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Preservative Efficacy Test


Test Report


No.: 13-081907

Date: August 26, 2013


1. Test Substance

Received July 23, 2013 – 1 sample

UMO Concentrated Solution


2. Test Method (According to JPXⅥ)

(1) Test Microorganisms

  • Escherichia coli NBRC 3972 (E. coli)

  • Pseudomonas aeruginosa NBRC 13275 (P. aeruginosa)

  • Staphylococcus aureus NBRC 13276 (S. aureus)

  • Candida albicans NBRC 1594 (C. albicans)

  • Aspergillus brasiliensis NBRC 9455 (A. brasiliensis)

(2) Preparation of Test Microbial Suspensions

Bacteria (E. coli, P. aeruginosa, S. aureus):Pre-cultured on SCD agar at 30°C for 20 hours. Cells were collected with a platinum loop, suspended in sterilized physiological saline, and adjusted to approximately 10⁸ cells/mL as the test suspension.

Yeast (C. albicans):Pre-cultured on potato dextrose agar at 25°C for 48 hours. Cells were collected with a platinum loop, suspended in sterilized physiological saline, and adjusted to approximately 10⁸ cells/mL as the test suspension.

Mold (A. brasiliensis):Pre-cultured on potato dextrose agar at 25°C for 7 days. Cells were collected with a platinum loop, suspended in 0.05% polysorbate 80 sterilized physiological saline, and adjusted to approximately 10⁷ cells/mL as the test suspension.

(3) Inoculation and StorageFor each test microorganism, 20 g of the test substance was placed in a sterilized vial, and 1% (0.2 mL) of the test microbial suspension was inoculated. Samples were stored at 25°C, and viable counts were measured on days 7, 14, 21, and 28.

(4) Measurement of Viable Cells

  • Bacteria: SCDLP agar plate count method

  • Fungi (yeast and mold): GPLP agar plate count method


3. Test Results

Table 1 – Viable Cell Counts at Receipt of Sample(Data from the original table; shows initial counts for each microorganism upon receipt)

Table 2 – Time Course of Viable Cell Counts After Inoculation(Data from the original table; shows counts on days 7, 14, 21, 28)


4. Summary

The test substance showed good preservative efficacy against E. coli, P. aeruginosa, S. aureus, and C. albicans.

For A. brasiliensis, the number of surviving cells was slightly higher, but no growth was observed, and therefore it is considered unlikely to pose any practical problems.


Note: This paper is translated from the following URL. The content is provided for reference on the scientific research of the raw material only. Whether APA raw materials are used or not, we hope this research will help increase understanding and awareness of body minerals.



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