Development of antibody functionalized magnetic nanoparticles for the immunoassay of carcinoembryonic antigen: a feasibility study for clinical use
© Yang et al.; licensee BioMed Central Ltd. 2014
Received: 10 August 2014
Accepted: 13 October 2014
Published: 26 November 2014
Magnetic nanoparticles functionalized antibodies are used for in-vitro assays on bio-markers. This work demonstrates the synthesis of high-quality magnetic nanoparticles coated with antibodies against carcinoembryonic antigen (CEA). Various characterizations, such as particle size, particle suspension, bio-activity and the stability of bio-magnetic nanoparticles suspended in liquid, are studied. The properties for the assay of CEA molecules in serum are also studied. The assay method used is so-called immunomagnetic reduction.
The results show that the effects of common materials in serum that interfere with detected signals are not significant. The low-detection limit is 0.21 ng/ml, which is well below the clinical threshold of 2.5 ng/ml.
The dynamic range for the assay of CEA molecules in serum is 500 ng/ml. By assaying serum CEA molecules from 24 normal controls and 30 colorectal-cancer patients, the threshold for the serum-CEA concentration to diagnose colorectal cancer is 4.05 ng/ml, which results in a clinical sensitivity of 0.90 and specificity of 0.87.
KeywordsBio-magnetic nanoparticles Carcinoembryonic antigen Assay Colorectal cancer
Bio-functionalized magnetic particles are used in biomedicines. Different bio-applications require different sizes of magnetic particles. For example, because each particle is strongly magnetized, magnetic particles with micrometer diameters are useful for in-vitro extraction or purification of bio-molecules such as antibodies, proteins and nucleic acids -. Magnetic nanoparticles with sub-micrometer diameters are used to sort specific cells in vitro, -. The main reason for the use of sub-micro-particles instead of micro-particles for cell sorting is to suppress the immunological responses from cells that are bound with magnetic particles. Nano-scaled magnetic particles are mostly used for in-vivo targeting or delivery, e.g. as a contrast medium for magnetic resonance imaging, vectors for drug delivery and for hyperthermia -. In the late 1990’s, the in-vitro quantitative detection of bio-molecules using antibody functionalized magnetic nanoparticles was proposed -. This is referred to as a magnetically labeled immunoassay (MLI).
There are several types of MLI: sandwiched MLI ,,, wash-free MLI , and single-probe MLI ,,. Different types of magnetic signals are detected for various types of MLI, including, ac magnetic susceptibility , magnetic relaxation , magnetic remanence , phase lag for ac magnetization , nuclear magnetic resonance  and magnetic reduction  and these are related to the concentrations of bio-molecules that are to be detected. In addition to this academic innovation, the literature shows that MLI is a promising method for in-vitro diagnosis in clinics. Since the early part of this century, some MLI technology has been commercialized in the US , France , Germany, Sweden , Japan, China  and Taiwan . There has been continuing investment in the development, the commercialization and the marketing of MLI, worldwide.
In a MLI, bio-functionalized magnetic nanoparticles are used as labeling markers to target molecules. If a test sample has more target molecules, more magnetic nanoparticles associate with target molecules. Ideally, each magnetic nanoparticle is identical. Every nanoparticle has the same size and magnetization. Each associated magnetic nanoparticle contributes equally to the magnetic signals. If more magnetic nanoparticles associate with target molecules, the magnetic signal is greater. The magnetic signals are exactly correlated to the number of target molecules. The precession of assay target molecules is high. However, if the magnetic nanoparticles obviously differ from each other and there is a broad variation in particle size, magnetic nanoparticles of different sizes contribute differently to the magnetic signals. This results in a significant variation in the magnetic signals for a fixed number of associated magnetic nanoparticles, so the precision the assay of target molecules is poor. For a MLI, it is important that the bio-functionalized magnetic nanoparticles are uniform. For a MLI, magnetic nanoparticles are suspended in solution as a reagent. When these nanoparticles agglomerate, the binding area between the nanoparticles and the target molecules is significantly reduced, which results in a reduced sensitivity and stability for detection, so the agglomeration of nanoparticles in a reagent must be inhibited.
