References
- J.L. Italia, V. Bhardwaj and M.N.V.R. Kumar, Diease, destination, dose and delivery aspects of ciclosporin: the state of the art, Drug Disco. Today, 11, 846-854 (2006) https://doi.org/10.1016/j.drudis.2006.07.015
- D. Faulds, K.L. Goa and P. Benfield, Cyclosporin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in immunoregulatory disorders, Drugs, 45, 953-1040 (1993) https://doi.org/10.2165/00003495-199345060-00007
- N.E. Taylor, A.E. Mark, P. Vallat, R.M. Brunne, B. Testa and W.F. Van Gunteren, Solvent dependent conformation and hydrogen bounding capacity of cyclosporin A: evidence from partition coefficient and molecular dynamics simulations, J. Med. Chem., 36, 3753-3764 (1993)
-
J.L. Italia, D.K. Bhatt, V. Bhardwaj, K. Tikoo and M.N.V. Ravi Kumar, PLGA nanoparticles for oral delivery of cyclosporine: Nephrotoxicity and pharmacokinetic studies in comparison to Sandimmune Neoral
$^{\circledR}$ , J. Control. Release, 119, 197-206 (2007) https://doi.org/10.1016/j.jconrel.2007.02.004 - M.H. El-Shabouri, Positively charged nanoparticles for improving the oral bioavailability of cyclosporin-A, Int. J. Pharm., 249, 101-108 (2002) https://doi.org/10.1016/S0378-5173(02)00461-1
- E. Ugazio, R. Cavalli and M.R. Gasco, Incorporation of cyclosporin A in solid lipid nanoparticles, Int. J. Pharm., 241, 341-344 (2002) https://doi.org/10.1016/S0378-5173(02)00268-5
- P.J. Carrigan and T.R. Bates, Biopharmaceutics of drugs administered in lipid-containing dosage forms I: GI absorption of griseofulvin from an oil-in-water emulsion in the rat, J. Pharm. Sci., 62, 1476-1479 (1973) https://doi.org/10.1002/jps.2600620918
-
J.F. Pinto and R.H. Muller, Pellets as carriers of solid lipid nanoparticles (
$SLN^{TM}$ ) for oral administration of drugs, Pharmazie, 54, 506-509 (1999) - K. Manjunath, V. Venkateswarlu, Pharmacokinetics, tissue distribution and bioavailability of nitrendipine solid lipid nanoparticles after intravenous and intraduodenal administration, J. Drug Target., 14, 632-645 (2006) https://doi.org/10.1080/10611860600888850
- M. Radtke and R.H. Müller, NLC-nanostructured lipid carriers: the new generation of lipid drug carriers, New Drugs, 2, 48-52 (2001)
- R.H. Muller, M. Radtke and S.A. Wissing, Nanostructured lipid matrices for improved microencapsulation of drugs, Int. J. Pharm., 242, 121-128 (2002) https://doi.org/10.1016/S0378-5173(02)00180-1
- L. Hu, X. Tang and F. Cui, Solid lipid nanoparticles (SLNs) to improve oral bioavailability of poorly soluble drugs, J. Pharm. Pharmacol., 56, 1527-1535 (2004) https://doi.org/10.1211/0022357044959
- Q.Y. Xiang, M.T. Wang, F. Chen, T. Gong, Y.L. Jian, Z.R. Zhang and Y. Huang, Lung-targeting delivery of dexamethasone acetate loaded solid lipid nanoparticles, Arch. Pharm.Res., 30, 519-525 (2007) https://doi.org/10.1007/BF02980228
- Y. Li, K.J. Zhu, J.X. Zhang, H.L. Jiang, J.H. Liu, Y.L. Hao, H. Yasuda, A. Ichimaru and K. Yamamoto, In vitro and in vivo studies of cyclosporin A-loaded microspheres based on copolymers of lactide and epsilon-caprolactone: comparison with conventional PLGA microspheres, Int. J. Pharm., 295, 67-76 (2005) https://doi.org/10.1016/j.ijpharm.2005.01.025
- C. Washington, Stability of lipid emulsions for drug delivery, Adv. Drug Deliv. Rev., 20, 131-145 (1996) https://doi.org/10.1016/0169-409X(95)00116-O
- K. Jores, W. Mehnert, M. Drechsler, H. Bunjes, C. Johann and K. Mader, Investigations on the structure of solid lipid nanoparticles (SLN) and oil-loaded solid lipid nanoparticles by photon correlation spectroscopy, field-flow fractionation and transmission electron microscopy, J. Control. Release, 95, 217-227 (2004) https://doi.org/10.1016/j.jconrel.2003.11.012
- J.X. Wang, X. Sun and Z.R. Zhang, Enhanced brain targeting by synthesis of 3',5'-dioctanoyl-5-fluoro-2'-deoxyuridine and incorporation into solid lipid nanoparticles, Eur. J. Pharm. Biopharm., 54, 285-290 (2002) https://doi.org/10.1016/S0939-6411(02)00083-8
- Cyclosporin emulsions, US Patent 5660858 (1997)