Abstract
Auditory diseases are disabling public health problems that afflict a significant number of people worldwide, and they remain largely incurable until now. Driven by continuous innovation in the fields of chemistry, physics, and materials science, novel materials that can be applied to hearing diseases are constantly emerging. In contrast to conventional materials, new materials are easily accessible, inexpensive, non-invasive, with better acoustic therapy effects and weaker immune rejection after implantation. When new materials are used to treat auditory diseases, the wound healing, infection prevention, disease recurrence, hair cell regeneration, functional recovery, and other aspects have been significantly improved. Despite these advances, clinical success has been limited, largely due to issues regarding a lack of effectiveness and safety. With ever-developing scientific research, more novel materials will be facilitated into clinical use in the future.
Introduction
According to the latest World Health Organization estimates, 466 million people around the world (over 5% of the world population) experience disabling hearing loss. By 2050, this number is projected to rise to approximately 900 million, and nearly 2.5 billion people are at risk of contracting auditory diseases (World Health Organization [WHO], 2021). The early detection, vaccination, accurate management, and timely treatment of auditory diseases can help improve clinical outcome. Nevertheless, therapeutic modalities and prevention strategies for the occurrence and development of auditory diseases are still limited currently. Hearing impairment caused by auditory diseases is categorized into three clinical types: conductive (CHL), sensorineural (SNHL), and mixed (MHL) hearing loss. CHL is known to result primarily from structural damage, blockage, and sclerosis of the outer and middle ear, eventually leading to aberrant signaling to the inner ear. Disruption of the inner ear, auditory nerve, central auditory nuclei, or cortex are classified as SNHL, with an elaborate pathology that includes loss of sensory hair cells, spiral ganglion neurons (SGNs), and stria vascularis cells in the inner ear, ultimately leading to the failure of auditory perception (). The established therapy for patients suffering from conductive deafness focuses on middle-ear infection, otosclerosis, etc. Research on curative therapies for sensorineural hearing loss mainly focuses on the repair and regeneration of hair cells, stria vascularis, and nerve synapses.
The practical application of new materials is continuously undergoing considerable advancements, and substantial success has been achieved in some aspects. Whereas the new materials are being applied to treat auditory diseases, the abundant advances made in the fields of diabetes, cardiovascular disease, and neuromuscular disease using new materials are progressing. Recently, the Food and Drug Administration (FDA) approved the first RNA interference-based gene silencing technology drug—Patisiran—which regulates gene expression by the delivery of RNA to target cells, improving the prognosis of patients with rare cardiac and neurologic disease (). For another example, with a fundamental role in the future repair or replacement of tissues defects (Zakrzewski et al., 2019), stem cells differentiate into insulin-producing cells after being implanted into the body, bringing considerable improvements to the prognosis of type 1 diabetes (). Regarding to stem cell therapy, graphene, with remarkable biocompatible and bioadhesive properties, can be fabricated as scaffolds for the proliferation and direct differentiation of stem cells (). Some scholars even propose stem cell engraftment as a highly feasible and fundamental curing method for sensorineural deafness (; ). Many prostheses formed out of new materials were reported to induce fewer immune responses and had a better overall prognosis than conventional materials after implantation (; ). This review will focus on the research progress of the novel materials employed for the treatment of CHL and SNHL (see Figure 1).
FIGURE 1
Treatment Orientation of Hearing Loss
Hearing loss is attributable to genetic factors, specific viral infections, chronic ear infections, birth complications, exposure to excessive noise, aging, and ototoxic drugs. CHL may occur as middle-ear effusion, tympanic membrane perforation, physical external trauma, infection, canal stenosis, cholesteatoma, otitis media, otosclerosis, ossicular erosions, and so on (). At present, treatment for CHL primarily involves surgery and drugs. Primary research directions for novel therapies are focused on new pharmaceuticals, materials, artificial auditory implantation, and other aspects. The artificial auditory implantation comprises middle-ear implant (MEI) and implantable bone-conduction devices (). The current widespread adoption of artificial auditory implantation includes bone-anchored hearing aids (BAHAs), subcutaneous bone bridges (BBs), vibrant sound bridges (VSBs), and semi-implantable middle-ear transducers. However, due to the pathway for bone conduction being more complex than air conduction, the following areas must be considered: percutaneous attenuation of high-frequency sound after the implantation of bone-conduction hearing aid devices; the susceptibility to infection of surgical sites after BAHA implantation; vibrator displacement after MEI implantation; ossicular necrosis; the wide fluctuation of postoperative gain, and so on. Therefore, further research aimed at bone-conduction audiology and more development of audiological assist devices are still required ().
Diseases that could contribute to SNHL are age-related hearing loss (ARHL), inherited hearing impairments, Meniere’s disease (endolymphatic hydrops), autoimmune inner-ear disease, ear infection, drug-induced deafness, ear trauma, and idiopathic SNHL (; ). In addressing sudden sensorineural hearing loss (SSNHL), current SSNHL management guidelines recommend glucocorticoids, psychotherapy, and intravenous agents that can improve microcirculation and neurotrophy, besides which numerous attempts for novel therapies have been reported. For instance, Vanwijck et al. (2019) summarized the efficacy of intratympanic injections of corticosteroids with a Silverstein tube to treat refractory SSNHL. They found that the topical application of corticosteroids with such a tube to the inner ear through the round window membrane can improve the hearing and clarity of patients who have failed in previous conventional therapies. However, therapies for SNHL remain clinically limited thus far, and the therapeutic effects remain less than satisfactory. Owing to the natural anatomical and physiological barriers of the cochlea, the supply and absorption of drugs reaching the targeting cochlea cells have been severely hindered (Zou et al., 2016; Yuan and Qi, 2018). An example is that the cochlea, surrounded by bones and located in a relatively closed environment, is difficult for drugs to access from the blood due to the presence of the blood labyrinth barrier (BLB). For local drug delivery to the cochlea, drug penetration through the oval window (OW) and round window membrane (RWM) becomes difficult due to their permselectivity. In addition, some of the drugs have a short half-life, and inter-individual differences in metabolism are marked, therefore limiting the benefits of drugs administered using traditional approaches.
In recent years, a range of new signaling pathways and genes playing essential roles in hair cell development and differentiation have been discovered that target therapies against SNHL (). For example, overexpressing Atoh1 can potentially reprogram supporting cells to become hair cells, subsequently promoting mammalian hair cell regeneration (). In cell cycle regulation, the absence of p27Kip1 drives the enhanced proliferation of supporting cells in adult mice, and inactivation of the retinoblastoma 1 (RB1) gene leads to the acquisition of newly generated hair cells originated from highly differentiated hair cells (). For other signaling pathways, the activator of the Wnt signal pathway—β-catenin, the overexpression of which triggers Lgr5-positive cell growth and mitosis—elevates hair cell regeneration (). When β-catenin and Atoh1 are co-expressed, the differentiation of Lg5-positive hair cells in neonatal mice is significantly advanced (). Furthermore, inhibition of the Notch pathway via γ-secretase inhibitors enables mice to regenerate hair cells in response to noise-induced damage, simultaneously gaining an improvement in their hearing level (). Furthermore, there is crosstalk between Notch and Wnt signaling (; ). Hence, various predictions can be hypothesized based on these theories; that is, gene targets that can be selectively modulated using small molecules or related drugs might drive the regeneration of hair cells.
Application of Novel Materials in Hearing Loss
Treatment of New Materials in Conductive Hearing Loss
In auricle-related disorders, the microtia is a congenital craniofacial malformation, ranking only second to cleft lip (). Traditional healing strategies employ autologous cartilage as conventional grafts (). used 3D printing technology and medical silicone to fabricate an auricular scaffold, and they found the scaffolds were implanted in vivo smoothly, with excellent bio-compatibility, affordable cost, and a simple preparation process. Presently, besides adipose-derived stem cell (ADSC) application for cartilage regeneration, cartilage stem/progenitor cells (CSPCs) have also been used for the successful ear reconstruction and modeling the pathogenesis of auricular deformities (Zhou G. et al., 2018; Zucchelli et al., 2020).
