TY - JOUR
T1 - Antibacterial efficacy of 6% green tea extract and 2% chlorhexidine against enterococcus faecalis biofilm in vitro
AU - Reflan, Fitri
AU - Meidyawati, Ratna
AU - Indrawati, Daru
N1 - Publisher Copyright:
© 2019 The Authors.
PY - 2019/4/1
Y1 - 2019/4/1
N2 - Objective: This study aimed to compare the antibacterial efficacy of green tea extract to chlorhexidine 2% against Enterococcus faecalis biofilm using real-time polymerase chain reaction (RT-PCR). Methods: E. faecalis strain ATCC 29212 colonies were collected from overnight cultures grown on brain–heart infusion agar (BHIA) and resuspended at 108 CFU/ml according to a 0.5 McFarland standard. Aliquots of bacterial suspension (50 μl) were then inoculated onto sterile nitrocellulose filter discs place on BHIA and incubated aerobically at 37°C for 72 h. After incubation, the discs were removed, transferred into 10-ml phosphate-buffered saline (PBS) to loosen planktonic bacteria, and then incubated for 10 min at 37°C in 10 ml of 6% green tea extract, 2% chlorhexidine, or sterile PBS (control). Surviving E. faecalis cells were then quantified by RT-PCR. Results: Green tea extract reduced bacterial survival compared to control but was not as effective as chlorhexidine 2%. Conclusion: Green tea extract may help reduce oral E. faecalis biofilm. Moreover, specific antimicrobial compounds in green tea extract such as epigallocatechin-3-gallate should be tested as non-toxic alternatives to chlorhexidine.
AB - Objective: This study aimed to compare the antibacterial efficacy of green tea extract to chlorhexidine 2% against Enterococcus faecalis biofilm using real-time polymerase chain reaction (RT-PCR). Methods: E. faecalis strain ATCC 29212 colonies were collected from overnight cultures grown on brain–heart infusion agar (BHIA) and resuspended at 108 CFU/ml according to a 0.5 McFarland standard. Aliquots of bacterial suspension (50 μl) were then inoculated onto sterile nitrocellulose filter discs place on BHIA and incubated aerobically at 37°C for 72 h. After incubation, the discs were removed, transferred into 10-ml phosphate-buffered saline (PBS) to loosen planktonic bacteria, and then incubated for 10 min at 37°C in 10 ml of 6% green tea extract, 2% chlorhexidine, or sterile PBS (control). Surviving E. faecalis cells were then quantified by RT-PCR. Results: Green tea extract reduced bacterial survival compared to control but was not as effective as chlorhexidine 2%. Conclusion: Green tea extract may help reduce oral E. faecalis biofilm. Moreover, specific antimicrobial compounds in green tea extract such as epigallocatechin-3-gallate should be tested as non-toxic alternatives to chlorhexidine.
KW - Chlorhexidine 2%
KW - Enterococcus faecalis
KW - Green tea extract
KW - Real-time polymerase chain reaction
UR - http://www.scopus.com/inward/record.url?scp=85068008876&partnerID=8YFLogxK
U2 - 10.22159/ijap.2019.v11s1.168
DO - 10.22159/ijap.2019.v11s1.168
M3 - Article
AN - SCOPUS:85068008876
SN - 0975-7058
VL - 11
SP - 64
EP - 66
JO - International Journal of Applied Pharmaceutics
JF - International Journal of Applied Pharmaceutics
ER -