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Cytarabine release

Assil, K. M., and Weinreb, R. N. (1987). Multi vesicular liposomes. Sustained release of the antimetabolite cytarabine in the eye. [Pg.317]

Kim, S., and Howell, S. B. (1987b). Multivesicular liposomes containing cytarabine for slow release s.c. administration, Cancer Treatm. Rep., 71. 447-450. [Pg.325]

Glantz, M., LaFollette, S., Jaeckle, K., Shapiro,W., Swinnen, L., Rozental, J., Phuphanich, S., Rogers, L., Gutheil, J., Batchelor, T., Lyter, D., Chamberlain, M., Maria, B., Schiffer, C., Bashir, R., Thomas, D., Cowens, W., and Howell, S. B. (1999), A randomized trial of a slow-release versus a standard formulation of cytarabine for the intrathecal treatment of lymphomatous meningitis, J. Clin. Oncol. 17, 3110-3116. [Pg.530]

Blanco, M.D. Trigo, R.M. Garcia, O. Teij6n, J.M. Controlled release of cytarabine from poly(2-hydroxyethyl methacrylate-co-A-vmyl-2-pyrrolidone) hydrogels. J. Biomater. Sci. Polym. Ed. 1997, 8, 709-719. [Pg.2037]

DepoCyt (Pacira Pharmaceuticals, San Diego, CA) is a slow release liposome-encapsulated cytarabine formulation, recently approved for intrathecal administration in the treatment of neoplastic meningitis and lymphomatous meningitis (30-32). The Depo-Foam platform used in DepoCyt , is essentially a spherical 20-pm multi-lamellar matrix comprised of phospholipids/ lipid mixture, similar to normal human cell membranes (phospholipids, triglycerides and cholesterol) (33). [Pg.5]

Glantz MJ et al (1999) A randomized controlled trial comparing intrathecal sustained-release cytarabine (DepoCyt) to intrathecal methotrexate in patients with neoplastic meningitis from solid tumors. Clin Cancer Res 5 3394-3402... [Pg.21]

Jaeckle KA et al (2002) An open label trial of sustained-release cytarabine (DepoCyt) for the intrathecal treatment of solid tumor neoplastic meningitis. J Neurooncol 57 231-239... [Pg.21]

The use of pharmaceuticals in form of emulsions is of special interest. Thus, for example, o/w emulsions stabilised by surfactants, such as mono- and diglycerides, are successfully used as pseuo-doxime-proxetil protection from intestinal lumen hydrolysis through oral administration [128]. Multiple w/o/w emulsions stabilised by Tween 20/Span 20 or Tween 80/Span 80 mixtures contributed to a prolonged retention of cytarabine in one of the phases, and its gradual release ensured a prolonged action of the drug [129]. [Pg.556]

Cytarabine loaded W/OAV multiple emulsions were prepared using nonionic surfactants (Tween and Span ) by the emulsification-sonication technique and characterized by studying the osmotic behavior. The system exhibited prolonged release pattern (Kim et al., 1995). [Pg.238]


See other pages where Cytarabine release is mentioned: [Pg.243]    [Pg.305]    [Pg.1194]    [Pg.226]    [Pg.1344]    [Pg.244]    [Pg.491]    [Pg.2033]    [Pg.1035]    [Pg.244]    [Pg.173]    [Pg.873]    [Pg.877]    [Pg.226]    [Pg.733]    [Pg.237]   
See also in sourсe #XX -- [ Pg.2033 ]




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