Recent Advances in Reactive Oxygen Species (ROS)-Responsive Polyfunctional Nanosystems 3.0 for the Treatment of Osteoarthritis.

Osteoarthritis (OA) is an inflammatory and degenerative joint disease with severe effects on individuals, society, and the economy that affects millions of elderly people around the world. To date, there are no effective treatments for OA; however, there are some treatments that slow or prevent its progression. Polyfunctional nanosystems have many advantages, such as controlled release, targeted therapy and high loading rate, and have been widely used in OA treatment. Previous mechanistic studies have revealed that inflammation and ROS are interrelated, and a large number of studies have demonstrated that ROS play an important role in different types of OA development. In this review article, we summarize third-generation ROS-sensitive nanomaterials that scavenge excessive ROS from chondrocytes and osteoclasts in vivo. We only focus on polymer-based nanoparticles (NPs) and do not review the effects of drug-loaded or heavy metal NPs. Mounting evidence suggests that polyfunctional nanosystems will be a promising therapeutic strategy in OA therapy due to their unique characteristics of being sensitive to changes in the internal environment.

Introduction

Osteoarthritis (OA), characterized by the progressive destruction of articular cartilage and joint dysfunction, is currently the second leading cause of disability in patients after cardiovascular disease.1,2 The increase in the elderly population and the prevalence of obesity across the world have incited a rising incidence of OA.3 According to an epidemiological investigation, the incidence of OA in the population over 65 years old can reach 50%, and the incidence among individuals over 80 years old is as high as 80%.4 Approximately 80% of OA patients have different degrees of movement impairment, and 25% have difficulties performing the activities in daily life.5 Consequently, OA has caused a huge burden on society, the economy, and individuals.

OA has a complex pathophysiological process. The main pathological manifestations are cartilage degeneration, bone remodeling, osteophyte formation and joint inflammation.6 OA can affect almost any joint, but it is most common in the hands, knees, hips and feet. Among them, excessive oxidative stress is an important factor in the pathological progression of OA. Mechanistically, reactive oxygen species (ROS), as a secondary messenger, gradually aggravate OA inflammation by activating the ROS/phosphoinositol-3 kinase (PI3K)/serine/threonine kinase (AKT),7 ROS/mitogen-activated protein kinase (MAPK)8 and reactive nitrogen species (RNS)/tumor necrosis factor-α (TNF)-α/nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathways.9,10 Excessive ROS can not only lead to the senescence and death of chondrocytes and destroy chondrocytes and the extracellular matrix (ECM) but also induce subchondral bone dysfunction. Moreover, ROS can promote M1 macrophage polarization. Synovial inflammation driven by M1 macrophages is thought to be one of the key causes of OA development and progression.11 M1 macrophages can secrete IL-1β, activating NF-κB to promote the secretion of TNF-α by chondrocytes, and this process is enhanced by interferon-γ via the JAK/STAT pathway.12–14 Furthermore, TNF-α regulates CXCL1 through 2 different pathways, one through JNK and its downstream AP-1 transcription factor influencing the expression of genes and the other affecting cellular CXCL1 secretion by p38 MAPK and PI3K activation.14 High CXCL1 expression leads to neutrophil infiltration,15 which can enhance the inflammatory response.

In addition, other joint tissues, such as the infrapatellar fat pad, synovial membrane and meniscus, all generate inflammatory changes after the onset of OA, contributing to the progression of OA. Increasing evidence has shown that synovial macrophage activation is one of the major destructive factors during the progression of OA.16 M1 macrophages, which promote synovial inflammation, secrete several proinflammatory cytokines, including IL-1β, IL-6, IL-12, and TNF-α, which cause cartilage degeneration.17 Moreover, advanced oxidation protein products (AOPPs), which are a sign of oxidative stress, upregulate the expression of MMP3 and MMP13 in the synovium, contributing to cartilage degradation.18 In addition, the meniscus is an important soft tissue in the etiology of knee OA (KOA). It has been reported that the severity of meniscal insufficiency is linked with the advancement of OA.19 IL-1β can promote meniscal cell apoptosis by inactivating c-JNK2 and suppressing autophagy, the production of which is elevated in meniscal cells under pathological conditions.20–22 Damage to the meniscus causes overload on the cartilage and thus accelerates the degeneration of chondrocytes. Furthermore, the infrapatellar pad is a new source of inflammatory factors and adipokines that contribute to KOA progression.23 The combination of inflammatory pathways and ROS signaling is well recognized in adipose dysfunction and metabolic syndrome.24 Lipid peroxidation produces a wide range of hydroperoxide and aldehyde compounds that are highly reactive with cell membrane and ECM components.25,26 Lipid radicals are also intracellular signaling molecules that affect a variety of cellular activities.27,28 For example, malondialdehyde (MDA), a hazardous aldehydic end product of lipid peroxidation, facilitates cartilage collagen oxidation, leading to cartilage degradation.29 The interactions of ROS with OA joint tissues are shown in Figure 1.

Figure 1

The interaction of ROS with OA joint tissues.

