Mg doped Li2FeSiO4/C nanocomposites synthesized by the solvothermal method for lithium ion batteries.

A series of porous Li2Fe1-xMgxSiO4/C (x = 0, 0.01, 0.02, 0.04) nanocomposites (LFS/C, 1Mg-LFS/C, 2Mg-LFS and 4Mg-LFS/C) have been synthesized via a solvo-thermal method using the Pluronic P123 polymer as an in situ carbon source. Rietveld refinement of the X-ray diffraction data of Li2Fe1-xMgxSiO4/C composites confirms the formation of the monoclinic P21 structure of Li2FeSiO4. The addition of Mg facilitates the growth of impurity-free Li2FeSiO4 with increased crystallinity and particle size. Despite having the same percentage of carbon content (∼15 wt%) in all the samples, the 1Mg-LFS/C nanocomposite delivered the highest initial discharge capacity of 278 mA h g-1 (∼84% of the theoretical capacity) at the C/30 rate and also exhibited the best rate capability and cycle stability (94% retention after 100 charge-discharge cycles at 1C). This is attributed to its large surface area with a narrow pore size distribution and a lower charge transfer resistance with enhanced Li-ion diffusion coefficient compared to other nanocomposites.

Functionalized nanoparticles enable tracking the rapid entry and release of doxorubicin in human pancreatic cancer cells.

Efficient drug delivery is critical to therapy. Using electron microscopy, X-ray, and light microscopy, we have characterized functionalized superparamagnetic iron oxide (SPIO) nanoparticles, and determined their ability for rapid entry and release of the cancer drug doxorubicin in human pancreatic cancer cells. Dextran-coated SPIO nanoparticle ferrofluid, functionalized with the red-autofluorescing doxorubicin and the green-fluorescent dye fluorescein isothiocyanate as a reporter, enables tracking the intracellular nanoparticle transport and drug release. This engineered nanoparticle enables a >20 fold rapid entry and release of the drug in human pancreatic cancer cells, holding therapeutic potential as an advanced drug delivery and imaging platform. The low extracellular pH of most tumors precluding the entry of a number of weakly basic drugs such as doxorubicin, conferring drug resistance, can now be overcome.

Fabrication of flexible and self-standing inorganic-organic three phase magneto-dielectric PVDF based multiferroic nanocomposite films through a small loading of graphene oxide (GO) and Fe3O4 nanoparticles.

Flexible inorganic-organic magneto-electric (ME) nanocomposite films (PVDF, PVDF-GO, PVDF-Fe3O4 and PVDF-GO-Fe3O4), composed of well-dispersed graphene oxide (GO 5 wt%) and magnetic Fe3O4 nanoparticles (5 wt%) embedded into a poly(vinylidene-fluoride) (PVDF) matrix, have been prepared by a solvent casting route. The magnetic, ferroelectric, dielectric, magneto-dielectric (MD) coupling and structural properties of these films have been systematically investigated. Magnetic (Ms = 2.21 emu g(-1)) and ferroelectric (P = 0.065 µC cm(-2)) composite films of PVDF-GO-Fe3O4 (PVDF loaded with 5% GO and 5% Fe3O4) with an MD coupling of 0.02% at room temperature (RT) showed a three times higher dielectric constant than that of the pure PVDF film, with a dielectric loss as low as 0.6. However, the PVDF-Fe3O4 film, which exhibited improved magnetic (Ms = 2.5 emu g(-1)) and MD coupling (0.04%) properties at RT with a lower dielectric loss (0.3), exhibited decreased ferroelectric properties (P = 0.06 µC cm(-2)) and dielectric constant compared to the PVDF-GO-Fe3O4 film. MD coupling measurements carried out as a function of temperature on the multi-functional PVDF-GO-Fe3O4 film showed a systematic increase in MD values up to 100 K and a decrease thereafter. The observed magnetic, ferroelectric, dielectric, MD coupling and structural properties of the nanocomposite films are attributed to the homogeneous dispersion and good alignment of Fe3O4 nanoparticles and GO in the PVDF matrix along with a partial conversion of nonpolar α-phase PVDF to polar ß-phase. The above multi-functionality of the composite films of PVDF-Fe3O4 and PVDF-GO-Fe3O4 paves the way for their application in smart multiferroic devices.