In tympanic-associated disorders, tympanic membrane perforation (TMP) is a commonly seen disease in otorhinolaryngology. Although the preferred autograft materials, such as temporal muscle, cartilage, and fat, have a variety of applications, they have also been reported to be highly susceptible to infection and have pronounced dependence on nutrients from the surrounding tissue (Teh et al., 2013). Therefore, an increasing emphasis is being placed on new materials that can decrease the rate of inflammation, foster tympanic membrane regeneration, and enhance the proliferation and migration of the epithelium. The current methods for tympanic membrane repair combine autologous tissue and novel materials, the latter including platelet-rich plasma (PRP), platelet-rich fibrin (PRF), hyaluronic acid (HA), epidermal growth factor (EGF), and basic fibroblast growth factor (bFGF). Among them, PRP and PRF have gained particular interest because they are enriched in growth factors, which are effective in inducing tissue regeneration and with a lower prevalence of infections (; ; ). Moreover, a study by found that recombinant human epidermal growth factor (rhEGF) in conjunction with a gelatin-based sponge scaffold can remarkably enhance the wound healing rate of chronic TMP, reduce improvement time, further improve hearing level, and has no toxic side effects on inner-ear function. Similar multiple studies have been performed for combining new materials into clinical practice, and correspondingly, an increased likelihood of TMP healing has been reported (). For example, heparin-binding epidermal growth factor (EGF)-like growth factor (), EGF-released nanofibrous patches (), bacterial cellulose (), chitosan patch scaffolds incorporated with insulin-like growth factor-binding protein 2 (), and a fibroblast growth factor (FGF)-infiltrated gelatin sponge (; ) have been documented to accelerate tympanic membrane (TM) perforation healing. As a type of novel material, have also reported that mesenchymal stem cells (MSCs) are promising candidates for therapy to treat TMP. Either separate engraftment of multipotent MSCs or a combination of these cells with biological materials and growth factors (GFs) can achieve faster TMP healing via increasing the activation of epidermal stem cell markers and stimulating the proliferation and migration of keratinocytes. MSCs, scaffolds, and GFs have a synergistic role in TM regeneration. The recent advancement of 3D- and 4D-printing technology has driven the development of a precise MSC-attached scaffold designed for the physical structure of patients. The direction of physical and chemical engineering may be incorporated in this advancement, further boosting the degree and rate of the target tissue regeneration (). The introduction of a cobalt-chromium (Co-Cr) coronary stent into the eustachian tube potentiates middle-ear ventilation, as validated in sheep (). A new class of tympanostomy stent made of nickel and titanium with a TiO2 coating has previously been shown to reduce Pseudomonas aeruginosa biofilm formation, resulting in a lower incidence of postoperative complications, such as deafness and catheter blockage after tympanotomy tube insertion ().
Tympanoplasty exerts significant actions on the treatment of auditory diseases such as chronic otitis mastoidea, tympanosclerosis, cholesteatomatous chronic otitis media, and middle-ear sound transmission defect caused by trauma. Adhesive otitis patients often require surgical interventions when they present with concomitant middle-ear atelectasis, structural adhesion in the tympanic chamber, sound transmission disorder, recurrent infection, and persistent otorrhea (). To avoid postoperative adhesion and to clean effusion, the filler materials are required for adhesion prevention after removal of tympanic sclerotic foci and middle-ear blockage caused by pathological factors; these materials can be divided into two categories: absorbable and non-absorbable. The most recent anti-adhesive materials include chitosan hydrogel within absorbable materials (Unsaler et al., 2016) and natural polymeric biomaterials–Naso Pore (). These two ingredients are otherwise used for nasal surgery and are of low ototoxicity, inflammatory response, and have strong anti-adhesion effects (). In the medical management of middle-ear cholesteatoma, traditional surgery combined with novel materials has been found to have superior efficacy. For mastoid postoperative tamponade, synthetic materials have clear advantages of easy accessibility, short procedure time, being less prone to contamination and so on, compared with traditional autologous materials, which are less accessible and unstable. Common filling synthetic materials in mastoid disorders include bioactive glass, hydroxyapatite, titanium, and silicon, with bioactive glass being most frequently used (; ). Tympanoplasty necessitates the use of transplanted materials, but classically employed autogenous materials are with high risk of shift, complete absorption, and residual cholesteatoma. determined that total (TORP) and partial (PORP) ossicular replacement prostheses can be biosynthesized and are stiff, safe, and stable. Compared with traditional materials, the hearing improvement after ossicular chain reconstruction is almost equivalent to using biosynthesizing materials, and the curative effect of myringoplasty is even superior to that of traditional autologous grafting materials (; ).
The ear is one of the predilection sites for keloids, frequently following trauma, surgery, burns, and ear piercing. Due to the high rate of recurrence, the search for excellent postoperative coverage materials and preventing recurrence has become a particular research hotspot in the treatment of keloids (). Park et al. proposed that employing hydrocolloid dressing as a wound coverage and pressurizing with a magnet during the early postoperative period, compared with traditional dressings used to cover wounds, could protect the wound tissue, facilitate the healing process, and reduce the water content inside the wound tissue (). Besides, more coverage materials to promote wound healing and reduce inflammation will become available in the coming years. For patients with CHL but normal hearing function of the inner ear, other assistive hearing devices are increasingly promising in addition to the aforementioned BAHA, BB, vibrant sound-bridge (VSB), and middle-ear transducers, such as ADHEAR–a new non-invasive bone-conduction hearing-assistive device, which uses a cohesive adaptor affixed to the skin surface behind the ear and applies no pressure to the skin ().
Treatment of New Materials in Sensorineural Hearing Loss
The loss of outer hair cells and spiral ganglion cell degeneration are major causes of sensorineural hearing loss (Wong and Ryan, 2015). The loss of hair cells, spiral ganglion cells, and auditory nerve fibers in the adult ear is irreversible, leading to permanent SNHL. The surgical implantation of a cochlear implant (CI) is envisaged as one of means to restore hearing, but the function of artificial cochlea is highly reliant on residue numbers of spiral ganglion cells. A recent study has found that superparamagnetic iron oxide (SPIO) nanoparticles can direct spiral ganglion neurites to orient to a CI electrode under the application of magnetic field modulation and maintain the survival of SGNs, producing a positive CI treatment effect (). Various other in vitro experiments have newly demonstrated that the cGMP-dependent atrial natriuretic peptide (ANP) and the permissive environment created by novel silicon micro-pillar substrates (MPS) could facilitate the survival and growth of SGNs (; ). Through in vivo experiments, mesenchymal stem cells (), valproic acid (VPA; 2-propylpentanoic acid) with growth factors (Wakizono et al., 2021), as well as neural stem cells () have been found to be beneficial for SGN growth.
Additionally, to achieve more SGNs and hair cell regeneration, researchers have been studying drug delivery systems (DDSs), gene therapy, and cell therapy from different perspectives () (see Figure 2).
