Bone Targeting Nanoparticles for the Treatment of Osteoporosis

Abstract

Osteoporosis (OP) affects millions of people worldwide, especially postmenopausal women and the elderly. Although current available anti-OP agents can show promise in slowing down bone resorption, most are not specifically delivered to the hard tissue, causing significant toxicity. A bone-targeted nanodrug delivery system can reduce side effects and precisely deliver drug candidates to the bone. This review focuses on the progress of bone-targeted nanoparticles in OP therapy. We enumerate the existing OP medications, types of bone-targeted nanoparticles and categorize pairs of the most common bone-targeting functional groups. Finally, we summarize the potential use of bone-targeted nanoparticles in OP treatment. Ongoing research into the development of targeted ligands and nanocarriers will continue to expand the possibilities of OP-targeted therapies into clinical application.

Graphical Abstract

Keywords:

• bone targeting
• nanomedicine
• osteoporosis therapy

Introduction

Osteoporosis (OP) is one of the most prevalent bone diseases characterized by a loss of bone calcium and matrix, leading to a decrease in bone density and degradation of bone tissue microstructure.^1,2 This condition can cause lower back pain, stooped posture, height loss, and fractures. Due to the loss of bone mass, patients with OP have an increased risk for bone fragility and fracture. If left unprevented or untreated, OP can progress painlessly and cause severe wrist, hip, and spinal fractures, leading to disability and death in the elderly.^3,4 Because bone and cartilage health are closely related, OP may affect the occurrence and development of osteoarthritis (OA). The decreased bone density and insufficient mineralization of bone trabeculae caused by OP can affect the normal structure of cartilage and subchondral bone. Therefore, treating OP is also necessary for preventing and treating OA.⁵ As the population ages, osteoporosis is gradually becoming a serious global health problem, affecting over 200 million people worldwide, according to statistics from the International OP Foundation.⁶ The etiology of OP is complex and involves a delicate balance between osteoblasts and osteoclasts in the body and multiple regulatory factors released by the osteocyte network that maintains bone remodeling homeostasis. The imbalance in any of these factors can lead to OP,⁷ highlighting the need for a clear understanding of its etiology to explore effective treatment options.

Currently, two main approaches are used to treat OP in clinical practice. These include preventing bone resorption using drugs like bisphosphonates, calcitonin, denosumab, and selective estrogen receptor modulators and directly increasing bone density using parathyroid hormone (PTH).^8,9 However, these commonly used drugs have limited efficacy and can result in inevitable toxic side effects. Table 1 summarizes their mechanisms and side effects. These drugs’ limitations restrict their efficacy in the body. On the one hand, these drugs have low biocompatibility once entering the body, making them susceptible to rejection reactions and difficult to transport to bone tissues.^10–12 On the other hand, most drugs lack targeting specificity and can not specifically recognize bone tissues, leading to high accumulation in organs, such as the liver and kidneys, causing toxic side effects and negatively impacting their therapeutic effectiveness.^13,14 Therefore, there is an urgent need to develop more refined and efficient treatment methods for OP.

Table 1 Characteristics and Side Effects of Various Drugs for OP Treatment

Type	Category	Representative Drug	Action Pathway	Side Effects	Ref
Anti-absorption regulators	Bisphosphonates	Risedronate (RDN)	Bind to bone surface, inhibit bone absorption by osteoclasts	Common side effects: gastrointestinal irritation, bone and joint pain or necrosis Long-term side effects: atypical fractures, esophageal cancer	[15–22]
	Selective estrogen receptor modulators	Raloxifene	Estrogen agonists that have cytokine activity and can inhibit bone absorption	Uterus and breast responses	[23–26]
		Bazedoxifene	Prevention of osteoporosis	NA	[27]
		Ipriflavone	Substitute for HRT and inhibit osteoclast differentiation	Both the uterus and breasts responses	[28]
	Receptor activator of NF-κB ligand (RANKL)	Denosumab	Block binding to RANK, inhibit formation and maturation of osteoclasts	Eczema, cellulitis, jawbone necrosis	[29,30]
	Calcitonin	Salmon calcitonin	Lower activity of active osteoclasts	Production of anti-calcitonin antibodies	[31,32]
Synthetic metabolic therapy	PTH analogs	Teriparatide (TPD)	Stimulate bone formation and conversion	Long-term injection increases risk of osteosarcoma	[33]
		Abaloparatide	For the treatment of women with postmenopausal osteoporosis	Nausea, orthostatic hypotension, and leg cramps	[34]

Nanotechnology is a rapidly growing research field that provides promising options for disease treatment. Currently, dozens of nanodrugs have been approved for clinical use, such as liposome-encapsulated doxorubicin (Doxil; Johnson & Johnson) for the treatment of ovarian cancer and Kaposi’s sarcoma,³⁵ while hundreds of other nanodrugs are in preclinical evaluation.³⁶ Nanomaterials are synthetic structures composed of inorganic or organic substances with at least two dimensions between 1 and 1000 nanometers.³⁶ The small size of nanoparticles (NPs) enables them to pass through biological barriers and reach ideal areas in the body, resulting in higher therapeutic efficiency. In addition, loading into nanomaterials can improve drugs’ solubility, thus greatly increasing drugs’ bioavailability.^37–39 By modifying NPs for drug delivery, they can be targeted to disease sites and released in specific locations.^40,41 This approach changes drugs’ pharmacokinetic characteristics, increases their time of existence in the disease area, and extends their biological effects.⁴² Because bone itself is a nanocomposite material, NPs have similarities with bone tissues and high surface areas and roughness, which facilitate protein and cell adsorption in bone tissue. Currently, strategies for targeting bone tissue focus on the bone surface, bone marrow and its endothelial cells. While more than 40 types of first-generation nanomaterials have been applied in clinical practice,⁴³ research on nanodrugs is still in its early stages, and future development and improvement of nanodrugs will require a massive undertaking. This review summarizes recent research progress on nanomaterials in OP treatment and mainly discusses two aspects of using nanomaterials for OP treatment: (i) various nanomaterials used for osteoporosis treatment, including liposomes, exosomes (Exos), Polymeric NPs such as poly (DL-lactide-co-glycolide) (PLGA) nanoparticles and Inorganic NPs, and (ii) exploring the potential of using various bone tissue-targeting modified nanomaterials for targeted drug delivery in OP treatment. Additionally, the potential challenges and prospects of using such nanomaterials for targeted OP treatment are also discussed.

