DOI:
10.1039/D4NA00014E
(Paper)
Nanoscale Adv., 2024,
6, 3367-3376
Enhancing MRI through high loading of superparamagnetic nanogels with high sensitivity to the tumor environment†
Received
5th January 2024
, Accepted 6th April 2024
First published on 29th April 2024
Abstract
Tumors pose a significant threat to human health, and their occurrence and fatality rates are on the rise each year. Accurate tumor diagnosis is crucial in preventing untimely treatment and late-stage metastasis, thereby reducing mortality. To address this, we have developed a novel type of hybrid nanogel called γ-Fe2O3@PNIPAM/PAm/CTS, which contains iron oxide nanoparticles and poly(N-isopropyl acrylamide)/polyacrylamide/chitosan. The rationale for this study relies on the concept that thermosensitive PNIPAM has the ability to contract when exposed to elevated temperature conditions found within tumors. This contraction leads to a dense clustering of the high-loading γ-Fe2O3 nanoparticles within the nanogel, thus greatly enhancing the capabilities of MRI. Additionally, the amino groups in chitosan on the particle surface can be converted into ammonium salts under mildly acidic conditions, allowing for an increase in the charge of the nanogel specifically at the slightly acidic tumor site. Consequently, it promotes the phagocytosis of tumor cells and effectively enhances the accumulation and retention of nanogels at the tumor site. The synthesis of the hybrid nanogels involves a surfactant-free emulsion copolymerization process, where vinyl-modified γ-Fe2O3 superparamagnetic nanoparticles are copolymerized with the monomers in the presence of chitosan. We have optimized various reaction parameters to achieve a high loading content of the superparamagnetic nanoparticles, reaching up to 60%. The achieved r2 value of 517.74 mM−1 S−1 significantly surpasses that of the clinical imaging contrast agent Resovist (approximately 151 mM−1 S−1). To assess the performance of these magnetic nanogels, we conducted experiments using Cal27 oral tumors and 4T1 breast tumors in animal models. The nanogels exhibited temperature- and pH-sensitivity, enabling magnetic targeting and enhancing diagnosis through MRI. The results demonstrated the potential of these hybrid nanogels as contrast agents for magnetic targeting in biomedical applications.
1 Introduction
Tumors pose a significant and persistent risk to human well-being, with high fatality rates over the years due to the population aging and an increasing incidence of cancer among younger people.1,2 Unfortunately, a major challenge lies in the delayed detection of tumors and the limitations of existing diagnostic techniques. As a result, diagnosis is often made at the late stage of tumors, when metastasis has already taken place or when tumors are difficult to control.3 Therefore, there is a pressing need to enhance the accuracy and sensitivity of tumor diagnosis in order to achieve precise tumor diagnosis and improve the efficacy of tumor treatment.
Currently, clinical tumor diagnosis primarily relies on imaging techniques such as computed tomography (CT), positron emission tomography (PET), single photon emission computed tomography (SPECT), and magnetic resonance imaging (MRI).4–6 While PET and SPECT offer high sensitivity and penetration depth, they can be costly and raise concerns about radiation exposure for patients. In contrast, MRI diagnosis is more widely utilized in clinical settings due to its non-invasiveness, safety, high spatial resolution, and absence of tissue penetration limitations. In many clinical procedures, particularly for tumor detection and diagnosis, MRI contrast agents are employed to enhance device resolution and differentiate between diseased and normal tissues, thereby achieving accurate diagnostic outcomes.7–9
Clinical magnetic resonance contrast agents are primarily categorized as positive or negative contrast agents. Positive contrast agents rely on paramagnetic substances based on rhenium or manganese, which produce bright images in T1-weighted mode. Negative contrast agents, on the other hand, predominantly consist of superparamagnetic nanoparticles that generate dark images in T2-weighted mode.10 The most commonly used MRI contrast agent in clinical practice is gadopentetate glucosamine (Gd-DTPA), known for its excellent thermodynamic stability and high relaxation rate.11 However, Gd-DTPA lacks specific distribution in the body. Moreover, in 2006, the US Food and Drug Administration (FDA) issued a statement highlighting the potential risk of renal systemic fibrosis associated with long-term use of the Gd-DTPA contrast agent in patients with renal insufficiency or transplantation, thereby limiting its applications.12
In comparison to paramagnetic substance-based positive contrast agents (rhenium or manganese), iron oxide-based negative contrast agents, particularly superparamagnetic iron oxide nanoparticles, have gained significant attention as a new generation of negative magnetic resonance contrast agents. These MRI contrast agents offer advantages such as excellent biocompatibility, high thermal stability, high relaxation rate, controllable size, good dispersibility, and easy surface functionalization.13–15 Various iron oxide-based magnetic resonance contrast agents have already found utility in clinical practice. For instance, ferumoxide is primarily used for liver and spleen imaging, while ferruglose is employed in angiography and tumor microvessel detection.