The most common clinical symptoms of OA are joint aches, swelling and stiffness. Therefore, the main objectives of OA treatment focus on easing pain, relieving joint swelling, improving the mobility of the joint, and minimizing disability. At present, conservative nonsurgical management of OA is divided into two main categories: pharmacological and physical intervention.30 Pharmacological intervention generally refers to oral or intra-articular injection of nonsteroidal anti-inflammatory drugs (NSAIDs) and intra-articular injection of corticosteroids and hyaluronan to suppress joint inflammation and relieve joint pain.31 However, oral drugs often cause adverse reactions such as gastrointestinal reactions and osteonecrosis, while intra-articular topical administration is shortened by the fact that drugs are rapidly cleared in synovial joints, resulting in a shortened duration of efficacy.32 Currently, there are still no effective therapeutic drugs for treating or slowing the progression of OA. Physical therapy consists mainly of interventions such as moderate exercise, weight loss, or occupational therapy.33,34 However, when patients present with severe joint damage and conservative treatment is insufficient to control symptoms, surgical treatment, such as arthroplasty and osteotomy, is usually the only option. As a result, there is an urgent need to clarify how the pathologically driven process of OA can be effectively suppressed. Drug delivery systems with controlled release can not only reduce the side effects and normal tissue exposure in OA treatment but also prolong the duration of drugs in the joint and avoid frequent drug administration through its sensitivity to changes in the microenvironment and cell targeting.

Therefore, we first emphasized the key role of ROS in the development of OA; then, we introduced the targeting effect of ROS-sensitive nanomaterials on chondrocytes and osteoclasts in the treatment of OA; finally, we summarized the advantages of nanotherapy in the treatment of OA to illustrate that multifunctional nanosystems will be a promising treatment strategy for OA in the future.

The Critical Role of ROS in the Development of OA

Excessive ROS production that is associated with oxidative stress plays an important role in OA. Oxidative stress has long been considered a significant factor in the induction of chondrocyte senescence and apoptosis in OA.35,36 The excess production of free radicals under oxidative stress is considered to be the main mechanism of cartilage damage,37 and therefore, the role of ROS in the pathogenesis of OA has become a primary concern of researchers.38,39

Sources of ROS and Related Enzymes Involved in Oxidative/Antioxidative Systems

ROS are an important factor that influences intracellular redox status. Common biologically relevant ROS include superoxide anion (O2−), hydroxyl free radical (HO−), and hydrogen peroxide (H2O2).

Endogenous and physiological ROS are mainly generated in the oxidative reaction process of the mitochondrial respiratory chain as byproducts of normal cellular metabolism. In animals, mitochondria and plasma membrane-bound nicotinamide adenine dinucleotide phosphate (NADPH) oxidases (NOXs) are the major sources of ROS, playing a central role in the induction of cell death.40 ROS can induce mitochondrial dysregulation by increasing mitochondrial membrane permeability, which further increases ROS production and leads to the release of ROS into the cytosol.41 Therefore, it is now well established that mitochondria are the major producers of ROS and the main targets of ROS. Defective mitochondrial function has been implicated in degenerative joint diseases such as OA.42 In addition to mitochondria, another source of cytoplasmic ROS is the cytochrome P450 enzyme (CYP) system, which responds to toxic substances. Moreover, the endoplasmic reticulum (ER) is also the source of ROS. ER oxidoreductase 1 (ERO1), which is associated with the inner ER membrane, has been shown to catalyze the formation of disulfide bonds in secretory proteins and associated H2O2 formation.43

Basic levels of ROS are essential for cellular signal transduction and physiological function. Excessive ROS that are caused by the imbalance between ROS production and antioxidants may induce severe damage to various biomolecules, such as protein oxidation, lipid peroxidation, and DNA fragmentation, which are associated with various inflammatory diseases, such as OA.9 These enzymes, including the NADPH oxidase family of enzymes (NOX), xanthine oxidase (XO), myeloperoxidase (MPO), and lipoxygenases, are responsible for the essential sources of ROS:44

In eukaryotes, critical enzymes for preventing ROS formation are superoxide dismutases (SODs), glutathione peroxidases (GPx), catalase (CAT) and glutathione reductase (GR). SOD and CAT are the best antioxidants in vivo. SODs can be classified into cytosolic CuZn-SOD (SOD1), mitochondrial Mn-SOD (SOD2) and extracellular SOD (SOD3). SOD can catalyze O2− into O2 and H2O2.45 GPxs reduce lipid hydroperoxides to their corresponding alcohols and mediate the breakdown of H2O2 to H2O. CAT, located mainly in peroxisomes, also mediates the decomposition of H2O2 to H2O and O2.46 GR catalyzes the reduction of glutathione disulfide (GSSG) to the sulfhydryl form of glutathione (GSH), which is a critical molecule in resisting oxidative stress.47 Recovering the appropriate ROS concentration by regulating ROS production or neutralizing ROS is a potentially effective means of preventing and treating diseases related to oxidative stress.48 The production and conversion of ROS are summarized in Figure 2.

Figure 2

A schematic diagram of reactive oxygen species including production and conversion.

