Hydrotropic Nanocarriers for Poorly Soluble Drugs
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[1] A. Lavasanifar,et al. Micelles of methoxy poly(ethylene oxide)-b-poly(epsilon-caprolactone) as vehicles for the solubilization and controlled delivery of cyclosporine A. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[2] D. Leslie-Pelecky,et al. Iron oxide nanoparticles for sustained delivery of anticancer agents. , 2005, Molecular pharmaceutics.
[3] Wim E Hennink,et al. Thermosensitive and biodegradable polymeric micelles for paclitaxel delivery. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[4] D. Taramelli,et al. Insights into the mechanism of action of ferroquine. Relationship between physicochemical properties and antiplasmodial activity. , 2005, Molecular pharmaceutics.
[5] X. Langlois,et al. Self-assembling PEG-p(CL-co-TMC) copolymers for oral delivery of poorly water-soluble drugs: a case study with risperidone. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[6] Kinam Park,et al. Hydrotropic polymer micelle system for delivery of paclitaxel. , 2005, Journal of controlled release : official journal of the Controlled Release Society.
[7] E. Tamiya,et al. Self-assembly of cholesterol-hydrotropic dendrimer conjugates into micelle-like structure: Preparation and hydrotropic solubilization of paclitaxel , 2005 .
[8] Kinam Park,et al. Hydrotropic dendrimers of generations 4 and 5: synthesis, characterization, and hydrotropic solubilization of paclitaxel. , 2004, Bioconjugate chemistry.
[9] Michael L Klein,et al. Self-assembly and properties of diblock copolymers by coarse-grain molecular dynamics , 2004, Nature materials.
[10] C. Daraio,et al. Dynamic Nanofragmentation of Carbon Nanotubes , 2004 .
[11] Kinam Park,et al. Hydrotropic Solubilization of Paclitaxel: Analysis of Chemical Structures for Hydrotropic Property , 2003, Pharmaceutical Research.
[12] J. Newton,et al. The Effect of Polyethylene Glycol 400 on Gastrointestinal Transit: Implications for the Formulation of Poorly-Water Soluble Drugs , 2001, Pharmaceutical Research.
[13] D. O. Kildsig,et al. Hydrotropic Solubilization— Mechanistic Studies , 1996, Pharmaceutical Research.
[14] Kinam Park,et al. Effects of ethylene glycol-based graft, star-shaped, and dendritic polymers on solubilization and controlled release of paclitaxel. , 2003, Journal of controlled release : official journal of the Controlled Release Society.
[15] Mark W Grinstaff,et al. Dendritic molecular capsules for hydrophobic compounds. , 2003, Journal of the American Chemical Society.
[16] Kinam Park,et al. Hydrotropic polymers: Synthesis and characterization of polymers containing picolylnicotinamide moieties , 2003 .
[17] T Andrew Taton. Two-way traffic , 2003, Nature materials.
[18] G. Kwon,et al. Polymeric micelles for delivery of poorly water-soluble compounds. , 2003, Critical reviews in therapeutic drug carrier systems.
[19] V. Torchilin,et al. Diacyllipid-Polymer Micelles as Nanocarriers for Poorly Soluble Anticancer Drugs , 2002 .
[20] R. Haag,et al. Dendritic polyglycerol: a new versatile biocompatible-material. , 2002, Journal of biotechnology.
[21] F. Szoka,et al. Polyester dendritic systems for drug delivery applications: design, synthesis, and characterization. , 2002, Bioconjugate chemistry.
[22] Francis C Szoka,et al. Polyester dendritic systems for drug delivery applications: in vitro and in vivo evaluation. , 2002, Bioconjugate chemistry.
[23] R. L. Baldwin,et al. Making a Network of Hydrophobic Clusters , 2002, Science.
[24] R. Liggins,et al. Polyether-polyester diblock copolymers for the preparation of paclitaxel loaded polymeric micelle formulations. , 2002, Advanced drug delivery reviews.