Other required properties for the use of suspended bio-functionalized magnetic nanoparticles as a reagent for in-vitro diagnosis in clinics are the life time, the interference, the low-detection limit, the sensitivity and the specificity. Most previous studies have focused on the development of either magnetic nanoparticles or detection methodologies, so there has been no complete study of the feasibility of the clinical use of bio-functionalized magnetic nanoparticles for in-vitro diagnosis. This study characterizes both the particle properties and the assay features of antibody functionalized magnetic nanoparticles. The target molecule is the carcinoembryonic antigen (CEA), which is the clinical bio-marker for the in-vitro diagnosis of colorectal cancer. The antibodies against CEA (anti-CEA) are immobilized on magnetic nanoparticles. Various characteristics, such as particle size, particle suspension, bio-activity and the stability of the anti-CEA functionalized magnetic nanoparticles suspended in liquid are studied. The assay method used is the so-called immunomagnetic reduction. Assaying CEA in serum allows features such as the interference, the low-detection limit, the dynamic range, the clinic sensitivity and the specificity to be determined.
Results and discussion
Stability of magnetic nanoparticle suspension
The factors that mainly affect the stability of a nanoparticle suspension in solution are the nano-size and the uniformity of the nanoparticles. If the nano-size is sufficient, the buoyancy of the nanoparticle is strong enough to cancel the gravitational force, so the nanoparticle is suspended in solution. However, for a certain magnetic nanoparticle in the reagent, there can be attractive or repulsive magnetic interactions between the magnetic nanoparticle and neighboring magnetic nanoparticles. If the magnetic nanoparticles are highly uniform, these magnetic interactions are isotropic. The resultant magnetic force that acts on this magnetic nanoparticle is zero and the magnetic interactions with these magnetic nanoparticles can be ignored. This nanoparticle is not attracted by other particles because there are no anisotropic magnetic forces. Magnetic nanoparticles do not agglomerate because of the isotropic magnetic interaction between particles, so highly uniform magnetic nanoparticles exhibit high stability in suspension in solution. The results shown in Figure 1(b) show the nano-size and the high degree of uniformity of the anti-CEA functionalized magnetic nanoparticles synthesized in this work. As a result, the CEA reagent is highly stable in a suspension in PBS solution.
Stability of magnetic nanoparticle bio-activity
In addition to the suspension stability, the other important measurement for the CEA reagent is the bio-activity during storage at 2–8°C. To measure this, the IMR signals for 5-ng/ml CEA solution were detected using the CEA reagent, during the storage period. The measurements for the storage period for the IMR signals for the 5-ng/ml CEA solution are plotted in Figure 2, using crosses. The IMR signals range from 1.67% to 1.76%, during storage at 2–8°C for nine months. There is no significant change in the IMR signal for the 5-ng/ml CEA solution during nine months of storage at 2–8°C. Therefore, the bio-activity of the CEA reagent is stable for at least nine months, if the CEA reagent is stored at 2–8°C.
Room-temperature stability of reagent
In clinics, serum is the sample that is used to assay CEA. There are many other materials in serum, besides CEA. These materials are referred as to interfering materials. Interfering materials can cause false IMR signals, because of the colors of bio-molecules or the non-specific associations between the interfering materials and antibodies on the magnetic nanoparticles. The accuracy of an assay is adversely affected if false IMR signals occur frequently, so the contributions of the interfering materials to IMR signals for the assay of CEA in serum must be determined.
Materials and concentrations used for interference tests for a CEA assay, using the IMR method
Mean IMR value(%)
Standard deviation of IMR(%)
Tegafur with uracil
The false IMR signal that is caused by interfering materials is mainly attributable to two factors: the color of the interfering materials and the non-specific associations between the interfering materials and antibodies on the magnetic nanoparticles. The detection signal used for IMR measurement is magnetic ac susceptibility, which is not affected by the colors of the samples, the reagents, or the interfering materials, so the color of the interfering materials does not cause false IMR signals to be generated.
The non-specific associations between the interfering materials and antibodies on the magnetic nanoparticles are inhibited if highly specific antibodies are used. An additional suppression mechanism is activated during IMR measurement. During the IMR measurement, the magnetic nanoparticles oscillate with the external ac magnetic fields. Both the target and other bio-molecules that are bound with antibodies on the oscillating magnetic nanoparticles experience centrifugal forces. At high oscillation frequencies, the centrifugal force is increased. If the centrifugal force is stronger than the binding force between the antibodies and non-target bio-molecules, the non-specific binding is broken, so the centrifugal force must be weaker than the specific binding force between the antibodies and the bio-molecules that are to be detected. As a result, the cross reactions are inhibited during IMR measurement. In principle, this suppression mechanism for non-specific binding between antibodies and non-target bio-molecules is independent of the concentration of the target molecules, such as CEA. A detailed discussion of this suppression mechanism is given in Ref. .
