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2000 | 05 | 4 |

Tytuł artykułu

Effect of liposome composition and cholesterol on the cellular uptake of stavudine by human monocyte-macrophages

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The objective of this study was to determine the cellular uptake of stavudine (an approved drug for AIDS treatment) by human monocyte/macrophages (U 937). The effect of lipid used, cholesterol concentration and the presence of charge on the liposome bilayer, on the cellular uptake by monocyte/macrophages was investigated. Liposomes employed in the study were prepared by reverse phase evaporation. The lipids egg PC, DMPC, DPPC, DSPC, DMPG and sphingomyelin were employed in this study. The effect of cholesterol on cellular uptake was studied by using liposomes containing a constant amount of lipid and varying amounts of cholesterol. Stearylamine or dicetylphosphate (10 mol%) was used to induce positive or negative charge on the bilayer. The cells were separated from liposomes by centrifugation in membrane filters and the amount of stavudine taken up by macrophages was estimated using tritium labeled drug as a marker. Stavudine uptake was found to be the maximum (approximately 950 ng/million cells) in liposomes containing dipalmitoyl phosphatidylcholine (DPPC). The presence of sphingomyelin, which increases bilayer rigidity decreased cellular uptake of stavudine and the presence of negative charge on the bilayer, enhanced the uptake of stavudine compared to positive charge. There is no apparent difference in uptake when varying amounts of cholesterol was added to liposomal formulations. The present study shows that the sensitivity of macrophages to different charge and lipid type can be used to either decrease or increase cellular uptake as desired.

Wydawca

-

Rocznik

Tom

05

Numer

4

Opis fizyczny

p.483-493,fig.,ref.

Twórcy

  • Auburn University, Auburn, AL 36849
autor
autor

Bibliografia

  • 1. Lasic, D. D. Liposomes. Am. Scientist 80 (1992) 20-31.
  • 2. Allen, T. M. Stealth Liposomes: Five years on. J. Liposome Res. 2 (1992) 289-305.
  • 3. Levy, J. A., Shimabukuro, J., McHugh, T., Casavant, C., Stites, D., and Oshiro, L. AIDS-associated retroviruses (ARV) can productively infect other cells besides human T helper cells. Virology 147 (1985) 441-448.
  • 4. Skowron, G. Biologic effects and safety of stavudine: Overview of phase I and II clinical trials. J. Infect. Dis. 171 (1995) S113-117.
  • 5. Mayer, L., Tai, L., and Bally, M. Characterization of liposomal systems containing doxorubicin. Biochim. Biophys. Acta 1025 (1990) 143-148.
  • 6. Kanter, P. M., Bullard, G. A., Pilkiewicz, F. G., Mayer, L. D., Cullis, P. R., and Pavelic, J. P. Preclinical toxicology study of liposome encapsulated doxorubicin: comparison with doxorubicin and empty liposomes in mice and dogs. In-vivo 7 (1993) 85-95.
  • 7. Lopez-Berestein, G., McQueen, T., and Mehta, K. Protective effect of liposomal amphotericin B against C. albicans infection. Cancer Drug Del. 2 (1985) 183-189.
  • 8. Szoka, F. C., Milhollan, D., and Barza, M. Effect of lipid composition and liposome size on toxicity and in vitro fungicidal activity of liposome intercalated Amphotericin B. Antimicro. Agents and Chemother. 31 (1987) 421-429.
  • 9. Allen, T. M., Austin, G. A., Chonn, A., Lin, L., and Lee, K. C. Uptake of liposomes by cultured bone marrow macrophages: influence of liposome composition and size. Biochim. Biophys. Acta 1061 (1991) 56-64.
  • 10. Szoka, F. C., and Papahadjopoulos, D. Procedure for preparation of liposomes with large internal aqueous space and high capture by reverse phase evaporation. Proc. Natl. Acad. Sci. USA 75 (1978) 494-498.
  • 11. Hsu, M. J and Juliano, R. L. Interactions of liposomes with the reticuloendothelial system. II: Nonspecific and receptor-mediated uptake of liposomes by mouse peritoneal macrophages. Biochim. Biophys. Acta 720 (1982) 411-419.
  • 12. Pagano., R. E., and Weinstein, J. N. Interactions of liposomes with mammalian cells. Ann. Rev. Biophys. Bioeng. 7 (1978) 435-468.
  • 13. Schroit, A. J., Madsen, J., and Nayar, R. Liposome-cell interactions: in vitro discrimination of uptake mechanism and in vivo targeting strategies to mononuclear phagocytes. Chem. Phys. Lipids 40 (1986) 373-393.
  • 14. Allen, T. M., and Chonn, A. Large unilamellar liposomes with low uptake into the reticuloendothelial system. FEBS Lett. 223, (1987) 42-46.
  • 15. Foong, W. C., and Green, K. L. Association of liposome-entrapped [3H]methotrexate with thioglycollate-elicited macrophages in vitro. J. Pharm. Pharmacol. 40 (1988) 171-175.
  • 16. Katragadda, A. K., Singh, M., and Betageri, G. V. Encapsulation, stability, and in vitro release characteristics of liposomal formulations of stavudine. Drug Delivery 6 (1999) 31-37.
  • 17. Raz., A, Bucana, C., Folger, W. E., Poste, G., and Fidler, I. J. Biochemical, morphological, and ultrastructural studies on the uptake of liposomes by murine macrophages. Cancer Res. 41 (1981) 487-494.
  • 18. Magee, W. E., Goff, C. W., Schoknecht, J., Smith, M. D., and Cherian, K. The interaction of cationic liposomes containing entrapped horseradish peroxidase with cells in culture. J. Cell. Biol. 63 (1974) 492-504.
  • 19. Roozemond, R. C., and Urli, D. C. Peculiar behaviour of rabbit thymocytes in interaction with liposomes of different compositions shown by fluorescence polarization studies, lipid analysis, and uptake of vesicle- entrapped carboxyfluorescein. Biochim. Biophys. Acta 689 (1982) 499-512.

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Bibliografia

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