Janus Nanocomposite for Enhanced Bone Tissue Engineering: Polyurethane Nanofibers with Zoledronic Acid-Silk Fibroin and Silver-Infused Chitosan Hydrogel

被引:0
作者
Khan, Rumysa Saleem [1 ]
Wani, Taha Umair [2 ,3 ]
Tramboo, Maida Lateef [1 ]
Khan, Anees Ellahi [1 ]
Rather, Anjum Hamid [1 ]
Shafi, Hasham [4 ]
Rafiq, Muheeb [1 ]
Rather, Sami-ullah [5 ]
Sheikh, Faheem A. [1 ]
机构
[1] Univ Kashmir, Dept Nanotechnol Nanostruct & Biomimet Lab, Srinagar 190006, Jammu And Kashm, India
[2] Jeonbuk Natl Univ Hosp, Biomed Res Inst, Nonclin Evaluat Ctr, Jeonju 54907, Jeollabuk Do, South Korea
[3] Res Inst Pharmaceut Sci, Coll Pharm, Jinju 52828, Gyeongsang, South Korea
[4] Florida Int Univ, Ctr Translat Sci, Port St Lucie, FL 34987 USA
[5] King Abdulaziz Univ, Dept Chem & Mat Engn, Jeddah 21589, Saudi Arabia
关键词
drug loadings; hydrogels; nanofibers; silk fibroin; zoledronic acid; DRUG-DELIVERY; IN-VITRO; ANTIMICROBIAL ACTIVITY; COMPOSITE NANOFIBERS; NANOPARTICLES; SCAFFOLDS; RELEASE; CELLS; BISPHOSPHONATE; EFFICACY;
D O I
10.1002/adem.202402466
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This work presents a hybrid material composed of a physically cross-linked poly(vinyl alcohol)/chitosan hydrogel with a pore size of 35 +/- 10 nm loaded with silver (Ag) nanoparticles (NPs) with a diameter of 83.4 nm. This hydrogel is physically integrated with polyurethane (PU) nanofibers with an average diameter of 0.93 +/- 0.5 mu m that is preloaded with silk fibroin (SF)-encapsulated zoledronic acid (ZA) NPs (99.11 nm). However, the hybrid composites are hydrophilic, showing contact angles of <90(o) due to incorporating hydrogel and NPs. Ultraviolet-visible spectrophotometry demonstrates a burst release of ZA from SF NPs within the first 6 h, followed by sustained release up to 48 h, after which the release rate declined. The degradation of hybrid composites in phosphate-buffered saline (PBS), protease type XIV, and human plasmin shows an increased degradation in the enzyme solutions of protease type XIV (42.6 +/- 1.4%) and plasmin (52.6 +/- 1.1%) than PBS (27.5 +/- 1.9%) after 40 days. Biocompatibility is assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide and staining, revealing viability of >300% and a higher cell density than the pure PU scaffold. These results suggest that the composite scaffolds offer a highly effective release of loaded NPs are suitable for healthcare products and devices for tissue engineering applications, especially deep wound defects involving bone injuries.
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页数:22
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