CEA-concentration dependent IMR signals
CEA concentrations, ϕ CEA , spiked in serum, for the detections of IMR signals
Mean IMR value(%)
Standard deviation of IMR(%)
Converted CEA concentration ϕCEA-IMR(ng/ml)
0.08 ± 0.07
0.24 ± 0.08
3.38 ± 0.21
5.58 ± 0.28
9.99 ± 0.43
49.49 ± 3.83
101.7 ± 15.0
482.6 ± 184.7
1269.6 ± 560
where A, B, ϕo and γ are fitting parameters. Fitting the data in Figure 4(a) to Eq. (1) gives values for these parameters of as A =1.05, B =3.22, ϕo =14.05, and γ =0.94. The fitting curve is plotted as a solid line in Figure 4(a). The coefficient of determination, R2, is 0.999.
The stability of the resulting logistic function Eq. (1) depends on the stability of the reagent. Several factors, such as the biodegradability of the antibodies on the magnetic nanoparticles, the agglomeration of the magnetic nanoparticles and the de-magnetization of the magnetic nanoparticles significantly affect the lifetime of the reagent. If these factors do not change, the characteristics of the logistic function Eq. (1) are retained.
In Figure 2, the high stability of the particles’ suspension and isolation in the reagent is demonstrated. The particle size is plotted as a function of the storage time at 2–8°C. The IMR signal for 5-ng/ml CEA solution is dependent on storage time, which demonstrates the bio-active stability of the antibodies on the magnetic nanoparticles. The magnetization of the magnetic nanoparticles does not change if the storage temperature remains lower than the Curie temperature of Fe3O4 (~585°C). The results in Figure 2 show that the factors that most greatly affect the lifetime of the reagent are unchanged, if the reagent is stored at 2–8°C for 12 months, so it is expected that the resultant logistic function Eq. (2) is stable over 12 months.
Low-detection limit of assaying serum CEA
In Eq. (1), A denotes the IMR signal as the CEA concentration approaches zero, so parameter A in Eq. (1) represents the background level for the detection of IMR signals. This non-zero background level is mainly due to the electronic noise of the IMR analyzer and the dynamic equilibrium for the association between the CEA molecules and anti-CEA on the magnetic nanoparticles. Using the 3-σ criterion, the low-detection limit for the assay of CEA in terms of the IMR signal is (1.05 + 3 × 0.014)% =1.09%, where 0.014% is the standard deviation of the IMR signals at low CEA concentrations, such as 0.1 ng/ml. Using Eq. (1), the CEA concentration that corresponds to the IMR signal of 1.09% is 0.21 ng/ml. Therefore, the low-detection limit for the assay of CEA in serum using IMR is 0.21 ng/ml. It is significant that the threshold of CEA concentration in serum for the diagnosis of colorectal cancer is 2.5 ng/ml. The IMR method allows sufficiently sensitive blood tests for the in-vitro diagnosis of colorectal cancer.
Linearity of assaying serum CEA
A careful inspection for Figure 4(a) shows that not every data point lies on the solid line. If the experimental IMR signals are used to derive the CEA concentration, using Eq. (1), the derived CEA concentrations, ϕCEA-IMR, are not exactly the same as those ϕCEA values that are shown in Table 2. It is noted that ϕCEA denotes the spiked CEA concentration in serum, but ϕCEA-IMR denotes the CEA concentration in serum, detected using the IMR method. The correlation between ϕCEA-IMR and ϕCEA is shown in Figure 4(b). Since the low-detection limit for the assay of CEA using IMR method is 0.21 ng/ml, a ϕCEA-IMR of 0.1-ng/ml CEA solution is not used in Figure 4(b). Figure 4(b) shows the linear relationship between ϕCEA-IMR and ϕCEA. If the ϕCEA-IMR values for CEA concentration ϕCEA values from 0.2 ng/ml to 1000 ng/ml are used in Figure 4(b), the slope of the ϕCEA-IMR-ϕCEA curve is 1.21 and the coefficient of determination, R2, is 0.989, as plotted with the dashed line in Figure 4(b). The US Food and Drug Administration (FDA) regulations state that the slope of the line in Figure 4(b) must be between 0.90 and 1.10. The slope of the dashed line in Figure 4(b) does not meet the requirement of the US FDA. However, if the ϕCEA-IMR for a CEA concentration ϕCEA of 1000 ng/ml is ignored, the curve for ϕCEA-IMR against ϕCEA is linear and is plotted with a solid line in Figure 4(b). The slope of this solid line is 0.97 and the coefficient of determination, R2, is 0.999. It is worthy of note that the slope of the solid line meets the requirement of the US FDA. The range of CEA concentrations used for the solid line in Figure 4(b) is from 0.2 ng/ml to 500 ng/ml, so the dynamic range of the CEA concentration for IMR assay is 500 ng/ml.
