TY - JOUR
T1 - Antibacterial Effect of Metabolites from Stem Cells from Human Deciduous Teeth with Alfa-Mangostin and EGCG on Streptococcus mutans and Staphylococcus aureus
AU - Sidarningsih,
AU - Yuliati,
AU - Diyatri, Indeswati
AU - Pratiwi, Reinaya Tifa
AU - Pongsumae, Dealtrini
AU - Aprilia, Sasha
AU - Fadilah, Oki
AU - Aljunaid, Mohammed Ahmed
AU - Ridwan, Rini Devijanti
N1 - Publisher Copyright:
© 2024 Universiti Putra Malaysia Press. All rights reserved.
PY - 2024/6
Y1 - 2024/6
N2 - Introduction: Stem cells from human exfoliated deciduous teeth (SHED) are currently receiving much attention because SHED has the potential to be widely used in regenerative medicine. The lineage-specific differentiation tendency of SHED, especially endothelial and neural differentiation, could be beneficial as neural innervation and blood vessel formation are essential in tissue regeneration. Streptococcus mutans (S. mutans) is the major bacterial cause of dental caries. At the same time, Staphylococcus aureus (S. aureus) is the bacterial cause of oral infections such as cheilitis, osteomyelitis, stomatitis, gingivitis, and dentoalveolar abscess. α-mangostin can inhibit bacterial growth by disrupting the cytoplasmic membrane of the bacteria. Epigallocatechin-3-gallate (EGCG) has a powerful antibacterial function, especially against gram-positive bacteria such as S. mutans and S. aureus. This study aimed to prove the inhibitory effect of SHED metabolite in combination with α-mangosteen and EGCG against S. aureus and S. mutans bacteria. Materials and methods: The study isolated and characterized metabolites from SHED in a specific medium. Subsequently, the combination of metabolites with α-mangostin and EGCG was made in a 1:1 ratio. The bacterial inhibition zones were measured on disk paper placed on bacterial growth media. Results: The combination of SHED metabolites with α-mangostin and EGCG significantly inhibited the growth of S. aureus and S. mutans bacteria. Conclusion: Combining SHED metabolites with α-mangostin and EGCG exhibits antibacterial properties against S. aureus and S. mutans bacteria. The combination of SHED metabolites with α-mangostin has higher inhibition results than the combination of SHED metabolites with EGCG.
AB - Introduction: Stem cells from human exfoliated deciduous teeth (SHED) are currently receiving much attention because SHED has the potential to be widely used in regenerative medicine. The lineage-specific differentiation tendency of SHED, especially endothelial and neural differentiation, could be beneficial as neural innervation and blood vessel formation are essential in tissue regeneration. Streptococcus mutans (S. mutans) is the major bacterial cause of dental caries. At the same time, Staphylococcus aureus (S. aureus) is the bacterial cause of oral infections such as cheilitis, osteomyelitis, stomatitis, gingivitis, and dentoalveolar abscess. α-mangostin can inhibit bacterial growth by disrupting the cytoplasmic membrane of the bacteria. Epigallocatechin-3-gallate (EGCG) has a powerful antibacterial function, especially against gram-positive bacteria such as S. mutans and S. aureus. This study aimed to prove the inhibitory effect of SHED metabolite in combination with α-mangosteen and EGCG against S. aureus and S. mutans bacteria. Materials and methods: The study isolated and characterized metabolites from SHED in a specific medium. Subsequently, the combination of metabolites with α-mangostin and EGCG was made in a 1:1 ratio. The bacterial inhibition zones were measured on disk paper placed on bacterial growth media. Results: The combination of SHED metabolites with α-mangostin and EGCG significantly inhibited the growth of S. aureus and S. mutans bacteria. Conclusion: Combining SHED metabolites with α-mangostin and EGCG exhibits antibacterial properties against S. aureus and S. mutans bacteria. The combination of SHED metabolites with α-mangostin has higher inhibition results than the combination of SHED metabolites with EGCG.
KW - Antimicrobial
KW - EGCG
KW - Health
KW - Medicine
KW - S. aureus
KW - S. mutans
KW - SHED metabolite
KW - α-mangostin
UR - http://www.scopus.com/inward/record.url?scp=85199719854&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:85199719854
SN - 1675-8544
VL - 20
SP - 151
EP - 156
JO - Malaysian Journal of Medicine and Health Sciences
JF - Malaysian Journal of Medicine and Health Sciences
ER -