1.Irradiation Time of Photodynamic Therapy to the Number of Lactobacillus acidophilus
Sri Kunarti ; Nunik Nuraini ; Farida Widhi Astuti ; Cecilia GJ Lunardi ; Lulytha Rahmanike Putri
Archives of Orofacial Sciences 2021;16(SUPP 1):33-36
ABSTRACT
Lactobacillus acidophilus (L. acidophilus) is one of the etiological agents for dental caries and dominant in
the deep carious lesion. L. acidophilus has also been identified in persistent root canal infection and also
related to the failure of endodontic treatment. Photodynamic therapy is a therapeutic process involving
the combination of a nontoxic photosensitizer and a light source. The excited photosensitizer reacts with
reactive oxygen species (ROS), which induce injury and death of the microorganism. This study aimed
to prove the effect of irradiation time of photodynamic therapy to the number of L. acidophilus. Forty-two Eppendorf tubes were treated with 0.5 ml L. acidophilus distributed into seven groups. Group 1 as
the control group received no treatment. Groups 2, 3, 4, 5, 6 and 7 were treated with a combination of
0.5 ml toluidine blue O (TBO) as a photosensitizer and 630 nm photoactivated (Fotosan®) exposure
time for 10, 20, 30, 40, 50 and 60 sec. Then, all were stored in an incubator of 37ºC for 48 h. Later,
the colony-forming unit (CFU) was counted for each group. There were significant differences in the
number of L. acidophilus in CFU of the various irradiation times. The longer the photodynamic therapy
irradiation was, the lesser the number of live L. acidophilus became. At 50 sec and 60 sec irradiation,
none of the L. acidophilus was found alive.
Photochemotherapy
;
Lactobacillus acidophilus
2.Stirring Time Effect of Beta-TCP Nanoencapsulation Synthesized from Anadara granosa Shells on Particle Size and Calcium Level
Aprilia ; Sri Kunarti ; Theresia Indah Budhy S ; Anggun Prawira Khoirunissak ; Wa Ode Siti Amaliyah Wulandari ; Rima Parwati Sari ; Linda Rochyani
Malaysian Journal of Medicine and Health Sciences 2020;16(Supp 4, July):111-115
Introduction: Anadara-granosa synthesization through hydrothermal-method produces beta-tricalcium(beta-TCP), a
biomaterial that is able to provide a pathway for calcium-ions in dentin reparative formation thus qualifies TCP as
pulp-capping material.Nanoencapsulation is needed as calcium-ions have shown its rapid solubility which is the
main cause of high probability risk of tunnel defect.The present study aimed to understand the correlation between
stirring time, particle size and level of calcium of beta-TCP nanoencapsulation synthesized from Anadara-granosa-shells. Methods: Anadara-granosa-shells powder was hydrothermically-processed for 18hours and sintered for
3hours. After homogenous beta-TCP powder mixed with aquadest in magnetic stirrer acquired, Na-alginate was added during the stirring process following CaCl2 drop by drop into the mixture.Sample divided into 6-test groups according to the stirring time; P1-one hours;P2-two hours;P3-three hours;P4-four hours;P5-five hours;P6-six hours.All
samples centrifuged at 2500rpm for 6minutes and freeze-dried for 12hours.PSA-test and Calcium level-test were performed on the sample test groups, followed by ANOVA-test and post hoc with significance level of P-value=0,05. Results: Data showed average of particle-sizes P1=±336.44; P2=±325.7; P3=±340.94; P4=±452.6; P5=±556.6; P6=±
593.93.ANOVA-test result indicated a significant difference and backed up by Gomes howell test result.Significant
differences were found between group first-second-third and group four-five-six also between group five and group
six. Calcium level test result was P1=±10.41; P2=±9.53; P3=±9.87; P4=±5.52; P5=±5.33; P6=±5.25.ANOVA-test
showed a significant difference and supported by post-hoc LSD-test.Significant differences noted between group one
and other groups also between group-two-three and group-four-five-six. Conclusion: In the process of Nanoencapsulation of Anadara-granosa-shells, particle size gradually increased and calcium level gradually decreased along with
the longer stirring time was performed.