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. 2020 Jan 6;2020(1):1. doi: 10.1186/s13662-019-2438-0

Dynamics analysis of a delayed virus model with two different transmission methods and treatments

Tongqian Zhang 1, Junling Wang 1, Yuqing Li 1, Zhichao Jiang 2, Xiaofeng Han 1,
PMCID: PMC7100214  PMID: 32226454

Abstract

In this paper, a delayed virus model with two different transmission methods and treatments is investigated. This model is a time-delayed version of the model in (Zhang et al. in Comput. Math. Methods Med. 2015:758362, 2015). We show that the virus-free equilibrium is locally asymptotically stable if the basic reproduction number is smaller than one, and by regarding the time delay as a bifurcation parameter, the existence of local Hopf bifurcation is investigated. The results show that time delay can change the stability of the endemic equilibrium. Finally, we give some numerical simulations to illustrate the theoretical findings.

Keywords: Cell-to-cell transmission, Delayed virus model, Treatment, Hopf bifurcation

Introduction and model formulation

Infectious diseases are still important diseases that endanger human health [2]. Not only do some ancient infectious disease pathogens continue to mutate and change, but new pathogens are also emerging, bringing many difficulties for us to discover, diagnose, and prevent infectious diseases. Studies have shown that many diseases are caused by viruses. Of more than 4000 viruses discovered so far, more than 100 can directly threaten human health and life. For example, rabies, a zoonotic disease caused by rabies virus, can cause severe encephalitis. Because the virus invades the central nervous system, if the treatment is not taken in time, the mortality rate is almost 100%. Another example is the Ebola virus, which causes Ebola hemorrhagic fever with a mortality rate from 50% to 90%. In addition, recent research has shown that several viruses have been found to link with cancer in humans, even that can push the cell toward becoming cancerous, such as human papilloma viruses (HPVs) which are considered to be the biggest factor that causes various cancers such as cervical cancer [35], anal cancer [6, 7], and oropharyngeal cancers [8]. The sudden outbreak of the SARS virus and the Ebola virus in the past 20 years has given us a major warning that public health issues are no longer just health issues, but also an important part of national security and urban security systems.

Using mathematical models to help discover the mechanism of viral transmission to predict the development of infectious diseases has become the mainstream method for controlling and preventing infectious diseases [912]. Therefore, for over a century, lots of mathematical models have been established to explain the evolution of the free virus in a body, and mathematical analysis was implemented to explore the threshold associated with eradication and persistence of the virus; for example, [1316] studied the global dynamic behavior of HIV models, [1724] analysed the global dynamics of HBV models [2528]. A general class of models describing the process of virus invading the target cells and release of the virus due to the infected cell apoptosis has been established and analyzed by Perelson et al. [29, 30] and Nelson et al. [31] as follows:

{dxdt=Λdxαvx,dydt=αvxay,dvdt=kyuv, 1

where x, y, and v represent the concentrations of uninfected target cells, infected cells, and virus, respectively. Λ and d are the generation rate and mortality rate of uninfected target cells respectively, α is the infection rate, a is the mortality rate of infected cells, k and u are the generation rate and mortality rate of free virus respectively.

However, the above model only considers that free viruses can infect uninfected cells by direct contact with them. Recent studies have shown that virus can be transmitted directly from cell to cell by virological synapses, i.e., cell-to-cell transmission [3239]. Spouge et al. [40] built a model to characterize this phenomenon:

{dCdt=rCC(1C+I+γMCm)kIIC,dIdt=kIICμII,dMdt=μCC+μII, 2

where C, I, M represent the concentrations of uninfected cells, infected cells, and dead cells, respectively. kI is the rate constant for cell-to-cell spread, rC is the reproductive rate of uninfected cell. μI, μC are the rate constants at which uninfected or infected cells die respectively, and the term kIIC represents the cell-to-cell transmission. However, research [41] shows that there is a delay between the time an uninfected cell becomes infected and when it begins to infect other uninfected cells, then Culshaw et al. [42] improved the model by introducing a distributed delay into model (2) and got the following model:

{dCdt=rCC(t)(1C(t)+I(t)CM)kIC(t)I(t),dIdt=kItC(u)I(u)F(tu)duμII(t),

where F(u) is the delay kernel.

