참고문헌
- S.H. Yallkowsky, Techniques of Solubilization of Drugs, Marcel Dekker, Inc., pp. 15-157 (1981).
- D.Q.M. Craig, The mechanism of drug release from solid dispersion in water-soluble polymers, Int. J. Pharm., 231, 131-144 (2002). https://doi.org/10.1016/S0378-5173(01)00891-2
- Adamo Fini and Antonio M. Rabasco, Diclofenac salts, Solids dispersion in PEG 6000 and Gelucire 50/13, Eur. J. Pharm. Biopharm., 60, 99-111 (2005). https://doi.org/10.1016/j.ejpb.2004.11.005
- Mahmoud Badry and M. Fatthy, Improvement of solubility and dissolution rate of indomethacin by solid dispersions in gelucire 50/13 and PEG4000, J. Saudi. Pharmaceutical Society., 16, 117-125 (2009). https://doi.org/10.1016/j.jsps.2009.08.006
- N. Yuksel and Tamer Baykara, Enhanced bioavailability of piroxicam using Gelucire 44/14 and Labrasol : in vitro and in vivo evaluation, Eur. J. Pharm. Biopharm., 56, 453-459 (2003) https://doi.org/10.1016/S0939-6411(03)00142-5
- S.A. Barker and D.Q and M. Craig, An investigation into the structure and bioavailability of a-tocopherol dispersion in Gelucire 44/14, Js. Control. Release, 91, 477-488 (2003). https://doi.org/10.1016/S0168-3659(03)00261-X
- W.L. Chiou, W.L. and S. Riegelman, Pharmaceutical applications of solid dispersion systems, J. Pharm. Sci., 60, 1281-1302 (1971). https://doi.org/10.1002/jps.2600600902
- A. Forster, J. and I. Hempenstall, Selection of excipients for melt extrusion with two poorly water-soluble drugs by solubility parameter calculation and thermal analysis, Int. J. Pharm., 226, 147-161 (2001). https://doi.org/10.1016/S0378-5173(01)00801-8
- J. Patterson, A. Bary and T. Rades, physical stability and solubility of the thermotropic mesophase of fenoprofen calcium as pure drug and in a tablet formulation, Int. J. Pharm., 247, 147-157 (2002). https://doi.org/10.1016/S0378-5173(02)00402-7
- G. Pavel and H. Amnon, Uptake of lipophilic drugs by plasma derived isolated dhylomicrons: Linear correlation with intestinal lymphatic bioavailability, Euro. J. Pharm. Sci., 26, 394-404 (2005). https://doi.org/10.1016/j.ejps.2005.07.011
- R. Peter, E.D. Jo-Anne, J.B. Michael and F.H. David, In vitro hydrolysis of polyunsaturated fatty acid N-acyloxymethyl deravetives of theophylline, Int. J. Pharm., 165, 87-96 (1998). https://doi.org/10.1016/S0378-5173(98)00007-6
- E.A. Schmitt, K. Peck, Y. Sun and J-M. Geoffroy, Rapid, practical and predictive excipient compatibility screening using isothermal microcalorimetry, Thermochimica Acta., 380, 175-184 (2001). https://doi.org/10.1016/S0040-6031(01)00668-2
- "Lacidipine tablets", British Pharmacoepia, 2713-2715 (2009).
- M. Mosharraf and C. Nystrom, The effect of particle size and shape on the surface specific dissolution rate of micronized practically insoluble drugs, Int. J. Pharm., 122, 35-47 (1995). https://doi.org/10.1016/0378-5173(95)00033-F
- T. Mizoe, S. Beppu, T. Ozeki and H. Okada, One-step preparation of drug-containing microparticles to enhance the dissolution and absoption of poorly water-soluble drugs using a 4-fluid nozzle spray drier, J. Control. Release., 120,205-210 (2007). https://doi.org/10.1016/j.jconrel.2007.05.002