In vitro cytotoxicity of two novel oral formulations of Amphotericin B (iCo-009 and iCo-010) against Candida albicans, human monocytic and kidney cell lines
- Carlos G Leon†1,
- Jinkyung Lee†1,
- Karen Bartlett2,
- Pavel Gershkovich1,
- Ellen K Wasan3,
- Jinying Zhao1,
- John G Clement4 and
- Kishor M Wasan1Email author
© Leon et al; licensee BioMed Central Ltd. 2011
Received: 15 July 2011
Accepted: 20 August 2011
Published: 20 August 2011
Invasive fungal infections such as candidiasis constitute an increasingly important medical problem. Drugs currently used for the treatment of candidiasis include polyenes (such as Amphotericin B) and azoles. Amphotericin B (AmpB) presents several limitations such as its nephrotoxicity and limited solubility. We have developed two novel lipid-based AmpB formulations which in vivo show less nephrotoxicity and enhanced solubility compared to Fungizone™ a commercial AmpB formulation.
The purpose of this study was to determine the cytotoxicity of Fungizone™, Ambisome™ and two novel AmpB formulations (iCo-009 and iCo-010) against Candida albicans, human kidney (293T) cells and monocytic (THP1) cells.
Cell cytotoxicity to the AmpB formulations was evaluated by MTS and LDH assays. In vitro anti-Candida albicans activity was assessed after a 48 h drug incubation.
None of the AmpB formulations tested showed cytotoxicity against 293T cells. In the case of THP1 cells only Fungizone™ and Ambisome™ showed cytotoxicity at 500 μg/L (n = 4-10, p < 0.05).
The calculated EC50 to Candida albicans for the different formulations was as follows: 26.8 ± 2.9 for iCo-010, 74.6 ± 8.9 for iCo-009, 109 ± 31 for Ambisome™ and 87.1 ± 22 for Fungizone™ (μg of AmpB/L, n = 6-12, p < 0.05).
The AmpB formulations analyzed were not cytotoxic to 293T cells. Cytotoxicity in THP1 cells was observed for Fungizone™ and Ambisome™, but not with the novel AmpB formulations. iCo-010 had higher efficacy compared to other three AmpB formulations in the Candida albicans model.
The absence of cytotoxicity as well as its higher efficacy for the Candida model compared to Fungizone™ and Ambisome™ suggest that iCo-010 has potential in treating candidiasis.
KeywordsAmphotericin B Candida cytotoxicity monocytes.
Invasive fungal infections constitute an increasingly important medical problem due to the growth of immunodeficient populations, the development of antifungal resistance and limitations in the efficacy and toxicity of current antifungals . Candida species are the most common cause of nosocomial invasive mycosis and are the leading cause of related mortality . An increasing rate of candidaemia  as well as the emergence of drug resistant strains  support the efforts in discovering novel therapeutic approaches .
Drugs currently used for the treatment of candidiasis include polyenes (such as Amphotericin B AmpB), azoles (fluconazole), echinocandins and flucytosine. Limited therapeutic efficiency and drug resistance have led to consider new therapeutic approaches, in particular the use of new analogs of existing drugs .
Amphotericin B (AmpB) is a treatment of choice for systemic fungal infections . The mechanism of action of AmpB involves its binding to ergosterol in the fungal cell membrane, producing pores in the membrane which leads to ion loss and cell death . Recently it has been described that AmpB can also elicit cell death through the induction of a strong oxidative burst . Acquired resistance to Amphotericin B in Candida species, though rare, has been reported previously [8, 9]. This AmpB resistance has been correlated with decreased levels of ergosterol in the plasma membrane and has been accompanied with azole resistance [10, 11].
One of the major limitations associated with AmpB is its nephrotoxicity . Another issue related to AmpB is its poor solubility that limits its route of administration . The development of an effective, safe, and inexpensive oral formulation of amphotericin B would have many applications for the treatment of fungal diseases. The new oral amphotericin B formulations developed by our group, iCo-009 and iCo-010, show efficacy in vivo against leishmaniasis [14, 15], aspergillosis and candidiasis .
