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Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2023 Apr 20;3:100179. doi: 10.1016/j.health.2023.100179

A caputo fractional order epidemic model for evaluating the effectiveness of high-risk quarantine and vaccination strategies on the spread of COVID-19

Morufu Oyedunsi Olayiwola 1, Adedapo Ismaila Alaje 1,, Akeem Yunus Olarewaju 1, Kamilu Adewale Adedokun 1
PMCID: PMC10118058  PMID: 37101804

Abstract

The recent global Coronavirus disease (COVID-19) threat to the human race requires research on preventing its reemergence without affecting socio-economic factors. This study proposes a fractional-order mathematical model to analyze the impact of high-risk quarantine and vaccination on COVID-19 transmission. The proposed model is used to analyze real-life COVID-19 data to develop and analyze the solutions and their feasibilities. Numerical simulations study the high-risk quarantine and vaccination strategies and show that both strategies effectively reduce the virus prevalence, but their combined application is more effective. We also demonstrate that their effectiveness varies with the volatile rate of change in the system’s distribution. The results are analyzed using Caputo fractional order and presented graphically and extensively analyzed to highlight potent ways of curbing the virus.

Keywords: Caputo-derivative, Laplace Adomian decomposition method, Homotopy perturbation method, COVID-19, High-risk quarantine, Vaccination

1. Introduction

In accordance with a report on global health crises by the World Health Organization (WHO) [1], COVID-19 is caused by the SARS-CoV-2 virus and has had a substantial impact on public health, healthcare systems, and the global economy [2]. The virus is highly infectious and is mainly transmitted through respiratory droplets, resulting in a pandemic that has affected millions of individuals worldwide [2]. COVID-19 can manifest a variety of symptoms, ranging from mild flu-like symptoms to severe respiratory illness and even death [3]. Preventive measures such as wearing of masks, practicing physical distancing, and frequently washing of hands [4] are critical to enhance prevention of the virus’s spread. Moreover, individuals with underlying health conditions such as diabetes, hypertension, and obesity are at greater risk of severe illness and death from COVID-19 [5]. It is, therefore, essential to safeguard vulnerable populations and provide appropriate medical care. It has also been observed that people who initially have mild symptoms of COVID-19 can as well develop long-term health complications, which include chronic fatigue, respiratory issues, and neurological problems. Consequently, ongoing medical care and monitoring of individuals who have recovered from COVID-19 are necessary.

Currently, COVID-19 vaccines are crucial tools in the fight against the ongoing pandemic caused by the SARS-CoV-2 virus [6]. Since the first COVID-19 case was reported in late 2019 [7], researchers and scientists worldwide have been working tirelessly to develop and distribute effective vaccines [8]. As at March 2023, several authorized COVID-19 vaccines have been made available, these include Pfizer-BioNTech, Moderna, Johnson & Johnson, AstraZeneca, Sinovac, and Sinopharm. These vaccines work by activating the body’s immune system to recognize and fight the SARS-CoV-2 virus if exposed [8]. Most COVID-19 vaccines require two doses, spaced several weeks apart, to achieve maximum effectiveness, while some vaccines, such as those from Johnson & Johnson, only require a single dose [9].

Clinical trials have demonstrated that COVID-19 vaccines are highly effective in preventing severe illness, hospitalization, and death from COVID-19. For instance, the Pfizer-BioNTech vaccine has shown over 90% effectiveness in preventing COVID-19 infection, while the Moderna vaccine has shown over 95% effectiveness. Johnson & Johnson vaccine has also been shown to be highly effective in preventing severe illness, hospitalization, and death [9]. Despite the high efficacy rate of COVID-19 vaccines, concerns and misconceptions regarding their safety and effectiveness still exist. Some individuals are hesitant to receive vaccinations because of concerns about side effects, the pace of development, or the vaccines’ unknown long-term effects. However, it is important to note that COVID-19 vaccines have undergone rigorous safety testing and extensive clinical trials before receiving authorization for emergency use [10]. The pace of development was a result of unprecedented global collaboration and funding, not because of shortcuts in safety testing. Adverse effects are generally mild and short-lived, such as soreness at the injection site, fever, and fatigue, with severe allergic reactions observed to be rare. Getting vaccinated against COVID-19 is a vital step in protecting oneself, loved ones, and the community from the virus. Even after vaccination, it is essential to continue practicing preventive measures such as wearing of masks, practicing physical distancing, and washing hands frequently. Vaccination is not only a personal decision but also a community responsibility in order to achieve herd immunity and end the pandemic [11].

2. Literature review

Researchers and mathematicians utilize mathematical modeling to study the transmission dynamics of infectious diseases [12]. These models can be stochastic or deterministic, and various types, including compartmental, individual-based, and network models, have been explored [13]. The benefits and drawbacks of each model type, such as the difficulty of fitting models to data and interpreting model results, have been discussed [14]. Furthermore, researchers have studied the transmission and control of COVID-19 using these mathematical models, considering within-host dynamics and between-host transmission [15]. For example, a conceptual study of the concurrent application of therapy, vaccine, and human compliance to physical limitation using a five-compartment model of coronavirus disease was conducted [16]. Additionally, an analysis of the effect of vaccination in controlling the spread of COVID-19 was studied in [17], where vaccination was shown to be an effective criterion to enable the disease to cease in the system. Recently, research developments in epidemiology have witnessed an array of applications of fractional derivatives, which generalize the standard concepts of classical derivatives and have helped researchers understand related volatile changes [18], [19], [20]. In [21], it was discussed that the effectiveness of vaccination depends not only on the vaccine itself but also on the distribution of the vaccine and the population’s response to it. Thus, several researchers often extend the use of fractional derivatives such as [22], [23], [24], [25], [26] to model the dynamics of vaccination, taking into account factors such as the rate of vaccine distribution and the rate of vaccine uptake. For example, the Caputo derivative was applied in a mathematical analysis of a coronavirus disease model in [27] to examine the dynamic reaction of the population group to vaccine uptake and distribution. The fractional-order derivative proved vital as the dynamics of each class of the population were effectively modeled using some fitted data. Apart from vaccination, high-risk immunity is another factor often considered during the eradication of diseases and refers to the quarantine of individuals who are at higher risk of contracting the disease, such as susceptible people living in infected zones, the elderly, and individuals with pre-existing medical conditions [28]. Several studies have been published on predicting COVID-19’s trajectory in the presence of high-risk immunity. A study of the effect of quarantine on the transmission of COVID-19 through a systematic review and meta-analysis was conducted in [29]. Their study, from an epidemiological point of view, analyzed quarantine strategies applicable to both travelers and contacts based on a test-and-release protocol. It was shown that through high-risk quarantine, fewer people in the population are liable to get infected by COVID-19.