Recently, magnetic nanoparticles have emerged as highly promising nanomaterials for enhancing tumor MRI, magnetic targeting, and tumor hyperthermia.16–20 The effectiveness of MRI induced by magnetic nanoparticles is influenced by various factors, including particle size, morphology, chemical composition, surface modification, and nanoparticle aggregation.21–25 Extensive research efforts have been devoted to increasing the T2 value of magnetic nanoparticles to improve MRI. For instance, adjusting the particle size of iron oxide has enabled the development of superparamagnetic nanoparticles with both T1 and T2 imaging capabilities.26 Additionally, hybrid iron oxide nanoparticles incorporating manganese have been fabricated to achieve higher relaxation values.27 Furthermore, the T2 value can be significantly enhanced by achieving high loading or concentration of magnetic nanoparticles in the tumor region.28 Therefore, it is highly desirable to employ magnetic nanoparticles with a high magnetic moment and saturation magnetization, as they exhibit rapid response to an external magnetic field. However, the strong magnetic attraction between magnetosome particles can lead to aggregation and precipitation in water as well as biological fluid environments. Thus, the preparation of magnetic particles with a high loading of superparamagnetic nanoparticles and good particle stability remains a challenge.
Our approach to addresses the above-mentioned challenge is to form magnetic nanogels. The nanogel particles have a high swelling capacity in water, which results in a particle density close to that of water. This high swelling capability enhances the stability of the magnetic nanoparticles within the nanogel, preventing their sedimentation or aggregation. This stability also ensures that the magnetic nanoparticles are uniformly dispersed within the nanogel matrix. Furthermore, we utilize temperature-sensitive polymers with a cloud point temperature (Tcp) close to the body temperature to ensure that the nanogel remains stable and expanded under normal physiological conditions. However, in hyperthermic tumor environments, the nanogel undergoes shrinkage, leading to aggregation of the magnetic nanoparticles within the nanogel, thus improving MRI. Poly(N-isopropylacrylamide) (PNIPAM) is a well-known polymer that exhibits a reversible hydration–dehydration transition in its aqueous solution, causing phase separation above 32 °C.29,30 Studies have shown that copolymerization of N-isopropylacrylamide (NIPAM) with a hydrophilic monomer such as acrylamide (Am) can increase the cloud point temperature (Tcp) in water.31 Acrylamide imparts hydrophilicity to the copolymer, thereby increasing its water solubility. This increased hydrophilicity affects the intermolecular interactions and hydrogen bonding between the copolymer and water molecules, leading to an increase in the Tcp of the copolymer in water. Therefore, the Tcp of the copolymer can be tuned by adjusting the composition of NIPAM and acrylamide in the copolymerization process. By increasing the Tcp of the copolymer to a temperature close to the physiological body temperature (37 °C), the copolymer becomes responsive to temperature changes in the body. This feature is desirable for applications such as MRI, where the nanogel can remain stable at lower temperatures but undergo a phase transition and form a compact structure at higher temperatures, thus facilitating the MRI of the tumor.
In addition, the core–shell nanogel containing a water-soluble chitosan shell provides pH-sensitive properties to the magnetic nanogel. Chitosan is a biocompatible and biodegradable polysaccharide derived from chitin, and it possesses pH-sensitive properties.32 At the slightly acidic tumor site, the chitosan coating undergoes a pH-dependent transformation. The amino groups present in chitosan can be converted into ammonium salts due to the lower pH in the tumor microenvironment. This conversion leads to an increase in the nanogel's charge, making it more positively charged. This design strategy enables the particles to specifically respond to the acidic tumor microenvironment, enhancing their accumulation and retention at the tumor site.33–36 Furthermore, having a water-soluble polymer on the particle surface improves the behaviour of particles in the bloodstream by enhancing stability, prolonging circulation time, improving biodistribution, and increasing biocompatibility. These advantages contribute to the overall efficacy and safety of the particles for MRI imaging. Therefore, the combination of enhanced MRI and responsive particles holds great promise for advancing tumor theranostics.37–39
In this study, we aim to develop a novel type of magnetic nanogel particle for accurate tumor diagnosis through MRI. The designed particle encompasses several desirable characteristics: (1) highloading capacity of superparamagnetic nanoparticles and saturation magnetization with good particle stability, (2) temperature sensitivity with a cloud point above the physiological temperature of 37 °C, enabling them to respond to temperature changes, (3) pH responsiveness to specifically respond to the acidic tumor microenvironment, thus enhancing the cellular uptake within the acidic milieu around the tumor, and (4) good biocompatibility. To fulfil these requirements, we synthesized a magnetic nanogel, namely iron oxide/poly(N-isopropyl acrylamide)/polyacrylamide/chitosan (γ-Fe2O3@PNIPAM/PAm/CTS) using a surfactant-free emulsion copolymerization method. This involved combining vinyl-modified γ-Fe2O3 nanoparticles, water-soluble chitosan, N-isopropyl acrylamide, and acrylamide in the presence of a crosslinker through a step-wise feeding process. The chemical crosslinking between the polymer and the magnetic nanoparticles enabled high loading while minimizing leakage of the iron oxide nanoparticles. Furthermore, the resulting γ-Fe2O3@PNIPAM/PAm/CTS nanogels exhibited a three-dimensional structure with a porous network. These core–shell nanogels with water-soluble chitosan on the particle surface could absorb water, reaching a density similar to that of water, thereby ensuring good stability in an aqueous system, as well as in blood circulation. The performance of the temperature and pH-sensitive magnetic nanogels was assessed through MRI using animal models with Cal27 oral and 4T1 breast tumors. Meanwhile, a magnetic field was used at the tumor site for magnetic targeting imaging. The results demonstrated the potential of these hybrid nanogels as contrast agents for magnetic targeting and enhanced MRI.
