Viability of human dental pulp stem cells: The potential of L‑arginine‑based culture media (Record no. 20620)

000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20240118163628.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 240118b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 22824
Author Lay, Sammy Henry
245 ## - TITLE STATEMENT
Title Viability of human dental pulp stem cells: The potential of L‑arginine‑based culture media
250 ## - EDITION STATEMENT
Volume, Issue number Vol.14(4), Oct-Dec
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Wolter Kluwer
Year 2023
300 ## - PHYSICAL DESCRIPTION
Pagination 306-310p.
520 ## - SUMMARY, ETC.
Summary, etc. Dental pulp is built by proteins that have various roles in the biological process of
pulp, such as structural protein, regulation protein, and catalytic protein. L‑arginine,
an amino acid and one of the building blocks of proteins, regulates pro‑inflammatory
and anti‑inflammatory activity. Therefore, L‑arginine‑based culture has potential
to promote dental pulp regeneration. This study aimed to investigate the potential
of L‑arginine‑based culture in improving the viability of human dental pulp stem
cells (hDPSCs). We evaluated the viability of hDPSCs in culture media supplemented
with different concentrations of L‑arginine amino acid (250, 300, 350, and 400 μmol/L)
and Dulbecco’s Modified Eagle Medium plus fetal bovine serum 10% (control)
using a 3‑(4,5‑dimethylthiazol‑2‑yl)‑2,5‑diphenyltetrazolium bromide assay after
24‑h incubation time. Statistical analysis was conducted using a one‑way analysis of
variance and post hoc least significant difference test. In qualitative analysis, the 4´,
6‑diamidino‑2‑phenylindole staining method was used. The evaluation has shown a
significant result when 250, 300, and 350 μmol/L concentration of L‑arginine amino acid
culture media compared with control, and 400 μmol/L has the best result and was not
significantly different with control toward viability of hDPSCs.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 22825
Co-Author Margono, Anggraini
773 0# - HOST ITEM ENTRY
Title Journal of advanced pharmaceutical technology and research
International Standard Serial Number 2231-4040
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10723171/pdf/JAPTR-14-306.pdf
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2024-01-18 2024-0089 2024-01-18 2024-01-18 Articles Abstract Database
Unique Visitors hit counter Total Page Views free counter
Implemented and Maintained by AIKTC-KRRC (Central Library).
For any Suggestions/Query Contact to library or Email: librarian@aiktc.ac.in | Ph:+91 22 27481247
Website/OPAC best viewed in Mozilla Browser in 1366X768 Resolution.

Powered by Koha