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International Journal of Nanomedicine logoLink to International Journal of Nanomedicine
. 2012 Sep 27;7:5137–5149. doi: 10.2147/IJN.S36197

Targeted delivery of tissue plasminogen activator by binding to silica-coated magnetic nanoparticle

Jyh-Ping Chen 1,✉, Pei-Ching Yang 1, Yunn-Hwa Ma 2, Su-Ju Tu 3, Yu-Jen Lu 1,4
PMCID: PMC3463402  PMID: 23055726

Abstract

Background and methods

Silica-coated magnetic nanoparticle (SiO2-MNP) prepared by the sol-gel method was studied as a nanocarrier for targeted delivery of tissue plasminogen activator (tPA). The nanocarrier consists of a superparamagnetic iron oxide core and an SiO2 shell and is characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, superconducting quantum interference device, and thermogravimetric analysis. An amine-terminated surface silanizing agent (3-aminopropyltrimethoxysilane) was used to functionalize the SiO2 surface, which provides abundant –NH2 functional groups for conjugating with tPA.

Results

The optimum drug loading is reached when 0.5 mg/mL tPA is conjugated with 5 mg SiO2-MNP where 94% tPA is attached to the carrier with 86% retention of amidolytic activity and full retention of fibrinolytic activity. In vitro biocompatibility determined by lactate dehydrogenase release and cell proliferation indicated that SiO2-MNP does not elicit cytotoxicity. Hematological analysis of blood samples withdrawn from mice after venous administration indicates that tPA-conjugated SiO2-MNP (SiO2-MNP-tPA) did not alter blood component concentrations. After conjugating to SiO2-MNP, tPA showed enhanced storage stability in buffer and operation stability in whole blood up to 9.5 and 2.8-fold, respectively. Effective thrombolysis with SiO2-MNP-tPA under magnetic guidance is demonstrated in an ex vivo thrombolysis model where 34% and 40% reductions in blood clot lysis time were observed compared with runs without magnetic targeting and with free tPA, respectively, using the same drug dosage. Enhanced penetration of SiO2-MNP-tPA into blood clots under magnetic guidance was confirmed from microcomputed tomography analysis.

Conclusion

Biocompatible SiO2-MNP developed in this study will be useful as a magnetic targeting drug carrier to improve clinical thrombolytic therapy.

Keywords: magnetic nanoparticles, drug delivery, thrombolysis, tissue plasminogen activator, silica

Introduction

Superparamagnetic iron oxide (Fe3O4) is a promising candidate for biomedical applications because of its strong magnetic properties and biocompatibility, as well as its unique multifunctional properties.1,2 Magnetic nanoparticle (MNP) based on Fe3O4 can be applied in drug delivery, bioseparation, biosensing, contrast agents for magnetic resonance imaging (MRI), and for magnetically induced cancer hyperthermia.3–7 As a drug carrier, MNP is usually composed of a superparamagnetic Fe3O4 core and a polymer coating layer, which provides functional groups facilitating drug binding, inhibiting aggregation, and increasing colloidal stability.8–10 Other than polymer coating, silica has been known to be one of the most ideal coating layers for Fe3O4-MNP due to its reliable chemical stability, biocompatibility, and reactivity with various coupling agents, making them suitable for conjugation with drugs for in vivo applications.11 In addition, amorphous silica particles have surface hydroxyl groups that render them intrinsically hydrophilic, which should decrease oxide particle clearance by the reticuloendothelial system, and thus increase their circulation time in the blood.12 When used as the coating material, silica is not subject to microbial attack and neither swells nor changes porosity in response to environmental pH values.13 There are few reports using silica-coated magnetic nanoparticle (SiO2-MNP) in targeted drug-delivery systems.14–16 Typically, there are two kinds of methods by which to prepare SiO2-MNP. The first method is based on the microemulsion system, in which the Fe3O4-MNP is restricted in the water droplets dispersed in a continuous organic phase and SiO2-MNP is formed by hydrolysis and condensation of tetraethoxysilane (TEOS), which diffuses from the surrounding organic phase into the water droplet.17,18 The microemulsion method will allow better control to achieve the composite particles with tunable size and shell thickness. However, it is hard to produce magnetic composite particles with submicron size with this method.19 The second method is based on the Stöber process, in which silica is formed by the hydrolysis and condensation of TEOS in an ethanol–ammonia mixture.20,21 The Stöber process is the prevailing choice for coating Fe3O4-MNP with silica, and has been proved to be an easy and efficient way to acquire silica-coated magnetic spheres.19

Myocardial infarction and venous thromboembolism are the major causes of cardiovascular mortality, which results in over 1 million deaths each year in the US.22,23 Thrombosis, beginning with endothelial injury followed by platelet activation, is responsible for most of the pathophysiology of these diseases. Thrombolytic drug therapy can reduce mortality, and this therapeutic approach has been widely used in thrombosis treatment.24 Although a number of thrombolytic drugs are currently available, tissue plasminogen activator (tPA) is currently the only US Food and Drug Administration-approved therapy for lysis of fibrin clot in treating ischemic stroke.25 tPA is a serine protease that converts the zymogen plasminogen to plasmin, which then initiates the process of lysis of the fibrin clot (fibrinolysis).26 As tPA has a very short life in plasma (half-life ≈5 minutes),27 it needs to be administered at a high dose for a prolonged period of time in order to maintain an effective drug level during thrombolytic drug therapy, which leads to degradation of clotting factors and hemorrhage.28 It will therefore be highly desirable to deliver tPA under guidance for targeted thrombolysis, which will allow tPA to be localized to the target site and reduce its hemorrhagic side effects.29–31 Target delivery of tPA using MNP as a drug carrier could meet this need by retaining the drug under magnetic guidance.32 Thus, delivery of tPA by binding the thrombolytic drug to SiO2-MNP will ensure that the drug is delivered under magnetic guidance and retained in a local area in circulation, which is potentially useful for targeting fibrin clot in vivo.