2 Materials and methods
2.1. Materials
The following chemicals including ferrous chloride tetrahydrate (FeCl2·4H2O, Aldrich), anhydrous ferric chloride (FeCl3, Fluka), ammonia solution (NH3·H2O, concentration of 32 w/w%, VWR), nitric acid (HNO3, 65 w/w%, Merck), trisodium citrate dihydrate (Na3C6H5O7·2H2O, Riedel-de Haën), tetraethyl orthosilicate (TEOS, Sigma), 3-(trimethoxysilyl)propyl methacrylate (MPS, 98%, Sigma), chitosan (CTS, medium molecular weight, Aldrich), acetic acid solution (0.6 v/v%), hydrogen peroxide (H2O2, 0.1 M); acrylamide (Am, 98.5%, Acros), and N,N′-methylenebisacrylamide (MBA, 97%, BDH Chemicals Ltd) were all used as received. N-Isopropylacrylamide powder (NIPAM, Tokyo Chemical Industry Co. Ltd) was purified through recrystallization in hexane before use. Deionized water (DI water) from a Milli-Q Gradient System was used in all experiments.
Female Balb/c mice (6–8 weeks old) and nude female Balb/c mice (6–8 weeks old) were purchased from Beijing HFK Bioscience Co. Ltd, China. They were fed with water and standard laboratory chow. The animal housing area was maintained at 24 °C for 12 h in a light/dark cycle. All animal procedures complied with the guidelines of the Institutional Animal Care and Use Committee (code number: WCHSIRB-D-2019-074) and were approved by the Animal Care and Use Committee of West China Hospital of Stomatology, Sichuan University, P. R. China.
2.2. Synthesis of vinyl-coated γ-Fe2O3 nanoparticles
The vinyl-coated γ-Fe2O3 nanoparticles (MPS-γ-Fe2O3) were first synthesized according to our previously established method.40 The procedure is described in detail in the ESI.† The as-prepared MPS-γ-Fe2O3 nanoparticles were purified by dialysis and then dispersed in ethanol for subsequent use.
2.3. Synthesis of γ-Fe2O3@PNIPAM/CTS nanogels
The γ-Fe2O3@PNIPAM/CTS hybrid nanogels were synthesized by free-radical grafting and crosslinking polymerization of chitosan and NIPAM in aqueous solutions. The chitosan powder (0.5 g) was dissolved in 44 mL of acetic acid (0.6 w/w%) under sonication and stirred at 300 rpm for 10 minutes. The purified MPS-γ-Fe2O3 solution (3.0 mL, 2.3 wt% in ethanol) was added to the chitosan solution dropwise. The mixture was then sonicated and stirred at 300 rpm for 30 min. The chitosan/MPS-γ-Fe2O3 mixture was then transferred to a three-necked water-jacketed reaction flask equipped with a magnetic stirrer, a condenser, and a nitrogen inlet. The mixture was diluted with an acetic acid solution (46 g, 0.6 v/v%), followed by stirring at 360 rpm at 80 °C under nitrogen for 30 min. The aqueous solution of NIPAM (0.52 g) and MBA (0.0028 g) was prepared by dissolving them in 5 mL of DI-water and purging solution with N2 for 15 min at room temperature. The prepared monomer solution was then added into the reaction flask dropwise, followed by the addition of H2O2 solution (51 μL, 0.1 M). The reaction was allowed to react for 8 h at 80 °C under a nitrogen atmosphere.
2.4. Synthesis of γ-Fe2O3@PNIPAM/PAm/CTS nanogels
A similar procedure to that described in Section 2.3 was used except that the monomers were charged to the reaction mixture via a step-wise feeding method. An acrylamide monomer (0.1228 g), which was pre-dissolved in 2 mL of DI water and purged with N2 for 15 min, was added into a three-necked water-jacketed reaction flask dropwise, followed by addition of 25 μL of H2O2 solution (0.1 M). After reacting for 30 min, a NIPAM monomer solution, which was prepared by dissolving 0.1228 g of purified NIPAM powder and 0.0028 g of MBA in 3 mL of DI-water and purged with N2 for 15 min, was added into the flask dropwise, followed by addition of another 26 μL of H2O2 solution (0.1 M). The reaction was allowed to react for 8 h at 80 °C under a nitrogen atmosphere. The product was purified by centrifugation three times with DI water. Monomer conversion was calculated gravimetrically according to the following equation:
Here, Cm is the monomer conversion; Wp is the weight of the product; WCST is the weight of chitosan; Wc is the weight of the crosslinker; Wm is the weight monomer added.
2.5. Characterization of magnetic nanogels
2.5.1. Structure analysis and morphology observation.
Chemical structures were identified using a Nicolet Avatar 360 FTIR spectrophotometer. Morphologies of the hybrid particles were observed using transmission electron microscopy (TEM) (JEOL, JEM-2011) at an acceleration voltage of 100 kV. The samples were prepared by wetting a carbon-coated grid with a small drop of dilute dispersion (70 to 100 ppm), followed by drying the solution at room temperature.
