs with dendrimer nanocarriers: an assessment of the merits of covalent conjugation compared to noncovalent encapsulation
Lisa M Kaminskas, Victoria M McLeod, Christopher J H Porter, et al.
Journal of Pharmaceutical Sciences
|
February 15, 2003
Separation and characterization of the colloidal phases produced on digestion of common formulation lipids and assessment of their impact on the apparent solubility of selected poorly water-soluble drugs
Greg A Kossena, Ben J Boyd, Christopher J H Porter, et al.
Page
of 24
Search research articles
Search
Showing results (41-50 of 232) with videos related to
Sort By:
Page
of 24
Journal of Controlled Release : Official Journal of the Controlled Release Society
|
April 19, 2011
Nanostructured liquid crystalline particles provide long duration sustained-release effect for a poorly water soluble drug after oral administration
Tri-Hung Nguyen, Tracey Hanley, Christopher J H Porter, et al.
The Journal of Pharmacy and Pharmacology
|
February 9, 2002
Evaluation of the in-vitro digestion profiles of long and medium chain glycerides and the phase behaviour of their lipolytic products
Leab Sek, Christopher J H Porter, Ann Marie Kaukonen, et al.
Journal of Pharmaceutical Sciences
|
April 18, 2014
Lipid-based formulations solidified via adsorption onto the mesoporous carrier Neusilin® US2: effect of drug type and formulation composition on in vitro pharmaceutical performance
Hywel D Williams, Michiel Van Speybroeck, Patrick Augustijns, et al.
Drug Delivery and Translational Research
|
March 20, 2015
Nanostructured reverse hexagonal liquid crystals sustain plasma concentrations for a poorly water-soluble drug after oral administration
Tri-Hung Nguyen, Tracey Hanley, Christopher J H Porter, et al.
Pharmaceutical Research
|
April 28, 2011
Fatty acid binding proteins: potential chaperones of cytosolic drug transport in the enterocyte?
Natalie L Trevaskis, Gary Nguyen, Martin J Scanlon, et al.
The Journal of Pharmacy and Pharmacology
|
June 1, 2006
Examination of the impact of a range of Pluronic surfactants on the in-vitro solubilisation behaviour and oral bioavailability of lipidic formulations of atovaquone
Leab Sek, Ben J Boyd, William N Charman, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society
|
February 26, 2004
Influence of physicochemical properties on the patterns of association of a series of aliphatic esters of halofantrine with plasma lipoproteins
Michelle P McIntosh, William N Charman, Michael Campbell, et al.
Molecular Pharmaceutics
|
March 17, 2021
Digestion of Lipid-Based Formulations Not Only Mediates Changes to Absorption of Poorly Soluble Drugs Due to Differences in Solubilization But Also Reflects Changes to Thermodynamic Activity and Permeability
Yusuke Tanaka, Tri-Hung Nguyen, Estelle J A Suys, et al.
Molecular Pharmaceutics
|
January 19, 2012
Association of chemotherapeutic drugs with dendrimer nanocarriers: an assessment of the merits of covalent conjugation compared to noncovalent encapsulation
Lisa M Kaminskas, Victoria M McLeod, Christopher J H Porter, et al.
Journal of Pharmaceutical Sciences
|
February 15, 2003
Separation and characterization of the colloidal phases produced on digestion of common formulation lipids and assessment of their impact on the apparent solubility of selected poorly water-soluble drugs
Greg A Kossena, Ben J Boyd, Christopher J H Porter, et al.
Page
of 24