Botulinum neurotoxin subtype A (BoNT-A) has been part of the urology treatment arsenal since it was first used in the treatment of detrusor-sphincter dyssynergia more than 30 years ago. BoNT-A has been recommended as an effective treatment for neurogenic detrusor overactivity and overactive bladder. However, direct intradetrusor injection of BoNT-A using cystoscopy after anesthesia may cause hematuria, pain, and infection; these adverse events have motivated urologists to find less invasive and more convenient ways to administer BoNT-A. The development of nanotechnology has led to the advancement of intravesical drug delivery. Using versatile nanocarriers to transport BoNT-A across the impermeable urothelium is a promising therapeutic option. In this review, we discuss the effectiveness and feasibility of liposomes, thermosensitive polymeric hydrogels, and hyaluronan-phosphatidylethanolamine as carriers of BoNT-A for intravesical instillation. To date, these carriers have not reached a similar efficacy as intradetrusor injections in long-term observations. Hopefully, researchers will make a breakthrough with new nanomaterials to develop clinical applications in the future.
Botulinum neurotoxin subtype AOveractive bladderNanocarriersIntravesical drug deliveryINTRODUCTION
Overactive bladder (OAB) is a clinical syndrome defined by the International Continence Society as “urgency, with or without urge incontinence, usually with frequency and nocturia, in the absence of other underlying pathology, including urinary tract infection (UTI)” [1]. OAB is a prevalent urinary disorder with a major impact on daily activities and quality of life. It is estimated that OAB affects the urinary health of 12% to 17% of the total population, and its prevalence increases with age [2,3]. The causes of OAB may be neurogenic, myogenic, urotheliogenic, or integrative [4,5].
Patient education and behavioral therapy are recommended as the first-line standard treatments for OAB. Subsequently, pharmacologic treatments, including antimuscarinic agents or β3-agonists, are administered [6]. However, many patients cannot adhere to conservative treatments owing to dissatisfactory efficacy or intolerable side effects such as dry mouth and constipation. When the previously mentioned treatments are insufficient, several minimally invasive surgical techniques can be considered, such as intravesical botulinum toxin type A (BoNTA) injection, posterior tibial nerve stimulation, and sacral neuromodulation. As a last resort, specialized surgical treatments, including augmentation cystoplasty and urinary diversion, are available for refractory urgency urinary incontinence induced by OAB.
Botulinum toxin is a neurologically destructive neurotoxin synthesized by the bacterium Clostridium botulinum [7]. Seven subtypes of botulinum toxin (A-G) are available for clinical use. Given its long effect duration, BoNT-A is used more often than the other botulinum toxin subtypes in urology. Because the molecular weight of BoNT-A is 150 kDa, it cannot access the submucosal nerve plexus in solution. Clinically, BoNT-A is directly injected, bypassing the urothelium to achieve botulinum toxin administration. However, BoNT-A injection therapy has many common and bothersome adverse events (AEs), such as leakage or uneven distribution of the drug, hematuria, pain, and risk of infection [8,9]. The incidence of these AEs varies among the results of many trials. Kuo et al. [10] reported that the most common AEs after botulinum toxin injection in 217 patients with refractory idiopathic detrusor overactivity (DO) were straining to void (46.5%), large postvoid residual (PVR) >150 mL (47.5%), UTIs (14.3%), and gross hematuria (7.8%). In a systematic review regarding intradetrusor Botox injections in patients with neurogenic DO, the most common reported AEs were injection site pain, UTIs (2%–32%), mild hematuria (2%–21%), and increased PVR, potentially resulting in urinary retention (0%–33%) or de novo intermittent self-catheterization (6%–88%) [11]. The diffusion of botulinum toxin beyond the injection site is also linked to a variety of life-threatening complications, such as generalized muscle weakness, dysphagia, and breathing difficulties, which are observed in rare cases after lower urinary tract injections of botulinum toxin [12,13]. Therefore, a safe and effective botulinum toxin preparation or delivery method to replace the traditional direct injection is urgently needed.
