Biomaterials Translational最新文献

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Targeting tumour-osteoclast interactions: a trigger-explosion system to combat bone metastasis. 靶向肿瘤破骨细胞相互作用:一种对抗骨转移的触发爆炸系统。
Biomaterials Translational Pub Date : 2024-09-28 eCollection Date: 2024-01-01 DOI: 10.12336/biomatertransl.2024.03.009
Ang Gao, Huaiyu Wang
{"title":"Targeting tumour-osteoclast interactions: a trigger-explosion system to combat bone metastasis.","authors":"Ang Gao, Huaiyu Wang","doi":"10.12336/biomatertransl.2024.03.009","DOIUrl":"10.12336/biomatertransl.2024.03.009","url":null,"abstract":"","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 3","pages":"328-330"},"PeriodicalIF":0.0,"publicationDate":"2024-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11681184/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142904214","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Corrigendum: Enhanced angiogenesis in porous poly(ε-caprolactone) scaffolds fortified with methacrylated hyaluronic acid hydrogel after subcutaneous transplantation. 更正:皮下移植后多孔聚(ε-己内酯)支架与甲基丙烯酸透明质酸水凝胶的血管生成增强。
Biomaterials Translational Pub Date : 2024-06-28 eCollection Date: 2024-01-01 DOI: 10.12336/biomatertransl.2024.02.011
{"title":"Corrigendum: Enhanced angiogenesis in porous poly(ε-caprolactone) scaffolds fortified with methacrylated hyaluronic acid hydrogel after subcutaneous transplantation.","authors":"","doi":"10.12336/biomatertransl.2024.02.011","DOIUrl":"10.12336/biomatertransl.2024.02.011","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.12336/biomatertransl.2024.01.006.].</p>","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 2","pages":"95"},"PeriodicalIF":0.0,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438606/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142333490","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Advanced nanoparticles in osteoarthritis treatment. 先进纳米粒子在骨关节炎治疗中的应用。
Biomaterials Translational Pub Date : 2024-06-28 eCollection Date: 2024-01-01 DOI: 10.12336/biomatertransl.2024.02.002
Qiushi Liang, Zhiliang Cheng, Ling Qin
{"title":"Advanced nanoparticles in osteoarthritis treatment.","authors":"Qiushi Liang, Zhiliang Cheng, Ling Qin","doi":"10.12336/biomatertransl.2024.02.002","DOIUrl":"10.12336/biomatertransl.2024.02.002","url":null,"abstract":"<p><p>Osteoarthritis (OA) is the most prevalent degenerative joint disorder, affecting hundreds of millions of people globally. Current clinical approaches are confined to providing only symptomatic relief. Research over the past two decades has established that OA is not merely a process of wear and tear of the articular cartilage but involves abnormal remodelling of all joint tissues. Although many new mechanisms of disease have been identified in the past several decades, the efficient and sustainable delivery of drugs targeting these mechanisms in joint tissues remains a major challenge. Nanoparticles recently emerged as favoured delivery vehicles in OA treatment, offering extended drug retention, enhanced drug targeting, and improved drug stability and solubility. In this review, we consider OA as a disease affecting the entire joint and initially explore the pathophysiology of OA across multiple joint tissues, including the articular cartilage, synovium, fat pad, bone, and meniscus. We then classify nanoparticles based on their composition and structure, such as lipids, polymers, inorganic materials, peptides/proteins, and extracellular vesicles. We summarise the recent advances in their use for treatment and diagnosis of OA. Finally, we discuss the current challenges and future directions in this field. In conclusion, nanoparticle-based nanosystems are promising carriers that advance OA treatment and diagnosis.</p>","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 2","pages":"95-113"},"PeriodicalIF":0.0,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438607/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142333488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dynamic regulation of the wound repair process: achieving one-stop scar-free repair. 伤口修复过程的动态调节:实现一站式无疤痕修复。
