Novel Solid State Nitric Oxide Sensor Using Siloxane-Poly(Oxypropylene) (PPO)
Rondinelli D. Herculano, Carlos A. Brunello, Jair P. Melo Jr., Mayler Martins, Felipe A. Borges, Leila A. Chiavacci, Carlos F. O. Graeff
Departamento de Ciências Biológicas, Faculdade de Ciências e Letras de Assis, Universidade Estadual Paulista “Júlio de Mesquita Filho”, Assis, Brazil.
Departamento de Fármacos e Medicamentos, Faculdade de Ciências Farmacêuticas, Universidade Estadual Paulista “Júlio de Mesquita Filho”, Araraquara, Brazil.
Departamento de Física, Faculdade de Ciências, Universidade Estadual Paulista “Júlio de Mesquita Filho”, Bauru, Brazil.
Departamento de Física, Faculdade de Filosofia, Ciências e Letras de Ribeir?o Preto, Universidade de S?o Paulo, Ribeir?o Preto, Brazil.
Departamento de Física, Faculdade de Filosofia, Ciências e Letras de Ribeir?o Preto, Universidade de S?o Paulo, Ribeir?o Preto, Brazil.
DOI: 10.4236/msa.2013.411085   PDF    HTML   XML   4,372 Downloads   6,170 Views   Citations

Abstract

In this paper, a novel solid state Nitric Oxide (NO) sensor made of a spin trap (iron(II)-diethyldithiocarbamate complex, FeDETC) encapsulated in a siloxane-poly(oxypropylene) (PPO) matrix was developed. Nitric oxide (NO), a free radical molecule, has numerous roles in various physiological functions, such as the regulation of blood pressure, immune response to bacterial infection, and nervous systems. Siloxane-polyether hybrid materials, for example siloxane-poly(oxypropylene) (PPO), are easy to prepare, transparent and flexible. The combination of all these characteristics in a unique material allows it to be used in several scientific and technological areas, including human health. NO radical is trapped in FeDETC, which allows its detection by electron paramagnetic resonance (EPR). FeDETC was added while PPO was a sol, which was then left in air for gelation. The novel sensor was dived directly into a solution of NO, when the NO-FeDETC complex was formed. Our results show that the novel sensor responds to NO, with similar sensitivity as previously published sensors. PPO sensors present a strong EPR signal and a high stability, keeping its signal for 45 days. We have studied ways to accelerate the NO release from the sensor, in order to study its potential as a drug delivery system. We observed an acceleration in NO release by using a modulated magnetic field of 40 G at 100 kHz; as well as by UV irradiation. Thermal induced NO release was also tested by heating NO-FeDETC PPO up to 50°C, with good results.

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R. Herculano, C. Brunello, J. Melo Jr., M. Martins, F. Borges, L. Chiavacci and C. Graeff, "Novel Solid State Nitric Oxide Sensor Using Siloxane-Poly(Oxypropylene) (PPO)," Materials Sciences and Applications, Vol. 4 No. 11, 2013, pp. 683-688. doi: 10.4236/msa.2013.411085.

1. Introduction

Nitric oxide (NO) is a free radical with multiples physiological functions [1-3], and few decades ago, NO was just another toxic molecule, one of a lengthy list of environmental pollutants such as cigarette smoke and smog. Over the past few years, diverse lines of evidence have converged to show that this sometime toxic pollutant gas plays a fundamental role in numerous biological processes in the body [4]. NO is synthesized by three differentially gene-encoded nitric oxide synthase (NOS) enzymes [4,5]. It serves as a key signaling molecule in various physiological processes including vasodilatation, respiration, cell migration, immune response and apoptosis. Over recent years, it has become apparent that NO has important effects on bone cell function [6,7]. On the other hand, excessive and unregulated NO synthesis has been implicated as causal or contributing factor to various pathophysiological conditions including cancer [8- 10]. Detection of NO presents a series of challenges since it is highly reactive, which means it has short lifetimes in living organisms, depending on the environment from milliseconds to minutes, before it reacts and consequently is found in low quantities in biological systems [11]. One way to measure NO is the use of spin traps like iron complexes with dithiocarbamates and porphyrins due to the affinity between NO and the iron complexes allowing the use of electron paramagnetic resonance (EPR) to radical detection. However, these complexes are unstable for long-term measurements. In previous works of our group [11-13], we proposed the encapsulation of iron(II)-diethyldithiocarbamate (FeDETC) in different matrixes for either the measurement of NO or its release.