Since the dynamics, behaviors, and trends of diseases in physical systems can be gained through numerical simulation, the use of computational algorithms to approximate solutions to mathematical models that describe a wide range of phenomena, such as the homotopy perturbation method, has proved powerful because it often yields good convergent simulation results [30], [31], [32], [33], [34]. For example, an analysis of the effect of two-stage vaccination was studied in [18], and the simulation process was carried out using the precise approximate results generated by the homotopy perturbation method. Their results successfully revealed the effectiveness of the method. Additionally, numerical methods such as the Laplace-Adomian decomposition method have been widely used by researchers to solve nonlinear problems involving complex geometries and initial conditions. Some studies on this can be found in [35], [36], [37], [38], [39], [40], and as evidenced in [41], where the dynamics of Lassa fever transmission were studied using the Laplace-Adomian decomposition method, the method equally produced effective simulation results that shed light on ways of curbing the virus.

The significance of vaccines and high-risk immunity in limiting the spread of COVID-19 has been emphasized by several literature sources. However, the combined effect of these two factors in the event of a re-emergence has not been examined by researchers. This study aims to fill this gap by evaluating the effectiveness of vaccine uptake, vaccine distribution, and high-risk quarantine strategies in preventing the spread of the virus. Our motivation for providing an alternative strategy for curbing the spread of COVID-19 virus in Nigeria stems from the tension and damages caused by the last pandemic on the country’s healthcare system. To achieve this goal, a mathematical model of COVID-19 is proposed, taking into account high-risk quarantine, vaccination parameters, and Caputo derivatives. The Laplace-Adomian decomposition method is employed to simulate the results of this model numerically using reported data from the Nigeria Centre for Disease Control. Therefore, the study seeks to identify effective methods of reducing virus transmission and protecting high-risk individuals to achieve herd immunity in the system.

In summary, the main objective of this study is to offer new perspectives on the effectiveness of combining vaccines and high-risk immunity to mitigate the spread of COVID-19 in Nigeria, making it a distinct research endeavor. The study plans to accomplish this by utilizing a mathematical model and numerical simulations to fill the existing research gap and provide valuable information to inform public health strategies for managing the virus in Nigeria.

Preliminaries

We discuss some essential ideas of fractional calculus applicable in this study here.

Definition 1 [42]

A real function ψ(x), for x>0, exists in the space δν,νR if a real number k>ν exists such that ψ(x)=xkψ1(x).  Where ψ1(x)δ(0,), and ψ(x) is said to exists in space δvα if and only if ψαδν,αN.

Definition 2 [42]

The Riemann–Liouville fractional integration of order γ0 for a real positive function ψ(x)δν,ν1x>0 is defined as:

Iγψ(x)=1Γ(γ)0x(tx)γ1ψ(t)dt.

The Riemann–Liouville fractional integral operator Iγ for ψ(x)δν,ν1γ,α0 and β1 satisfies the following properties:

1.IγIαψ(x)=Iγ+αψ(x),2.IγIαψ(x)=IαIγψ(x),3.Iγtβ=Γ(β+1)Γ(γ+β+1)tγ+β.

Definition 3 [42]

For a positively defined real function ψ(x)δν, the Caputo fractional derivative can mathematically be expressed as;

Dγψ(x)=1Γ(αγ)0x(xt)αγ1ψα(t)dt,α1<γα,αN.

The fractional order integral operator of Caputo derivative for α1<γα,   αN,ψδ1α,   ν1 is :

IγDγψ(x)=ψ(x)m=0α1ψm(0)tmm!.

Definition 4 [41]

Let φ(t) be a function defined for all positive real number t0

  • i

    The Laplace transform of φ(t) is the function φ(s): φ(s)=0estφ(t)dt

  • ii
    The Laplace transform of function φ(t) with order η is defined as
    L[φη(t)]=αηL[φ(t)]αη1φ(0)αη2φ(0)αη3φ(0)
  • iii

    The inverse Laplace transform of φ(s)s is L1φ(s)s=0tφ(t)dt

  • iv
    The Laplace transform of f(t)=tλ is L(tλ)=Γ(λ+1)sλ+1, and the inverse transform is
    L11sλ+1=tλΓ(λ+1)

Definition 5 [41]

The Adomian polynomials denoted by A0,A1,.An, consists in the decomposition of the unknown function y(t) whose series can be expressed as y(t)=y0+y1+y2+yn is given as:

An=1ndndλnG(t)j=0nyjλjλ=0

3. Methods

This section outlines the methodology flowchart and algorithm utilized for solving the proposed COVID-19 epidemic model. The two methods employed for this purpose are the Laplace Adomian decomposition method and the homotopy perturbation method (see Fig. 1).

Fig. 1.

Fig. 1

Flowchart of the methodology.

3.1. Laplace-Adomian decomposition method

Consider the following nonlinear coupled fractional order differential equation [41]

tcDαfk(t)=Lk(f1,f2,f3,,fk)+Nk(f1,f2,f3,,fk), (1)

subject to

ykik(0)=cik, for k=1,2,3m, and nk1αnk.

where tcDαfk(t) is the Caputo-derivative of k numbers of some unknown functions f(t), Lk and Nk respectively represents the linear and nonlinear operators.