[25] John Samuel,et al. Poly(ethylene oxide)-block-poly(L-amino acid) micelles for drug delivery. , 2002, Advanced drug delivery reviews.
[26] J. Fréchet,et al. Dendrimers and Other Dendritic Polymers: Frechet/Dendrimers , 2001 .
[27] G. Kwon,et al. Micelles self-assembled from poly(ethylene oxide)-block-poly(N-hexyl stearate L-aspartamide) by a solvent evaporation method: effect on the solubilization and haemolytic activity of amphotericin B. , 2001, Journal of controlled release : official journal of the Controlled Release Society.
[28] T. Okano,et al. Development of the polymer micelle carrier system for doxorubicin. , 2001, Journal of controlled release : official journal of the Controlled Release Society.
[29] G. Richmond,et al. Water at Hydrophobic Surfaces: Weak Hydrogen Bonding and Strong Orientation Effects , 2001, Science.
[30] Jean M. J. Fréchet,et al. Dendrimers and other dendritic polymers , 2001 .
[31] K. Kono,et al. Synthesis of polyamidoamine dendrimers having poly(ethylene glycol) grafts and their ability to encapsulate anticancer drugs. , 2000, Bioconjugate chemistry.
[32] J Dressman,et al. Improving drug solubility for oral delivery using solid dispersions. , 2000, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[33] R. Haag,et al. An Approach to Glycerol Dendrimers and Pseudo-Dendritic Polyglycerols , 2000 .
[34] Mikiharu Kamachi,et al. Self-association of cholesterol-end-capped poly(sodium 2-(acrylamido)-2-methylpropanesulfonate) in aqueous solution , 2000 .
[35] Christine Allen,et al. Nano-engineering block copolymer aggregates for drug delivery , 1999 .
[36] M. Jones,et al. Polymeric micelles - a new generation of colloidal drug carriers. , 1999, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
[37] Rodrigo Corrêa da Silva,et al. Investigations on the mechanism of aqueous solubility increase caused by some hydrotropes , 1999 .
[38] Takaaki Sato,et al. Dynamical structure of oligo(ethylene glycol)s-water solutions studied by time domain reflectometry , 1998 .
[39] H. Sunada,et al. Mechanistic studies on hydrotropic solubilization of nifedipine in nicotinamide solution. , 1998, Chemical & pharmaceutical bulletin.
[40] M. Sugimoto,et al. Improvement of dissolution characteristics and bioavailability of poorly water-soluble drugs by novel cogrinding method using water-soluble polymer , 1998 .
[41] K. Akiyoshi,et al. Microscopic structure and thermoresponsiveness of a hydrogel nanoparticle by self-assembly of a hydrophobized polysaccharide , 1997 .
[42] Teruo Okano,et al. Polymeric micelles as new drug carriers , 1996 .
[43] Teruo Okano,et al. Introduction of cisplatin into polymeric micelle , 1996 .
[44] G. Buckton,et al. Dissolution behaviour of sulphonamides into sodium dodecyl sulfate micelles: a thermodynamic approach. , 1996, Journal of pharmaceutical sciences.
[45] M. Hussain,et al. Complexation of moricizine with nicotinamide and evaluation of the complexation constants by various methods. , 1993, Journal of pharmaceutical sciences.
[46] A. A. Rasool,et al. Solubility enhancement of some water-insoluble drugs in the presence of nicotinamide and related compounds. , 1991, Journal of pharmaceutical sciences.
[47] Manish Sharma,et al. Aggregation behavior of hydrotropic compounds in aqueous solution , 1989 .
[48] M. Groves,et al. The solubility of 17 β‐oestradiol in aqueous polyethylene glycol 400 , 1984 .
[49] H. Ringsdorf,et al. Watersoluble polymers in medicine , 1984 .
[50] M. Tute,et al. Rationalization of drug complexation in aqueous solution by use of Hückel frontier molecular orbitals. , 1980, Journal of pharmaceutical sciences.