Cell Function is Impaired by ROS at the Cellular and Molecular Levels

ROS are produced mainly by NOXs at low levels in normal articular chondrocytes. However, many pathological factors, such as inflammatory factors and mechanical pressure, will cause a high concentration of ROS production. Excessive ROS production can induce irreversible damage to articular cartilage and apoptosis of chondrocytes, which is the main cause of OA.49–51 The downstream molecular targets of ROS include nucleic acids, proteins, and lipids. Elevated ROS levels lead to hyperperoxidation, protein carbonylation and DNA damage, leading to the functional loss of chondrocytes.39,52 A recent study suggested that cell senescence was also closely related to OA development.53 Chondrocytes from human cartilage explants cultured in the presence of hydrogen peroxide exhibited senescence hallmarks.54 Exogenous senescence is induced by a variety of stresses, such as DNA damage and oxidative stress.55

Furthermore, studies have demonstrated that elevated ROS levels can promote the catabolism of chondrocytes by increasing the production of MMPs, resulting in the destruction of the cartilage matrix, including collagen, proteoglycans and hyaluronan, in OA.39,56 Therefore, studies have shown that targeting ROS effectively suppresses the severity of OA in vivo.57 Bardoxolone methyl (BM), a semisynthetic triterpenoid, has been proven to alleviate OA progression by preventing oxidative stress-induced chondrocytes apoptosis and ECM degradation, such as aggrecan and collagen II degradation.58,59 In addition, irisin, an 8-pentenyl flavonoid glycoside, repressed inflammation-mediated oxidative stress and extracellular matrix underproduction by retaining mitochondrial biogenesis, dynamics and autophagic programs.60

The Mutual Influences Between Inflammation and Oxidative Stress

ROS and inflammation are interdependent and interact with each other, and thus, they are both ideal targets for the treatment of OA. Local inflammatory responses along with aging and/or mechanical load can contribute to increased oxidative stress with the accumulation of ROS, O2−, H2O2, and concomitant failure in the expression of antioxidant enzymes and ROS scavenging systems.61 Various proinflammatory mediators, such as cytokines TNF-α and interleukin (IL)-1β, −8, −6, −15, −17, −18, −21, and −33), are increased in the joint tissue of OA patients and have been shown to induce oxidative stress, apoptosis and catabolic gene expression in OA individuals.62,63 These proinflammatory cytokines stimulate chondrocytes and osteoclasts to activate cartilage degradation pathways, thereby driving OA pathogenesis.64

The NOD-like receptor (NLR) family pyrin domain containing 3 (NLRP3) inflammasome is one of the most studied inflammasome sensors and a master regulator of inflammation in OA.65 A recent study suggested that intracellular ROS are elevated by various NLRP3 stimulators and that enhanced ROS in turn activate the NLRP3 inflammasome.66 ROS production has also been reported to stimulate NLRP3 inflammatory body assembly in a ROS-sensitive manner.67 Accumulated ROS also activate the NLRP3 inflammasome in synovial membrane macrophages and increase the expression of the proinflammatory cytokines IL-18 and IL-1β.68

Some compounds have exhibited both antioxidant and anti-inflammatory effects in the treatment of OA. Engeletin is a natural compound with anti-inflammatory and antioxidant effects on other diseases. Pretreatment with engeletin alleviated TNF-α-induced inhibition of ECM synthesis (collagen II and aggrecan) and upregulation of matrix catabolic enzymes (MMP9 and MMP3) and scavenged intracellular ROS by activating the Nrf2 pathway.69 Tempol (4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl) has excellent antioxidant and anti-inflammatory effects by decreasing superoxide ion levels in LPS-induced macrophages.70 In addition, resveratrol has a strong protective effect against B[a]P-induced intracellular ROS generation by increasing mitochondrial content and function.71 Furthermore, ascorbic acid reduces H2O2 production and lipid peroxidation by inhibiting the NF-κB pathway.72

ROS Play an Important Role in OA

OA can be classified as primary and secondary. Aging plays a major role in primary OA, while obesity and joint injury are the two most relevant risk factors for secondary OA.73

Aged-related NOXs are rarely detected in young individuals, but the levels increase with age. The degree of cartilage degradation is correlated with the activity of NOXs in age-related OA.74 Advanced oxidation protein products (AOPPs) are also considered biomarkers of oxidative stress, and intra-articular injections accelerate cartilage degeneration in rabbit OA models.18 AOPPs have been reported to activate the NOXs-mediated oxidative stress pathway in oxidation-associated diseases.75 The excessive production of ROS is attributed to mitochondrial dysfunction, and the decline in antioxidant enzymes such as catalase (CAT) and superoxide dismutases (SODs) with age has also been implicated in the development of aging-related OA.76,77

In addition, type II diabetes mellitus (T2DM) is the most common subtype of diabetes in diabetic patients, accounting for >90% of the total number, and most of the patients are obese. In recent years, the incidence of T2DM with OA has gradually increased. The symptoms in OA patients with diabetes are more severe than those in nondiabetic patients with OA.78 The possible reason may be linked to the increased proinflammatory cytokines that are secreted by adipocytes and invading macrophages in adipose tissue.79 Adipokines increase the number of activated macrophages that generate proinflammatory cytokines, such as IL-1β, TNF-α and ROS, by acting on the synovial membrane of the joint.80,81 Moreover, chronic hyperglycemia induces the production of ROS, leading to increased ROS and reduced synthesis of type II collagen (COL-II).82

Moreover, the aberrant overproduction of ROS is also a potential component of the biochemical inflammatory response to joint injury. In the inflammatory response, overproduction of ROS is potentially harmful to tissues and may sensitize the joint to the development of posttraumatic osteoarthritis (PTOA).83 After joint injury, the inflammatory mediators in synovial fluid increased significantly and subsequently decreased gradually. Within 24 hours of acute ligament tear, cytokine (IL-1β, TNF-α) and keratin sulfate levels rise rapidly and remain high for 7 days.84,85 These inflammatory factors could contribute to oxidative stress.86,87 For example, IL-1β has been shown to reduce ATP-binding cassette transporter A (ABCA-1) mRNA expression and enhance intracellular lipid retention to promote M1 macrophage polarization.88 Therefore, inhibiting aberrant ROS signaling in the inflammatory response after joint injury may have the potential to protect normal joint tissues and decrease early changes associated with the development of PTOA.83

