<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(12)</volume><submitter>Jing Z</submitter><funding>Ministry of Science and Technology of the People&amp;apos;s Republic of China</funding><pubmed_abstract>Surgical resection and perioperative adjuvant chemotherapy-based therapies have improved the prognosis of patients with osteosarcoma; however, intraoperative bone defects, local tumour recurrence, and chemotherapy-induced adverse effects still affect the quality of life of patients. Emerging 3D-printed titanium alloy (Ti&lt;sub>6&lt;/sub>Al&lt;sub>4&lt;/sub>V) implants have advantages over traditional implants in bone repair, including lower elastic modulus, lower stiffness, better bone conduction, more bone in-growth, stronger mechanical interlocking, and lager drug-loading capacity by their inherent porous structure. Here, cisplatin, a clinical first-line anti-osteosarcoma drug, was loaded into Ti&lt;sub>6&lt;/sub>Al&lt;sub>4&lt;/sub>V implants, within a PLGA-PEG-PLGA thermo-sensitive hydrogel, to construct bone substitutes with both anti-osteosarcoma and bone-repair functions. The optimal concentrations of cisplatin (0.8 and 1.6 mg/mL) were first determined &lt;i>in vitro&lt;/i>. Thereafter, the anti-tumour effect and biosafety of the cisplatin/hydrogel-loaded implants, as well as their bone-repair potential were evaluated &lt;i>in vivo&lt;/i> in tumour-bearing mouse, and bone defect rabbit models, respectively. The loading of cisplatin reduced tumour volume by more than two-thirds (from 641.1 to 201.4 mm&lt;sup>3&lt;/sup>) with negligible organ damage, achieving better anti-tumour effects while avoiding the adverse effects of systemic cisplatin delivery. Although bone repair was hindered by cisplatin loading at 4 weeks, no difference was observed at 8 weeks in the context of implants with versus without cisplatin, indicating acceptable long-term stability of all implants (with 8.48%-10.04% bone in-growth and 16.94%-20.53% osseointegration). Overall, cisplatin/hydrogel-loaded 3D-printed Ti&lt;sub>6&lt;/sub>Al&lt;sub>4&lt;/sub>V implants are safe and effective for treating osteosarcoma-caused bone defects, and should be considered for clinical use.</pubmed_abstract><journal>Bioactive materials</journal><pagination>4542-4557</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8138733</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Practical strategy to construct anti-osteosarcoma bone substitutes by loading cisplatin into 3D-printed titanium alloy implants using a thermosensitive hydrogel.</pubmed_title><pmcid>PMC8138733</pmcid><pubmed_authors>Zheng Y</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Jing Z</pubmed_authors><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>Wei Q</pubmed_authors><pubmed_authors>Ni R</pubmed_authors><pubmed_authors>Lin X</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Cai H</pubmed_authors><pubmed_authors>Fan D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Practical strategy to construct anti-osteosarcoma bone substitutes by loading cisplatin into 3D-printed titanium alloy implants using a thermosensitive hydrogel.</name><description>Surgical resection and perioperative adjuvant chemotherapy-based therapies have improved the prognosis of patients with osteosarcoma; however, intraoperative bone defects, local tumour recurrence, and chemotherapy-induced adverse effects still affect the quality of life of patients. Emerging 3D-printed titanium alloy (Ti&lt;sub>6&lt;/sub>Al&lt;sub>4&lt;/sub>V) implants have advantages over traditional implants in bone repair, including lower elastic modulus, lower stiffness, better bone conduction, more bone in-growth, stronger mechanical interlocking, and lager drug-loading capacity by their inherent porous structure. Here, cisplatin, a clinical first-line anti-osteosarcoma drug, was loaded into Ti&lt;sub>6&lt;/sub>Al&lt;sub>4&lt;/sub>V implants, within a PLGA-PEG-PLGA thermo-sensitive hydrogel, to construct bone substitutes with both anti-osteosarcoma and bone-repair functions. The optimal concentrations of cisplatin (0.8 and 1.6 mg/mL) were first determined &lt;i>in vitro&lt;/i>. Thereafter, the anti-tumour effect and biosafety of the cisplatin/hydrogel-loaded implants, as well as their bone-repair potential were evaluated &lt;i>in vivo&lt;/i> in tumour-bearing mouse, and bone defect rabbit models, respectively. The loading of cisplatin reduced tumour volume by more than two-thirds (from 641.1 to 201.4 mm&lt;sup>3&lt;/sup>) with negligible organ damage, achieving better anti-tumour effects while avoiding the adverse effects of systemic cisplatin delivery. Although bone repair was hindered by cisplatin loading at 4 weeks, no difference was observed at 8 weeks in the context of implants with versus without cisplatin, indicating acceptable long-term stability of all implants (with 8.48%-10.04% bone in-growth and 16.94%-20.53% osseointegration). Overall, cisplatin/hydrogel-loaded 3D-printed Ti&lt;sub>6&lt;/sub>Al&lt;sub>4&lt;/sub>V implants are safe and effective for treating osteosarcoma-caused bone defects, and should be considered for clinical use.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2024-11-21T00:48:19.683Z</modification><creation>2022-02-10T11:39:48.915Z</creation></dates><accession>S-EPMC8138733</accession><cross_references><pubmed>34027239</pubmed><doi>10.1016/j.bioactmat.2021.05.007</doi></cross_references></HashMap>