The purpose of the present study was to determine if four different formulations of AmpB (iCo-009, iCo-010, Fungizone™ and Ambisome™) were cytotoxic in human monocytic, human kidney cells and Candida albicans.
2. Results and Discussion
Previously, others  have described a difference in the degree of cellular activation by AmpB in the 293 and THP1 cell lines. This disparity was accounted by the differential expression of the TLR2, highly expressed in THP1 cells and expressed at very low levels in 293 cells. The new oral formulations, iCo-009 and iCo-010, did not show any evidence of toxicity at the highest concentration analyzed in 293T cells (10,000 μg/L, Figure 1). The limited TLR2 expression in 293T cells may explain this lack of cytotoxicity that was observed even at large doses of AmpB compared with a cytotoxic effect of AmpB in THP1 cells at a lower concentration (500 μg/L).
The difference in cytotoxicity found in THP1 cells between the LDH and MTS assays could be accounted by the fact that the MTS assay relies on the accessibility of the substrate to the respiratory machinery of the cell (i.e. expression and activity of transporters). In the case of LDH there is no active transport factor(s) as it is an index of the cell breakdown and the release of LDH enzyme to the medium. The drug concentration that elicits toxicity in the THP1 monocytes with Fungizone™ and Ambisome™ can be compared with the serum drug levels obtained in patients. After a standard dose of AmpB (0.3 mg/kg on days 1 and 2 followed by increasing doses to 0.5 mg/kg) for patient therapy, the expected serum AmpB levels can reach 200 μg/L . Few studies have assessed the AmpB-induced cytotoxicity in monocytes and macrophages. Sesana et al.,  examined the in vitro activity of AmpB cochleates against Leishmania chagasi and the cytotoxic effect on mouse peritoneal macrophages using AmpB deoxycholate (Fungizone™) as a control. They found that the AmpB deoxycholate (Fungizone™) was cytotoxic to mouse peritoneal macrophages at a concentration of 1250 μg/L, while the AmpB cochleates were not toxic at that AmpB concentration.
EC50 for AmpB formulations (mean ± SD, expressed in μ g/L of AmpB, n = 6-12, * p < 0.05) tested in the Candida model
Mean ± SD
87.1 ± 22
109 ± 31
74.6 ± 8.9
26.8 ± 2.9 *
iCo-009 was previously compared to Abelcet® in an in vivo study in Candida albicans-infected male rats . In that report, iCo-009 exhibited significant reduction in viable colony forming units of Candida from kidney homogenates compared to Abelcet®.
We have tested the cytotoxicity and efficacy of four AmpB formulations in two human cell lines and a Candida albicans model, respectively. Fungizone™ and Ambisome™, but not iCo-009 and iCo-010, show cytotoxicity in human monocytes at a concentration of 500 μg/L. iCo-010 shows a higher efficacy compared to iCo-009, Ambisome™ and Fungizone™ in the Candida albicans model. The lack of toxicity and efficacy of iCo-010, a novel oral AmpB formulation, warrant future in vivo Candida albicans studies to determine its therapeutic index.
4. Materials and methods
4.1. Novel lipid oral Amphotericin B formulations
The description of the composition and development of the two novel lipid oral Amphotericin B formulations can be found elsewhere iCo-009  and iCo-010 . AmpB concentration was analyzed by HPLC as previously described . For the cytotoxicity and efficacy studies we used as negative controls medium alone and medium containg the vehicle controls for both iCo-009 and iCo-010. No cytotoxicity was found when any of these controls were used (data not shown).
