Biosynthesis of gold nanoparticles, characterization and their loading with zonisamide as a novel drug delivery system for the treatment of acute spinal cord injury

التفاصيل البيبلوغرافية
العنوان: Biosynthesis of gold nanoparticles, characterization and their loading with zonisamide as a novel drug delivery system for the treatment of acute spinal cord injury
المؤلفون: Wenbin Zhang, Chao Jiang, Hongjie Li, Ziping Ma, Chunyang Fang, Liqiu Chen
المصدر: Journal of photochemistry and photobiology. B, Biology. 190
سنة النشر: 2018
مصطلحات موضوعية: 030303 biophysics, Biophysics, Nanoparticle, Metal Nanoparticles, 02 engineering and technology, Cell Line, 03 medical and health sciences, Drug Delivery Systems, Spectroscopy, Fourier Transform Infrared, Animals, Radiology, Nuclear Medicine and imaging, Fourier transform infrared spectroscopy, Solubility, Spinal Cord Injuries, 0303 health sciences, Radiation, Radiological and Ultrasound Technology, Chemistry, Green Chemistry Technology, 021001 nanoscience & nanotechnology, Calcium Channel Blockers, Rats, Kinetics, Transmission electron microscopy, Colloidal gold, Zonisamide, Drug delivery, Acute Disease, Particle size, Gold, Selected area diffraction, 0210 nano-technology, Nuclear chemistry
الوصف: In the present work, a facile biosynthetic approach for the synthesis of AuNPs using bark extract of Juglans regia (J. regia) is reported. Ultra-violet visible (UV–vis) absorption spectroscopic studies exhibited and narrow SPR absorption band at 540 nm, represented the isotropy in particle size. The transmission electron microscopy (TEM) and X-ray diffraction (XRD) analysis, confirmed the fabrication of spherical and crystalline nanoparticles of average size of about 14 nm. Also, typical characteristic selected area electron diffraction (SAED) pattern showed the crystalline nature of AuNPs. The prepared AuNPs were loaded with zonisamide which can be used for future spinal cord injury repair applications. The fourier transform infrared spectroscopy (FTIR) analysis represented the zonisamide loading onto AuNPs. The biological preparation of AuNPs using the bark extract of J. regia is prominent approach because of its eco friendly nature without using any toxic chemicals. The controlled-release of zonisamide-AuNPs was about 43.0 ± 2.2 nm with high stability and solubility under room temperature conditions. Further, the cytotoxicity results showed the comparatively higher toxicity of zonisamide-AuNPs towards CTX TNA2 cells than free zonisamide. Hence, zonisamide-AuNPs may act as very good clinical drug for future therapeutic treatment of spinal cord injury.
تدمد: 1873-2682
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28706e6969c462b15618c85b5b52fc40
https://pubmed.ncbi.nlm.nih.gov/30502587
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....28706e6969c462b15618c85b5b52fc40
قاعدة البيانات: OpenAIRE