Heng Zheng
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Heng Zheng has a total of 21 co-authors. Here are the top co-authors by number of shared publications:
- Guoyu Lv
College of physics, Sichuan University, Chengdu 610065, China
3 shared publications - Aiping Yang
College of physics, Sichuan University, Chengdu 610065, China
2 shared publications - Hong Li
College of physics, Sichuan University, Chengdu 610065, China
2 shared publications Junqin Mao
College of Physics, Sichuan University , Chengdu 610065
2 shared publicationsAiping Yang
College of physics, Sichuan University, Chengdu 610065, China
1 shared publication- Guoyu Lv
College of Physics, Sichuan University , Chengdu 610065
1 shared publication
Latest Publications
- Open Access
- 22 January 2026
- Published by Oxford University Press (OUP) in Regenerative Biomaterials
- Vol. 13
Electrospun PPDO-BG/PVDF fibrous membranes with piezoelectric synergistic bioactive ion controlled release for enhanced bone repair
Bone defects caused by trauma, infection or tumors remain challenging in clinics. Conventional methods cannot simultaneously regulate the electrical microenvironment, ionic microenvironment and extracellular matrix (ECM) microenvironment during osteogenesis. This study reports a piezoelectric and bioactive glass (BG)-loaded fibrous membrane (PVO) fabricated via electrospinning from polyvinylidene fluoride (PVDF) and poly(p-dioxanone) (PPDO). The PVDF component provides piezoelectric stimulation to build the electrical microenvironment, while BG-loaded PPDO enables sustained ion release to optimize the ionic microenvironment. The fibrous structure mimics the ECM microenvironment. In vitro osteogenic differentiation experiments using bone marrow mesenchymal stem cells (BMSCs) showed that the PVO fibrous membrane doped with 0.5% BG exhibited the highest alkaline phosphatase (ALP) content after 14 days of electrical stimulation combined with BG treatment, with substantial calcium nodules formed by day 21. In vivo implantation experiments in rat skull defect models further validated its therapeutic potential, with new bone formation observed in the PVO-0.5 group up to day 28. Its structure, piezoelectric performance and ion release synergistically improve osteogenic activity, making the PVO membrane an ideal scaffold for bone tissue engineering and providing an effective solution for bone repair.
- 22 January 2026
- Published by Oxford University Press (OUP) in Regenerative Biomaterials
- Vol. 13
Open AccessElectrospun PPDO-BG/PVDF fibrous membranes with piezoelectric synergistic bioactive ion controlled release for enhanced bone repair
Bone defects caused by trauma, infection or tumors remain challenging in clinics. Conventional methods cannot simultaneously regulate the electrical microenvironment, ionic microenvironment and extracellular matrix (ECM) microenvironment during osteogenesis. This study reports a piezoelectric and bioactive glass (BG)-loaded fibrous membrane (PVO) fabricated via electrospinning from polyvinylidene fluoride (PVDF) and poly(p-dioxanone) (PPDO). The PVDF component provides piezoelectric stimulation to build the electrical microenvironment, while BG-loaded PPDO enables sustained ion release to optimize the ionic microenvironment. The fibrous structure mimics the ECM microenvironment. In vitro osteogenic differentiation experiments using bone marrow mesenchymal stem cells (BMSCs) showed that the PVO fibrous membrane doped with 0.5% BG exhibited the highest alkaline phosphatase (ALP) content after 14 days of electrical stimulation combined with BG treatment, with substantial calcium nodules formed by day 21. In vivo implantation experiments in rat skull defect models further validated its therapeutic potential, with new bone formation observed in the PVO-0.5 group up to day 28. Its structure, piezoelectric performance and ion release synergistically improve osteogenic activity, making the PVO membrane an ideal scaffold for bone tissue engineering and providing an effective solution for bone repair.
- Open Access
- 26 December 2025
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 27 (1) , 276
Polyethylene Glycol (PEG)-Based Wet-Adhesive Absorbable Bone Wax for Osseous Hemostasis and Repair
The non-absorbability and biological inertia of traditional bone wax often result in foreign body retention, inhibit bone healing, and increase the risk of infection. Herein, a novel absorbable bone wax was developed by mixing polyethylene glycol (PEG), tannic acid (TA), sodium carboxymethyl cellulose (CMC), and low-molecular-weight poly-L-lactic acid (PLLA) via one-pot method. Among them, PEG functions as the matrix, endowing it with plasticity and hydrophilicity, thereby facilitating its facile, close fit to the surface of bone defects. TA, with its profusion of phenolic hydroxyl groups, bestows the material with exceptional adhesion properties. The hydroxyl and carboxyl groups in the CMC molecular structure are capable of forming hydrogen bond networks with PEG and TA. Concurrently, hydrophobic PLLA reinforces the hydrogen bond network structure. Absorbable bone wax maintains excellent adhesion in water. The obtained wax shows an adhesion strength of 27.07 kPa and can maintain adhesion to pig bone for 6.0 h in an aqueous environment. In particular, after being soaked in water for 24 h, the bone wax only dissolves on the surface, while the core remains intact. The results of the porcine sternum implantation experiment showed that the hemostatic performance of this bone wax was comparable to that of non-absorbable bone wax. Furthermore, the absorbable bone wax was gradually absorbed, leading to better bone tissue healing. This absorbable formulation could eliminate the 5–15% infection rate associated with traditional bone wax.
