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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The treatment of infectious bone defects requires simultaneous resolution of bacteria-associated antibiotic resistance, inflammatory microenvironment dysregulation, and impaired bone regeneration. Here, we developed an injectable, self-assembling designed gelatin micro-/nano-sphere system (GHMs@G1-N-A/T) that addresses the tripartite challenges of infectious bone defects through innovative material engineering: Antibacterial module featuring aptamer-conjugated gelatin nanospheres (AGN-Apt/Te) for MRSA-specific targeting, coupled with dual enzyme/pH-responsive release mechanisms (gelatinase-triggered nanosphere detachment and MgO-derived ROS generation); A self-assembling microsphere scaffold (GHMs) constructed through vanillin-mediated crosslinking and nano-hydroxyapatite (n-HA)/MgO incorporation, enabling sequential release of Mg/Ca; and A gelatinase-sensitive peptide (G-1) interface that dynamically links these components, ensuring microenvironment-responsive functionality. Results demonstrated that gelatinase-triggered AGN-Apt/Te nanospheres detachment enabled bacteria-specific antibiotic delivery, achieving greater than 95 % eradication of S. aureus and MRSA through synergistic biofilm disruption (via MgO-derived ROS bursts) and Te-mediated membrane damage. In vitro, self-assembling GHMs scaffold ensured sustained release of Mg/Ca, thereby promoting HUVEC tube formation (1.9-fold) and osteogenic differentiation of BMSCs. In a rat osteomyelitis model, GHMs@G1-N-A/T demonstrated sequential therapeutic efficacy: rapid infection control (greater than 95 % reduction within 7 days) followed by functional bone regeneration (46.32 % BV/TV at day 28). This work offers a new multifunctional biomaterial design that integrates hierarchical modular assembly, infection microenvironment-responsive logic and sequential transition from antibacterial to regenerative for the repair of complex infectious bone defects.
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http://dx.doi.org/10.1016/j.biomaterials.2025.123642 | DOI Listing |