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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In tissue engineering, scaffolds are designed to mimic the extracellular matrix (ECM), creating three-dimensional (3D) microenvironments that support cell adhesion and growth. However, the precise fabrication of heterogenenous ECM-mimicking 3D microstructures remains an unsolved challenge. To address this, high-precise sericin-based scaffolds were developed via femtosecond laser direct writing (FsLDW) technology. Chemically modified sericin served as a monomer in the FsLDW process, achieving nanoscale precision and enabling the fabrication of arbitrary 3D sericin microstructures. Biomimetic 3D models, derived from natural tissue matrices, were employed to construct heterogenenous sericin bioscaffolds. These anisotropic scaffolds effectively supported cell directional growth and differentiation. This advancement greatly enhances the precision of sericin-based tissue-engineered scaffolds, enabling the creation of heterogenenous, multifunctional microenvironments that mimic natural ECM to support functional tissue development and address challenges in accurately simulating ECM microstructures in tissue regeneration.
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Source |
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http://dx.doi.org/10.1021/acs.nanolett.5c00346 | DOI Listing |