Personalized Porous Gelatin Methacryloyl Sustained-Release Nicotinamide Protects Against Noise-Induced Hearing Loss.
Baoyi FengTingting DongXinyu SongXiaofei ZhengChenxi JinZhenzhe ChengYiqing LiuWenjie ZhangXueling WangYong TaoHao WuPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
There are no Food and Drug Administration-approved drugs for treating noise-induced hearing loss (NIHL), reflecting the absence of clear specific therapeutic targets and effective delivery strategies. Noise trauma is demonstrated results in nicotinamide adenine dinucleotide (NAD+) downregulation and mitochondrial dysfunction in cochlear hair cells (HCs) and spiral ganglion neurons (SGNs) in mice, and NAD+ boosted by nicotinamide (NAM) supplementation maintains cochlear mitochondrial homeostasis and prevents neuroexcitatory toxic injury in vitro and ex vivo, also significantly ameliorated NIHL in vivo. To tackle the limited drug delivery efficiency due to sophisticated anatomical barriers and unique clearance pathway in ear, personalized NAM-encapsulated porous gelatin methacryloyl (PGMA@NAM) are developed based on anatomy topography of murine temporal bone by micro-computed tomography and reconstruction of round window (RW) niche, realizing hydrogel in situ implantation completely, NAM sustained-release and long-term auditory preservation in mice. This study strongly supports personalized PGMA@NAM as NIHL protection drug with effective inner ear delivery, providing new inspiration for drug-based treatment of NIHL.
Keyphrases
- hearing loss
- drug delivery
- drug administration
- tissue engineering
- computed tomography
- drug induced
- air pollution
- high glucose
- hyaluronic acid
- diabetic rats
- oxidative stress
- induced apoptosis
- high fat diet induced
- bone regeneration
- spinal cord
- cell proliferation
- type diabetes
- bone mineral density
- metal organic framework
- spinal cord injury
- highly efficient
- neuropathic pain
- cell death
- emergency department
- metabolic syndrome
- soft tissue
- endoplasmic reticulum stress
- optical coherence tomography