In one of these matrixes, a NO sensor was made encapsulating FeDETC in a sol-gel matrix [14]. Sensors entrapped in gels offer numerous advantages when compared with liquid based systems: they are easier to manipulate, allow species detection and concentrations measurements with less contamination of the sample, can be used for continuous sensing and are normally more stable. In our case [14], the idea was to combine the specificity and high sensitivity of EPR, with the conveniences of working with a spin trap in the solid state. For EPR, measurement of special interest is the fact that solutions are in general hard to measure since liquids have high dielectric losses, or in other words they absorb microwaves, which limits severely the detection. EPR quartz liquid cells are necessary when liquids are to be measured by EPR, which are expensive and impose restrictions in what concerns the concentration of paramagnetic species. Therefore, entrapping the paramagnetic species in a solid is of great interest for EPR.

In another work [12,13], natural rubber latex (NRL) was used as a matrix for the sustained and controlled delivery of NO. NRL is an important inductor of the healing process of wounds, being used in various biomedical applications like prosthetics and bone grafts [15-18]. Results showed that one can have sustained delivery of NO from NRL matrix for up to 350 hours. FTIR spectroscopy showed that NO/FeDETC when encapsulated in NRL has its properties and structure preserved [19].

In this work, we present a novel EPR NO sensor based on a siloxane-poly(oxypropylene) (PPO) matrix. The sensor was obtained by the spin trap iron(II)-diethyldithiocarbamate complex (FeDETC) encapsulated in a siloxane-poly(oxypropylene) PPO matrix. This same system is used for the sustained and controlled delivery of NO. This material is flexible, transparent and easily manipulated. We have tested different ways to do accelerated and controlled release of NO. The PPO-FeDETC system was exposed to ambient atmosphere (humidity 60%, 25˚C), ultraviolet, temperature at 50˚C, dark room, and magnetic field (amplitude modulation) of 40 G. The EPR signal of NO in the matrix was monitored as function of time.

2. Materials and Methods

First The PPO used in this work was obtained by sol-gel. All chemical reagents used are commercially available (Fluka, Aldrich). Succinctly, 3-isocyanatopropyltriethoxysilane (IsoTrEOS) and O,O’Bis(2-aminopropyl(polyoxypropylene)) in the molar ratio 2:1 were stirred together in tetrahydrofuran (THF) under reflux at 80˚C for 6 h to form the hybrid precursor 3(EtO)Si-(PPO)- Si(OEt)3 [20,21].

The sol was obtained by mixing the precursor with the spin trap FeDETC in an ethanol solution containing HCl or NH4F. Hydrolysis was promoted by water addition followed by polycondensations reactions. This process was adopted for PPO polymers with molecular weight (MW) of 300 and 2000 g/mol (labeled as PPO300 and PPO2000).

For the FeDETC solution, iron(III) chloride hexahydrate (FeCl3∙6H2O), dimethylformamide (DMF, C3H7ON) and sodium dietyldithiocarbamate (DETC, C5H10NNaS2∙3H2O) were used. DMF and DETC were obtained from Acrós Organics (Belgium). The solution was prepared using 12 mg of iron chloride and 20 mg of DETC in 3 mL of DMF under magnetic agitation during 10 minutes. The entrapment of FeDETC in the matrix was obtained by mixing the PPO solution with FeDETC solution. After this, the solution was left in air for 2 day to complete the polymerization process resulting in a solid matrix. NO was generated in an aqueous solution by mixing NaNO2 10 mM (250 μL), deionized water (750 μL) and Na2S2O4 (145 mg) in an eppendorf tube of 1.5 mL. In the presence of sodium dithionite (Na2S2O4) nitrite is reduced to NO. The saturated concentration of NO in this solution is 2.2 mM.

