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Fluconazole flz

Manufactured by Merck Group
Sourced in United States

Fluconazole (FLZ) is an antifungal medication used in the treatment of various fungal infections. It functions as a triazole antifungal agent, inhibiting the synthesis of ergosterol, a critical component of the fungal cell membrane.

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4 protocols using fluconazole flz

1

Antifungal Susceptibility of Candida parapsilosis

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We calculated the minimum inhibitory concentration (MIC) and the minimum fungicidal concentration (MFC) of the twelve clinical strains of C. parapsilosis using Fluconazole (FLZ; Sigma-Aldrich, St. Louis, MO, USA), Amphotericin B (AmB; Sigma-Aldrich, USA), Nystatin (NYST; Sigma-Aldrich, USA), and Caspofungin (CAS; Sigma-Aldrich, USA). A broth microdilution assay was performed under the guidelines recommended in the standard M27 document (4th ed.) presented by the Clinical and Laboratory Standard Institute [14 ]. The stock solution of the prior mentioned drugs was prepared using dimethyl sulfoxide (DMSO; Merck, RSA) and the test concentration ranged from 1250 to 9.77 µg/mL for FLZ, 62.5 to 0.49 µg/mL for AmB, 250 to 19.5 µg/mL for NYST, and 8 to 0.06 µg/mL for CAS. Sterility and growth control were included for comparison. The plates were incubated at 37 °C for 48 h. The MIC results were determined by visual observation, where antifungal drugs with the lowest concentration inhibited the fungal growth when compared to the growth control was considered as MIC value.
For estimating MFC, 10 µL from the wells with different concentrations of antifungal drugs were subcultured onto Sabouraud dextrose agar (SDA; Merck, RSA) plates followed by incubation at 37 °C for 48 h. The MFC was determined by observing the lowest concentration with no growth on the agar plate [15 (link)].
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2

Antifungal activity of C18 peptide

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The novel synthesized Ceropin-4 derived peptide, C18(LWKIGKKIWRVLWNWR), showed high activity against C. albicans, with reference in our previous study (Peng et al., 2021 (link)). Consequently, C18 was synthesized by Gil Biochemical Co., Ltd. (Shanghai, China) with purity >95%, as verified by high-performance liquid chromatography (HPLC) and mass spectrometry. Fluconazole (FLZ) was purchased from Sigma-Aldrich. Other reagents were obtained from solarbio (Beijing, China) unless indicated otherwise.
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3

Antifungal Susceptibility Testing Protocol

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To determine the MIC values of each species, the broth microdilution method using CLSI-M27/A3 was followed [19 ]. AFST included the following antifungals; fluconazole (FLZ) (Sigma-Aldrich, St. Louis, MO, USA), voriconazole (VRZ) (Sigma-Aldrich, St. Louis, MO, USA), itraconazole (ITZ) (Sigma-Aldrich, St. Louis, MO, USA) anidulafungin (AND) (Pfizer, NY, USA), micafungin (MFG) (Astellas, Munich, Germany), and amphotericin B (AMB) (Sigma-Aldrich, St. Louis, MO, USA). MIC values were visually read after 24 h of incubation at 35 °C, and Pichia kudriavzveii (ATCC 6258) and C. parapsilosis (ATCC 22019) were used for quality control purposes. MIC data were interpreted in a species-specific manner as suggested [20 (link)].
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4

Evaluation of Duloxetine and Fluconazole against Cryptococcus neoformans

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C. neoformans H99 (ATCC 208821) was used for the experiments. Candida krusei ATCC 6258 was used as a quality control strain for the broth microdilution assay. Duloxetine hydrochloride (DH) (Galena, Campinas, Brazil), a selective serotonin and norepinephrine reuptake inhibitor class, and the antifungal fluconazole (FLZ) (Sigma-Aldrich, St Louis, MO) were used to assess susceptibility and synergistic effects in C. neoformans.
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