Summary
Colloidal drug carriers such as liposomes and nanoparticles are easily taken up by phagocytic cells and accumulate in the organs of the reticuloendothelial system. Therefore, they hold promise as carriers for the treatment of intracellular infections with antibiotics that would normally not find easy access to intracellular sites. Consequently, inin vitro andin vivo experiments the therapeutic efficacy of substances such as amphotericin B, dihydrostreptomycin, amikacin, ampicillin, stibogluconate against a number of microorganisms includingLeishmania donovani, Candida albicans, Staphylococcus aureus, Mycobacterium avium, Listeria monocytogenes, andSalmonella typhimurium was increased significantly by binding to liposomes and nanoparticles.
Zusammenfassung
Kolloidale Arzneistoffträger wie Liposomen und Nanopartikeln werden leicht von phagozytierenden Zellen aufgenommen und reichern sich somit in den Organen des retikuloendothelialen Systems an. Aus diesem Grunde sind sie vielversprechende Träger für Antibiotika zur Therapie intrazellulärer Infektionen, die sonst kaum oder nicht in diese Zellen gelangen können. Entsprechend wurdein vitro wie auchin vivo durch Bindung von Substanzen wie Amphotericin B, Dihydrostreptomycin, Amikacin, Ampicillin und Wismutgluconat an Liposomen und Nanopartikeln eine wesentliche Verbesserung der therapeutischen Effizienz gegen eine Reihe von Mikroorganismen wieLeishmania donovani, Candida albicans, Staphylococcus aureus, Mycobacterium avium, Listeria monocytogenes, undSalmonella typhimurium erreicht.
Similar content being viewed by others
References
Kreuter, J.: Nanoparticles — preparation and applications. In:Donbrow, M. (ed.): Microencapsulation in medicine and pharmacy. CRC Press, Boca Raton (in press).
Hässander, U. K., Storm, G., Peeters, P. A. M., Crommelin, D. J. A.: Liposomes. In:Chasin, M., Langer, R. (eds.): Biodegradable polymers as drug delivery systems. M. Decker, New York (in press).
Kreuter, J. Evaluation of nanoparticles as drug-delivery systems. I. Preparation methods. Pharm. Acta Helv. 58 (1983) 196–209.
Lenaerts, V., Nagelkerke, J. F., van Berkel, T. J. C., Couvreur, P., Grislain, L., Roland, M., Speiser, P. In vivo uptake of polyisobutylcyanoacrylate nanoparticles by rat liver Kupffer, endothelial, and parenchymal cells. J. Pharm. Sci. 73 (1984) 980–983.
Kreuter, J. Evaluation of nanoparticles as drug-delivery systems. II. Comparison of the body distribution of nanoparticles with the body distribution of microspheres (diameter < 1 µm), liposomes, and emulsions. Pharm. Acta Helv. 58 (1983) 217–226.
Couvreur, P., Tulkens, P., Roland, M., Trouet, A., Speiser, P. Nanocapsules: A new type of lysosomotropic carrier. FEBS Lett. 84 (1977) 323–326.
Tröster, S. D., Müller, U., Kreuter, J. Modification of the body distribution of poly(methyl methacrylate) nanoparticles in rats by coating with surfactants. Int. J. Pharm. 61 (1990) 85–100.
Trouet, A., Tulkens, P. Intracellular penetration and distribution of antibiotics: The basis for an improved chemotherapy of intracellular infections. In:Ninet, L., Bost, P. E., Bouanchand, D. H., Florent, J. (eds.): The future of antibiotherapy and antibiotic research. Academic Press, London 1981, pp. 337–349.
Brajtburg, J., Powderly, W. G., Kobayashi, G. S., Medoff, G. Amphotericin B: Delivery systems. Antimicrob. Agents Chemother. 34 (1990) 381–384.