Lai et al. [43] proposed a model containing two different types of infection as follows:

{dTdt=rT(t)(1T(t)+αT(t)TM)β1T(t)V(t)β2T(t)T(t),dTdt=β1T(t)V(t)+β2T(t)T(t)dTT(t),dVdt=kT(t)dVV(t),

where T, T, and V are the concentrations of uninfected cells, infected cells, and free virus, respectively. β1 is the infection rate of cell-free virus transmission and β2 is the infection rate of cell-to-cell transmission. For more details on parameters, please see [43]. The authors proved that a Hopf bifurcation can occur under certain conditions. Recently, Zhang et al. [1] proposed an ordinary differential equations virus model with both two different types of infection and cure rate as follows:

{dxdt=πdx(βy+αv)x+ρy,dydt=(βy+αv)x(a+ρ)y,dvdt=kyuv, 3

where x, y, and v represent the concentrations of uninfected cells, infected cells, and free virus respectively. π is the regeneration rate of uninfected cells, d, a, u are the death rates of three kinds of cells. ρ represents the cure rate, ky is the rate at which infected cells produce free viruses. By constructing suitable Lyapunov function, the authors proved that the equilibria are globally asymptotically stable under some conditions. However, the authors did not consider the time delay in model (3). In order to understand whether the introduction of time delay or not will change the stability of the equilibria, then motivated by the works [42, 43] and based on [1], we further consider model (4) by introducing a discrete delay into model (3) as follows:

{dxdt=πdx(t)(βy(tτ)+αv(tτ))x(tτ)+ρy(t),dydt=(βy(tτ)+αv(tτ))x(tτ)(a+ρ)y(t),dvdt=ky(t)uv(t), 4

where τ is time delay. βxy is the term of cell-to-cell transmission. αvx represents cell-free virus transmission. For more details on parameters, please see [1]. Considering the biological meanings, we analyze model (4) in region A={(x,y,v)R+3|0x+yπ/λ,v0}, where λ=min{a,d}.

The paper is organized as follows. Firstly, we summarize some basic results about model (4) in Sect. 2. The local stability of the free equilibrium and Hopf bifurcation of the system are discussed in Sect. 3. We give the properties of Hopf bifurcation in Sect. 4. Finally, we perform some numerical simulations to verify the results in Sect. 5.

Some basic results

From [1], we can conclude some basic results and summarize them in the following theorem in this section.

Theorem 2.1

  • (i)

    Model (3) or (4) always has a virus-free equilibrium E0=(x0,0,0), where x0=π/d.

  • (ii)
    If R>1, model (3) or (4) has a unique endemic equilibrium E1(x,y,v), where
    x=πdR,y=πa(11R),v=kuy,
    and
    R=π(αk+βu)du(a+ρ)
    is the basic reproduction number.

Local stability of the free equilibrium and Hopf bifurcation

Theorem 3.1

For model (4), if R<1, E0is locally stable, and if R>1, then E0is unstable.

Proof

Letting X=xx0, Y=y, V=v in (4) yields

{dXdt=πd(X(t)+x0)(βY(tτ)+αV(tτ))(X(tτ)+x0)+ρY(t),dYdt=(βY(tτ)+αV(tτ))(X(tτ)+x0)(a+ρ)Y(t),dVdt=kY(t)uV(t). 5

Then linearization at the original results in a characteristic equation is as follows:

(λ+d)[λ2+(u+a+ρ)λ+(a+ρ)u+(βx0λβux0αkx0)eλτ]=0. 6

Clearly, it has a root λ=d<0. Thus we only need to analyze the distribution of roots, which determines the stability of solution of system (5) of the equation

P1(λ)+P2(λ)eλτ=0, 7

where

P1(λ)=λ2+Aλ+B,P2(λ)=Cλ+D

and

A=a+ρ+u>0,B=(a+ρ)u>0,C=βx0<0,D=(βu+αk)x0<0.

When τ=0, (7) reduces to

λ2+(A+C)λ+B+D=0. 8

Since R=(αk+βu)x0(a+ρ)u<1 implies A+C>0 and B+D>0, we know the two roots of (8) always have a negative real part. Next, we assume that equation (7) with τ0 has two pure imaginary roots ±iϖ (ϖ>0), which implies that the equation

F(ϖ)=ϖ4+(A2C22B)ϖ2+B2D2=0 9

has at least one positive solution.

