au.\*:("DAVIES, Nigel M")
Results 1 to 14 of 14
Selection :
Encapsulation of lipopeptides within liposomes : Effect of number of lipid chains, chain length and method of liposome preparationLIANG, Ming T; DAVIES, Nigel M; TOTH, Istvan et al.International journal of pharmaceutics. 2005, Vol 301, Num 1-2, pp 247-254, issn 0378-5173, 8 p.Article
A novel method for preparing immune stimulating complexes (ISCOMs) by hydration of freeze-dried lipid matrixMINGTAO LIANG; TOTH, Istvan; DAVIES, Nigel M et al.European journal of pharmaceutics and biopharmaceutics. 2008, Vol 68, Num 3, pp 840-845, issn 0939-6411, 6 p.Article
Factors influencing the entrapment of hydrophilic compounds in nanocapsules prepared by interfacial polymerisation of water-in-oil microemulsionsPITAKSUTEEPONG, Tasana; DAVIES, Nigel M; TUCKER, Ian G et al.European journal of pharmaceutics and biopharmaceutics. 2002, Vol 53, Num 3, pp 335-342, issn 0939-6411Article
Analysis of Quil A-phospholipid mixtures using drift spectroscopyDEMANA, Patrick H; DAVIES, Nigel M; HOOK, Sarah et al.International journal of pharmaceutics. 2007, Vol 342, Num 1-2, pp 49-61, issn 0378-5173, 13 p.Article
In-vitro release and oral bioactivity of insulin in diabetic rats using nanocapsules dispersed in biocompatible microemulsionWATNASIRICHAIKUL, Suchat; RADES, Thomas; TUCKER, Ian G et al.Journal of pharmacy and pharmacology. 2002, Vol 54, Num 4, pp 473-480, issn 0022-3573Article
Synthesis of cationic derivatives of Quil A and the preparation of cationic immune-stimulating complexes (ISCOMs)PHAM, Hoang L; ROSS, Benjamin P; MCGEARY, Ross P et al.International journal of pharmaceutics (Print). 2009, Vol 376, Num 1-2, pp 123-133, issn 0378-5173, 11 p.Article
A method for the incorporation of ovalbumin into immune stimulating complexes prepared by the hydration methodKÖNNINGS, Stephanie; COPLAND, Melissa J; DAVIES, Nigel M et al.International journal of pharmaceutics. 2002, Vol 241, Num 2, pp 385-389, issn 0378-5173Article
Incorporation of ovalbumin into ISCOMs and related colloidal particles prepared by the lipid film hydration methodDEMANA, Patrick H; DAVIES, Nigel M; BERGER, Bianca et al.International journal of pharmaceutics. 2004, Vol 278, Num 2, pp 263-274, issn 0378-5173, 12 p.Article
Quil A-lipid powder formulations releasing ISCOMs and related colloidal stuctures upon hydrationDEMANA, Patrick H; DAVIES, Nigel M; HOOK, Sarah et al.Journal of controlled release. 2005, Vol 103, Num 1, pp 45-59, issn 0168-3659, 15 p.Article
Pseudo-ternary phase diagrams of aqueous mixtures of Quil A, cholesterol and phospholipid prepared by the lipid-film hydration methodDEMANA, Patrick H; DAVIES, Nigel M; VOSGERAU, Uwe et al.International journal of pharmaceutics. 2004, Vol 270, Num 1-2, pp 229-239, issn 0378-5173, 11 p.Article
Development of a Novel Method for Formulating Stable siRNA-Loaded Lipid Particles for In vivo UseWU, Sherry Y; PUTRAL, Lisa N; MINGTAO LIANG et al.Pharmaceutical research. 2009, Vol 26, Num 3, pp 512-522, issn 0724-8741, 11 p.Article
Liposomal delivery of antigen to human dendritic cellsCOPLAND, Melissa J; BAIRD, Margaret A; RADES, Thomas et al.Vaccine. 2003, Vol 21, Num 9-10, pp 883-890, issn 0264-410X, 8 p.Conference Paper
Preparation of poly (alkylcyanoacrylate) nanoparticles by polymerization of water-free microemulsionsKRAUEL, Karen; GRAF, Anja; HOOK, Sarah M et al.Journal of microencapsulation. 2006, Vol 23, Num 5, pp 499-512, issn 0265-2048, 14 p.Article
Characterizing colloidal structures of pseudoternary phase diagrams formed by oil/water/amphiphile systemsALANY, Raid G; TUCKER, Lan G; DAVIES, Nigel M et al.Drug development and industrial pharmacy. 2001, Vol 27, Num 1, pp 31-38, issn 0363-9045Article