4.2. Cytotoxicity assay on 293T cells
Human embryonic kidney cells (293T ATCC CRL 11268) were kindly provided by Dr JS Hill (St Paul's Hospital, UBC, Vancouver, BC). Cells were grown in complete DMEM without phenol red at 37°C (5% CO2) in T75 flasks. At near confluency, the cells were trypsinized and transferred to either additional flasks or to 96-well plates (previously coated with Poly L-lysine and seeded at a density of 10,000 cells/well). Twenty four hours post seeding, the adherent cells were washed and incubated with different concentrations of AmpB formulations (250 to 10,000 μg/L of AmpB) for 48 h. Percent AmpB-mediated cytotoxicity was determined using the MTS conversion assay (Promega Corp, Madison, WI), as previously described .
4.3. Cytotoxicity assay on THP1 cells
Human monocytic THP1 cells (ATCC TIB-202) were kindly provided by Dr JS Hill (St Paul's Hospital, UBC, Vancouver, BC). Cells were grown in complete RPMI without phenol red at 37°C (5% CO2) in T75 flasks. Before the cells reached a concentration of one million per mL, the cells were transferred to either additional flasks or to 96-well plates and seeded at a density of 20,000 cells/well with the addition of PMA (10 ng/mL final) to allow the cells to differentiate overnight. Twenty four hours post seeding, the differentiated cells were washed and the different concentrations of AmpB formulations were added (31 to 500 μg/L of AmpB) for 48 h. After a 90 min incubation with the MTS reagent, percent AmpB-mediated cytotoxicity was determined using the MTS conversion assay (Promega Corp, Madison, WI), as previously described  or the LDH assay (Promega Corp, Madison, WI) as outlined by the manufacturer specifications. The MTS and LDH results were corrected by the amount of protein present in the respective wells. Purified LDH from the manufacturer kit was used as a positive control (data not shown).
4.4. Minimum inhibitory concentration determination of the AmpB formulations on Candida growth in liquid medium
RPMI without phenol red and supplemented with 10% Fetal bovine serum, 2% dextrose plus penicillin and streptomycin was used to prepare dilutions of AmpB (31.25, 62.5, 125, 250 and 500 μg/L- final drug concentration) from Fungizone™, Ambisome™, iCo-009 and iCo-010 (AmpB concentration in the formulations was determined by HPLC). A vehicle control of iCo-009 and iCo-010 was used as a negative control. RPMI is the standard medium used in microplate drug susceptibility assays and is commonly used for testing of drug sensitivity for both Candida albicans and Cryptococcus neoformans . A limitation of the RPMI medium is that there are frequent overlaps between the EC50 ranges for isolates that are putatively resistant or susceptible to Amphotericin B. The supplementation of RPMI medium with 2% glucose has lead to higher fungal growth rates and better separation of EC50s for isolates that are putatively resistant to fluconazole . This is the methodology that we have used for our experiments.
The Candida albicans (ATCC reference strain 18804) inoculum was prepared as follows. The fungal cell concentration was determined using a hematocytometer. One hundred microlitres of a 5 × 105/mL preparation of Candida in RPMI was placed in the 96 well plates for a final concentration of 2.5 × 105 cells/mL. Each concentration was analyzed in eight replicates per experiment (n = 6-12 independent experiments).
The plates were incubated for 48 h at 37°C protected from the light before analyzing the growth pattern using a spectrophotometer at 650 nm. A new Candida agar plate was streaked each week to ensure the viability of the culture.
This work was supported by a grant-in-aid from iCo Therapeutics Inc., Vancouver, BC Canada and a Canadian Institutes of Health Research (CIHR) grant awarded to KMW.
