Magnetic hydroxyapatite: a promising multifunctional platform for nanomedicine application

Abstract

In this review, specific attention is paid to the development of nanostructured magnetic hydroxyapatite (MHAp) and its potential application in controlled drug/gene delivery, tissue engineering, magnetic hyperthermia treatment, and the development of contrast agents for magnetic resonance imaging. Both magnetite and hydroxyapatite materials have excellent prospects in nanomedicine with multifunctional therapeutic approaches. To date, many research articles have focused on biomedical applications of nanomaterials because of which it is very difficult to focus on any particular type of nanomaterial. This study is possibly the first effort to emphasize on the comprehensive assessment of MHAp nanostructures for biomedical applications supported with very recent experimental studies. From basic concepts to the real-life applications, the relevant characteristics of magnetic biomaterials are patented which are briefly discussed. The potential therapeutic and diagnostic ability of MHAp-nanostructured materials make them an ideal platform for future nanomedicine. We hope that this advanced review will provide a better understanding of MHAp and its important features to utilize it as a promising material for multifunctional biomedical applications.

Introduction

The increased application of nanomaterials in our everyday work increases human interactions with nanoparticles. Since Freeman et al introduced the concept of using magnetism in medicine in the 1960s, a vast amount of research has been performed, leading to the design of several magnetic nanoparticles and vectors.¹ Recent progress in the field of magnetic nanoparticles for therapeutic applications has considerably surpassed expectations. The ability to specifically target and easily recover excess or unused drugs by an external magnetic field makes these nanoparticles particularly interesting for researchers.

The key factor for magnetism solely depends on the orbital and spin motions of electrons and the in-between interactions of electrons. Magnetic materials are classified into the following five major groups according to the behavior of a material in a magnetic field: diamagnetic, paramagnetic, ferromagnetic, ferrimagnetic, and antiferromagnetic. Magnetic targeting is established on the following two key aspects: a magnetically responsive carrier and a magnetic field gradient (magnetic force) that is liable for attracting or placing magnetically responsive carriers inside a body system. Superparamagnetism is an extremely important characteristic for a magnetic material, which allows strong instant magnetization (during magnetization, all magnetic atoms align parallel to the direction of an applied magnetic field). There should be no residual magnetization (remanence) remaining after removal of the magnetic force. When a magnetic material is positioned in a magnetic field H, specific atomic moments in the material give their overall response to the magnetic induction (B):

$$B={\mu }_0(H+M)$$

where μ₀ represents the free space permeability and M (magnetization) = m/V which denotes the magnetic moment per unit volume.² The force applied to a magnetic carrier with magnetic moment $\overrightarrow{m}$ is given by the following equation:³

$$\overrightarrow{F}=(\overrightarrow{m}\cdot \nabla \overrightarrow{B})\overrightarrow{B}$$

where $\overrightarrow{F}=\text{magnetic force}$, $\overrightarrow{m}=\text{magnetic moment}$, $\overrightarrow{B}=\text{magnetic field}$, and $\nabla \overrightarrow{B}=\text{high magnetic field gradients}$.

The versatile fundamental characteristics of magnetic nanoparticles facilitate numerous therapeutic applications such as controlled and specific targeted drug delivery, detoxification of biological fluids, magnetic resonance imaging (MRI), cancer therapy, magnetic fluid hyperthermia, environmental application (adsorption or catalysis), and isolation of pathogens and macromolecules and as sensors. The most common types of magnetic nanoparticles are based on iron oxides. Investigations have also been performed on magnetic nanoparticles based on other dopants. Magnetic nanoparticles are broadly categorized into the following eight different categories: (1) iron oxide (Fe₃O₄, Fe₂O₃); (2) iron doped; (3) Fe and platinum co-doped; (4) barium, manganese, and Fe doped; (5) cobalt-ferrite (CoFe₂O₄); (6) gadolinium–neodymium co-doped; (7) samarium (¹⁵³Sm) lexidronam and Gd incorporated; and (8) iron oxide, Fe, and copper doped. Superparamagnetic iron oxide nanoparticles exhibit superior characteristics compared with other magnetic compounds, such as less toxicity, high magnetic saturation, and easy fabrication, which attracts a great deal of attention.

All the magnetic materials used for different application purposes, especially for the biomedical application, have some merits and demerits (Table 1). A demerit of magnetic materials such as Nd, Gd, and Sm is that they need large external fields and controlled environment to influence. Materials with efficient magnetization and great susceptibility are preferred for applications such as drug targeting and magnetic separation. Transition metals (like cobalt) possess a potential magnetic property; however, owing to their toxicity, these types of materials are less used in biological research. Manganese, another suitable metal, has been used as a bone-reconstructing and bone loss-inhibiting agent. However, manganese substitution does not affect the magnetic properties of composite materials. Different magnetic nanomaterials have been produced for different functional aspects. In biomedical applications, nanoparticles could not be directly used in the body system. They require some precautions such as surface modification by means of coating, before their medicinal application.

Table 1.

Advantages and disadvantages of different types of MHAp nanostructures for biomedical application

S no	Materials	Advantages	Disadvantages	Study
1	Iron oxide HAp	Magnetic hyperthermia, drug delivery application, superparamagnetic behavior, etc.	Core shell HAp-coated iron oxide synthesis is difficult and associated with multiple steps	Trandafir et al4
2	Fe-doped HAp	Magnetic hyperthermia, drug delivery application, etc.	Fe-HAp exhibits very low crystallinity and a structural coherence at the nanometer length scale together with very low thermal stability	Tampieri et al5
3	Fe and Pt co-doped HAp	Good catalytic activity, used in sensors, high stability, etc.	Limited biological application due to toxicity	Tseng et al6
4	Mn- and Fe-doped	Useful for hyperthermia applications, to treat bone cancer, MRI contrast agent	Manganese substitution does not affect the magnetic properties in composite materials	Pon-On et al7
5	Cobalt-ferrite (CoFe2O4)-doped HAp	Bioimaging property, MRI contrast agent	Metal toxicity to biometabolism	Petchsang et al8
6	Gd–Nd co-doped	Good luminescent property for bioimaging. Electrical conductivity of HAp is improved because of the high polarizability of Nd (III) and Gd (III)	Need large external fields and controlled environment to influence	Syamchand and Sony9
7	Samarium (153Sm) lexidronam and Gd incorporated	Used for bioimaging specially for SPECT/MRI dual-imaging probe	Need large external fields and controlled environment to influence	Liu et al10
8	Iron oxide, Fe- and Cu-doped HAp	Drug delivery ability, pro-osteogenic and proangiogenic activities	The size and morphology varies with different dopant compositions. The solubility in water media is also variable	Kuda et al11

Abbreviations: MHAp, magnetic hydroxyapatite; HAp, hydroxyapatite; MRI, magnetic resonance imaging; SPECT, single-photon emission computed tomography.