In this study, we examine the preparation of SiO2-MNP by the sol-gel method and the feasibility to use it as a magnetic nanocarrier for delivery of tPA. SiO2-MNP consisting of a superparamagnetic core and an SiO2 shell was synthesized and characterized. An amine-terminated surface silanizing agent (3-aminopropyltrimethoxysilane) was used to functionalize the SiO2 surface, which provides abundant –NH2 functional groups for conjugating with tPA. After covalent binding to SiO2-MNP, tPA showed high activity retention and enhanced storage and operation stability. Effective thrombolysis with SiO2-MNP-tPA under magnetic guidance substantially reduced blood clot lysis time compared with runs without magnetic targeting and with free tPA using the same drug dosage. The results demonstrate that SiO2-MNP is a useful magnetic targeting drug carrier for tPA delivery, and SiO2-MNP-tPA may provide a new form of thrombolytic drug that is potentially useful for treatment of thrombus.

Materials and methods

Materials

The raw Fe(II) chloride tetrahydate (99%) and Fe(III) chloride hexahydrate (97%) were purchased from Acros (Geel, Belgium). tPA ( Actilyse®) was obtained from Boehringer Ingelheim (Mannheim, Germany). TEOS was obtained from Fluka (Buchs, Germany). The crosslinking agent glutaraldehyde (GA) was obtained from Merck & Co (Whitehouse Station, NJ). 3-aminopropyltriethoxysilane (APTES), o-phthaldialdehyde, thrombin, fibrinogen, and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) were obtained from Sigma-Aldrich (St Louis, MO). The chromogenic substrate H-D-Isoleucyl-L-prolyl-L-arginine-p-nitroaniline (S-2288) was obtained from Chromogenix (Milano, Italy). All the chemicals were of reagent grade and used without further purification.

Synthesis of Fe3O4 magnetic nanoparticles and silica-coated magnetic nanoparticles

Fe3O4-MNP was obtained by reacting 0.22 M FeCl3 · 6H2O and 0.11 M of FeCl2 · 4H2O (Fe+3:Fe+2 = 2:1) in distilled deionized (DDI) water at 60°C under nitrogen atmosphere for 1 hour. Four milliliters of 25% NH4OH was added to the solution, after which the color of the mixture turned from yellow to black immediately, and the solution was stirred at 400 rpm for another 20 minutes. The synthesized Fe3O4-MNP was washed three times with DDI and separated by magnetic decantation, dialyzed (MWCO = 3500) for 7 days against DDI water with daily water change, and stored at 4°C. SiO2-MNP was prepared by mixing 50 mL ethanol, 1 mL DDI water, and 1.5 mL TEOS in a 250 mL four-neck flask in a 40°C water bath under mechanical stirring for 20 minutes at 1500 rpm. Two milliliters of 25% NH4OH was added to the solution under stirring and reacted for 20 minutes, followed by adding 60 mL Fe3O4-MNP (0.18 mg/mL) under stirring for another 6 hours. SiO2-MNP was isolated with a magnet to eliminate the homogeneous silica nucleus and dried at 90°C under vacuum after being washed three times with ethanol.

Amine-derived SiO2-MNP was prepared by modifying SiO2-MNP with APTES to introduce surface amine groups (Figure 1, step 1). Fifteen milligrams of SiO2-MNP was treated in 4 mL ethanol/1 mL DDI water for 30 minutes with an ultrasonic processor (Misonix Sonicator 4000; Qsonica, LLC, Newtown, CT) at 600 W, and 0.25 mL APTES and 0.25 mL dimethylformamide was added. The solution was shaken at 200 rpm in an incubator for 2 hours, and SiO2-MNP was isolated with a magnet after washing with phosphate-buffered saline (PBS) three times and stored in PBS at 1 mg/mL.

Figure 1.

Figure 1

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A schematic diagram showing the surface modification of silica-coated magnetic nanoparticle (SiO2-MNP) with 3-aminopropyltriethoxysilane (APTES) (step 1), activation with glutaraldehyde (step 2), and immobilization of tissue plasminogen activator (tPA) (step 3).

Characterization of magnetic nanoparticles

The particle size and morphology of MNP were examined by transmission electron microscopy (TEM) (JEM-2000 EX II; JEOL, Tokyo, Japan). An aqueous dispersion of the particles was drop-cast on to a carbon-coated copper grid, and the grid was air-dried at room temperature before loading into the microscope. Alternatively, the sample was stained with 2% phosphotungstic acid (PTA) aqueous solution for 3 minutes before analysis.