Obviously, B2D2>0, then we can see that

A2C22B=(a+ρ+u)2(βx0)22(a+ρ)u=(a+ρ)2+u2(βx0)2>0,

where a+ρ>βx0 is used. Then we can conclude that when R<1, equation (9) has no positive real root, which leads to that equation (7) does not have a pure imaginary root. Thus, all the roots of (7) always have negative real parts. Therefore, E0 is locally stable. When R>1, it is easy to see B+D<0, then equation (7) has at least one positive root, thus E0 is unstable. This proof is completed. □

Next we discuss the existence of Hopf bifurcation. For this purpose, we let X=xx, Y=yy, V=vv, to shift the equilibrium to the original. Then linearization at the original results in a characteristic equation is as follows:

Δ(λ,τ)=λ3+b2λ2+b1λ+b0+(c2λ2+c1λ+c0)eλτ=0, 10

where

b0=d(a+ρ)u,b1=d(a+ρ+u)+(a+ρ)u,b2=d+a+ρ+u,c0=au(βy+αv)d(βux+αkx),c1=(u+a)(βy+αv)x(βu+αk)dβx,c2=βy+αvβx.

When τ=0, (10) reduces to

Δ(λ,0)=f(λ)=λ3+a2λ2+a1λ+a0=0,

where

a2=b2+c2=d+a+ρ+u+βy+αvβx=d+u+βy+αv+αk/ux>0,a1=b1+c1=d(a+ρ+u)+(a+ρ)u+(u+a)(βy+αv)x(βu+αk)dβx=du+(u+a)(βy+αv)+dαk/ux>0,a0=b0+c0=au(βy+αv)>0,

here (a+ρ)u=(βu+αk)x is used. And

a2a1a0=(d+u+βy+αv+αk/ux)(du+(u+a)(βy+αv)+αk/ux)au(βy+αv)=(d+βy+αv+αk/ux)(du+(u+a)(βy+αv)+αk/ux)+u(du+u(βy+αv)+αk/ux)>0.

Then all the roots of f(λ)=0 have negative real parts by using the Routh–Hurwitz criterion [44], which implies the local asymptotic stability of E for τ=0.

For τ>0, let (ω>0) be the root of (10), we get

{sinωτ=c2ω5+(b2c1b1c2c0)ω3+(b1c0b0c1)ω(c2ω2c0)2+c12ω2=P(ω),cosωτ=(c1b2c2)ω4+(b0c2+b2c0b1c1)ω2b0c0(c2ω2c0)2+c12w2=Q(ω). 11

By setting μ=ω2, we get

G(μ)=μ3+d2μ2+d1μ+d0=0, 12

where

d0=b02c02,d1=b12+2c0c22b0b2c12,d2=b222b1c22.

By the method in [45], we get the following lemmas.

Lemma 3.1

  • (i)

    If conditions b0>c0and d223d10hold, then (12) has no positive root.

  • (ii)

    If conditions b0>c0, (H1)d223d1>0, z1>0, and G(z1)<0hold, then (12) has two positive roots, where z1=d2+d223d13.

  • (iii)

    If condition b0<c0holds, then (12) has at least one positive root.

If b0>c0 and (H1) hold, suppose z1<z2, then dGdz1<0 and dGdz2>0. Substituting ωk=zk (k=1,2) into (11), we have

τk(j)={1ωk[arccos(Q(ωk))+2jπ],P(ωk)0,1ωk[2πarccos(Q(ωk))+2jπ],P(ωk)<0,j=0,1,2,. 13

Lemma 3.2

If (H1) holds, then dαdτ1<0and dαdτ2>0, where λ(τ)=α(τ)+iω(τ)is the root of (10) and α(τk(j))=0, ω(τk(j))=ωk (k=1,2; j=0,1,2,).

Proof

Substituting λ(τ) into (10), we get

[dαdτk(j)]1=3ω04+2d2ω02+d1c1ω02+(c0c2ω02)2ω02=dGdZkc1ω02+(c0c2ω02)2ω02.

Obviously, Signdαdτk(j)=SigndGdzk. Since dGdz1<0 and dGdz2>0, then we have dαdτ1<0 and dαdτ2>0. The proof is completed. □

About the existence of Hopf bifurcation, we have the following theorem.