Importance of coating over magnetic nanoparticles

The issues regarding biocompatibility and toxicity limit the choice of materials for biomedical application; however, coatings may make the use of these materials feasible. Biocompatible polymers, metals, ceramics, or composites are generally used as coatings to render the materials nontoxic and nonimmunogenic. Moreover, coatings help in reducing aggregation and preventing magnetic particles from being directly exposed to the body. In addition, coatings are used as matrix for drugs, nucleotides, or genetic materials to deliver them to target sites. Different types of coatings have been employed for nanoparticles to make them suitable for different applications. These coatings and their consequent geometric structure on nanoparticles control their complete size, which also regulates the biodistribution of nanoparticles in a body system. Coatings are chosen based on their application, for example, to induce a response to inflammation, in tissue engineering, or as anticancer agents. Coated magnetic nanoparticles can bind to proteins, enzymes, nucleotides, drugs, and antibodies, and could also be directed toward a target site by an external magnetic field.¹² All coating materials have some advantages and limitations (Table 2). Based on the experimental data, it was observed that polymers were the first choice of researchers as coating materials. Iafisco et al synthesized magnetic hollow micro-nanospheres (2 μm to 500 nm) coated with polymeric shell of poly(L-lactic) acid for potential application as scaffolds for hard tissue regeneration as well as carriers for biomolecules.¹³ Taccola et al reported a single-step fast free-standing, flexible nanofilm preparation process for poly(L-lactic) acid-coated iron oxide nanocomposite for biomedical application.¹⁴ Polyacrylic acid (PAA)-coated iron oxide nanoparticles (sizê9 nm) were used together with first-line anti-TB drug rifampicin in Mycobacterium as efflux inhibitors to overcome drug resistance.¹⁵ Ma et al synthesized PAA-coated magnetite nanoparticles (PAA-MNPs, 246 nm) and studied magnetically targeted thrombolysis with recombinant tissue plasminogen activator bound to PAA-MNPs.¹⁶ Denizot et al reported the synthesis of phosphorylcholine-coated iron oxide nanoparticles (5 nm) for use as MRI contrast agent. In this study, phosphorylcholine facilitated a thin-wall coating over iron oxide nanoparticles.¹⁷ During the synthesis of nanomaterials, some polymers like polyvinyl pyrrolidone (PVP), polyvinyl alcohol, polystyrene, and dextran control the size, shape, and growth of nanoparticles.^18–27 Liu et al used PVP as a surfactant in one-pot polyol process to synthesize mono-size PVP-coated iron oxide nanoparticles for biomedical application.¹⁸ Sun et al reported the synthesis of polyethylene glycol (PEG)-coated iron oxide nanoparticle for specific targeting of glioma tumors via the surface-bound targeting peptide, chlorotoxin.²³ Nazli et al reported the synthesis of PEG hydrogel-coated iron oxide nanoparticles for enhanced intracellular uptake by HeLa cells.²⁴ Jarrett et al and Yu et al synthesized dextran-coated iron oxide nanoparticles controlling the particle sizes.^25,26 Progress in development of nanoparticle-based therapeutic and diagnostic platforms is expected to offer incredible potential for advanced diagnosis and tumor treatment. Starch, ethyl cellulose, chitosan, and gelatin polysaccharides are also used by several researchers to coat iron oxide nanoparticles for MRI, drug delivery, and different biomedical applications.^28–35 Saboktakin et al used iron oxide nanoparticles of 10 nm diameter coated with starch for MRI.²⁸ Saikia et al studied the pH-sensitive drug delivery potentiality of starch-coated iron oxide nanoparticles (8–20 nm),²⁹ whereas Ma et al and Bekaroğlu et al reported the successful application of hydroxyethyl cellulose-coated iron oxide nanoparticles in targeted drug delivery.^30,31 Gaihre et al reported gelatin-coated doxorubicin-loaded iron oxide nanoparticles and their drug-loading and drug-releasing kinetics with variable pH.^32,33 In food industry, fatty acid-coated iron oxide nanoparticles are widely used as biocatalyst because of their excellent catalytic activity and easy separation of the catalyst post-reaction by applying an external magnetic field.^36,37 Kalidasan et al reported enhanced biocompatibility and magnetic hyperthermia performance of bovine serum albumin-coated iron oxide nanoparticles.³⁸ For targeted drug delivery, it is very important to improve surface functionality with specific functional groups. Zhang et al enhanced intracellular uptake of iron oxide nanoparticles by successful immobilization of folic acid over their surface. Along with folic acid, they coated PEG over the iron oxide surface and studied the uptake by RAW 264.7 (mouse macrophage) and BT20 (human breast cancer) cell lines.³⁹ Gupta et al reported the synthesis of insulin-coated iron oxide nanoparticles where insulin acted as a surface ligand to prevent endocytosis.⁴⁰ Liu and Huang synthesized a novel liposome-coated magnetic hydroxyapatite (MHAp) drug vehicle with ultrasound-triggered MRI contrast-changing property.⁴¹ The advantages of polymers are that they are easy to fabricate and easy to coat over nanoparticles, and a wide variety of polymers are available with different functional groups. However, some serious disadvantages of polymers restrict ~95% of experimental results obtained in laboratory from translating to clinical application. The three major problems associated with polymers are as follows: (1) they are usually very unstable (affected by varying pH and temperature), (2) they have agglomerating and adherence properties (cause toxic and immunogenic effects), and (3) the hydrodynamic flow inside the body system retards their movement (mostly dissolved in body fluids and degraded because of enzyme activity). Using metals as sole coating agents is strongly discouraged owing to their toxic effects, fabrication difficulties, and synthesis-associated costs. The advancement of nanotechnology has led to the development of metallic nanostructure surfaces or materials for biomedical applications. Metals such as gold, silver, zinc, and platinum show good prospects to enhance magnetization and optical and electrochemical properties of materials.^42–46 Silva et al and Elsherbini et al reported the synthesis and biomedical applications, such as drug delivery, hyperthermia, photothermal therapy, and imaging, of gold-coated iron oxide nanoparticles.^42,43 Silver is an excellent antibacterial agent. Mahmoudi and Serpooshan reported the synthesis of antimicrobial magnetic silver ring-coated nanoparticles which were targeted to bacterial biofilm by an external magnetic field.⁴⁴ Platinum coating over magnetic nanoparticle is very less reported, but Kwon et al synthesized platinum-coated magnetic nanoparticles for colorimetric detection of pathogenic bacteria and magnetophoretic chromatography application.⁴⁵ Thomas et al developed zinc-doped iron oxide nanocrystals with mesoporous silica framework as drug delivery vehicle for controlled release of drug molecules achieved by external magnetic hyperthermia effect.⁴⁶ For magnetic nanoparticles to be efficiently used in medicine, they should be extremely biocompatible, stable, and securely eliminated from the body system. Researchers are currently paying more attention to bioceramic coatings which have many added advantages over conventional polymeric coatings. Metal oxides such as TiO₂ and SiO₂ including calcium phosphate coating over nanoparticles are well studied by several researchers.^47–49 Yang et al synthesized mesoporous and nonmesoporous silica-coated iron oxide nanoparticles for luminescent and drug delivery applications.⁴⁷ Ye et al reported the synthesis of mesoporous silica-coated iron oxide nanoparticles for use as nontoxic MRI contrast agent.⁴⁸ Calcium phosphate is a well-known bioceramic for biomedical application, specifically for bone tissue engineering. Pareta et al reported calcium phosphate-coated iron oxide nanoparticles with increasing osteoblast density which could be a promising material for bone tissue engineering application.⁵⁰ Bioactive coating with hydroxyapatite is an important condition to enhance biological functionality which favors the adhesion and proliferation of osteoblasts over implant materials.⁵¹ Among different bioceramics, HAp is the prime choice for researchers because of its high biocompatibility and osteoconductivity. Kumar et al elucidated the synthesis, mechanical property, biological property, and application of different three-dimensional (3D) HAp scaffolds developed by different techniques such as 3D printing and rapid prototyping.^52,53 Maganti et al and Thein-Han and Misra reported freezing and lyophilization techniques to prepare chitosan-nanohydroxyapatite scaffold for bone tissue engineering application.^54–56 In spite of various positive aspects as a suitable biomaterial, low mechanical property is a serious disadvantage of HAp. Kumar et al reported electroconductive HAp and titanium disilicide composite system to overcome the fracture toughness from 0.6 MPa·m^1/2 (HAp) to 1.2 MPa·m^1/2 (titanium disilicide composite HAp).⁵⁷ The study further extended to explain the increased electrical conductivity of titanium disilicide HAp composite which stimulated myoblast proliferation.^57–59 Depan et al studied the cellular response with electrical stimulation effect of different electroactive nanostructure composites.⁵⁸ Mondal et al reported natural-origin and synthetic hydroxyapatite for different biomedical engineering and scaffold development applications.^60–64

Table 2.