Johnson, J. D., Hand, W. L., Francis, J. B., King-Thompson, N., Corwin, R. W. Antibiotic uptake by alveolar macrophages. J. Lab. Clin. Med. 95 (1980) 429–439.
Barza, M. Principles of tissue penetration of antibiotics. J. Antimicrob. Chemother. 8 (Suppl. C) (1981) 7–28.
Eltahawy, A. T. The penetration of mammalian cells by antibiotics. J. Antimicrob. Chemother. 11 (1983) 293–298.
Lam, C., Mathison, G. E. Intraphagocytic protection of staphylococci from extracellular penicillin. J. Med. Microbiol. 15 (1982) 373–385.
New, R. R. C., Chance, M. L., Health, S. Antileishmanial activity of amphotericin B and other antifungal agents entrapped in liposomes. J. Antimicrob. Chemother. 8 (1981) 371–381.
Taylor, R. L., Williams, D. M., Craven, P. C., Graybill, J. R., Drutz, D. J., Magee, W. E. Amphotericin B in liposomes: A novel therapy for histoplasmosis. Am. Rev. Respir. Dis. 145 (1982) 748–752.
Graybill, J. R., Craven, P. C., Taylor, R. L., Williams, D. M., Magee, W. E. Treatment of murine cryptococcosis with liposomal-associated amphotericin B. J. Infect. Dis. 45 (1982) 748–752.
Lopez-Berestein, G., Mehta, R., Hofer, R. L., Mills, K., Kasi, L., Mehta, K., Fainstein, V., Luna, M., Hersh, E. M., Juliano, R. Treatment and prophylaxis of disseminated infection due toCandida albicans in mice with liposomal-encapsulated amphotericin B. J. Infect. Dis. 147 (1983) 939–944.
Lopez-Berestein, G., Fainstein, V., Hopfer, R., Mehta, K., Sullivan, M. P., Keating, M., Rosenblum, M. G., Mehta, R., Luna, M., Hersh, E. M., Reuben, J., Juliano, R. M., Bodey, G. P. Liposomal amphotericin B for the treatment of systemic fungal infections in patients with cancer: A preliminary study. J. Infect. Dis. 151 (1985) 704–710.
Lopez-Berestein, G., Bodey, G. P., Frankel, L. S., Mehta, K. Treatment of hepatosplenic fungal infections with liposomal amphotericin B. J. Clin. Oncol. 5 (1987) 310–317.
Sculier, J. P., Coune, A., Meunier, F., Brassinne, C., Laduron, C., Hollaert, C., Collette, N., Heyman, C., Klastersky, J. Pilot study of amphotericin B entrapped into sonicated liposomes in cancer patients with fungal infections. Eur. J. Cancer Clin. Oncol. 24 (1988) 527–538.
Bonventre, P. F., Gregoriadis, G. Killing ofStaphylococcus aureus by dihydrostreptomycin entrapped within liposomes. Antimicrob. Agents Chemother. 13 (1978) 1049–1051.
Barsoum, I. S., Reich, M. The effect of liposome-entrapped penicillin G onStaphylococcus aureus infection in mice. Pharmacology 10 (1982) 358.
Bermudez, L. E. M., Wu, M., Young, L. S. Intracellular killing ofMycobacterium avium complex by rifapentine and liposome-encapsulated amikacin. J. Infect. Dis. 156 (1987) 510–513.
Cynamon, M. H., Swenson, S. W., Palmer, G. S., Ginsberg, R. S. Liposome encapsulated-amikacin therapy ofMycobacterium avium complex infection in beige mice. Antimicrob. Agents Chemother. 33 (1989) 1179–1183.
Bakker-Woudenberg, I. A. J. M., Lokerse, A. F., Vink-van den Berg, J. C., Roerdink, F. H. Liposome-encapsulated ampicillin againstListeria monocytogenes in vivo andin vitro. Infection 16 (Suppl. 2) (1988) 165–170.
