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Table 1.

Plants studied.

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Table 2.

Minimum inhibitory concentrations (MICs) of 10% DMSO and acetone dissolved extracts of plant species identical to those reported in the literature.

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Table 2 Expand

Table 3.

Minimum inhibitory concentrations (MICs) of 10% DMSO and acetone dissolved extracts of plant species reported to those reported in the literature.

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Table 3 Expand

Table 4.

Semi-quantitative evaluation of solubility of crude extracts in 10% DMSO and acetone.

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Table 4 Expand

Fig 1.

An overlay of UV chromatograms of acetone (blue) and DMSO (red) based working solutions of an n-hexane rhizomes extract of C. longa.

Qualitative similarity and higher quantities of phytochemicals observed in the acetone based working solution, which had better solubility compared to that of DMSO.

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Fig 2.

a. An overlay of UV chromatograms of acetone (blue) and DMSO (red) based working solutions of a methanol leaves extract of G. tinctoria, which had better solubility in acetone. Higher quantities of phytochemicals are observed in the acetone based working solution towards a less polar region of the chromatogram. b. Comparison of base peak chromatograms of acetone (blue) and DMSO (red) based working solutions of a methanol leaves extract of G. tinctoria, which had a better solubility in acetone. At least three additional compounds (marked A) are visible in the less polar region of acetone based working solution’s chromatogram.

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Fig 2 Expand

Fig 3.

a. An overlay of UV chromatograms of acetone (blue) and DMSO (red) based working solutions of a methanol barks extract of F. carica, which had a better solubility in 10% DMSO. Higher quantities of phytochemicals are seen in the in a DMSO based working solution. b. Comparison of base peak chromatograms of acetone (blue) and DMSO (red) based working solutions of a methanol barks extract of F. carica, which had a better solubility in 10% DMSO. At least 4 (marked A) and 1 (marked B) additional compound(s) are visible in the chromatograms of acetone and DMSO based working solutions, respectively.

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Fig 3 Expand

Fig 4.

a. Frequency of missing key information/aspects in the referred articles (n = 20). b. Variations in methodological approaches in antimicrobial susceptibility testing with respect to identities of studied bacteria, origins of test methods and visualization techniques for ascertaining the MIC values (n = 20).

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Fig 4 Expand