Injectable, Antibacterial, and Hemostatic Tissue Sealant Hydrogels

Author:

Haghniaz Reihaneh123,Montazerian Hossein123,Rabbani Atiya234,Baidya Avijit56,Usui Brent17,Zhu Yangzhi1,Tavafoghi Maryam23,Wahid Fazli8,Kim Han‐Jun19,Sheikhi Amir1011ORCID,Khademhosseini Ali1

Affiliation:

1. Terasaki Institute for Biomedical Innovation 11570 W Olympic Blvd Los Angeles CA 90024 USA

2. Department of Bioengineering University of California, Los Angeles 410 Westwood Plaza Los Angeles CA 90095 USA

3. California NanoSystems Institute University of California, Los Angeles 570 Westwood Plaza Los Angeles CA 90095 USA

4. Akhtar Saeed Medical College Bahria Golf City 46000 Pakistan

5. Department of Chemical and Biomolecular Engineering University of California, Los Angeles Los Angeles CA 90095 USA

6. Department of Chemistry Faculty of Engineering and Technology SRM Institute of Science and Technology Kattankulathur Tamil Nadu 603203 India

7. Franklin W. Olin College of Engineering 1000 Olin Way Needham MA 02492 USA

8. Department of Biomedical Sciences Pak‐Austria Fachhochschule Institute of Applied Sciences and Technology Haripur 22620 Pakistan

9. College of Pharmacy Korea University Sejong 30019 Republic of Korea

10. Department of Chemical Engineering The Pennsylvania State University University Park PA 16802 USA

11. Department of Biomedical Engineering The Pennsylvania State University University Park PA 16802 USA

Abstract

AbstractHemorrhage and bacterial infections are major hurdles in the management of life‐threatening surgical wounds. Most bioadhesives for wound closure lack sufficient hemostatic and antibacterial properties. Furthermore, they suffer from weak sealing efficacy, particularly for stretchable organs, such as the lung and bladder. Accordingly, there is an unmet need for mechanically robust hemostatic sealants with simultaneous antibacterial effects. Here, an injectable, photocrosslinkable, and stretchable hydrogel sealant based on gelatin methacryloyl (GelMA), supplemented with antibacterial zinc ferrite (ZF) nanoparticles and hemostatic silicate nanoplatelets (SNs) for rapid blood coagulation is nanoengineered. The hydrogel reduces the in vitro viability of Staphylococcus aureus by more than 90%. The addition of SNs (2% w/v) and ZF nanoparticles (1.5 mg mL−1) to GelMA (20% w/v) improves the burst pressure of perforated ex vivo porcine lungs by more than 40%. Such enhancement translated to ≈250% improvement in the tissue sealing capability compared with a commercial hemostatic sealant, Evicel. Furthermore, the hydrogels reduce bleeding by ≈50% in rat bleeding models. The nanoengineered hydrogel may open new translational opportunities for the effective sealing of complex wounds that require mechanical flexibility, infection management, and hemostasis.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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