N. Davies

T. Rades, I. Tucker, N. Davies, 2002, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Synthetic lipopeptides formulated in liposomes: effect on their immune stimulatory capacity in vitro

I. Toth, S. Hook, N. Davies, 2006, 2006 International Conference on Nanoscience and Nanotechnology.

Enzymatic degradation of luteinizing hormone releasing hormone (LHRH) by mucosal homogenates from the intestine of the common brushtail possum (Trichosurus vulpecula).

I. Tucker, B. Mcleod, N. Davies, 2002, Life sciences.

Protein and peptide degradation in the intestine of the common brushtail possum (Trichosurus vulpecula)

I. Tucker, B. Mcleod, N. Davies, 2002, Journal of Comparative Physiology B.

Hydration of lipid films with an aqueous solution of Quil A: a simple method for the preparation of immune-stimulating complexes.

T. Rades, N. Davies, M. J. Copland, 2000, International journal of pharmaceutics.

Quil A-lipid powder formulations releasing ISCOMs and related colloidal structures upon hydration.

T. Rades, S. Hook, N. Davies, 2005, Journal of controlled release : official journal of the Controlled Release Society.

Incorporation of ovalbumin into ISCOMs and related colloidal particles prepared by the lipid film hydration method.

T. Rades, N. Davies, P. Demana, 2004, International journal of pharmaceutics.

Considerations in the developability of peptides for oral administration when formulated together with transient permeation enhancers.

H. Edlund, N. Davies, Staffan Berg, 2022, International journal of pharmaceutics.

Impact of Intestinal Concentration and Colloidal Structure on the Permeation-Enhancing Efficiency of Sodium Caprate in the Rat

Christel A. S. Bergström, B. Abrahamsson, F. Seeliger, 2021, Molecular pharmaceutics.

A combined approach of chemical enhancers and sonophoresis for the transdermal delivery of tizanidine hydrochloride.

S. Mutalik, N. Udupa, H. Parekh, 2009, Drug delivery.

Intestinal Absorption of FITC-Dextrans and Macromolecular Model Drugs in the Rat Intestinal Instillation Model

Christel A. S. Bergström, B. Abrahamsson, H. Bönisch, 2022, Molecular pharmaceutics.

Fusion of Interleukin‐2 to Subunit Antigens Increase their Antigenicity In Vitro Due to an Interleukin‐2 Receptor β‐Mediated Antigen Uptake Mechanism

G. Buchan, N. Davies, M. Baird, 2003, Scandinavian journal of immunology.

Evaluation of Mucoadhesive Polymers in Ocular Drug Delivery. I. Viscous Solutions

J. Hadgraft, I. Kellaway, N. Davies, 1991, Pharmaceutical Research.

The effect of complexation on characteristics and drug release from PLGA microspheres loaded by cyclosporine-cyclodextrin complex

B. Malaekeh-Nikouei, M. Jaafari, N. Davies, 2006 .

Evaluation in pig of an intestinal administration device for oral peptide delivery.

Christel A. S. Bergström, A. Larsson, Xiaoqiu Wu, 2022, Journal of controlled release : official journal of the Controlled Release Society.

Poly(acrylic acid) microspheres containing beta-cyclodextrin: loading and in vitro release of two dyes.

I. Tucker, N. Davies, D. Bibby, 1999, International journal of pharmaceutics.

Synthesis of cationic derivatives of Quil A and the preparation of cationic immune-stimulating complexes (ISCOMs).

R. McGeary, P. N. Shaw, H. Pham, 2009, International journal of pharmaceutics.

Considerations in the use of hydroxypropyl-beta-cyclodextrin in the formulation of aqueous ophthalmic solutions of hydrocortisone.

I. Tucker, N. Davies, A. R. Bary, 2000, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Evaluation of a hydrocortisone/hydroxypropyl-β-cyclodextrin solution for ocular drug delivery

Guangji Wang, I. Tucker, N. Davies, 1997 .

Cyclodextrin-Crosslinked Poly(Acrylic Acid): Adhesion and Controlled Release of Diflunisal and Fluconazole from Solid Dosage Forms

J. Stokes, M. Boehm, R. McGeary, 2013, AAPS PharmSciTech.

Effects of alcohols and diols on the phase behaviour of quaternary systems.

T. Rades, S. Agatonovic-Kustrin, I. Tucker, 2000, International journal of pharmaceutics.

Analysis of Quil A-phospholipid mixtures using drift spectroscopy.

T. Rades, S. Hook, N. Davies, 2007, International journal of pharmaceutics.

Biopharmaceutical Considerations In Topical Ocular Drug Delivery

N. Davies, N M Davies, 2000, Clinical and experimental pharmacology & physiology.

A combined approach of chemical enhancers and sonophoresis for the transdermal delivery of tizanidine hydrochloride

S. Mutalik, H. Parekh, U. Nayanabhirama, 2009 .

Evaluation of Mucoadhesive Polymers in Ocular Drug Delivery. II. Polymer-Coated Vesicles

J. Hadgraft, I. Kellaway, N. Davies, 1992, Pharmaceutical Research.

Pilocarpine bioavailability from a mucoadhesive liposomal ophthalmic drug delivery system

I. Kellaway, N. Davies, M. Thomas, 1992 .

W/O microemulsions for ocular delivery: evaluation of ocular irritation and precorneal retention.

