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Quantum dots for bone tissue engineering 用于骨组织工程的量子点
IF 8.7 1区 医学
Materials Today Bio Pub Date : 2024-08-03 DOI: 10.1016/j.mtbio.2024.101167
{"title":"Quantum dots for bone tissue engineering","authors":"","doi":"10.1016/j.mtbio.2024.101167","DOIUrl":"10.1016/j.mtbio.2024.101167","url":null,"abstract":"<div><p>In confronting the global prevalence of bone-related disorders, bone tissue engineering (BTE) has developed into a critical discipline, seeking innovative materials to revolutionize treatment paradigms. Quantum dots (QDs), nanoscale semiconductor particles with tunable optical properties, are at the cutting edge of improving bone regeneration. This comprehensive review delves into the multifaceted roles that QDs play within the realm of BTE, emphasizing their potential to not only revolutionize imaging but also to osteogenesis, drug delivery, antimicrobial strategies and phototherapy. The customizable nature of QDs, attributed to their size-dependent optical and electronic properties, has been leveraged to develop precise imaging modalities, enabling the visualization of bone growth and scaffold integration at an unprecedented resolution. Their nanoscopic scale facilitates targeted drug delivery systems, ensuring the localized release of therapeutics. QDs also possess the potential to combat infections at bone defect sites, preventing and improving bacterial infections. Additionally, they can be used in phototherapy to stimulate important bone repair processes and work well with the immune system to improve the overall healing environment. In combination with current trendy artificial intelligence (AI) technology, the development of bone organoids can also be combined with QDs. While QDs demonstrate considerable promise in BTE, the transition from laboratory research to clinical application is fraught with challenges. Concerns regarding the biocompatibility, long-term stability of QDs within the biological environment, and the cost-effectiveness of their production pose significant hurdles to their clinical adoption. This review summarizes the potential of QDs in BTE and highlights the challenges that lie ahead. By overcoming these obstacles, more effective, efficient, and personalized bone regeneration strategies will emerge, offering new hope for patients suffering from debilitating bone diseases.</p></div>","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":null,"pages":null},"PeriodicalIF":8.7,"publicationDate":"2024-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S259000642400228X/pdfft?md5=8c34011c4b845fc942241e1e69e6a383&pid=1-s2.0-S259000642400228X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141931420","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","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 to ‘Injectable and high-strength PLGA/CPC loaded ALN/MgO bone cement for bone regeneration by facilitating osteogenesis and inhibiting osteoclastogenesis in osteoporotic bone defects’ [Mater. Today Bio 26, June 2024, 101092] 骨质疏松性骨缺损中通过促进成骨和抑制破骨细胞生成实现骨再生的可注射高强度 PLGA/CPC 负载 ALN/MgO 骨水泥"[《今日材料》,生物 26,2024 年 6 月,101092]更正
IF 8.7 1区 医学
Materials Today Bio Pub Date : 2024-08-02 DOI: 10.1016/j.mtbio.2024.101171
{"title":"Corrigendum to ‘Injectable and high-strength PLGA/CPC loaded ALN/MgO bone cement for bone regeneration by facilitating osteogenesis and inhibiting osteoclastogenesis in osteoporotic bone defects’ [Mater. Today Bio 26, June 2024, 101092]","authors":"","doi":"10.1016/j.mtbio.2024.101171","DOIUrl":"10.1016/j.mtbio.2024.101171","url":null,"abstract":"","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":null,"pages":null},"PeriodicalIF":8.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590006424002321/pdfft?md5=c62009d2fbba765b34041529eec7a302&pid=1-s2.0-S2590006424002321-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142314150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
CD47-SIRPα signaling-inspired engineered monocytes for preventing the progression of atherosclerotic plaques CD47-SIRPα 信号启发工程单核细胞用于预防动脉粥样硬化斑块的进展
IF 8.7 1区 医学
Materials Today Bio Pub Date : 2024-08-02 DOI: 10.1016/j.mtbio.2024.101178
{"title":"CD47-SIRPα signaling-inspired engineered monocytes for preventing the progression of atherosclerotic plaques","authors":"","doi":"10.1016/j.mtbio.2024.101178","DOIUrl":"10.1016/j.mtbio.2024.101178","url":null,"abstract":"<div><p>The accumulation of foam cells in the subendothelial space of the vascular wall to form plaques is the real cause of atherosclerotic lesions. Conventional interventions, such as statins and anti-cytokine or anti-inflammatory therapies, suffer problems in terms of their short therapeutic outcomes and potential disruption of the immune system. The development of more efficient therapeutics to restrict the initial progression of plaques appears to be crucial for treating and preventing atherosclerosis. Decreasing foam cell formation by reversing the excessive phagocytosis of modified low-density lipoprotein (LDL) in macrophages is highly