In view of applying the Laplace-Adomian decomposition method to obtain the solution of system (1), we initiate the algorithm by first taking the Laplace transform of (1):

LtcDαfk(t)=LLk(f1,f2,f3,,fk)+Nk(f1,f2,f3,,fk). (2)

By Definition 4, Eq. (2) yields:

SαkLfk(t)i=0m1Sαki1cik=LLk(f1,f2,f3,,fk)+Nk(f1,f2,f3,,fk). (3)

Applying the Adomian decomposition method, the unknown functions fk(t) is decomposed as:

fk(t)=j=0fkj(t),k=1,2,3,m, (4)

and the nonlinear terms

Nk(f1,,fm)=j=0Akj(t),k=1,2,,m. (5)

where Akj is the Adomian polynomial defined in Definition 5. Thus evaluating (3) with (4), (5) yields:

Lj=0fkj(t)=1Sαki=0m1Sαki1cik+1SαkLLkj=0f1j(t),,j=0fmj(t)+1SαkLj=0Akj(t). (6)

Next, we utilize the linearity property of the Laplace transform and establish a recursive formula as follows:

Lfk0=1sαkj=0m1Sαki1cik,k=1,2,3,m,

and

Lfk(j+1)(t)=1sαkLLkj=0f1j(t),,j=0fmj(t)+1SαkLj=0Akj(t). (7)

Taking the inverse Laplace transform of both sides yields f1j,f2j,,fn,j,j0 such that

fk0(t)=L11sαkj=0m1Sαki1cik,k=1,2,3,m, (8)

and

fk(j+1)(t)=L11sαkLLkj=0f1j(t),,j=0fmj(t)+1SαkLj=0Akj(t). (9)

3.2. Homotopy perturbation method

To extend the theory of HPM to (17), consider a general coupled differential equation of Caputo fractional order α defined as:

cdSiα1(t)dtα1=f(t,S1,S2,S3,,Sn)iN (10)

A homotopy can be constructed for (10), such that

1pcdSiα1(t)dtα1pcdSiα1(t)dtα1f(t,S1,S2,S3,,Sn)=0,iN. (11)

Eq. (11) can be simplified such that

cdSiα1(t)dtα1=pf(t,S1,S2,S3,,Sn), (12)

where p(0,1) is an embedding parameter. At p=0, Eq. (12) becomes linear such that the following equation is obtained:

cdSiα1(t)dtα1=0. (13)

At p=1, the original equation in (12) is obtained. Let assume a solution series embedding the parameter p for (10) such that

Si(t)=si0+psi1+p2si2+p3si3,,pnsin, (14)

substituting (14) into (12) and comparing the coefficients of equal powers of p, the following series of equations is obtained;

p0::cdSi0α1(t)dtα1=0p1:cdSi2α1(t)dtα1=fi1(t,s10,s20,s30,,sn0),p2:cdSi3α1(t)dtα1=fi2(t,s10,s20,s30,,sn0,s11,s21,s31,,sn1), (15)

and so on. In turn, these systems of equation in (15) can be solved by applying the Riemann–Liouville fractional integral operator Iα1 to obtain the values of si1(t),si2(t),si3(t) Thus, the solution of (10) is obtained as:

SiN(t)=k=0N1sik(t). (16)

4. Model formulation, description and analysis

The proposed mathematical model represents the transmission dynamics of COVID-19 in a physical system, the classes of the model includes S(t) which are the susceptible individuals, exposed individuals E(t), infected people of the population I(t), and the recovered population R(t). We introduced parameter c which measures the vaccination rate of susceptible individuals living in infected zone given by c=τSN, where τ is the vaccination rate, S is the susceptible population and N is the total population. The immunization of vulnerable persons is represented by parameter ρ, and conceptually we agree with [6] by assuming that all susceptible people including the current and newly recruited members of the class are administered vaccine in order to fully examine its influence on the disease prevalence. The described dynamics is represented by the following flow diagram (see Fig. 2):

Fig. 2.

Fig. 2

Schematic diagram of the proposed model.

The system of non-linear, fractional-order ordinary differential equations that follows is the proposed model’s dynamics (see Table 2).

cdα1S(t)dtα1=Λβ(1c)S(t)I(t)(μ+ρ)S(t)cdα2E(t)dtα2=β(1c)S(t)I(t)(μ+ɛ)E(t)cdα3I(t)dtα3=ɛE(t)(μ+γ+d)I(t)cdα3R(t)dtα3=γI(t)μR(t)+ρS(t) (17)

Table 2.

Values of the model’s parameters and references.

Parameters Value References
Λ 750day1 [43]
β 0.0000124day1 [43]
σ 0.010939586day1 [43]
γ 4.013000000×108day1 [43]
θ 0.0766169day1 [43]
μ 0.001466848day1 [43]
c 0.05
ρ 0.05

4.1. Model analysis

In this section, we shall conduct the qualitative analysis of the mathematical model, and we shall do this in an integer order α=1 to fully study the properties of the mathematical model and show its potential for real-life applications.

4.1.1. Existence and uniqueness of solution

Theorem 1

Let

m1=f1(s1,s2,s3,,sn,t),s1(t0)=s10,m2=f2(s1,s2,s3,,sn,t),s2(t0)=s20,m3=f3(s1,s2,s3,,sn,t),s3(t0)=s30,.mk=fn(s1,s2,s3,,sn,t),sk(t0)=sk0.

Suppose D exist in domain of (k+1) dimensional space for time t and space x and the partial derivative fsi where i=1,2,3,....n are continuous in D={(s,t):tt0a,ss0b} then there exist a constant ɛ0 such that a unique solution exists for continuous vector. m=[s1(t),s2(t),s3(t)sk(t)] in the interval tt0ɛ

Proof

A Lipchitz criterion will be employed to ensure that the solution exists and is unique. Thus from Eq. (17), let:

m1=Λμ+ρSβ1cSI,m2=1cβSI(μ+ɛ)E,m3=ɛEγ+μ+dI,m4=γIμR+ρS. (18)

Following the criterion, we obtain the system’s partial derivatives.

The partial derivatives of m1=Λμ+ρSβ1cSI with respect to the classes yields:

|m1S|=|μ+ρ|<,|m1E|=|0|<,|m1I|=|β1cS|<,|m1R|=|0|<.

Similarly for m2=1cβSI(μ+ɛ)E we obtain:

|m2S|=|1cβI|<,|m2E|=|(ɛ+μ)|<,|m2I|=|1cβS|<,|m2R|=|0|<.

For m3=ɛEγ+μ+dI,

|m3S|=|0|<,|m3E|=|ɛ|<,|m3I|=|μ+γ+d|<,|m3R|=|0|<.

For m4S=γIμR+ρS,

|m4S|=|ρ|<,|m4E|=|0|<|m4I|=|γ|<,|m4R|=|μ|<.

The partial derivatives of these functions exist and are continuous and bounded; therefore, system (18) exists and has a unique solution in 5.

4.1.2. Positivity of invariant region

The feasible domain for the stability of solution of an epidemiological model is the invariant region. At an increasing time t0, we prove that the region covered by the model solution remain positively invariant. Thus, let the total human population be:

N(t)=S(t)+E(t)+I(t)+R(t). Since the human population varies throughout time, therefore:

dNdt=dSdt+dEdt+dIdt+dRdt.