To investigate the crystal structure of the NP, wide-angle X-ray diffraction (XRD) spectra were registered with a Siemens D5005 diffractometer (Siemens AG, Erlangen, Germany) composed of a CuKα source, a quartz monochrometer, and a geniometric plate at a scanning speed of 2° min−1 from 15° to 70°. The zeta potential and the particle size distributions were determined using laser dynamic light scattering with Malvern Zetasizer ZA 90 (Malvern Instruments, Malvern, UK) in water at 25°C. The magnetization of the NP was measured by a superconducting quantum interference device (SQUID) magnetometer (MPMS XL-7; Quantum Design, San Diego, CA) at 25°C and ±10,000 G applied magnetic field. For Fourier transform infrared spectroscopy (FTIR) measurement using a Horiba FT-730 spectrometer, the samples were blended with KBr and then compressed to form a pellet. The transmission spectra were obtained from 450 to 4000 cm−1 with a resolution of 4 cm−1. Concentrations of amino groups on the surface of SiO2-MNP were determined by the ο-phthaldialdehyde method, which is based on the reaction of primary amines with an excess of ο-phthaldialdehyde and β-mercaptoethanol and subsequent quantitative determination of unreacted ο-phthaldialdehyde by reaction with glycine.33 The iron contents of SiO2-MNP were analyzed by inductively coupled plasma optical emission spectroscopy (Optima 2100 DV; PerkinElmer, Waltham, MA). Thermogravimetric analysis (TGA) was conducted with TGA 2050 from TA instruments (New Castle, DE).

For in vitro biocompatibility test, the cytotoxic effect of SiO2-MNP was tested on a mouse embryonic fibroblast cell line (3T3). 3T3 cells were cultured using 24-well culture plates (1.0 × 104 cells/well) in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum and incubated at 37°C in a 5% CO2 atmosphere. After 24 hours of culture, the medium in the wells was replaced with fresh medium containing SiO2-MNP at a concentration ranging from 10−4 to 106 ng/mL and cultured for another 3 days before measuring mitochondria activity by MTT assays. Forty microliters of MTT solution (5 mg/mL in 0.1 M phosphate buffer, pH 7.4) and 200 μL PBS were added to each well. After 3 hours’ incubation at 37°C in 5% CO2, the medium was removed and the formazan crystals were dissolved in 1 mL of dimethylsulfoxide. The solution was mixed vigorously to dissolve the crystal product. The optical density (OD) of solution in each well was recorded on a microplate reader (BioTek Synergy HT; BioTek, Winooski, VT) at 570 nm (OD570). For detection of cell damage caused by SiO2-MNP, the same procedure was followed, except 50 μL of medium was removed 1 day after adding SiO2-MNP to measure the lactate dehydrogenase (LDH) concentration secreted by cells with a commercial LDH assay kit from Promega (Madison, WI) using a microplate reader at 490 nm (OD490). 3T3 cells without contacting SiO2-MNP were used as the control.

MRI was carried out in C57BL/6 mice to show that asprepared NP could be used as an imaging agent and visualized in MRI. The experiments were improved by the Institutional Animal Care and Use Committee of Chang Gung Memorial Hospital (Kwei-San, Taoyuan, Taiwan) and adhered to the experimental care guidelines. Animals were assessed by MRI 120 minutes after tail vein injection of 0.1 mL of PBS (control) or 0.1 mL of 10 mg/mL SiO2-MNP in PBS. All MR images were acquired on a 3-T scanner (MAGNETOM Trio, A Tim System; Siemens Healthcare, Erlangen, Germany) using the standard wrist coil with an inner diameter of 13 cm. The animals were anesthetized with 2% isoflurane throughout the MRI process, placed in an acrylic holder, and positioned at the center of the magnet.

Immobilization and activity assays of tissue plasminogen activator

tPA was immobilized using GA as a crosslinking agent to promote the formation of imide bonds between the aldehyde groups of GA and amino groups of SiO2-MNP or tPA. Five milligrams of SiO2-MNP suspension was mixed with 0.1 mL of 0.5% GA for 30 minutes in 0.5 mL PBS (pH 7.4) with shaking (200 rpm) at 30°C, followed by washing twice with 1 mL PBS (pH 7.4) to prepare activated SiO2-MNP (Figure 1, step 2). Two hundred and fifty microliters of activated SiO2-MNP (20 mg/mL) was then mixed with 0.25 mL of tPA solution for 12 hours at 4°C using a rotator at 6 rpm to obtain SiO2-MNP-tPA (Figure 1, step 3). Immobilized tPA could be obtained after magnetic separation from the solution and washing with PBS. The amount of tPA immobilized to SiO2-MNP was determined by measuring unbound tPA protein concentrations in the supernatant and the washing solution by a colorimetric method at 595 nm with the Protein Assay Kit from Bio-Rad (Hercules, CA). Protein loading efficiency was defined as the percentage of tPA protein bound to SiO2-MNP in comparison with that added initially during the immobilization step.

Amidolytic activity of tPA was measured spectrophotometrically using the protease substrate S-2288, a specific chromogenic substrate for tPA, according to the manufacturer’s instruction. Activity retention after immobilization was defined as the percentage of specific activity (U/mg) of immobilized tPA compared with that of free tPA, which is 2.43 U/mg. Fibrinolytic activity of tPA was determined from fibrin clot lysis assay using fibrin-containing agarose plates.34 The plates were prepared by mixing 10 mL low melting temperature agarose solution (5%) containing 2.5 U thrombin with 5.0 mL fibrinogen solution (5 mg/mL) at 50°C. The reaction mixture was poured into a 9 cm culture dish and cooled at 4°C for 30 minutes until the fibrin clot became visible. To perform the assays, 0.1 mL solution (tPA or SiO2-MNP-tPA) was added into the round sample wells (3 mm diameter) made on the solid fibrin–agarose gel and incubated at 37°C for 1 hour. The degree of fibrin lysis was quantified by comparing the size of the fibrinolysis zone around sample wells containing equivalent tPA concentrations. A linear calibration curve could be established for the diameter of fibrin lysis zone versus tPA concentration from 0 to 2 mg/mL.