Nanoparticles, materials with a scale of 1 to 1,000 nm, have been developed rapidly in recent years. Nanomaterials are versatile in several research fields because of their characteristics, including a high surface-area-to-volume ratio, flexible construction, good biocompatibility, and biodegradability [14]. Nanomedicine, which incorporates different medical disciplines, has emerged as an especially promising discipline in the field of drug delivery. Advancements in intravesical drug delivery (IDD) systems have been significant for the treatment of urinary system diseases. Dose reduction increases drug effectiveness by targeting the site of the drug’s action. The other advantages of IDD include uniform delivery of the active agent, maximization of the therapeutic effect, and minimization of systemic side effects [15,16]. Specifically, compared to BoNT-A injection, the development of IDD as a method of BoNT-A administration for patients could simplify the treatment procedure by avoiding the need for anesthesia and cystoscopy and thus drastically reduce the treatment costs for patients with refractory OAB. More importantly, this procedure may improve AEs. However, the efficacy of intravesical delivered BoNT-A is restricted by its residence time and the extent to which it attaches to the bladder wall and penetrates into it. Researchers have tried to develop penetration enhancers to improve efficacy to some extent by using physical or chemical methods, such as electromotive force, chitosan, and dimethyl sulfoxide, which have yet to be optimized for large-scale use [17].
Interest has recently increased in intravesically administered agents carried by nanostructured systems, which can provide effective and safe therapy for bladder disorders. Therefore, in this review, we discuss recent developments in nanostructured IDD systems, the most recent formulation technologies, and the feasibility and physicochemical characteristics of the systems, providing prospects for progress in this field.
BLADDER PERMEABILITY BARRIER
The 4 layers of the bladder wall, from inside to outside, are the mucosa, the submucosa consisting of lamina propria and muscularis mucosae, the muscular layer consisting of the detrusor, and the serous layer [18]. As the main component of the bladder mucosal layer, the transitional urothelium acts as a physiological barrier between components of urine and the submucosal layers [19]. The urothelium is comprised of 3 layers of cells, including basal cells, intermediate cells, and the characteristically shaped surface umbrella cells. Tight junctions connecting the umbrella cells, densely packed plaques, and the glycosaminoglycan (GAG)-mucin layer form the bladder permeability barrier (BPB) (Fig. 1) [20].
The BPB is significant for the design of effective IDD. The bladder epithelium is regenerated by the differentiation of basal cells into the intermediate layer, with subsequently differentiation into the superficial epithelial layer, which contains polarized umbrella cells [21]. The diameter of umbrella cells can change from 50 to 120 μm, according to the degree of bladder expansion. The tight junctions connecting umbrella cells may reduce the permeability of ions, waste solutes, and some lipids [22], while the plaques covering the apical membrane can block small molecules such as water and urea. The hexagonal plaques consist of 4 uroplakins arranged in an orderly manner: UPIa (27 kDa), UPIb (28 kDa), UPII (15 kDa), and UPIII (47 kDa) (Fig. 1) [23,24].
The GAG layer serves as an antiadherence and anti-infection barrier on the urothelial surface, preventing solutes from reaching underneath the tight junctions and cell membranes [25,26]. The submucosal layer is made up of interstitial cells, blood vessels, myofibroblasts, and afferent sensory nerve endings in the lamina propria, tightly arranged under the basal membrane (Fig. 1). Meanwhile, the BPB structure of the urothelium restricts the adhesion and penetration of drugs after intravesical delivery, leading to elimination of the drug’s active ingredient. Hence, many drugs fail to reach their site of action in the bladder and ultimately cannot achieve the desired therapeutic effects.
MECHANISM OF ACTION OF BoNT-A
Structurally, BoNT-A consists of a 50-kDa light chain and a 100-kDa heavy chain linked by a noncovalent disulfide bond [27]. The process of BoNT-A entering the cell begins with recognition by 2 types of receptors on the cell membrane surface: gangliosides and synaptic vesicle glycoprotein 2 (SV2). Recent studies have also predicted that fibroblast growth factor receptor 3 may be an alternative receptor for BoNT-A [28]. The heavy-chain C-terminal of BoNT-A recognizes and binds to SV2 on the synaptic membrane of the nerve terminals, and BoNT-A is internalized into the nerve terminal by endocytosis [29].
After being transported into the cytosol, the disulfide bond of BoNT-A is cleaved in the synaptic vesicle. The N-terminal of the heavy chain binds to the endosomal membrane, and the light chain is transported from the endosome to the cytosol as the true active moiety of BoNT-A. Then the light chain cleaves synaptosome-associated protein 25 (SNAP-25), blocking the function of the soluble N-ethylmaleimide-sensitive factor attachment receptor family, which is essential for the transport of vesicles and signal transduction. Hence, BoNT-A inhibits neurotransmitter release by disrupting the fusion of vesicles with the neuron cell membrane, paralyzing the affected neuromuscular junctions (Fig. 2) [29].