Chondrocytes and Osteoclasts as Targets for OA Treatment

Synovitis is one of the typical manifestations of OA. The synovial tissue is mainly composed of synovial macrophages and synoviocytes. Macrophage-mediated synovial inflammation is the main driving factor for the occurrence and progression of OA. The increased number of macrophages results in an imbalance between the synthesis and degradation of the ECM in cartilage by upregulating the expression levels of proinflammatory factors, thus damaging the function of the cartilage.33,34

However, the inflammatory response in OA depends mainly on activated osteoclasts, which can secrete ROS molecules, and persistent oxidative stress is the source of inflammation.64 Recent studies have also indicated that ROS are important components regulating the differentiation process of osteoclasts.89,90 In a hypoxic environment, the accumulation of mitochondrial ROS is essential for osteoclast differentiation.91,92 NOX has been identified as one of the key sources of ROS. It has also been reported that the decreased production of ROS by silencing NOX1 (a member of the NOX family) in bone marrow mononuclear macrophages inhibited osteoclasts differentiation.93 In addition to osteoclasts from synovial tissue, osteoclasts from subchondral bone also play an important role in OA. The abnormal mechanical overload caused by anterior cruciate ligament tears leads to an increase in osteoclast activity and bone resorption in subchondral bone, which finally triggers the occurrence of OA.94 Inhibition of hyperactivated osteoclast activity in subchondral bone can ameliorate OA severity.95 Betaine maintains the structural integrity of subchondral bone and slows the progression of OA by reducing the production of ROS and inhibiting the activity of osteoclasts.96 Therefore, osteoclasts are an important target in the treatment of OA.

Chondrocytes, the only cell type present in articular cartilage, are responsible for cartilage homeostasis by maintaining a balance between the synthesis and degradation of ECM comprising primarily type II collagen and aggrecan. It has been reported that ROS components detected in OA joints that can directly destroy hyaline include O2−, HO−, peroxide, and hydroxyproline.97 H2O2 inhibited proteoglycan production in chondrocytes by inhibiting mitochondrial oxidative phosphorylation and ATP generation and subsequently induced chondrocyte cell death in a dose-dependent manner.98,99 Furthermore, oxidative stress causes apoptosis in superficial cartilage areas, resulting in hypertrophic chondrocytes in deeper places and affecting normal endochondral ossification and matrix repair.100 Hence, early intervention for oxidative stress is necessary to prevent cartilage damage. Antioxidative agents hold great potential in OA treatment for a considerably high level of oxidative stress that was associated with the development of OA.39,101 Free radical scavengers with excellent biocompatibility and lower cytotoxicity will expand their further applications in OA therapy.

Polyfunctional Nanosystems 3.0 means that the third generation of nanocarriers was stimuli-responsive or activated by local environmental changes such as decreased pH, imbalanced redox state, temperature, and external stimuli such as light, ultrasound and magnetic field. Here, we focus on the third generation of nanomaterials that are ROS-responsive in treating OA.

The ROS-responsive nanomaterials for targeting chondrocytes and osteoclasts in OA are shown in Table 1.

Table 1

The ROS Responsive Biomaterials for OA Therapy

Nanomaterial	Platform	Target Cells	Main Structure Components	Function	Ref
RRHMs	Hollow microsphere	Osteoclasts	1. C2H5OH(ROS-responsive)2. DEX-P (drug)3. SBC4. FeCl25. PLGA	Triggered by the conversion of ethanol into acetic acid, releasing SBC-derived CO2, disrupting the shell wall of the HMs, and releasing DEX-P	[105]
PTKU@DEXNPs	NPs	Osteoclasts	1. Polythioketal(PTK)(ROS-responsive)2. DEX(drug)3. Diisocyanate	ROS-responsive group PTK is cleavable, then release DEX.	[108]
PEG-PTK-PEG@DA	Micelle	Osteoclasts	1. PTK (ROS-responsive)2. Dexamethasone acetate(drug)3. PEG4. Hydrogel	PTK is ROS-specific cleavable for the subsequent releasing dexamethasone acetate.	[109]
CPHs	Dendrimers	Osteoclasts	1. CORM-401(ROS-responsive, drug)2. PDNs3. FA-modified HA	The CO release from CORM-401 is oxidation-responsive in the presence of oxidants (H2O2), and consumes a large amount of H2O2.	[110]
DEX@PPNP	NPs	Osteoclasts	1. Boronate(ROS-responsive)2. Dex(drug)3. Polyphenol–poloxamer	The DEX@PPNP can be broken together with the boronate by ROS, leading to dexamethasone release.	[111]
DHMP/M	Micelle	Chondrocytes	1. PDA(ROS-responsive)2. Melanin(drug)	The PDA shell is responsive to ROS and slowly degraded by endogenous ROS, releasing melanin for scavenging free radicals.	[115]
TKCP@DEX	NPs	Chondrocytes	1. PEG-thioketal-BHQ-3(ROS-responsive)2. Dexamethasone(drug)3. Cartilage-targeting peptide-Cy5.5	ROS-responsive group TK is cleavable, then release DEX.	[116]
DLNPs	Micelle	Chondrocytes	1. PLGA-SeSe-mPEG(ROS-responsive)2. Dexamethasone(drug)3 CDMP-1(drug)	SeSe-group is fractured upon exposure to ROS in arthritis lesions, then DEX and CDMP-1 are released.	[117]
Dex-pPADN	NPs	Chondrocytes	1. Phenylboronic acid(ROS-responsive)2. Dex(drug)3. PEG	Dex-pPADN is dissociated from the ROS-responsive phenylboronic acid group, and the structure transformation of pPADN triggers the release of DEX.	[119]

