Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Atomic force microscopy (AFM) is used to measure live cells. Changes in the biomechanical properties of a single cell under mycelium extract () treatment play a critical role in drug efficacy evaluation and drug development, but they remain underexplored. In this study, ethanol-damaged human gastric mucosal cells (GES-1) treated with were examined through AFM to investigate the physical changes. GES-1 cells were exposed to 5% ethanol to create a cell damage model. -induced physical changes in the cell damage model were evaluated using AFM, including cell surface morphology, adhesion force, Young's modulus, and cell surface roughness. For comparison, the GES-1 cells were treated with various concentrations of as a normal group. The scratch assay and colony-forming assay were conducted to determine the growth-promoting effects of . The results show that 200 μg mL of is the optimal dosage, exhibiting the best repair capacity. This study presents a single-cell approach for evaluating the drug efficacy of , and the methodology used in this study is expected to investigate the effects of other drugs and physical and chemical factors.
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Source |
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http://dx.doi.org/10.1039/d5ay00836k | DOI Listing |