Enhanced magneto-dielectric coupling in multiferroic Fe and Gd codoped PbTiO3 nanorods synthesized via microwave assisted technique.

The quest for new multiferroic materials is on the rise due to their potential application in spintronics and futuristic multiple state memory devices. Here we report the microwave synthesis of iron/gadolinium co-doped PbTiO3 nanorods, which display multiferroic behavior. Both the undoped and doped PbTiO3 samples have been characterized using powder X-ray diffraction, energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) techniques. The morphology of the samples has been studied using transmission electron microscopy (TEM) and high resolution transmission electron microscopy (HRTEM), which confirmed the formation of nanorods. The substitution of Fe ions for Ti and Gd ions for Pb enhances the ferromagnetic and ferroelectric properties of this system. The reasons for this observation have been explored in detail. The ferroelectric, magnetic and magneto-capacitive measurements at room temperature substantiate the multiferroic nature of the codoped samples with significant magnetoelectric coupling observed in case of nano PbTiO3:Gd(3+)(0.5%):Fe(3+)(5%).

Vision 20/20: the role of Raman spectroscopy in early stage cancer detection and feasibility for application in radiation therapy response assessment.

Raman spectroscopy is an optical technique capable of identifying chemical constituents of a sample by their unique set of molecular vibrations. Research on the applicability of Raman spectroscopy in the differentiation of cancerous versus normal tissues has been ongoing for many years, and has yielded successful results in the context of prostate, breast, brain, skin, and head and neck cancers as well as pediatric tumors. Recently, much effort has been invested on developing noninvasive "Raman" probes to provide real-time diagnosis of potentially cancerous tumors. In this regard, it is feasible that the Raman technique might one day be used to provide rapid, minimally invasive real-time diagnosis of tumors in patients. Raman spectroscopy is relatively new to the field of radiation therapy. Recent work involving cell lines has shown that the Raman technique is able to identify proteins and other markers affected by radiation therapy. Although this work is preliminary, one could ask whether or not the Raman technique might be used to identify molecular markers that predict radiation response. This paper provides a brief review of Raman spectroscopic investigations in cancer detection, benefits and limitations of this method, advances in instrument development, and also preliminary studies related to the application of this technology in radiation therapy response assessment.

Quantitative skin color measurements in acanthosis nigricans patients: colorimetry and diffuse reflectance spectroscopy.

Tristimulus colorimetry and diffuse reflectance spectroscopy (DRS) are white-light skin reflectance techniques used to measure the intensity of skin pigmentation. The tristimulus colorimeter is an instrument that measures a perceived color and the DRS instrument measures biological chromophores of the skin, including oxy- and deoxyhemoglobin, melanin and scattering. Data gathered from these tools can be used to understand morphological changes induced in skin chromophores due to conditions of the skin or their treatments. The purpose of this study was to evaluate the use of these two instruments in color measurements of acanthosis nigricans (AN) lesions. Eight patients with hyperinsulinemia and clinically diagnosable AN were seen monthly. Skin pigmentation was measured at three sites: the inner forearm, the medial aspect of the posterior neck, and anterior neck unaffected by AN. Of the three, measured tristimulus L*a*b* color parameters, the luminosity parameter L* was found to most reliably distinguish lesion from normally pigmented skin. The DRS instrument was able to characterize a lesion on the basis of the calculated melanin concentration, though melanin is a weak indicator of skin change and not a reliable measure to be used independently. Calculated oxyhemoglobin and deoxyhemoglobin concentrations were not found to be reliable indicators of AN. Tristimulus colorimetry may provide reliable methods for respectively quantifying and characterizing the objective color change in AN, while DRS may be useful in characterizing changes in skin melanin content associated with this skin condition.

Defect stabilization in ZnO nanorods by Mg2+ doping.

Luminescent ZnO and Zn0.95Mg0.05O nanorods with length around 0.5 to 3 microm and diameter 100-150 nm were prepared by a facile solvothermal method. On hydriding at room temperature, a change of morphology from nanorods with aspect ratio 5-10 to particles of sizes 100 nm has been observed in both ZnO and Zn0.95Mg0.05O. While hydrided Zn0.95Mg0.05O showed an enhanced defect related green emission, the same got suppressed in hydrided ZnO. Even though it is observed that zinc vacancies are present in both as prepared ZnO and Zn0.95Mg0.05O, luminescence studies indicate that zinc vacancies get stabilized in Zn0.95Mg0.05O on hydrogenation.