Storage stability, operation stability, and blood compatibility of SiO2-MNP-tPA

Storage stability of free and immobilized tPA was determined from the residual activity of tPA after storage in PBS at 4°C. Ten milliliters of PBS containing free tPA (1 mg/mL tPA) or 10 mg/mL SiO2-MNP-tPA solution (equivalent to 1 mg/mL tPA) was incubated under static condition. Samples (0.1 mL) were withdrawn at times and assayed for residual amidolytic activity. Relative activity was determined by normalizing the residual activity measured for each sample at different times with its initial amidolytic activity.

Operation stability was determined by preparing 10 mL whole blood containing free tPA (2 mg/mL tPA) or 20 mg/mL SiO2-MNP-tPA (equivalent 2 mg/mL tPA) and incubated at 37°C under static condition. Samples (0.3 mL) were withdrawn at 5, 10, 30, and 45 minutes and assayed for residual fibrinolytic activity by comparing the diameter of the fibrinolysis zone around sample wells.

For blood compatibility, hematological measurements were carried out in C57BL/6 mice. The experiments were approved by the Institutional Animal Care and Use Committee of Chang Gung University and adhered to the experimental care guidelines. One milliliter of blood samples was collected via the tail vein 120 minutes after venous administration of 0.1 mL PBS (control), tPA in PBS (1 mg/mL), 10 mg/mL SiO2-MNP in PBS, or 10 mg/mL SiO2-MNP-tPA in PBS (equivalent to 1 mg/mL tPA). Concentrations of red blood cells (RBCs), white blood cells (WBCs), platelets, hemoglobin, and hematocrit were determined by an automated hematology system (Sysmex XE-5000; Sysmex Co, Kobe, Japan).

Blood clot lysis and micro-CT analysis

Blood clot lysis induced by free tPA or SiO2-MNP-tPA was determined by an ex vivo thrombolysis model driven by a constant pressure gradient at 37°C (Figure 2), which is similar to the condition that maintains blood circulation in vivo.35 A 0.02 × 0.2 × 30 mm collagen-coated glass capillary tube (Vitrotube; Vitrocom, Mountain Lakes, NJ) was vertically mounted below a reservoir (ID = 0.75 cm) and immersed in a PBS bath. Whole blood samples (0.5 mL) were mixed with 0.1 mL of 0.9% NaCl and 0.15% CaCl2 solution containing 50 U thrombin to produce a 0.8 cm height blood clot at the bottom of the reservoir. A solution of 0.2 mg/mL tPA, 2 mg/mL SiO2-MNP, or 2 mg/mL SiO2-MNP-tPA ( equivalent to 0.2 mg tPA/mL) was prepared in whole blood and introduced above the blood clot in the reservoir to a height of 0.2 cm. For magnetic targeting, a magnet (6000 G) was placed next to the bottom of the reservoir and rotated at 6 rpm to introduce a magnetic guidance force down the blood clot at intervals. Blood generated from the clot was allowed to drain from the reservoir, through the capillary, into the PBS bath. Time to blood flow was recorded as the time when blood first exited from the capillary into the PBS bath.

Figure 2.

Figure 2

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An ex vivo thrombolysis model for determining the thrombolysis efficacy of tissue plasminogen activator.

Abbreviation: PBS, phosphate-buffered saline.

Micro-CT studies were carried out to delineate the penetration depth of SiO2-MNP-tPA into the blood clots in a static lysis model and to demonstrate the dissemination of MNP within the clot matrix. Six hundred microliters of whole blood and 0.1 mL thrombin solution (10 U/mL) was mixed in a 2 mL plastic tube (3 cm height × 1 cm diameter and sealed with 1 cm height polydimethylsiloxane silicone elastomer at the bottom) to form a blood clot. The individual blood clot was placed at the bottom of the tube, which allowed the clot to occupy the complete inner tube circumference, restricting the various treatments to remain in contact only with the clot surface. Two hundred microliters of SiO2-MNP or SiO2-MNP-tPA (10 mg/mL) in PBS was placed on top of the blood clot. A 6000 G magnet (1 × 1 × 8 cm) was placed at the tube bottom for magnetic targeting when needed. After 8 hours, the tube was incubated at 80°C to inactivate tPA and fix the NP, and the tube was subject to micro-CT imaging. A micro-CT scanner system (SkyScan 1076; SkyScan, Kontich, Belgium) was used in the imaging experiments. In micro-CT images, each pixel is associated with a linear attenuation coefficient that is a quantity to characterize the strength for a photon to pass through a material. For iron-based MNP, the physics of photoelectric effect is enhanced to generate contrast between NP and soft tissues. In this study, imaging energy of 50 keV, projection number of 720, a metal filter of aluminum with 0.5 mm thickness, spatial resolution of 8.9 μm, and reconstruction algorithm of filtered backprojection were used.

Statistical analysis

Values are expressed as mean ± standard error and examined by one-way analysis of variance and Tukey’s HSD test. Statistical significance was declared at P < 0.05.

Results and discussion

Preparation and properties of silica-coated magnetic nanoparticles

The chemical coprecipitation of ferrous and ferric cations in an alkaline solution is a classical method widely used for the preparation of Fe3O4-MNP. For further coating with silica using the Stöber method,36 due to the strong dipole–dipole interactions among the Fe3O4-MNP and increased ionic strength during the hydrolysis of TEOS, a first silica layer deposited on the Fe3O4-MNP surface is usually necessary to improve the dispersibility of the MNP before carrying out the silica coating by hydrolysis and condensation of TEOS.37 SiO2-MNP was prepared in this study by direct introduction of Fe3O4-MNP into the Stöber process upon formation of the primary silica particles. When the Fe3O4-MNP was added into the reaction mixture at the appropriate time, the primary particles can quickly aggregate with the Fe3O4-MNP, thus suppressing the dipole–dipole interactions among the NP effectively and allowing the synthesis of composite SiO2-MNP with defined structure by further deposition of a silica layer. The prepared SiO2-MNP possesses excellent colloidal stability in solution and withstands repeated centrifugation/redispersion cycles without aggregation, which is the characteristic required for a magnetic nanosized carrier for tPA to effectively interact with fibrin clots.