Abbreviations: ROS, reactive oxygen species; RRHMs, ROS-responsive hollow microspheres; HMs, hollow microspheres; DEX, dexamethasone; DEX-P, dexamethasone sodium phosphate; PLGA, poly (D,L-lactic acid-co-glycolic acid); SBC, sodium bicarbonate; PTKU, polythioketal urethane; NPs, nanoparticles; PEG, poly(ethylene glycol); DA, dexamethasone acetate; CORMs, CO release molecules; PDNs, peptide dendrimers nanogel; CPH, a multifunctional anti-inflammatory drug; FA, folic acid; HA, hyaluronic acid; PPNPs, polyphenol–poloxamer NPs; DHMP/M, a smart dual-responsive hybrid micelle with free radical scavenger melanin in the micellar core and polydopamine on the shell; TKCP, materials formed by Cy5.5-modified cartilage-targeting peptide (CAP, DWRVIIPPRPSA) and PEG-modified oxidation-responsive thioketal linkers (TK); BHQ-3, Black Hole Quencher 3; DLNP, NPs composed of SeSe-group, DEX and cartilage-derived-morphogenetic-protein-1 (CDMP-1); pPADN, phenylboronicacid modified L-DOPA pro-antioxidant nanoparticles.

ROS-Responsive Nanomaterials for Osteoclasts

Dexamethasone sodium phosphate (DEX-P) is widely used in the treatment of OA to relieve inflammation and prevent cartilage ECM loss.102 The main difficulty of clinical application is that soluble drugs (DEX-P) are easy to clear; thus, frequent administration of DEX-P (once daily) is required.103 Poly (D,L-lactic acid-co-glycolic acid) (PLGA) has been extensively used in drug delivery, and its drug release is relatively slow in the absence of initiating factors, which will affect the therapeutic effect.104 The ultrasensitive ROS-responsive hollow PLGA microspheres (HM) contain the anti-inflammatory drugs DEX-P, ethanol, ferrous chloride (FeCl2), and sodium bicarbonate (SBC) as bubble-generating agents. Excessive H2O2 converted encapsulated ethanol into acetic acid in the presence of Fe2+ by the Fenton reaction to form an acidic milieu (acetic acid) in OA tissue. The SBC is decomposed into CO2 in an acidic environment, which subsequently destroys the PLGA shell and releases the internal DEX-P.105

It has been found that macrophage polarization is a crucial component of the joint inflammatory microenvironment, which is a therapeutic target for OA.106,107 Other researchers synthesized a novel polythioketal urethane (PTKU) using diisocyanate and polythioketal (PTK), which is sensitive to ROS. PTKU, as a drug delivery carrier, is loaded with the anti-inflammatory drug DEX to form NPs (PTKU@DEXNPs). It can significantly inhibit the intracellular level of ROS in the articular cavity and reduce the destruction of oxidative stress, which results in a lower ratio of inflammatory M1 macrophages to anti-inflammatory M2 macrophages. PTKU@DEXNPs show good cartilage protection and elimination of inflammation in a monosodium iodoacetate (MIA)-induced OA model.108

Based on the ROS-responsive property of PTK, a ROS-scavenging and drug-release platform was synthesized by encapsulating dexamethasone acetate (DA)-loaded ROS-erasable poly(ethylene glycol)-b-polythioketal-b-poly(ethylene glycol) (PEG-PTK-PEG) micelles (PDM) into an injectable hydrogel. To achieve a self-healing property for viscosupplementation, the hydrogel (HDH@PDM) was created using a Schiff base reaction between hydrazide-grafted hyaluronic acid (HA-ADH) and aldehyde-modified dextran (Dex-ALH). Intra-articular injections of a multifunctional hydrogel potently reduced inflammation through the depletion of ROS, the suppression of inflammatory cytokines, and the downregulation of the proinflammatory M1 macrophage ratio in a rat OA model109 (Figure 3).

Figure 3

Schematic diagram showing the fabrication of hyaluronic (HA) and dextran (Dex) Schiff base hydrogel loaded with dexamethasone acetate (DA)-encapsulated PEG-PTK-PEG micelles (PDM) for OA therapy in vivo.

A possible enhancement of OA therapy could be achieved by using ROS clearance to stimulate anti-inflammatory drug release in response to oxidation. The therapeutic effect is further increased by targeting the membrane receptor in macrophages and subsequently releasing anti-inflammatory drugs. Here, a multifunctional anti-inflammatory drug (CPH) was constructed by physically encapsulating CO release molecules 401(CORM-401) as a CO donor, folic acid (FA)-modified hyaluronic acid (HA) as the targeting ligand, and peptide dendrimers nanogels (PDNs) as a carrier. The oxidation-responsive release of CO from CORM-401 is significantly accelerated in the presence of relevant oxidants, such as H2O2. CPHs enter activated macrophages via FA-modified HA and rapidly release large amounts of CO that suppress the secretion of inflammatory factors by inhibiting cell proliferation, protect articular cartilage and suppress the degradation of ECM by deleting ROS in OA joints and inhibit proinflammatory signaling pathways.110

