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

MARC details
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<br/>pulp, such as structural protein, regulation protein, and catalytic protein. L‑arginine,<br/>an amino acid and one of the building blocks of proteins, regulates pro‑inflammatory<br/>and anti‑inflammatory activity. Therefore, L‑arginine‑based culture has potential<br/>to promote dental pulp regeneration. This study aimed to investigate the potential<br/>of L‑arginine‑based culture in improving the viability of human dental pulp stem<br/>cells (hDPSCs). We evaluated the viability of hDPSCs in culture media supplemented<br/>with different concentrations of L‑arginine amino acid (250, 300, 350, and 400 μmol/L)<br/>and Dulbecco’s Modified Eagle Medium plus fetal bovine serum 10% (control)<br/>using a 3‑(4,5‑dimethylthiazol‑2‑yl)‑2,5‑diphenyltetrazolium bromide assay after<br/>24‑h incubation time. Statistical analysis was conducted using a one‑way analysis of<br/>variance and post hoc least significant difference test. In qualitative analysis, the 4´,<br/>6‑diamidino‑2‑phenylindole staining method was used. The evaluation has shown a<br/>significant result when 250, 300, and 350 μmol/L concentration of L‑arginine amino acid<br/>culture media compared with control, and 400 μmol/L has the best result and was not<br/>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)
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Koha item type Articles Abstract Database
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 18/01/2024   2024-0089 18/01/2024 18/01/2024 Articles Abstract Database
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