Nanocarriers for OP

The development of nanotechnology has opened exciting possibilities for the treatment of OP, with nanomaterials severing as effective delivery vehicles for growth factors, nucleic acids, and proteins that have demonstrated therapeutic benefits.^44–48 Such delivery can be achieved through various methods, including oral administration, injection, or local injection. High-quality nanocarriers offer several excellent characteristics, such as (1) protecting drugs from degradation, (2) enhancing their penetration into the body, (3) targeted delivery of therapeutic substances and improved topical drug penetration and release in the affected area, and (4) excellent biocompatibility and biodegradability.⁴⁸ These unique properties make nanotechnology a promising player in the development of effective treatments for OP. Nanomaterials-based therapies offer several advantages in biomedical applications. Firstly, their smaller size allows for enhanced drug penetration and mobility within the body, leading to improved therapeutic outcomes. Secondly, their natural structure and good biocompatibility make them less susceptible to immune responses and degradation, leading to longer circulation time in the body. Lastly, their relative non-toxicity compared to conventional drug delivery systems can result in fewer side effects and improved patient safety. Moreover, modifying nanocarriers makes drug delivery more efficient and precise.^49–51 Currently, there are several types of nanocarriers employed for treating OP, including lipid carriers, Exos, and various synthetic NPs. While each of these nanocarriers has unique advantages, combining their advantages through particle modification or nanocomposite assembly is a promising direction for future research.Figure 1 and Table 2 provides an overview of the characteristics of various nanocarriers and related research. By developing more sophisticated and effective nanocarrier systems, researchers can potentially enhance drug delivery and improve the outcomes of OP treatments.

Table 2 Various Nanocarriers and Their Applications in the Treatment of OP

Nanocarriers	Characteristics	Carrier	Therapeutic Agent	Results	Ref
Lipid nanocarriers	Easily modified, high loading efficiency	Liposome	Antagomir-148a	Inhibiting osteoclast bone resorption	[52]
		Lipid nanoparticle (LNP)	SiRNA-GNAS	Enhanced differentiation of MSCs into osteoblasts	[53]
		Ionizable LNP	BMP-9 gene	Exhibited the safety and bone regeneration efficiency	[54]
		Nanostructure lipid carrier	RLX hydrochloride, Vitamin D	Improving drug permeability	[55]
		Solid LNP(SLNP)	RLX hydrochloride	Stronger drug effects	[56]
		Bioadhesive nanoparticle	RLX	Improve oral bioavailability of drugs	[57]
		LNP	SIM	Enhance the bone-formation effect of SIM	[58]
		Bilosome	Risedronate (RDN)	Improving drug permeability and reducing drug toxicity	[59]
Exos	Rich source, capable of autologous transplantation	iPSC-Exo	SiRNA-Shn3	Silencing of Shn3 gene, reducing autologous RANKL expression, and inhibiting osteoclast formation	[60]
		Hybrid Exo (Exo with liposome)	Antagomir-188	Promoting osteogenic differentiation of BMSCs and preventing bone loss	[61]
		BMSC-derived exosomal	MiR-29a	Promote osteogenesis	[62]
		Blood cell extracellular vesicles (RBCEVs)	Anti-miR-214	Inhibit osteoblasts and enhance osteogenesis	[63]
SPIONs	Superparamagnetic, promote bone regeneration and inhibit bone loss	nHAP-based composite co-doped with SPIONs	MiR-21, miR-124	Increased osteoblast activity and inhibited osteoclast activity	[64]
		silk Fibroin/hydroxyapatite scaffolds incorporated with SPIONs	BMSCs	Promoting BMSC adhesion and growth, and enhancing osteogenic effects	[65]
nHAP	Structurally similar to bone tissue and has a natural bone cement effect	nHAP	PTH	Synergistically increasing bone matrix	[66]
		nHAP	RhBMP-2	Synergistically stimulating bone formation	[67]
		nHAP	bisphosphonate	Promote bisphosphonate-induced inhibition of bone resorption	[68]
		nHAP	SCT	Excellent bone repair in vivo	[69]
		nHAP	ZOL	Inhibit bone loss, maintain of trabecular structure and strengthening of bone	[70]
		Zinc-nHAP	RDN	Preserve the structure of cortical and trabecular bone	[71]
PLGA nanoparticles	Easily degraded, good drug release kinetics	AL sodium-mPEG-PLGA	Astragaloside	Improving oral bioavailability and anti-osteoporosis effect of AS	[72]
		Tetracycline decorated PLGA NPs	Simvastatin	Increasing bone density of OP rats	[73]
		PLGA NPs	Estradiol	Enhance the estradiol concentration in the blood for more effective treatment of OP	[74]
		PLGA NPs	MSC-Sec	Inhibit osteoclast differentiation and promote osteoblast proliferation	[75]
		PLGA/HAP	BMP	Increasing mouse bone formation	[76]
CS-NPs	Storage stable, widely existing in nature	CS-NPs	RLX, PTH, RDN	Increasing drug oral bioavailability and reducing bone loss	[77–79]
		CS-NPs	PTH-134	Biocompatibility, high embedding efficiency and delivery efficiency	[80]
		CS-NPs	SWE	Enhance the anti-OP effect of SWE	[81]
		hyaluronic acid-CS-NPs	RDN and TPD	Synergistically enhancing bone regeneration	[82]

Figure 1 NPs are classified into different categories according to their properties, shape or size. Each class of NPs has several subclasses, with advantages and limitations are presented here.

Lipid Nanocarriers

Lipid nanocarriers are a type of drug delivery system primarily composed of solid lipid matrices with hydrophilic and lipophilic phases, offering excellent drug-loading capacity and easy modification. They represent the second generation of lipid-based drug delivery systems, aiming to overcome the limitations of previous systems.^55,83 Among them, liposomes are the most widely used lipid nanocarriers in clinical applications. These spherical vesicles can encapsulate hydrophilic or hydrophobic therapeutic molecules, exhibit good biocompatibility and biodegradability, and possess easily modifiable structures, improved drug solubility and pharmacokinetics, and reduced drug toxicity.^84–87

In 1995, the US Food and Drug Administration (FDA) approved the first clinical nanodrug for chemotherapy, Doxil^®,⁸⁸ which is a pegylated liposome formulation of doxorubicin. The drug has proven effective in reducing the cardiotoxicity associated with doxorubicin.⁸⁹ Other liposome formulations subsequently approved for clinical use include Myocet™⁹⁰ and Marqibo^®.⁹¹ Extensive research has been conducted on modifying lipid nanocarriers, providing inspiration for developing lipid nanocarriers for treating OP. One interesting development is the use of liposome-based thermosensitive nanocarriers that release loaded drugs at high temperatures. ThermoDox, a lipid-based thermosensitive nanocarrier containing doxorubicin, is currently undergoing Phase II trials for the treatment of breast cancer and liver metastases and Phase III trials for the treatment of liver cancer.⁹²