Boronate-stabilized polyphenol–poloxamer NPs are used as drug delivery systems (PPNPs). Dexamethasone is loaded into PPNP to form nanodrugs (DEX@PPNP) for OA treatment that exhibit ROS-responsive drug release behavior and ROS scavenging capabilities. In lipopolysaccharide-activated RAW264.7 macrophages, nanodrugs inhibit ROS and nitric oxide production efficiently and modulate M2 polarization. Treating monosodium iodoacetate-induced OA mice with this nanodrug reduced the inflammation associated with angiogenesis and arthritis scores and inhibited cartilage degradation and bone erosion in the joints.111

ROS-Responsive Nanomaterials for Chondrocytes

Melanin can scavenge ROS due to its abundant reductive functional groups, such as catechol, amine, and imine. Artificial melanin-like NPs prepared by dopamine polymerization also exhibit the potential to neutralize ROS and reduce joint inflammation.112–114 A smart dual responsive hybrid micelle with free radical scavenger melanin in the micellar core and polydopamine (PDA) on the shell (DHMP/M) has been developed for photoacoustic imaging-guided OA microenvironmental regulation. The PDA shell on the surface of the HM/M core is responsive to ROS and slowly degraded by endogenous ROS. Subsequently, this drug delivery system will gradually release melanin for a long time under chronic inflammation and be manually activated explosively by near-infrared (NIR) irradiation during acute inflammation. These two methods are very important for personalized therapy at specific time points.115

Recently, the ROS-responsive linker thioketal has attracted considerable interest for its sensitivity and responsiveness to downregulate endogenous ROS. TKCP is formed by Cy5.5-modified cartilage-targeting peptide (CAP, DWRVIIPPRPSA) and PEG-modified oxidation-responsive thioketal linkers (TK), which contain Black Hole Quencher 3 (BHQ-3) as a quencher for Cy5.5, and then encapsulated with DEX to form TKCP@DEX NPs. The advantage of TKCP@DEX Ns is that they specifically target chondrocytes through CAP, cleaving the thioketal linkages in response to high levels of ROS and resulting in the gradual dissociation of the polymer to release Cy5.5 and DEX in inflamed tissues. The released Cy5.5 from the polymer makes it a long distance between the quencher (BHQ-3) and Cy5.5, which enables a stronger fluorescence signal from Cy5.5 without the quenching action from BHQ-3. Conversely, the low level of ROS in normal tissue does not cleave thioketal linkers. BHQ-3 played an important role in quenching Cy5.5 over a short distance. This smart cartilage-targeting ROS-responsive theranostic nanoprobe is promising for OA therapy116 (Figure 4).

Figure 4

Schematic illustration of the self-assembly of ROS-responsive NPs for bioimaging and targeted therapy of OA in vivo.

In addition, the NPs named DLNPs were composed of SeSe-group, DEX and cartilage-derived-morphogenetic-protein-1 (CDMP-1). The SeSe group, as the ROS response component, will be fractured when encountering a high concentration of oxygen free radicals in arthritis lesions, and then DEX and CDMP-1, as the main pharmacophore, will be released to eliminate joint inflammation and induce cartilage repair.117 The drug-loaded micelles exhibited an anti-inflammatory effect by inhibiting the proliferation of activated macrophages, inducing macrophage apoptosis, and promoting bone marrow mesenchymal stem cells (BMSC) differentiation into chondrocytes.

Previous studies proved that phenylboronic acid is an efficient ROS-responsive group.118 Dex-pPADN NPs are constructed by modifying L-DOPA with phenylboronic acid and PEGylating to self-assemble into NPs (pPADN) and subsequently loading and dual-responsive delivery of Dex,119 inducing the inhibition of proinflammatory factors, the scavenging of ROS, and the activation of a NIR photoacoustic (PA) signal. In a rat OA model, Dex-pPADN markedly alleviated synovial inflammation and inhibited joint destruction and cartilage matrix degradation. Moreover, the structural transformation of pPADN makes it a suitable tool to monitor therapeutic effects such as photoacoustic imaging.

ROS-Responsive Nanomaterials for Other Cells

Other intra-articular tissues, such as the infrapatellar pad, meniscus and synovium, in OA have contributed to the progression of OA,16,19,28 but relatively little research using NPs has been done in these tissues.

To control intracellular gases, researchers created encapsulated S-methylisothiourea hemisulfate salt (SMT) and CAT ZIF-8 NPs. These NPs were additionally modified with anti-CD16/32 antibody (Ab) to target M1 macrophages and extend the retention duration of NPs in the synovium. ZIF-8 NPs breakdown into the acidic environment of endosomes after being ingested by M1 macrophages and release CAT and SMT. In addition, CAT may breakdown extracellular H2O2 to produce O2, which is required for mitochondrial respiration.120 Hypoxia-inducible factor 1α (HIF1α), which is crucial for M1 macrophage polarization, can also be inhibited by O2121. More notably, modified NPs prevented cartilage degradation in vivo and inhibited macrophage conditioned medium (CM)-induced chondrocyte hypertrophy in vitro.

The Advantages of Nanotherapy in OA

Traditional injection or oral intake of antioxidants usually cannot manifest therapeutic effects because of rapid clearance, degradation, and low bioavailability. For example, intra-articular injection takes at least once a week for 8 weeks, but effectiveness cannot be guaranteed due to the rapid clearance and degradation of drug molecules.122,123 However, systematic administration often requires a high dosage and frequent drug administration to ensure curative effects, resulting in obvious side effects.33,124 Nanotechnology refers to the development and use of small nanometer-sized objects based on their various properties, the size of which ranges from 1–100 nm or their volume-specific surface area is larger than 60 m2/cm2. NPs have been used as drug delivery systems, where they are capable of reaching targeted organs or sites by recognizing receptors on the target cells’ cellular pathways.125 The advantages of nanodrug delivery systems in the treatment of OA are summarized as follows.