2.5.2. Particle size and surface charges.
The particle size and size distribution of samples were measured on a Malvern™ Zetasizer Nano S9 based on electrophoretic dynamic light scattering (DLS) at 658 nm wavelength and 30 mV with the scattering angle at 174°. The concentration of the samples dispersed in DI water was adjusted to around 20 ppm with a pH between 5 and 6. The surface charges of the samples were also measured using the Malvern™ Zetasizer Nano S9 with a scattering angle at 173°. The concentration of the samples was diluted to 20 ppm.
2.5.3. Temperature sensitivity of the nanogels.
The percentage of shrinking volume was calculated according to the following equation where Rt is the hydrodynamic particle size at t °C and R0 is the particle size at a specific temperature (25 or 37 °C). The shrinking volume was calculated according to the following equation:
2.5.4. Determination of encapsulated iron oxide content.
The loading content of iron oxide nanoparticles was determined by thermogravimetric analysis (TGA) using a thermogravimetric analyzer (Mettler Toledo™ TGA/DSC3+). The dried sample (∼5 mg) was placed in a ceramic holder, followed by heating from 25 to 900 °C at a heating rate of 10 °C min−1 under 20 mL per min nitrogen flow. The iron oxide content was calculated based on the following equation:
2.5.5. Vibrating sample magnetometry (VSM) analysis.
The saturation magnetization of the γ-Fe2O3@PNIPAM/PAm/CTS nanogels was measured with a vibrating sample magnetometer (VSM) (PPMS model 6000 Quantum Design, San Diego, USA). The measurement was conducted at room temperature under an external magnetic field H ranging from 0 to ±300
000 Oe.
2.6.
In vitro cytotoxicity
In vitro cytotoxicity of the γ-Fe2O3@PNIPAM/PAm/CTS nanogels was investigated using mouse embryonic fibroblast (3T3) and human tongue squamous carcinoma cells (CAL-27). Cells were seeded into a 96-well plate (5 × 103 cells per well, 100 μL), followed by incubation at 37 °C for 24 h. Subsequently, the cells were treated with γ-Fe2O3@PNIPAM/PAm/CTS nanogels of different concentrations ranging from 1.58 to 200 μg mL−1. After incubation for 24 h, the cells were washed with PBS three times, and the cell viability was determined based on the absorbance of cell counting kit-8 (CCK-8) at 450 nm.
2.7. Cell uptake study
Cell uptake of γ-Fe2O3@PNIPAM/PAm/CTS nanogels was studied using Cal27 oral tumor cells. The cells were rinsed with PBS when the confluence reached 80%. 50 μg per mL nanogels were then incubated with cells at 37 °C for 2 h, according to the literature studies.41,42 The medium pH was set at either 7.40 (control) or 6.86. Then, the cells were gently washed with PBS to remove free nanogels and fixed with 4% paraformaldehyde. The magnetic nanogels taken up by the cells were stained with Prussian blue, and cells were stained with nuclear fast red. The cell images were recorded with an inverted fluorescence microscope (Leica, Germany).
2.8. The hemolysis study
The hemolysis study was conducted using a New Zealand white rabbit, which was anesthetized with pentobarbital sodium. The whole blood was drawn by an injection syringe from the heart of the rabbit. The blood was stirred with a glass rod in a beaker for 10 minutes to get rid of the fibrinogen. Subsequently, the blood was diluted with more than ten times the volume of normal saline. The diluted blood was centrifuged at 1000 rpm for 15 min until the supernatant was clear. The obtained erythrocytes were further diluted to 2% with normal saline for final use. γ-Fe2O3@PNIPAM/PAm/CTS nanogels in different concentrations were mixed with erythrocyte solution and incubated at 37 °C for 3 h. The positive and negative controls were water and normal saline, respectively. Finally, all samples were centrifuged and photographed. The morphology of red blood cells (RBCs), which had been incubated with saline or γ-Fe2O3@PNIPAM/PAm/CTS nanogels, was analyzed with an inverted light microscope.
2.9. Systemic toxicity of γ-Fe2O3@PNIPAM/PAm/CTS nanogels
Female BALB/c mice (3 mice per group) were administered with saline and γ-Fe2O3@PNIPAM/PAm/CTS nanogels (30 mg kg−1) through tail vein injection. After two weeks, the blood and serum were collected, and the blood hematology and biochemistry were evaluated using an automatic animal blood analyzer (Mindray BC-2800Vet) and blood cell analyzer (Roche Cobas 6000-C501), respectively. Furthermore, mice were sacrificed to obtain their major organs (heart, lungs, liver, spleen, and kidneys) for toxicity analysis. Tissues were fixed with 10% formalin, embedded in paraffin, sectioned, and stained with hematoxylin and eosin (H&E).
2.10.
In vitro MRI test
The in vitro MRI analysis was performed by using different concentrations of nanogels to calculate the transverse relaxivity (r2). Before MRI, the nanogel samples were dispersed in an HNO3/HCl solution (1
:
3). The iron concentrations were determined by inductively coupled plasma-atomic emission spectroscopy (ICP-AES). MRI was performed with a 7.0 T magnetic field using an MRI instrument (Bruker, German). The T2-weighted MRI images of the nanogels with various iron concentrations (0, 0.012, 0.024, 0.048, 0.072, 0.096, and 0.120 mM) were obtained by using a T2-weighted fast-recovery fast spin-echo (FR-FSE) sequence. The parameters for T2 relaxivity measurement were as follows: repetition time (TR) = 2500.0 ms, echo time (TE) = 33.0 ms, and field of view (FOV) = 3.50 cm. The r2 value was calculated through the curve fitting of 1/T2 relaxation time against the iron concentration.