Comparison of the low-detection limit and the dynamic range of a CEA assay using commercially available kits (e.g. Siemens, Abbott, and Roche) and those for this work (denoted as this work)
Siemens/ADVIA Centuar CEA assay
0.5 - 100 ng/ml
Abbott/AXSYM system CEA assay
0.5 - 500 ng/ml
Roche/Elecsys CEA assay
0.2 - 1,000 ng/ml
0.21 - 500 ng/ml
Clinical tests for assaying serum CEA
Antibodies against carcinoembryonic antigen (CEA) are conjugated onto magnetic nanoparticles, to synthesize a magnetic reagent for the assay of CEA in serum. The reagent gives a highly stable particle suspension in pH-7.4 phosphate buffered saline (PBS) solution and CEA molecules with a highly stable bio-activity, when the reagent is stored at 2–8°C. The immunomagnetic reduction method gives a low-detection threshold for the assay of CEA is 0.21 ng/ml and the dynamic range is 500 ng/ml. There is no significant interference with the assay of CEA in serum by bio-molecules that commonly occur in serum, or by frequently used drugs or chemicals. The results for CEA concentration in 54 serum samples show that the clinical sensitivity and the specificity for the diagnosis of colorectal cancer are 0.90 and 0.87, respectively, with a threshold of 4.05 ng/ml.
Synthesis of bio-magnetic nanoparticles
The protocol for the synthesis of magnetic Fe3O4 nanoparticles is proposed by MagQu Co., Ltd . A ferrite solution containing ferrous sulphate hepta-hydrate (FeSO4⋅7H2O) and ferric chloride hexa-hydrate (FeCl3⋅6H2O) in a stoichiometric ratio of 1:2 was mixed with an equal volume of aqueous dextran, which acts as a surfactant for Fe3O4 particles dispersed in water. The mixture was heated to 70–90°C and titrated with a strong base solution, to form black Fe3O4 particles. Aggregates and excess unbound dextran were removed by centrifugation and gel filtration chromatography, to produce a highly concentrated homogeneous magnetic fluid. The reagent (MF-DEX-0060, MagQu) with the desired magnetic concentration was obtained by diluting the highly concentrated magnetic fluid with pH-7.4 phosphate buffered saline (PBS) solution. To ensure that the antibodies against carcinoembryonic antigen (CEA) for colorectal cancer, i.e. anti-CEA (AT-CEA, MagQu), bound to the dextran on the outmost shell of magnetic nanoparticles, NaIO4 solution was added into the magnetic solution to oxidize the dextran, which then creates aldehyde groups (−CHO). The dextran then reacts with anti-CEA via the linking of –CH = N-, so anti-CEA is bound covalently to dextran, as schematically shown in Figure 1(a). Unbound anti-CEA was separated from the solution by magnetic separation.
Characterizations of bio-magnetic nanoparticles
For each IMR signal measurement, 40-μl reagent and 60-μl CEA solution or sample were used.
According to Ref. , the total number of antibody functionalized magnetic nanoparticles in 1-ml, 8-mg-Fe/ml magnetic bio-reagent is roughly 1013 particles. There are averagely 6 antibodies immobilized on one magnetic nanoparticle. For IMR measurement, the used volume of reagent is 40 μl. Hence, 2.4 × 1012 anti-CEA molecules are used for each IMR test.
Preparation of standard CEA solutions
Standard CEA (Human CD66e) protein was obtained from AdD Serotec (Cat. No. PHP282). Various concentrations of CEA protein were prepared by serially diluting standard CEA protein with PBS buffer or normal free serum and the resulting solution was stored at −80°C. The concentration of CEA protein was then quantified using a spectrophotometer (NanoDrop2000; Thermo Scientific.).
Assessment of human serum CEA
24 serum samples from healthy subjects (Normal control) and 30 serum samples from patients with colorectal cancer (CRC) were used for the CEA assay. The CEA concentrations in human serum samples will be determined using the IMR signals. CRC patients were identified using either pathological evidence or an immunoassay. All of the enrolled patients provided informed consent before undergoing the procedure and this study was approved by National Taiwan University Hospital Research Ethics Committee (No.201105996RC).
This work is supported by the Ministry of Economic Affairs of Taiwan, under Grant Numbers 101-EC-17-A-17-I1-0074, 1Z970688 and 1Z0990415 (SBIR), by New Taipei City Government, under Grant Number 103049, and by the Council of Agriculture, under Grant Number 103-a5.2-08.
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