desirable. Here, we developed a strategy based on engineered monocytes to dynamically regulate lipid uptake by macrophages inspired by a CD47–SIRPα signaling-induced defect in the phagocytosis of lesional macrophages at the advanced stage of AS. Briefly, a complex called CD47p-GQDs-miR223, which is designed to interact with SIRPα, was synthesized to remodel monocytes by decreasing the uptake of oxidized LDL through the activation of CD47-SIRPα signaling. After injection, these monocytes compete for recruitment to atherosclerotic plaques, release gene drugs and mediate anti-inflammatory phenotypic remodeling of the aboriginal macrophages, effectively inhibiting the development of foam cells. Our strategy provides a new therapeutic for preventing the progression of atherosclerosis.</p></div>","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":null,"pages":null},"PeriodicalIF":8.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590006424002394/pdfft?md5=1a5106f4d1cd4387660cafc36ef3af12&pid=1-s2.0-S2590006424002394-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141931478","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Curcumin loaded hydrogel with double ROS-scavenging effect regulates microglia polarization to promote poststroke rehabilitation 具有双重清除 ROS 作用的姜黄素负载水凝胶可调节小胶质细胞极化,促进中风后康复
IF 8.7 1区 医学
Materials Today Bio Pub Date : 2024-08-02 DOI: 10.1016/j.mtbio.2024.101177
{"title":"Curcumin loaded hydrogel with double ROS-scavenging effect regulates microglia polarization to promote poststroke rehabilitation","authors":"","doi":"10.1016/j.mtbio.2024.101177","DOIUrl":"10.1016/j.mtbio.2024.101177","url":null,"abstract":"<div><p>Cyclodextrins are used to include curcumin to form complex, which is subsequently loaded into a reactive oxygen species (ROS) responsive hydrogel (Cur gel). This gel exhibits a dual ROS scavenging effect. The gel can neutralize extracellular ROS to lead to a ROS-sensitive curcumin release. The released curcumin complex can eliminate intracellular ROS. Furthermore, the Cur gel effectively downregulates the expression of CD16 and IL-1β while upregulating CD206 and TGF-β in oxygen and glucose-deprived (OGD) BV2 cells. Additionally, it restores the expression of synaptophysin and PSD95 in OGD N2a cells. Upon injection into the stroke cavity, the Cur gel reduces CD16 expression and increases CD206 expression in the peri-infarct area of stroke mice, indicating an <em>in vivo</em> anti-inflammatory polarization of microglia. Colocalization studies using PSD95 and VGlut-1 stains, along with Golgi staining, reveal enhanced neuroplasticity. As a result, stroke mice treated with the Cur gel exhibit the most significant motor function recovery. Mechanistic investigations demonstrate that the released curcumin complex scavenges ROS and suppresses the activation of the ROS-NF-κB signaling pathway by inhibiting the translocation of p47<em>-phox</em> and p67<em>-phox</em> to lead to anti-inflammatory microglia polarization. Consequently, the Cur gel exhibits promising potential for promoting post-stroke rehabilitation in clinics.</p></div>","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":null,"pages":null},"PeriodicalIF":8.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590006424002382/pdfft?md5=0c692b842980f59ab096ced5763c38ff&pid=1-s2.0-S2590006424002382-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141931479","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cationic homopolypeptides: A versatile tool to design multifunctional antimicrobial nanocoatings 阳离子均聚多肽:设计多功能抗菌纳米涂层的通用工具
IF 8.7 1区 医学
Materials Today Bio Pub Date : 2024-08-02 DOI: 10.1016/j.mtbio.2024.101168
{"title":"Cationic homopolypeptides: A versatile tool to design multifunctional antimicrobial nanocoatings","authors":"","doi":"10.1016/j.mtbio.2024.101168","DOIUrl":"10.1016/j.mtbio.2024.101168","url":null,"abstract":"<div><p>Postoperative infections are the most common complications faced by surgeons after implant surgery. To address this issue, an emerging and promising approach is to develop antimicrobial coatings using antibiotic substitutes. We investigated the use of polycationic homopolypeptides in a layer-by-layer coating combined with hyaluronic acid (HA) to produce an effective antimicrobial shield. The three peptide-based polycations used to make the coatings, poly(<span>l</span>-arginine) (PAR), poly(<span>l</span>-lysine), and poly(<span>l</span>-ornithine), provided an efficient antibacterial barrier by a contact-killing mechanism against Gram-positive, Gram-negative, and antibiotic-resistant bacteria. Moreover, this activity was higher for homopolypeptides containing 30 amino-acid residues per polycation chain, emphasizing the impact of the polycation chain length and its mobility in the coatings to deploy its contact-killing antimicrobial properties. However, the PAR-containing coating emerged as the best candidate among the three selected polycations, as it promoted cell adhesion and epithelial monolayer formation. It also stimulated nitric oxide production in endothelial cells, thereby facilitating angiogenesis and subsequent tissue regeneration. More interestingly, bacteria did not develop a resistance to PAR and (PAR/HA) also inhibited the proliferation of eukaryotic pathogens, such as yeasts. Furthermore, <em>in vivo</em> investigations on a (PAR/HA)-coated hernia mesh implanted on a rabbit model confirmed that the coating had antibacterial properties without causing chronic inflammation. These impressive synergistic activities highlight the strong potential of PAR/HA coatings as a key tool in combating bacteria, including those resistant to conventional antibiotics and associated to medical devices.