Which yields:

dNdt=Λμ(S+E+I+R) (19)
Theorem 2

The resulting solutions provided analytically for Eq. (17) are feasible in Π for t0 .

Proof

Let D=S,E,I,R4 contains the solution of (17) for S(t),E(t),I(t),R(t)0, assume that the population is devoid of infection, then E, I, and Q are set to zero:

dNdt=ΛμN,

and

dNdtΛμN. (20)

Separating the variables and integrating both sides of Eq. (20) yields:

1μlin(ΛμN)t. (21)

Such that

lin(ΛμN)μt.

Thus, solving for the total human population N in (21),

Λ=μN+eμt.
As t we have NΛμ. (22)

This implies that the suggested model in (17) may be investigated in the viable zone

Π=S,E,I,R4:NΛμ.

4.1.3. Non-negativity of solution

Theorem 3

Given S>0,E>0,I>0,R>0 , then the solutions S,E,I,R4:NΛμ are positively invariant for t0 .

Proof

From Eq. (17),

dS(t)dtμ+ρ+β(1c)IS(t).

Separating the variables,

dS(t)S(t)(μ+ρ+β(1c)I)dt.

Integrating both sides and applying the initial conditions,

S(t)s0eμ+ρ+β(1c)It0. This indicates that S(t)>0 for all t0.

Following the same procedure, we demonstrate the positivity of the other classes.

E(t)e0e(μ+ɛ)t0,I(t)i0eμ+d+γt0.,R(t)R0eμt0.

Thus S(t),E(t),I(t),R(t)>0,t0inS(t),E(t),I(t),R(t)4;and NΛμ.

The solutions are positive and this completes the proof.

After satisfying all of the fundamental requirements for an epidemiology model, we conclude that the suggested model is appropriate for studying the dynamics of COVID-19 in the general population.

4.2. Equilibrium analysis

4.2.1. Disease free equilibrium

At disease free equilibrium, there is no infection in the system. Thus, E=I=0. Thus, concurrently solving for S,E,I,R at these points, the disease free threshold of the model class are.

S=Λμ+ρ,E=0,I=0,R=Λρ(μ+ρ)μ

4.2.2. Endemic equilibrium points

At these point, there is transmission of infection in the system. Hence, EI0 and the following thresholds are obtained.

S=(μ+ɛ)(γ+μ+d)β(1c)ɛ,E=β(1c)ɛΛ(μ+ρ)(μ+ɛ)(γ+μ+d)β(1c)ɛ(μ+ɛ)ɛ,I=β(1c)ɛΛ(μ+ρ)(μ+ɛ)(γ+μ+d)β(1c)(μ+ɛ)(μ+γ+d),R=β(1c)ɛ2Λγ(μ+ρ)(μ+ɛ)(γ+μ+d)ɛγ+(μ+ɛ)2(γ+μ+d)2ρβ(1c)(μ+ɛ)(γ+μ+d)ɛμ. (23)

4.3. Basic reproduction number

The reproduction ratio of the SEIR model is associated with the reproductive power of the disease and is defined by R0=ρ(G) where ρ is the spectral radius of the next generation matrix G=FV1.

The basic reproductive ratio of the model equation (1) at disease free equilibrium point is obtained as:

R0=βΛ(1c)ɛ(μ+ρ)(μ+ɛ)(μ+γ+d)

Remark

If R0<1 the disease will cease to exist in the system and if R0>1, epidemic will occur.

Without the implementation of the control parameter, the ratio is evaluated as R0=35.74811197, which is large and can cause rapid progression of the disease in the system; thus, we investigate the effect of raising the levels of the two introduced mitigating factors on R0 (see Table 3).

Table 3.

Response of R0 to control parameters.

c,ρ R0
0 35.74811197
0.03 1.616378873
0.06 0.80188346895
0.09 0.5216772740

4.4. Stability analysis

We shall study the stability of the model equilibrium points by finding the eigenvalues of the Jacobian matrix of system (1)

Definition 6

The equilibrium point v¯ is stable if the reproductive ratio R0 is positive and the following are true R<R0 an r on the interval 0<r<R such that v(0) is inside S(v¯,R), whenever v¯(t) is inside S(v¯,R) t>0

Definition 7

An equilibrium point v¯ is unstable if it is not stable. Thus v¯ is unstable R0>0 for which the following is true. For every R<R0 there exist r on 0<r<R, such that v(0) is inside S(v¯,R) when v¯(t) is inside S(v¯,R) t>0.

Lemma 1

The model’s disease-free equilibrium is locally asymptotically stable if R0<1 and unstable if R0>1 .

Proof

For brevity, let β(1c)=A,(μ+ρ)=D,(μ+ɛ)=F,(μ+γ+d)=G in Eq. (1). Thus the Jacobian of Eq. (1) after evaluation at the disease free equilibrium points yields:

J1=D0ΛAD00FΛA00ɛG0ρ0γμ (24)

and the eigenvalues of the matrices are obtained as:

λ1=D,
λ2=μ
λ3=12DF+DG+4ADΛɛ+D2F22D2FG+D2G2D
λ4=12DF+DG4ADΛɛ+D2F22D2FG+D2G2D

Remark

The disease-free equilibrium is locally asymptotically stable since all eigenvalues are negative.

5. Numerical solution

By means of qualitative analysis, we have verified the uniqueness and existence of the solution to the model and its suitability for addressing physical problems. Thus, we proceed with the application of the methodology outlined in Section 4 to numerically compute the solution of the Caputo derivative mathematical model through the utilization of the Laplace-Adomian decomposition method and the homotopy perturbation method.

5.1. The homotopy perturbation method

Following the iterative scheme of the homotopy perturbation method described in the methodology section, we can construct a homotopy for (1):

cdα1S(t)dtα1=p(Λβ(1c)S(t)I(t)(μ+ρ)S(t)),cdα2E(t)dtα2=pβ(1c)S(t)I(t)(μ+ɛ)E(t),cdα3I(t)dtα3=pɛE(t)(μ+γ+d)I(t),cdα3R(t)dtα3=pγI(t)μR(t)+ρS(t). (25)

We assume the following series results for the system state variables:

S(t)=s0(t)+ps1(t)+p2s2(t)+pnsn(t),E(t)=e0(t)+pe1(t)+p2e2(t)+pnen(t),I(t)=i0(t)+pi1(t)+p2i2(t)+pnin(t),R(t)=r0(t)+pr1(t)+p2r2(t)+pnrn(t). (26)

Eq. (17) is evaluated with (18), and the coefficients of pn are compared such that for

p0:cdα1s0(t)dtα1=0,cdα1e0(t)dtα1=0,cdα1i0(t)dtα1=0,cdα1r0(t)dtα1=0.