- Calugi C, Trabocchi A, Guarna A: Novel small molecules for the treatment of infections caused by Candida albicans: a patent review 2. Expert Opin Ther Pat. 2011, 21 (3): 381-97. 10.1517/13543776.2011.551116View ArticlePubMedGoogle Scholar
- Marr KA: Fungal infections in oncology patients: update on epidemiology, prevention, and treatment. Curr Opin Oncol. 2010, 22 (2): 138-42. 10.1097/CCO.0b013e328335a755View ArticlePubMedGoogle Scholar
- Rodriguez-Creixems M, Alcala L, Munoz P, Cercenado E, Vicente T, Bouza E: Bloodstream infections: evolution and trends in the microbiology workload, incidence, and etiology, 1985-2006. Medicine (Baltimore). 2008, 87 (4): 234-49. 10.1097/MD.0b013e318182119b.View ArticleGoogle Scholar
- Niimi M, Firth NA, Cannon RD: Antifungal drug resistance of oral fungi. Odontology. 2010, 98 (1): 15-25. 10.1007/s10266-009-0118-3View ArticlePubMedGoogle Scholar
- Oura M, Sternberg TH, Wright ET: A new antifungal antibiotic, amphotericin B. Antibiot Annu. 1955, 3: 566-73.PubMedGoogle Scholar
- Baginski M, Sternal K, Czub J, Borowski E: Molecular modelling of membrane activity of amphotericin B, a polyene macrolide antifungal antibiotic. Acta Biochim Pol. 2005, 52 (3): 655-8.PubMedGoogle Scholar
- Sangalli-Leite F, Scorzoni L, Mesa-Arango AC, Casas C, Herrero E, Soares Mendes Gianinni MJ, Rodriguez-Tudela JL, Cuenca-Estrella M, Zaragoza O: Amphotericin B mediates killing in Cryptococcus neoformans through the induction of a strong oxidative burst. Microbes Infect. 2011, 13 (5): 457-67. 10.1016/j.micinf.2011.01.015View ArticlePubMedGoogle Scholar
- Krcmery V, Barnes AJ: Non-albicans Candida spp. causing fungaemia: pathogenicity and antifungal resistance. J Hosp Infect. 2002, 50 (4): 243-60. 10.1053/jhin.2001.1151View ArticlePubMedGoogle Scholar
- Kelly SL, Lamb DC, Kelly DE, Manning NJ, Loeffler J, Hebart H, Schumacher U, Einsele H: Resistance to fluconazole and cross-resistance to amphotericin B in Candida albicans from AIDS patients caused by defective sterol delta5, 6-desaturation. FEBS Lett. 1997, 400 (1): 80-2. 10.1016/S0014-5793(96)01360-9View ArticlePubMedGoogle Scholar
- Barker KS, Crisp S, Wiederhold N, Lewis RE, Bareither B, Eckstein J, Barbuch R, Bard M, Rogers PD: Genome-wide expression profiling reveals genes associated with amphotericin B and fluconazole resistance in experimentally induced antifungal resistant isolates of Candida albicans. J Antimicrob Chemother. 2004, 54 (2): 376-85. 10.1093/jac/dkh336View ArticlePubMedGoogle Scholar
- Chamilos G, Kontoyiannis DP: Update on antifungal drug resistance mechanisms of Aspergillus fumigatus. Drug Resist Updat. 2005, 8 (6): 344-58. 10.1016/j.drup.2006.01.001View ArticlePubMedGoogle Scholar
- Safdar A, Ma J, Saliba F, Dupont B, Wingard JR, Hachem RY, Mattiuzzi GN, Chandrasekar PH, Kontoyiannis DP, Rolston KV, Walsh TJ, Champlin RE, Raad II: Drug-induced nephrotoxicity caused by amphotericin B lipid complex and liposomal amphotericin B: a review and meta-analysis. Medicine (Baltimore). 2010, 89 (4): 236-44. 10.1097/MD.0b013e3181e9441b.View ArticleGoogle Scholar
- Thornton SJ, Wasan KM: The reformulation of amphotericin B for oral administration to treat systemic fungal infections and visceral leishmaniasis. Expert Opin Drug Deliv. 2009, 6 (3): 271-84. 10.1517/17425240902802861View ArticlePubMedGoogle Scholar
