Scopus
🔓 Açık Erişim YÖKSİS DOI Eşleşti
SJR Q3
Evaluation of Dual Effect of Sodium Borohydride (NaBH4) as a Reducing and Crosslinking Agent for Development of Novel Silver Nanoparticles (AgNPs) Loaded Chitosan-Poly (Vinyl Alcohol) (CS-PVA) Hydrogels for Wound Healing Activity
Journal of Pharmaceutical Innovation · Haziran 2026
Özet
Purpose: Hydrogels are three-dimensional, crosslinked polymeric systems with high hydrophilicity and biocompatibility, making them ideal materials for wound healing applications. In this study, a silver nanoparticle (AgNP)-loaded chitosan–poly (vinyl alcohol) (CS–PVA) hydrogel was developed using a novel, simple, and cost-effective approach. In this approach, sodium borohydride (NaBH₄) simultaneously acts as a reducing agent for AgNP synthesis and as a physical crosslinking agent for hydrogel formation. Methods: AgNPs were synthesized via NaBH₄-mediated reduction and characterized by dynamic light scattering and UV–Vis spectroscopy. The resulting hydrogels were evaluated by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), Energy-dispersive X-ray (EDS) spectroscopy, swelling, porosity and mechanical test. In vitro biocompatibility and wound healing potential were assessed using cell viability assays and a scratch wound assay. Results: Among all formulations, M30, an AgNP-loaded CS–PVA hydrogel, prepared with medium molecular weight (MMW) chitosan and 30 mL of AgNP suspension, had the best overall performance with the highest swelling degree, favorable mechanical performance. It maintained cell viability above 80% at 24 and 48 h, and showed the greatest wound closure rate, even at low AgNP concentration. Conclusion: The results demonstrate that AgNP-loaded CS–PVA hydrogels prepared using NaBH₄ as a dual-function agent exhibit promising biocompatibility and wound healing potential even at low AgNP content. To the best of our knowledge, this study is the first to demonstrate the dual functionality of NaBH₄ in a single-step approach as both a reducing and physical crosslinking agent, providing a simple and promising strategy for the development of next-generation wound dressing materials without need for additional chemical crosslinkers.
YÖKSİS Kayıtları
Evaluation of Dual Effect of Sodium Borohydride (NaBH4) as a Reducing and Crosslinking Agent for Development of Novel Silver Nanoparticles (AgNPs) Loaded Chitosan-Poly (Vinyl Alcohol) (CS-PVA) Hydrogels for Wound Healing Activity
Journal of Pharmaceutical Innovation · 2026 SCI-Expanded
Dr. Öğr. Üyesi YAKUP GÜLTEKİN →
YÖKSİS Kayıtları — ISSN Eşleşmesi
Bu dergide (ISSN eşleşmesi) kurumun 4 kaydı bulundu.
YÖKSİS Kayıtları — ISSN Eşleşmesi
Bu dergide (ISSN eşleşmesi) kurumun 4 kaydı bulundu.
Evaluation of Dual Effect of Sodium Borohydride (NaBH4) as a Reducing and Crosslinking Agent for Development of Novel Silver Nanoparticles (AgNPs) Loaded Chitosan-Poly (Vinyl Alcohol) (CS-PVA) Hydrogels for Wound Healing Activity
2026 ISSN: 1872-5120 SCI-Expanded Q2
Dr. Öğr. Üyesi YAKUP GÜLTEKİN →
Development of Film Formulations of Acyclovir as Safe and Effective Antiviral Agent: Optimization, In Vitro Characterization and Antialphaherpesviral Efficacy
2026 ISSN: 1872-5120 SCI-Expanded Q2
Dr. Öğr. Üyesi DİLARA ÖRGÜL →
Preparation and Evaluation of Nicotine and Quercetin Loaded Polyvinyl Alcohol Nanofiber Wound Dressings
2025 ISSN: 1872-5120 SCI-Expanded Q2
Dr. Öğr. Üyesi YAKUP GÜLTEKİN →
Preparation and Evaluation of Nicotine and Quercetin Loaded Polyvinyl Alcohol Nanofiber Wound Dressings
2025 ISSN: 1872-5120 SCI-Expanded Q2
Dr. Öğr. Üyesi DİLARA ÖRGÜL →
Makale Bilgileri
Toplam Atıf
0 atıf
· Scopus
ISSN18725120
Yayın TarihiHaziran 2026
Cilt / Sayfa21
Scopus ID2-s2.0-105033882393
Erişim🔓 Açık Erişim
Kurumlar
Hacettepe Üniversitesi
Ankara Turkey
Hitit University
Corum Turkey
Inönü Üniversitesi
Malatya Turkey
Selçuk Üniversitesi
Selçuklu Turkey
Yeditepe University
Istanbul Turkey
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Scimago Dergi (ISSN Eşleşmesi)
Journal of Pharmaceutical Innovation
Q3
SJR Skoru0,367
H-Index43
YayıncıSpringer
ÜlkeUnited States
Drug Discovery (Q3)
Pharmaceutical Science (Q3)