Different coating and doping materials for iron oxide nanoparticles

S no	Coating and doping materials	Advantages	Disadvantages	References
Polymer coatings over iron oxide
1	Poly (D,L-lactide)	Enhanced biocompatibility	Usually very unstable (affected with varying pH and temperature); agglomeration and adherence property (causing toxic and immunogenic effects); inside body system, hydrodynamic flow retards its movement (mostly dissolved in body fluids and degradation due to enzyme activity)	13, 14
2	Polyacrylic acid	Improves bioadhesion		15, 16
3	Phosphorylcholine	Initiates coagulation		17
4	Polyvinyl pyrrolidone	Improves functionalization		18
5	Polyvinyl alcohol	Increases monodisperse particle formation		19–22
6	Polyethylene glycol	Improves biocompatibility		23, 24
7	Dextran	Biocompatible, controlling particle size and shapes		25, 26
8	Polystyrene	Uniform cluster formation, controlling particle size and shapes		27
9	Starch	Biocompatible, coating material		28, 29
10	Ethyl cellulose	Enhances drug uptake, good functional property		30, 31
11	Gelatin	Natural, biocompatible		32–34
12	Chitosan	Natural, biocompatible		35
13	Fatty acids	Terminal group functionalization, biocatalyst		36, 37
14	Bovine serum albumin	Biocompatible		38
15	Folic acid	Targets cancer cells, less immunogenic		39
16	Insulin	Improves gene therapy		40
17	Liposome	Long circulatory time in body system		41
Metal and metal oxide coatings over iron oxide
1	Gold	Enhances optical properties and stabilization	Toxic effects, fabrication difficulties, and cost associated with its synthesis	42, 43
2	Silver	Enhances optical properties and antimicrobial activity		44
3	Platinum	Enhances optical and electrochemical properties		45
4	Zinc	Enhances magnetic property		46
5	SiO2	Increases surface area and binding affinity	Increases oxidative stress and agglomerates	47, 48
6	TiO2	Photocatalytic activity	Nonbiological application only	49
7	Calcium phosphate coating	Biocompatible, osteoconductive	Difficult to control coating layer thickness	50
8	Hydroxyapatite	Biocompatible, stable, osteoconductive	Difficult to control coating layer thickness	65–107

HAp is a well-recognized nontoxic biocompatible material that has good stability and a flexible structure that allows easy assimilation of magnetic ions. Iron is the most frequently used metal for imparting HAp with magnetic properties. This review addresses recent advances in the use of MHAp and the possibilities and limitations from fabrication to biomedicinal applications. In addition, different synthetic routes and surface modifications of desired MHAp for application in drug delivery, tissue engineering, and scaffold development are carefully discussed (Table 3).^65–87 The use and effect of an applied magnetic field for drug delivery and release, mechanical cell stimulation, and hyperthermia effects are also discussed.^65–87

Table 3.

Different synthetic routes of MHAp and its applications

S no	Synthesis route	Application	Magnetic saturation (Ms)	References
1	Solution intercalation method	Gene therapy and drug delivery	–	62
2	Template-assisted self-assembly	Gene delivery	–	63
3	Wet precipitation	Biomedicine application, hyperthermia study	7.23–20.92 emu/g	65, 69
4	Ion exchange procedure	Theoretical calculation	–	71
5	Pulsed plasma deposition	Biofilm formation	0.26 emu/g	73
6	Hydrothermal method	Biomedical orthopedic applications	Approximately 0.32 emu/g	74
7	Spray-drying technique	Medical diagnosis and imaging	Approximately 12 emu/g	75
8	Microwave-assisted route	pH-responsive drug release	18.9 emu/g	76
9	Four-step synthesis associated with wet precipitation, ultrasonication, hydrothermal method, and layer-by-layer coating	Magnetic resonance imaging, drug delivery	Approximately 4–7 emu/g	77
10	Hydrothermal method	pH-dependent protein adsorption release carrier	11.5–15.5 emu/g	78
11	Polymer-templated electrospun method	Biomedical and hyperthermia treatment	27.20 emu/g	79
12	Mechanochemical method	Hyperthermia treatments	–	80
13	Ultrasonic irradiation technique	Biomedicine application	7.40 emu/g	81
14	Other synthetic routes (electrophoretic deposition, biogenic source, chemical precipitation)	Solid-phase extraction of plasmid DNA, medical imaging	–	65, 69, 82–95

Abbreviation: MHAp, magnetic hydroxyapatite.

Different synthesis routes of magnetic HAp

The synthesis of HAp and iron oxide nanoparticles by different routes has already been well discussed by many researchers worldwide. However, the synthesis of MHAp is less researched compared with that of HAp and iron oxide. This review attempts to focus on almost every aspect of synthesis procedures of MHAp, which are opted by researchers, and their application to date. Wu et al reported the synthesis of MHAp nanoparticles using a two-step wet chemical process. Calcium hydroxide [Ca(OH)₂] was reacted with orthophosphoric acid for 20 h in an inert (Ar) condition to synthesize HAp nanocrystals. Next, FeCl₂·4H₂O was added and stirred at an ambient environment (80°C and pH 8.0–8.5) for 10 h to obtain a Ca/Fe molar ratio of 0.75. The obtained MHAp was washed several times to achieve a neutral pH for further gene delivery studies.⁶⁵ Shan et al reported a similar wet precipitation method for synthesizing MHAp for solid-phase plasmid DNA (pDNA) extraction.⁶⁶ Zuo et al synthesized laminated MHAp via a solution intercalation method. In their study, 1.0 g sodium dodecyl sulfonate was dissolved in 15 mL deionized (DI) water with 30 mL ethanol, followed by heating at 60°C. Next, 15 mL of 3.3 M calcium nitrate and 30 mL of 1 M diammonium hydrogen phosphate were added to 30 mL of ethanol. Then, 20 mL of 2.5 M NaOH and 20 mL of ethanol were added to the mixture and stirred for 30 min. To synthesize magnetic nanoparticles, 7.5 mL of 2.4 M iron (III) chloride, 7.5 mL of 1.2 M iron (II) chloride, and 30 mL of 3 M NaOH were mixed, after which 45 mL of ethanol was added. The mixture was refluxed for 14 h at 85°C and left at room temperature for 21 days to develop laminated MHAp.⁶⁷ Xiong et al synthesized self-assembled lamellar MHAp for gene delivery application following a similar synthetic method by Zuo et al.⁶⁸ The synthesized MHAp lamellar structure was further loaded with a DNA molecule for gene delivery application. Gopi et al dissolved iron (II) perchlorate and iron (III) perchlorate in DI water (1:2 M ratio), which resulted in the formation of a pale yellow-colored solution. Next, this solution was ultrasonicated (28 kHz at 150 W), and after 5 min, HAp nanoparticles were dispersed in it. A little amount of DI water was added to the gel formed via sonication, and the pH of the solution adjusted to 8 by adding 1 M sodium hydroxide. A black color precipitate immediately appeared owing to the formation of MNPs. Ultrasonic irradiation was continued for the formation of homogenized MHAp in an inert atmosphere. Hou et al followed the similar pathway of Wu et al for synthesizing MHAp nanoparticles in an in vivo hyperthermia study with the mice model.⁶⁹ Laranjeira et al prepared MHAp nanoparticles doped with different magnetic dopants (Gd, Co, and Fe) by wet precipitation method. First, they used calcium hydroxide as the calcium precursor and then added gadolinium chloride hexahydrate, cobalt nitrate hexahydrate, iron nitrate nonahydrate, and iron chloride tetrahydrate (2.5%–10%) to phosphoric acid at pH 7.4 with stirring for 2 h and overnight aging. They performed separate reactions for separate doping and reported that 10% of Gd and Fe (III) offered maximum magnetic saturation, although the exact value was not mentioned. The study also assessed cytotoxic, hemocompatibility, hemolytic, and thrombogenic effects of various MHAp, of which Gd-doped MHAp was the most biocompatible.⁷⁰ Zilm et al reported the wet chemical synthesis of HAp using calcium nitrate (225 mM) and diammonium hydrogen phosphate (80 mM) in a basic (pH 11) condition. The synthesized HAp was further used for an ion exchange procedure to synthesize MHAp. The study reported that different salts (FeCl₂, CoCl₂, and MnCl₂) with a concentration of 0.02 M were used for synthesizing different MHAp. The synthesized HAp was mixed with different salt solutions and sonicated at room temperature for 1 h. Then, the synthesized MHAp was washed and collected for further use.⁷¹ Iannotti et al synthesized iron-doped MHAp by the chemical precipitation method. In a calcium hydroxide suspension (20.40 g in 400 mL H₂O), iron (II) (6.03 g in 75 mL H₂O) and iron (III) chloride (8.28 g in 75 mL H₂O) solutions were simultaneously added. Phosphoric acid solution (20.75 g in 300 mL H₂O) was added very slowly to the mixture. Next, the solution was heated at 45°C for 3 h and finally left for 24 h at room temperature for aging. The synthesized MHAp samples were washed and used for further experiments.⁷² Gambardella et al fabricated a magnetite-augmented MHAp film via the pulsed plasma deposition method, in which the biofilm formed was used to study bacterial adhesion. A mixture of HAp and magnetite (90:10 wt.%) was ball milled with 1.5 wt.% Dolapix CE-64 (dispersant) and finally sintered at 1,200°C for 1 h. This sintered material was further used with PPD system to make a film layer.⁷³ Tran and Webster synthesized MHAp nanoparticles by dissolving FeCl₂·4H₂O and FeCl₃·6H₂O (1:2 molar ratio) in DI water in the presence of HCl. The solution was then added dropwise to an ammonium hydroxide solution (N₂ atmosphere with vigorous stirring), resulting in the formation of black MNPs, and citric acid was mixed as a surfactant with the mixture. After washing and separation, the MNPs were added to 1 M CaNO₃·4H₂O solution. This mixture was added dropwise to 0.6 M potassium phosphate while stirring, and finally, the precipitated materials were hydrothermally treated for 20 h at 200°C. Finally, the obtained MHAp was used for an increased osteoblast study.⁷⁴ Researchers employed a co-precipitation method with chloride salts to synthesize iron MNPs. Instantly, HAp nanoparticles were synthesized by using CaHPO₄·2H₂O and CaCO₃ through mechanochemical wet milling. MNPs were integrated into the HAp matrix during the milling process. The researchers only reported the saturation magnetization of synthesized iron oxide nanoparticles, which was 47 emu/g. However, after coating with HAp, no magnetic saturation was reported. Donadel et al reported a HAp coating of iron oxide magnetic particles by spray-drying. MNPs were synthesized by the alkaline co-precipitation of ferric (0.25 mol/L) and ferrous (0.125 mol/L) solutions in the presence of NaOH solution (1 mol/L) at a high pH with vigorous stirring. MHAp nanoparticles were synthesized by adding diammonium hydrogen phosphate and calcium nitrate into the solution containing iron oxide nanoparticles (previously synthesized). The synthesized MHAp nanoparticles were spray-dried and atomized using the Büchi B-191 dryer with an inlet temperature of 170 and 90°C and a pressure of 5 bar gauge.⁷⁵