Electron Paramagnetic Resonance (EPR) experiments were done in a computer interfaced Varian E-4 X-band spectrometer at room temperature. For EPR measurements, the films were removed from the solution, dried and inserted in a quartz tube. For all samples the only signal observed was of the NO-FeDETC complex. To maximize signal to noise ratio various spectra were summed up, typically at least 10. To avoid sample repositioning induced errors for the measurements following the EPR signal with time, the sample was kept inside the resonant cavity. A reference sample with a known and stable amount of spins was used before each measurement.

3. Results and Discussion

In recent years, the study of organic-inorganic nanocomposites became a mushrooming field of investigation due to the promising applications of these materials in optics, electronics, electrochemistry and biology [22-26]. These hybrids are considered as biphasic materials, the organic and inorganic phases being mixed at a nanometric scale. A family of hybrids, which recently attracted interest, consists of siloxane-polyether nanometer scale composites (Figure 1), in which the organic and inorganic phases are bonded by urea bridges, thus named ureasils [27]. These transparent materials were originally

Figure 1. Siloxane-Poly(Oxypropylene) (PPO) monomer, with n = 34 for PPO2000 and n = 5 for PPO300 [31].

synthesized to be used in photochromic devices [28] as solid electrolytes [29,30] because the covalent bonds between the polymer and the siloxane backbone hinder phase separation, preserving the stability of mechanical and thermal properties.

Gradzielski et al. [32] studied the aqueous aggregation behavior of several nonionic and ionic siloxane surfactants. They found micellar and lyotropic liquid crystal phases in siloxane surfactant/water systems similar to the phases found in hydrocarbon surfactant colloidal systems, although some of these siloxane surfactants have irregular branched structures.

We shall start by comparing the EPR signal of FeDETC:NO in different matrixes. [11-13]. In Figure 2 the EPR signal of the FeDETC:NO in a matrix of Latex and SiOx is shown. SiOx is a sol-gel matrix from siloxane. In the same figure the EPR signal of FeDETC:NO at different temperatures is also shown. Notice the similarities of the spectra measured in the matrixes at room temperature with the one in the solution measured at 77 K.

In Figure 3, the EPR signal of the FeDETC:NO in different concentrations inside of the PPO300 matrix is shown. Notice that the signal increases as the FeDETC concentration is also increased. Another important parameter, which concerns the sensitivity of the NO delivery system, is the density of spin traps [14] incorporated into the PPO matrix. In this case, the function of FeDETC is to trap NO. As already mentioned, to maximize signal to noise ratio various spectra were summed up, typically at least 10. All sensors were immersed in a saturated NO solution for 2 h prior to starting the measurements. These spectra were taken after leaving the sample in the dark for 24 h after immersion in the NO solution. Figure 3(a) shows the EPR signal amplitude as a function of FeDETC concentration for the PPO matrix. The experimental data in Figure 3(b) were fitted using an exponential decay function.

In Figure 4, the PPO300 sensor was immersed in a 2.5 mM NO solution for 2 hours. The EPR signal amplitude just after the sensor was taken from the NO solution is plotted as a function of time in different conditions: 1) left in the dark at room temperature, 2) under ultraviolet illumination, 3) left at 50˚C and 4) dark room. As can be seen, the signal decreases with time until it vanishes for temperature at 50˚C and dark room. However, the EPR signal increase for samples preserved at room tempera-

Figure 2. Typical EPR spectra from FeDETC:NO in solution and inside the Latex matrix, and SiOx matrix. For the spectra in solution (dashed lines) the measurement temperatures were 300 K and 77 K [13].

(a)(b)

Figure 3. EPR signal from FeDETC:NO of  PPO matrix as a function of FeDETC concentration: (a) Amplitude intensity; (b) Amplitude as a function of time. Notice that FeDETC:NO signal amplitudes are essentially dependent of FeDETC concentration.

Figure 4. EPR signal intensity of PPO300 sensor as a function of time.

ture and UV.

In Figure 5, the EPR signal amplitude just after the PPO2000 sensor was taken from the NO solution is plotted as a function of time in different conditions: 1) UV, 2) dark room, 3) temperature at 50˚C and 4) magnetic field (Amplitude Modulation) of 40 G. As can be seen, the signal decreases with time until it vanishes all samples.

