Nanoparticles loaded with antifungal drug for the treatment of skin infection

https://doi.org/10.53730/ijhs.v6nS4.10742

Authors

  • Sushma Verma Associate Professor, Faculty at Noida Institute of Engineering and Technology (Pharmacy Institute), Institutional Area, Knowledge Park II, Greater Noida, Uttar Pradesh 201306, India
  • Tushar Agarwal Master of Pharmacy, Noida Institute of Engineering and Technology (Pharmacy Institute), Institutional Area, Knowledge Park II, Greater Noida, Uttar Pradesh 201306, India
  • Gaurav Sharma Master of Pharmacy, Noida Institute of Engineering and Technology (Pharmacy Institute), Institutional Area, Knowledge Park II, Greater Noida, Uttar Pradesh 201306, India

Keywords:

amphotericin B, bioavailability, nanotechnology, skin disease

Abstract

Recent studies have concentrated on different formulations of polymeric nanoparticles. The oral bioavailability of water-insoluble medications has also increased because to advancements made possible by nanotechnology. Evaporation of the solvent and interfacial polymerization are two more methods that can be used in addition to these. Because of its nature as a macrolide pharmaceutical substance, it is especially prone to deterioration when exposed to organic solvents and heat; hence, these processes might not be optimal. On the other hand, coacervation is a sort of encapsulation that is less severe and more straightforward. There are two distinct types of nanoparticulate compositions. Although these formulations are more costly, researchers claim that they cause less damage to the kidneys. Many different resources have created delivery strategies that are both less dangerous to the kidneys and less costly. The current work utilized polyelectrolyte complexation technology in order to generate nanoparticle dosage forms with the intention of maximizing the oral bioavailability of amphotericin B (AmB). Oral bioavailability can be increased thanks to these polymers, which are also biocompatible and biodegradable.

Downloads

Download data is not yet available.

References

Allugunti V.R (2022). A machine learning model for skin disease classification using

convolution neural network. International Journal of Computing, Programming and Database

Gondal JA, Swartz RP, Rahman A. Therapeutic evaluation of free and liposome-encapsulated amphotericin B in the treatment of systemic candidiasis in mice. Antimicrob Agents Chemother. 1989 Sep;33(9):1544–1548.

Graybill JR, Craven PC, Taylor RL, Williams DM, Magee WE. Treatment of murine cryptococcosis with liposome-associated amphotericin B. J Infect Dis. 1982 May;145(5):748–752.

Graybill JR, Palou E, Ahrens J. Treatment of murine histoplasmosis with UK 49,858 (fluconazole). Am Rev Respir Dis. 1986 Oct;134(4):768–770

Holmberg K, Meyer RD. Fungal infections in patients with AIDS and AIDS-related complex. Scand J Infect Dis. 1986;18(3):179–192.

Hospenthal DR, Rogers AL, Beneke ES. Effect of attachment of anticandidal antibody to the surfaces of liposomes encapsulating amphotericin B in the treatment of murine candidiasis. Antimicrob Agents Chemother. 1989 Jan;33(1):16–18.

hrens J, Graybill JR, Craven PC, Taylor RL. Treatment of experimental murine candidiasis with liposome-associated amphotericin B. Sabouraudia. 1984;22(2):163–166.

Janoff AS, Boni LT, Popescu MC, Minchey SR, Cullis PR, Madden TD, Taraschi T, Gruner SM, Shyamsunder E, Tate MW, et al. Unusual lipid structures selectively reduce the toxicity of amphotericin B. Proc Natl Acad Sci U S A. 1988 Aug;85(16):6122–6126.

Katz NM, Pierce PF, Anzeck RA, Visner MS, Canter HG, Foegh ML, Pearle DL, Tracy C, Rahman A. Liposomal amphotericin B for treatment of pulmonary aspergillosis in a heart transplant patient. J Heart Transplant. 1990 Jan-Feb;9(1):14–17.

Kirsh R, Goldstein R, Tarloff J, Parris D, Hook J, Hanna N, Bugelski P, Poste G. An emulsion formulation of amphotericin B improves the therapeutic index when treating systemic murine candidiasis. J Infect Dis. 1988 Nov;158(5):1065–1070.

