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
98%
921
2 minutes
20
A critical prerequisite for translating circulating tumor cells (CTCs) detection technologies into clinical practice is achieving high-efficiency capture and non-destructive release of low-abundance CTCs in blood. In recent years, innovative designs and surface modification of bioinspired topological micro/nanostructured materials have provided efficient solutions to capture and release CTCs. Motivated by pollen morphology and multimodal regulation, this study designed pollen-inspired spiky topological magnetic nanoparticles (IP-GSMNs) based on dual-recognition interface and intelligent-response modulation for high-efficiency capture and non-destructive release of CTCs from peripheral whole blood. The spiky protrusions on the surface of IP-GSMNs structurally match the extended filopodia of CTCs. Furthermore, IP-GSMNs were functionalized via gradient surface modification with intelligent-response materials, antifouling brush layers, and specific targeting molecules. These components collectively promoted multivalent interactions between IP-GSMNs and CTCs. A maximum CTC capture efficiency of 96.36 % ± 0.36 % was achieved while CTCs were released with an efficiency of 90.23 % ± 4.91 %, and viability of the released CTCs reached 99.77 % ± 0.40 %. Meanwhile, an intelligent-response multimodal regulatory platform integrating structural adaptation, interface regulation, molecular recognition, and dynamic dissociation was constructed. This platform achieved CTC capture counts ranging from 4 to 29 across 14 cancer patient blood samples while maintaining viability and integrity of released CTCs during dissociation. Importantly, this CTC capture-release platform established a non-invasive tumor profiling system for early diagnosis, therapeutic efficacy monitoring and personalized treatment, providing both scientific value and clinical significance for the development of precision oncology.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.bios.2025.117932 | DOI Listing |