Xu et al reported the use of MHAp nanoworms for diagnosing acute hepatic injury by MRI. They briefly discussed four steps for synthesizing MHAp nanoworms. In step 1, HAp nanowillows were prepared using 0.303 g urea in 20 mL ethanol–water (3:1), after which CaCl₂ and NaH₂PO₄ were added under a heating condition of 80°C (pH 11.9) for 24 h. In step 2, after washing, the obtained HAp nanowillows, ~30 mg, were suspended and ultrasonicated in DI water. Next, poly(sodium-p-styrenesulfonate) (PSS) was dissolved in 0.04 M NaCl solution. From this, 0.6 mL PSS-NaCl solution and 0.3 mL NaCl were added with vortexing for 2 min. After 30 min, the samples were washed and freeze-dried for use in step 3. In step 3, HAp and iron oxide nanocomposites were prepared by dispersing HAp-PSS in 30 mL triethylene glycol and ultrasonicating the mixture, after which 30/60/90 mg iron (III) 2,4-pentanedionate was added. The solution was heated at 135°C for 30 min while vigorously stirring. Finally, the solution was autoclaved at 220°C for 4 h and washed. In step 4, the obtained MHAp nanoworms were redispersed in 3 mL DI water with ultrasonication, and 3 mL chitosan was added for 2 min. After washing, the obtained MHAp chitosan nanoworms were dispersed in a sodium alginate solution. The chitosan and sodium alginate coating steps were repeatedly performed four times for layer-by-layer coating of MHAp nanoworms.⁷⁶

Bharath et al prepared MHAp via the hydrothermal route using iron (II) and (III) chloride salts as magnetite precursors and calcium chloride dihydrate and diammonium hydrogen phosphate as HAp precursors (Figure 1A and C). First, 0.01 M diammonium hydrogen phosphate and 0.1 M N-cetyl-N,N,N-trimethyl ammonium bromide (CTAB) were mixed in 10 mL DI water. Simultaneously, 0.03 M of calcium chloride dihydrate was prepared by dissolving in 10 mL DI water, and previously prepared CTAB phosphate solution was added to this solution with vigorous stirring at pH 10.5. To this solution, 0.01 M iron (II) and 0.015 M iron (III) chloride solutions were added with basic pH 10.5. Similarly, different concentrations of other iron chloride salts were used to prepare two different concentrations of iron oxide-loaded HAp (MHAp:MHAp =0.5:1 M). After vigorous stirring, the solution was autoclaved at 180°C for 12 h. Two different concentrations of (0.5 and 1 M, Fe:HAp) MHAp were prepared. The final MHAp particles were washed and used for further experimental study of a pH protein delivery carrier.⁷⁷

Figure 1.

Different synthesis routes of MHAp nanostructures. Schematic illustration of (A) formation mechanism of one-dimensional MHAp nanorods, (B) synthesis of ultrathin MHAp nanosheet (HAPUN/MNs), and (C) chemical precipitation and hydrothermal synthesis of MHAp. (A) Reproduced from Bharath G, Prabhu D, Mangalaraj D, Viswanathan C, Ponpandian N. Facile in situ growth of Fe₃O₄ nanoparticles on hydroxyapatite nanorods for pH dependent adsorption and controlled release of proteins. RSC Adv. 2014;4(92):50510–50520 with permission of The Royal Society of Chemistry.⁷⁷ (B) Reproduced from Chen F, Li C, Zhu YJ, Zhao XY, Lu BQ, Wu J. Magnetic nanocomposite of hydroxyapatite ultrathin nanosheets/Fe₃O₄ nanoparticles: microwave-assisted rapid synthesis and application in pH-responsive drug release. Biomater Sci. 2013;1(10):1074–1081 with permission of The Royal Society of Chemistry.⁷⁸

Abbreviations: MHAp, magnetic hydroxyapatite; HAp, hydroxyapatite; CTAB, N-cetyl-N,N,N-trimethyl ammonium bromide.

Chen et al prepared HAp ultrathin nanosheets (HAPUN/MNs) comprising Fe₃O₄ magnetic nanoparticles by rapid microwave method (Figure 1B). In a solvent system of 15 mL DI water and 15 mL ethylene glycol, 1 mmol Ca(CH₃COO)₂, 0.10 g poly(L-lactic acid)-methoxy PEG, and 0.05 g Fe₃O₄ nanoparticles were dissolved. Next, 10 mL of 1 mmol NaH₂PO₄·2H₂O solution was added dropwise to the previous mixture. Finally, the mixture was poured into a Teflon-lined steel chamber and microwave heated to 120°C for 30 min. The synthesized material was washed and separated using a magnet for a further drug delivery study.⁷⁸

Singh et al reported the synthesis of MHAp nanotubes by poly(caprolactone) template electrospun method. The experimental study was performed by preparing a 10% (w/v) suspension of poly(caprolactone) in MNPs (20 wt.%) containing dichloromethane–ethanol solvent. This mixture was then electrospun (field strength, 15 kV/10 cm) into a nanofiber mesh, and the obtained nanofibers were activated in 2 M NaOH solution for 4 h. Next, the nanofibers were alternatively soaked in 150 mM CaCl₂ and Na₂HPO₄ solutions followed by apatite mineralization by dipping in a 1.5 times-simulated body fluid solution for a week at 37°C. The obtained MHAp nanofibers were finally calcined at 500°C for 5 h to obtain hollow MHAp nanofibers.⁷⁹

Different methods of synthesizing MHAp produce different types of nanostructures. Researchers have also been tailoring MHAp nanostructures according to their nature of applications (Figure 2). The very interesting part of such MHAp nanoparticles is their equally important multifunctional property suitable for many different applications such as environmental and biomedical applications, adsorption, and catalysis.

Figure 2.