2.11.
In vivo MRI and magnetic targeting imaging
The tumor-bearing nude mice were established by injection Cal27 cells in the armpit of mice. When the tumors grow to approximately 4 mm in diameter, the mice were administered with γ-Fe2O3@PNIPAM/PAm/CTS nanogels (10 mg kg−1, 0.2 mL). In one group of mice, a magnet was attached to the tumor site for magnetic targeting imaging. The magnetic targeting strategy was not adopted for the other group. Before injection, the T2-weighted MRI was taken as control. At 1, 2, and 4 h post-injection, the MRI images obtained were compared for their magnetic targeting and non-targeting effects.
Meanwhile, in vivo MRI diagnosis was performed on Balb/c mice with 4T1 breast tumors. The mice were taken for imaging at 1 and 4 h. The parameters of the MRI in vivo test were as follows: TR = 2500.0 ms, TE = 33.0 ms, FOV = 3.00 cm, matrix = 256, slice thickness = 1 mm, and flip-angle = 90°. The signal intensities were measured in the region of interest (ROI) of tumor tissue and the liver at different time intervals.
2.12. Statistical analysis
The statistical data were based on at least three independent repeated experiments, and Student's t-test was used for statistical comparisons. Statistical significance was considered when the p-value was less than 0.05.
3 Results and discussion
3.1. Synthesis of magnetic hybrid nanogels
The magnetic nanogels were synthesized using a previously established method for the preparation of γ-Fe2O3@poly(methyl methacrylate)/CTS particles.40Scheme 1A illustrates the reaction steps involved in the synthesis process. Initially, positively charged chitosan and negative charged vinyl-coated γ-Fe2O3 nanoparticles were mixed together in a weight ratio of 7.25 to 1, resulting in the formation of chitosan/γ-Fe2O3 complexes. Subsequently, grafting and crosslinking copolymerization of N-isopropyl acrylamide, acrylamide, and N,N′-methylenebisacrylamide monomers were initiated using H2O2 as the initiator. Since the polymerization occurred at a temperature of 80 °C, which exceeded the phase transition temperature of PNIPAM, the growing chitosan/PNIPAM graft copolymer surpassed their water solubility. This led to the assembly of amphiphilic copolymers into particles, facilitating the copolymerization of NIPAM and vinyl-coated γ-Fe2O3 nanoparticles in the presence of the MBA crosslinker. Consequently, crosslinked nanogel particles were formed. The prepared nanogels were then evaluated by injecting into tumor-bearing mice for MRI (Scheme 1B).
![image file: d4na00014e-s1.tif](/image/article/2024/NA/d4na00014e/d4na00014e-s1.gif) |
| Scheme 1 (A) Illustration of the synthesis process of γ-Fe2O3@PNIPAM/PAm/CTS nanogels; (B) nanogels were injected into tumor-bearing mice for MRI. | |
We conducted a systematic study on the synthesis of magnetic nanogels, investigating the effects of various factors, including the addition method (one-shot or step-wise), reaction time (2, 8, 24 hours), chitosan to monomer weight ratio (3.46
:
1, 1.98
:
1, 0.82
:
1), and crosslinking percentage to NIPAM (2.3% and 5%). The results are shown in the ESI (Tables S1 and S2†). The optimal procedure and conditions for the synthesis process were that the graft copolymerization of acrylamide from the chitosan/γ-Fe2O3 complexes occurred first, using H2O2 as the initiator. Subsequently, N-isopropylacrylamide and N,N′-methylenebisacrylamide monomers were added. The optimal chitosan to monomer weight ratio was approximately 2
:
1, with 5% crosslinking. The polymerization took place at 80 °C for 8 hours, and the monomer conversion was above 70% as determined gravimetrically.
3.2. Characterization of γ-Fe2O3@PNIPAM/PAm/CTS nanogels
TEM images in Fig. 1A show the morphology of the γ-Fe2O3@PNIPAM/PAm/CTS nanogels, exhibiting a spherical shape with a rough surface as well as sizes below 200 nm in the dry state. The cores and surfaces of the nanogels contain numerous γ-Fe2O3 nanoparticles (visible as dark dots). The stability of the nanogels was assessed by measuring their surface charge. The ζ-potential of the γ-Fe2O3@PNIPAM/PAm/CTS nanogels was determined to be +43.5 mV within a pH range of 5 to 6. The highly positive charge observed in acidic solutions indicates that chitosan effectively covers the nanogels' surface, resulting in good particle stability. To determine the loading content of magnetic nanoparticles in the nanogels, a thermogravimetric analysis (TGA) was conducted, and the results are presented in Fig. 1B. The weight change before 110 °C can be attributed to the loss of residual solvent and water molecules. The PNIPAM molecules decomposed between 210 and 400 °C,43 while chitosan and polyacrylamide decomposed in the range of 200 to 500 °C.44,45 The remaining weight at 900 °C corresponds to the presence of the γ-Fe2O3 nanoparticles. The TGA analysis indicates that the iron oxide content within the hybrid nanogels was up to 60%. This high loading content suggests that our polymerization approach can efficiently encapsulate magnetic nanoparticles through copolymerization.