FIGURE 2
The clinical advancement of DDS has been hindered by a short biological half-life, poor pharmacokinetics, and low permeability through the biological barriers of nerve growth factor (NGF). Hence, developing highly efficient and inexpensive materials is of substantial importance (; ). Currently, the nanotechnology-based ongoing development of novel NGF delivery systems covers nanogels, hydrogels, micelles, microspheres, electrospun nanofibers, nanoparticles, and supraparticles. NGF could be immobilized in nanomaterials via physical trapping, adsorption, or electrostatic interactions, then the sustained release can be obtained using diffusion of NGF and/or degradation of carriers, with the aim of local, sustained drug release (). One such nanoscaled drug delivery system could be used in targeted drug delivery. By constructing degradable and non-toxic nanoparticle loading drugs, ligands for the specific recognition and delivery into targeted organs or tissues, nanoscaled drug delivery systems show the stability and property of sustained release (; ). Moreover, supraparticles have increased volume in comparison to nano-onions, which have yet to be fully translated into clinical practice. The supraparticles have a larger capacity for the delivery of drugs and provide sustained drug release, concurrently spreading to particular targeted areas (). However, several challenges persist for the clinical application of nanoparticle drug delivery systems, such as drug delivery risk assessments through the RWM or OW routes and the implementation of controlled release and targeted nano-drug delivery. For example, intratympanic medication injection or nanoparticle delivery may access the inner ear more through the RWM approach (; ), but OW shows higher permeability than RWM (, ; Zou et al., 2012). Chen et al. also found similar results in that fluorescence traceable chitosan nanoparticles (CS-NPs) were more quickly transported into the inner ear through OW, with less damage exhibited (), but further validation regarding nanomaterials and loaded drugs for optimum routes of delivery is still necessary. In gene therapy, the introgressed gene in the inner ear typically involves the basic helix-loop-helix (bHLH) family transcription factor () as well as neurotrophic (Sun et al., 2011), anti-apoptotic (; ), antioxidant (), connexin (; Sun et al., 2009), cochlear protein-related, interleukin, and other (Zhuo et al., 2008) genes. To cross the BBB and blood labyrinth barrier successfully and transfer functional genes into the mammalian inner ear, both viral and non-viral vectors are the most common tools for transgene delivery. Viral vectors consist of adenovirus (AV), adeno-associated virus (AAV), herpes simplex virus type I, vaccinia virus, and so on. Non-viral vectors can be categorized into liposomes, cationic polymers, peptide-based nanoparticles, and other synthetic vectors (Sun and Wu, 2013). Other vectors, such as viral and non-viral composite carriers, as well as bacterial vectors, are being studied (). AAV2/Anc80L65, a recently discovered synthetic viral vector, targets the inner and outer hair cells of the cochlea with high efficiency and elicits only a weak immune response when compared to other viral vectors with low transfection ability (Zinn et al., 2015). Tan et al. designed a variant of AAV—AAV-inner ear (AAV-ie). The variant not only achieved 90% successful transfection to supporting cells but also expanded the number of mice hair cells via carrying the Atoh1 gene, which did not affect the numbers of hair cells or hearing level (Tan et al., 2019). MicroRNA regulates gene expression in vivo by means of inhibiting protein translation and promoting mRNA degradation, the primary function of which is to play a suppressor role post-transcriptionally (Wu et al., 2020). Luo et al. constructed MicroRNA-146a (miR-146a) lentiviral recombinant vectors and found that miR-146a could significantly mitigate inflammatory injury and auditory dysfunctions of the inner ear after being injected into the inner ear through the scala tympani (). A single microRNA can regulate hundreds of different transcription processes, by which the regeneration of damaged hair cells in the inner ear and treating hearing loss are major focuses of much recent research (Zhou W. et al., 2018). Autoimmune inner ear disease (AIED) is an independent disorder, the main clinical manifestation of which is bilateral, rapidly progressive sensorineural hearing loss. Distinct from conventional systemic glucocorticoid treatment, Cai et al. injected adenoviral-mediated interleukin-10 (IL-10) through the RWM. The authors found that adenoviral carrying IL-10 can be imported into the inner ear of guinea pigs and express the gene products, consequently attenuating inflammatory injury and impairment in the auditory function of the inner ear to some extent (). Therapies for sensorineural hearing loss by replacement of damaged or lost cells and secreting neurotrophic factors, cytokines, immunoregulatory protein, etc., with the transplanted cells hold promise in a wide variety of fields (; ). Mesenchymal (MSCs), embryonic (ESCs), and induced pluripotent (iPSCs) stem cells are the most frequently used sources for regenerative medicine in the field of otology. Nevertheless, in contrast, the potential tumorigenicity and immune rejection response caused by ESCs and iPSCs, MSCs have a higher safety profile, anti-apoptotic properties, and characteristics of easy amplification; hence, MSCs have become a particular focus of regenerative medicine research (). The application of MSCs promotes BDNF secretion and increases the expression of connexin26 and connexin30, contributing to the alleviation of inflammation, oxidative stress, and apoptosis, the recovery of cell-cell junctions, an increased number of SGNs differentiated into neural progenitor cells and specific lineages of neurons, and significantly decreased hearing threshold and improved audial function (; ; Young et al., 2018; ). In regenerative medicine, scaffolds are essential for cell growth and could provide a three-dimensional structure for cell differentiation and migration to restore the normal function of damaged organs (). The preparation of scaffolds can be accomplished with various source materials, including decellularizing tissue (), 3D printing technologies (Wang and Yang, 2021), tailored hydrogels (), and electrospinning (). Recent studies have used biological scaffolds comprising 3D graphene and artificial photonic crystals for stem cell culture. Scaffolds mimicking the microenvironment of cell growth in vivo can positively regulate stem cell growth, proliferation, and differentiation (Yang et al., 2013; ; ). Other novel materials yielding similarly supportive effects for stem cells include 3D polydopamine-functionalized carbon microfibrous scaffolds (Yang et al., 2020), Ti3C2TxMxene membranes (), microfluidic chip platforms (), and anisotropy inverse opals (). Suggested mechanisms of the aforementioned materials include the promotion of cell growth, expansion, development and cell-cell adhesion, alignment, and connection.
In terms of hearing ancillary equipment, the application of CI for bilateral severe-to-profound SNHL has also reached maturity. However, implantation surgery can potentially cause invasive damage. Recent studies have increasingly found that degradable cell coatings for CI electrodes can increase neuronal survival by persistently releasing BDNF from cell-coated surfaces (). In addition, the local delivery of dexamethasone into the inner ear or coating Cis with dexamethasone during cochlear implantation may alleviate inflammation in the surgical sites (; ).
Other Novel Materials for Treating Auditory-Related Conditions
The control of tinnitus by external noise stimuli has become a therapy of particular interest. Tinnitus afflicts approximately 15% of the general population worldwide, and there is currently no cure for this disorder. Attempts have been made to ameliorate tinnitus with individually applied spectrally optimized near-threshold noise (), with most patients stating that subjective tinnitus loudness was suppressed during the noise stimulation.
