Fluorescent polymer as a biosensing tool for the diagnosis of microbial pathogens.

Diseases and diagnoses are predominant in the human population. Early diagnosis of etiological agents plays a vital role in the treatment of bacterial infections. Existing standard diagnostic platforms are laborious, time-consuming, and require trained personnel and cost-effective procedure, though they are producing promising results. These shortcomings have led to a thirst for rapid diagnostic procedures. Fluorescence-based diagnosis is one of the efficient rapid diagnostic methods that rely on specific and sensitive bacterial detection. Emerging bio-sensing studies on conducting polymers (CPs) are gaining popularity in medical diagnostics due to their promising properties of high fluorescence efficiency, good light stability, and low cytotoxicity. Poly[2-methoxy-5-(2'-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV), is the first identified soluble polymer and model material for understanding the fundamental photophysics of conventional CPs. In this present study, MEH-PPV is used as a fluorescent dye for direct pathogen detection applications by interacting with the microbial cell surface. An optimized concentration of MEH-PPV solution used to confirm the presence of selective bacterial structures. The present study endeavours towards bacterial detection based on the emission from bacteria due to interfacial interaction between polymer and bacterial surface.

Nanocarriers of solid lipid from micelles of amino acids surfactants coated with polymer nanoparticles.

Polymer nanoparticle coated micelle assemblies of lauryl ester of tyrosine (LET) act as potential nanocarriers for the model solid lipid stearyl alcohol. The coating is afforded by a simple methodology of heterophase polymerization reaction of styrene or the mixture of styrene and butyl acrylate at a mole ratio of 0.8:0.2 in the presence of 200 mM LET in water. On the contrary, the polymer nanoparticles produced under similar conditions in the presence of a structurally similar surfactant, lauryl ester of phenyl alanine (LEP), failed to act as nanocarrier. The micelle templates of LET and LEP favored polymerization under controlled conditions as observed from the near monodisperse distribution of molecular weight and size of the polymers. The particle size distribution of poly(styrene) (PS) and poly(styrene-co-butyl acryalte) (PS-co-PBA) nanoparticles from LET was smaller at 24 and 20 nm in comparison to those from LEP. The encapsulation efficiency of polymer nanoparticles from LET surfactant is explained on the basis of difference in the coating of micelle assemblies, which we believe must be arising due to difference in the solubilization site of the monomers in the surfactant micelles before polymerization reaction. The solubilization of the model monomer, benzene at different regions, varying between shell and core of LET and LEP micelles is established from (1)H nuclear magnetic resonance spectra. The evidence for the coating of micelle assemblies from surface tension measurements and the encapsulation of stearyl alcohol in the polymer nanoparticle dispersions from LET drawn from transmission electron microscopy, differential scanning calorimetry, and thermogravimetric analysis is discussed.

pH-responsive aggregation states of chiral polymerizable amphiphiles from L-tyrosine and L-phenyl alanine in water.

Sodium salts of maleamic acid derivatives of lauryl ester of tyrosine (MTNa) and phenyl alanine (MPNa) in water exhibited strong pH-responsive behaviors of viscosity and specific conductivity that originate from the concentration and pH dependence of their aggregation states. The aggregates were characterized by a novel spin-probe-partitioning electron paramagnetic resonance (SPPEPR) method and dynamic light scattering (DLS). Results of high-precision fitting of the second-harmonic EPR spectra of the small spin probe di-tert-butyl nitroxide (DTBN) in these aggregates together with viscosity, conductivity, and DLS showed that, at pH ~ 7.54, MTNa formed micelles and MPNa vesicles and MTNa exhibited a pH-induced micelle to vesicle transition as pH was lowered toward 6. MTNa, at pH ~ 7.54, formed small micelles at low concentrations that transformed to long worm-like micelles for concentrations ≥ 0.05 M, accompanied by a 30-fold increase in solution viscosity. The hydrodynamic radii from DLS confirmed the presence of small micellar aggregates of radius ~ 2 nm in MTNa at pH ~ 7.54 at the lower concentrations, with coexisting micelles (~2 nm) and vesicles (~50 nm) at pH near 6.5, vesicles (radii ~ 70 nm) at pH near 6, and large vesicles (85 nm) in MPNa at pH ~ 7.60. Both MTNa and MPNa precipitated upon reduction of pH below 6 and below 7, respectively. The rate of transfer of DTBN between the aqueous phase and the aggregate was calculated from the high-field Lorentzian linewidths of the electron paramagnetic resonance (EPR) spectra. The activation energy for the transfer determined from the temperature dependence of the rate of transfer is 12.7 kJ/mol for MTNa vesicles (pH ~ 6) and 20.6 ± 1.3 kJ/mol for MPNa (pH ~ 7.60). The pH-induced transformations were reversible.

Formation of self-aggregated structures of different types in water of chiral polymerizable amphiphiles from L-tyrosine and L-phenylalanine.