![image file: d4na00014e-f1.tif](/image/article/2024/NA/d4na00014e/d4na00014e-f1.gif) |
| Fig. 1 (A) The TEM images of γ-Fe2O3@PNIPAM/PAm/CTS nanogels; (B) the TGA thermogram of γ-Fe2O3@PNIPAM/PAm/CTS nanogels; (C) the magnetization loop of γ-Fe2O3@PNIPAM/PAm/CTS nanogels measured by VSM analysis. | |
The chemical structures of the vinyl-modified magnetic nanoparticles (MPS-γ-Fe2O3) and γ-Fe2O3@PNIPAM/PAm/CTS nanogels were identified using an FT-IR spectrometer. Fig. S1 in the ESI† displays characteristic peaks associated with MPS-coated iron oxides (red curve in the figure), including stretching vibrations of O–H (3417 cm−1), C–H (2800–3000 cm−1), C
O ester (1716 cm−1), COO− (1634 cm−1), Si–O (1100 cm−1), and Fe–O (400–650 cm−1). The spectrum of the γ-Fe2O3@PNIPAM/PAm/CTS nanogels (black curve in Fig. S1†) exhibits characteristic peaks that can be attributed to the presence of chitosan, PAm, PNIPAM, and iron oxide (γ-Fe2O3). These peaks include: amine N–H and O–H stretching (3452 cm−1), C–H stretching (2926 cm−1), C
O ester (1716 cm−1), C
O amide (1634 cm−1), N–H bending (1557 cm−1), C–N stretching, CH2– and CH3– bending vibrations (between 1350 and 1460 cm−1), C–O stretching (1128 cm−1), and iron oxide (γ-Fe2O3, 637 cm−1). Based on these peaks, it can be confirmed that the nanogels consist of chitosan, PAm, PNIPAM, and iron oxide components.
The magnetic properties of the γ-Fe2O3@PNIPAM/PAm/CTS nanogels were assessed using vibrating sample magnetometry (VSM) analysis. In Fig. 1C, an S-shaped magnetization loop is observed, indicating the superparamagnetic nature of the nanogels. No hysteresis loops were observed, further confirming the superparamagnetic behaviour. The saturation magnetization (Ms) of the magnetic nanogels was measured to be 19.4 emu per gram of particles. By subtracting the weight of the polymer in the hybrid nanogels, the saturation magnetization of the encapsulated γ-Fe2O3 nanoparticles was calculated to be 98.1 emu per gram of maghemite. This value is higher than that of the citrate-coated γ-Fe2O3 nanoparticles (87.9 emu g−1), indicating that the chemical modifications and polymerization processes did not alter the magnetic properties of the maghemite. The increase in saturation magnetization suggests an improvement in the magnetic performance of the hybrid nanogels, which could potentially enhance MRI capabilities.
The temperature sensitivity of the γ-Fe2O3@PNIPAM/PAm/CTS nanogels was investigated by measuring their sizes and size distribution (PDI) at various temperatures ranging from 25 to 55 °C. As depicted in Fig. 2A, at 25 °C, the nanogels exhibited an average size of 509.9 nm (PDI = 0.06). As the solution temperature was increased to 40 °C, there was only a slight reduction in the nanogel sizes. However, upon further increasing the temperature above 40 °C, the nanogels underwent significant shrinkage. At 55 °C, the average size of the nanogels decreased to 434.6 nm (PDI = 0.08), which corresponds to a 38% reduction in size compared to their original size. This size reduction can be attributed to the phase transition of the PNIPAM chain, which undergoes a transition from a random coil to a collapsed state. Therefore, the phase transition of the γ-Fe2O3@PNIPAM/PAm/CTS hybrid particles was found to occur around 40 °C. Additionally, the PDI values between 25 and 55 °C remained relatively consistent, ranging from 0.050 to 0.078. These results indicate that the nanogels maintained excellent stability during the phase transition process.
![image file: d4na00014e-f2.tif](/image/article/2024/NA/d4na00014e/d4na00014e-f2.gif) |
| Fig. 2 Effect of solution temperature between 25 and 55 °C on (A) hydrodynamic particle size, size distribution (PDI) and (B) zeta-potential of γ-Fe2O3@PNIPAM/PAm/CTS nanogels; (C) the changes of zeta-potential of γ-Fe2O3@PNIPAM/PAm/CTS nanogels with the pH changing from acidic to alkaline condition. | |
Furthermore, the zeta-potential of magnetic nanogels remained above +40 mV as the solution temperature increased from 25 to 50 °C (Fig. 2B). No noticeable agglomeration of the magnetic hybrid nanogels was observed in water. In Fig. 2C, it can be observed that the zeta-potential of the γ-Fe2O3@PNIPAM/PAm/CTS nanogels shifted from negative to positive charge as the pH changed from alkaline to acidic condition. This shift can be attributed to the conversion of the amino group of chitosan into quaternary ammonium ions in acidic environments. Therefore, the thermal-responsive and pH-sensitive properties of these magnetic nanogels make them highly desirable for stimuli-responsive drug release and sensing in tumor therapy.
3.3.
