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Restoring logic and data to phage-cures for infectious disease

  • Received: 12 June 2017 Accepted: 10 August 2017 Published: 15 August 2017
  • Antibiotic therapy for infectious disease is being compromised by emergence of multi-drug-resistant bacterial strains, often called superbugs. A response is to use a cocktail of several bacteria-infecting viruses (bacteriophages or phages) to supplement antibiotic therapy. Use of such cocktails is called phage therapy, which has the advantage of response to bacterial resistance that is rapid and not exhaustible. A procedure of well-established success is to make cocktails from stockpiles of stored environmental phages. New phages are added to stockpiles when phage therapy becomes thwarted. The scientific subtext includes optimizing the following aspects: (1) procedure for rapidly detecting, purifying, storing and characterizing phages for optimization of phage cocktails, (2) use of directed evolution in the presence of bacteriostatic compounds to obtain phages that can be most efficiently used for therapy in the presence of these compounds, (3) phage genome sequencing technology and informatics to improve the characterization of phages, and (4) database technology to make optimal use of all relevant information and to rapidly retrieve phages for cocktails that will vary with the infection(s) involved. The use of phage stockpiles has an established record, including a recent major human-therapy success by the US Navy. However, I conclude that most research is not along this track and, therefore, is not likely to lead to real world success. I find that a strong case exists for action to rectify this situation.

    Citation: Philip Serwer. Restoring logic and data to phage-cures for infectious disease[J]. AIMS Microbiology, 2017, 3(4): 706-712. doi: 10.3934/microbiol.2017.4.706

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  • Antibiotic therapy for infectious disease is being compromised by emergence of multi-drug-resistant bacterial strains, often called superbugs. A response is to use a cocktail of several bacteria-infecting viruses (bacteriophages or phages) to supplement antibiotic therapy. Use of such cocktails is called phage therapy, which has the advantage of response to bacterial resistance that is rapid and not exhaustible. A procedure of well-established success is to make cocktails from stockpiles of stored environmental phages. New phages are added to stockpiles when phage therapy becomes thwarted. The scientific subtext includes optimizing the following aspects: (1) procedure for rapidly detecting, purifying, storing and characterizing phages for optimization of phage cocktails, (2) use of directed evolution in the presence of bacteriostatic compounds to obtain phages that can be most efficiently used for therapy in the presence of these compounds, (3) phage genome sequencing technology and informatics to improve the characterization of phages, and (4) database technology to make optimal use of all relevant information and to rapidly retrieve phages for cocktails that will vary with the infection(s) involved. The use of phage stockpiles has an established record, including a recent major human-therapy success by the US Navy. However, I conclude that most research is not along this track and, therefore, is not likely to lead to real world success. I find that a strong case exists for action to rectify this situation.


    1. Introduction

    Recently the Polyvinylidene fluoride (PVDF) is studied extensively due to its interesting piezoelectric and pyroelctric properties. PVDF based composites found application in lithium ion batteries, capacitors, hydrophones and variety of sensors [1,2,3]. The most attractive property of PVDF is polymorphism. It exists in five α, β, γ, δ, ϵ phases but the first two phases are dominate phases [4,5,6]. The piezoelectric and pyrolectric properties are mainly governed by α and β phase. So researchers are investigating the various methods to promote these phases. Fillers/dopants are used to make PVDF composite film so as to improve the dielectric, magnetic and mechanical properties. The addition of dopant in polymer enhances the physical properties, thus widening the application are of PVDF polymer. In various studies, the researchers confirm the changes in the morphology and crystalline structure of PVDF doped with different types of fillers/dopant [7,8]. For PVDF film having dominated α, and β phase the prepared films were to be mechanical stretched as well as poled [9]. This technique enhances the piezoelectric response which is desirable for sensing applications. Plasma treatment was also used to enhance the hydrophilic property of PVDF membranes [10]. Different types of organic and inorganic fillers were utilized to investigate the effect on various physical and chemical properties of PVDF. The degree of crystallinity and electrical response of PVDF also depends upon the weight percentage of fillers [11]. Few researches have added nanoclay as filler to PVDF so as to study the changes in structure PVDF matrix [12,13]. Some groups focused on use of high polarity solvent used for casting the PVDF film. Recently Zeolite was actively used as filler to develop a Zeolilite/PVDF composite. Additions of Zeolite improvise the tensile strength as well as mechanical properties of PVDF thin films, thus widening the application are of these composites [14]. Some of the common fillers used as dopant includes Ba, Co, Mn, Fe, Cr, Ti, Li and so on [15,16,17,18]. In this research work, the MgCl2 is selected as dopant material. It was revealed that addition of MgCl2 significantly modifies the crystalline structure and reduction in crystalline structure was observed. The other objective was to evaluate the effect of MgCl2 on the dielectric constant and application of sensing properties of PVDF composite films.


