Amidon GL, Lennernas H, Shah VP, Crison JR. A theoretical basis for biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res. 1995;12:413–20.
Article
CAS
PubMed
Google Scholar
Ware EC, Lu DR. An automated approach to salt selection for new unique trazodone salts. Pharm Res. 2004;21:177–84.
Article
CAS
PubMed
Google Scholar
Thompson DO. Cyclodextrins-enabling exicipients: their present and future use in pharmaceuticals. Crit Rev Ther Drug Carrier Syst. 1997;14:1–104.
CAS
PubMed
Google Scholar
Liversidge GG, Cundy KC. Particle size reduction for improvement of oral bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of nanocrystalline danazol in beagle dogs. Int J Pharm. 1995;125:91–7.
Article
CAS
Google Scholar
Fleisher D, Bong R, Stewart BH. Impoved oral drug delivery: solubility limitations overcome by the use of prodrugs. Adv Drug Deliv Rev. 1996;19:115–30.
Article
CAS
Google Scholar
Pouton CW. Lipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and ‘self-microemulsifying’ drug delivery systems. Eur J Pharm Sci. 2000;11:S93–8.
Article
CAS
PubMed
Google Scholar
Serajuddin ATM. Solid dispersions of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs. J Pharm Sci. 1999;88:1058–66.
Article
CAS
PubMed
Google Scholar
Noyes AA, Whitney WR. The rate of dissolution of solid substances in their own solution. J Am Chem Soc. 1897;19:930–4.
Article
Google Scholar
Motoyama S, Saito AS, Yasumi H, Sudo E, Takasaka Y, Tsujino T. Process for the preparation of activated pharmaceuticals, U.S. Pat. No. 4,540,602 (1985).
Liversidge GG, Cundy KC, Bishop JF. Surface modified drug nanoparticles, U.S. Pat. No.5,145,684 (1992).
Merisko-Liversidge E, Liversidge GG. Toxicol Pathol. 2008;36(1):43–8.
Article
CAS
PubMed
Google Scholar
Merisko-Liversidge E, Liversidge GG, Cooper ER. Eur J Pharm Sci. 2003;18(2):113–20.
Article
CAS
PubMed
Google Scholar
http://www.elandrugtechnologies.com/
Eerdenbrugh BV, Vand den Mooter G, Augustijns P. Int J Pharm. 2008;364:64–75.
Article
PubMed
Google Scholar
Habib MJ (Ed). Pharmaceutical solid dispersion technology, (Technomic, Lancaster, PA, (2001).
Lyons J, Ko F. Nanofibers. Encycl Nanosci Nanotech. 2004;6:727–38.
CAS
Google Scholar
Formhals A. Method and apparatus for the production of fibers, U. S. Pat. No. 2,116,942 (1938)
Reneker DH, Chun I. Nanometer diameter fibers of polymer, produced by electrospinning. Nanotechnology. 1996;7:216–23.
Article
CAS
Google Scholar
Langer R, Tirrell DA. Designing materials for biology and medicine. Nature. 2004;428:487–92.
Article
CAS
PubMed
Google Scholar
Ignatious F, Baldoni J. Electrospun pharmaceutical compositions, WO0154667 (2001).
Ignatious F, Sun L. Electrospun amorphous pharmaceutical compositions, WO 2004014304 (2004).
Verreck G, Chun I, Peeters J, Rosenblatt J, Brewster ME. Preparation and characterization of nanofibers containing amorphous drug dispersions generated by electrostatic spinning. Pharm Res. 2003;20:810–7.
Article
CAS
PubMed
Google Scholar
Verreck G, Chun I, Peeters J, Rosenblatt J, Dijck AV, Mensch J, et al. Incorporation of drugs in an amorphous state into electrospun nanofibers composed of a water-insoluble nonbiodegradable polymer. J Control Release. 2003;92:349–60.
Article
CAS
PubMed
Google Scholar
Kenawy El-R, Abdel-Hay FI, Wnek GE. Processing of nanofibers through electrospinning as drug delivery systems. Mater Chem Phys. 2009;113:296–302.
Article
CAS
Google Scholar
Battisti WP, Katz NP, Weaver AL, Matsumoto AK, Kivitz AJ, Polis AB, et al. Pain management in osteoarthritis: a focus on onset of efficacy—a comparison of refecoxib, celecoxib, acetaminophen, and nabumetone across four clinical trials. J Pain. 2004;5:511–20.
Article
CAS
PubMed
Google Scholar
Cummings P. Pharmaceutical composition comprising Nabumetone, WO0113889 (2001).
Kaur R, Grant DJW, Eaves T. J Pharm Sci. 1980;69:1317–21.
Article
CAS
PubMed
Google Scholar
Marsac PJ, Shamblin SL, Taylor LS. Pharm Res. 2006;23:2417–26.
Article
CAS
PubMed
Google Scholar
http://www.accessdata.fda.gov/scripts/cder/iig/index.cfm
Broman E, Khoo C, Taylor LS. A comparison of alternative polymer excipients and processing methods for making solid dispersions of a poorly water soluble drug. Int J Pharm. 2001;222:139–51.
Article
CAS
PubMed
Google Scholar