MHAp structure synthesized in different shapes (A–H). (A) Reproduced from Cui X, Green MA, Blower PJ, et al. Al(OH)₃ facilitated synthesis of water-soluble, magnetic, radiolabelled and fluorescent hydroxyapatite nanoparticles. Chem Commun (Camb). 2015;51(45):9332–9335 with permission of The Royal Society of Chemistry.⁸⁸ (B) Reproduced from Lin K, Chen L, Liu P, et al. Hollow magnetic hydroxyapatite microspheres with hierarchically mesoporous microstructure for pH-responsive drug delivery. CrystEngComm. 2013;15(15):2999–3008 with permission of The Royal Society of Chemistry.⁸⁹ (C) Reprinted with permission from Boda SK, Anupama AV, Basu B, Sahoo B. Structural and magnetic phase transformations of hydroxyapatite magnetite composites under inert and ambient sintering atmospheres. J Phys Chem C. 2015;119(2):6539–6555. Copyright 2015 American Chemical Society.⁹⁰ (D) Reproduced from Chen F, Li C, Zhu YJ, Zhao XY, Lu BQ, Wu J. Magnetic nanocomposite of hydroxyapatite ultrathin nanosheets/Fe₃O₄ nanoparticles: microwave-assisted rapid synthesis and application in pH-responsive drug release. Biomater Sci. 2013;1(10):1074–1081 with permission of The Royal Society of Chemistry.⁷⁸ (E) Reproduced from Lin K, Chen L, Liu P, et al. Hollow magnetic hydroxyapatite microspheres with hierarchically mesoporous microstructure for pH-responsive drug delivery. CrystEngComm. 2013;15(15):2999–3008 with permission of The Royal Society of Chemistry.⁸⁹ (F) Reprinted from Singh RK, El-Fiqi AM, Patel KD, Kim HW. A novel preparation of magnetic hydroxyapatite nanotubes. Mater Lett. 2012;75:130–133. Copyright 2012, with permission from Elsevier.⁷⁹ (G) Reproduced from Bharath G, Prabhu D, Mangalaraj D, Viswanathan C, Ponpandian N. Facile in situ growth of Fe₃O₄ nanoparticles on hydroxyapatite nanorods for pH dependent adsorption and controlled release of proteins. RSC Adv. 2014;4(92):50510–50520 with permission of The Royal Society of Chemistry.⁷⁷ (H) Reproduced from Cui X, Green MA, Blower PJ, et al. Al(OH)₃ facilitated synthesis of water-soluble, magnetic, radiolabelled and fluorescent hydroxyapatite nanoparticles. Chem Commun (Camb). 2015;51(45):9332–9335 with permission of The Royal Society of Chemistry.⁸⁸ (I) Reproduced from Bharath G, Prabhu D, Mangalaraj D, Viswanathan C, Ponpandian N. Facile in situ growth of Fe₃O₄ nanoparticles on hydroxyapatite nanorods for pH dependent adsorption and controlled release of proteins. RSC Adv. 2014;4(92):50510–50520 with permission of The Royal Society of Chemistry.⁷⁷

Abbreviation: MHAp, magnetic hydroxyapatite.

Synthesized MHAp nanomaterials are characterized by several sophisticated analytical methods such as X-ray diffraction, scanning and transmission electron microscopy, thermogravimetric and differential thermal analysis, energy-dispersive X-ray spectroscopy, Fourier transformed infrared spectroscopy, and vibrating sample magnetometer analysis to determine their phase purity, morphology, thermal stability, qualitative chemical composition, functional groups, and magnetic saturation, respectively.

Biomedical scaffold

The main objective of tissue engineering is the development of novel orthopedic strategies based on a multidisciplinary approach for the augmentation, restoration, and regeneration of damaged or diseased tissues.⁹¹ MHAp scaffolds have been proposed as an advanced tissue engineering tool to increase bone regeneration by providing a fixed platform for controlled accumulation, delivery, and release of essential growth factors, stem cells, or other bioactive molecules directly to the implantation site. Many researchers have already demonstrated the external biophysical stimulations (ultrasound, magnetic pulse, electrical stimulation, etc.) which may act as an important factor for new bone cell regeneration.⁹² Study reports suggest that compared to conventional scaffold materials, MHAp scaffolds have more potential to control the cell growth and scaffold architecture after implantation by external magnetic field stimulation for bone tissue engineering.^92–95 MHAp nanoparticles at nanoscale level act as a single magnetic domain to facilitate micromotion at the interface between cells and scaffold, which might trigger the ion channels on the cell membrane, and activate the mechanotransduction pathway, leading to increase in cell growth, proliferation, and differentiation.⁹⁶

Panseri et al demonstrated a novel method for facilitating the fixation of MHAp collagen-based scaffolds by reducing micromotion at the scaffold–tissue interface. The scaffold architecture orientation based on magnetic forces is clearly described in their study. By employing two approaches, two types of scaffolds were fabricated with a diameter and height of 4 mm each. In the first method, biomagnetic apatite, that is, 7 wt.% magnetic nanoparticles with collagen fibrils, was used as the magnetic scaffold A (MAG-A). The second-type HAp collagen porous scaffold immersed in magnetic ferrofluid was used as the magnetic scaffold B (MAG-B). The in vivo experimental study was performed in 12 healthy male rabbits by inducing surgical defects (2.0 mm diameter and 12.0 mm depth) and positioning the scaffold in the trauma region. The authors explained how magnetic scaffolds implanted in an in vivo system could enhance controlled bone tissue regeneration in a 3D pattern according to the applied very low static magnetic field of 1.2 T (Figure 3A and B[a]). Moreover, the authors hypothesized the fixation of a scaffold using a small pin made of permanent magnets to avoid scaffold micromotion and to facilitate enhanced tissue regeneration (Figure 3B[b]).⁹²

Figure 3.

(A) SEM images of new bone tissue growing inside and around magnetic scaffolds: (a) MAG-A; (b) a detail of MAG-A; and (c) MAG-B at 4 weeks. Scaffold delimited by yellow dashed line; red arrows show mineralization. (b′ and d) Osteocyte lacunae (indicated by asterisks) in the new bone grown inside MAG-A and MAG-B, respectively. Scale bars: (a and c) 1.0 mm; (b) 300 μm; and (d) 100 μm. Reprinted from Panseri S, Russo A, Sartori M, et al. Modifying bone scaffold architecture in vivo with permanent magnets to facilitate fixation of magnetic scaffolds. Bone. 2013;56(2):432–439. Copyright 2013, with permission from Elsevier.⁹² (B) Merged images in (a) show magnetic field lines coming out from permanent magnet and resulting scaffold orientation. (b) Schematic presentation of magnet–scaffold fixation with four implanted permanent magnet pins (PM) that hold an osteochondral scaffold. Reprinted from Panseri S, Russo A, Sartori M, et al. Modifying bone scaffold architecture in vivo with permanent magnets to facilitate fixation of magnetic scaffolds. Bone. 2013;56(2):432–439. Copyright 2013, with permission from Elsevier.⁹²

Abbreviations: MAG-A, magnetic scaffold A; SEM, scanning electron microscopy.

Bock et al successfully transformed standard commercial scaffolds (collagen and HAp) to magnetic scaffolds by dip-coating in iron-containing aqueous ferrofluids (Figure 4). The nanoparticles were incorporated into the scaffold structure, facilitating a magnetization value of 15 emu/g at 10 kOe. This developed magnetic scaffold did not have any structural damage and maintained its specific porosity and shape. Moreover, the magnetic scaffold did not release magnetic particles under a constant flow of simulated body fluids over a period of 8 days. The authors also observed a good biological activity of the magnetic scaffolds supporting adhesion and proliferation of human bone marrow stem cells in vitro.⁹⁷

Figure 4.

Schematic presentation of scaffolds magnetization process: (1) scaffold is immersed in 1 mL of ferrofluid for 15 min; (2) scaffold is freeze-dried for 24 h; (3) scaffold is rinsed with deionized water under ultrasonication for 20 min; (4) scaffold is freeze-dried for 24 h; and (5) magnetized scaffold is obtained.