For bone diseases, researchers hope to develop lipid nanocarriers targeting bone tissue. Song et al⁹³ and Ferreira et al⁹⁴ have respectively developed pamidronate-conjugated liposomes and alendronate salt-conjugated PEGylated liposomes and demonstrated that the former exhibited an increased affinity for bone tissue, and the latter had the bone-targeting ability. Currently, researchers are exploring the use of liposomes to treat OP. A recent study utilized modified liposomes to load antagomir-148a, a miRNA modulator that suppresses the osteoclastogenic miR-148a (a miRNA modulator suppressing the osteoclastogenic miR-148a) and found that the modified liposomes accumulated mainly in bone and downregulated miR-148a expression in osteoclasts, inhibiting bone absorption in mice with OP.⁵² In another study on lipid nanoparticle delivery of nucleic acids, the authors used LNP delivery of siRNA to silence the GNAS gene in MSCs. Ex vivo and in vivo experiments demonstrated that this LNP-siRNA delivery system effectively silenced the GNAS gene and enhanced the potential of MSCs to differentiate into osteoblasts. This delivery strategy provides promise option for the treatment of OP.⁵³ A novel ionizable lipid with a C18 tail and ionizable head group was developed for delivery of bone morphogenetic protein-9 (BMP-9) gene for OP treatment. In this study, Ionizable LNP showed excellent delivery efficacy, and ex vivo and in vivo experiments confirmed the transfection efficiency and safety of the BMP-9 gene for the reversal of OP.⁵⁴

While drugs commonly used to orally treat OP have good pharmacological advantages, their gastrointestinal effects often lead to lower bioavailability and toxic side effects.⁹⁵ Researchers have designed a lipid nanocarrier to simultaneously carry Raloxifene (RLX) hydrochloride and Vitamin D (Vit.D), two classic drugs, to address the low bioavailability of these drugs. After testing the pharmacokinetic parameters of healthy volunteers who took the drugs orally, they found that compared to traditional commercial products, these nanolipid carriers increased the bioavailability of RLX by 385.6%, and the average level of Vit.D metabolites from 91±29 nmol/L to 174±36 nmol/L. The increased bioavailability of these drugs may be due to the lipid carriers being absorbed via the interaction of the drug and bile salts after being decomposed by enzymes in the intestine, which protects the drug from premature metabolism.⁵⁵ Similarly, to enhance the bioavailability of RLX hydrochloride, researchers invented a double emulsion solvent evaporation (DESE) to encapsulate RLX hydrochloride into solid lipid nanoparticles (SLNPs). This drug-loading method can encapsulate RLX hydrochloride in SLNPs with appropriate physicochemical and biological properties, which enhances the drug’s effect.⁵⁶ Another lipid NP is a bioadhesive nanoparticle composed of Carbopol 940, glyceryl distearate, and TGPS. This lipid nanodelivery system was able to firmly encapsulate RLX internally and demonstrated higher biological utilization in rat experiments, suggesting an excellent OP drug delivery vehicle.⁵⁷ Simvastatin (SIM), which has been shown to treat OP through osteoblast differentiation and mineralization, has poor bone targeting and low bioavailability for in vivo application. However, the in vivo application of SIM has poor bone targeting and low bioavailability. Therefore, LNP, which is combined with a targeting peptide, was used as a carrier to deliver SIM to the bone tissue and to enhance the bone-enhancing effect of SIM. This demonstrated that LNP is an effective carrier for the treatment of OP.⁵⁸

In a separate study, researchers added bile salts and cholesterol to lipids and designed a new type of lipid nanocarrier called bilosomes. They then evaluated the advantages of bilosomes carrying sodium alendronate. Compared with regular liposomes, the addition of cholesterol and bile salts improved the stability of the bilosomes, protecting them from external digestive damage and reducing the toxicity of oral drugs. This significantly enhanced the efficacy of sodium alendronate in treating OP.⁵⁹

Exosomes

Exos are lipid bilayer-enclosed structures with diameters ranging from 40 to 160 nm.⁹⁶ Scientists believe that cells use Exos to package proteins, mRNA, microRNAs (miRNAs), and lipids for intercellular communication.^97,98 Due to their natural communication carrier properties, researchers are considering developing drug delivery systems based on Exos. In addition to the advantages of small size, structural stability, and low toxicity possessed by nanomaterials, as previously mentioned, Exos are widely available and exist in all bodily fluids and tissues.⁹⁷ This provides a continuous source of carriers, and delivering drugs through autologous Exos does not raise ethical issues or cause immune rejection reactions.⁶⁰ Another advantage of using Exos as drug carriers is their ability to exert regulatory effects. Specifically, Exos secreted by bone marrow stromal cells (BMSCs), osteoclasts, and osteoblasts have been shown to participate in bone regulation.⁹⁹ Exos derived from osteoclasts have bone-inhibiting effects,^100,101 while those from BMSCs and osteoblasts can enhance bone formation.¹⁰² Another key element is that Exos can be highly engineered. After engineering, Exos have cell and tissue specificity, making them better suited for drug delivery.^63,103–109

Researchers are investigating the potential of engineered Exos carrying therapeutic molecules as a new treatment option for osteoporosis. In one study, researchers developed a delivery system based on Exos derived from human induced pluripotent stem cells (iPSCs) to combat OP. They used these MSC-derived Exos to fight against OP and modified them to target and deliver siRNA of the Shn3 gene (siShn3) to osteoblasts. This downregulated the expression of the Shn3 gene in osteoblasts, enhanced osteoblast differentiation, and decreased the expression of receptor activator of nuclear factor-κB ligand (RANKL), thereby inhibiting osteoclast formation from achieving an anti-osteoporotic effect.⁶⁰ Similarly, stem cell-derived exosomes were chosen as the subject by Lu et al. In their work, BMSC-derived exosomes loaded with miR-29a showed potent osteogenic capacity, suggesting the potential for therapeutic OP.⁶² In addition, a new study selected red blood cell derived extracellular vesicles as delivery vehicles and achieved the targeting of osteoclasts with a bifunctional peptide to deliver anti-miR-214. The experimental results suggested the bone-targeting ability of the delivery vehicle, as well as the inhibition of osteoclasts and the enhancement of osteogenesis. The use of red blood cell derived extracellular vesicles as carriers for OP treatment is a promising direction.⁶³ Hu et al fused Exos with liposomes to form hybrid Exos and delivered antagomir-188 to the skeleton via C-X-C motif chemokine receptor 4 (CXCR4), which promotes BMSC osteoblastic differentiation, thus reversing the age-related loss of trabecular bone.⁶¹