The discovery of novel pharmaceuticals is one of the important directions for future research. Today, drug candidates with potential therapeutic applications for hearing loss include antioxidants, regulators of mitochondrial function, ion channel modulators, hair-cell protectants, and anti-inflammatory drugs (). Other potentially effective drugs that have been experimentally validated are N-acetylcysteine (NAC) (), melatonin (), resveratrol (Xiong et al., 2015), mineralocorticoid aldosterone (ALD) (; ), teprenone (GGA) (), aspirin (Verschuur et al., 2014), and salicylic acid () et al. One example is age-related hearing loss (ARHL); SAMP8 mice models demonstrated notably decreased auditory brainstem response (ABR) thresholds, increased distortion product otoacoustic emission (DPOAE) amplitudes, and memory improvement after the administration of NAC, suggesting that NAC has protective effects on hair cells and neurons of the central nervous system (CNS) (). Some systemic diseases are accompanied by damage to the inner ear, such as the microvascular and nerve damage caused by long-term diabetes, further leading to neurovascular injury in the cochlear. found resveratrol to be effective in preventing cell apoptosis and reducing diabetes damage to the inner ear by hypoglycemic activities, anti-dyslipidemic effects, and inhibiting anti-oxidative stress, ICAM-1, and VEGF expression. GGA was found to up-regulate heat-shock proteins (HSPs), and many experimental studies have demonstrated the protective effect of HSPs against cochlear damage induced by noise exposure, ototoxic drugs, and heat stress. In addition, a decline of ABR thresholds was observed in presbycusis mice (). ARHL models of DBA/2J mice were given injections of 200 mg/kg salicylic acid, and the expression of prestin, hair-cell survival, and function of the cochlea were significantly better than in saline-treated controls (). However, although antioxidants, such as resveratrol, ferulic acid (), and glutathione () are currently under active research, Sha Suhua et al. expressed caution that long-term or excessive intake of exogenous antioxidants or vitamin supplements is not only hazardous to hearing but also increases the risk of developing cancer (). Additionally, and Polanski et al. identified that various antioxidants such as Ginkgo biloba extract (GBE), alpha-lipoic acid (AL), and vitamins A, E, and C do not result in hearing improvement (). For other novel agents, bioactive peptides from Rapana venosa were found to exert an antioxidant effect, as demonstrated via the diminishing hair-cell uptake of gentamicin, activating Nrf2-Kcap1-ARE, up-regulation of Nrf2, and the expression of related antioxidant genes without damaging mechanoelectrical transduction channels (Yan, 2021). It has been suggested that rapamycin can slow the onset of ARHL through the inhibition of mTORC1 hyperactivation (). Multiple previous studies have also shown that rapamycin reduces cisplatin- and gentamicin-induced nephrotoxicity (; ) and alleviates noise-induced hearing loss (NIHL) by reducing oxidative stress (Yuan et al., 2015). However, rapamycin has many side effects as an immunosuppressant. New drugs can simulate the antioxidant activity of rapamycin with fewer side effects, and such classes of drugs are currently undergoing clinical experimentation. Traditional herbal medicines have been used in China for thousands of years. However, to date, the efficacy of these medicines has yet to be confirmed, and their action mechanisms remain unclear. Modern pharmacological studies have also spurred intense research programs targeting the auditory diseases. For instance, Xuan et al. (2018) demonstrated that composite Jianer formulations, mainly consisting of Puerariae Lobatae Radix (Gegen in Chinese), Scutellariae Radix (Huangqin in Chinese), and Salvia miltiorrhiza (Danshen in Chinese), reduced the level of malondialdehyde (MDA), the main product of lipid peroxidation, to exhibit an antioxidant effect in adult mice. Besides, the composite Jianer formulations ameliorated mtDNA damage and the release of Cyt-c, thereby attenuating caspase-mediated apoptosis through the mitochondrial pathway and playing a protective role against age-related decline in hair cells and spiral ganglion neurons. Furthermore, traditional Chinese herbal medicine (TCHM) seems to be associated with few adverse effects (Xuan et al., 2018). Another active ingredient extracted from traditional Chinese medicine Flos puerariae (Gehua in Chinese)—total flavonoids of Pueraria lobata—has been found to suppress the inflammatory response. The total flavonoids of Pueraria lobata reduce isoprenaline-induced damage to the inner ear of the rat via inhibiting the expression of TNF-α, IL-4, and Bax and up-regulating ACTH proteins, at the same time regulating auditory system homeostasis and improving the microvasculature circulation of the inner ear and the ischemia conditions of tissue cells in rats (Zhao and Liang, 2018). Thus, TCHM has substantial potential for treating auditory diseases. The development of new classes of novel antibiotics is valuable for the treatment of hearing loss. For example, for severe chronic suppurative otitis media, new antibiotics are required for effective anti-infectious therapeutics owing to the constant emergence of drug-resistant bacteria. A kind of new cephalosporin— “ceftolozane-tazobactam”—has particularly good therapeutic benefits for moderate to severe suppurative otitis media caused by multidrug- and extensively drug-resistant (MDR and XDR) P. aeruginosa ().
This study has highlighted some bottlenecks in the application of therapeutic materials for auditory diseases, such as the tumorigenicity of repair-promoting substances, immune reaction to implanted materials, high cost, and a difficult fabrication process. More research combining materials science, basic medicine, and clinical medicine is required to address these bottlenecks, with the aim of obtaining more cost-effective and safer new materials for treating hearing loss.
Conclusion
Presently, various deficiencies still exist regarding insufficient treatment options and their modest efficacy for auditory diseases, leading to CHL and SNHL. Nevertheless, the development and application of novel materials are gradually improving the condition. The novel materials are able to hasten perforated tympanic membrane healing, tympanoplasty of the middle ear, and repair of the microtia, as well as promote the regeneration of inner hair cells, spiral ganglion cells, and the synaptic ribbons, decrease inflammation level, and modify hearing level adjunctively. Although the efficacy and safety of novel materials in clinical application remain to be verified, with more progression of research and substantial technological innovation, these novel materials will be continuously improved, and more refined materials could be employed to treat hearing loss clinically.
Publisher’s Note
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Statements
Author contributions
ML conceived and wrote the manuscript. YD modified the manuscript. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by grants from Science Foundation of Union Hospital (2021XHYN113).
Acknowledgments
The authors thank Yang Zhang for his assistance in the preparation of all figures.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
1
AdamsD.Gonzalez-DuarteA.O’RiordanW. D.YangC. C.UedaM.KristenA. V.et al (2018). Patisiran, an RNAi therapeutic, for hereditary transthyretin amyloidosis.N. Engl. J. Med.37911–21. 10.1056/NEJMoa1716153
2
AkinD.SturgisJ.RaghebK.ShermanD.BurkholderK.RobinsonJ. P.et al (2007). Bacteria-mediated delivery of nanoparticles and cargo into cells.Nat. Nanotechnol.2441–449. 10.1038/nnano.2007.149
3
AnX.ZhaD. (2020). Advances in research on nanoparticle delivery systems for inner ear targeted drug delivery and therapy.Chin. J. Otol.18409–413.
4
AnkamS.LimC. K.YimE. K. (2015). Actomyosin contractility plays a role in MAP2 expression during nanotopography-directed neuronal differentiation of human embryonic stem cells.Biomaterials4720–28. 10.1016/j.biomaterials.2015.01.003
5
BartelR.CruellasF.HamdanM.Gonzalez-ComptaX.CisaE.DomenechI.et al (2018). Hearing results after type III tympanoplasty: incus transposition versus PORP. A systematic review.Acta Otolaryngol.138617–620. 10.1080/00016489.2018.1425901
6
BartusR. T. (2012). Translating the therapeutic potential of neurotrophic factors to clinical ‘proof of concept’: a personal saga achieving a career-long quest.Neurobiol. Dis.48153–178. 10.1016/j.nbd.2012.04.004
7
BicharaD. A.O’SullivanN. A.PomerantsevaI.ZhaoX.SundbackC. A.VacantiJ. P.et al (2012). The tissue-engineered auricle: past, present, and future.Tissue Eng. Part B Rev.1851–61. 10.1089/ten.TEB.2011.0326
8
BirkenhagerR.ZimmerA. J.MaierW.SchipperJ. (2006). [Pseudodominants of two recessive connexin mutations in non-syndromic sensorineural hearing loss?].Laryngorhinootologie85191–196. 10.1055/s-2005-870302
9
BrillI. T.BrillS.StarkT. (2019). [New options for rehabilitation of conductive hearing loss: tests on normal-hearing subjects with simulated hearing loss].HNO67698–705. 10.1007/s00106-019-0685-8
10
CaiW.TanW. (2015). Adenovirus-mediated IL-10 gene for the treatment of autoimmune inner ear disease——an experimental study.J. Audiol. Speech Pathol.23602–606.
11
Campos-BanalesE. M.Lopez-CamposD.de Serdio-AriasJ. L.Esteban-RodriguezJ.Garcia-SainzM.Munoz-CortesA.et al (2015). [A comparative study on efficacy of glucocorticoids, mineralocorticoids and vasoactive drugs on reversing hearing loss in patients suffering idiopathic sensorineural cochlear hypoacusis. A preliminary clinical trial].Acta Otorrinolaringol. Esp.6665–73. 10.1016/j.otorri.2014.05.008
12
ChanD. K.LiebermanD. M.MusatovS.GoldfeinJ. A.SelesnickS. H.KaplittM. G. (2007). Protection against cisplatin-induced ototoxicity by adeno-associated virus-mediated delivery of the X-linked inhibitor of apoptosis protein is not dependent on caspase inhibition.Otol. Neurotol.28417–425. 10.1097/01.mao.0000247826.28893.7a
13
ChenK.DaiP.YangL.ZhangT. (2014). Progress in middle ear implants.Progr.Biomed. Eng.3523–27.