Figure 3A and B illustrates the TEM micrographs of the prepared SiO2-MNP, which show uniform spherical particle morphology with ~100 nm diameter. The NP has a core shell structure with a core electronic dense part (magnetite) surrounded by a silica shell of 10 nm thickness. Selected area electron diffraction pattern exhibits spots and rings of well-crystallized magnetite NPs within SiO2-MNP, indicating successful coating of Fe3O4-MNP surface with silica (Figure 3B, insert). The TEM micrograph of SiO2-MNP after conjugating tPA is shown in Figure 3C after PTA staining. Dynamic light scattering measurements show the hydrodynamic diameters of the SiO2-MNP to be about 200.5 ± 3.1 nm with a rather monodisperse particle size distribution (polydispersive index = 0.138). Fe3O4 content as determined by inductively coupled plasma is 57.1 wt% Fe3O4 in SiO2-MNP. Electrophoretic mobility measurements give a highly negative zeta potential after silica coating where the zeta potentials changed from 18.8 ± 0.9 mV for Fe3O4-MNP to −27.0 ± 0.4 mV for SiO2-MNP due to the presence of the negatively charged surface silanol group. After modifying SiO2-MNP surface with 3-aminopropyltriethoxysilane, the zeta potential of amine-derived SiO2-MNP changes again to 33.2 ± 1.8 mV with the introduction of abundant positively charged amine groups on the surface. The surface density of –NH2 groups of amine-derived SiO2-MNP could be determined quantitatively to be 1.19 ± 0.02 μmole/mg particle. The abundance of –NH2 groups hanging from the particle surface can facilitate the immobilization of tPA by glutaraldehyde-mediated imide bond formation. The size of amine-derived SiO2-MNP remains unchanged at 191.0 ± 5.1 nm (polydispersive index = 0.195).

Figure 3.

Figure 3

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Transmission electron microscope images of (A and B) silica-coated magnetic nanoparticle (SiO2-MNP) and (C) tissue plasminogen activator (tPA) bound to SiO2- MNP (SiO2-MNP-tPA) after staining with phosphotungstic acid. Characterization of superparamagnetic iron oxide magnetic nanoparticle (Fe3O4-MNP) and SiO2-MNP with (D) Fourier transform infrared spectroscopy analysis, (E) X-ray diffraction patterns, and (F) superconducting quantum interference device magnetization curves.

Notes: (A) Magnification = 100,000, bar = 100 nm; (B and C) magnification = 300,000, bar = 50 nm. Insert in (B) is electron diffraction pattern; insert in (C) is a blowup of the circled area.

The FTIR spectra of different NPs are presented in Figure 3D. For Fe3O4-MNP, an absorption band at 572 cm−1 corresponding to the Fe–O–Fe vibration relates to the magnetite phase. The peak at 1632 cm−1 represents N–H bond formation during the chemical coprecipitation of Fe+2 and Fe+3 salts induced by the addition of NH4OH base. For SiO2-MNP the existence of the characteristic peaks at 792, 967, and 1084 cm−1, due to the symmetric and asymmetric stretching vibration of framework and terminal Si–O–groups, is direct evidence to verify the formation of the silica shell. The characteristic Fe–O–Fe peak shifts from 572 cm−1 to 589 cm−1 in the spectrum of SiO2-MNP, indicating that the silica shell is linked to the surface of the Fe3O4-MNP by Fe–O–Si chemical bonds. Also, the peak at 1551 cm−1 corresponds with the –NH2 characteristic peak in amine-derived SiO2-MNP. All diffraction peaks of the XRD patterns of the prepared NP can be easily indexed to a pure cubic phase of Fe3O4 (JCPDS No 65-3107) (Figure 3E). The characteristic peaks at 2θ = 30.2°, 35.4°, 43.1°, 53.2°, 56.9°, and 62.5° for pure Fe3O4-MNP, which represent corresponding indices (220), (311), (400), (422), (511), and (440), are also observed for SiO2-MNP. Surface coating Fe3O4-MNPs with silica thus did not lead to their phase change. It should be noted that only minor broad reflection at low 2θ values (20°~30°), originating from the amorphous silica matrix, appears in SiO2-MNP XRD patterns after silica coating due to the thin silica coating layer (Figure 3B).38 The average particle size calculated using the Debye–Scherrer formula from the reflection peak of (311) is about 13.9 nm,39 consistent with the result measured from the TEM images. The results of SQUID analysis at room temperature indicate a saturation magnetization value of 48.9 emu/g for SiO2-MNP, which is lower than that of bare Fe3O4-MNP (68.3 emu/g) due to the coated shell (Figure 3F). This can be explained by considering the diamagnetic contribution of the silica shell surrounding the magnetite, which was also observed in a previous study.40 Generally, the saturation magnetization would decrease when the particle surface was covered by coating materials. The high magnetization value will greatly enhance the ability for magnetic guidance and complete magnetic blood clot penetration by the NP.41 From the magnetization curve, the remanence (residue magnetization) and coercive force (the applied field that reduces magnetization to zero) were zero, and there was no magnetic hysteresis loop observed, indicating the characteristic superparamagnetic behavior.