Theorem 3.2

If R>1, b0>c0, and (H1)hold, then system (4) undergoes a Hopf bifurcation at Ewhen τ=τk(j) (k=1,2; j=0,1,2,). Furthermore, Eis stable when τ[0,τ0)and unstable when τ>τ0. τ0is the Hopf bifurcation value.

Property of Hopf bifurcation at E

From Theorem 3.2, we got the sufficient conditions for the Hopf bifurcation to appear. We assume that when τ=τ0, system (4) produces a Hopf bifurcation at E. Next by the normal form theory and the center manifold [46], we try to establish the explicit formula determining the directions, stability, and period of periodic solutions bifurcating from E at τ=τ0 and ω(τ0)=ω0.

Let ω0=ω(t0), τ=τ0+ς, ςR, then ς=0 is the Hopf bifurcation value of model (4). Let w1(t)=xx, w2(t)=yy, w3(t)=vv, then (4) becomes

{dw1dt=dw1(t)+ρw2(t)(βy+αv)w1(tτ)βxw2(tτ)αxw3(tτ)dw1dtβw1(tτ)w2(tτ)tαw1(tτ)w3(tτ),dw2dt=(a+ρ)w2(t)+(βy+αv)w1(tτ)+βxw2(tτ)+αxw3(tτ)dw2dt+βw1(tτ)w2(tτ)+αw1(tτ)w3(tτ),dw3dt=kw2(t)uw3(t). 14

Let C=C([τ,0],R3), we have

w˙t=Lςwt+F(ς,wt), 15

where wt(θ)=w(t+θ)C and Lς is given by

Lςφ=B1φ(0)+B2φ(τ0),

where φ=(φ1,φ2,φ3)T,

B1=(dρ00(a+ρ)00ku),B2=((βy+αv)βxαxβy+αvβxαx000),F(ς,wt)=(βw1(tτ)w2(tτ)αw1(tτ)w3(tτ)βw1(tτ)w2(tτ)+αw1(tτ)w3(tτ)0).

By using the Riesz representation theorem, we have a function ζ(θ,ς) such that, for φC,

Lςφ=τ00dζ(θ,ς)φ(θ),

where ζ(θ,ς) is a bounded variation function for [τ0,0]. And we can choose

ζ(θ,ς)=B1δ(θ)B2δ(θ+τ),

where

δ(θ)={1,θ=0,0,θ0.

For φC1=C([0,τ],R3), let us define

H(ς)φ={φ˙(θ),θ(τ0,0),τ00dζ(s,ς)φ(s),θ=0,

and

R(ς)φ={0,θ[τ,0),F(ς,φ),θ=0

is the nonlinear part of the right-hand side of system (15), where

F(ς,φ)=(βφ1(τ)φ2(τ)αφ1(τ)φ3(τ)βφ1(τ)φ2(τ)+αφ1(τ)φ3(τ)0).

For ψC1([0,τ0],R3) and φC([τ0,0],R3), define

Hψ(s)={ψ˙(s),s(0,τ0],τ00dζT(t,0)ψ(t),s=0,

and

ψ,φ=ψ¯(0)φ(0)τ00ξ=0θψ¯T(ξθ)dζ(θ)φ(ξ)dξ,

where ζ(θ)=ζ(θ,0). We have that H and H=H(0) are adjoint operators. Then ±iω0 are eigenvalues of H(0) when τ=τ0. Thus they are also eigenvalues of H. Also, we can get q(θ)=(1,q2,q3)eiω0θ and q(s)=D¯(1,q2,q3)eiω0s, which are the eigenvectors of H and H corresponding to iω0 and iω0, respectively, and

h2=iω0+diω0+a,h3=(iω0+a+ρβxeiω0τ0)h2(βy+αv)eiω0τ0αxeiω0τ0,q2=(iω0u)(ρ+βxeiω0τ0)kαxeiω0τ0(iω0u)[iω0(a+ρ)+βxeiω0τ0]+kαxeiω0τ0,h3=αxeiω0τ0αxeiω0τ0h2iω0u,

and

h(s),h(θ)=1,h(s),h¯(θ)=0,

where

D={1+h2h2¯+h3h3¯+τ0A}1,H=(βy+αv)eiω0τ0βxeiω0τ0h2αxeiω0τ0h3+h2¯((βy+αv)eiω0τ0+βxeiω0τ0h2+αxeiω0τ0h3).

