Yanfeng Li

Dr. Yanfeng Li


Research Focus & Metrics

Academic Career Length

4Years (2023-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 December 2023 in Advanced Science
Verified
Journal Article
Open access
XWXuan Wang
Xuan Wang
ALAobo Liu
Aobo Liu
ZZZhenbao Zhang
Zhenbao Zhang
DHDazhong Hao
Dazhong Hao
YLYijie Liang
Yijie Liang
YLYanfeng Li
Yanfeng Li
The combination of bioactive Zn‐2Mg alloy and additively manufactured porous scaffold is expected to achieve customizable biodegradable performance and enhanced bone regeneration. Herein, Zn‐2Mg alloy scaffolds with different porosities, including 40% (G‐40‐2), 60% (G‐60‐2), and 80% (G‐80‐2), and different unit sizes, including 1.5 mm (G‐60‐1.5), 2 mm (G‐60‐2), and 2.5 mm (G‐60‐2.5), are manufactured by a triply periodic minimal surface design and a reliable laser powder bed fusion process. With the same unit size, compressive strength (CS) and elastic modulus (EM) of scaffolds substantially decrease with increasing porosities. With the same porosity, CS and EM just slightly decrease with increasing unit sizes. The weight loss after degradation increases with increasing porosities and decreasing unit sizes. In vivo tests indicate that Zn‐2Mg alloy scaffolds exhibit satisfactory biocompatibility and osteogenic ability. The osteogenic ability of scaffolds is mainly determined by their physical and chemical characteristics. Scaffolds with lower porosities and smaller unit sizes show better osteogenesis due to their suitable pore size and larger surface area. The results indicate that the biodegradable performance of scaffolds can be accurately regulated on a large scale by structure design and the additively manufactured Zn‐2Mg alloy scaffolds have improved osteogenic ability for treating bone defects.

5 June 2025 in Biomaterials
Verified
Journal Article
Closed access
YLYijie Liang
Yijie Liang
JDJiabao Dai
Jiabao Dai
ZZZhenbao Zhang
Zhenbao Zhang
ALAobo Liu
Aobo Liu
JXJing Xu
Jing Xu
YLYanfeng Li
Yanfeng Li

14 March 2025 in Acta Biomaterialia
Verified
Journal Article
Closed access
ALAobo Liu
Aobo Liu
ZZZhenbao Zhang
Zhenbao Zhang
YLYijie Liang
Yijie Liang
XWXuan Wang
Xuan Wang
LCLi Chen
Li Chen
PWPeng Wen
Peng Wen

28 August 2024 in Bioengineering
Verified
Journal Article
Open access
PDF file
YZYu Zhou
Yu Zhou
LYLi Yuan
Li Yuan
YLYanfeng Li
Yanfeng Li
JYJiannan Yu
Jiannan Yu
Background: Intraoral scans (IOS) provide precise 3D data of dental crowns and gingival structures. This paper explores an application of IOS in human identification. Methods: We propose a dental biometrics framework for human identification using 3D dental point clouds based on machine learning-related algorithms, encompassing three stages: data preprocessing, feature extraction, and registration-based identification. In the data preprocessing stage, we use the curvature principle to extract distinguishable tooth crown contours from the original point clouds as the holistic feature identification samples. Based on these samples, we construct four types of local feature identification samples to evaluate identification performance with severe teeth loss. In the feature extraction stage, we conduct voxel downsampling, then extract the geometric and structural features of the point cloud. In the registration-based identification stage, we construct a coarse-to-fine registration scheme in order to realize the identification task. Results: Experimental results on a dataset of 160 individuals demonstrate that our method achieves a Rank-1 recognition rate of 100% using complete tooth crown contours samples. Utilizing the remaining four types of local feature samples yields a Rank-1 recognition rate exceeding 96.05%. Conclusions: The proposed framework proves effective for human identification, maintaining high identification performance even in extreme cases of partial tooth loss.

1 February 2025 in Bioactive Materials
Verified
Journal Article
Open access
JXJing Xu
Jing Xu
ZZZhenbao Zhang
Zhenbao Zhang
JWJianhui Wang
Jianhui Wang
YQYuhan Qi
Yuhan Qi
XQXiaohong Qi
Xiaohong Qi
YLYanfeng Li
Yanfeng Li
Zn-based biodegradable metals (BMs) are regarded as revolutionary biomaterials for bone implants. However, their clinical application is limited by insufficient mechanical properties, delayed in vivo degradation, and overdose-induced Zn2+ toxicity. Herein, innovative multi-material additive manufacturing (MMAM) is deployed to construct a Zn/titanium (Ti) hetero-structured composite. The biodegradation and biofunction of Zn exhibited intriguing characteristics in composites. A potential difference of about 300 mV naturally existed between Zn and Ti. This natural potential difference triggered galvanic coupling corrosion, resulting in 2.7 times accelerated degradation of Zn. The excess release of Zn2+ induced by accelerated degradation enhanced the antibacterial function. A voltage signal generated by the natural potential difference also promoted in vitro osteogenic differentiation through activating the PI3K-Akt signaling pathway, and inhibited the toxicity of overdose Zn2+in vivo, significantly improving bone regeneration. Furthermore, MMAM technology allows for the specific region deployment of components. In the future, Ti and Zn could be respectively deployed in the primary and non-load-bearing regions of bone implants by structural designs, thereby achieving a functionally graded application to overcome the insufficient mechanical properties of Zn-based BMs. This work clarifies the functional optimization mechanism for multimetal bone implants, which possibly breaks the application dilemma of Zn-based BMs.

21 April 2026 in Frontiers in Pharmacology
Verified
Journal Article
Open access
PDF file
YQYuhan Qi
Yuhan Qi
QFQue Feng
Que Feng
YWYan Wu
Yan Wu
JXJing Xu
Jing Xu
XZXin Zhang
Xin Zhang
YLYanfeng Li
Yanfeng Li
Background: Delayed healing of maxillofacial soft tissue wounds is closely associated with inffammatory injury and mitochondrial dysfunction in fibroblasts, while effective therapeutic strategies remain limited. This study investigated whether activation of the mechanosensitive ion channel Piezo1 by Yoda1 could promote wound healing. Methods: An LPS-induced inflammatory model was established in human gingival fibroblasts (HGFs) and treated with Yoda1. Intracellular calcium influx, cell viability, oxidative stress, mitochondrial membrane potential, apoptosis, migration, wound closure, and type I collagen expression were assessed. The involvement of the PINK1/Parkin-mediated mitophagy pathway was analyzed. An in vivo inflammatory wound model was used to evaluate therapeutic efficacy. Results: Yoda1 significantly increased intracellular calcium influx, improved cell viability, reduced oxidative stress, restored mitochondrial membrane potential, and inhibited apoptosis in LPS-treated HGFs. It also enhanced HGFs migration, wound closure, and type I collagen expression in vitro . Mechanistically, these effects were associated with activation of the PINK1/Parkin-mediated mitophagy pathway. In vivo , Yoda1 accelerated wound closure, accompanied by increased collagen deposition and improved tissue regeneration. Conclusion: Activation of Piezo1 by Yoda1 can alleviate its inflammatory damage by restoring mitochondrial homeostasis and regulating the cellular functions of HGFs. Piezo1 may be a promising therapeutic target for promoting maxillofacial wound repair.