Applying operator Iα1, the following initial approximations are obtained:

s(t)=s0,e(t)=e0,i(t)=i0,r(t)=r0.

Also, the coefficient of p1

cdα1s1(t)dtα1=p(Λβ(1c)s0(t)i0(t)(μ+ρ)s0(t))cdα2e1(t)dtα2=pβ(1c)s0(t)i0(t)(μ+ɛ)e0(t)cdα3i1(t)dtα3=pɛs0(t)(μ+γ+d)i0(t)cdα3r1(t)dtα3=pγi0(t)μr0(t)+ρs0(t) (27)

The Riemann–Liouville integral operator Iα1 is equally applied on (19) to give the first approximation results which yields:

s1(t)=(Λβ(1c)s0(t)i0(t)(μ+ρ)s0(t))tα1Γα1+1,e1(t)=β(1c)s0(t)i0(t)(μ+ɛ)e0(t)tα2Γα2+1,i1(t)=ɛs0(t)(μ+γ+d)i0(t)tα3Γα3+1,r1(t)=γi0(t)μr0(t)+ρs0(t)tα4Γα4+1. (28)

After computing the second approximation, the following solutions are equally obtained:

s2(t)=β2c2i022β2ci02s0+β2i02s02βcμi0s02βcρi0s0+Λβci0+2βρi0s0Λβi0+μ2s0+2μρs0+ρ2s0ΛμΛρt2α1Γ(2α1+1)βs0(cdi0cɛe0+cγi0+cμi0di0+ɛe0γi0μi0)tα1+α3Γ(α1+α3+1),
e2(t)=β2c2i022β2ci02s0+β2i02s0βcμi0s0βcρis0+βΛc+βρs0Λβ+μβs0tα1+α2Γ(α1+α2+1)βcs0ɛi0+μ2e0+βcμ0i0s0βci0ɛe0e0ɛ2+2ɛμe0×t2α13Γ(2α1+1)+βs0cdi0βs0cɛe0+βs0cγi0+βs0cμi0βs0di0+βs0e0ɛ+βs0γi0βs0μi0tα2+α3Γ(α2+α3+1),
i2(t)=ɛβci0s0+ɛβi0s0ɛ2e0ɛμe0tα2+α3Γ(α2+α3+1)d2i0dɛe0+2dγi0+2dμi0ɛe0γ+ɛe0μ+γ2i0+2γμi0+μ2i0t2α3Γ(2α3+1),
r2(t)=γdi0+γɛe0γ2i0μγi0tα4+α3Γ(α4+α3+1)μγi0μr0+ρμs0t2α4Γ(2α4+1)+ρβci0s0ρβi0s0ρμs0ρ3s0+Λρtα4+α4Γ(α4+α1+1).

The third iteration was equally computed using MATHEMATICA 12 software package, and the approximate solution of each class is obtained by adding the iterative solutions:

S(t)=n=03sn(t),C(t)=n=03cn(t).I(t)=n=03in(t),
R(t)=n=03rn(t),Q(t)=n=03qn(t)

5.2. The Laplace Adomian decomposition method

Again, the iterative scheme of the Laplace-Adomian decomposition method will be applied to obtain the model’s solution. Thus, following the algorithm of the method as described in the methodology,

cDα1S(t)=ΛμS(t)βS(t)I(t)(1c)ρS(t),cDα2E(t)=βS(t)I(t)(1c)(μ+ɛ)E(t),cDα3I(t)=ɛE(t)(γ+μ+d)I(t),cDα4R(t)=γI(t)μR(t)+ρS(t). (29)

Subject to initial conditions e0(t)=s0,e0(t)=e0,i0(t)=i0,r0(t)=r0.

We initiate the process by taking the Laplace transforms of class of the system such that

L{cDα1S(t)}=L{Λ}L{μS(t)βS(t)I(t)(1c)ρS(t)},L{cDα2E(t)}=L{βS(t)I(t)(1c)(μ+ɛ)E(t)},L{cDα3I(t)}=L{ɛE(t)(γ+μ+d)I(t)},L{cDα5R(t)}=L{γI(t)μR(t)+ρS(t)}. (30)

Applying Definition (4) on (30) yields

α1LS(t)α11S(0)=L{Λ}L{μS(t)βS(t)I(t)(1c)ρS(t)},α2LE(t)α21E(0)=L{βS(t)I(t)(1c)(μ+ɛ)E(t)},α3LI(t)α31I(0)=L{ɛE(t)(γ+μ+d)I(t)},α4LR(t)α41R(0)=L{γI(t)μR(t)+ρS(t)}. (31)

Such that we have

LS(t)=s0+1α1L{Λ}L{μS(t)βS(t)I(t)(1c)ρS(t)},LE(t)=e0+1α2L{βS(t)I(t)(1c)(μ+ɛ)E(t)},LI(t)=i0+1α3L{ɛE(t)(γ+μ+d)I(t)},LR(t)=r0+1α4L{γI(t)μR(t)+ρS(t)}. (32)

The solution of each class can be represented by an infinite series given by:

S(t)=n=0sn(t),E(t)=n=0en(t),I(t)=n=0in(t),.R(t)=n=0rn(t), (33)

the infinite series of the nonlinear term I(t)S(t) is represented with:

I(t)S(t)=n=0Xn (34)

where Xn(t) is the Adomian polynomial of the nonlinear term given by

Xn=1Γ(n+1)dndtc=0nλcIcc=0nλcSc. (35)

Evaluating Eq. (32) with expressions in (33), (34) and taking the inverse Laplace transform of both sides yields the recurrence relations:

n=0Sn+1(t)=s0+Λtα1Γ(α1+1)+L11α1LμSnβXn(1c)ρSn,n=0En+1(t)=e0+L11α2LXn(1c)(μ+ɛ)En,n=0In+1(t)=i0+L11α3LɛEn(γ+μ+α)In,n=0Rn+1(t)=r0+L11α4LγInμRn+ρSn. (36)

