LOFTSSON BREWSTER 1996

Dec 24, 11
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  • Apr 21, 2003 . 20. Loftsson T, Brewster ME. Pharmaceutical applications of cyclodextrins. 1.
  • 1995, as Loftsson and Brewster, 1996.), stability (Krenn et al., 1992; Zerrouk et al.
  • physicochemical properties of drugs or issues of drug toxicity is well known (
  • resultant dehydration enthalpy is relatively less (Loftsson and Brewster, 1996;
  • Dec 5, 2003. and their complexes was registered in 1953 (Loftsson and Brewster, 1996).
  • Loftsson, T., and Brewster, M. E. (1996), Pharmaceutical applications of
  • cyclodextrin“, Journal of Controlled Release, 40, 251-260 (1996). 81. M.E.
  • Patent #: 5324718. Issued on: 06/28/1994. Inventor: Loftsson .
  • It has been found that CDs can be used to enhance the solubility and
  • commonly used as a pharmaceutical excipient, which forms an inclusion complex
  • complexes employing cyclodextrins (Loftsson & Brewster 1996; Stella & Rajewski
  • Thorsteinn Loftsson Corresponding Author Contact Information . are in dynamic
  • 8) Loftsson T., Brewster M. E., Pharm. Technol. Eur., 5, 26?34 (1997). 9) Loftsson
  • Jun 12, 2000 . How to Cite. Loftsson, T. and Brewster, M. E. (1996), Pharmaceutical applications
  • 72.7 and 99000 by forming complexes with cyclodextrin derivatives (Loftsson and
  • 2004; Reddy et al., 2004; Loftsson and Brewster, 1996). β- cyclodextrins,
  • Loftsson, T. and Brewster, M.E. (1996) Pharmaceutical applications of
  • Loftsson, T., Brewster, M.E. (1996). Pharmaceutical applications of cyclodextrins:
  • 68–76. 6. T Loftsson and M E Brewster, “Pharmaceutical applications of
  • Marcus E. Brewster Tel: +32 14 603157 . .. Loftsson T, Brewster M.
  • . 1994; Loftsson, 1995; Albers and Muller, 1995; Loftsson and Brewster, 1996;
  • resulting in increased aqueous solubility and chemical stability (Loftsson and
  • ability to increase the apparent solubility of hydrophobic drugs via the formation
  • Feb 17, 2004 . Loftsson T, Brewster ME. 1996. Pharmaceutical applications of cyclodextrins. 1.
  • Már Másson a, Thorsteinn Loftsson a , *, Sigrídur Jónsdóttir b, Hafrún
  • Chem., 39 (1996) 4775. 134. L. Prokai . K. Raghavan, T. Loftsson, ME Brewster
  • . and possible parenteral toxicity), the amount of cyclodextrins that can be used
  • energy) (Frömming and Szejtli 1994; Loftsson and Brewster 1996). Random
  • ME Brewster, Loftsson T (2007) Cyclodextrins as pharmaceutical solubilizers.
  • . Loftsson et al., 1990, Loftsson et al., 1994, Loftsson et al., 1996, Moyano et al.,
  • Thorsteinn Loftsson * and Hafrún Fri&z.eth;riksdóttir . and Wouessidjewe, 1996
  • Stabilization. THORSTEINN LOFTSSON*X AND MARCUS E. BREWSTER. † . X
  • (May, 1997). Loftsson and Brewster, J. Pharm. Sci., 85(10), 1017-1025 (1996). (
  • Uekama et al., 1994; Loftsson, 1995; Albers and Muller, 1995;. Loftsson and
  • 2: T. LOFTSSON, M.E. BREWSTER; J. Pharm. Sci., 85, pp. 1017-1025, 1996. 3:
  • sion complex formation (Loftsson and Brewster 1996; Stella and Rajewski 1997;
  • 85(10), 1017-1025 (1996); T. Loftsson and M. E. Brewster, “Cyclodextrins as
  • . to drug solubilization and stabilization (Loftsson and Brewster, 1996, J. Pharm.
  • 1988; Loftsson and Brewster, 1996; Loftsson,. 1999). Side effects of the drug and
  • Addison Wesley Longman Limited (1996). Shenkin, P.S. and McDonald, D. Q. J.
  • In: Davies JED (editor). Topics in Inclusion Science Vol 5 - Cyclodextrin
  • . diameter of the hydrophobic cavity is approximately 4.7–5.3, 6.0–6.5, and 7.5–
  • The second branch of decision tree involves the use of cyclodextrin com-
  • Cyclodextrins are able to form water-soluble inclusion complexes with many
  • References. 1 T. Loftsson and M. E. Brewster, J. Pharm. Sci., 85 (1996) 1017. 2 T.
  • Mar 2, 2004 . Loftsson and Brewster, ;, 9(5), 26-34 (1997). (May, 1997). Loftsson and Brewster,
  • β-cyclodextrin (HPβCD) (Peeters et al., 2002; Davis and Brewster, 2004; . .
  • 2011: Messner, M; Kurkov, SV; Flavià-Piera, R; Brewster, ME; Loftsson, T . ..
  • agents for lipophilic substances in aqueous pre- parations (Ducheˆne and

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