Biomaterials Translational Pub Date : 2024-06-28 eCollection Date: 2024-01-01 DOI: 10.12336/biomatertransl.2024.02.010
Min Wang, Xianwen Wang
{"title":"Dynamic regulation of the wound repair process: achieving one-stop scar-free repair.","authors":"Min Wang, Xianwen Wang","doi":"10.12336/biomatertransl.2024.02.010","DOIUrl":"10.12336/biomatertransl.2024.02.010","url":null,"abstract":"","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 2","pages":"200-202"},"PeriodicalIF":0.0,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438611/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142333492","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Decellularised extracellular matrix-based injectable hydrogels for tissue engineering applications. 用于组织工程应用的基于细胞外基质的脱细胞可注射水凝胶。
Biomaterials Translational Pub Date : 2024-06-28 eCollection Date: 2024-01-01 DOI: 10.12336/biomatertransl.2024.02.003
Wan-Ying Guo, Wei-Huang Wang, Pei-Yao Xu, Ranjith Kumar Kankala, Ai-Zheng Chen
{"title":"Decellularised extracellular matrix-based injectable hydrogels for tissue engineering applications.","authors":"Wan-Ying Guo, Wei-Huang Wang, Pei-Yao Xu, Ranjith Kumar Kankala, Ai-Zheng Chen","doi":"10.12336/biomatertransl.2024.02.003","DOIUrl":"10.12336/biomatertransl.2024.02.003","url":null,"abstract":"<p><p>Decellularised extracellular matrix (dECM) is a biomaterial derived from natural tissues that has attracted considerable attention from tissue engineering researchers due to its exceptional biocompatibility and malleability attributes. These advantageous properties often facilitate natural cell infiltration and tissue reconstruction for regenerative medicine. Due to their excellent fluidity, the injectable hydrogels can be administered in a liquid state and subsequently formed into a gel state in vivo, stabilising the target area and serving in a variety of ways, such as support, repair, and drug release functions. Thus, dECM-based injectable hydrogels have broad prospects for application in complex organ structures and various tissue injury models. This review focuses on exploring research advances in dECM-based injectable hydrogels, primarily focusing on the applications and prospects of dECM hydrogels in tissue engineering. Initially, the recent developments of the dECM-based injectable hydrogels are explained, summarising the different preparation methods with the evaluation of injectable hydrogel properties. Furthermore, some specific examples of the applicability of dECM-based injectable hydrogels are presented. Finally, we summarise the article with interesting prospects and challenges of dECM-based injectable hydrogels, providing insights into the development of these composites in tissue engineering and regenerative medicine.</p>","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 2","pages":"114-128"},"PeriodicalIF":0.0,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438603/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142333491","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
"Yin-Yang philosophy" for the design of anticancer drug delivery nanoparticles. 设计抗癌药物输送纳米粒子的 "阴阳哲学"。
Biomaterials Translational Pub Date : 2024-06-28 eCollection Date: 2024-01-01 DOI: 10.12336/biomatertransl.2024.02.005
Yanwen Ai, Yuan Tian, Jiaming Qiao, Changnan Wang, Huafei Li
{"title":"\"<i>Yin-Yang</i> philosophy\" for the design of anticancer drug delivery nanoparticles.","authors":"Yanwen Ai, Yuan Tian, Jiaming Qiao, Changnan Wang, Huafei Li","doi":"10.12336/biomatertransl.2024.02.005","DOIUrl":"10.12336/biomatertransl.2024.02.005","url":null,"abstract":"<p><p>Understanding the in vivo transport process provides guidelines for designing ideal nanoparticles (NPs) with higher efficacy and fewer off-target effects. Many factors, such as particle size, morphology, surface potential, structural stability, and etc., may influence the delivering process of NPs due to the existence of various physiological barriers within the body. Herein, we summarise the distinct influences of