From (36), the initial approximations are:

s0(t)=s0+Λtα1Γ(α1+1),e0(t)=e0,i0(t)=i0,r0(t)=r0

Matching both sides of (36) to obtain subsequent approximations terms of n0, at n=0, we have

s1(t)=L11α1LμS0βX0(1c)ρS0,e1(t)=L11α2LX0(1c)(μ+ɛ)E0,i1(t)=L11α3LɛE0(γ+μ+α)I0,r1(t)=L11α4LγI0μR0+ρS0. (37)

Which leads to the following first approximate results obtained as:

s1(t)=(Λμs0βs0i0(1c)ρs0)tα1Γ(α1+1),e1(t)=β(1c)s0(t)i0(t)(μ+ɛ)e0(t)tα2Γα2+1,i1(t)=ɛs0(t)(μ+γ+d)i0(t)tα3Γα3+1,r1(t)=γi0(t)μr0(t)+ρs0(t)tα4Γα4+1. (38)

At n=1, we have

s2(t)=L11α1Lμs1βX1(1c)ρs1,e2(t)=L11α2LX1(1c)(μ+ɛ)e1,i2(t)=L11α3Lɛe1(γ+μ+α)i1,r2(t)=L11α4Lγi1μr1+ρs1. (39)

Such that the following solutions are obtained:

s2(t)=(μ+ρ)β(1c)(Λμs0βs0i0(1c)ρs0)t2α1Γ(2α1+1)β(1c)s0(ɛe0(γ+μ+d)i0)×tα1+α3Γ(α1+α3+1)+i0(Λμj1βs0s0ρs0(1c))t2α1Γ(2α1+1)
e2(t)=β(1c)s0ɛe0β(1c)(γ+μ+d)i0tα2+α3Γ(α2+α3+1)+i0Λμs0ρs0βs0i0(1c)×tα2+α1Γ(α2+α1+1)βα1α3(1c)+ɛ(μ+ɛ)α2μt2α2Γ(2α2+1)
i2(t)=ɛβs01i0(1c)(μ+ɛ)e0tα3+α2Γ(α2+α3+1)(γ+μ+α)i0(ɛe0(γ+μ+α)i0)t2α31Γ(2α3+1)
r2(t)=γɛe0γ(γ+μ+α)i0tα4+α3Γ(α4+α3+1)μ(γi0μr0+ρs0)×tα4Γ(α4+1)+ρΛμs0βs0i0(1c)ρs0tα4+α1Γ(α4+α1+1)

We also computed the third-order approximation of each class using the MATHEMATICA 12 software package, and the approximate results of the classes are obtained as follows: i.e., 

i.e., S(t)=n=03sn(t),C(t)=n=03cn(t).I(t)=n=03in(t),
R(t)=n=03rn(t),Q(t)=n=03qn(t)

6. Results

The model’s raw series results, produced via the homotopy perturbation method and Laplace Adomian decomposition methods in Sections 5.1, 5.2, are examined with live COVID-19 data from Nigeria’s Center for Disease Control [44]. The outcomes, presented in the subsequent section, offer a third-order polynomial function with two key control parameters introduced in the model.

6.1. Numerical results of the homotopy perturbation method

S(t)470200+4.70200105ρ+2425.479680c2365.169040t+2425.479680cρ+9.565559022+2740.169040ρ+2.35100105ρ2+6.255797190c215.86558804ct2217.08728806cρ6.255797191ρc2+1212.739840cρ20.05987847224+0.1283929616c1432.584520ρ210.97060904ρ78366.66667ρ30.07924949775c2+0.01075663474c3t36+
E(t)2003+2425.479680c+2422.516842t+1212.739840ρc9.6226375076.255797191c2+15.88062601c1212.739840ρt220.01075663474c312.94152250cρ+4.170531461ρc2404.2466133cρ2+0.068651806730.1460992507c+404.2466133ρ2+8.770991040ρ+0.08820299825c2t36+
I(t)416+.5936732694t0.01503797402c+0.01546094232t22+0.00002585729505c2+0.005012658004cρ+00000.7309276088c0.005012658004ρ0.0004743603205t36+
R(t)115+470200ρ+0.1686803306t1527.429200ρ+0.0001237089633+1212.739840ρc2.35100000000ρ2t222.011579657.1011c+0.0004123673942+2.085265730ρc2808.4932267ρc2+78366.66667ρ3+398.9580840ρc77453.27699ρ2505.9545470ρt36+

6.2. Numerical results of the Laplace adomian decomposition method

S(t)470200+2365.1690399+2425.47968c470200ρt+5.746065097++235100ρ25.240246921129955c1212.73984ρc+1902.4292ρt220.00368077427032960020.0036807742703296002ct36+
E(t)2003+2425.479680c+2422.516842t+5.2530935804569965.253093580456996ct2+0.00368077427032960020.0036807742703296002ct3+
I(t)416+0.5936732694t0.0154609423225633220.015037974015999999ct2+0.000029375250495871813+0.000029174684271396126ct3+
R(t)115+470200ρ0.1686803306t5.240246921129955c+235100ρ21212.73984ρc+1902.4292ρt20.00365139901983372850.0036515995860582043ct3+

6.3. Error analysis

Performing an analysis of the model solution generated by HPM and LADM is crucial to determining which method is most appropriate for numerical simulation. In this section, an error analysis of both methods is performed to observe their convergence rates. Additionally, comparison plots of the two methods are provided to evaluate their agreement, while ensuring that all parameters retain their baseline values as defined in Table 1. The following results were obtained:

SH(t)4702002365.169040t+5.565559020t20.05987847222t3SL(t)4702002365.17t+5.746060810t2+0.003680775000t3
EH(t)2003+2422.516842t5.593447004t20.02495188340t3EL(t)2003+2422.52t5.253090810t20.0036807750t2 (40)
IH(t)4160.5936732694t+0.01546094232t20.00004743603205t3IL(t)=4160.593673t+0.0154609t20.0000293753t3
RH(t)115.1686803306t+0.0001237089632t20.00004123673942t3RL(t)=115.016868t+0.000123709t20.00000006.04648t8

Table 1.

Variables, parameters, and descriptions.