Superparamagnetic Iron Oxide Nanoparticles

In the 1970s, Freeman et al were the first to combine magnetism with medical applications, and since then, extensive research on magnetic NPs has been conducted.¹¹⁰ Superparamagnetic iron oxide nanoparticles (SPIONs) have become one of the most widely studied targeted nanomaterials due to their many advantages. Firstly, SPIONs are synthesized from a single raw material and are easy to synthesize, with good chemical stability.¹¹¹ SPIONs also exhibit good biocompatibility and biological safety and are relatively non-toxic compared to nanoparticles containing manganese and gadolinium.^112,113 Furthermore, SPIONs exhibit excellent superparamagnetic, allowing them to be accumulated in a designated area through an external magnetic field.¹¹⁴ These magnetic particles lose their magnetism and scatter when the external magnetic field disappears, thus avoiding possible immune system attacks and enhancing local effects and half-life in circulation.¹¹⁵ Currently, SPIONs have mainly been applied in two areas of clinical biomedical research. One is in magnetic resonance imaging (MRI), where SPIONs serve as contrast agents to assist in diagnosing early diseases.¹¹⁶ The other area of interest is using SPIONs as excellent drug-target delivery vehicles, especially for tumor-targeted radiotherapy and chemotherapy.^117,118

While acting as carriers, SPIONs also play an essential role in anti-OP. Previous in vitro studies have shown that SPIONs can promote osteoblast differentiation and inhibit osteoclast formation. In vivo experiments have demonstrated that these nanoparticles can accelerate bone defect repair and prevent bone loss.^111,119,120 These studies further illustrate the advantages of using SPIONs for the treatment of OP. SPIONs can deliver bioactive molecules (such as antibodies, proteins, drugs, etc.) or cells, which opens up more possibilities for bone regenerative medicine.¹²¹

Marycz et al designed a dual-target scaffold carrier doped with SPIONs and HAP nanoparticles (nHAP) for delivering miR-21 and miR-124.⁶⁴ Under the action of the carrier and the magnetic field, miRNA targets accumulate and then release, increasing osteoblast activity and inhibiting osteoclast activity, enhancing the regeneration of osteoporotic bone. In another study, researchers incorporated SPIONs into silk fibroin/hydroxyapatite scaffolds and implanted BMSCs into the backs of nude mice using this scaffold. The results showed that BMSCs could adhere and grow well and promote bone formation. SPIONs not only enhance the stability of silk fibroin/hydroxyapatite scaffolds but also show a stronger bone-forming effect by incorporating magnetic particles. In addition, bone regeneration can be monitored non-invasively by MRI.⁶⁵

Hydroxyapatite Nanoparticles

Hydroxyapatite (HAP), with the chemical formula of Ca₁₀(OH)₂(PO₄)₆, has a unique structure that closely resembles bone tissue, making it a promising material for biomedical applications in bone diseases. One potential application of HAP is as a bone cement and bone graft due to its osteoconductive and injectable properties, as proposed by Ginebra et al (1999). Numerous studies have explored the use of bone cement to strengthen osteoporotic bones.^122–126 HAP-based bone cement offers several advantages, such as low-temperature solidification reactions and inherent porosity, which enable it to carry drugs or active ingredients for joint action.¹²⁷ Panzavolta et al^128,129 have successfully combined bisphosphonates with HAP, resulting in drug-carrying bone cement with good mechanical properties. This combination of drugs and HAP has the potential to resist bone resorption, which can be beneficial in relieving osteoporosis.

Recently, researchers have synthesized HAP nanoparticles (nHAP) and combined them with various polymers to create bio composite materials with enhanced osteoconductive properties.^122,130 These nanoscale biomaterials are crucial in orthopedic surgery as they have a small size and possess structure and chemical properties similar to natural bone, which allows them to remain stable in the acidic and alkaline environment of the body and resist degradation by enzymes. In addition, the inherent degradation products of Ca²⁺ and PO₄^3- in the body are not non-toxic and do not cause immune reactions.

Researchers are hopeful that nHAP can serve as a carrier for delivering drugs and therapeutic proteins for the treatment of OP.^131–133 Besides its role as a drug carrier, nHAP is also expected to supplement bone defects. Dave et al synthesized nHAP carriers loaded with PTH, achieving targeted delivery of PTH to osteoporotic bones.⁶⁶ The nanocarriers dissolve in the osteoporotic bone, enhancing the matrix components of the bone while playing a role in PTH synthesis and metabolism locally. Furthermore, nHAP has been combined with recombinant human bone morphogenetic protein-2 (rhBMP-2) in another study. The nanocarrier carrying rhBMP-2 was implanted into rabbits’ unilateral radial bone defects, and it was found that nHAP with growth factors could stimulate more bone formation, highlighting its excellent growth factor carrier performance.⁶⁷ The advantages of bisphosphonates in the treatment of OP have become the focus of research by scientists. Delivery of bisphosphonates with nHAP as a carrier has a favorable anti-OP effect. In vitro experiments confirmed that nHAP could enhance the function of bisphosphonates to inhibit osteoclast formation, and the combination with hydrogel could induce mineralization, which is a new bone repair material.⁶⁸ Surface-stabilized nHAP prepared by aqueous precipitation was used to deliver salmon calcitonin (SCT), and the nHAP showed high loading efficiency, permeability, and stability. In an osteoporotic rat model, the nHAP delivered SCT demonstrated excellent bone repair ability and is an injectable treatment for OP.⁶⁹ Similarly, by loading novel zoledronic acid (ZOL) in nHAP (ZOL-nHAP) by the classical adsorption method, researchers explored the role of ZOL-nHAP in osteoporotic rats. After three months of treatment, it was found that treating OP rats with nHAP-delivered ZOL was more effective than ZOL alone. Apparently, ZOL-nHAP better reversed bone loss, better preserved trabecular structure and improved mechanical strength in the OP rat model.⁷⁰

In addition, researchers are keen on modifying various substances in combination with nHAP to enhance the performance of nanoparticles on the original basis. For example, zinc is a suitable combination with nHAP. For example, Risedronate (RDN), which is a high-quality osteogenic drug, was loaded onto zinc-nHAP by researchers through adsorption. Using an animal model of OP, the researchers compared the effects of zinc-nHAP delivered RDN and RDN alone for the treatment of OP. The results strongly suggest that preparations of zinc-nHAP-delivered RDN have a therapeutic advantage over administration alone, with better preservation of cortical and trabecular bone structures.⁷¹

Overall, the potential applications of nHAP in orthopedic surgery are vast and promising, and ongoing research may uncover additional benefits.