NP physicochemical properties on the four consecutive in vivo transport steps: (1) navigating with bloodstream within blood vessels, (2) transport across vasculature walls into tumour tissues, (3) intratumoural transport through the interstitial space, and (4) cellular uptake & intracellular delivery by cancerous cells. We found that the philosophy behind the current consensus for NP design has certain similarities to the \"Yin-Yang\" theory in traditional Chinese culture. Almost all physicochemical properties, regardless of big or small sizes, long or short length, positive or negative zeta potentials, are double-edged swords. The balance of potential benefits and side effects, drug selectivity and accessibility should be fully considered when optimising particle design, similar to the \"Yin-Yang harmony\". This paper presents a comprehensive review of the advancements in NPs research, focusing on their distinct features in tumour targeting, drug delivery, and cell uptake. Additionally, it deliberates on future developmental trends and potential obstacles, thereby aiming to uncover the ways these characteristics influence the NPs' biological activity and provide theoretical guidance for the targeted delivery of NPs.</p>","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 2","pages":"144-156"},"PeriodicalIF":0.0,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438609/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142333477","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Artificial intelligence-enabled studies on organoid and organoid extracellular vesicles. 人工智能驱动的类器官和类器官细胞外囊泡研究。
Biomaterials Translational Pub Date : 2024-06-28 eCollection Date: 2024-01-01 DOI: 10.12336/biomatertransl.2024.02.001
Han Liu, James T Triffitt, Zhidao Xia, Jiacan Su
{"title":"Artificial intelligence-enabled studies on organoid and organoid extracellular vesicles.","authors":"Han Liu, James T Triffitt, Zhidao Xia, Jiacan Su","doi":"10.12336/biomatertransl.2024.02.001","DOIUrl":"10.12336/biomatertransl.2024.02.001","url":null,"abstract":"","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 2","pages":"93-94"},"PeriodicalIF":0.0,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438610/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142333489","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Self-rectifying magnetoelectric device for remote neural regeneration and function restoration. 用于远程神经再生和功能恢复的自校正磁电装置。
Biomaterials Translational Pub Date : 2024-06-28 eCollection Date: 2024-01-01 DOI: 10.12336/biomatertransl.2024.02.009
Yuanhao Tong, Yuanming Ouyang, Cunyi Fan, Yun Qian
{"title":"Self-rectifying magnetoelectric device for remote neural regeneration and function restoration.","authors":"Yuanhao Tong, Yuanming Ouyang, Cunyi Fan, Yun Qian","doi":"10.12336/biomatertransl.2024.02.009","DOIUrl":"10.12336/biomatertransl.2024.02.009","url":null,"abstract":"","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 2","pages":"197-199"},"PeriodicalIF":0.0,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438602/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142333496","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Exosome-loaded biomaterials for tendon/ligament repair. 用于肌腱/韧带修复的外泌体负载生物材料。
Biomaterials Translational Pub Date : 2024-06-28 eCollection Date: 2024-01-01 DOI: 10.12336/biomatertransl.2024.02.004
Haohan Wang, Yonglin Guo, Yiwen Jiang, Yingyu Ge, Hanyi Wang, Dingyi Shi, Guoyang Zhang, Jinzhong Zhao, Yuhao Kang, Liren Wang