Using the same notations as in [47], we can obtain

g20=2D(1,h2¯,h3¯)((βh2+αh3)e2iω0τ0(βh2+αh3)e2iω0τ00)=2D[(βh2+αh3)e2iω0τ0+h2¯(βh2+αh3)e2iω0τ0],g11=D(1,h2¯,h3¯)(β(h2¯+h2)α(h3¯+h3)β(h2¯+h2)+α(h3¯+h3)0)=D[β(h2¯+h2)+α(h3¯+h3)](h2¯1),g02=2D(1,h2¯,h3¯)((βh2¯+αh3¯)e2iω0τ0(βh2¯+αh3¯)e2iω0τ00)=2D(βh2¯+αh3¯)e2iω0τ0(h2¯1),g21=2D(1,h2¯,h3¯)(BC0),

where

B=β[w11(2)(τ0)eiω0τ0+12w20(2)(τ0)eiω0τ0+12w20(1)(τ0)h2¯eiω0τ0+w11(1)(τ0)h2eiω0τ0]α[w11(3)(τ0)eiω0τ0+12w20(3)(τ0)eiω0τ0+12w20(1)(τ0)h3¯eiω0τ0+w11(1)(τ0)h3eiω0τ0],C=β[w11(2)(τ0)eiω0τ0+12w20(2)(τ0)eiω0τ0+12w20(1)(τ0)h2¯eiω0τ0+w11(1)(τ0)h2eiω0τ0]+α[w11(3)(τ0)eiω0τ0+12w20(3)(τ0)eiω0τ0+12w20(1)(τ0)h3¯eiω0τ0+w11(1)(τ0)h3eiω0τ0],w20(θ)=ig20ω0h(0)eiω0θ+ig20¯3ω0h¯(0)eiω0θ+E1e2iω0θ,w11(θ)=ig11ω0h(0)eiω0θ+ig11¯ω0h¯(0)eiω0θ+E2,

with

E1=(2iω0+d+(βy+αv)e2iω0τ0βxe2iω0τ0ρdxe2iω0τ0(βy+αv)e2iω0τ02iω0+a+ρβxe2iω0τ0αxe2iω0τ00k2iω0+u)1×((βh2+αh3)e2iω0τ0(βh2+αh3)e2iω0τ00),

and

E2=(d(βy+αv)ρβxαxβy+αvβx(a+ρ)αx0ku)1(β(h2¯+h2)+α(h3¯+h3)β(h2¯+h2)α(h3¯+h3)0).

By substituting E1 and E2 into W20(θ) and W11(θ), respectively, g21 can be expressed by the parameters. Then each gij can be determined by the parameters. Therefore we get the following expression:

C1(0)=i2ω0(g20g112|g11|213|g02|2)+g212,μ2=Re{C1(0)}Reλ(τ0),T2=Im{C1(0)}+μ2Imλ(τ0)ω0,β2=2Re{C1(0)}.

Thus, we have from [47] the following theorem.

Theorem 4.1

  • (i)

    μ2determines the direction of Hopf bifurcation. If μ2>0 (<0), then Hopf bifurcation is supercritical (subcritical).

  • (ii)

    β2determines the stability of the bifurcated periodic solutions. If β2<0 (>0), then the bifurcated periodic solutions are orbitally stable (unstable).

  • (iii)

    T2determines the period of the bifurcated periodic solutions. If T2>0 (<0), then the period increases (decreases).

Conclusion and numerical simulations

In this paper, we have mainly considered the effect of time delay on the dynamics of a virus model with two different transmission methods and treatments. Our results show that the introduction of time delay has a significant effect on the dynamics of the system. However, it can be seen from [1] that when there is no time delay in system (3), the positive equilibrium E of system (3) is asymptotically stable if it exists. The appearance of the time delay causes the positive equilibrium of the model (4) to be inverted from stable to unstable, and a periodic solution of small amplitude is generated near the positive equilibrium E. Biologically, the number of healthy, infected, and free viruses exhibits periodic changes.