PLGA Nanoparticles

Poly(DL-lactide-co-glycolide) (PLGA) is a biocompatible material that has been used as a growth factor carrier in the 1990s.¹³⁴ It can be easily synthesized and modified to optimize polymer degradation and drug release kinetics.¹³⁵ With advances in nanotechnology, PLGA NPs are being extensively investigated as drug delivery carriers.¹³⁶ For instance, to improve the bioavailability of hydrophobic drugs, Xi et al successfully encapsulated Astragaloside (AS) in the hydrophobic core of PLGA NPs and enabled them bone-targeting properties by conjugated PLGA nanocarrier with Alendronate (AL) sodium via polyethylene glycol.⁷² In vivo and in vitro experiments have demonstrated the improved oral bioavailability and anti-OP effect of this nanocarrier, with the addition of AL further enhancing its bone targeting properties.

PLGA nanoparticles are also being explored as carriers for simvastatin, a drug that enhances bone formation and density but has limited use due to its hydrophobic and non-targeted nature.^137,138 To overcome this, researchers have combined PLGA NPs with tetracycline to give the nanocarrier bone targeting properties. In vivo experiments have shown that simvastatin-loaded tetracycline-modified PLGA NPs significantly increase bone density in osteoporotic rats compared to free simvastatin and non-targeted NPs.⁷³ Similarly, using PLGA NPs as carriers, the researchers delivered estradiol to OP rats and administered the drug via iontophoresis. The results showed that the negative ions on the surface of the PLGA NPs combined with the special delivery method could enhance the concentration of estradiol in the blood and treat the OP rats more effectively.⁷⁴ Zhang et al loaded secretome (Sec) from MSC into PLGA NPs and endowed the carrier with bone targeting via CXCR4. In the OP rat model, they found that this NP accumulated in the bone and exhibited inhibition of osteoclast differentiation and promotion of osteoblast proliferation, which reduced bone attenuation from the surgical model.⁷⁵

In another study, composite nanocarriers of PLGA/HAP were implanted subcutaneously in mice to deliver BMPs, resulting in increased mouse bone formation.⁷⁶ The PLGA/HAP nanofiber exhibited good morphology and mechanical strength and using it as a carrier allowed BMP to be released while maintaining good biological activity in vivo.¹³⁹

Chitosan Nanoparticles

Chitosan, a natural polysaccharide derived from chitin found in crustaceans, insects, and fungi, is known for its hydrophilicity, biocompatibility, and biodegradability.^77,140,141 Chitosan nanoparticles (CS-NPs) have gained popularity as drug carriers due to their small size, high encapsulation efficiency, and loading capacity,^142–144 and ability to combine with a wide range of molecules, including plant components, nanomaterials, hormones, and proteins.^145,146

To overcome the low bioavailability and toxic side effects of drugs commonly used in clinics, like RLX, lipid nanocarriers have been effectively used for delivery. Saini et al used CS-NPs to deliver RLX, which improved its oral bioavailability.⁷⁷ Similarly, PEGylated chitosan nanoparticles were used to deliver PTH, yielding similar effects.⁷⁸ CS-NPs were also used to deliver bisphosphonates, resulting in a significant improvement in bone density and microstructure in osteoporotic rats, while cortical porosity on bone surfaces decreased.⁷⁹ CS-NPs were used to load Human Parathyroid hormone 1–34 (PTH1-34), and the experimental results suggested the biocompatibility and high encapsulation efficiency of this delivery strategy. In addition, the researchers affirmed the efficiency of oral CS-NPs in delivering PTH1-34, and this strategy is a potential way to treat OP in the future.⁸⁰ Shilajit is a class of natural minerals whose extracts (SWE) have been shown to affect bone development. In a study, researchers utilized CS-NPs encapsulated with SWE and evaluated the efficacy of the pair combination in OP rats.The results suggested that CS-NPs encapsulated SWE could enhance the anti-OP effects of SWE.CS NPs delivered SWE could be recommended as a potential treatment for OP.⁸¹

In another study, researchers sought to deliver RDN and TPD together in a targeted manner using CS-NPs as carriers, with the carrier surface modified with hyaluronic acid. This carrier, which loaded both RDN and TPD, could be stably preserved at low temperatures and exhibited stronger bone regeneration effects, indicating a promising new strategy for treating OP.⁸²

Bone-Targeted Nanoparticles for the Treatment of Osteoporosis

In clinical practice, there are several drugs available for the treatment of OP, as outlined in Table 1. However, these drugs face limitations when administered orally or intravenously, as they struggle to target specific tissues for release. Most drugs are absorbed or excreted by other organs in circulation, making it difficult to achieve the therapeutic effect.^147–149 Consequently, higher drug doses or more frequent administration may be required, leading to adverse reactions and organ toxicity. To overcome these limitations, targeted drug delivery strategies are required, with the combination of targeted delivery and nanotechnology offering a more effective approach. For OP, scientists need to focus on bone targeting as the primary strategy. Since the concept of “bone targeting” was first proposed in 1986 by Pierce et al,¹⁵⁰ research in this area has developed rapidly.

Bone tissue has a surface-mineralized extracellular matrix primarily that primarily consists of HAP and hosts a variety of movements, such as ion exchange, crystal growth, dissolution, and combinations of foreign molecules on the bone surface. Therefore, this mineralized component offers an option for bone targeting.^14,151 Studies indicate that the crystal size of HAP in the bone tissue of osteoporotic patients is larger,¹⁵² making targeted treatment of the bone surface with drugs more feasible.

Bone targeting strategies involve binding the target molecule to HAP in bone, enabling NPs carrying the drug to aggregate and exert their effects on bone tissue.¹⁵¹ The surface of these NPs can also be modified with cell/tissue-targeting groups, such as bisphosphonates or osteoclast/osteoblast-targeting peptides, to enhance the biological distribution of the drug in bone tissue. Additionally, bone marrow presents itself as a potential target for bone-targeting delivery systems. Figure 2 illustrates the bone targeting strategy, which, when combined with nanocarrier delivery systems, can offer a more satisfactory drug treatment for OP. Understanding the bone targeting strategy is essential to develop effective targeted drug delivery systems for OP. Table 3 summarizes typical examples of the targeted strategy of nanoparticles to enhance the treatment of OP.