Variable Description
S(t) Time relying count of vulnerable individuals
E(t) Time relying count of exposed individuals
I(t) Time relying count of infected individuals
R(t) Time relying count of recovered individuals

Incorporated parameters Description

c High risk immunity rate
ρ Vaccination rate of susceptible Covid-19 population

Parameters Description

Λ Influx rate
β Effective transmission rate
ɛ Rate of progression from exposed to infected
γ Progression rate from infected to recovered
μ Natural death rate
d Disease induced death rate

Eq. (40) represents the evaluated results of the homotopy perturbation method and the Laplace-Adomian decomposition method, respectively, on the susceptible class at classical order α=1.

Convergence

The convergence of the methods strictly depends on the contraction of the approximation solution to the exact solution [45].

Theorem

Let there exist a mapping k:mn defined on two Banach spaces m , n for all s,tm then k(s)k(t)nδstm , 0<δ<1 such that the sequence sr+1=kn(s0)=τ(s0) for some s0m which converges to a unique fixed point k

Proof

We consider a Picard sequence sr+1=k(sr)n to prove the theorem. It is required to show that sr is convergent in n for all rν such that srsvsrsr+1+sr+1sr+2++sr+2sr+3+ +sr1sv. The proof is defined by applying mathematical induction on the contractive property of contraction c such that srsr+1δrs0s1. This implies, limvsrsvδr1+δs0s1=0asr.

This proves that (sr) is Convergent in n and through completeness of n, we can find ωn: limr(sr)=ωn. Clearly, contraction C ensures the continuity of k. Thus ω=limrsr+1=sv.

Lemma

The proposed mathematical model’s convergence of sr to sv cannot be asserted since no exact solution to the model exists.

Proof

This rate can be examined using Maclaurin’s error approximation [46] hence it follows:

Definition 8

Let, φ(x) be a polynomial of order k with k+1 derivatives on the interval |x|ɛ and |φk+1(x)|B, The Maclaurin’s truncation error of the kth order Maclaurin’s polynomial of a function has the following bound as maximum error [46]

δn(t)=maxx[0,ɛ]B(k+1)!|x|k+1.

We apply this definition to compute the 3rd order maximum truncation error of the model’s series results for each class on an interval [0,1]. Hence, we construct the following functions (see Table 4, Table 5):

S3(t)=maxt[0,1]d3S(t)dt3|t|33!E3(t)=maxt[0,1]d3E(t)dt3|t|33!,
I3(t)=maxt[0,1]d3I(t)dt3|t|33!,
R3(t)=maxt[0,1]d3R(t)dt3|t|33!,

Table 4.

3rd order maximum truncation error for t[0,1].

t SL3(t) SH3(t) EL3(t) EH3(t) IL3(t) IH3(t) RL3(t) RH3(t)
0 0 0 0 0 0 0 0 0
0.2 0.00000294 0.000479 0.0000294 0.0002 0.0000000235 0.0000000379 0.000000000484 0.0000000329894
0.4 0.000236 0.003832 0.000236 0.001597 0.000000188 0.000000304 0.00000000387 0.000000263915
0.6 0.000795 0.012934 0.000795 0.00539 0.000000635 0.00000102 0.00000000131 0.000000890714
0.8 0.001885 0.030658 0.001885 0.012775 0.00000015 0.000000243 0.00000000317 0.00000211132
1.0 0.003681 0.059878 0.003681 0.024952 0.000000294 0.000000474 0.0000000605 0.00000412367

Table 5.

Error range of each class at t[0,1].

Se3(t) 0EL103 0EH102
Ee3(t) 0EL103 0EH102
Ie3(t) 0EL107 0Er107
Re3(t) 0EL108 0Er106

The error analysis of the approximation series shows the model is suitable for actual data simulation with a small error from third-order approximation. LADM had a lower error compared to HPM, indicating it is the best method for numerical simulation.

Comparison plots

Fig. 3 reflects the comparison and extent of agreement of the results produced by the two methods. A good correlation of the results is measured early on the graph before the graph diverges dramatically over time. Overall, it follows that the results of the two methods for the four classes follow the same trend. The error analysis performed showed that the third-order truncation error of the LADM is of lower order when compared to that of the HPM. Hence, we proceed to conduct the numerical simulation of the mathematical model using the LADM.

Fig. 3.

Fig. 3

Comparison plots of HPM and LADM on the model classes.

6.4. Numerical simulation

In this section, we mainly emphasize the effects of the parameters: High risk immunity c, vaccination control ρ and the fractional-order of the system in the presence of live COVID-19 data acquired from the Nigeria Centre for Disease Control on 1st December 2020 given that E(0)=2003, I(0)=416, Q(0)=404, R(0)=115 [26]. We shall conduct a case study on the real life acquired population of Ikeja Lagos, Nigeria [47] given that S(0)=470200. The dynamics are studied to determine the impact of the Caputo fractional order derivative on the distribution of the model population, as well as the impact of high-risk immunity and vaccination of susceptible individuals, in order to examine the effects on methods of controlling the COVID-19 virus and preventing its epidemic outbreak or future proliferation. Two scenarios are specifically examined to determine the influence of the factors on viral propagation.

The scenarios are:

  • A.

    effective analysis of control applications which involves:

  • i.

    effects of varying 0c<1 on the model classes to study the population response and distributions to high risk immunity;

  • ii.

    analysis of variation of 0ρ<1 on the Susceptible, Exposed, infected and recovered humans for proposed controls scheme;

  • iii.

    analysis of fractional order effect of combinations of both controls on the model class.

  • B.

    analysis of model population reaction in the presence of combined

  • i.

    implemented control strategies;

  • ii.

    unimplemented control strategies;

6.4.1. Simulation outcome of scenario A

  • 1.

    In this analysis, the effectiveness of vaccination in controlling the spread of the disease is examined by simulating the model class population. The data presented below was obtained through numerical simulations of each model equation.

It is worth noting that increasing vaccination rates in the population may not have a drastic impact on reducing the number of infected cases. The data recorded in the table suggests that increasing the vaccination rate can potentially decrease the number of exposed and susceptible individuals, but not necessarily in a significant way (see Table 6).

Table 6.

Dynamical variation in population response to vaccination ρ.

Class ρ=0 ρ=0.3 ρ=0.9
Susceptible 346 607.0930 254 624.9961 179 323.1486
Exposed 4091.154396 3839.110328 3659.830648
Infected 415.4067058 415.3924197 415.3781336
Recovered 12 176.72336 21 398.21368 28 945.49406
  • 1.