14
ChenM.LiS. (2020). Advances in diagnosis and treatment of adhesive otitis media.Chin. J. Ophthalmol. Otorhinolaryngol.20493–497.
15
ChengC.WangY.GuoL.LuX.ZhuW.MuhammadW.et al (2019). Age-related transcriptome changes in Sox2+ supporting cells in the mouse cochlea.Stem Cell Res. Ther.10:365. 10.1186/s13287-019-1437-0
16
DiensthuberM.StoverT. (2018). Strategies for a regenerative therapy of hearing loss.HNO66(Suppl. 1) 39–46. 10.1007/s00106-017-0467-0
17
Diken TurksayarA. A.SaglamS. A.BulutA. C. (2019). Retention systems used in maxillofacial prostheses: a review.Niger. J. Clin. Pract.221629–1634. 10.4103/njcp.njcp_92_19
18
DingS.XieS.ChenW.WenL.WangJ.YangF.et al (2019). Is oval window transport a royal gate for nanoparticle delivery to vestibule in the inner ear?Eur. J. Pharm. Sci.12611–22. 10.1016/j.ejps.2018.02.031
19
DingY.MengW.KongW.HeZ.ChaiR. (2020). The role of FoxG1 in the inner ear.Front. Cell. Dev. Biol.8:614954. 10.3389/fcell.2020.614954
20
DuG.ZhuJ. (2015). Ear keloid and clinical research progress.J. Clin. Otorhinolaryngol. Head Neck Surg. (China)29770–772.
21
DuX.ChenK.KuriyavarS.KopkeR. D.GradyB. P.BourneD. H.et al (2013). Magnetic targeted delivery of dexamethasone acetate across the round window membrane in guinea pigs.Otol. Neurotol.3441–47. 10.1097/MAO.0b013e318277a40e
22
EbnoetherE.RamseierA.CortadaM.BodmerD.Levano-HuamanS. (2017). Sesn2 gene ablation enhances susceptibility to gentamicin-induced hair cell death via modulation of AMPK/mTOR signaling.Cell Death Discov.3:17024. 10.1038/cddiscovery.2017.24
23
FangB.XiaoH. (2014). Rapamycin alleviates cisplatin-induced ototoxicity in vivo.Biochem. Biophys. Res. Commun.448443–447. 10.1016/j.bbrc.2014.04.123
24
FangQ.ZhangY.ChenX.LiH.ChengL.ZhuW.et al (2019). Three-dimensional graphene enhances neural stem cell proliferation through metabolic regulation.Front. Bioeng. Biotechnol.7:436. 10.3389/fbioe.2019.00436
25
FarhadiM.JalessiM.SalehianP.GhaviF. F.EmamjomehH.MirzadehH.et al (2013). Dexamethasone eluting cochlear implant: histological study in animal model.Cochlear Implants Int.1445–50. 10.1179/1754762811Y.0000000024
26
FetoniA. R.MancusoC.EramoS. L.RalliM.PiacentiniR.BaroneE.et al (2010). In vivo protective effect of ferulic acid against noise-induced hearing loss in the guinea-pig.Neuroscience1691575–1588. 10.1016/j.neuroscience.2010.06.022
27
FuX.SunX.ZhangL.JinY.ChaiR.YangL.et al (2018). Tuberous sclerosis complex-mediated mTORC1 overactivation promotes age-related hearing loss.J. Clin. Invest.1284938–4955. 10.1172/JCI98058
28
GaoH.QuY.ZhangX.MuJ.ZhangP.WangX.et al (2018). The protective effects and its mechanisms of resveratrol on inner ear damage in diabetes rats.J. Audiol. Speech Pathol.29409–413.
29
GhonchehM.LilliG.LenarzT.MaierH. (2016). Outer ear canal sound pressure and bone vibration measurement in SSD and CHL patients using a transcutaneous bone conduction instrument.Hear. Res.340161–168. 10.1016/j.heares.2015.12.019
30
Gisselsson-SolenM.TahtinenP. A.RyanA. F.MulayA.KariyaS.SchilderA. G. M.et al (2020). Panel 1: biotechnology, biomedical engineering and new models of otitis media.Int. J. Pediatr. Otorhinolaryngol.130(Suppl. 1):109833. 10.1016/j.ijporl.2019.109833
31
GuoR.XiaoM.ZhaoW.ZhouS.HuY.LiaoM.et al (2020). 2D Ti3C2TxMXene couples electrical stimulation to promote proliferation and neural differentiation of neural stem cells.Acta Biomater.S1742–7061, 30749–30752. 10.1016/j.actbio.2020.12.035
32
GurO. E.EnsariN.OzturkM. T.BoztepeO. F.GunT.SelcukO. T.et al (2016). Use of a platelet-rich fibrin membrane to repair traumatic tympanic membrane perforations: a comparative study.Acta Otolaryngol.1361017–1023. 10.1080/00016489.2016.1183042
33
HalonenJ.HintonA. S.FrisinaR. D.DingB.ZhuX.WaltonJ. P. (2016). Long-term treatment with aldosterone slows the progression of age-related hearing loss.Hear. Res.33663–71. 10.1016/j.heares.2016.05.001
34
HashemiS. S.JowkarS.MahmoodiM.RafatiA. R.MehrabaniD.ZareiM.et al (2018). Biochemical methods in production of three-dimensional scaffolds from human skin: a window in aesthetic surgery.World J. Plast. Surg.7204–211.
35
HeZ.DingY.MuY.XuX.KongW.ChaiR.et al (2021). Stem cell-based therapies in hearing loss.Front. Cell. Dev. Biol.9:730042. 10.3389/fcell.2021.730042
36
HuY.LiD.WeiH.ZhouS.ChenW.YanX.et al (2021). Neurite extension and orientation of spiral ganglion neurons can be directed by superparamagnetic iron oxide nanoparticles in a magnetic field.Int. J. Nanomed.164515–4526. 10.2147/IJN.S313673
37
HuangG.ChenX.JiangH. (2011). Effects of NasoPore packing in the middle ear cavity of the guinea pig.Otolaryngol. Head Neck Surg.145131–136. 10.1177/0194599811400834
38
HuangJ.YuanZ.HuS.LvC.HuY.ShenY. (2021). The effectiveness and research progress of platelet-rich concentrate products in tympanic membrane perforation.Chin. J. Cell Biol.431700–1704.
39
JangS.ChoH. H.KimS. H.LeeK. H.JunJ. Y.ParkJ. S.et al (2015). Neural-induced human mesenchymal stem cells promote cochlear cell regeneration in deaf Guinea pigs.Clin. Exp. Otorhinolaryngol.883–91. 10.3342/ceo.2015.8.2.83
40
JiL.ShenQ.ZhaoL. (2021). Progress in treatment of presbycusis.J. Otol.19662–665.
41
JiaoT.ZhangF. (2001). The present situation of auricular prostheses.Chin. J. Dent. Mater. Devices10213–215.
