Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Jan 25:2022:8930709.
doi: 10.1155/2022/8930709. eCollection 2022.

Solidified Reverse Micellar Solution- (SRMS-) Based Microparticles for Enhanced Oral Bioavailability and Systemic Antifungal Efficacy of Miconazole Nitrate in Immunocompromised Mice

Affiliations

Solidified Reverse Micellar Solution- (SRMS-) Based Microparticles for Enhanced Oral Bioavailability and Systemic Antifungal Efficacy of Miconazole Nitrate in Immunocompromised Mice

Emmanuel Maduabuchi Uronnachi et al. Biomed Res Int. .

Abstract

Purpose: To assess the improvement in oral bioavailability and efficacy in systemic candidiasis treatment of miconazole nitrate (MN) formulations in murine models of candidiasis.

Methods: Selected formulations containing 5% of Softisan + Phospholipon 90H lipid matrix with 3% of MN (A 1), 5% of stearic acid + Phospholipon 90H lipid matrix with 3% of MN (B 1), and 5% Softisan + stearic acid + Phospholipon 90H with 3% of MN (C 1) from the in vitro investigation were used for the study. Their acute toxicity was assessed using Lorke's method (with slight modification) while bioavailability was determined using the bioassay method. The optimized batch (A 1) was tested in murine systemic candidiasis induced in cyclophosphamide-immunosuppressed mice. The mice were treated with a single oral dose (100 mg/kg) of the formulations for five days. Serum fungal counts (cfu/mL) were determined on days 1, 3, and 5 of the treatment period. Haematological assessments were done.

Results: The lipid formulations were safer than MN powder with LD50 values of 3162.8 and 1118.3 mg/kg. Bioavailability determination revealed a higher area under the curve (AUC) value for formulations A 1 (6.11 μg/hr/mL) and B 1 (4.91 μg/hr/mL) while formulation C 1 (1.80 μg/hr/mL) had a lower AUC than MN (4.46 μg/hr/mL). Fungi were completely cleared from the blood of animals treated with the optimized formulation by day 3 as opposed to the controls (MN and Tween® 20) which still had fungi on day 5. No significant increase (p > 0.05) in haematological parameters was observed in mice treated with A 1.

Conclusion: Formulation A 1 successfully cleared Candida albicans from the blood within a shorter period than miconazole powder. This research has shown the potential of orally administered MN-loaded SRMS-based microparticles in combating systemic candidaemia.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests in the research work.

Figures

Figure 1
Figure 1
Calibration plot of miconazole nitrate against Candida albicans.
Figure 2
Figure 2
Bioavailability determination of selected formulations.
Figure 3
Figure 3
Blood colony counts of Candida albicans in immune suppressed mice. Group 1: immunosuppressed mice induced with candidiasis and administered miconazole solution (100 mg/kg). Group 2: immunosuppressed mice induced with candidiasis and administered Batch A1 (100 mg/kg). Group 3: mice induced with candidiasis and administered 1% Tween® 20 solution.

References

    1. Kabir M. A., Ahmad Z. Candida infections and their prevention. ISRN Preventive Medicine . 2013;2013 doi: 10.5402/2013/763628.763628 - DOI - PMC - PubMed
    1. Stevens D. A. Azoles in the management of systemic fungal infections. Infectious Diseases in Clinical Practice . 2004;12:81–92.
    1. Shadkchan Y., Segal E. Antifungal activity of amphotericin B-lipid admixtures in experimental systemic candidosis in naive mice. The Journal of Antimicrobial Chemotherapy . 1999;44(6):787–790. doi: 10.1093/jac/44.6.787. - DOI - PubMed
    1. Dupont B. Overview of the lipid formulations of amphotericin B. The Journal of Antimicrobial Chemotherapy . 2002;49(supplement 1):31–36. doi: 10.1093/jac/49.suppl_1.31. - DOI - PubMed
    1. Semis R., Mendlovic S., Polacheck I., Segal E. Activity of an intralipid formulation of nystatin in murine systemic candidiasis. International Journal of Antimicrobial Agents . 2011;38:336–340. - PubMed

Supplementary concepts