    Here the impact of high-risk quarantine is analyzed on the model population to observe the population distribution towards its implementation

The findings from the simulation suggest that high-risk quarantine has an impact on the population comparable to vaccination but with a slower rate of effectiveness. This highlights the importance of vaccination in controlling the spread of the disease, particularly in protecting susceptible individuals who may be at high risk of exposure in infected areas. Even in situations where a complete curfew cannot be implemented, it is suggested that other health regulations, such as social distancing and regular hand washing should be strictly enforced in order to reduce the transmission of the disease (see Table 7).

Table 7.

Dynamical variation in population response to vaccination ρ=0.

Class c=0 c=0.3 c=0.9
Susceptible 398 003.4643 401 075.3989 400 969.9147
Exposed 9760.772200 2953.560982 3106.563423
Infected 413.2887348 415.4126917 413.0775985
Recovered 64 843.43772 65 084.51221 65 326.99425
  • 2.

    Population distributions with respect to combined fractional implementation of vaccination and imposition of high risk quarantine

6.4.2. Simulation outcome of scenario B:

Here, we do some mathematical analysis and present some comparison plots of the results obtained for the combined maximum applications of mitigation strategies and various responses that were received for each class at both classical order α=1 and fractional order α=0.75.

The result of the analysis shows that the implementation of control strategies, particularly vaccination, has a significant impact on reducing the spread of the disease in the population. In the susceptible class, a decline was observed when control measures were implemented, with a more drastic reduction in population when the control measure was implemented at a classical derivative α=1. This takes more time than when control measures are implemented at a fractional level α=0.75. Similarly, in the infected class, a sharp decline was observed after a month of control implementation at α=1. The number of infected individuals (390) recorded at α=1 is much lower (406) than when control measures are implemented at α=0.75. The recovered class also shows the importance of the control measures studied, with a steady increase in population observed in both cases, although the progression is higher when the control measure is implemented at an integer derivative.

7. Discussion

This section provides a detailed discussion of our analysis results on the transmission control of the COVID-19 virus, which were obtained through numerical simulations using real-time data from Nigeria’s Ikeja region. The evaluation of the basic reproductive ratio in the area is relatively high, making it an ideal setting for investigating the efficacy of vaccination and high-risk quarantine measures in reducing disease prevalence and new cases. Our results reveal that the combination of both vaccination and quarantine measures produces a faster decline in disease prevalence and new cases, as depicted in Fig. 4, Fig. 5. It was found that in the initial phases of the pandemic, the effectiveness of vaccines did not have a significant influence on transmission. Nevertheless, as the pandemic entered remission, a more potent vaccination implementation was linked to a faster decline in cases. Vaccinating susceptible individuals is particularly effective in preventing disease spread and decreasing overall prevalence, as demonstrated in scenario A. In addition, we investigated the impact of a high-risk quarantine period on the transmission of COVID-19. The findings, as presented in Fig. 5, suggest that a longer period of high-risk quarantine can aid in preventing the spread of the pandemic. Although high-risk quarantine measures offer protection, their efficacy is lower than that of vaccination. Moreover, we explored the impact of fractional ordering on control measures and observed that higher orders result in a greater decrease in disease prevalence. In scenario B, we studied the effects of maximum and zero control implementation on susceptible, infected, and recovered individuals. Our findings, as observed in Fig. 6, suggest that full control implementation at classical orders lead to a slower spread of the disease than fractional orders. Fig. 7 provides evidence that the dual implementation of vaccination and high-risk quarantine measures produces a rapid and positive response in reducing the reproductive ratio. Hence, we recommend a dual implementation of vaccination and high-risk quarantine measures to significantly reduce disease transmission and spread. Moreover, it is essential to ensure that vaccines are widely distributed to the masses and that the rate of vaccine uptake among them is high.

Fig. 4.

Fig. 4

Reaction of the four population class to vaccination at time variations.

Fig. 5.

Fig. 5

Impact of high risk quarantine on the model classes.

Fig. 6.

Fig. 6

Fractional order dynamics of vaccination and high risk quarantine on recovered population.

Fig. 7.

Fig. 7

Shows the reaction of SIR population class to control strategies at a Caputo classical order α=1 and fractional order α=0.75.

8. Conclusion

The proposed model of COVID-19 transmission dynamics has been analyzed to investigate the combined effects of high-risk quarantine and vaccination. A separate study [48] titled “vaccination and quarantine effect on COVID-19 transmission dynamics incorporating the Chinese spring festival travel rush” suggests that a minimum of 61.38% of people must be vaccinated to achieve herd immunity. When vaccination and quarantine are implemented simultaneously, a quarantine rate of 38.74 percent is necessary to prevent further spread of the disease. These findings are consistent with our simulation results, which demonstrate the efficacy of combining these two methods. Additionally, a higher number of vaccinations and greater vaccine effectiveness lead to a more significant positive effect, while a longer immune protection period helps to help suppress the spread of the pandemic.

Theoretical and practical implications

Our analysis indicates that combining vaccination measures with high-risk quarantine could be an effective strategy for reducing the spread of the virus. These measures may involve protecting vulnerable populations and minimizing the negative impact of the pandemic, which could potentially require implementing temporary curfews. However, it is crucial to ensure the welfare of those living in affected regions to gain their cooperation with the proposed measures. Furthermore, careful planning, resource allocation, and ongoing development of vaccine distribution are essential to ensure timely access to protection against the virus and prevent prolonging any curfew measures. Implementing our research findings could lead to several positive outcomes, including lower hospitalization and mortality rates as well as economic recovery.

Recommendations for future research

Our future goal is to develop a model that integrates screening and vaccination protocols for immigrants, providing a more accurate assessment of COVID-19 transmission within a larger population that incorporates vaccines and quarantine measures. Through this research, we intend to offer valuable insights to policymakers who seek effective strategies for preventing the spread of COVID-19. Ultimately, our findings are believed to play a vital role in shaping public health policies aimed at curbing the transmission of this pandemic.

CRediT authorship contribution statement

Morufu Oyedunsi Olayiwola: Innovation, Model design, Read and approve the manuscript. Adedapo Ismaila Alaje: Model solution, Computations, Read and approve the manuscript. Akeem Yunus Olarewaju: Qualitative analysis, Editing, Read and approve the manuscript. Kamilu Adewale Adedokun: Simulations, Results discussion, Read and approve the manuscript.

Declaration of Competing Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgment

The efforts of all academic colleagues in the Department of Mathematical sciences of Osun State university, Osogbo is acknowledged.

Funding

No funding has been received.

Data availability

Data will be made available on request.

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