Table 3 Targeting Group-Modified Nanoparticles Enhance the Therapeutic Potential of Drugs to Treat OP

Targeting Moiety	Nanocarrier	Delivery Agent	Outcome	References
(Asp)14 or (AspSerSer)6	Cationic liposomes	siRNA CKIP-1	(AspSerSer)6 is favorable for binding to the bone formation surface, enhancing CKIP-1 gene silencing, significantly increasing osteoblast activity, and improving bone mass and trabecular structure.	[184]
CH6 aptamer	LNPs	siRNA CKIP-1	CH6 aptamer can specifically target osteoblasts, delivering siRNA to induce efficient gene knockdown and enhance bone metabolism	[185]
SDSSD	Nanomicelles	Anti-miR-214	Anti-miR-214 promotes bone formation, improves bone microstructure, and increases bone mass in a mouse OP model with ovariectomy	[182]
SDSSD	Exos	siRNA-Shn3	siRNA-Shn3 inhibits osteoclast formation to treat OP	[60]
(DSS)6	Liposomes	quercetin	Osteotropic delivery of quercetin can effectively enhance the clearance of senescent cells and promote bone formation.	[198]
C11 peptide, CH6 aptamer	Dendrimer	N.A	The drug can quickly accumulate in the bone, especially in the sites of active osteoblasts.	[199]
CXCR4	Hybrid Exo-liposomes	Antagomir-188	CXCR4 can accumulate rapidly in bone, especially in areas of active osteoblasts. It also aggregates in bone marrow, promoting osteoblast differentiation and inhibiting adipocyte differentiation, thereby reversing age-related bone loss.	[61]
GLG1	Exos	Wnt agonist	GLG1-NP can reside in bone tissue over an extended period and has good bone targeting and BMSC targeting properties.	[197]

Figure 2 Targeted ligands and their targets for the treatment of OP. Bone-targeted nano-delivery systems can be specifically delivered to bone matrix, bone marrow, osteoblasts, and osteoclasts by using various targeting ligands, including BPs, peptides, antibodies, and many other synthetic chemical molecules.

Tartrate-Resistant acid Phosphatase

Tartrate-resistant acid phosphatase (TRAP) is an acid hydrolysis enzyme mainly found in osteoclasts, making it a useful indicator for identifying these cells.^153,154 Moreover, TRAP is secreted by osteoclasts towards the bone surface and can be detected on the bone surface and in the bone matrix,^155,156 making it a potential therapeutic target. Wang et al designed a peptide TPLSYLKGLVTVG with a high affinity for TRAP and coupled it to the corona of a nanosphere.¹⁵⁷ They delivered a GSK-3β inhibitor to the site of bone fractures in mice, resulting in higher drug accumulation, activation of the β-catenin pathway in MSCs and osteoblasts, increased formation of bone bridges and deposition of bone mass. This targeted approach enhanced the healing ability of bone fractures. As mentioned above, a bifunctional peptide, TBPCP05, binds to the surface of EVs, causing them to display TRAP-binding peptides on the surface, and in vivo and in vitro experiments have demonstrated the ability of such EVs to target osteoclasts. This vector carrying anti-miR-214 can focus on osteoclasts and exert anti-OP effects.⁶³

Although targeting TRAP is still in its early stages of research, these successful examples provide valuable insight for future directions in using TRAP-based peptide and NP coupling for drug delivery to treat bone diseases.

Tetracycline

Tetracycline is a yellow crystalline amphipathic substance derived from the metabolism of Streptomyces rimosus, and it was first used as a broad-spectrum antibiotic in the 1940s.^158,159 It is effective in inhibiting bacterial growth at high concentrations and plays an important role in the prevention and treatment of human and animal infections.¹⁶⁰ Shortly after tetracycline was used in medicine, an interesting phenomenon was discovered where bright yellow fluorescence could be observed under UV light in the bones of animals treated with tetracycline.¹⁶¹ This fluorescent property of tetracycline made it a target marker carrier.¹⁶² Tetracycline’s ability to deposit in bone tissue also sparked an interest. Initially, it was thought that tetracycline interacted with the organic matrix of bones, but later evidence showed that it mainly binds to HAP on the bone surface.^163,164 Tetracycline’s bone-binding ability is a double-edged sword. On the one hand, pigmentation was observed in the teeth of young people who had taken tetracycline, which may lead to a decrease in tooth hardness and enamel damage, limiting its clinical use.¹⁶⁵ On the other hand, due to tetracycline’s high affinity for HAP, researchers began exploring its potential as an effective compound for bone targeting.

In recent years, the drug delivery strategy for OP based on the combination of tetracycline bone-targeting agents and nanocarriers has been widely studied. Que et al used TC-mPEG-PLGA to establish a bone-targeting nanodrug delivery system and loaded it with astragaloside to treat OP.¹⁶⁶ In vivo and in vitro results showed that TC-mPEG-PLGA effectively increased the accumulation of astragaloside in bone and improved bone density in ovariectomized rats compared to free astragaloside. Similarly, Wang et al used TC-PLGA NPs to load SIM to treat OP and demonstrated higher bone-targeting efficiency and improved efficacy in restoring bone density.⁷³ In addition, tetracycline can also serve as a bone-targeting agent for another type of nanocarrier. Researchers have constructed tetracycline-modified and SIM-loaded amorphous calcium carbonate (ACC) hybrid nanoparticles (TC/ACC/SIM) and found that TC/ACC/SIM can enhance its accumulation in osteoporotic sites and synergistically promote bone formation with calcium supplementation and SIM.¹⁶⁷

Although tetracycline combined with nanocarriers has shown good results in treating OP, its side effects, complex chemical structure, and poor stability during chemical modification seem to hinder further utilization of tetracycline as a bone-targeting agent.¹⁶⁸ Therefore, researchers hope to develop molecules with similar tetracycline-like abilities but with fewer side effects and greater stability. As a result, a minimized chemical structure B (3-amino-2,6-dihydroxy-benzamide) derived from tetracycline was designed, which has significantly fewer side effects compared to tetracycline while retaining 50% of its bone-binding ability.¹⁶⁸ Moreover, molecule C, which is a derivative of B with a succinate linker, has an even greater bone-binding ability than tetracycline. The structures of tetracycline and modified tetracycline molecules are shown in Figure 3.

Figure 3 General structures of bisphosphonate, tetracycline, Asp-rich peptides, and its analogues with variable groups extending the function for bone target.