A similar research was also reported by Tampieri et al, where they developed magnetic biohybrid porous scaffolds. The main constituents of the developed scaffolds were type I collagen (equine tendon extraction) as an organic matrix and HAp; in contrast, the MHAp collagen scaffold was prepared by adding MHAp (synthesized by the chemical precipitation method) to a collagen matrix and was cross-linked with 1,4-butanediol diglycidyl ether and cast in a fabricated mold, after which it was freeze-dried at −25°C, under vacuum conditions. Although the reported magnetic saturation of the developed composite material was very low (0.07 emu/g), the bulk approach of developing MHAp collagen scaffolds remains very promising for the future study.⁹⁸

Scaffold fixation is one of the most important challenges in osteogenic corrective surgery. The fixation should be done efficiently to hold the scaffold in a fixed position and for the bone–scaffold interface to facilitate enhanced tissue regeneration. For small-defect repair, fixation is not a major problem, but for large defects (>2 cm²), fixation is a big challenge. Russo et al described an innovative magnetic fixation approach based on the application of MHAp scaffold. Mathematical finite element modeling was employed to explore the fixation effectiveness. Three magnetic configurations were utilized as follows: (1) near the joint defect, an external permanent magnet ring was placed around the leg; (2) four small permanent magnet pins were used to fix the bone and scaffold; and (3) similar four stainless steel pins were implanted with an induced external magnetic field (Figure 5). In this study, the scaffolds comprised HAp and collagen immersed and impregnated with biocompatible magnetite ferrofluid. The scaffold size was 3×3×1 cm, with a magnetic saturation of 17 emu/g. Based on the designed experimental study, the most appropriate magnetic materials and optimized magnet–scaffold positioning via a magnetic force facilitated sufficient scaffold fixation for treating osteochondral defects.⁹⁹ Another study from Russo et al reported the enhanced osteoconductive property of MHAp scaffold compared to HAp scaffold studied in vivo in rabbit model after 4 weeks of surgery. The HAp and MHAp scaffolds were able to induce bone tissue development without any adverse effects. The histological analysis of 4-week-implanted HAp and MHAp scaffold showed embedded newly developed bone tissues on scaffold surface (Figure 5A–D). In 12-week implantation study, both types of scaffold surfaces were covered with new bone tissues connected directly with the scaffold materials without any inflammation (Figure 5E–H). The interesting result of this study shows the better mechanical property of MHAp scaffold obtained which is an important criterion for tissue engineering application.¹⁰⁰

Figure 5.

Representative histological views of (A, C, E, and G) HAp and (B, D, F, and H) MHAp scaffolds stained with toluidine blue, acid fuchsin, and fast green at (A–D) 4 and (E–H) 12 weeks from implantation. The low magnification reported in images (A, B, E, and F) allows the displaying of the entire scaffold (dark) and of the implant site. Scale bar is 1 mm in (A, B, E, and F) and 500 mm in (C, D, G, and H). Reproduced from Russo A, Bianchi M, Sartori M, et al. Bone regeneration in a rabbit critical femoral defect by means of magnetic hydroxyapatite macroporous scaffolds. J Biomed Mater Res B Appl Biomater. Epub 2017 Feb 15. Copyright 2017 Wiley.¹⁰⁰

Abbreviations: HAp, hydroxyapatite; MHAp, magnetic hydroxyapatite.

Tran and Webster reported an interesting study on MHAp nanoparticles and their enhanced osteoblast activity. This study showed the synthesis of HAp-coated iron oxide nanoparticles by the wet precipitation method, followed by the hydrothermal method with an average particle size of 170 nm. The magnetic saturation of synthesized MHAp nanoparticles was very less (~0.32 emu/g). In a biological study with human osteoblasts (ATCC, CRL-11372), synthesized MHAp nanoparticles showed improved collagen synthesis, calcium deposition, and good alkaline phosphatase activity, which are clear indications of enhanced osteoblast activity for treating bone-related disorders.⁷⁴

Zhu et al investigated the in vitro and in vivo development of protein coronas on HAp and MHAp scaffolds and their controlling effects on cell proliferation (Figure 6). HAp disks (14 mm diameter and 2 mm height) were immersed in 10.0 wt.% MNPs colloidal solution for 24 h and vacuum-dried to form MHAp scaffolds. The saturation magnetization of developed MHAp scaffolds was ~2 emu/g. In this study, MC3T3-E1 cells were used to study the formation of protein corona and its regulatory effect on cell proliferation. This study revealed the significant increase in proteins that regulated cell proliferation. More significantly, the MAPK/ERK signaling pathway, along with two more signaling pathways MEK1/2 and ERK1/2, was triggered in the presence of HAp and MHAp scaffolds. Through a critical investigation of the expression of different proteins, the molecular mechanism of cell proliferation by MHAp was revealed. This study will definitely help in understanding the scaffold-specific cellular activity and in selecting materials for future tissue engineering application.¹⁰¹

Figure 6.

Schematic diagram of MHAp scaffold-enhanced MC3T3-E1 cell proliferation, showing that MAPK/ERK signaling pathway was activated by the protein corona formed on the surface of MHAp scaffold to promote cell proliferation. Reprinted with permission from Zhu Y, Yang Q, Yang M, et al. Protein corona of magnetic hydroxyapatite scaffold improves cell proliferation via activation of mitogen-activated protein kinase signaling pathway. ACS Nano. 2017;11(4):3690–3704. Copyright 2017 American Chemical Society.¹⁰¹

Abbreviations: MHAp, magnetic hydroxyapatite; HAp, hydroxyapatite.

Drug delivery, imaging, and magnetic hyperthermia

For drug delivery application, particle sizes should be small enough to be introduced into the blood circulation system, so that they can easily pass through the capillary systems.

Lin et al developed mesoporous hollow MHAp micro-structure by hydrothermal treatment for pH-responsive drug delivery application. With 50% of magnetite-loaded scaffold, the maximum magnetic saturation obtained was ~58.78 emu/g. Vancomycin was used as the model drug, and the maximum drug-loading capacity was 28.84–35.92 mg/g on mesoporous hollow MHAp. A drug release study was performed at different pH of 3.4, 5.4, and 7.4. During the first 9 h, 19% of drug was released because of the burst effect, and the subsequent release remarkably decreased by 26%–29% on the next 2 days at pH 7.4. At pH 3.4, the release of loaded vancomycin was maximum at ~70 wt.%, whereas at pH 5.4, the final release capacity was ~40 wt.%. This study concluded that with decreasing pH, the drug release efficiency increased, which indicated a suitable condition for magnetic-guided pH-responsive drug delivery.⁸⁹

Chen et al synthesized an MHAp ultrathin nanosheet via a microwave-assisted rapid synthesis route for pH-responsive drug and protein delivery. In this study, docetaxel (Dtxl) and hemoglobin (Hb) were used as model drugs which were adsorbed on the high surface area of nanosheet (~92.8 m²/g, calculated by the Brunauer–Emmett–Teller analysis). The maximum concentration of Hb adsorbed was 150 mg/g, and the maximum release was about 84.1% during the 8-hour study. In contrast, the Dtxl-loading capacity of the MHAp nanocomposite was ~56 mg/g, and the release rate was regulated by two pH parameters (pH 7.4 and pH 4.5). At pH 7.4, ~30% of the drug was released, whereas at pH 4.5, ~98% of the drug was released during the 108-hour study (Figure 7A and B). Because of a well-regulated pH-responsive drug delivery and high biocompatibility, this MHAp ultrathin nanocomposite will be an ideal drug delivery agent for cancer treatment.⁷⁸

Figure 7.