42
JoeH.SeoY. J. (2018). A newly designed tympanostomy stent with TiO2 coating to reduce Pseudomonas aeruginosa biofilm formation.J. Biomater. Appl.33599–605. 10.1177/0885328218802103
43
KaboodkhaniR.MehrabaniD.Karimi-BusheriF. (2021). Achievements and challenges in transplantation of mesenchymal stem cells in otorhinolaryngology.J. Clin. Med.10:2940. 10.3390/jcm10132940
44
KanemaruS. I.KanaiR.YoshidaM.KitadaY.OmaeK.HiranoS. (2018). Application of regenerative treatment for tympanic membrane perforation with cholesteatoma, tumor, or severe calcification.Otol. Neurotol.39438–444. 10.1097/MAO.0000000000001701
45
KanzakiS. (2018). Gene delivery into the inner ear and its clinical implications for hearing and balance.Molecules23:2507. 10.3390/molecules23102507
46
KanzakiS.ToyodaM.UmezawaA.OgawaK. (2020). Application of mesenchymal stem cell therapy and inner ear regeneration for hearing loss: a review.Int. J. Mol. Sci.21:5764. 10.3390/ijms21165764
47
KashioA.AmanoA.KondoY.SakamotoT.IwamuraH.SuzukiM.et al (2009). Effect of vitamin C depletion on age-related hearing loss in SMP30/GNL knockout mice.Biochem. Biophys. Res. Commun.390394–398. 10.1016/j.bbrc.2009.09.003
48
KawamotoK.ShaS. H.MinodaR.IzumikawaM.KuriyamaH.SchachtJ.et al (2004). Antioxidant gene therapy can protect hearing and hair cells from ototoxicity.Mol. Ther.9173–181. 10.1016/j.ymthe.2003.11.020
49
KenryLeeW. C.LohK. P.LimC. T. (2018). When stem cells meet graphene: opportunities and challenges in regenerative medicine.Biomaterials155236–250. 10.1016/j.biomaterials.2017.10.004
50
KhalinI.AlyautdinR.KochergaG.BakarM. A. (2015). Targeted delivery of brain-derived neurotrophic factor for the treatment of blindness and deafness.Int. J. Nanomedicine.103245–3267. 10.2147/IJN.S77480
51
Khodakaram-TaftiA.MehrabaniD.Shaterzadeh-YazdiH. (2017). An overview on autologous fibrin glue in bone tissue engineering of maxillofacial surgery.Dent. Res. J. (Isfahan)1479–86.
52
KingE. B.SaltA. N.EastwoodH. T.O’LearyS. J. (2011). Direct entry of gadolinium into the vestibule following intratympanic applications in Guinea pigs and the influence of cochlear implantation.J. Assoc. Res. Otolaryngol.12741–751. 10.1007/s10162-011-0280-5
53
KingE. B.SaltA. N.KelG. E.EastwoodH. T.O’LearyS. J. (2013). Gentamicin administration on the stapes footplate causes greater hearing loss and vestibulotoxicity than round window administration in guinea pigs.Hear. Res.304159–166. 10.1016/j.heares.2013.07.013
54
KuoB. R.BaldwinE. M.LaymanW. S.TaketoM. M.ZuoJ. (2015). In vivo cochlear hair cell generation and survival by coactivation of beta-catenin and atoh1.J. Neurosci.3510786–10798. 10.1523/JNEUROSCI.0967-15.2015
55
LaremA.HaidarH.AlsaadiA.AbdulkarimH.AbdulraheemM.ShetaS.et al (2016). Tympanoplasty in adhesive otitis media: a descriptive study.Laryngoscope1262804–2810. 10.1002/lary.25987
56
LeeH. B.LimH. J.ChoM.YangS. M.ParkK.ParkH. Y.et al (2013). Clinical significance of beta-tricalcium phosphate and polyphosphate for mastoid cavity obliteration during middle ear surgery: human and animal study.Clin. Exp. Otorhinolaryngol.6127–134. 10.3342/ceo.2013.6.3.127
57
LeeJ.IsmailH.LeeJ. H.KelG.O’LearyJ.HampsonA.et al (2013). Effect of both local and systemically administered dexamethasone on long-term hearing and tissue response in a Guinea pig model of cochlear implantation.Audiol. Neurootol.18392–405. 10.1159/000353582
58
LiC.WangB.ZhangH.YangS.YangT.HanX.et al (2021). Advances in the surgical treatment of cholesteatoma of the middle ear.J. Clin. Otorhinolaryngol. Head Neck Surg. (China)35952–956.
59
LiS.WuK.JiY. (2020). Protective effect of long-term injection of salicylic acid on presbycusis.Chin. J. Otol.18755–762.
60
LiW.WuJ.YangJ.SunS.ChaiR.ChenZ. Y.et al (2015). Notch inhibition induces mitotically generated hair cells in mammalian cochleae via activating the Wnt pathway.Proc. Natl. Acad. Sci. U.S.A.112166–171. 10.1073/pnas.1415901112
61
LinY.YinF.ChenJ.BaiZ.LiuS.ZhangJ. (2013). The clinical effect of recombinant human epidermal growth factor in treatment of chronic tympanic membrane perforation.J. Kunming Med. Univ.34102–104, 109.
62
LiuH.ChenS.ZhouY.CheX.BaoZ.LiS.et al (2013). The effect of surface charge of glycerol monooleate-based nanoparticles on the round window membrane permeability and cochlear distribution.J. Drug Target.21846–854. 10.3109/1061186X.2013.829075
63
LuoC.LiT.TanC.HuangH. (2016). Local injection of the microRNA-146a recombinant lentiviral vector into the inner ear for immune-mediated inner ear disease in guinea pigs.J. Med. Postgra29801–807.
64
MaY.BjornmalmM.WiseA. K.Cortez-JugoC.RevalorE.JuY.et al (2018). Gel-mediated electrospray assembly of silica supraparticles for sustained drug delivery.ACS Appl. Mater. Interfaces1031019–31031. 10.1021/acsami.8b10415
65
MaY.WiseA. K.ShepherdR. K.RichardsonR. T. (2019). New molecular therapies for the treatment of hearing loss.Pharmacol. Ther.200190–209. 10.1016/j.pharmthera.2019.05.003
66
MaharajanN.ChoG. W.JangC. H. (2020). Application of mesenchymal stem cell for tympanic membrane regeneration by tissue engineering approach.Int. J. Pediatr. Otorhinolaryngol.133:109969. 10.1016/j.ijporl.2020.109969
67
MaharajanN.ChoG. W.JangC. H. (2021). Therapeutic application of mesenchymal stem cells for cochlear regeneration.In Vivo3513–22. 10.21873/invivo.12227
68
MalikS.SundarrajanS.HussainT.NazirA.RamakrishnaS. (2021). Role of block copolymers in tissue engineering applications.Cells Tissues Organs1–14. 10.1159/000511866
69
MandourY. M. H.MohammedS.MenemM. O. A. (2019). Bacterial cellulose graft versus fat graft in closure of tympanic membrane perforation.Am. J. Otolaryngol.40168–172. 10.1016/j.amjoto.2018.12.008
70
MarieA.MeunierJ.BrunE.MalmstromS.BaudouxV.FlaszkaE.et al (2018). N-acetylcysteine treatment reduces age-related hearing loss and memory impairment in the senescence-accelerated prone 8 (SAMP8) mouse model.Aging Dis.9664–673. 10.14336/AD.2017.0930
71
MatsuokaA. J.KondoT.MiyamotoR. T.HashinoE. (2007). Enhanced survival of bone-marrow-derived pluripotent stem cells in an animal model of auditory neuropathy.Laryngoscope1171629–1635. 10.1097/MLG.0b013e31806bf282
72
MattottiM.MicholtL.BraekenD.KovacicD. (2015). Characterization of spiral ganglion neurons cultured on silicon micro-pillar substrates for new auditory neuro-electronic interfaces.J. Neural Eng.12:026001. 10.1088/1741-2560/12/2/026001
73
MehrabaniD.Mojtahed JaberiF.ZakeriniaM.HadianfardM. J.JalliR.TanidehN.et al (2016). The healing effect of bone marrow-derived stem cells in knee osteoarthritis: a case report.World J. Plast. Surg.5168–174.