Bisphosphonates and Analogues

Bisphosphonates (BPs) are a class of drugs that inhibit bone resorption and are widely used in skeletal diseases such as OP.^169,170 At the cellular level, the mechanism of action of BPs, especially their effect on osteoclasts, is mainly manifested as the inhibition of cell activity, shortening of cell lifespan, and inhibition of their recruitment and adhesion to the mineral matrix.¹⁷¹ Additionally, BPs act as bone-targeting agents.¹⁷² Studies have shown that BPs are similar to pyrophosphates (P-O-P), which naturally exist in the bone matrix. Pyrophosphate is a non-metabolic endogenous substance composed of an oxygen atom and two phosphate groups, while BPs are composed of a carbon atom and two phosphate groups (P-C-P).¹⁷³ The molecular structures of BPs and their analogs are shown in Figure 3. The two phosphonate groups on BPs have a strong affinity for Ca²⁺ in HAP and can bidentate bind to the bone. For most BPs, if R₁ is a hydroxyl or amino group, it can trigger tridentate binding to HAP, which makes it have a higher bone-binding affinity.^174,175 With the deepening exploration of BPs, three generations of BPs have been approved for clinical use. The second generation contains nitrogen-containing BPs, such as alendronate (ALN), and the third generation contains nitrogen-containing heterocycles, such as risedronate. The nitrogen-containing group on the R₂ side chain exhibits a higher affinity for HAP through hydrogen bonding.¹⁷⁶ Therefore, BPs have the dual advantages of being bone-targeting agents and anti-bone resorption agents and are widely used as targeting ligands for anti-OP NPs. For example, Hoque et al used ALN as a bone-targeting agent for the nanocarrier loaded with adenosine, which was administered systemically to ovariectomized mice.¹⁷⁷ Compared with the non-targeted nanocarrier, ALN could guide more than 45% of the nanocarrier to accumulate in the mouse vertebrae and restore the trabecular bone characteristics of ovariectomized mice to the level of the healthy group. Furthermore, similar to the study of TC-mPEG-PLGA loaded with astragaloside discussed in the previous chapter, researchers replaced the targeting agent from tetracycline with ALN. The targeted nanocarrier greatly improved the affinity and bone tissue concentration of astragaloside to HAP, and the oral bioavailability of astragaloside was significantly improved. The addition of ALN made the prevention and treatment of OP more effective.⁷²

Targeting Other Bone-Formation Surfaces

In addition to the typical targeting of bone surface ligands mentioned above, the affinity between certain bone proteins and HAP in nature has also sparked interest in bone-targeting strategies. Some studies have found that non-collagenous proteins in the bone matrix, such as bone sialoprotein and osteopontin, play important regulatory roles in the growth and dissolution of HAP and have an affinity for HAP to bind to it.¹⁷⁸ These proteins share a common feature of repetitive acidic amino acid sequences of L-aspartic acid (L-Asp) and L-glutamic acid (L-Glu).¹⁷⁹ In 2000, Kagugai et al found that when administered systemically, peptides containing repeating Asp or Glu amino acid residues can selectively deliver drugs to bone tissue.¹⁸⁰ Compared with peptides and proteins, oligopeptides have higher stability, better tissue penetration, and lower immunogenicity.¹⁸¹ Compared with BPs containing P-C-P bonds, oligopeptides have a shorter half-life, do not produce long-term adverse reactions, and do not form micelles with metal ions, making them easier to be enzymatically metabolized into non-toxic substances.¹²

Using acidic oligopeptides as bone-targeting agents to modify NPs also shows promising prospects. Sun et al designed a five-amino acid motif oligopeptide Ser-Asp-Ser-Ser-Asp (SDSSD), which has a binding affinity with osteoblast membrane inhibitor (also known as osteoblast-specific factor 2, OSF-2) expressed by osteoblasts.¹⁸² They combined it with polyurethane (PU) nanomicelles to create a targeted nanocapsule, SDSSD-PU, that can target the bone formation surface to deliver anti-miR-214 to osteoblasts. This can increase bone formation, improve bone microstructure, and increase bone mass in ovariectomized osteoporotic mice without causing obvious toxicity or triggering an immune response in the body. Similarly, using this bone-targeting oligopeptide to modify MSC-Exos and loading siRNA targeting Shn3 can specifically inhibit the expression of the Shn3 gene in osteoblasts and inhibit osteoclast formation, providing inspiration for cell-free therapy for OP.⁶⁰ Kagugai et al found that fluorescently labeled Asp₆ only accumulated in bone and teeth after systemic administration to rats for 24 hours.¹⁸⁰ Using the targeting ability of the peptide, a novel drug conjugated with L-Asp-hexapeptide and estradiol exhibited a good anti-OP treatment effect in the ovariectomized mice.¹⁸³ Tao et al used L-aspartic acid oligopeptide Asp₆ as a bone-targeting peptide to deliver SIM-loaded novel LNPs to the osteoporotic bone, significantly enhancing the therapeutic effect of OP and demonstrating the advantages of bone-targeted drug delivery systems.⁵⁸

In addition, Zhang et al found that aspartic acid, serine, and six repeat sequences of serine (AspSerSer)₆ have a very high affinity for mineralized nodules of osteoblasts and amorphous calcium phosphate. They connected these sequences to DOTAP cationic liposomes to develop a targeted delivery system that can specifically deliver siRNA to the surface of bone formation. The Plekho1 gene is an intracellular negative regulator of bone formation. Zhang et al encapsulated Plekho1-siRNA in liposomes connected to (AspSerSer)₆ for targeted delivery. In vivo experiments found that the siRNA selectively accumulated on the bone surface, reduced the levels of Plekho1mRNA and protein in selective osteoblasts, significantly promoted bone formation, enhanced bone microstructure, and increased bone mass in healthy and osteoporotic rats. Bioimaging analysis further showed that this method was effective.¹⁸⁴

Similarly, Liang et al screened for a specific adapter molecule, CH6, for osteoblasts and developed a CH6-lipid nanoparticle (LNP)-Plekho1-siRNA delivery system for targeted Plekho1 delivery. By functionalizing the LNP with the adapter molecule CH6, the system achieved specific delivery of Plekho1-siRNA to osteoblasts. The CH6-LNP-siRNA targeting system showed higher accumulation in bone tissue, and its application in osteoporotic rats that underwent ovariectomy revealed significantly improved bone mineral density (BMD), relative bone mass (BV/TV), trabecular thickness (Tb.Th), trabecular separation (Tb.Sp), trabecular number (Tb.N), and structure model index (SMI), demonstrating good osteoblast specificity.¹⁸⁵

Overall, targeted group-modified nanodelivery systems can improve microstructure, increase bone mass, enhance bone mechanical properties, and significantly reduce side effects in OP models. Gene targeting modification can further enhance the function of targeted delivery systems from tissue specificity to cellular specificity, making it more precise and effective, which is beneficial for the clinical application of osteoporosis metabolism therapy.