Increased Bioavailability in vivo by Improving Drug Solubility

Polyethylene glycol (PEG) has been proven to increase drug solubility and is widely used in polymer-drug conjugates due to its negligible toxicity and immunogenicity.126 Formononetin (FMN), a phytoestrogen from natural herbal plants, can effectively decrease proteoglycan loss in IL-1β-induced catabolic chondrocytes.127 PEGylation of FMN followed by coupling with cartilage-targeting peptide (CollBP) showed good anti-inflammatory and chondroprotective effects in IL-1β-stimulated chondrocytes and OA rat joints.128 However, the bioavailability of FMN is low due to its poor water solubility, but the loading rate of FMN in PEG-CollBP-FMN (PCFMN) is nearly 9%.

High Loading Rate of Drugs

Numerous studies have shown that a higher drug loading of biomaterials is linked to a higher pore surface area. The mesoporous structure in the NPs was constructed to enhance the drug loading, such as CaP coated mesoporous polydopamine nanoparticles with responsive membrane permeation ability realizing high siRNA loading capacity (10 wt%) and mesoporous polydopamine nanoparticles (MPDA) have properties of a high payload of doxorubicin hydrochloride (up to 2000 μg mg−1).129–131 The superiority of improving the loading rate of the drug in NPs can effectively reduce the number of intra-articular injections, which will avoid further damage to cartilage.

Precise Drug Targeting to Organ or Tissue

Synovial inflammation is a major indication of OA. In particular, macrophages in the synovium have attracted considerable attention.132–134 Several targeting peptides have been described in recent studies. Liposomes containing phosphatidylserine (PS) (PS-containing liposomes; PSL), as a biomaterial carrier, show the ability to target macrophages and anti-inflammatory function both in vivo and in vitro.132 A 4-phenyl borate-cyclodextrin biomaterial loaded with dexamethasone (Dex/Oxi-αCDNPs) reduced joint swelling and cartilage destruction by targeting synovial macrophages.133 CEL-loaded PRNPs (CEL-PRNPs), which were composed of celastrol (CEL), enzyme-responsive NPs (termed PRNPs) and RGD-modified NPs (termed RNPs) covered with cleavable PEG chains, selectively induced the apoptosis of osteoclasts and inflammatory macrophages in arthritic joints.134

Controlled Release for NPs

External environmental factors, such as near-infrared light (NIR, λ= 700–1100 nm), can be used as influencing factors for precise and controllable drug release. NIR can penetrate inflammatory tissue, the treatment of which is of particular interest because it is relatively harmless.135,136

The intra-articular drug delivery nanosystem MoS2@CS@Dex (MCD) was constructed by using chitosan (CS)-modified molybdenum disulfide (MoS2) nanosheets as NIR photoresponsive carriers loaded with the anti-inflammatory drug dexamethasone (Dex). MCD was in response to NIR light both in vitro and in vivo and released Dex through photothermal conversion. Injecting MCD into the articular cavity followed by NIR radiation downregulated the secretion levels of TNF-α and IL-1β, thus protecting chondrocytes and articular cartilage from injury.137

Loading and Delivering Multiple Drugs Simultaneously

The onset and development of OA are affected by multiple factors. Therefore, different drugs that target different factors are essential in OA treatment to achieve remarkable effects. For example, RB@MPMW refers to a metal organic framework (MOF)-decorated mesoporous polydopamine (MPDA)-based dual-drug delivery system that has bilirubin (Br) loaded onto the MOF shell and rapamycin (Rap) loaded into the mesopores, which are responsible for enhancing autophagy activation and scavenging reactive oxygen species (ROS), respectively.138 Rapamycin, an autophagy activator, protects chondrocytes from harmful stressors and apoptosis,138 and bilirubin inhibits the polarization of M1 macrophages, which release proinflammatory cytokines.139,140 Furthermore, as little as 10 nM bilirubin protects against 10,000-fold higher concentrations of H2O2.141

Theranostic NPs for OA

The nanoprobe with the features of bioimaging and targeted therapy in treating OA shows different fluorescence intensities depending on the physiologic state. The fluorescent signal from the ROS-responsive nanoprobe following intra-articular injections was strong in the OA microenvironment but extremely weak in normal chondrocytes and joints, indicating that the level of the fluorescence signal correlates with the ROS content. This smart cartilage-targeting ROS-responsive nanoprobe with diagnosis and treatment is especially suitable for OA therapy.116

The OA microenvironment includes excessive inflammation and the overproduction of ROS, which mainly destroys ECM synthesis in the development of OA.142 The abnormality of the antioxidant defense system in OA patients is an important factor that makes tissues susceptible to oxidative stress and causes joint oxidative pathological damage.117,138,143 Hence, ROS might be a potential therapeutic target in clinical application. Ideal treatment should be sensitive and activated by changes in the tissue microenvironment, leading to a controlled release of the drug and satisfying OA therapy.144

Although nanotherapy has many advantages over conventional treatment, it still has many limitations. 1) NPs can be transferred via the bloodstream throughout the body and then accumulate in various organs, affecting their functions after entering the body,145 which is prevalent, as is the case for ROS-responsive NPs. 2) The synthesis of some NPs is complicated, and this method requires high cost, such as liposomes.146 The manufacturing process, reproducibility, and quality are difficult to control.146 3) Some NPs become unstable in close to neutral pH circumstances, such as chitosan.147 4) The NPs may be present in the joint cavity for only a short amount of time due to rapid clearance.148 The advantages and disadvantages of Nanotherapy in OA are summarized in Table 2.