74
NadolJ. B.Jr.MerchantS. N. (2001). Histopathology and molecular genetics of hearing loss in the human.Int. J. Pediatr. Otorhinolaryngol.61, 1–15. 10.1016/s0165-5876(01)00546-8
75
MikuriyaT.SugaharaK.SugimotoK.FujimotoM.TakemotoT.HashimotoM.et al (2008). Attenuation of progressive hearing loss in a model of age-related hearing loss by a heat shock protein inducer, geranylgeranylacetone.Brain Res.12129–17. 10.1016/j.brainres.2008.03.031
76
MittalR.OcakE.ZhuA.PerdomoM. M.PenaS. A.MittalJ.et al (2020). Effect of bone marrow-derived mesenchymal stem cells on cochlear function in an experimental rat model.Anat. Rec. (Hoboken)303487–493. 10.1002/ar.24065
77
MizutariK.FujiokaM.HosoyaM.BramhallN.OkanoH. J.OkanoH.et al (2013). Notch inhibition induces cochlear hair cell regeneration and recovery of hearing after acoustic trauma.Neuron7758–69. 10.1016/j.neuron.2012.10.032
78
NakagawaT.ItoJ. (2005). Cell therapy for inner ear diseases.Curr. Pharm. Des.111203–1207. 10.2174/1381612053507530
79
NappiF.IervolinoA.SinghS. S. A. (2021). The new challenge for heart endocarditis: from conventional prosthesis to new devices and platforms for the treatment of structural heart disease.Biomed. Res. Int.2021:7302165. 10.1155/2021/7302165
80
OhinataY.YamasobaT.SchachtJ.MillerJ. M. (2000). Glutathione limits noise-induced hearing loss.Hear. Res.14628–34. 10.1016/s0378-5955(00)00096-4
81
OmaeK.KanemaruS. I.NakataniE.KanedaH.NishimuraT.TonaR.et al (2017). Regenerative treatment for tympanic membrane perforation using gelatin sponge with basic fibroblast growth factor.Auris Nasus Larynx44664–671. 10.1016/j.anl.2016.12.005
82
Ontario Health. (2020). Implantable devices for single-sided deafness and conductive or mixed hearing loss: a health technology assessment.Ont. Health Technol. Assess. Ser.201–165.
83
ParkJ.KimS.ParkS. I.ChoeY.LiJ.HanA. (2014). A microchip for quantitative analysis of CNS axon growth under localized biomolecular treatments.J. Neurosci. Methods221166–174. 10.1016/j.jneumeth.2013.09.018
84
ParkT. H.ChangC. H. (2013). Early postoperative magnet application combined with hydrocolloid dressing for the treatment of earlobe keloids.Aesthetic Plast. Surg.37439–444. 10.1007/s00266-013-0076-6
85
PettinatoG.WenX.ZhangN. (2015). Engineering strategies for the formation of embryoid bodies from human pluripotent stem cells.Stem Cells Dev.241595–1609. 10.1089/scd.2014.0427
86
PfannenstielS. C.PraetoriusM.PlinkertP. K.BroughD. E.StaeckerH. (2009). Bcl-2 gene therapy prevents aminoglycoside-induced degeneration of auditory and vestibular hair cells.Audiol. Neurootol.14254–266. 10.1159/000192953
87
PohlF.SchuonR. A.MillerF.KampmannA.BultmannE.HartmannC.et al (2018). Stenting the eustachian tube to treat chronic otitis media - a feasibility study in sheep.Head Face Med.14:8. 10.1186/s13005-018-0165-5
88
PolanskiJ. F.CruzO. L. (2013). Evaluation of antioxidant treatment in presbyacusis: prospective, placebo-controlled, double-blind, randomised trial.J. Laryngol. Otol.127134–141. 10.1017/S0022215112003118
89
RichardsonR. T.AtkinsonP. J. (2015). Atoh1 gene therapy in the cochlea for hair cell regeneration.Expert Opin. Biol. Ther.15417–430. 10.1517/14712598.2015.1009889
90
RichardsonR. T.WiseA. K.ThompsonB. C.FlynnB. O.AtkinsonP. J.FretwellN. J.et al (2009). Polypyrrole-coated electrodes for the delivery of charge and neurotrophins to cochlear neurons.Biomaterials302614–2624. 10.1016/j.biomaterials.2009.01.015
91
SageC.HuangM.KarimiK.GutierrezG.VollrathM. A.ZhangD. S.et al (2005). Proliferation of functional hair cells in vivo in the absence of the retinoblastoma protein.Science3071114–1118. 10.1126/science.1106642
92
Santa MariaP. L.KimS.VarsakY. K.YangY. P. (2015). Heparin binding-epidermal growth factor-like growth factor for the regeneration of chronic tympanic membrane perforations in mice.Tissue Eng. Part A211483–1494. 10.1089/ten.TEA.2014.0474
93
SaracaL. M.Di GiuliC.SicariF.PrianteG.LavagnaF.FrancisciD. (2019). Use of ceftolozane-tazobactam in patient with severe medium chronic purulent otitis by XDR Pseudomonas aeruginosa.Case Rep. Infect. Dis.2019:2683701. 10.1155/2019/2683701
94
SchillingA.KraussP.HannemannR.SchulzeH.TziridisK. (2021). [Reducing tinnitus intensity: pilot study to attenuate tonal tinnitus using individually spectrally optimized near-threshold noise].HNO69891–898. 10.1007/s00106-020-00963-5
95
SeonwooH.ShinB.JangK. J.LeeM.ChooO. S.ParkS. B.et al (2019b). Epidermal growth factor-releasing radially aligned electrospun nanofibrous patches for the regeneration of chronic tympanic membrane perforations.Adv. Healthc. Mater.8:e1801160. 10.1002/adhm.201801160
96
SeonwooH.KimS. W.ShinB.JangK. J.LeeM.ChooO. S.et al (2019a). Latent stem cell-stimulating therapy for regeneration of chronic tympanic membrane perforations using IGFBP2-releasing chitosan patch scaffolds.J. Biomater. Appl.34198–207. 10.1177/0885328219845082
97
SerraL. S. M.AraujoJ. G.VieiraA. L. S.SilvaE. M. D.AndradeR. R.KuckelhausS. A. S.et al (2020). Role of melatonin in prevention of age-related hearing loss.PLoS One15:e0228943. 10.1371/journal.pone.0228943
98
ShaS. H.SchachtJ. (2017). Emerging therapeutic interventions against noise-induced hearing loss.Expert Opin. Investig. Drugs2685–96. 10.1080/13543784.2017.1269171
99
ShahjalalH. M.Abdal DayemA.LimK. M.JeonT. I.ChoS. G. (2018). Generation of pancreatic beta cells for treatment of diabetes: advances and challenges.Stem Cell Res. Ther.9:355. 10.1186/s13287-018-1099-3
100
ShangJ.JiangT.TangL.WangZ. (2016). Key technology of transplantable human auricular scaffold based on 3D printing.J. Natl. Univ. Defense Technol.38175–180.
101
ShiF.HuL.EdgeA. S. (2013). Generation of hair cells in neonatal mice by beta-catenin overexpression in Lgr5-positive cochlear progenitors.Proc. Natl. Acad. Sci. U.S.A.11013851–13856. 10.1073/pnas.1219952110
102
ShouJ.ZhengJ. L.GaoW. Q. (2003). Robust generation of new hair cells in the mature mammalian inner ear by adenoviral expression of Hath1.Mol. Cell. Neurosci.23169–179. 10.1016/s1044-7431(03)00066-6
103
SlaughterB. V.KhurshidS. S.FisherO. Z.KhademhosseiniA.PeppasN. A. (2009). Hydrogels in regenerative medicine.Adv. Mater.213307–3329. 10.1002/adma.200802106
104
SorourS. S.MohamedN. N.Abdel FattahM. M.ElbaryM. E. A.El-AnwarM. W. (2018). Bioglass reconstruction of posterior meatal wall after canal wall down mastoidectomy.Am. J. Otolaryngol.39282–285. 10.1016/j.amjoto.2018.03.007
105
StavrakasM.KarkosP. D.MarkouK.GrigoriadisN. (2016). Platelet-rich plasma in otolaryngology.J. Laryngol. Otol.1301098–1102. 10.1017/S0022215116009403
106
SunF.ZhouK.TianK. Y.WangJ.QiuJ. H.ZhaD. J. (2020). Atrial natriuretic peptide improves neurite outgrowth from spiral ganglion neurons in vitro through a cGMP-dependent manner.Neural Plast.2020:8831735. 10.1155/2020/8831735
107
SunH.WuX. (2013). Current status and prospects of non-viral vector in inner ear gene therapy.J. Clin. Otorhinolaryngol. Head Neck Surg. (China)271339–1342.