Previous research has confirmed the distribution of SV2 and SNAP-25 in the submucosa and detrusor, but with no expression in the urothelium [30]. SV2 and SNAP-25 are expressed more abundantly in cholinergic than in parasympathetic fibers, with less than 50% of expression in the sensory and sympathetic nerves. Another study has demonstrated that the cleaved SNAP-25 is predominantly expressed in the parasympathetic nerve and that botulinum toxin mainly cleaves the SNAP-25 protein in cholinergic fibers [31]. These observations indicate that the parasympathetic nerves are the main target of BoNT-A action in the human bladder and that cleaved SNAP-25 is considered an important marker of sites of BoNT-A action for future research [30,31]. Other clinical studies and animal models have demonstrated that SV2 and SNAP-25 are expressed in the urothelial cells and mucosa of the rat and human bladder [32,33]. Because the urothelium is also an important signal transducer [18], many findings indicate that the IDD of BoNT-A may exert a therapeutic effect by acting on the urothelium through inhibition of neurotransmitter release from urothelial cells [34,35].
After BoNT-A is injected into the detrusor, the release of acetylcholine at the neuromuscular junction is temporarily blocked, and the actions of α and γ motor neurons innervate the extrafusal and the intrafusal muscle fibers, respectively. A randomized controlled trial on the effect of onabotulinum toxin A detrusor injections on postsynaptic muscular receptors in the human bladder with neurogenic DO showed downregulation of M2, M3, P2X2, and P2X3 receptors in the detrusor muscle after onabotulinum toxin A injections [36]. Traditionally, the therapeutic effects of BoNT-A on OAB have been attributed to the inhibition of detrusor or urethral sphincter contractions, suggesting that BoNT-A inhibits DO by affecting sensory and motor signal transmission.
Recent studies have revealed that BoNT-A injections can inhibit bladder sensory nerve function by reducing the expression of different receptors on afferent nerve fibers, including the ATP receptor P2X3 and the transient receptor potential vanilloid subfamily-1 (TRPV1) [37]. The decrease of TRPV1 and P2X3 immunoreactivity is correlated to fewer urgency episodes [37]. Other studies have shown that intravesical BoNT-A injections significantly inhibited the release of ATP and neurotrophin while increasing the release of nitric oxide from the urothelium [35,38].
NANOTECHNOLOGY IN INTRAVESICAL DRUG DELIVERY OF BoNT-A
Many studies have shown that direct intravesical instillation of BoNT-A cannot exert therapeutic effects [31,39]. Some factors prevent BoNT-A from penetrating the mucosa: First, the passive diffusion of BoNT-A is limited by tight junctions due to its large molecular weight (150 KDa). Second, the intact BPB blocks the adherence and permeation of BoNT-A, and third, the dilution and flushing effect of urine prevents BoNT-A from remaining localized in the bladder [40]. As previously mentioned, BoNT-A injections are associated with AEs in patients. Therefore, urologists have tried to overcome these obstacles with different approaches. The goal of these studies has been to achieve deep penetration of BoNT-A into the bladder and sufficient residence time in the bladder.
Currently, IDD, combined with nanotechnological approaches, is a potential tool to improve BoNT-A therapies. Nanomaterials, categorized into carbon-based materials (e.g., carbon nanotubes, carbon nanofibers, graphene), inorganic-based materials (e.g., gold, titanium oxide, silicon), organic-based materials (e.g., dendrimers, micelles, liposomes, polymer nanoparticles), and composite-based materials, have versatile properties as nanocarriers that enable penetration or retention in many tissues, including the urothelium [41,42]. Several nanoparticle formulations of BoNT-A have been investigated to improve IDD (Fig. 3).
Liposome Formulation of BoNT-A
Liposomes are spherical vesicles made up of an aqueous core surrounded by 1 or more phospholipid layers. Liposomes can load both lipophilic drugs (e.g., capsaicin) and hydrophilic drugs (e.g., botulinum toxin) [43,44]. Subsequently, liposomes penetrate the urothelium via endocytosis for IDD [45]. Empty liposomes have been shown to partially reverse high micturition frequency in a rat model of bladder hyperactivity induced by potassium chloride irritation after protamine sulfate intravesical instillation [46]. This indicates that empty liposomes may enhance the BPB by forming a protective lipid film on the urothelial surface against irritant penetration. Treatment with liposomes alone had no toxic effects on the urothelium. Liposomes were also found to protect urothelial cells from acrolein damage [47].