Sodium salts of maleamic acid derivatives from lauryl esters of L-tyrosine (MTNa) and L-phenylalanine (MPNa) were synthesized and characterized. The aggregated structures of MTNa and MPNa in water were investigated, employing several independent methods. MPNa showed secondary aggregated structures in contrast to MTNa at concentrations of >1 × 10(-3) M. The results from dynamic light scattering, transmittance, conductivity, and viscosity measurements suggested the formation of aggregated structures of different types in MTNa and MPNa solutions. The measured fluorescence anisotropy (r) at 0.180 of the fluoroprobe, 1,6-diphenyl-1,3,5-hexatriene (DPH), and the d spacing of 38 Å from small-angle X-ray diffraction (SAXD) experiments confirmed the bilayer structures in MPNa. Scanning electron microscope (SEM) images provided the morphological features. The emulsion produced using MPNa solution was more stable. The confocal fluorescence microscopy image of the emulsion from MPNa confirmed the entrapment of water-soluble dye, rhodamine. The models of MTNa and MPNa molecules and the aggregated structures are presented.

High performance controlled reactors from micellar assemblies of aromatic amino acid amphiphiles for nanoparticle synthesis.

The micellar assemblies of lauryl esters of tyrosine (LET) and phenylalanine (LEP) show extraordinary emulsification properties. The structural similarity in respect of the aromatic ring between the dispersed phase, styrene, and the surfactants facilitates solubilization of styrene up to four times the weight of LEP and 11 times that of LET. We propose that the solubilization site varies between core in the LEP and shell in the LET micelles. LET affords double emulsions, water in oil in water (w/o/w) over a narrow phase composition, for example at R=7.15, where R represents ratio of weight of styrene to LET. A schematic model depicting the solubilization site of styrene at different regions in LET and LEP micelles has been proposed. On polymerization, the emulsions with LET and LEP micelles generated high molecular weight polymer nanoparticles of size 12-49 nm with low polydispersity index (P(d)). This demonstrates that micellar assemblies act as templating controlled reactors for the polymerization reaction. We demonstrate that PS nanoparticle dispersion of size 49 nm with polymer weight fraction as high as 42.80% could be produced from emulsions with the LET surfactant, in contrast to LEP that is 50% less efficient. Polymerization of these emulsions occurs predominantly through a micellar nucleation mechanism. It is significant to note that under the same conditions, the control experiments with sodium dodecylsulfate (SDS) micelles resulted in polymers with broad distribution, P(d)>3.0 in molecular weight.

Self-organization at the interface and in aqueous solution of a cationic gemini surfactant from the dioctyl ester of cystine.

The cationic surfactant, dioctyl ester of cystine hydrochloride (DOEC), was characterized for interfacial adsorption and aggregation behavior in water. The cmc of DOEC was measured as 1.42±0.27×10(-5) mol dm(-3) using the techniques of tensiometry, conductivity and fluorimetry. From specific conductivity measurements, the degree of dissociation (α) of the amine hydrochloride was measured as 0.612. The standard free energy change of micellization (ΔG(m)(°)) and adsorption (ΔG(a)(°)) were calculated to be -25.07 and -44.37 kJ mol(-1), respectively. The aggregated structures provide non-polar microdomains as inferred from the I(3)/I(1) emission intensity ratio of 1.05 of pyrene fluoroprobe and also a blue shift of fluorescence emission wave length (λ(emi.)) maximum down to 470 nm with enhanced intensity of ANS probe in micellar solutions. From Langmuir film balance experiments, it is shown that DOEC forms stable viscoelastic films at the interface with A(0) at 0.69 nm(2)molecule(-1) that agree with the result from surface tension measurements. Molecular modeling suggests the tilted orientation of DOEC at the interface. A large packing parameter (P) of 0.58 and the fibril structures as observed from microscopy studies demonstrate that DOEC favors one-dimensional growth to form elongated micelles.

Adsorption and emulsification properties of amphiphilic poly(styrene-co-octadecyl maleamic acid salt) with comb-like architecture.

Amphiphilic poly(styrene-co-octadecyl maleamic acid salt) (PS-co-ODMAS) with a comb-like architecture was synthesized employing a heterophase aqueous polymerization reaction. The side-chain comonomer from octadecyl maleamic acid salt exhibited hydrogelation characteristics and provided conditions for a controlled polymerization reaction. PS-co-ODMAS polymers consisting of 5 and 10 mol% side-chain monomer showed a high molecular weight on the order of 10(6) and narrow polydispersity index at 1.33+0.02. The polymer consisting of 10 mol% side-chain monomer was shown to exhibit properties that are significantly different from those with 5 mol%, and the control poly(styrene) synthesized using sodium dodecyl sulfate surfactant. The polymer consisting of 10 mol% side-chain monomer formed hollow spherical spheres of 30 nm size. It also showed close-packed structures of the side-chain monomer on the polymer surface. Detailed adsorption studies at the liquid/liquid interface were carried out to evaluate and understand the scope for modification in surface energy characteristics of polymers in the presence of additives drawn from simple surfactants. Triton X-100 was shown to undergo effective adsorption on the polymer consisting of 10 mol% side-chain monomer and thus could generate stable emulsions with different volume fractions of heptadecane. The results from electron microscopy studies and viscosity of emulsions are discussed.