Investigations on the transfer of porphyrin from o/w emulsion droplets to liposomes with two different methods

References

• Müller RH, Mäder K, Gohla S. Solid lipid nanoparticles (SLN) for controlled drug delivery – a review of the state of the art. Eur J Pharm Biopharm 2000;50:161–77
   PubMed Web of Science ®Google Scholar
• Westesen K. Novel lipid-based colloidal dispersions as potential drug administration systems – expectations and reality. Colloid Polym Sci 2000;278:608–18
   Web of Science ®Google Scholar
• Davis SS, Washington C, West P, et al. Lipid emulsions as drug delivery systems. Ann NY Acad Sci 1987;507:75–88
   PubMed Web of Science ®Google Scholar
• Boyd BJ. Characterisation of drug release from cubosomes using the pressure ultrafiltration method. Int J Pharm 2003;260:239–47
   PubMed Web of Science ®Google Scholar
• Cui F, Shi K, Zhang LQ, et al. Biodegradable nanoparticles loaded with insulin-phospholipid complex for oral delivery: preparation, in vitro characterization and in vivo evaluation. J Control Release 2006;114:242–50
   PubMed Web of Science ®Google Scholar
• Hu FQ, Yuan H, Zhang HH, Fang M. Preparation of solid lipid nanoparticles with clobetasol propionate by a novel solvent diffusion method in aqueous system and physicochemical characterization. Int J Pharm 2002;239:121–8
   PubMed Web of Science ®Google Scholar
• D’Souza SS, DeLuca PP. Development of a dialysis in vitro release method for biodegradable microspheres. AAPS PharmSciTech 2005;6:E323–8
   PubMed Web of Science ®Google Scholar
• Levy MY, Benita S. Drug release from submicronized o/w emulsion – a new invitro kinetic evaluation model. Int J Pharm 1990;66:29–37
   Web of Science ®Google Scholar
• Washington C. Drug release from microdisperse systems: a critical review. Int J Pharm 1990;58:1–12
   Web of Science ®Google Scholar
• D’Souza SS, DeLuca PP. Methods to assess in vitro drug release from injectable polymeric particulate systems. Pharm Res 2006;23:460–74
   PubMed Web of Science ®Google Scholar
• Washington C, Koosha F. Drug release from microparticulates – deconvolution of measurement errors. Int J Pharm 1990;59:79–82
   Web of Science ®Google Scholar
• Washington C, Evans K. Release rate measurements of model hydrophobicsolutes from submicron triglyceride emulsion. J Control Release 1995;33:383–90
   Web of Science ®Google Scholar
• Lanza GM, Yu X, Winter PM, et al. Targeted antiproliferative drug delivery to vascular smooth muscle cells with a magnetic resonance imaging nanoparticle contrast agent implications for rational therapy of restenosis. Circulation 2002;106:2842–7
   PubMed Web of Science ®Google Scholar
• Shabbits JA, Chiu GNC, Mayer LD. Development of an in vitro drug release assay that accurately predicts in vivo drug retention for liposome-based delivery systems. J Control Release 2002;84:161–70
   PubMed Web of Science ®Google Scholar
• Dawoud M. Transfer of a lipophilic drug model from lipid nanoparticle carriers to a lipophilic acceptor compartment. Am J PharmTech Res 2013;3:370–86
   Google Scholar
• Fahr A, van Hoogevest P, May S, et al. Transfer of lipophilic drugs between liposomal membranes and biological interfaces: consequences for drug delivery. Eur J Pharm Sci 2005;26:251–65
   PubMed Web of Science ®Google Scholar
• Petersen S, Fahr A, Bunjes H. Flow cytometry as a new approach to investigate drug transfer between lipid particles. Mol Pharmaceutics 2010;7:350–63
   PubMed Web of Science ®Google Scholar
• McLean LR, Phillips MC. Mechanism of cholesterol and phosphatidylcholine exchange or transfer between unilamellar vesicles. Biochemistry 1981;20:2893–900
   PubMed Web of Science ®Google Scholar
• Fahr A, Seelig J. Liposomal formulations of cyclosporin A: a biophysical approach to pharmacokinetics and pharmacodynamics. Crit Rev Ther Drug 2001;18:141–72
   PubMed Web of Science ®Google Scholar
• Fliszar KA, Wuelfing WP, Li Z, Reed RA. Profiling of medium chain glycerides used in pharmaceutical formulation development by reversed-phase HPLC. J Pharm Biomed Anal 2006;40:896–900
   PubMed Web of Science ®Google Scholar
• Fahr A, Liu X. Utilization of liposomes for studying drug transfer and uptake. Methods Mol Biol 2010;606:1–10
   PubMedGoogle Scholar
• Westesen K, Siekmann B. Investigation of the gel formation of phospholipid-stabilized solid lipid nanoparticles. Int J Pharm 1997;151:35–45
   Web of Science ®Google Scholar
• Drew J, Liodakis A, Chan R, et al. Preparation of lipid emulsions by pressure extrusion. Biochem Int 1990;22:983–92
   PubMedGoogle Scholar
• Ferezou J, Lai NT, Leray C, et al. Lipid-composition and structure of commercial parenteral emulsions. BBA Lipid Lipid Met 1994;1213:149–58
   PubMed Web of Science ®Google Scholar
• Rotenberg M, Rubin M, Bor A, et al. Physicochemical characterization of intralipid emulsions. Biochim Biophys Acta 1991;1086:265–72
   PubMed Web of Science ®Google Scholar
• Hellings JA, Kamp HH, Wirtz KWA, Vandeene Ll. Transfer of phosphatidylcholine between liposomes. Eur J Biochem 1974;47:601–5
   PubMedGoogle Scholar
• Vandenbesselaar A, Helmkamp GM, Wirtz KW. Kinetic model of protein-mediated phosphatidylcholine exchange between single bilayer liposomes. Biochemistry 1975;14:1852–8
   PubMed Web of Science ®Google Scholar
• de Araujo SC, de Mattos ACA, Teixeira HF, et al. Improvement of in vitro efficacy of a novel schistosomicidal drug by incorporation into nanoemulsion’s. Int J Pharm 2007;337:307–15
   PubMed Web of Science ®Google Scholar
• Wiehe A, Shaker YM, Brandt JC, et al. Lead structures for applications in photodynamic therapy. Part 1: synthesis and variation of m-THPC (Temoporfin) related amphiphilic A(2)BC-type porphyrins. Tetrahedron 2005;61:5535–64
   Web of Science ®Google Scholar
• Liu XY, Yang Q, Kamo N, Miyake J. Effect of liposome type and membrane fluidity on drug-membrane partitioning analyzed by immobilized liposome chromatography. J Chromatogr A 2001;913:123–31
   PubMed Web of Science ®Google Scholar