Kreuter, J., Speiser, P. P. New adjuvants on a polymethylmethacrylate base. Infect. Immunity 13 (1976) 204–210.
Kreuter, J., Berg, U., Liehl, E., Soliva, M., Speiser, P. P. Influence of the particle size on the adjuvant effect of particulate polymeric adjuvants. Vaccine 4 (1986) 125–129.
Kreuter, J., Liehl, E. Protection induced by inactivated influenza vaccines with polymethylmethacrylate adjuvants. Med. Microbiol. Immunol. 165 (1978) 111–117.
Kreuter, J., Mauler, R., Gruschkau, H., Speiser, P. P. The use of new polymethylmethacrylate adjuvants for split influenza vaccines. Exp. Cell Biol. 44 (1978) 12–19.
Kreuter, J., Liehl, E. Long-term studies of micro-encapsulated and adsorbed influenza vaccine nanoparticles. J. Pharm. Sci. 70 (1981) 367–371.
Kreuter, J., Haenzel, I. Mode of action of immunological adjuvants: Some physicochemical factors influencing the effectivity of polyacrylic adjuvants. Infect. Immunity 19 (1978) 667–675.
Kreuter, J., Liehl, E., Berg, U., Soliva, M., Speiser, P. P. Influence of hydrophobicity on the adjuvant effect of particulate polymeric adjuvants. Vaccine 6 (1988) 253–256.
Baillie, A. J., Coombs, G. H., Dolan, T. F., Hunter, C. A., Laakso, T., Sjöholm, I., Stjärnkvist, P. Biodegradable microspheres: polyacryl starch microparticles as a delivery system for the antileishmanial drug, sodium stibogluconate. J. Pharm. Pharmacol. 39 (1978) 832–835.
Stjärnkvist, P., Artursson, P., Brunmark, A., Laakso, T., Sjöholm, I. Biodegradable microspheres. VIII. Killing ofLeishmania donovani in cultured macrophages by microparticle-bound primaquine. Int. J. Pharm. 40 (1987) 215–222.
Fouarge, M., Dewulf, M., Couvreur, P., Roland, M., Vranckx, H. Development of dehydroemetine nanoparticles for the treatment of visceral leishmaniasis. J. Microencapsul. 6 [1989] 29–34.
Labhasetwar, V. D., Dorle, A. K. Nanoparticles — colloidal drug delivery system for primaquine and metronidazole. J. Controlled Rel. 12 (1990) 113–119.
Lherm, C., Couvreur, P., Loiseau, P., Bories, C., Gayral, P. Unloaded polyisobutylcyanoacrylate nanoparticles: efficiency against bloodstream trypanosomes. J. Pharm. Pharmacol. 39 (1986) 650–652.
Youssef, M., Fattal, E., Alonso, M.-J., Roblot-Treupel, L., Sauzières, J., Tancrède, C., Omnès, A., Couvreur, P., Andremont, A. Effectiveness of nanoparticle-bound ampicillin in the treatment ofListeria monocytogenes infections in athymic nude mice. Antimicrob. Agents Chemother. 32 (1988) 1204–1207.
Fattal, E., Rojas, J., Andremont, A., Couvreur, P.: Efficacité comparée de nanoparticles et de liposomes chargés en ampicilline dans le traitement de la listériose et de la salmonellose expérimentales chez la souris. Proc. 5th Int. Conf. Pharm. Technol., Paris 1989, Vol. III, APGI, Chatenay Malabry 1989, pp. 72–79.
Fattal, E., Youssef, M., Couvreur, P., Andremont, A. Treatment of experimental salmonellosis in mice with ampicillin-bound nanoparticles. Antimicrob. Agents Chemother. 33 (1989) 1540–1543.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Kreuter, J. Liposomes and nanoparticles as vehicles for antibiotics. Infection 19 (Suppl 4), S224–S228 (1991). https://doi.org/10.1007/BF01644038
Issue Date:
DOI: https://doi.org/10.1007/BF01644038