Another interesting discovery is that bones are rich in Ca²⁺ and carry positive charges, making an ideal material for targeting bone surfaces with negative charges, which facilitates its affinity with positively charged bone. Researchers found that nHAP-loaded PTH with negative zeta potential can promote its affinity for Ca²⁺-rich bone tissue, enabling targeted localization and exerting anti-OP effects.⁶⁶

Targeting Bone Marrow

The development of bone-targeted delivery systems has the potential to improve the treatment of OP by targeting both bone surface and bone marrow. It is essential to have a clear understanding of the relationship between bone marrow and OP to achieve this. Increasing evidence suggests that bone loss in postmenopausal women and ovariectomized animals is always accompanied by abnormal accumulation of marrow adipose tissue (MAT).^186–189 Anti-OP drugs such as BPs, RLX, and TPD have been shown to reduce bone marrow adiposity.^187,189,190 The bone marrow microenvironment contains various types of cells, including adipocytes, stromal matrix cells, hematopoietic cells, osteoblasts, and osteoclasts, and can secrete various cytokines to regulate bone remodeling,¹⁹¹ highlighting the importance of targeting the bone marrow.

NPs with a neutral surface charge and small size are promising candidates for targeted drug delivery to the bone marrow, where they can accumulate and release drugs over an extended period.¹⁹² Researchers have identified various potential targeting ligands for bone marrow receptors, including pregnancy zone protein (PZP) in the exosomes secreted by endothelial cells¹⁹³ and E-selectin expressed on the surface of bone marrow endothelial cells.¹⁹⁴ Although the use of PZP to treat bone tumors has been explored, the use of PZP and E-selectin to treat osteoporosis has not been investigated and might become a novel direction for future research. Researchers have also modified LNPs with anionic amphiphiles. The hydrophilic head group on the modified NP can be recognized by scavenger receptors expressed on bone marrow macrophages, providing another potential target for the bone marrow.^195,196

It has been found that stromal cell-derived factor 1 (SDF1) in the bone marrow has been found to recruit CXCR4⁺ hematopoietic stem cells (HSCs) and promote bone metastasis of CXCR4⁺ tumor cells. In a prospective study, researchers have used this finding to develop a targeted drug delivery approach, as discussed in the exosome section.⁶¹ Hu et al genetically engineered NIH-3T3 cells to secrete Exos with high CXCR4 expression. They found that these Exos are selectively accumulated in the bone marrow. They then fused these Exos with liposomes carrying antagomir-188 to form hybrid Exos, which could accumulate antagomir-188 in the bone marrow. This approach promoted osteogenesis and inhibited BMSCs from differentiating into adipocytes, thereby reversing age-related bone loss.

Based on the receptor-ligand binding theory and inspired by the molecular mechanism of prostate cancer bone metastasis, scientists have expressed GLG1 (Golgi glycoprotein) on the surface of Exos and collected GLG1⁺ Exos from a tool cell line to construct GLG1⁺ drug-loaded nanoparticles (GLG1-NP) carrying Wnt pathway activator Wnt agonist 1. The results showed that peripheral administration of GLG1-NP achieved specific distribution in bone tissue. In a mouse model of OP induced by chronic colitis, GLG1-NP significantly improved bone mass, mechanical properties, BMSC osteogenic differentiation, and bone formation. Additionally, GLG1-NP promoted fracture healing in mice with ulcerative colitis and reduced bone marrow fat accumulation, achieving significant therapeutic effects in bone complications of mice with ulcerative colitis.¹⁹⁷

In summary, the utilization of NPs to enhance drug delivery across biological barriers and improve the efficacy of precision medicine holds the potential to accelerate the clinical translation of targeted NPs for the treatment of OP. Developing nanobiomaterials for precision medicine in OP requires carefully designed methods to adjust the composition of NPs, examine the pharmacokinetics of therapeutic drugs, and optimize drugs’ solubility, administration, and biological distribution. This highly customizable platform has the potential to accelerate the clinical translation of targeted NPs for OP treatment.

Conclusion and Outlook

The high prevalence of OP is a significant health concern, posing a tremendous burden on patients, their families, and society. Although current conventional clinical medications provide some symptomatic relief, their limitations and adverse effects remain unresolved, severely restricting their use. Therefore, finding low-toxic, stable, specific and efficient drug delivery methods for the treatment of osteoporosis has become a key area of research. Fortunately, in the past few decades, the development of nanomedicine has created new possibilities for the diagnosis and treatment of many diseases. In particular, the application of nanotechnology for bone targeting has been successful in the field of bone tumors, but the application of nanocarrier bone-targeted drug delivery in osteoporosis treatment is still at an early stage.

In this review, we introduce bone-targeted nano-delivery carriers, modification strategies for bone targeting, and their applications in OP therapy. Currently, the most studied nanocarriers for OP include LPS, Exos, SPIONs, PLGA NPs, nHAP, and CS-NPs. Among them, Exos, as cell-derived nanomaterials with low immunogenicity, good barrier penetration, and targeting properties, is expected to overcome the disadvantages of traditional nanomaterials such as potential cytotoxicity, poor biodegradability, and uncontrolled drug release and other drawbacks, showing great promise for effective treatment of OP. In addition, the plasticity of nanocarriers allows us to integrate their advantages to create more desirable nanocarriers, such as the fusion of multiple nanocarriers (eg, hybrid liposomes and Exos), which is a future direction for the optimization of biocompatible nanocarriers. However, these nanodrug release mechanisms need to be further explored, and we need to fully understand the effect of magnetic field variations on drug release, but many other factors such as temperature, pH, light, linkage modifications between the drug and the carrier, and bone-specific enzymes may also regulate drug release. Future studies should focus on these factors to better understand drug release from bone-targeted nanocarriers. Follow-up studies are needed to accurately address all aspects of a mature bone-targeted nanodrug delivery system if clinical applications are to be realized as soon as possible. We eagerly anticipate that bone-targeted delivery of nanomedicines will benefit every osteoporosis patient in the future.

Disclosure

The authors declare that they have no competing interests.

Additional information

Funding

This project was partly supported by National Natural Science Foundation of China (82102607); Taishan Young Scholar Foundation of Shandong Province (NO. tsqnz20231256); Shandong Provincial Natural Science Foundation (ZR2023QH148); PhD Research Foundation of Affiliated Hospital of Jining Medical University (2022-BS-03, 2022-BS-04), Engineering Research Center of Shandong Higher Education Institutions ([2022] No. 2), the NSFC cultivation project of Jining Medical University (JYP2019KJ33).