</p></div>","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":null,"pages":null},"PeriodicalIF":8.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590006424002291/pdfft?md5=296707409863368ddb37e8dba84213cc&pid=1-s2.0-S2590006424002291-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141931480","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Melatonin-loaded bioactive microspheres accelerate aged bone regeneration by formation of tunneling nanotubes to enhance mitochondrial transfer 褪黑素生物活性微球通过形成隧道纳米管来促进线粒体转移,从而加速老化骨再生
IF 8.7 1区 医学
Materials Today Bio Pub Date : 2024-08-02 DOI: 10.1016/j.mtbio.2024.101175
{"title":"Melatonin-loaded bioactive microspheres accelerate aged bone regeneration by formation of tunneling nanotubes to enhance mitochondrial transfer","authors":"","doi":"10.1016/j.mtbio.2024.101175","DOIUrl":"10.1016/j.mtbio.2024.101175","url":null,"abstract":"<div><p>The repair of bone defects in the elderly individuals is significantly delayed due to cellular senescence and dysfunction, which presents a challenge in clinical settings. Furthermore, there are limited effective methods available to promote bone repair in older individuals. Herein, melatonin-loaded mesoporous bioactive glasses microspheres (MTBG) were successfully prepared based on their mesoporous properties. The repair of bone defects in aged rats was significantly accelerated by enhancing mitochondrial function through the sustained release of melatonin and bioactive ions. MTBG effectively rejuvenated senescent bone marrow mesenchymal stem cells (BMSCs) by scavenging excessive reactive oxygen species (ROS), stabilizing the mitochondrial membrane potential (ΔΨm), and increasing ATP synthesis. Analysis of the underlying mechanism revealed that the formation of tunneling nanotubes (TNTs) facilitated the intercellular transfer of mitochondria, thereby resulting in the recovery of mitochondrial function. This study provides critical insights into the design of new biomaterials for the elderly individuals and the biological mechanism involved in aged bone regeneration.</p></div>","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":null,"pages":null},"PeriodicalIF":8.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590006424002369/pdfft?md5=585ec9eaeeadaf6c8442f58a29385384&pid=1-s2.0-S2590006424002369-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141931482","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biomimetic design and integrated biofabrication of an in-vitro three-dimensional multi-scale multilayer cortical model 体外三维多尺度多层皮质模型的仿生设计和综合生物制造
IF 8.7 1区 医学
Materials Today Bio Pub Date : 2024-08-02 DOI: 10.1016/j.mtbio.2024.101176
{"title":"Biomimetic design and integrated biofabrication of an in-vitro three-dimensional multi-scale multilayer cortical model","authors":"","doi":"10.1016/j.mtbio.2024.101176","DOIUrl":"10.1016/j.mtbio.2024.101176","url":null,"abstract":"<div><p>The lack of accurate and reliable <em>in vitro</em> brain models hinders the development of brain science and research on brain diseases. Owing to the complex structure of the brain tissue and its highly nonlinear characteristics, the construction of brain-like <em>in vitro</em> tissue models remains one of the most challenging research fields in the construction of living tissues. This study proposes a multi-scale design of a brain-like model with a biomimetic cortical structure, which includes the macroscopic structural features of six layers of different cellular components, as well as micrometer-scale continuous fiber structures running through all layers vertically. To achieve integrated biomanufacturing of such a complex multi-scale brain-like model, a multi-material composite printing/culturing integrated bioprinting platform was developed in-house by integrating cell-laden hydrogel ink direct writing printing and electrohydrodynamic fiber 3D printing technologies. Through integrated bioprinting, multi-scale models with different cellular components and fiber structural parameters were prepared to study the effects of macroscopic and microscopic structural features on the directionality of neural cells, as well as the interaction between glial cells and neurons within the tissue model in a three-dimensional manner. The results revealed that the manufactured <em>in vitro</em> biomimetic cortical model achieved morphological connections between the layers of neurons, reflecting the structure and cellular morphology of the natural cortex. Micrometer-scale (10 μm) cross-layer fibers effectively guided and controlled the extension length and direction of the neurites of surrounding neural cells but had no significant effect on the migration of neurons. In contrast, glial cells significantly promoted the migration of surrounding PC12 cells towards the glial layer but did not contribute to the extension of neurites. This study provides a basis for the design and manufacture of accurate brain-like models for the functionalization of neuronal tissues.