پديد آورندگان :
MEHRGAN HADI نويسنده , ELMI FERIAL نويسنده , FAZELI MOHAMMAD REZA نويسنده , SHAHVERDI AHMAD-REZA نويسنده , Samadi Nasrin نويسنده
چكيده لاتين :
The purpose of this research was to study the neutralization efficacy of a universal
neutralizer proposed by the CTPA on a range of antimicrobial agents and its potential
toxicity for microorganisms that are used for antimicrobial preservation testing. Several
types of antimicrobial agents including a mixture of methylisothiazolinone and its
5-chloro derivative, dimethylol dimethyl hydantoin, Quaternium-l SיP, Bronopol", benzalkonium
chloride, phenoxyethanol, methyl and propyl paraben, chlorhexidine, imidazolidinyl urea,
triclosan and thiomersal built-in pharmaceutical, cosmetic or health care products, as well as
6 types of these antimicrobials, i.e. a combination of methyl paraben (0.18% w/v) and propyl
paraben (0.02%), imidazolidinyl urea (0.3%), chlorhexidine (0.01%), benzalkonium chloride
(0.02%), Bronopol" (0.1%) and thiomersal (0.02%) in their pure and soluble form were
tested. Validation of microbial recovery was carried out according to the US Pharmacopeia 27
guidelines. The universal neutralizer could inactivate all the studied antimicrobial agents against
different strains tested except Staphylococcus aureus. With regards to this microorganism,
only seven preservative chemicals consisting of parabens, dimethylol dimethyl hydantoin,
Quaternium-l SיP, Bronopolי", benzalkonium chloride, Phenonipf and imidazolidinyl urea
were effectively inactivated. In addition, a pure solution of 0.02% thiomersal retained its
antimicrobial properties against all studied microorganisms. The neutralizer solution showed
no toxicity on any of the test organisms. In conclusion, CTPA proposed neutralizing solution
is not an inclusive neutralizer. Moreover, each organism to be used in the test must be included
in the validation study.