- Wasan KM, Wasan EK, Gershkovich P, Zhu X, Tidwell RR, Werbovetz KA, Clement JG, Thornton SJ: Highly effective oral amphotericin B formulation against murine visceral leishmaniasis. J Infect Dis. 2009, 200 (3): 357-60. 10.1086/600105View ArticlePubMedGoogle Scholar
- Wasan EK, Gershkovich P, Zhao J, Zhu X, Werbovetz K, Tidwell RR, Clement JG, Thornton SJ, Wasan KM: A novel tropically stable oral amphotericin B formulation (iCo-010) exhibits efficacy against visceral Leishmaniasis in a murine model. PLoS Negl Trop Dis. 2010, 4 (12): e913- 10.1371/journal.pntd.0000913PubMed CentralView ArticlePubMedGoogle Scholar
- Wasan EK, Bartlett K, Gershkovich P, Sivak O, Banno B, Wong Z, Gagnon J, Gates B, Leon CG, Wasan KM: Development and characterization of oral lipid-based amphotericin B formulations with enhanced drug solubility, stability and antifungal activity in rats infected with Aspergillus fumigatus or Candida albicans. Int J Pharm. 2009, 372 (1-2): 76-84. 10.1016/j.ijpharm.2009.01.003View ArticlePubMedGoogle Scholar
- Razonable RR, Henault M, Lee LN, Laethem C, Johnston PA, Watson HL, Paya CV: Secretion of proinflammatory cytokines and chemokines during amphotericin B exposure is mediated by coactivation of toll-like receptors 1 and 2. Antimicrob Agents Chemother. 2005, 49 (4): 1617-21. 10.1128/AAC.49.4.1617-1621.2005PubMed CentralView ArticlePubMedGoogle Scholar
- Atkinson AJ, Bennett JE: Amphotericin B pharmacokinetics in humans. Antimicrob Agents Chemother. 1978, 13 (2): 271-6.PubMed CentralView ArticlePubMedGoogle Scholar
- Sesana AM, Monti-Rocha R, Vinhas SA, Morais CG, Dietze R, Lemos EM: In vitro activity of amphotericin B cochleates against Leishmania chagasi. Mem Inst Oswaldo Cruz. 2011, 106 (2): 251-3. 10.1590/S0074-02762011000200022View ArticlePubMedGoogle Scholar
- Rex JH, Pfaller MA, Galgiani JN, Bartlett MS, Espinel-Ingroff A, Ghannoum MA, Lancaster M, Odds FC, Rinaldi MG, Walsh TJ, Barry AL: Development of interpretive breakpoints for antifungal susceptibility testing: conceptual framework and analysis of in vitro-in vivo correlation data for fluconazole, itraconazole, and candida infections. Subcommittee on Antifungal Susceptibility Testing of the National Committee for Clinical Laboratory Standards. Clin Infect Dis. 1997, 24 (2): 235-47. 10.1093/clinids/24.2.235View ArticlePubMedGoogle Scholar
- Rodriguez-Tudela JL, Martinez-Suarez JV: Improved medium for fluconazole susceptibility testing of Candida albicans. Antimicrob Agents Chemother. 1994, 38 (1): 45-8.PubMed CentralView ArticlePubMedGoogle Scholar
- Chang HC, Chang JJ, Chan SH, Huang AH, Wu TL, Lin MC, Chang TC: Evaluation of Etest for direct antifungal susceptibility testing of yeasts in positive blood cultures. J Clin Microbiol. 2001, 39 (4): 1328-33. 10.1128/JCM.39.4.1328-1333.2001PubMed CentralView ArticlePubMedGoogle Scholar
- Zager RA: Polyene antibiotics: relative degrees of in vitro cytotoxicity and potential effects on tubule phospholipid and ceramide content. Am J Kidney Dis. 2000, 36 (2): 238-49. 10.1053/ajkd.2000.8967View ArticlePubMedGoogle Scholar
- Anaissie EJ, Paetznick VL, Ensign LG, Espinel-Ingroff A, Galgiani JN, Hitchcock CA, LaRocco M, Patterson T, Pfaller MA, Rex JH, Rinaldi MG: Microdilution antifungal susceptibility testing of Candida albicans and Cryptococcus neoformans with and without agitation: an eight-center collaborative study. Antimicrob Agents Chemother. 1996, 40 (10): 2387-91.PubMed CentralPubMedGoogle Scholar
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