Abstract
A nanosomal formulation of moxifloxacin has been prepared by anionic polymerization of poly(butyl-2-cyanoacrylate) in the presence of the drug. The poly(butyl-2-cyanoacrylate) nanoparticles absorb effectively moxifloxacin with a high total content and have a considerable capacity (> 45%). The influence of reaction parameters such as pH and drug-to-polymer ratio on the nanoparticle characteristics has been studied. The efficacy of the novel formulation has been evaluated in mice infected with M. tuberculosis. It is shown that the efficacy of the proposed nanosomal formulation for i.v. administration evaluated by a decrease in the lung mycobacteria count is more than twice that of a reference preparation.
Similar content being viewed by others
References
H. Pinto-Alphandary, A. Andremont, and P. Couvreur, Int. J. Antimicrob. Agents, 13, No. 3, 155–168 (2000).
R. Pandey and G. K. Khuller, Indian J. Exp. Biol., 44, No. 5, 357–366 (2006).
R. Pandey, S. Sharma, and G. K. Khuller, Tuberculosis (Edinb.), 85, No. 5–6, 415–420 (2005).
R. Rastogi, Y. Sultana, A. Ali, et al., Curr. Drug Delivery, 3, No. 1, 121–128 (2006).
S. Gelperina, K. Kisich, M. D. Iseman, et al., Am. J. Respir. Crit. Care Med., 15, 172, No. 12, 1487–1490 (2005).
J. Kreuter, ed., “Nanoparticles,” in: Colloidal Drug Delivery Systems, Marcel Dekker, New York (1994), pp. 291–342.
C. Vautheir, C. Dubernet, E. Fattal, et al., Adv. Drug Delivery Rev., 55, No. 4, 519–548 (2003).
E. Fattal, M. Youssef, P. Couvreur, et al., Antimicrob. Agents Chemother., 33, No. 9, 1540–1543 (1989).
I. N. Skidan, S. E. Gel(perina, S. E. Severin, et al., Antibiot. Khimioter., 48, No. 1, 23–26 (2003).
M. Youssef, E. Fattal, M.-J. Alonso, et al., Antimicrob. Agents Chemother., 32, No. 8, 1204–1207 (1988).
E. A. Oganesyan, A. P. Bud(ko, Yu. V. Stukalov, et al., Antibiot. Khimioter., 50, No. 8–9, 15–19 (2005).
F. Fawaz, F. Bonini, J. Maugein, et al., Int. J. Pharm., 168, 225–259 (1998).
M. I. Perel(man, G. B. Sokolova, G. N. Mozhokhina, et al., Antibiot. Khimioter., 49, No. 6, 20–24 (2004).
L. S. Strachunskii and V. A. Krechikov, Klin. Mikrobiol. Antimicrob. Khimioter., 3, 3–40 (2001).
S. J. Douglas, L. Illum, S. S. Davis, et al., J. Colloid Interface Sci., 101, No. 1, 149–175 (1984).
F. Fawaz, M. Guyot, A. M. Lagueny, et al., Int. J. Pharm., 154, 191–203 (1997).
M. Fresta, G. Puglisi, G. Giammona, et al., J. Pharm. Sci., 84, No. 7, 895–901 (1995).
C. M. Shoen, M. S. DeStefano, M. R. Sklaney, et al., Int. J. Antimicrob. Agents, 53, No. 4, 641–645 (2004).
Author information
Authors and Affiliations
Additional information
__________
Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 42, No. 3, pp. 43–47, March, 2008.
Rights and permissions
About this article
Cite this article
Shipulo, E.V., Lyubimov, I.I., Maksimenko, O.O. et al. Development of a nanosomal formulation of moxifloxacin based on poly(butyl-2-cyanoacrylate). Pharm Chem J 42, 145–149 (2008). https://doi.org/10.1007/s11094-008-0073-2
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11094-008-0073-2