In a rat model of acetic acid-induced bladder hyperactivity, Chuang et al. [44] demonstrated that liposome-encapsulated BoNT-A significantly reduces bladder overactivity. Rats that received liposome-encapsulated BoNT-A (lipotoxin) had a larger decrease in the intercontraction interval (ICI) response to acetic acid instillation than liposome- or BoNT-A–pretreated rats, without compromising voiding function. Furthermore, intravesical lipotoxin instillation can cleave SNAP-25, inhibiting the release of calcitonin gene-related peptide from afferent nerves. The results indicate that BoNT-A with liposome as a vehicle can effectively and safely cross the BPB without a direct injection. Similar results were observed in animal studies with liposomes encapsulating capsaicin [43].
Furthermore, Kuo et al. [33] reported a double-blind randomized controlled pilot trial in 24 OAB patients at a single center to assess the safety and efficacy of lipotoxin. In this study, lipotoxin-containing 80-mg liposomes and 200 U of BoNT-A or normal saline were intravesically instilled and voiding diaries, Overactive Bladder Symptom Scores, urodynamic parameters, and AEs were assessed. At 1 month posttreatment, urinary frequency every 3 days and urgency significantly improved in the lipotoxin treatment group when compared to the control group. Taken together, the results showed no increase in PVR or risk of UTI in the lipotoxin-treated group. Immunohistochemistry and western blot studies showed the expression of SV2 and SNAP25 in urothelial cells and suburothelial tissues. However, no differential expression of SV2 or SNAP25 was observed between responders and nonresponders 3 months after treatment.
In a subsequent 2-center, placebo-controlled trial using the same lipotoxin, Chuang et al. [48] enrolled 62 participants with OAB inadequately managed with antimuscarinics to investigate whether intravesical instillation of lipotoxin could significantly decrease OAB symptoms and urinary frequency every 3 days without the AEs of dysuria, increased PVR, or UTI. However, lipotoxin treatment did not change the frequency of urgency urinary incontinence episodes in the 2 clinical trials. We could infer from the trials and the animal model that the penetration depth of intravesically instilled lipotoxin is not as deep as that of detrusor injections. Future studies could help determine whether the action of lipotoxin is restricted to the urothelium or lipotoxin is further transported to the submucosa for action. A larger randomized controlled trial is also needed to validate the effectiveness of lipotoxin in OAB.
Other studies have considered the application of lipotoxin for bladder sensory disorders such as interstitial cystitis/bladder pain syndrome (IC/BPS). However, Chuang et al. [49] demonstrated that the therapeutic effect of a single intravesical instillation of lipotoxin for patients with moderate to severe IC/BPS was likely due to a significant placebo effect. A study with a rat model of ketamine-induced cystitis showed that repeated intravesical instillation of lipotoxin can ameliorate bladder overactivity in ketamine-treated rats and restore the urothelial tight junction and adhesion proteins [50].
Thermosensitive Hydrogel Delivery of BoNT-A
Thermosensitive polymeric hydrogel stays in a liquid state at room temperature or below but converts to a semisolid state at a higher temperature (e.g., body temperature [37°C]). Thus, it can be injected in its liquid state and forms a hydrogel in situ in the bladder at higher body temperatures [51]. The triblock copolymer poly(ethylene glycol)-poly(lactic acid-co-glycolic acid)-poly(ethylene glycol) was used to form a polymeric hydrogel, which can be modified to acquire more hydrophobic characteristics and withstand urine components [52]. Because the hydrogel has the advantages of easy synthesis, good biocompatibility, and biodegradability, it can be used as an effective nanocarrier for IDD to maintain a prolonged release of drugs to the urothelium.
A double-blind randomized pilot study evaluated the effect of BoNT-A embedded in an inert TC-3 hydrogel in patients with idiopathic OAB [53]. The results revealed that intravesical instillation of 200 U BoNT-A in 50 mL of TC-3 gel can decrease urgency and leakage episodes and improve Overactive Bladder Questionnaire and Patient Perception of Bladder Condition total scores in patients with OAB after 1 month of treatment. Rappaport et al. [54] conducted a pilot study in 2018 to evaluate the feasibility and safety of a single intravesical instillation of 200 U of BoNT-A in 40 mL of TC-3 gel for IC/BPS patients. The study reported that intravesical instillation of BoNT-A could reduce the Visual Analog Scale for pain, Interstitial Cystitis Symptom Index, and Interstitial Cystitis Problem Index at week 12 compared with baseline, with transient and mild AEs. However, there was a borderline therapeutic effect on nocturia and urge episodes upon returning to baseline at week 12.
