Synergistic preservative compositions, process for preparing the same and method of use thereof
A technology of preservatives and compositions, applied in the field of synergistic preservative compositions, which can solve problems such as inability to protect end-user products
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Embodiment 1
[0078] Example 1: Synergistic effect / efficacy of preservative formulations containing PC (propylene carbonate), CHA (octanoylhydroxamic acid) and IPMP (isopropylmethylphenol).
[0079] Tables 1 to 3 below provide the different synergistic compositions prepared for the purposes of the present invention:
[0080] Table 1: Synergistic composition 1
[0081]
[0082] Table 2: Synergistic composition 2
[0083]
[0084] Table 3: Synergistic composition 3
[0085]
Embodiment 2
[0086] Example 2: Synergistic activity:
[0087] The synergistic activity of PC and (CHA+IPMP) compounds was performed on selected microbial strains. The synergistic effect of these compositions was demonstrated by testing a wide range of concentrations and ratios of the compounds as follows.
[0088] Tryptic Soy Broth (TSB) medium was used for bacterial evaluation and Yeast Malt Broth (YMB) was used for fungal evaluation. An IPMP solution was prepared by mixing 0.25% IPMP with 20% DMSO and water (qs. to 100%). A CHA solution was prepared by mixing 0.5% CHA with 20% DMSO and water (qs. to 100%). Compounds were then added to medium (50 [mu]L) and serially diluted. Add the same amount of PC (eg, 50 μL of a 6.25% solution) to all wells. Add 100 μl of the test bacterial or fungal suspension to a final concentration of about 10 in the double concentrated medium 6 CFU / ml. The inoculated medium was then incubated at 32°C for 2-5 days for bacteria, or 3-7 days at 28°C for fungi....
Embodiment 3
[0102] Embodiment 3: efficacy data
[0103]Efficacy data for synergistic preservative compositions were generated in different products following a 28-day double inoculation challenge trial. Briefly, with Gram-positive bacteria (Staphylococcus aureus 6538), Gram-negative bacteria complex (bacteria complex) (Escherichia coli 8739, Pseudomonas aeruginosa 9027 and Burkholderia cepacia 25416 ) or mold complexes (mold complexes) (C. albicans 10231 and Aspergillus brasiliensis 16404) were inoculated with samples containing synergistic preservative compositions or controls (no preservatives). Bacteria were inoculated on days 0 and 21 to a final concentration of approximately 10^ 6-7 cfu / ml, inoculate the fungal complex on days 0 and 21 to a final concentration of approximately 10^ 5-6 spores / ml. Inoculated samples were plated on days 2, 7, 14, 21 and 28. Recovery media was Lee's agar for bacteria and potato dextrose agar for fungi.
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