{"title":"Exosome-loaded biomaterials for tendon/ligament repair.","authors":"Haohan Wang, Yonglin Guo, Yiwen Jiang, Yingyu Ge, Hanyi Wang, Dingyi Shi, Guoyang Zhang, Jinzhong Zhao, Yuhao Kang, Liren Wang","doi":"10.12336/biomatertransl.2024.02.004","DOIUrl":"10.12336/biomatertransl.2024.02.004","url":null,"abstract":"<p><p>Exosomes, a specialised type of extracellular vesicle, have attracted significant attention in the realm of tendon/ligament repair as a potential biologic therapeutic tool. While the competence of key substances responsible for the delivery function was gradually elucidated, series of shortcomings exemplified by the limited stability still need to be improved. Therefore, how to take maximum advantage of the biological characteristics of exosomes is of great importance. Recently, the comprehensive exploration and application of biomedical engineering has improved the availability of exosomes and revealed the future direction of exosomes combined with biomaterials. This review delves into the present application of biomaterials such as nanomaterials, hydrogels, and electrospun scaffolds, serving as the carriers of exosomes in tendon/ligament repair. By pinpointing and exploring their strengths and limitations, it offers valuable insights, paving the way the future direction of biomaterials in the application of exosomes in tendon/ligament repair in this field.</p>","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 2","pages":"129-143"},"PeriodicalIF":0.0,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438604/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142333494","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abalone shell-derived Mg-doped mesoporous hydroxyapatite microsphere drug delivery system loaded with icariin for inducing apoptosis of osteosarcoma cells. 鲍鱼壳衍生的掺镁介孔羟基磷灰石微球给药系统负载冰片苷,用于诱导骨肉瘤细胞凋亡。
Biomaterials Translational Pub Date : 2024-06-28 eCollection Date: 2024-01-01 DOI: 10.12336/biomatertransl.2024.02.008
Kaihua Liu, Meiqi Cheng, Hao Huang, Hui Yu, Shiyao Zhao, Jinnuo Zhou, Dan Tie, Jianhua Wang, Panpan Pan, Jingdi Chen
{"title":"Abalone shell-derived Mg-doped mesoporous hydroxyapatite microsphere drug delivery system loaded with icariin for inducing apoptosis of osteosarcoma cells.","authors":"Kaihua Liu, Meiqi Cheng, Hao Huang, Hui Yu, Shiyao Zhao, Jinnuo Zhou, Dan Tie, Jianhua Wang, Panpan Pan, Jingdi Chen","doi":"10.12336/biomatertransl.2024.02.008","DOIUrl":"10.12336/biomatertransl.2024.02.008","url":null,"abstract":"<p><p>Hydroxyapatite (HAP) porous microspheres with very high specific surface area and drug loading capacity, as well as excellent biocompatibility, have been widely used in tumour therapy. Mg<sup>2+</sup> is considered to be a key factor in bone regeneration, acting as an active agent to stimulate bone and cartilage formation, and is effective in accelerating cell migration and promoting angiogenesis, which is essential for bone tissue repair, anti-cancer, and anti-infection. In this study, abalone shells from a variety of sources were used as raw materials, and Mg<sup>2+</sup>-doped abalone shell-derived mesoporous HAP microspheres (Mg-HAP) were prepared by hydrothermal synthesis as Mg<sup>2+</sup>/ icariin smart dual delivery system (ICA-Mg-HAP, IMHA). With increasing of Mg<sup>2+</sup> doping, the surface morphology of HAP microspheres varied from collapsed macroporous to mesoporous to smooth and non-porous, which may be due to Mg<sup>2+</sup> substitution or coordination in the HAP lattice. At 30% Mg<sup>2+</sup> doping, the Mg-HAP microspheres showed a more homogeneous mesoporous morphology with a high specific surface area (186.06 m2/g). The IMHA microspheres showed high drug loading (7.69%) and encapsulation rate (83.29%), sustained Mg<sup>2+</sup> release for more than 27 days, sustained and stable release of icariin for 60 hours, and good responsiveness to pH (pH 6.4 > pH 5.6). In addition, the IMHA delivery system stimulated the rapid proliferation of bone marrow mesenchymal stem cells and induced apoptosis in MG63 cells by blocking the G2 phase cycle of osteosarcoma cells and stimulating the high expression of apoptotic genes (Bcl-2, caspase-3, -8, -9). This suggests that the abalone shell-based IMHA may have potential applications in drug delivery and tumour therapy.</p>","PeriodicalId":58820,"journal":{"name":"Biomaterials Translational","volume":"5 2","pages":"185-196"},"PeriodicalIF":0.0,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438601/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142333487","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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