Drug and protein release kinetics of different MHAp nanostructures at different pH conditions. (A) The cumulative drug release percentages of docetaxel from the HAPUN/MNs nanocomposite drug delivery system in PBS with different pH values of 7.4 and 4.5. Reproduced from Chen F, Li C, Zhu YJ, Zhao XY, Lu BQ, Wu J. Magnetic nanocomposite of hydroxyapatite ultrathin nanosheets/Fe₃O₄ nanoparticles: microwave-assisted rapid synthesis and application in pH-responsive drug release. Biomater Sci. 2013;1(10):1074–1081 with permission of The Royal Society of Chemistry.⁷⁸ (B) Cell viability tests of the HAPUN/MNs without and with docetaxel drug loading. Reproduced from Chen F, Li C, Zhu YJ, Zhao XY, Lu BQ, Wu J. Magnetic nanocomposite of hydroxyapatite ultrathin nanosheets/Fe₃O₄ nanoparticles: microwave-assisted rapid synthesis and application in pH-responsive drug release. Biomater Sci. 2013;1(10):1074–1081 with permission of The Royal Society of Chemistry.⁷⁸ Cumulative release of hemoglobin loaded on (C) Fe₃O₄/HAp-1 and (D) Fe₃O₄/HAp-2 nanocomposites at different initial pH values of 7.4 and 9.0 in PBS at room temperature. Reproduced from Bharath G, Prabhu D, Mangalaraj D, Viswanathan C, Ponpandian N. Facile in situ growth of Fe₃O₄ nanoparticles on hydroxyapatite nanorods for pH dependent adsorption and controlled release of proteins. RSC Adv. 2014;4(92):50510–50520 with permission of The Royal Society of Chemistry.⁷⁷

Abbreviations: MHAp, magnetic hydroxyapatite; PBS, phosphate buffer solution; HAp, hydroxyapatite; Hb, hemoglobin; Dtxl, docetaxel; HAPUN/MN, HAp ultrathin nanosheet.

Bharath et al reported the synthesis of two different MHAp nanorods (two different concentrations of iron loading on HAp) for pH-controlled protein transport by means of protein adsorption and release. The detailed MHAp nanorod synthesis procedure using different synthesis routes is discussed in the earlier section. In this study, Hb was used as the model protein, the maximum adsorption of which was reported to be 200.07 mg/g. The researchers revealed that increased MNP concentration increased the protein adsorption capacity. The phosphate buffer solution (PBS) of different pH values (4.0, 7.4, and 9.0) was employed to study the protein release kinetics during 25 h of the total study period (Figure 7C and D). The maximum protein release (~87%–95%) was observed at pH 4.0 for synthesized MHAp nanorods. This excellent pH-sensitive protein release property will help in transporting drugs and releasing them at tumor- or cancer-specific target cell sites.⁷⁷

Chen et al studied the use of multifunctional Eu³⁺/Gd³⁺ dual-doped HAp nanorods for in vivo imaging of nude mice with computed tomography (CT) for monitoring the release and distribution of ibuprofen at the injected sites (Figure 8).¹⁰² A similar study was done by Pan et al with iron oxide-coated fluoridated HAp/Ln³⁺ (Ln = Eu or Tb) nanocomposites for biological applications.¹⁰³ Due to isotropic electronic ground-state ⁸S_7/2 and half-filled f-orbitals, both the trivalent gadolinium and europium ions retained a high magnetic moment and proton relaxation (both transverse and longitudinal) even at low magnetic fields. These electronic structures of rare earth ions make doped MHAp nanostructures an ideal biomarker for MRI and CT scan.¹⁰²

Figure 8.

In vivo PL imaging of the mice after subcutaneous injection (A) without and (B) with Eu³⁺/Gd³⁺-HAp (Eu³⁺:Gd³⁺ =1:2) nanorods. (C) PL emission images of Eu³⁺/Gd³⁺-HAp nanorods at different concentrations. The excitation wavelength was 430 nm. Reprinted from Chen F, Huang P, Zhu YJ, Wu J, Zhang CL, Cui DX. The photolu minescence, drug delivery and imaging properties of multifunctional Eu³⁺/Gd³⁺ dual-doped hydroxyapatite nanorods. Biomaterials. 2011;32(34):9031–9039. Copyright 2011 with permission from Elsevier.¹⁰²

Abbreviations: PL, photoluminescence; HAp, hydroxyapatite.

Xu et al reported a novel synthesis method for magnetic functionalized HAp nanocomposites (MHAp nanoworms) for magnetic resonance diagnosis of the acute hepatic injury. The detailed four-stage fabrication of MHAp nanoworms is discussed in the previous section. The fabrication methodology associated with layer-by-layer modifications with chitosan and sodium alginate enhanced solubility and biocompatibility. The incorporation of iron oxide nanocrystals resulted in the improved performance of MRI. The study was further extended to intravenous injection of MHAp nanoworms, to study the contrast-to-noise ratio of hepatic in vivo MRI (Figure 9). The improved MRI clearly distinguished the hepatic injury grading which indicated the future use of this synthesized material as a potential contrast agent for MRI.⁷⁶

Figure 9.

T2-weighted MR images of liver: (A) stage I, normal liver, (B) stage II, acute hepatic injury which is 4 h after CCl₄ gavage, and (C) stage III, with the contrast enhancement of the HAp-ION-90 nanoworm. Histochemical analysis of (D) normal hepatic area and (E) injured hepatic area. All scale bars: 20 μm. Reproduced from Xu YJ, Dong L, Lu Y, et al. Magnetic hydroxyapatite nanoworms for magnetic resonance diagnosis of acute hepatic injury. Nanoscale. 2016;8(3):1684–1690 with permission of The Royal Society of Chemistry.⁷⁶

Abbreviations: MR, magnetic resonance; HAp, hydroxyapatite; i, Stage I; ii, Stage II; iii, Stage III.

Tampieri et al reported the doping of Fe²⁺/Fe³⁺ on HAp nanostructures for synthesizing MHAp nanoparticles for biomedical applications. The authors aimed to study the potential application of developed nanoparticles using magnetic hyperthermia to treat cancers and to use materials in magnetic scaffolds for tissue engineering application. The hyperthermia study of developed MHAp nanoparticles showed a temperature increase of 40°C in 60 s when exposed to alternating magnetic field (hyperthermia).⁵

Hou et al reported the in vivo performance of synthesized MHAp nanoparticles in hyperthermia therapy for treating cancer in mouse model. MHAp synthesized by co-precipitation method with the addition of Fe²⁺ and pure HAp nanoparticles were mixed with PBS. This mixture was then injected into the tumor region. The hyperthermia treatment was initiated by placing the mouse into an inductive heater with an applied alternating magnetic field. The 15-day treatment period revealed that the mouse injected with only MHAp showed a dramatic reduction of tumor volume (Figure 10). The blood cytotoxicity study of the mouse showed that MHAp nanoparticles have good biocompatibility with very less toxicity when subcutaneously injected.⁶⁹

Figure 10.

The clinical photographs of the mouse treated with MHAp on magnetic field exposure. The tumor on (A) day 1, (B) day 5, and (C) day 14 is shown. Reprinted from Hou CH, Hou SM, Hsueh YS, Lin J, Wu HC, Lin FH. The in vivo performance of biomagnetic hydroxyapatite nanoparticles in cancer hyperthermia therapy. Biomaterials. 2009;30(23–24):3956–3960. Copyright 2009, with permission from Elsevier.⁶⁹

Abbreviation: MHAp, magnetic hydroxyapatite.

Kamitakahara et al successfully synthesized spherical HAp granules that contained composites of magnetic and HAp nanoparticles via a hydrothermal process.¹⁰⁴ The obtained composite nanoparticles were expected to generate enough heat to kill cancer cells under an alternating magnetic field. The authors assessed hyperthermia using a model experiment, in which synthesized nanoparticles were dispersed in an agar gel solution and an alternating magnetic field of 300 Oe at 100 kHz was used. Because of the generated hyperthermia effect, the temperature increased to more than 45°C within a very short time period of 80 s.