Hyaluronan-Phosphatidylethanolamine Delivery of BoNT-A
Ubiquitously distributed in biological fluids and tissues, hyaluronic acid (hyaluronan, HA) is a hydrophilic polysaccharide formed from disaccharide units containing N-acetyl-D-glucosamine and glucuronic acid. It has interesting rheological, viscoelastic, and biological properties, which are attributed to its polymeric and polyelectrolyte characteristics [55-57]. Topically applied HA has poor penetration for its molecular weight of 50 kDa. Thus, linking HA to phosphatidylethanolamine (PE) to develop a nonparticulate formula can enhance its penetrating properties and HA levels throughout epidermal cell layers [58]. Its high viscosity makes HA-PE an excellent carrier for transferring BoNT-A through the urothelium.
In 2017, El Shatoury et al. [59] examined the effect of intravesical instillation of BoNT-A embedded in HA-PE in a rat model of hyperactive bladder induced by 1% acetic acid instillation. The results proved that bladder instillation of 10 U BoNT-A embedded in 0.4 or 0.5 g of HA-PE for 60 minutes, instead of BoNT-A with a lower HA-PE dose or a shorter instillation time, transferred BoNT-A throughout the bladder urothelium. In this study, both HA-PE–embedded and intradetrusor-injected BoNT-A showed comparable cleavage of SNAP-25, and rats in both groups showed a comparable effect on the prolongation of ICI compared with baseline. These results all suggested that adequate HA-PE with a sufficient instillation time favors the ability of BoNT-A embedded in HA-PE to penetrate the bladder mucosa and reach comparable efficacy as intradetrusor injection.
OTHER NANOCARRIERS FOR INTRAVESICAL DRUG DELIVERY
Nanotechnology in IDD is not only applied to lower urinary tract dysfunction, but is widely used in chemotherapy and bacillus Calmette-Guérin immunotherapy against bladder cancer. The nanocarriers developed for bladder cancer intravesical therapy were mainly based on microparticles and nanoparticles, carbon nanotubes, hydrogels, nanogels, liposomes, and micelles [60]. These nanocarriers can transport the active agent of drugs to the target sites and provide controlled release, and their biocompatible and biodegradable natures enable them to be used in IDD [61-65]. Currently studied nano-scale materials with great potential include chitosan, dendrimers, and lipid, protein, polymeric, magnetic, and inorganic nanoparticles [16,20,66,67]. For their excellent mucosal adhesion and penetration characteristics, they may be able to be used as a carrier of botulinum toxin to achieve safe and effective submucosal administration. However, different drugs have distinct physicochemical and pharmacodynamic characteristics, which determine their unique clinical efficiency and side effects [68]. Given the pathological differences between bladder cancer and OAB, ongoing experiments are needed to verify the feasibility of these nanocarriers.
CONCLUSIONS AND FUTURE PROSPECTS
Nanotechnology in IDD, directing the instillation of botulinum toxin with nanocarriers into the urinary bladder via catheters, is an effective alternative to intradetrusor injections. This method, which can maximize local therapeutic effects while minimizing adverse effects, relies on the development of nanocarriers that can effectively penetrate the urothelial barrier to reach the submucosa and deeper layers, stably release drugs, and be safe to the bladder tissue. In this review, suitable nanocarriers for transferring BoNT-A into the bladder were discussed. The effectiveness of liposome-encapsulated BoNT-A has been investigated in animal models and clinical trials. However, intravesical instillation of lipotoxin did not reach a similar efficacy as intradetrusor injection, and the therapeutic effect of lipotoxin lasted only 1 month. Clinical trials of thermosensitive hydrogelembedded BoNT-A were only marginally satisfactory, and clinical trials of HA-PE are needed to prove its efficacy. However, each type of nanocarrier has specific disadvantages, and it is difficult to decide which nanocarrier would be most promising. Research on liposomes is the earliest and most detailed, yet the potential of other nanocarriers should not be dismissed. Further research is required to discover potential nanocarriers with excellent mucosal adhesion and penetration abilities for intravesical instillation-based therapy. We hope that these safe, efficient carriers can be developed and become clinically available to patients with bladder dysfunction in the near future.
Conflict of Interest
No potential conflict of interest relevant to this article was reported.