Figure 4A shows the TGA curves of MNPs. All samples show an initial small mass loss at temperatures below 200°C due to desorption of adsorbed water and CO2. At temperatures above 200°C, there is negligible weight loss for Fe3O4-MNP with no observable peak temperature for the highest weight loss in the differential weight loss curve (Figure 4B). In contrast, SiO2-MNP samples showed distinct behavior due to the decomposition of functional groups. Peak temperatures at 345°C and 310°C were found for SiO2-MNP and amine-derived SiO2-MNP, respectively, due to decomposition of the organic parts (hydroxyl and propylamine groups) from the NP surface (Figure 1). The mass loss of amine-derived SiO2-MNP is 6.2 wt% (Figure 4A). Under the assumption that all the ethoxy groups were eliminated during silica formation and that only the organic part of the linker (propylamine) contributes to the mass loss for amine-derived SiO2-MNP, this weight loss corresponds to 1.07 μmol/mg, which is in fairly good agreement with the value obtained from the surface density of –NH2 groups (1.19 μmol/mg). The cytotoxicity of SiO2-MNP on 3T3 fibroblast cells was examined using the MTT method for cell proliferation and the LDH assay for cell damage. The MTT assay is a simple nonradioactive colorimetric assay to measure the level of cell viability. The LDH assay is a convenient method to evaluate cell damage from the release of LDH from lysed cells. Figure 5 shows that SiO2-MNP mediated very low cytotoxicity within the concentration range studied. There is no statistical difference in OD570 or OD490 from the control (3T3 cells without contacting SiO2-MNP) when 3T3 cells were exposed to different concentrations of SiO2-MNP (P < 0.05). Since the threshold cytotoxic concentration of MNP has been reported to be within our testing range,42 the in vitro biocompatibility test indicated that SiO2-MNP elicited no cytotoxicity.

Figure 4.

Figure 4

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Thermogravimetric analysis of superparamagnetic iron oxide magnetic nanoparticle (Fe3O4-MNP), silica-coated magnetic nanoparticle (SiO2-MNP), SiO2-MNP surface modified with 3-aminopropyltriethoxysilane (amine-derived SiO2-MNP), and tissue plasminogen activator (tPA) bound to SiO2-MNP (SiO2-MNP-tPA).

Figure 5.

Figure 5

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Cytotoxicity analysis of silica-coated magnetic nanoparticles (SiO2-MNP) by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) (A) and lactate dehydrogenase (LDH) (B) assays. (A) 3T3 cells were contacted with SiO2-MNP at indicated concentration for 3 days before measuring mitochondria activity by MTT assay at 570 nm (OD570). (B) 3T3 cells were contacted with SiO2-MNP at indicated concentration for 1 day before measuring released LDH concentration at 490 nm (OD490).

Note: 3T3 cells without contacting SiO2-MNP were used as the control.

Figure 6 shows the T2-weighted MRI images of B6 mice after tail vein injection of PBS (control) or 10 mg/mL SiO2-MNP suspended in PBS. After intravenous injection, the liver was darkened significantly for mice administrated with SiO2-MNP in comparison with that of control, indicating that SiO2-MNP could be used as an imaging agent and visualized in MRI.

Figure 6.

Figure 6

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In vivo T2-weighted magnetic resonance images of silica-coated magnetic nanoparticles (SiO2-MNP) in mice 2 hours after injection of phosphate-buffered saline (PBS) (control) or SiO2-MNP in PBS.

Preparation and properties of tPA immobilized to silica-coated magnetic nanoparticles

One of the major challenges of enzyme immobilization to MNP is the loss of enzyme activity after immobilization.43 Covalent immobilization of tPA to SiO2-MNP may potentially involve amino acids necessary for substrate recognition or catalytic activity, which will result in loss of the enzyme activity after immobilization. The effect of the amount of tPA used for immobilization was studied and the results are shown in Figure 7. The protein loading efficiency and the activity retention remain >95% up to 0.3 mg tPA, which subsequently decrease at higher tPA loadings. The immobilized tPA activity per mg of SiO2-MNP will be important in order to use the least amount of NP during in vivo application. This value also reaches a plateau at around 0.5 mg tPA. The optimum drug loading is therefore reached when 0.5 mg tPA is reacted with 5 mg SiO2-MNP, by which 94% tPA is attached to the carrier with 86% retention of its amidolytic activity.

Figure 7.

Figure 7

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The effects of the amount of tissue plasminogen activator ( tPA) added during immobilization on the protein loading efficiency and activity retention of tPA immobilized to silica-coated magnetic nanoparticles (SiO2-MNP) (5 mg).

In this study, tPA activator was immobilized to amine-derived SiO2-MNP by a two-step process using GA as a crosslinking agent. Previously, tPA was immobilized to polyacrylic acid-coated MNP by using carbodiimide-mediated amide bond formation between carboxylic acid groups of polyacrylic acid and amine groups of tPA.31 For amine-derived SiO2-MNP, imide bond formation between tPA and SiO2-MNP could be achieved with GA or genipin. Although genipin may be preferable to reduce the associated toxicity of GA, it may not equate to GA’s ability to immobilize and promote the formation of imide bonds between the aldehyde groups of GA and amine groups of SiO2-MNP or tPA.44 Considering GA as a crosslinking agent in clinical application, bioprostheses made of GA-treated bovine pericardium or porcine heart valve tissues have been used for more than 20 years.45 A recent study used N-hydroxysulfosuccinimide and tresyl chloride to conjugate tPA to MNP. However, the protein loading efficiency (63%) and the activity retention (45%) are much lower than those in current study using GA.46

Due to the selective staining of silica and protein with PTA, tPA molecules (gray region) could be observed to attach to the surface of SiO2-MNP (black region) (Figure 3C). TGA analysis of SiO2-MNP-tPA indicates additional weight loss after conjugating tPA and a new peak temperature at 500°C (Figure 4B), which can be assigned to the decomposition of tPA protein moiety. The weight percentage of tPA in SiO2-MNP-tPA preparation could be calculated to be 8.3% from the difference between the weight loss of amine-derived SiO2-MNP and SiO2-MNP-tPA (Figure 4A), which could be compared with 8.6% calculated from protein assay.