Table 2

Advantages and Disadvantages of Nanotherapy in OA

Advantages	Ref	Disadvantages	Ref
Increased bioavailability	[128]	Accumulation in various organs via the bloodstream	[145]
High loading rate	[129–131]	High cost, complicated synthesis and uncontrollable quality	[146]
Precisely targeting to organ or tissue	[132–134]	Unstable at neutral pH	[147]
Controlled release	[137]	Rapid joint clearance	[148]
Loading multiple drugs	[138]

Abbreviation: pH, potential of hydrogen.

Discussion and Future Perspectives

Recently, ROS-responsive nanomaterials have attracted considerable attention in basic research of many diseases, such as cancer, inflammation and neurodegenerative diseases. Remarkable progress has been made in ROS-responsive biomaterials for cancer treatment. However, relatively few studies are available on OA treatment with ROS-responsive biomaterials. Previous studies have demonstrated that inflammation stimulates oxidative stress and vice versa. Theoretically, anti-inflammatory drugs such as DEX also possess the property of removing ROS. In this review, we found that DEX has been used in almost all ROS-responsive nanodrug delivery systems for clearing excess free radicals in OA tissue.

However, DEX has limited clinical applications due to its side effects at high doses in short-term use or side effects at low doses in long-term use, which often cause muscular atrophy, bone fractures, and osteonecrosis. Controlling the release of DEX precisely and responsively in OA treatment is still a great challenge. Melanin, a natural antioxidative metabolite, has also been applied in OA treatment, which efficiently diminishes inflammatory cytokine release and cartilage degradation.112 Nevertheless, melanin-based/like biomaterials are linked to poor stability due to the autoxidation of catechol in aqueous solution. Given the unsatisfactory clinical efficacy of OA treatment, it is urgent to discover novel drugs targeting inflammation and ROS.

Compared with unresponsive delivery systems, ROS-responsive systems remain stable in normal tissue, preventing their release to noninflamed tissues, which suggests their specificity in inflammation sites. OA is characterized by the degeneration of the whole joint, which is especially suitable for intra-articular injection of ROS-responsive nanomedicine, realizing controlled release and targeted therapy without affecting other tissues or organs through blood circulation. Generally, this approach entailed the endogenous or exogenous stimulus-responsive release of bioactive agents to the target tissue and reduced the side effects.149,150

There are currently a number of clinical trials using NPs. For example, a Phase 3 controlled trial using doxorubicin-loaded NPs for patients with advanced hepatocellular carcinoma after sorafenib treatment failure (RELIVE) showed the dose-dependent toxicity of doxorubicin, and this first phase 3 study did increase overall survival.151 However, there are few clinical trials using NPs in OA. For example, a randomized controlled trial showed that P. amarus NP gel was effective for reducing pain and improving the results of the six-minute walk test (6-MWT) in patients with OA knees.152 This means that NPs are very promising in the treatment of OA, and there is a lot of work to do.

However, difficulties in clinical transformation still exist. 1) The effectiveness and safety of ROS-responsive nanomaterials need to be considered for long-term use. The best choice for clinical application is the drug carrier from natural polymers such as chitosan, dextran, alginate, pullulan, and HA, all of which are FDA-approved natural polymers for their noncytotoxicity, nonimmunogenicity, biocompatibility, and biodegradability. In particular, biomaterials from the components of cartilage tissue (HA) may be more preferred. 2) The biological mechanism underlying OA should be well understood. OA is a multifactorial disease for which it is difficult to achieve the desired therapeutic effect using single-modal therapy. Multimodal therapy is an attractive treatment method, especially when paired with precise treatments. 3) The changes in physiological behavior and tissue structure in experimental animals are different from those in humans, and different patients respond differently to ROS-responsive nanomedicines because of the complexity of biological systems.

In addition, all these platforms, including the delivery efficiency of current drug carriers for scavenging ROS, in vivo therapeutic effects and controlled drug release profiles of the current drug delivery system, are still unsatisfactory due to their insufficient responsiveness and rapid joint clearance.

Although NPs can respond to the microenvironment when they enter the human body, there is a lack of long-term, comprehensive analysis of the in vivo toxicity of nanomaterials. Future work should focus on chemistry, new biomaterials, specific targets for therapy, and effective free radical scavenging drugs. Moreover, mitochondria are responsible for the main source of ROS. Conventional antioxidants fail to ameliorate the severity of ROS-related diseases, which may be a result of their inability to concentrate in mitochondria. Thus, it seems to be a worthwhile strategy to develop mitochondria-targeted antioxidants in the future. Furthermore, considering the rapid clearance of the joint cavity, NPs should be designed to maximize the retention time in the joint cavity.

As previously mentioned, the infrapatellar pad, meniscus and synovium promote the development of OA. However, there are very few studies using ROS-responsive nanoparticles in these tissues. Therefore, novel nanomaterials that target these tissues can be considered.

Conclusion

ROS-responsive polyfunctional nanosystems 3.0 are a promising therapy for the treatment of OA. Given the effects proven by the current study, this is very prospective for clinical applications.