Gene, protein, and plasmid delivery

In the last century, the delivery of genetic materials, such as DNA, RNA, proteins, and plasmids, was considered to be complex and be helpful for controlling, protecting, or enriching the biological property of living beings. Hopefully, the present era establishes distinctive controls and improves human life by using different new technologies such as recombinant DNA technology. This technology helps in improving the genetic property by directly delivering new proteins, genes, or plasmids to the target site. There are many technologies associated with delivery of genes, proteins, or plasmids, but in this review we mainly focus on magnetic field-assisted delivery (magnetofection) via MHAp nanoparticles (Figure 10). The suitability and advantages of MHAp nanoparticles are also discussed. In the year 2000, Mah et al first reported regarding the magnetic microparticle-associated genetic material transfer, which helped improve transduction efficiency.¹⁰⁵

Different strategies, including use of cleavable linkers, electrostatic interactions, and integration of vector with degradable property, could be executed after targeting specific cells. The most promising approaches for binding genetic materials to the surface of magnetic particles are based on electrostatic interactions. Here, the coating of HAp plays a key role and gives the added advantage over conventional coating materials. Most importantly, the nontoxic HAp surface exhibits a tunable property that allows to change its surface charge (positive, negative, or neutral) by very simple modifications (eg, aminododecanoic acid); moreover, a large number of target molecules have good affinity and adherence to the HAp surface.¹⁰⁶

Shan et al attempted to formulate HAp–iron oxide nanocomposites to reduce the complexity of the purification of pDNA from crude Escherichia coli lysates. DNA is expected to bind with HAp, and this binding involves the phosphate bond moieties of DNA and the surface calcium sites of HAp. The binding efficiency of DNA and MHAp in pure water was 0.42 μg pDNA/mg MHAp, and the static binding efficiency in sodium acetate solution was 3.96 μg pDNA/mg MHAp at 10 mM. This method of MHAp synthesis is simple, fast, and cost-effective without the requirement of further purification via centrifugation and hazardous chemical solvents.⁶⁶

Zuo et al synthesized laminated MHAp/DNA nanohybrid using a solution intercalation method. The prepared laminated MHAp exhibited an effective DNA-protecting property. The laminated MHAp preparation method is already described in the previous synthesis section. After the intercalation of salmon sperm DNA, the size expansion study of laminated MHAp (from 3.1 to 3.8 nm) proved the DNA attachment. The authors reported the DNA-protecting property of laminated MHAp during the exposure of attached DNA to DNase I enzyme. This laminated MHAp has prospective application in gene therapy because of its stable protective behavior.⁶⁷

Wu and Lin synthesized MHAp nanoparticles by adding iron into HAp using wet precipitation method. MHAp nanoparticles have a binding affinity to pDNA to form a transfection composite. Three different transfection approaches have been studied, namely 1) traditional transfection without a magnetic field (as the control), 2) combined transfection with application of a magnetic field for initial 15 min, and 3) a combined transfection with a 4 h co-culture (during co-culture, a magnetic field was applied for 5 min in each hour). pDNA-MHAp nanoparticles showed an increase in gene delivery efficacy across the cell membrane and demonstrated specific localization under the control of a magnetic field. Based on this study, MHAp nanoparticles were confirmed to have good potential as a nonviral vector for gene delivery.¹⁰⁷

Xiong et al synthesized lamellar MHAp nanoparticles by template-assisted self-assembly procedure, the DNA loading and transfection efficiencies of which were compared with those of HAp lamellar nanostructures without magnetite. The MHAp lamellar structure showed 47% more (14.16% compared to 9.64%) transfection efficiency. The mouse L929 fibroblast cell line was used for transfection and cell cytotoxicity study. In their study, zeta (ζ) potential was critically evaluated, and the authors concluded that a higher ζ-potential results in a higher transfection efficiency. The synthesized lamellar MHAp is a promising magnetic-guided gene delivery agent for a new-generation virus-free transfection method (Figure 11).⁶⁸

Figure 11.

(A) Schematic representation of magnetofection for gene delivery. (B) Schematic illustration of DNA loading into lamellar MHAp nanoparticles for nucleic acid delivery.

Abbreviation: MHAp, magnetic hydroxyapatite.

Scope of future applications

The nature of surface modifications and their consequent geometric orientation on the nanoparticles crucially determine the sizes and shapes of these nanoparticles, and also play a significant role in their biokinetics and biodistribution inside the body system. To this end, most studies have focused on improving the biocompatibility of materials, but very few scientific studies have reported the refining of magnetic particles after coating or formation of a composite structure. After the surface modification of MHAp nanoparticle, the saturation magnetization dramatically decreased. For a medical-grade drug delivery agent, a better method needs to be identified for improving the magnetic property while ensuring that the other characteristics are unaffected. Important applications, including many interesting biomedicinal uses of MHAp, have already been discussed. Different facile synthetic routes and their mode of action, as well as close integration with surrounding molecules, need to be evaluated in a more comprehensive study. More critical studies are warranted to formulate more cost-effective but good-quality MHAp nanoparticles without any protracted purification stages. In vivo and analytical applications need specific MHAp particles with predefined properties (quantity, geometric arrangement, etc.). The safety and biocompatibility of MHAp nanoparticles need to be assessed over a long time duration prior to applications in human, and hence, more in-depth toxicity studies should be conducted. Futuristic nanotechnology will also perceive medical prosthetics as another sector for improved biomedical implants such as multifunctional drug-loaded implants with external magnetic control.

The potentials of MHAp nanoparticles in biomedical and environmental applications that have been emphasized in a vast number of recent publications and demonstrated through filed and offered patents particularly during the last 7 years (2010–2017) are enlisted in Table 4.

Table 4.

A list of granted patents on MHAp nanomaterials during 2010–2017

S no	Patents (application potentials)	Number and grant date	Application area
1	Magnetic nano-hydroxyapatite adsorbent, preparation and application thereof	CN101703917A (May 12, 2010)	Environmental
2	Biodegradable macromolecule composite material with shape memory function and its preparation method and use	CN101240116B (Mar 30, 2011)	Biomedical
3	Ordered porous magnetic hydroxyapatite material, preparation method thereof and applications	CN101337665B (Apr 06, 2011)	Biomedical
4	Method for preparing magnetic fluorescence hydroxyapatite nanocomposite structure	CN102020258A (Apr 20, 2011)	Biomedical
5	Magnetic cationic surfactant-modified chitosan/hydroxyapatite/zeolite composite and preparation method and application thereof	CN102500333A (Jun 20, 2012)	Environmental
6	Method for preparing magnetic hydroxyapatite nanotubes	KR20120068802A (Nov 13, 2013)	Biomedical and environmental
7	Coliform detection process and kit for use therein	US8741595B2 (Jun 03, 2014)	Biomedical
8	Coated metal powder, powder magnetic core, and a process for their production	JP5565595B2 (Aug 06, 2014)	Biomedical
9	Preparation and application of magnetic hydroxyapatite/graphene oxide adsorbent	CN104289181A (Jan 21, 2015)	Environmental
10	Underground water fluoride-removing device based on magnetic hydroxyapatite	CN104386859A (Mar 04, 2015)	Environmental
11	Magnetic nanoporous composite bone tissue engineering support material and preparation method thereof	CN103480044B (May 06, 2015)	Biomedical
12	Preparation method of magnetic, luminescent bifunctional core-shell structure nano-hydroxyapatite particles	CN103820102B (Apr 13, 2016)	Biomedical
13	Intrinsically magnetic hydroxyapatite	US13812741 (May 03, 2016)	Biomedical
14	A magnetic ball of hydroxyapatite whisker preparation method	CN103541005B (Jun 22, 2016)	Biomedical and environmental
15	Biomedical materials	US9561960B2 (Feb 07, 2017)	Biomedical

Abbreviation: MHAp, magnetic hydroxyapatite.

Conclusion

This review on the nano-biomedical applications of nanoparticles focuses on tailoring new materials through facile synthetic methods or refining conventional synthetic routes to obtain reproducible MHAp nanoparticles with optimum morphology (shape and size), stability, and biocompatibility, in addition to superior magnetic saturation. The ultimate goal of using MHAp in biomedicine is to help patients, by introducing selective treatments through guided drug delivery systems. In addition to drug delivery, the use of multifunctional MHAp in simultaneous imaging, hyperthermia, and gene/plasmid delivery is going to drastically improve the diagnosis and therapy of diseases. HAp coating over magnetic nanoparticles offers several advantages such as excellent biocompatibility and high stability in a broad pH and temperature range; moreover, it protects nanoparticles such as polymers from agglomeration. The stability of HAp at high pH range helps in regulating drug release kinetics during a pH-mediated drug delivery inside the body system. In regenerative tissue engineering applications, using MHAp nanoparticles to prepare scaffold materials stimulates remote actuation for regulating bioactive molecules and magneto-mechanical cell stimulation, cell seeding, and cell patterning. Besides the advances, the exhilarating milestones made in these areas seek attention for critical evaluation before being regularized in the medical sector. However, we trust that the coming few years will see huge advances in the number of MHAp-based diagnostics and medicines being used in the clinics. This review critically revealed the recent status, efficiency, and future prospects of MHAp nanomaterials in biomedical applications.