From fibrin clot lysis assay, the fibrinolytic activity of SiO2-MNP-tPA is not different from free tPA (P < 0.05) for concentrations up to 1 mg/mL tPA, suggesting that all fibrinolytic activity of tPA could be preserved after immobilization to SiO2-MNP (Figure 8). Covalent binding of tPA to SiO2-MNP hence fully preserved its fibrinolytic activity, which is critical for effective thrombolysis in vivo.

Figure 8.

Figure 8

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Fibrinolytic activities of tissue plasminogen activator (tPA) and tPA bound to silica-coated magnetic nanoparticles (SiO2-MNP-tPA) by fibrin clot lysis assays.

To provide a readily available tPA formulation for immediate thrombolysis application, it is important that tPA immobilized to SiO2-MNP could be stored in PBS and preserve a reasonable residue activity when needed. Thus, the storage stability of free tPA and SiO2-MNP-tPA was determined by measuring the residual activity in PBS at 4°C (Figure 9). After 72 days, the residual activities are 43.6% and 91.0% for free and immobilized t-PA, respectively. The activity decay could be modeled with first-order enzyme inactivation kinetics.47 The inactivation rate constants (kd) determined from the data are 1.092 × 10−2 d−1 (r2 = 0.995) and 1.152 × 10−3 d−1 (r2 = 0.933) for free and immobilized tPA, respectively. The calculated half-life (ln 2/kd) is thus 63.5 d and 601.6 d. In general, immobilization of enzyme with MNP as support material has been considered as one of the efficient methods to improve enzyme stability.48 In the current study, the stability of tPA in solution at 4°C was enhanced 9.5-fold as a result of binding to SiO2-MNP. Possible mechanisms leading to enhanced storage stability of tPA could be ascribed to the restriction of the conformation change of the drug after covalent binding with SiO2-MNP, thus preventing distortion and activity loss of the enzyme molecule.49,50 The increased storage stability of bound tPA is crucial to extend the period during which it could fully exert its therapeutic effects in vivo when needed.

Figure 9.

Figure 9

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Storage stability of tissue plasminogen activator (tPA) and tPA bound to silica-coated magnetic nanoparticles (SiO2-MNP-tPA).

Notes: The residual amidolytic activity after incubation in phosphate-buffered saline at 4°C for time indicated was determined by chromogenic substrate assay. Relative activity was defined as percentage activity of tPA and SiO2-MNP-tPA, respectively, at day 0.

However, it is not known whether MNP-bound tPA may exert a prolonged half-life in vivo compared with that of free tPA. To simulate in vivo conditions, the operation stability was determined from the residual fibrinolytic activity of tPA after incubating the drug in whole blood for a specific time (Figure 10). The diameter of fibrin lysis zone for free and immobilized tPA showed statistical difference if the incubation time in blood is longer than 5 minutes. At 45 minutes’ incubation time in blood, the diameter is 0.42 cm and 0.15 cm for free tPA and SiO2-MNP-tPA, respectively, corresponding to a 2.8-fold increase in stability in blood using immobilized tPA. Results of previous studies have shown that coupling tPA to RBCs increased its intravascular life span compared with soluble tPA.51 One possible explanation for this surprising result is that coupling to RBCs renders tPA less susceptible to plasma tPA inhibitors,52 including the most physiologically relevant plasminogen activator inhibitor 1 (PAI-1). Further studies affirm the greater fibrinolytic potency of bound tPA compared with soluble tPA in mouse blood, and indicate that coupling to RBCs protects tPA against physiological and pathological concentrations of PAI-1,53 and inhibition by other serpins (α2-macroglobulin and α1-antitrypsin). As the interaction of tPA and PAI-1 may be stabilized through salt bridges formed between cationic amino acid in tPA and anionic residues in PAI-1,54 the authors propose that the protection is due to charge-mediated masking of vulnerable sites on tPA molecules by the negatively charged components of glycocalyxon on the surface of RBCs. This is consistent with the negative surface potential (−27.0 ± 0.4 mV) of SiO2-MNP due to the presence of negatively charged surface silanol groups. Sensitivity to inhibitors is one of the factors that may control the longevity of SiO2-MNP-tPA activity in vivo.

Figure 10.

Figure 10

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Operation stability of tissue plasminogen activator (tPA) and tPA bound to silica-coated magnetic nanoparticles (SiO2-MNP-tPA).

Notes: The residual fibrinolytic activity after incubation in blood at 37°C for time indicated was determined by fibrin clot lysis assay. *P < 0.05 compared with corresponding tPA value.

For blood compatibility, the results of hematological analysis are illustrated in Table 1. The platelet counts of tPA and SiO2-MNP were different from the control (P < 0.05). WBCs of SiO2-MNP were also elevated (P < 0.05). However, other counts of RBCs, WBCs, hemoglobin, and hematocrit were not different among groups. Target thrombolysis with SiO2-MNP-tPA will therefore be well suited for in vivo applications.