Possible weak ferromagnetism in pure and M (Mn, Cu, Co, Fe and Tb) doped NiGa2O4 nanoparticles.

We report on the structural and magnetic properties of nanoparticles of NiGa2O4 and 5 at.% M doped (M = Mn2+, Cu2+, Co2+, Fe3+ and Tb3+) at Ga site of NiGa2O4, synthesized by gel-combustion method. The particle size, as investigated by X-ray diffraction and transmission electron microscopy, could be fine tuned by a controlled annealing process. Weak ferromagnetism becomes significant, when the particles are in the nano regime (5-7 nm). The magnetization becomes insignificant at larger particle size ( 150 nm). Cu2+ and Tb3+ doped NiGa2O4 nanoparticles showed relatively large room temperature ferromagnetism compared to other doped (Fe, Mn and Co) and undoped NiGa2O4 samples. The weak ferromagnetism observed in the nanoparticles of NiGa2O4, which is antiferromagnetic in the bulk, is due to the surface disordered states with uncompensated spins.

Critical comparison of diffuse reflectance spectroscopy and colorimetry as dermatological diagnostic tools for acanthosis nigricans: a chemometric approach.

Quantification of skin changes due to acanthosis nigricans (AN), a disorder common among insulin-resistant diabetic and obese individuals, was investigated using two optical techniques: diffuse reflectance spectroscopy (DRS) and colorimetry. Measurements were obtained from AN lesions on the neck and two control sites of eight AN patients. A principal component/discriminant function analysis successfully differentiated between AN lesion and normal skin with 87.7% sensitivity and 94.8% specificity in DRS measurements and 97.2% sensitivity and 96.4% specificity in colorimetry measurements.

Improving a high-resolution fiber-optic interferometer through deposition of a TiO2 reflective coating by simple dip-coating.

Fiber-optic based interferometers are used to detect small displacements, down to the subnanometer range. Coating the end of the optical fiber with a partially reflecting thin film greatly improves the resolution of interferometers by increasing the multiple reflections between the fiber end and the measured object. In this work, we present a quick and easy thin film deposition technique to coat the end of a single optical fiber by dip-coating a metal-organic precursor, which is then decomposed in a propane flame. The coated fiber was tested for morphology and usefulness for interferometric application. We found that this coating technique is much faster and easier than conventional thin coating techniques, and yields results that are comparable or better than can be achieved with sputtering or thermal evaporation.

Magnetic-field-induced optical anisotropy in ferrofluids: a time-dependent light-scattering investigation.

We report an experimental investigation of time dependent anisotropic light scattering by an aqueous suspension of tetramethyl ammonium hydroxide coated Fe3O4 nanoparticles (approximately 6 nm) under the ON-OFF transient of an external dc magnetic field. The study employs the synchronized recording and measurement of the two magnetic-field-induced light-scattering patterns produced by two identical orthogonal He-Ne laser beams passing through the ferrofluid sample and propagating parallel and perpendicular to the applied field, respectively. From these patterns, we extract the time dependence of the induced optical anisotropy, which provides a measure of the characteristic time scale and kinematic response for field-induced structure formation in the sample. We propose that the time evolution of the scattering patterns, which is very fast at short times and significantly slower at long times, can be explained using a model based on a two-stage chain formation and coarsening processes.

Evaluation of pancreatic cancer with Raman spectroscopy in a mouse model.

OBJECTIVES: Detection of neoplastic changes using optical spectroscopy has been an active area of research in recent times. Raman spectroscopy is a vibrational spectroscopic technique that can be used to diagnose various tumors with high sensitivity and specificity. We evaluated the ability of Raman spectroscopy to differentiate normal pancreatic tissue from malignant tumors in a mouse model. METHODS: We collected 920 spectra, 475 from 31 normal pancreatic tissue and 445 from 29 tumor nodules using a 785-nm near-infrared laser excitation. Discriminant function analysis was used for classification of normal and tumor samples. RESULTS: Using principal component analysis, we were able to highlight subtle chemical differences in normal and malignant tissue. Using histopathology as the gold standard, Raman analysis gave sensitivities between 91% and 96% and specificities between 88% and 96%. CONCLUSIONS: Raman spectroscopy along with discriminant function analysis is a useful method to detect cancerous changes in the pancreas. Pancreatic tumors were characterized by increased collagen content and decreased DNA, RNA, and lipids components compared with normal pancreatic tissue.