AUTHOR CONTRIBUTION STATEMENT
·Conceptualization: LL
·Data curation: QL
·Formal analysis: LL
·Funding acquisition: LL
·Methodology: QL
·Project administration: LL
·Visualization: QL
·Writing-original draft: QL
·Writing-review & editing: LL
REFERENCESAbramsPCardozoLFallMGriffithsDRosierPUlmstenUThe standardisation of terminology of lower urinary tract function: report from the Standardisation Sub-committee of the International Continence Society20022116778LinkCLSteersWDKusekJWMcKinlayJBThe association of adiposity and overactive bladder appears to differ by gender: results from the Boston Area Community Health survey201118595563IrwinDEKoppZSAgatepBMilsomIAbramsPWorldwide prevalence estimates of lower urinary tract symptoms, overactive bladder, urinary incontinence and bladder outlet obstruction201110811328PeyronnetBMironskaEChappleCCardozoLOelkeMDmochowskiRA comprehensive review of overactive bladder pathophysiology: on the way to tailored treatment2019759881000MengELinWYLeeWCChuangYCPathophysiology of overactive bladder20124 Suppl 14855LightnerDJGomelskyASouterLVasavadaSPDiagnosis and treatment of overactive bladder (non-neurogenic) in adults: AUA/ SUFU Guideline Amendment 2019201920255863FranciosaGFloridiFMauglianiAAureliPDifferentiation of the gene clusters encoding botulinum neurotoxin type A complexes in Clostridium botulinum type A, Ab, and A(B) strains20047071929MehnertUBoySSchmidMReitzAvon HesslingAHodlerJA morphological evaluation of botulinum neurotoxin A injections into the detrusor muscle using magnetic resonance imaging200927397403KuoHCUrodynamic evidence of effectiveness of botulinum A toxin injection in treatment of detrusor overactivity refractory to anticholinergic agents20046386872KuoHCLiaoCHChungSDAdverse events of intravesical botulinum toxin a injections for idiopathic detrusor overactivity: risk factors and influence on treatment outcome20105891926KarsentyGDenysPAmarencoGDe SezeMGaméXHaabFBotulinum toxin A (Botox) intradetrusor injections in adults with neurogenic detrusor overactivity/neurogenic overactive bladder: a systematic literature review20085327587OrasanuBMahajanSTThe use of botulinum toxin for the treatment of overactive bladder syndrome201329211De LaetKWyndaeleJJAdverse events after botulinum A toxin injection for neurogenic voiding disorders2005433979MaddoxMLiuJMandavaSHCallaghanCJohnVLeeBRNanotechnology applications in urology: a review201411465360TyagiPWuPCChancellorMYoshimuraNHuangLRecent advances in intravesical drug/gene delivery2006336979ZacchèMMSrikrishnaSCardozoLNovel targeted bladder drugdelivery systems: a review2015716978GiannantoniADi StasiSMChancellorMBCostantiniEPorenaMNew frontiers in intravesical therapies and drug delivery200650118393discussion 1193BirderLAnderssonKEUrothelial signaling20139365380LewisSAEverything you wanted to know about the bladder epithelium but were afraid to ask2000278F86774GuhaSarkarSBanerjeeRIntravesical drug delivery: challenges, current status, opportunities and novel strategies201014814759BirderLAMore than just a barrier: urothelium as a drug target for urinary bladder pain2005289F48995HaynesMDMartinTAJenkinsSAKynastonHGMatthewsPNJiangWGTight junctions and bladder cancer (review)20051639WuXRLinJHWalzTHänerMYuJAebiUMammalian uroplakins. A group of highly conserved urothelial differentiationrelated membrane proteins19942691371624YuJLinJHWuXRSunTTUroplakins Ia and Ib, two major differentiation products of bladder epithelium, belong to a family of four transmembrane domain (4TM) proteins199412517182SolerRBruschiniHMartinsJRDreyfussJLCamaraNOAlvesMTUrinary glycosaminoglycans as biomarker for urothelial injury: is it possible to discriminate damage from recovery?20087293742PoggiMMJohnstonePAConnerRJGlycosaminoglycan content of human bladders. a method of analysis using cold-cup biopsies200052347RossettoOPirazziniMMontecuccoCBotulinum neurotoxins: genetic, structural and mechanistic insights20141253549BenoitRMFreyDHilbertMKevenaarJTWieserMMStirnimannCUStructural basis for recognition of synaptic vesicle protein 2C by botulinum neurotoxin A201450510811DongMYehFTeppWHDeanCJohnsonEAJanzRSV2 