Kobayashi GS, Travis SJ, Medoff G. Comparison of fluconazole and amphotericin B in treating histoplasmosis in immunosuppressed mice. Antimicrob Agents Chemother. 1987 Dec;31(12):2005–2006.

Kumar, S. (2022). A quest for sustainium (sustainability Premium): review of sustainable bonds. Academy of Accounting and Financial Studies Journal, Vol. 26, no.2, pp. 1-18

Kusumawati, A. H., Wulan, I. R., & Ridwanuloh, D. (2020). Formulation and physical evaluation sheet mask from red rice (Oryza Nivara) and virgin coconut oil (Cocos Nucifera L). International Journal of Health & Medical Sciences, 3(1), 60-64. https://doi.org/10.31295/ijhms.v3n1.148

Lopez-Berestein G, Bodey GP, Fainstein V, Keating M, Frankel LS, Zeluff B, Gentry L, Mehta K. Treatment of systemic fungal infections with liposomal amphotericin B. Arch Intern Med. 1989 Nov;149(11):2533–2536.

Lopez-Berestein G, Bodey GP, Frankel LS, Mehta K. Treatment of hepatosplenic candidiasis with liposomal-amphotericin B. J Clin Oncol. 1987 Feb;5(2):310–317.

Lopez-Berestein G, Fainstein V, Hopfer R, Mehta K, Sullivan MP, Keating M, Rosenblum MG, Mehta R, Luna M, Hersh EM, et al. Liposomal amphotericin B for the treatment of systemic fungal infections in patients with cancer: a preliminary study. J Infect Dis. 1985 Apr;151(4):704–710.

Lopez-Berestein G, Hopfer RL, Mehta R, Mehta K, Hersh EM, Juliano RL. Liposome-encapsulated amphotericin B for treatment of disseminated candidiasis in neutropenic mice. J Infect Dis. 1984 Aug;150(2):278–283.

Lopez-Berestein G, Mehta R, Hopfer RL, Mills K, Kasi L, Mehta K, Fainstein V, Luna M, Hersh EM, Juliano R. Treatment and prophylaxis of disseminated infection due to Candida albicans in mice with liposome-encapsulated amphotericin B. J Infect Dis. 1983 May;147(5):939–945.

Management 3(1), 141-147

Mardon DN, Gunn JL, Robinette E., Jr Variation in the lethal response in mice to yeast-like and pseudohyphal forms of Candida albicans. Can J Microbiol. 1975 Nov;21(11):1681–1687.

Patterson TF, Miniter P, Dijkstra J, Szoka FC, Jr, Ryan JL, Andriole VT. Treatment of experimental invasive aspergillosis with novel amphotericin B/cholesterol-sulfate complexes. J Infect Dis. 1989 Apr;159(4):717–724.

Sculier JP, Coune A, Meunier F, Brassinne C, Laduron C, Hollaert C, Collette N, Heymans C, Klastersky J. Pilot study of amphotericin B entrapped in sonicated liposomes in cancer patients with fungal infections. Eur J Cancer Clin Oncol. 1988 Mar;24(3):527–538.

Suryasa, I. W., Rodríguez-Gámez, M., & Koldoris, T. (2021). Health and treatment of diabetes mellitus. International Journal of Health Sciences, 5(1), i-v. https://doi.org/10.53730/ijhs.v5n1.2864

Szoka FC, Jr, Milholland D, Barza M. Effect of lipid composition and liposome size on toxicity and in vitro fungicidal activity of liposome-intercalated amphotericin B. Antimicrob Agents Chemother. 1987 Mar;31(3):421–429.

Taylor RL, Williams DM, Craven PC, Graybill JR, Drutz DJ, Magee WE. Amphotericin B in liposomes: novel therapy for histoplasmosis. Am Rev Respir Dis. 1982 May;125(5):610

Published

16-07-2022

How to Cite

Verma, S., Agarwal, T., & Sharma, G. (2022). Nanoparticles loaded with antifungal drug for the treatment of skin infection. International Journal of Health Sciences, 6(S4), 7966–7978. https://doi.org/10.53730/ijhs.v6nS4.10742

Issue

Section

Peer Review Articles