    2. Materials and Methods


    2.1. Preparation of PVDF Composite Films

    The PVDF composite films were prepared by solution casting technique. The MgCl2 powder was dissolved in DMF for 30 minutes on magnetic stirrer. PVDF powder was dissolved in DMF for 60 minutes at temperature of 60 °C. Then the dopant solution is mixed with appropriate amount of PVDF solution. The mixed solution of MgCl2/PVDF was again stirred continuously for 30 minutes. The solutions of different weight percentage were casted on the glass slides and placed in furnace for 6 hrs at temperature of 70 °C. PVDF composite films were then peeled off from the glass slides and washed with DI water to remove any solvent traces. Then the films of different wt% of MgCl2 were coated with Al on both sides using vacuum coating unit and poled subsequently. The detailed regarding different weight percentage of MgCl2 is given in Table 1.

    Table 1.Solution composition of MgCl2/PVDF composite.
    SolutionMgCl2 wt%PVDF wt%DMF
    S00%10%100 ml
    S12%10%100 ml
    S24%10%100 ml
    S36%10%100 ml
     | Show Table
    DownLoad: CSV

    2.2. Characterization and Measurement

    The phase structure of MgCl2/PVDF composite was analysed using X ray diffractometer (PANalytical). The FTIR spectra were carried out using spectrum 400 (Perkin Elmer). The dielectric parameters were measured using LCR meter (Hioki 3532). Vacuum coating unit were used to deposit Al on both sides of films. The sensor response was observed using Digital oscilloscope (Yokoga DL9140). The poling of PVDF samples were done using setup shown in Figure 1. Poling was done in two fold process. The samples were initially placed in temperature controlled furnace. Firstly 250 volts DC was applied at temperature of 70 °C for 1 hour. After 1 hour the temperature was brought down to the room temperature and electric field was still applied for another 30 minutes. After this two fold process the PVDF samples were removed from furnace for sensing and dielectric measurements.

    Figure 1. Schematic of PVDF Poling.

    3. Results and Discussion


    3.1. XRD Analysis

    The XRD scans of MgCl2/PVDF composite for pure and various wt% of dopant is shown in Figure 2. The pure PVDF exhibits the semi crystalline structure comprising of both amorphous and crystalline phase. The peaks at 18.40°, 26.50°, 38.60° corresponds to α phase. The peak at 20.2° indicates the presence of β phase [2,19]. As the concentration of filler increase to 6 wt%, all other peaks disappeared only one broader peak related to β phase remains present. The piezoelectric property of PVDF is affected by crystallinity appreciably. Without crystallinity, the PVDF would not exhibit any piezoelectric properties. The level of crystallinity is key parameter affecting the PVDF chemical, piezoelectric, mechanical and thermodynamic properties. The crystallinity is calculated using relation (1).

    Xc=Kc(A1+A2)Kc(A1+A2)+Ka(A3)×100 (1)
    Figure 2. XRD scans of Pure and MgCl2 doped PVDF.

    Where A3 is the area concerned with amorphous hump, A1 & A2 is area of two crystalline peaks as depicted in Figure 3. Ka & Kc are proptionallity constant for amorphous and crystalline phases [20,21]. The crystallinity of Pristine PVDF as determined from XRD is 51.8%. With the addition of MgCl2 into PVDF, the crystallinity decrease to 42.6%. The decrease in crystallinity indicates the modification in crystalline structure with the addition of MgCl2.

    Figure 3. XRD pattern illustrating calculation of crystallinity.

    3.2. FTIR

    The FTIR scans for pure and doped PVDF is shows in Figure 4. Most of the peaks at frequency corresponds to α and β phase. The peaks at 610 cm−1, 760 cm−1 and 1420 cm−1 belong to α phase [22,23]. The other peaks at 508 cm−1and 836 cm−1 related to β phase. With increase in dopant concentration to higher level, some of peaks intensity reduces to lower level.

    Figure 4. FTIR Spectra of Pure and doped PVDF composite.

    3.3. Dielectric Constant and Force Sensing

    The dielectric constant or permittivity ε′(ω) is a measure of the polarization of the medium between two charges when an electric field is applied. The dielectric constant of a PVDF polymer depends on structural morphology and presence fillers in crystalline structure. The dielectric constant ε′(ω) was calculated using following equation:

    Cp=ε0εAD (2)

    Where, ε0 is the dielectric constant/permittivity (8.86 × 10−12 F/cm) for free space, d (in cm) is thickness and A (in cm2) is the cross sectional area of PVDF thin films. As the dopant wt% increase to 6 wt% (Figure 5), the dielectric constant increase indicating the large polarization in PVDF composite. As the frequency increase to higher level, the decrease in dielectric constant was observed. Figure 6(a) and 6(b) shows the output voltage from pristine and doped PVDF composite sensor when force of 19 N was applied to the surface.

    Figure 5. Dielectric constant vs. frequency.
    Figure 6. Voltage output of (a) Pristine PVDF, (b) MgCl2/PVDF sensor.

    4. Conclusion

    The present work shows the MgCl2 has significantly affected the structural properties of the PVDF composite films. The reduction in crystallinity was also observed which confirms the modification in morphology of PVDF films. The enhancement in dielectric constant was observed as the dopant concentration reaches to higher level. This present study reveals the application of PVDF composite in sensing areas which includes tactile as well as pressure sensing.


    Acknowledgments

    This work was supported by Department of Instrumentation, Kurukshetra University via TEQIP-II World Bank grant.


    Conflict of Interest

    The authors declare no conflicts of interest regarding this paper.


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