is the protein receptor for botulinum neurotoxin A20063125926CoelhoADinisPPintoRGorgalTSilvaCSilvaADistribution of the high-affinity binding site and intracellular target of botulinum toxin type A in the human bladder20105788490CoelhoACruzFCruzCDAvelinoASpread of onabotulinumtoxinA after bladder injection. Experimental study using the distribution of cleaved SNAP-25 as the marker of the toxin action201261117884Hanna-MitchellATWolf-JohnstonASBarrickSRKanaiAJChancellorMBde GroatWCEffect of botulinum toxin A on urothelial-release of ATP and expression of SNARE targets within the urothelium2015347984KuoHCLiuHTChuangYCBirderLAChancellorMBPilot study of liposome-encapsulated onabotulinumtoxina for patients with overactive bladder: a single-center study201465111724ApostolidisADasguptaPFowlerCJProposed mechanism for the efficacy of injected botulinum toxin in the treatment of human detrusor overactivity20064964450CruzFTargets for botulinum toxin in the lower urinary tract201433318Schulte-BauklohHPriefertJKnispelHHLawrenceGWMillerKNeuhausJBotulinum toxin A detrusor injections reduce postsynaptic muscular M2, M3, P2X2, and P2X3 receptors in children and adolescents who have neurogenic detrusor overactivity: a singleblind study20138110527ApostolidisAPopatRYiangouYCockayneDFordAPDavisJBDecreased sensory receptors P2X3 and TRPV1 in suburothelial nerve fibers following intradetrusor injections of botulinum toxin for human detrusor overactivity200517497782discussion 982-3YiangouYFacerPFordABradyCWisemanOFowlerCJCapsaicin receptor VR1 and ATP-gated ion channel P2X3 in human urinary bladder2001877749KheraMSomogyiGTSalasNAKissSBooneTBSmithCPIn vivo effects of botulinum toxin A on visceral sensory function in chronic spinal cord-injured rats20056620812ChenPYLeeWCWangHJChuangYCTherapeutic efficacy of onabotulinumtoxinA delivered using various approaches in sensory bladder disorder20201275JeevanandamJBarhoumAChanYSDufresneADanquahMKReview on nanoparticles and nanostructured materials: history, sources, toxicity and regulations20189105074MartinDTHoimesCJKaimakliotisHZChengCJZhangKLiuJNanoparticles for urothelium penetration and delivery of the histone deacetylase inhibitor belinostat for treatment of bladder cancer20139112434TyagiPChancellorMBLiZDe GroatWCYoshimuraNFraserMOUrodynamic and immunohistochemical evaluation of intravesical capsaicin delivery using thermosensitive hydrogel and liposomes20041714839ChuangYCTyagiPHuangCCYoshimuraNWuMKaufmanJUrodynamic and immunohistochemical evaluation of intravesical botulinum toxin A delivery using liposomes200918278692ChenPYLeeWCWangHJChuangYCTherapeutic efficacy of onabotulinumtoxinA delivered using various approaches in sensory bladder disorder20201275FraserMOChuangYCTyagiPYokoyamaTYoshimuraNHuangLIntravesical liposome administration--a novel treatment for hyperactive bladder in the rat20036165663NirmalJWolf-JohnstonASChancellorMBTyagiPAnthonyMKaufmanJLiposomal inhibition of acrolein-induced injury in rat cultured urothelial cells201446194752ChuangYCKaufmannJHChancellorDDChancellorMBKuoHCBladder instillation of liposome encapsulated onabotulinumtoxina improves overactive bladder symptoms: a prospective, multicenter, double-blind, randomized trial201419217439ChuangYCKuoHCA prospective, multicenter, double-blind, randomized trial of bladder instillation of liposome formulation onabotulinumtoxina for interstitial cystitis/bladder pain syndrome201719837682LeeWCSuCHTainYLTsaiCNYuCCChuangYCPotential orphan drug therapy of intravesical liposomal onabotulinumtoxinA for ketamine-induced cystitis by mucosal protection and anti-inflammation in a rat model201885795TyagiPLiZChancellorMDe GroatWCYoshimuraNHuangLSustained intravesical drug delivery using thermosensitive hydrogel2004218327JeongBBaeYHKimSWDrug release from biodegradable injectable thermosensitive hydrogel of PEG-PLGA-PEG triblock copolymers20006315563KrhutJNavratilovaMSykoraRJurakovaMGärtnerMMikaDIntravesical instillation of onabotulinum toxin A embedded in inert hydrogel in the treatment of idiopathic overactive bladder: A double-blind randomized pilot