Table 1.

Hematological measurements in rats treated with 0.1 mL phosphate-buffered saline (PBS) (control), tissue plasminogen activator (tPA) in PBS (1 mg/mL), 10 mg/mL silica-coated magnetic nanoparticle (SiO2-MNP) in PBS, or 10 mg/mL SiO2-MNP-tPA in PBS (equivalent to 1 mg/mL tPA)

Treatment RBC (106/μL) WBC (103/μL) Platelet (103/μL) HGB (g/dL) HCT (%)
Control 9.4 ± 0.5 5.2 ± 0.2 1054 ± 50 12.1 ± 0.6 48.9 ±1.4
tPA 8.9 ± 0.4 5.0 ± 0.3 850 ± 29* 11.6 ± 0.5 47.2 ± 1.0
SiO2-MNP 9.1 ± 0.3 6.9 ± 0.1* 804 ± 48* 11.7 ± 0.7 49.8 ± 1.3
SiO2-MNP-tPA 9.2 ± 0.4 5.3 ± 0.3 1100 ± 76 11.8 ± 0.4 48.2 ± 1.2
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Notes: Concentrations of red blood cells (RBC), white blood cells (WBC), platelets, hemoglobin (HGB), and hematocrit (HCT) were determined by automated hematology system (values presented as mean ± standard error).

*

P < 0.05 compared with control.

Blood clot lysis and micro-CT analysis

The efficacy of thrombolysis by SiO2-MNP-tPA was studied with an ex vivo intravascular thrombolysis model. The time to blood flow from capillary is shown in Figure 11. Runs with SiO2-MNP (with or without magnet) show no difference in blood flow time from that of control (blood only). The thrombolysis efficacy of free and bound tPA in blood was compared using the same tPA drug dosage (0.2 mg/mL). Although the activity of SiO2-MNP-tPA is 86% that of free tPA (Figure 7), the blood flow times are 157 and 144 minutes for free tPA and SiO2-MNP-tPA, respectively. This improvement in thrombolysis ability is consistent with the enhanced fibrinolytic activity retention in whole blood for the bound drug (Figure 9). Magnetic guidance can further reduce the blood flow time of SiO2-MNP-tPA to 95 minutes, which is 66% that of the run without magnetic targeting and 60% that of the free tPA run. Magnetic targeting delivery of SiO2-MNP-tPA can therefore effectively shorten the thrombolysis time compared with the conventional treatment with free tPA under the same drug dosage. Alternatively, a reduced dosage of tPA could be used in vivo to reach the same thrombolysis effect by delivering SiO2-MNP-tPA under magnetic guidance, which can prevent the hemorrhagic side effect of tPA.

Figure 11.

Figure 11

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The efficacy of thrombolysis studied with an ex vivo thrombolysis model as shown in Figure 2.

Notes: The time to blood flow from capillary with or without magnet for magnetic guidance is shown. *P < 0.05 compared with tissue plasminogen activator bound to silica-coated magnetic nanoparticles (SiO2-MNP-tPA) with magnet; #P < 0.05 compared with SiO2-MNP-tPA without magnet.

Micro-CT studies were used to provide semiquantitative estimates about the spatial distribution of MNP within a whole blood clot (Figure 12). Magnetic targeting was employed by placing a magnet below the clot at the tube bottom. Exposure of the clots to SiO2-MNP with or without magnetic fields showed no difference in penetration depth with minimum downward movement (Figure 12A and B). In contrast, SiO2-MNP-tPA delineated a considerable increase in clot penetration from the passage trajectories of MNP ( Figure 12C). Similar to previous studies when blood clots were exposed to tPA alone,39 SiO2-MNP-tPA penetration depth and lysis zone are restricted to the top layer of the thrombus due to limited drug delivery into the thrombus with the presence of tight fibrin meshwork.55–57 In contrast, the combination of SiO2-MNP-tPA and a magnetically driven force delineated a substantial increase in clot penetration (Figure 12D). The frontal shape was not flat in the image of micro-CT under magnetic guidance with the nonuniformity of external magnetic field in contrast to without magnetic field where a flat front was observed with the continued lysis of clots with tPA bound to the NPs. These experiments provided direct evidence that not only tPA bound to SiO2-MNP exerted thrombolysis activity but also the exposure of the thrombus to magnetic fields resulted in enhanced penetration of MNP into the clot, supporting the improved clot lysis efficacy of SiO2-MNP-tPA under magnetic guidance (Figure 11).

Figure 12.

Figure 12

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Microcomputed tomography imaging of the penetration of silica-coated magnetic nanoparticles into blood clot with or without immobilized tissue plasminogen activator (tPA) and with or without a magnet at the clot bottom for magnetic guidance.

Note: The red arrows indicate imaging boundaries.

Conclusion

Biocompatible SiO2-MNP could be prepared and used for covalent immobilization of tPA with a high protein loading efficiency and activity retention. The results presented herein demonstrate the characteristic of SiO2-MNP to make it useful as a magnetic targeting drug carrier. By conjugating tPA to an SiO2-MNP surface, a new form of thrombolytic drug potentially useful for treatment of thrombus was achieved and is expected to improve clinical thrombolytic therapy.

Acknowledgments

Financial support from National Science Council (NSC99-2120-M-182-001), National Health Research Institute (NHRI-EX101-9937EI), Department of Health (DOH101-TD-PB-111-TM009), and Chang Gung Memorial Hospital was highly appreciated.

Footnotes

Disclosure

The authors report no conflicts of interest in this work.

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