T. Rades, I. Tucker, R. Alany, 2006, Journal of controlled release : official journal of the Controlled Release Society.

Characterizing Colloidal Structures of Pseudoternary Phase Diagrams Formed by Oil/Water/Amphiphile Systems

T. Rades, I. Tucker, R. Alany, 2001, Drug development and industrial pharmacy.

Cyclodextrin-crosslinked poly(acrylic acid): Synthesis, physicochemical characterization and controlled release of diflunisal and fluconazole from hydrogels.

R. McGeary, P. N. Shaw, B. Ross, 2013, International journal of pharmaceutics.

Formulation and stability of pilocarpine oral solution

I. Tucker, J. P. Fawcett, N. Davies, 1994 .

Current challenges and future perspectives in oral absorption research: An opinion of the UNGAP network.

Clive G. Wilson, B. Griffin, P. Artursson, 2021, Advanced drug delivery reviews.

In‐vitro release and oral bioactivity of insulin in diabetic rats using nanocapsules dispersed in biocompatible microemulsion

T. Rades, I. Tucker, N. Davies, 2002, The Journal of pharmacy and pharmacology.

Enhanced delivery of immunoliposomes to human dendritic cells by targeting the multilectin receptor DEC-205.

A. Badiee, Kylie J. McDonald, N. Davies, 2007, Vaccine.

A novel method for preparing immune stimulating complexes (ISCOMs) by hydration of freeze-dried lipid matrix.

I. Toth, N. Davies, M. Liang, 2007, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Preparation and characterization of beta-cyclodextrin and poly(acrylic acid) microspheres.

I. Tucker, I G Tucker, N. Davies, 1998, Journal of microencapsulation.

Gastrointestinal transit in the common brushtail possum measured by gamma scintigraphy.

I. Tucker, A. McDowell, N. Davies, 2005, International journal of pharmaceutics.

Saponins from Quillaja saponaria Molina: isolation, characterization and ability to form immuno stimulatory complexes (ISCOMs).

R. McGeary, P. N. Shaw, H. Pham, 2006, Current drug delivery.

Particulate systems as adjuvants and carriers for peptide and protein antigens.

I. Toth, N. Davies, J. Blanchfield, 2006, Current drug delivery.

Liposomal delivery of antigen to human dendritic cells.

P. Tyler, T. Rades, F. Reck, 2003, Vaccine.

Functionalized lipid nanoparticles for subcutaneous administration of mRNA to achieve systemic exposures of a therapeutic protein

A. Dabkowska, A. Radulescu, M. Johansson, 2021, Molecular therapy. Nucleic acids.

Lipid based particulate formulations for the delivery of antigen

Thomas Rades, T. Rades, Melissa J Copland, 2005, Immunology and cell biology.

Preparation and Characterization of PLGA Microspheres Loaded by Cyclosporine-Cyclodextrin Complex

B. Malaekeh-Nikouei, M. Jaafari, N. Davies, 2005 .

In vitro and in vivo evaluation of 3D printed capsules with pressure triggered release mechanism for oral peptide delivery.

Christel A. S. Bergström, W. Weitschies, B. Abrahamsson, 2020, Journal of pharmaceutical sciences.

Pseudo-ternary phase diagrams of aqueous mixtures of Quil A, cholesterol and phospholipid prepared by the lipid-film hydration method.

Thomas Rades, T. Rades, Nigel M Davies, 2004, International journal of pharmaceutics.

Investigations into the structure and composition of beta-cyclodextrin/poly(acrylic acid) microspheres.

I. Tucker, N. Davies, D. Bibby, 1999, International journal of pharmaceutics.

Development of a Novel Method for Formulating Stable siRNA-Loaded Lipid Particles for In vivo Use

S. Wu, N. McMillan, L. Putral, 2009, Pharmaceutical Research.

A method for the incorporation of ovalbumin into immune stimulating complexes prepared by the hydration method.

T. Rades, Melissa J Copland, N. Davies, 2002, International journal of pharmaceutics.

Encapsulation of lipopeptides within liposomes: effect of number of lipid chains, chain length and method of liposome preparation.

Istvan Toth, I. Toth, Nigel M Davies, 2005, International journal of pharmaceutics.

Preparation of immuno-stimulating complexes (ISCOMs) by ether injection.

P. N. Shaw, H. Pham, N. Davies, 2006, International journal of pharmaceutics.

A comparison of pseudo‐ternary diagrams of aqueous mixtures of Quil A, cholesterol and phospholipid prepared by lipid‐film hydration and dialysis

T. Rades, N. Davies, P. Demana, 2004, The Journal of pharmacy and pharmacology.

Effects of formulation variables on characteristics of poly (ethylcyanoacrylate) nanocapsules prepared from w/o microemulsions.

T. Rades, I. Tucker, N. Davies, 2002, International journal of pharmaceutics.

Enhancing absorption of fluorescein and LHRH across hindgut epithelia in a marsupial, the common brushtail possum Trichosurus vulpecula.

I. Tucker, N. Davies, J. Wen, 2007, Journal of pharmaceutical sciences.

Preparation of poly (alkylcyanoacrylate) nanoparticles by polymerization of water-free microemulsions

T. Rades, S. Hook, N. Davies, 2006, Journal of microencapsulation.