study2016502005RappaportYHZismanAJeshurun-GutshtatMGerassiTHakimGVinshtokYSafety and feasibility of intravesical instillation of botulinum toxin-A in hydrogel-based slow-release delivery system in patients with interstitial cystitis-bladder pain syndrome: a pilot study2018114605KoganGSoltésLSternRGemeinerPHyaluronic acid: a natural biopolymer with a broad range of biomedical and industrial applications2007291725VoigtJDriverVRHyaluronic acid derivatives and their healing effect on burns, epithelial surgical wounds, and chronic wounds: a systematic review and meta-analysis of randomized controlled trials20122031731SternRMaibachHIHyaluronan in skin: aspects of aging and its pharmacologic modulation20082610622SymonetteCJKaur MannATanXCTolgCMaJPereraFHyaluronan-phosphatidylethanolamine polymers form pericellular coats on keratinocytes and promote basal keratinocyte proliferation20142014727459El ShatouryMGDeYoungLTurleyEYazdaniADaveSEarly experimental results of using a novel delivery carrier, hyaluronanphosphatidylethanolamine (HA-PE), which may allow simple bladder instillation of botulinum toxin A as effectively as direct detrusor muscle injection201814172.e1172.e6OliveiraMBVilla NovaMBruschiMLA review of recent developments on micro/nanostructured pharmaceutical systems for intravesical therapy of the bladder cancer201823112BarthelmesJPereraGHombachJDünnhauptSBernkop-SchnürchADevelopment of a mucoadhesive nanoparticulate drug delivery system for a targeted drug release in the bladder201141633945LuSNeohKGKangETMahendranRChiongEMucoadhesive polyacrylamide nanogel as a potential hydrophobic drug carrier for intravesical bladder cancer therapy2015725768PoinardBLamSAENeohKGKahJCYMucopenetration and biocompatibility of polydopamine surfaces for delivery in an ex vivo porcine bladder201930016173LiGWangSDengDXiaoZDongZWangZFluorinated chitosan to enhance transmucosal delivery of sonosensitizer-conjugated catalase for sonodynamic bladder cancer treatment postintravesical instillation202014158699WangBZhangKWangJZhaoRZhangQKongXPoly (amidoamine)-modified mesoporous silica nanoparticles as a mucoadhesive drug delivery system for potential bladder cancer therapy2020189110832QiuXCaoKLinTChenWYuanAWuJDrug delivery system based on dendritic nanoparticles for enhancement of intravesical instillation201712736574ChengCJTietjenGTSaucier-SawyerJKSaltzmanWMA holistic approach to targeting disease with polymeric nanoparticles20151423947SunDZhouSGaoWWhat went wrong with anticancer nanomedicine design and how to make it right2020141228190Figures
Schematic diagram of the bladder wall and bladder permeability barrier (BPB). The bladder wall consists of the mucosa, submucosa (lamina propria and muscularis mucosae), muscular layer (detrusor), and serous layer. The urothelium consists of 3 layers of cells, including basal cells, intermediate cells, and the characteristic surface umbrella cells. The composition of the BPB includes umbrella cells joined by tight junctions, dense plaques, and a glycosaminoglycan (GAG)-mucin layer on the surface. The plaque subunit comprises 4 types of uroplakins (UPs) arranged in an orderly manner.
Botulinum toxin type A (BoNT-A) inhibits neurotransmitter release from nerve terminals. The heavy chain of BoNT-A recognizes and binds to synaptic vesicle glycoprotein 2 (SV2) on the synaptic membrane of the nerve terminals, then BoNT-A is internalized into the nerve terminal by endocytosis. In the synaptic vesicle, the disulfide bond of BoNT-A is cleaved, and the light chain is released from the endosome to the cytosol. Light chain cleaves synaptosome-associated protein 25 (SNAP-25) and blocks the function of SNARE, thereby inhibiting neurotransmitter transportation within vesicles. HC, heavy chain; LC, light chain; VAMP, vesicle-associated membrane protein.
Illustration of different strategies using nanocarriers for Botulinum toxin type A (BoNT-A) intravesical delivery. Nanocarriers (liposomes, hyaluronan-phosphatidylethanolamine [HA-PE], and thermosensitive hydrogels) conjugated to BoNT-A facilitate urothelial penetration and retention of active ingredients.