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Original

Molecular Encapsulation of Thalidomide with Sulfobutyl Ether-7 β-Cyclodextrin for Immediate Release Property: Enhanced In Vivo Antitumor and Antiangiogenesis Efficacy in Mice

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Pages 149-156 | Published online: 11 Aug 2009

REFERENCES

  • Bauer K. S., Dixon S. C., Figg W. D. Inhibition of angiogenesis by thalidomide requires metabolic activation, which is species-dependent. Biochemical Pharmacology 1998; 55: 1827–1834
  • Chen T. L., Vogelsang G. B., Petty B. G., Brundrett R. B., Noe D. A., Santos G. W., Colvin O. M. Plasma pharmacokinetics and urinary excretion of thalidomide after oral dosing in healthy male volunteers. Drug Metabolism and Disposition 1989; 17: 402–405
  • Corrigan O I., Stanley T. Mechanism of drug dissolution enhancement from β-cyclodextrin-drug systems. Journal of Pharmacy and Pharmacology 1982; 34: 621–626
  • Dredge K., Horsfall R., Robinson S. P., Zhang L-H, Ling L., Yang T., Shirley M. A., Muller G., Schafer P., Stirling D., Dalgleish A. G., Bartlett J. B. Orally administered lenalidomide (CC-5013) is anti-angiogenic in vivo and inhibits endothelial cell migration and Akt phosphorylation in vitro. Microvascular Research 2005; 69: 56–63
  • Goosen C., Laing T. J., Plessis J., Du Goosen T. C., Lu G.W., Flynn G. L. Percutaneous delivery of thalidomide and its N-alkyl analogs. Pharmaceutical Research 2002; 19: 434–439
  • Grosse P. Y., Francoise B., Pinguet F. Methyl-b-cyclodextrin in HL-60 parental and multidrug-resistant cancer cell lines: Effect on the cytotoxic activity and intracellular accumulation of doxorubicin. Cancer Chemotherapy and Pharmacology 1997; 40: 489–494
  • Gutman M., Szold A., Ravid A., Lazauskas T., Merimsky O., Klausner J. M. Failure of thalidomide to inhibit tumor growth and angiogenesis in vivo. Anticancer Research 1996; 16: 3673–3677
  • Higuchi T., Connors K. A. Phase solubility analysis. Advances in. Analytica Chemistry and Instrumentation 1965; 4: 117–212
  • Hirayama F., Uekama K. Cyclodextrin-based controlled drug release system. Advanced Drug Delivery Reviews 1999; 36: 125–141
  • Kale R. D., Saraf M. N., Juvekar A. S., Tayade P. T. Decreased B16F10 melanoma growth and impaired tumor vascularization using quercetin-cyclodextrin binary system. Journal of Pharmacy and Pharmacology 2006, (In Press)
  • Khan K. A. The concept of dissolution efficiency. Journal of Pharmacy and Pharmacology 1975; 27: 48–49
  • Kim K. H., Frank M. J., Henderson N. L. Application of differential scanning calorimetry to the study of solid drug dispersions. Journal of Pharmaceutical Sciences 1985; 74: 283–289
  • Koch H. P., Steinacker C. Improvement of solubility and stability of thalidomide by inclusion complexation with cyclodextrins. Archives of Pharmazie 1988; 321: 371–373
  • Krenn M., Gamcsik M. P., Vogelsang G. B., Colvin O. M., Leong K. W. Improvements in solubility and stability of thalidomide upon complexation with hydroxypropyl-beta-cyclodextrin. Journal of Pharmaceutical Sciences 1992; 81: 85–689
  • Lipinski C. A., Lombardo F., Dominy B. W. Experimental and computatorial approaches to estimate solubility and permeability in drug discovery and development settings. Advanced Drug Delivery Reviews 2001; 46: 3–26
  • Loftsson T., Brewster M. E. Pharmaceutical applications of cyclodextrins: 1. Drug solubilization and stabilization. Journal of Pharmaceutical Sciences 1996; 85: 1017–1025
  • Marriott B. J., Westby M., Cookson S., Guckian M., Goodbourne S., Muller G., Shire M. G., Stirling D., Dalgleish A. G. CC-3052: A water-soluble analog of thalidomide and potent inhibitor of activation-induced TNF-α production. The Journal of Immunology 1998; 161: 4236–4243
  • Mura P., Faucci M. T., Parrini P. L., Furlanetto S., Pizauti S. Influence of the preparation method on the physicochemical properties of ketoprofen-cyclodextrin binary systems. International Journal of Pharmaceutics, 179: 117–128
  • Omura T., Sato R. The Carbon monoxide-binding pigment of liver microsomes I. Evidence for its hemoprotein nature. Journal of Biological Chemistry 1964; 239: 2370–2378
  • Physicians Desk Reference55th. Medical Economics, Inc, New Jersey, NJ 2001; 1081–1083
  • Pollard M. Thalidomide promotes metastasis of prostate adenocarcinoma cells (PA III) in L-W rats. Cancer Letters 1996; 101: 21–24
  • Simmons B. R., Lush R. M., Figg W. D. A reversed-phase high performance liquid chromatography method using solid phase extraction to quantitate thalidomide in human serum. Analytica Chimica Acta 1997; 339: 91–97
  • Szejtli J. Introduction and general overview of cyclodextrin chemistry. Chemical Reviews 1998; 98: 1743–1754
  • Tayade P., Saraf M., Kale R. Concept, mechanisms, and therapeutics of angiogenesis in cancer and other diseases. Journal of Pharmacy and Pharmacology 2003; 55: 1045–1053
  • Toyoda K., Shoda T., Uneyama C., Takada K., Takahashi M. Carcinogenicity study of β-cyclodextrin in F344 rats. Food Chemistry and Toxicology 1997; 35: 331–336
  • Uekama K., Hirayama F., Irie T. Cyclodextrin drug carrier systems. Chemical Reviews 1998; 98: 2045–2076
  • Walawalkar P., Serai P., Iyer K. Isolation and catalytic competence of different animal liver microsomal fractions prepared calcium-aggregation method. Indian Journal of Pharmaceutical Sciences 2006; 68: 262–265

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