</p></div>","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":null,"pages":null},"PeriodicalIF":8.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590006424002370/pdfft?md5=dc9c525c98f942dae9f6a5aadb28fdec&pid=1-s2.0-S2590006424002370-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141931477","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Virucidal activity of porphyrin-based metal-organic frameworks against highly pathogenic coronaviruses and hepatitis C virus 卟啉基金属有机框架对高致病性冠状病毒和丙型肝炎病毒的杀病毒活性
IF 8.7 1区 医学
Materials Today Bio Pub Date : 2024-08-02 DOI: 10.1016/j.mtbio.2024.101165
{"title":"Virucidal activity of porphyrin-based metal-organic frameworks against highly pathogenic coronaviruses and hepatitis C virus","authors":"","doi":"10.1016/j.mtbio.2024.101165","DOIUrl":"10.1016/j.mtbio.2024.101165","url":null,"abstract":"<div><p>The antiviral effect of four porphyrin-based Metal-Organic Frameworks (PMOFs) with Al and Zr, namely Al-TCPP, PCN-222, PCN-223 and PCN-224 was assessed for the first time against HCoV-229E, two highly pathogenic coronaviruses (SARS-CoV-2 and MERS-CoV) and hepatitis C virus (HCV). Infection tests <em>in vitro</em> were done under dark or light exposure for different contact times, and it was found that 15 min of light exposure were enough to give antiviral properties to the materials, therefore inactivating HCoV-229E by 99.98 % and 99.96 % for Al-TCPP and PCN-222. Al-TCPP diminished the viral titer of SARS-CoV-2 greater than PCN-222 in the same duration of light exposure, having an effect of 99.95 % and 93.48 % respectively. Next, Al-TCPP was chosen as the best candidate possessing antiviral properties and was tested against MERS-CoV and HCV, showcasing a reduction of infectivity of 99.28 % and 98.15 % respectively for each virus. The mechanism of the antiviral activity of the four PMOFs was found to be the production of singlet oxygen <sup>1</sup>O<sub>2</sub> from the porphyrin ligand TCPP when exposed to visible light, by using sodium azide (NaN<sub>3</sub>) as a scavenger, that can later attack the phospholipids on the envelope of the viruses, thus preventing their entry into the cells.</p></div>","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":null,"pages":null},"PeriodicalIF":8.7,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590006424002266/pdfft?md5=bd0760401ed9f6ff63ea3dbc120ef090&pid=1-s2.0-S2590006424002266-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141931481","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","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 to ‘Effective strategies to enhance the diagnosis and treatment of RCC: The application of biocompatible materials’ [Mater. Today Bio 27 (2024) 101149] 加强 RCC 诊断和治疗的有效策略:生物相容性材料的应用' [Mater. Today Bio 27 (2024) 101149] 的更正
IF 8.7 1区 医学
Materials Today Bio Pub Date : 2024-08-01 DOI: 10.1016/j.mtbio.2024.101155
{"title":"Corrigendum to ‘Effective strategies to enhance the diagnosis and treatment of RCC: The application of biocompatible materials’ [Mater. Today Bio 27 (2024) 101149]","authors":"","doi":"10.1016/j.mtbio.2024.101155","DOIUrl":"10.1016/j.mtbio.2024.101155","url":null,"abstract":"","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":null,"pages":null},"PeriodicalIF":8.7,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590006424002151/pdfft?md5=c18fde8b2569ec7226bd6650a4199a4e&pid=1-s2.0-S2590006424002151-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141851500","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","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 to targeted therapy and deep learning insights into microglia modulation for spinal cord injury 脊髓损伤的靶向治疗和深度学习对小胶质细胞调控的启示》勘误表
IF 8.7 1区 医学
Materials Today Bio Pub Date : 2024-08-01 DOI: 10.1016/j.mtbio.2024.101140
{"title":"Corrigendum to targeted therapy and deep learning insights into microglia modulation for spinal cord injury","authors":"","doi":"10.1016/j.mtbio.2024.101140","DOIUrl":"10.1016/j.mtbio.2024.101140","url":null,"abstract":"","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":null,"pages":null},"PeriodicalIF":8.7,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590006424001996/pdfft?md5=32e2d65f9b90ae3515a4ffd9e9c852d1&pid=1-s2.0-S2590006424001996-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141702731","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","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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