108
SunH.HuangA.CaoS. (2011). Current status and prospects of gene therapy for the inner ear.Hum. Gene Ther.221311–1322. 10.1089/hum.2010.246
109
SunY.TangW.ChangQ.WangY.KongW.LinX. (2009). Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea.J. Comp. Neurol.516569–579. 10.1002/cne.22117
110
TanF.ChuC.QiJ.LiW.YouD.LiK.et al (2019). AAV-ie enables safe and efficient gene transfer to inner ear cells.Nat. Commun.10:3733. 10.1038/s41467-019-11687-8
111
TehB. M.MaranoR. J.ShenY.FriedlandP. L.DilleyR. J.AtlasM. D. (2013). Tissue engineering of the tympanic membrane.Tissue Eng. Part B Rev.19116–132. 10.1089/ten.TEB.2012.0389
112
UnsalerS.BasaranB.Ozturk SariS.KaraE.DegerK.WormaldP. J.et al (2016). Safety and efficacy of chitosan-dextran hydrogel in the middle ear in an animal model.Audiol. Neurootol.21254–260. 10.1159/000447623
113
VanwijckF.RogisterF.Pierre BarriatS.CambyS.LefebvreP. (2019). Intratympanic steroid therapy for refractory sudden sensory hearing loss: a 12-year experience with the Silverstein catheter.Acta Otolaryngol.139111–116. 10.1080/00016489.2018.1532107
114
VerschuurC.Agyemang-PrempehA.NewmanT. A. (2014). Inflammation is associated with a worsening of presbycusis: evidence from the MRC national study of hearing.Int. J. Audiol.53469–475. 10.3109/14992027.2014.891057
115
WakizonoT.NakashimaH.YasuiT.NodaT.AoyagiK.OkadaK.et al (2021). Growth factors with valproic acid restore injury-impaired hearing by promoting neuronal regeneration.JCI Insight6:e139171. 10.1172/jci.insight.139171
116
WangZ.YangY. (2021). Application of 3D printing in implantable medical devices.Biomed. Res. Int.2021:6653967. 10.1155/2021/6653967
117
WongA. C.RyanA. F. (2015). Mechanisms of sensorineural cell damage, death and survival in the cochlea.Front. Aging Neurosci.7:58. 10.3389/fnagi.2015.00058
118
World Health Organization [WHO] (2021). WHO: 1 in 4 People Projected to Have Hearing Problems by 2050. Available online at: https://www.who.int/news/item/02-03-2021-who-1-in-4-people-projected-to-have-hearing-problems-by-2050(accessed March 2, 2021).
119
WuX.ZouS.WuF.HeZ.KongW. (2020). Role of microRNA in inner ear stem cells and related research progress.Am. J. Stem Cells916–24.
120
XiongH.PangJ.YangH.DaiM.LiuY.OuY.et al (2015). Activation of miR-34a/SIRT1/p53 signaling contributes to cochlear hair cell apoptosis: implications for age-related hearing loss.Neurobiol. Aging361692–1701. 10.1016/j.neurobiolaging.2014.12.034
121
XuanY.DingD.XuanW.HuangL.TangJ.WeiY.et al (2018). A traditional Chinese medicine compound (Jian Er) for presbycusis in a mouse model: Reduction of apoptosis and protection of cochlear sensorineural cells and hearing.Int. J. Herb. Med.6127–135.
122
YanG. (2021). Studies on the Protective Effects on Sensory Hair Cells of Bioactive Peptides from Rapana venosa, Vol. 10. 69. Jinan: Qilu University of Technology.
123
YangK.JungK.KoE.KimJ.ParkK. I.KimJ.et al (2013). Nanotopographical manipulation of focal adhesion formation for enhanced differentiation of human neural stem cells.ACS Appl. Mater. Interfaces510529–10540. 10.1021/am402156f
124
YangY.ZhangY.ChaiR.GuZ. (2020). A polydopamine-functionalized carbon microfibrous scaffold accelerates the development of neural stem cells.Front. Bioeng. Biotechnol.8:616. 10.3389/fbioe.2020.00616
125
YoungE.WesterbergB.YanaiA.Gregory-EvansK. (2018). The olfactory mucosa: a potential source of stem cells for hearing regeneration.Regen. Med.13581–593. 10.2217/rme-2018-0009
126
YuanF.QiW. (2018). Development of drug delivery to inner ear.Chin. J. Otol.16575–580.
127
YuanH.WangX.HillK.ChenJ.LemastersJ.YangS. M.et al (2015). Autophagy attenuates noise-induced hearing loss by reducing oxidative stress.Antioxid. Redox Signal.221308–1324. 10.1089/ars.2014.6004
128
ZakrzewskiW.DobrzynskiM.SzymonowiczM.RybakZ. (2019). Stem cells: past, present, and future.Stem Cell Res. Ther.10:68. 10.1186/s13287-019-1165-5
129
ZhaoJ.LiangY. (2018). Experimental study on the effect of total flavonoids of Pueraria lobata on inflammatory cytokines in rats with inner ear injury induced by iso-proterenol.Chin. J. Clin. Pharmacol. Ther.231003–1007.
130
ZhouG.JiangH.YinZ.LiuY.ZhangQ.ZhangC.et al (2018). In vitro regeneration of patient-specific ear-shaped cartilage and its first clinical application for auricular reconstruction.EBioMedicine28287–302. 10.1016/j.ebiom.2018.01.011
131
ZhouW.DuJ.JiangD.WangX.ChenK.TangH.et al (2018). microRNA183 is involved in the differentiation and regeneration of Notch signalingprohibited hair cells from mouse cochlea.Mol. Med. Rep.181253–1262. 10.3892/mmr.2018.9127
132
ZhuoX. L.WangY.ZhuoW. L.ZhangY. S.WeiY. J.ZhangX. Y. (2008). Adenoviral-mediated up-regulation of Otos, a novel specific cochlear gene, decreases cisplatin-induced apoptosis of cultured spiral ligament fibrocytes via MAPK/mitochondrial pathway.Toxicology24833–38. 10.1016/j.tox.2008.03.004
133
ZinnE.PacouretS.KhaychukV.TurunenH. T.CarvalhoL. S.Andres-MateosE.et al (2015). In silico reconstruction of the viral evolutionary lineage yields a potent gene therapy vector.Cell Rep.121056–1068. 10.1016/j.celrep.2015.07.019
134
ZouJ.PoeD.RamadanU. A.PyykkoI. (2012). Oval window transport of Gd-dOTA from rat middle ear to vestibulum and scala vestibuli visualized by in vivo magnetic resonance imaging.Ann. Otol. Rhinol. Laryngol.121119–128. 10.1177/000348941212100209
135
ZouJ.PyykkoI.HyttinenJ. (2016). Inner ear barriers to nanomedicine-augmented drug delivery and imaging.J. Otol.11165–177. 10.1016/j.joto.2016.11.002
136
ZucchelliE.BirchallM.BulstrodeN. W.FerrettiP. (2020). Modeling normal and pathological ear cartilage in vitro using somatic stem cells in three-dimensional culture.Front. Cell. Dev. Biol.8:666. 10.3389/fcell.2020.00666
Summary
Keywords
new materials, auditory diseases, conductive hearing loss, sensorineural hearing loss, therapy
Citation
Li M, Mu Y, Cai H, Wu H and Ding Y (2022) Application of New Materials in Auditory Disease Treatment. Front. Cell. Neurosci. 15:831591. doi: 10.3389/fncel.2021.831591
Received
08 December 2021
Accepted
22 December 2021
Published
31 January 2022
Volume
15 - 2021
Edited by
Zuhong He, Wuhan University, China
Reviewed by
Fuping Qian, Nantong University, China; Ling Lu, Nanjing Drum Tower Hospital, China
Updates
Copyright
© 2022 Li, Mu, Cai, Wu and Ding.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yanyan Ding, dingyanyande@163.com
This article was submitted to Cellular Neuropathology, a section of the journal Frontiers in Cellular Neuroscience
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