In vitro cytotoxicity and pH-sensitivity to the tumor environment
The cytotoxicity of the magnetic nanogels was evaluated based on the study of cell viability. Fig. 3A and B show less than 10% cell death in both 3T3 normal and Cal27 tumor cell lines when the concentration of the nanogels increased to up to 200 μg mL−1. The results indicate that the hybrid nanogels possess low cytotoxicity and good biocompatibility for biological application.
![image file: d4na00014e-f3.tif](/image/article/2024/NA/d4na00014e/d4na00014e-f3.gif) |
| Fig. 3 Cell viabilities of (A) 3T3 normal cells and (B) Cal27 cells treated with different concentrations of γ-Fe2O3@PNIPAM/PAm/CTS nanogels. (C) Microscopy images of Cal27 tumor cells after incubation with 50 μg per mL γ-Fe2O3@PNIPAM/PAm/CTS nanogels for 2 h (blue dots are the magnetic nanogels engrafted by tumor cells). Scale bar = 100 μm. | |
The γ-Fe2O3@PNIPAM/PAm/CTS nanogels developed in our study are expected to be pH-responsive in the acidic microenvironment of the tumor site. This is because the amino group of chitosan can be converted to quaternary ammonium ions under acidic conditions. The cationic nanogel surface is conducive to the phagocytosis of tumor cells and thus can effectively increase the accumulation and retention of the magnetic nanogels in the tumor region and cells. Fig. 3C compares in vitro intracellular uptake of the magnetic nanogels under different pH conditions with Prussian blue staining. The blue dots represent the magnetic nanogels stained with Prussian blue. The more blue dots there were, the more magnetic nanogels were taken up by tumor cells. Fig. S2† shows comparison of the cellular uptake ratio which means the cells with engulfed nanoparticles divided by all cells. The results show that a higher number of nanogels were engrafted by the tumor cells at pH 6.86 than at pH 7.40, indicating that the nanogels exhibit pH sensitivity to the tumor environment, which is promising for tumor theranostics.
3.4. Hemolysis study of γ-Fe2O3@PNIPAM/PAm/CTS nanogels
The hemolytic analysis of γ-Fe2O3@PNIPAM/PAm/CTS nanogels with concentrations ranging from 1 to 8 mg mL−1 was conducted. Fig. S3A† shows the supernatants of centrifuged erythrocyte samples. No significant difference was found when compared with the negative control group. The absorption of the supernatants was determined with a spectrophotometer at 540 nm. No hemolysis was observed even when the concentration of nanogels was up to 8 mg mL−1. Moreover, morphology analysis of RBC as shown in Fig. S3B† indicated that no obvious changes or membrane destruction were observed for the high concentration nanogel group. All the results suggest that the γ-Fe2O3@PNIPAM/PAm/CTS nanogels possess good blood compatibility.
3.5.
In vitro MRI
Fig. 4A shows in vitro T2-weighted MR images of the γ-Fe2O3@PNIPAM/PAm/CTS nanogels at different iron concentrations. Increasing concentrations from 0.012 to 0.120 mM resulted in darkening of images. The transverse relaxivity (r2), which is a measure of the change in the spin–spin relaxation rate (T2−1) per unit concentration,46 was determined by plotting the transverse relaxation rate versus iron concentration (Fig. 4B). The r2 value was then calculated based on the slope of the stimulated regression line to give 517.74 mM−1 S−1. This value is much higher than that of the clinical imaging contrast Resovist (r2 value is 151 mM−1 S−1). Since the r2 value is related to the particle size, morphology, surface modification and aggregation,21,23,25 the significant enhancement of the r2 value may be attributed to the following three reasons: (1) the high loading capacity of our magnetic nanogel, (2) the aggregation of iron oxide nanoparticles encapsulated in the nanogels, and (3) water penetration through swollen nanogels, thus enhancing the interaction between iron oxide nanoparticles and water molecules.
![image file: d4na00014e-f4.tif](/image/article/2024/NA/d4na00014e/d4na00014e-f4.gif) |
| Fig. 4 (A) In vitro T2-weighted MRI images of γ-Fe2O3@PNIPAM/PAm/CTS nanogels at different iron concentrations; (B) the plot of transverse relaxation rate versus iron concentration. The r2 value (transverse relaxivity) was calculated based on the slope of the stimulated regression lines. | |
3.6.
In vivo MRI
A high transverse relaxivity (r2) value of 517.74 mM−1 S−1 obtained from the in vitro MRI prompted us to conduct an in vivo test on Cal27 tumor-bearing mice. Fig. 5A shows that the T2-weighted images of the tumor treated with the γ-Fe2O3@PNIPAM/PAm/CTS nanogels were darker than the pre-images at different time intervals. This is due to the fact that the iron oxide nanoparticles are commonly classified as T2 negative contrast agents. This classification is based on their ability to reduce the signal intensity in T2-weighted images, resulting in darker areas or negative contrast.10,47Fig. 5B shows the results of signal intensities which were quantitatively analyzed using region of interest (ROI) within the tumor area. It was found that at 4 h post-injection, the magnetically targeted group has 1.28 times lower signal intensity than that of the non-targeting group. Therefore, the γ-Fe2O3@PNIPAM/PAm/CTS nanogels not only can be potential MRI contrast reagents, but they can also be used for magnetic-enhanced applications because of their sensitivity towards the tumor microenvironment and ability to accumulate in the tumor region under the guidance of magnetic targeting.