Next, we take some numerical simulations to validate our main results. We set the basic parameters as follows [48]: d=0.2, β=0.000024, α=0.000024, ρ=0.2, a=0.15, k=150, u=0.2. Firstly, we set π=2, direct calculations with Maple 14 show that R=0.514971<1 and E0=(10,0,0). By Theorem 3.1 the virus-free equilibrium E0 of the system is stable (see Figs. 14). Next, we change π to 10, direct calculations show that R=2.574857>1, then system (4) has two equilibria, i.e., the virus-free equilibrium E0=(50,0,0) and the virus equilibrium E=(19.4186,40.7753,30581.4470). It is easy to see that

b0=0.0140,c0=0.008048,G(0)=d0=b02c02=0.000131>0,Δ=0.148921>0,z1=0.240948,G(z1)=0.008284<0,

then equation (12) has two positive roots z1=0.0089 and z2=0.3680, and equation (11) has two positive roots ϖ1=0.09441603258 and ϖ2=0.6066529567. Therefore we have the Hopf bifurcation value τ20=3.828340005.

Figure 2.

Figure 2

Time series for y(t) with the initial value (19,40,30581), where R=0.514971<1

Figure 3.

Figure 3

Time series for v(t) with the initial value (19,40,30581), where R=0.514971<1

Figure 1.

Figure 1

Time series for x(t) with the initial value (19,40,30581), where R=0.514971<1

Figure 4.

Figure 4

3D phase for x(t), y(t), and v(t) with the initial value (19,40,30581), where R=0.514971<1

If we set τ=3.8<3.828340005, by Theorem 3.2, the virus equilibrium E is asymptotically stable (see Figs. 58). If we set τ=3.9>3.828340005, by Theorem 3.2, the virus equilibrium E is unstable and periodic oscillations occur (see Figs. 916 with different initial values).

Figure 6.

Figure 6

Time series for y(t) with the initial value (19,40,30581), where R=2.574857>1

Figure 7.

Figure 7

Time series for v(t) with the initial value (19,40,30581), where R=2.574857>1

Figure 10.

Figure 10

Time series for y(t) with the initial value (19,40,30581), where R=2.574857>1, τ=3.8<τ20

Figure 11.

Figure 11

Time series for v(t) with the initial value (19,40,30581), where R=2.574857>1, τ=3.8<τ20

Figure 12.

Figure 12

3D phase for x(t), y(t), and v(t) with the initial value (19,40,30581), where R=2.574857>1, τ=3.8<τ20

Figure 13.

Figure 13

Time series for x(t) with the initial value (30,75,29000), where R=2.574857>1, τ=3.9>τ20

Figure 14.

Figure 14

Time series for y(t) with the initial value (30,75,29000), where R=2.574857>1, τ=3.9>τ20

Figure 15.

Figure 15

Time series for v(t) with the initial value (30,75,29000), where R=2.574857>1, τ=3.9>τ20

Figure 5.

Figure 5

Time series for x(t) with the initial value (19,40,30581), where R=2.574857>1

Figure 8.

Figure 8

3D phase for x(t), y(t), and v(t) with the initial value (19,40,30581), where R=2.574857>1

Figure 9.

Figure 9

Time series for x(t) with the initial value (19,40,30581), where R=2.574857>1, τ=3.8<τ20

Figure 16.

Figure 16

3D phase for x(t), y(t), and v(t) with the initial value (30,75,29000), where R=2.574857>1, τ=3.9>τ20

Availability of data and materials

Data sharing not applicable to this article as all data sets are hypothetical during the current study.

Authors’ contributions

All authors read and approved the final manuscript.

Funding

Z.C. Jiang was supported by the National Natural Science Foundation of China (Nos. 11801014 and 11875001), the Natural Science Foundation of Hebei Province (No. A2018409004), Hebei province university discipline top talent selection and training program (SLRC2019020), and Talent Training Project of Hebei Province.

Competing interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Footnotes

Publisher’s Note

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Contributor Information

Tongqian Zhang, Email: zhangtongqian@sdust.edu.cn.

Junling Wang, Email: junlingwang@sdust.edu.cn.

Yuqing Li, Email: l_yq_i@126.com.

Zhichao Jiang, Email: jzhsuper@163.com.

Xiaofeng Han, Email: hanxiaofeng@sdust.edu.cn.

References

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