In Figures 4 and 5, we observed that EPR signal amplitudes (PPO300 and PPO2000) increase with the FeDETC quantify, but non-linearly. We demonstrated that diethyldithiocarbamates is presence in PPO support. FeDETC:NO signal amplitudes are essentially dependent of FeDETC concentration [12,14]. In addition, the PPO sensors present a stronger EPR signal and highest stability, keeping the NO signal intensity for more than 40 days. The ultraviolet radiation induces an increase in EPR signal in both matrixes. Moreover, modulated magnetic field of 40 G at 100 kHz, as well exposing the PPO2000 sensor to a temperature at 50˚C, accelerated the NO release from the sensor, i.e.; field magnetic induced release of NO has potential application as a drug delivery system. The acceleration in the NO release is due the hyperthermia magnetic.

Kumar & Mohammad [33] presented a case for broadening the meaning of the term “hyperthermia” by including thermotherapy as well as magnetically modulated controlled drug delivery. They provided a classification for controlled drug delivery using hyperthermia: The highlight of this work was to portray potential opportunities for the combination of hyperthermia-based therapy and controlled drug release paradigms-towards successful application in personalized medicine.

Lien & Wu [34] synthesized the multifunctional magnetic nanoparticles (SiO2/Fe3O4) containing thermosensitive polymers (PNIPAM, poly(N-isopropylacrylamide), generating thermosensitive and magnetic properties of

Figure 5. EPR signal intensity of PPO2000 sensor as a function of time.

nanocomposites. The magnetic properties of SiO2/Fe3O4 nanoparticles show superparamagnetic behavior. They observed that for thermosensitivity analysis, the phase transition temperatures of multifunctional nanoparticles measured using DSC was at around 34˚C - 36˚C.

Kim et al. [35] synthesized and characterized multifunctional chitosan-MnFe2O4 MNPs for hyperthermia and drug release behavior. They observed that these nanoparticles display significant heating for hyperthermia applications (which when adds to their already-reported use in MRI).

Already, others works have shown the magnetic field influence in drug delivery. Souza et al. [36] showed the influence of magnetic nanoparticles (SiO2/Fe3O4) on drug release kinetics with cisplatin, carboplatin, and atenolol under in vitro conditions in the absence and in the presence of an external magnetic field (0.25 T) by using NdFeB permanent magnet. The constant external magnetic field did not affect drug release significantly. The low-frequency alternating magnetic field had a large influence on the cisplatin release profile.

Chen et al. [37] (2008) grafted doxorubincin (DOX, anticancer agent) into surface of the core-shell nanoparticles (Fe3O4/SiO2). They showed that DOX-grafted Fe3O4/SiO2 core-shell structure nanoparticles presented a superparamagnetic property with a saturation magnetization value of 49.3 emu/g, indicating a great potential application in the treatment of cancer using magnetic targeting drug-delivery technology.

Souza et al. [38] (2008) showed that the magnetite nanoparticles (Fe3O4) are completely coated by wellordered mesoporous silica(SiO2) with free pores and stable (~8 nm thick) pore walls, and that the structural and magnetic properties of the Fe3O4 nanoparticles are preserved in the applied synthesis route.

PPOs associated to FeDETC-NO are easy to manipulate, allow species detection and concentrations measurements with few sample contamination. These characteristics indicate that PPO matrix may be a good choice for a NO delivery system, with superior mechanical properties [11-13]. The samples are very stable: the signal amplitude of NO could be detected even after 40 days exposed to ambient atmosphere. As NO is an early mediator of the inflammatory process associated to tissue regeneration presented interesting biological properties.

4. Conclusion

We propose a novel NO delivery system made of a spin trap (iron(II)-diethyldithiocarbamate complex, FeDETC) encapsulated in a PPO matrix. The rate release of NO in this system was observed by EPR, exposing the sample to ambient atmosphere. The results indicate that it is possible NO release for 40 days. Moreover, a system with modulated magnetic field of 40 G at 100 kHz in PPO sensor to a temperature at 50˚C, accelerated the NO release from the sensor, i.e. field magnetic, and induced release of NO, has potential application as a drug delivery system. The acceleration in the NO release is due to the hyperthermia magnetic. In addition, the matrix is flexible, transparent and easily manipulated.

5. Acknowledgements

We are grateful to J. L. Aziani for technical support. This work received financial support from FAPESP, CNPq and CAPES.

Conflicts of Interest

The authors declare no conflicts of interest.

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