Diagnosis of neuroblastoma and ganglioneuroma using Raman spectroscopy.

BACKGROUND: Raman spectroscopy has proven to be useful in studying premalignant and malignant lesions in adults. This is the first report to evaluate Raman spectroscopy in the diagnosis and classification of neuroblastoma in children. METHODS: A biopsy or resection of fresh tissue samples from normal adrenal glands, neuroblastomas, ganglioneuromas, nerve sheath tumors, and pheochromocytoma at our hospital were equally divided between routine histology and spectroscopic studies. At least 12 spectra were collected from different regions of each sample using a Renishaw Raman microscope. Raw spectra were processed to remove noise, fluorescence, and shot noise, and then analyzed using principle component analysis and discriminant function analysis. RESULTS: We collected 698 spectra from 16 neuroblastomas, 5 ganglioneuromas, 3 normal adrenal glands, 6 nerve sheath tumors, and 1 pheochromocytoma. Raman spectroscopy differentiated between normal adrenal gland, and neuroblastoma and ganglioneuroma with 100% sensitivity and 100% specificity. It correlated well with the Shimada histologic classification system with 100% sensitivity and 100% specificity. It was also able to differentiate neuroblastoma from nerve sheath tumors and pheochromocytoma with high sensitivity and specificity. CONCLUSION: This technique can differentiate neuroblastoma from ganglioneuroma and other tumors. It has a potential as a noninvasive real-time diagnostic tool in classifying pediatric tumors.

Raman spectroscopy can differentiate malignant tumors from normal breast tissue and detect early neoplastic changes in a mouse model.

Raman spectroscopy shows potential in differentiating tumors from normal tissue. We used Raman spectroscopy with near-infrared light excitation to study normal breast tissue and tumors from 11 mice injected with a cancer cell line. Spectra were collected from 17 tumors, 18 samples of adjacent breast tissue and lymph nodes, and 17 tissue samples from the contralateral breast and its adjacent lymph nodes. Discriminant function analysis was used for classification with principal component analysis scores as input data. Tissues were examined by light microscopy following formalin fixation and hematoxylin and eosin staining. Discriminant function analysis and histology agreed on the diagnosis of all contralateral normal, tumor, and mastitis samples, except one tumor which was found to be more similar to normal tissue. Normal tissue adjacent to each tumor was examined as a separate data group called tumor bed. Scattered morphologically suspicious atypical cells not definite for tumor were present in the tumor bed samples. Classification of tumor bed tissue showed that some tumor bed tissues are diagnostically different from normal, tumor, and mastitis tissue. This may reflect malignant molecular alterations prior to morphologic changes, as expected in preneoplastic processes. Raman spectroscopy not only distinguishes tumor from normal breast tissue, but also detects early neoplastic changes prior to definite morphologic alteration.

Raman spectroscopy for neoplastic tissue differentiation: a pilot study.

BACKGROUND: Several changes occur during the transformation of normal tissue to neoplastic tissue. Such changes in molecular composition can be detected by Raman spectroscopy. Raman spectroscopy is a nondestructive method of measuring these changes, which suggests the possibility of real-time diagnosis during medical procedures. METHODS: This study seeks to evaluate the ability of Raman spectra to distinguish tissues. The Raman signatures of normal kidney, lung, and liver tissue samples from pigs and rats were characterized in vitro. Further, a human neuroblastoma and a hepatoblastoma, obtained at resection were also studied. RESULTS: The Raman spectra of the animal samples of kidney, liver, and lung are distinctly different in the intensity distribution of the Raman peaks. Further, the spectra of a given organ from pigs and rats, although similar, were different enough to distinguish between the 2 animals. In the patient tissues, the Raman spectra of normal liver, viable tumor, and fibrotic hepatoblastoma were very different. Fibrotic tissue showed a greater concentration of carotenoids, whereas viable tissue was rich in proteins and nucleic acids. The normal tissue showed both components. Similar differences were also seen in the neuroblastoma tissue. CONCLUSIONS: The results of this study show the potential use of Raman spectroscopy in clinical diagnosis.