![image file: d4na00014e-f5.tif](/image/article/2024/NA/d4na00014e/d4na00014e-f5.gif) |
| Fig. 5 (A) In vivo T2-weighted MR images of nude mice bearing Cal27 oral tumors before and after injection with γ-Fe2O3@PNIPAM/PAm/CTS nanogels at different time intervals. The tumor site of the mice treated with the magnet set as the magnetic targeting group. (The red circles represent the tumor.) (B) Signal intensities of tumors in different groups before and after administration of magnetic nanogels. (*P < 0.05). | |
To further verify the enhancement of T2-weighted MRI using the magnetic nanogels, a breast tumor-bearing mice model was used, and the results are shown in Fig. 6A, with the tumor region and liver marked with a red and yellow dashed circle, respectively. The darkness of these two parts appeared to increase with prolonged blood circulation time. For quantitative analysis, the signal intensity of the tumor decreased to 75.26% at 1 h and to 70.43% at 4 h (Fig. 6B). On the other hand, the signal intensity of the liver significantly reduced to 15.55% at 1 h and to 14.88% at 4 h. These results suggest that the magnetic nanogels may be suitable for MRI for both the tumor and liver. The enhanced contrast effect could remain for up to 4 h. Thus, the γ-Fe2O3@PNIPAM/PAm/CTS nanogels may act as a long-lasting contrast agent for diagnosis of tumor and hepatic disease (especially hepatocellular carcinoma10).
![image file: d4na00014e-f6.tif](/image/article/2024/NA/d4na00014e/d4na00014e-f6.gif) |
| Fig. 6 (A) In vivo T2-weighted MR images of mice bearing 4T1 breast tumors before and after administration of γ-Fe2O3@PNIPAM/PAm/CTS nanogels at different time intervals (the red and yellow circles represent tumor and liver, respectively). (B) Comparison of signal intensities of the tumor and liver before and after administration of γ-Fe2O3@PNIPAM/PAm/CTS nanogels. (**P < 0.01). | |
3.7. Systemic toxicity of γ-Fe2O3@PNIPAM/PAm/CTS nanogels
The biocompatibility studies of the γ-Fe2O3@PNIPAM/PAm/CTS nanogels including blood analysis and tissue toxicity were conducted. Female BALB/c mice (3 mice per group) were administered with saline and magnetic nanogels (30 mg kg−1) through tail vein injection. At two-week post-injection, the blood and serum were collected for blood hematology and biochemistry. No mortality, adverse effects, or body weight loss in the animals were found during the period. The hematology parameters and blood biochemistry results were normal and within the normal reference range (Fig. S4†). The results indicated that γ-Fe2O3@PNIPAM/PAm/CTS nanogels were safe at the blood test level.
After blood analysis, the mice were sacrificed to obtain their major organs for histological analysis to assess the acute toxicity of γ-Fe2O3@PNIPAM/PAm/CTS nanogels. Fig. 7 shows that there is no significant damage in the tissues of the heart, kidneys, liver, lungs, or spleen. The in vivo results confirmed that the magnetic nanogels possessed no severe toxic effects on rodent animals.
![image file: d4na00014e-f7.tif](/image/article/2024/NA/d4na00014e/d4na00014e-f7.gif) |
| Fig. 7 Histological images of the major organs of Balb/c mice after treatment for 2 weeks. The scale bars at the right corner are 20 μm. | |
4 Conclusions
We have successfully prepared magnetic nanogels (γ-Fe2O3@PNIPAM/PAm/CTS) containing high loading of superparamagnetic iron oxide nanoparticles as well as a pH- and temperature-responsive polymer via the step-wise emulsion polymerization approaches. The magnetic nanogels contain high iron oxide loading of approximately 60% with good stability in aqueous systems. They showed high magnetic saturation strength (r2 value of 517.74 mM−1 S−1) and were responsive to the tumor microenvironment, thus leading to enhanced in vivo MRI. Systemic toxicity studies confirmed that the magnetic nanogels possessed no severe toxic effects on rodent animals. Our results demonstrated that the magnetic nanogels constructed in this study are promising contrast agents for magnetic targeting with enhanced MRI. Thus this study provides safe and improved contrast agents for tumor diagnosis.
Author contributions
Jinfeng Liao: writing – original draft, writing – review & editing, conceptualization, methods & methodology, formal analysis, investigation, data curation and funding acquisition. Liangyu Zhou: writing – original draft, writing – review & editing, methods & methodology, formal analysis, and data curation. Yongzhi Wu: data curation. Zhiyong Qian: writing – review & editing. Pei Li: writing – manuscript & editing, conceptualization, supervision, project administration, and funding acquisition. All authors have read and agreed to the published version of the manuscript.
Conflicts of interest
The authors declare no conflict of interest.
Acknowledgements
This work was financially supported by the Chengdu International Science and Technology Cooperation Project (2020-GH02-00048-HZ), the National Natural Science Foundation of China (32171354), NSFC/RGC Joint Research Scheme (N_PolyU533/14) and PolyU Lo Ka Chung Centre for Natural Anti-Cancer Drug Development. The authors would like to thank Dr Cheng-Hao Lee for his invaluable assistance in obtianing the TEM images presented in this work.
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Footnotes |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d4na00014e |
‡ Jinfeng Liao and Liangyu Zhou contributed equally to this work. |
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