- 26 December 2025
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 27 (1) , 276
Open AccessPolyethylene Glycol (PEG)-Based Wet-Adhesive Absorbable Bone Wax for Osseous Hemostasis and Repair
The non-absorbability and biological inertia of traditional bone wax often result in foreign body retention, inhibit bone healing, and increase the risk of infection. Herein, a novel absorbable bone wax was developed by mixing polyethylene glycol (PEG), tannic acid (TA), sodium carboxymethyl cellulose (CMC), and low-molecular-weight poly-L-lactic acid (PLLA) via one-pot method. Among them, PEG functions as the matrix, endowing it with plasticity and hydrophilicity, thereby facilitating its facile, close fit to the surface of bone defects. TA, with its profusion of phenolic hydroxyl groups, bestows the material with exceptional adhesion properties. The hydroxyl and carboxyl groups in the CMC molecular structure are capable of forming hydrogen bond networks with PEG and TA. Concurrently, hydrophobic PLLA reinforces the hydrogen bond network structure. Absorbable bone wax maintains excellent adhesion in water. The obtained wax shows an adhesion strength of 27.07 kPa and can maintain adhesion to pig bone for 6.0 h in an aqueous environment. In particular, after being soaked in water for 24 h, the bone wax only dissolves on the surface, while the core remains intact. The results of the porcine sternum implantation experiment showed that the hemostatic performance of this bone wax was comparable to that of non-absorbable bone wax. Furthermore, the absorbable bone wax was gradually absorbed, leading to better bone tissue healing. This absorbable formulation could eliminate the 5–15% infection rate associated with traditional bone wax.
- Open Access
- 14 May 2025
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 26 (10) , 4688
A Biomimetic Adhesive/Kaolin Material with Strong Adhesion, Sealing, and Active Coagulation Function for Arterial Hemostasis
Effective prehospital hemostasis is pivotal for improving survival outcomes in arterial hemorrhage. Existing hemostatic materials have limitations in terms of both efficiency and portability, particularly under complex wound conditions. This study engineered a kaolin-reinforced biomimetic adhesive composite powder (DTG-K), which achieved dual hemostatic mechanisms: mechanical occlusion via strong interfacial adhesion (lap-shear strength of 58.3 kPa) and biochemical activation of the intrinsic coagulation pathway through factor XII. In vitro evaluations confirmed its exceptional hemocompatibility, with a 0.93% hemolysis rate. When applied to femoral artery hemorrhage models in Bama swine, DTG-K demonstrated complete hemostasis within 30 s through synergistic physical sealing and biochemical coagulation. These findings demonstrate the potential of DTG-K as an innovative strategy for managing life-threatening arterial hemorrhage in prehospital emergency scenarios.
- 14 May 2025
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 26 (10) , 4688
Open AccessA Biomimetic Adhesive/Kaolin Material with Strong Adhesion, Sealing, and Active Coagulation Function for Arterial Hemostasis
Effective prehospital hemostasis is pivotal for improving survival outcomes in arterial hemorrhage. Existing hemostatic materials have limitations in terms of both efficiency and portability, particularly under complex wound conditions. This study engineered a kaolin-reinforced biomimetic adhesive composite powder (DTG-K), which achieved dual hemostatic mechanisms: mechanical occlusion via strong interfacial adhesion (lap-shear strength of 58.3 kPa) and biochemical activation of the intrinsic coagulation pathway through factor XII. In vitro evaluations confirmed its exceptional hemocompatibility, with a 0.93% hemolysis rate. When applied to femoral artery hemorrhage models in Bama swine, DTG-K demonstrated complete hemostasis within 30 s through synergistic physical sealing and biochemical coagulation. These findings demonstrate the potential of DTG-K as an innovative strategy for managing life-threatening arterial hemorrhage in prehospital emergency scenarios.
- 17 September 2024
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 280 (Pt 4) , 135722
A self-gelling alginate/chitosan based powder containing bioactive nanoparticles for non-compressible bleeding control and promoting wound healing
- 17 September 2024
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 280 (Pt 4) , 135722
A self-gelling alginate/chitosan based powder containing bioactive nanoparticles for non-compressible bleeding control and promoting wound healing