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Numerous methods are available to forensic scientists for detecting fingerprints in which the prints are treated with various agents to enhance the visual contrast between the print and the surface. In the present work, the spatial elemental imaging capabilities of micro-X-ray fluorescence (MXRF) were used to visualize fingerprint patterns based on inorganic elements present in the prints. A major advantage of using MXRF is that the prints are left unaltered for other analyses, such as deoxyribonucleic acid extraction or for archiving. Most of the fingerprints which were examined were imaged from the potassium and chlorine present in the print residue. Among the various prints studied, lower count rates were also observed in the elemental maps of Ca, Al, Na, Mg, Si, P, S, and the X-ray source scatter. A sebaceous oily fingerprint left by one subject was successfully imaged by MXRF, but sebaceous prints left by a different person were undetectable, indicating that print elemental composition may be person and/or diet dependent. Prints containing substances that might be found in real-world cases were also visualized including sweat, lotion, saliva, and sunscreen.

The focus of this study was to explore automated printing technology (APT) as an alternative means to manual methods for nanoliter dried spot sample preparation of liquid samples for micro x-ray fluorescence analysis (MXRF). APT was used successfully to dispense 20 and 50 nl volumes of multielemental standard solutions onto AP1 and Kapton film substrates. Automated droplet deposition was rapid and minimized operator skill and human error in the sample preparation process. Dried spots prepared by APT were generally circular in shape and similar in appearance to those prepared by manual dried spot deposition techniques. Furthermore, multiple dried spots could be accurately and reproducibly deposited in the same precise location on the film substrate surface, allowing for increased sample loadings within the MXRF analysis area for higher elemental sensitivity. The characteristics of the substrate did affect the quality of dried spot formation, with irregularly shaped spots forming on the thicker, more hydrophobic Kapton film, especially with higher droplet mass loadings. Adverse effects of irregular spot formation on quantitative analysis could be easily minimized by increasing the MXRF analysis area to encompass the entire dried spot residue. Nanoliter dried spot sample preparation is useful not only for MXRF analysis of liquid samples, but can also be applied to other analytical techniques such as IR, Raman or UV/fluorescence spectroscopy, the applications of which can benefit from rapid sample throughput and matrix reduction. Copyright © 2005 John Wiley & Sons, Ltd.

Micro X-ray fluorescence was used to study both homogeneous and heterogeneous particle systems. Specifically, homogeneous glass microspheres and heterogeneous soil particle samples were prepared by both bulk and single particle sample preparation methods for evaluation by micro X-ray fluorescence. Single particle sample preparation methods allow for single particles from a collected sample to be isolated and individually presented to the micro X-ray fluorescence instrument for analysis. Various particle dispersion methods, including immobilization onto Tacky Dot™ slides, mounting onto double-sided sticky tape affixed to polypropylene film, or attachment to polypropylene film using 3M Artist's Adhesive, were used to separate the sample particles for single particle analysis. These methods were then compared and evaluated for their ability to disperse the particles into an array of single separated particles for optimal micro X-ray fluorescence characterization with minimal background contribution from the particle mounting surface. Bulk methods of particle sample preparation, which included pellet preparation and aerosol impaction, used a large quantity of collected single particles to make a single homogeneous specimen for presentation to the instrument for analysis. It was found that single particle elemental analysis by micro X-ray fluorescence can be performed if the particles are well separated (minimum separation distance = excitation source beam diameter) down to a particle mass of ∼ 0.04 ng and a mean particle diameter of ∼ 0.06 μm. Homogeneous particulates can be adequately characterized by micro X-ray fluorescence using either bulk or single particle analysis methods, with no loss of analytical information. Heterogeneous samples are much harder to characterize, and both single particle as well as bulk analyses must be performed on the sample to insure full elemental characterization by micro X-ray fluorescence.

The analysis of the distribution of pharmaceutical materials in tablet formulations, such as drugs and matrix elements, is critical to product performance and is used in such areas as quality control, impurity testing, and process monitoring. Recently imaging techniques, such as Raman, near-IR, and fluorescence imaging, have become popular for “visualization” of pharmaceutical formulations, allowing for spatial and chemical composition information to be obtained simultaneously. These methods have been primarily focused on molecular imaging, or spatial analysis of the molecular characteristics of the tablet formulation. However, elemental species are also an important part of pharmaceuticals. Micro X-ray fluorescence (MXRF) elemental imaging offers complementary information to molecular imaging techniques. In this study, MXRF was used for the elemental imaging of various commercial pharmaceutical drug and vitamin supplements. Specifically, elemental composition and heterogeneity were monitored for each different tablet.

Space Shuttle orbiter thrusters fabricated from C-103 niobium alloy rely on a fused chromium disilicide coating as protection from high-temperature oxidation. Coating voids caused by high-temperature spalling, micrometeorite damage, or other impact damage must first be detected, and then characterized to measure the amount of remaining coating materials, since service life is directly proportional to coating thickness. Existing techniques to estimate the thickness of this diffusion layer are labor intensive, prone to error, and require contact with the coating. Alternative non-contact methods are sought that can automate the detection and characterization of coating defects. Micro X-ray fluorescence (MXRF) imaging is evaluated in this study as a potential NDE method to inspect the chromium disilicide coating. MXRF imaging, a relatively new technique to map the elemental composition of a surface, creates a high spatial resolution multispectral image that can be analyzed to detect coating voids and to quantify the remaining coating materials diffused in the alloy. Analysis of image data collected from sectioned thruster samples confirms that MXRF imaging is a viable detection and characterization method for the thruster coating inspection problem.

In this study, the nanoliter dried spot method was applied to semiconductor contamination analysis to enhance vapor phase decomposition processes with total reflection X-ray fluorescence detection. Nanoliter-sized droplets (10 and 50 nl) were deposited onto native silicon oxide wafer surfaces in a clean room environment from both single and multielemental standards containing various concentrations of iron in different matrices. Direct comparisons were made to droplets formed by conventional VPD with similar iron standards. Nanoliter dried spots could be reproducibly deposited and dried in air with typical drying times ranging from 20 s to 2 min depending on the nanoliter volume deposited, compared to VPD spots which have drying times ranging from tens of minutes to several hours. Both types of residues showed a linear relationship between Fe intensity and mass deposited. Variable angle experiments showed that both nanoliter and VPD deposits of single element standards were film-like in character, while residues formed from much more complex matrices and higher mass loadings were particulate in character. For the experimental conditions used in this study (30 kV, 100 mA), typical TXRF spectral Fe limits of detection were calculated to be on the order of picograms or ∼1×1010 atoms/cm2 for a 0.8 cm2 X-ray excitation beam area for both nanoliter dried spots and VPD spots prepared from single elemental standards. Calculated Fe detection limits for 200 mm diameter silicon wafers used in this study were in the ∼1×108 atoms/cm2 range. By using nanoliter sized droplets, the required sample volume is greatly reduced resulting in higher sample throughput than with conventional VPD methods.

Micro X-ray fluorescence (MXRF) offers the analyst a new approach to materials characterization. The range of applications is expanding rapidly. Single point analysis has been demonstrated for nanoliter volumes with detection limits at the 0.5 ng level. MXRF can be used as an element specific detector for capillary electrophoresis. Elemental imaging applications include analysis of sample corrosion and polymers, use as a combinatorial chemistry screening tool, and integration with molecular spectroscopic imaging methods to provide a more comprehensive characterization. Three-dimensional elemental imaging is a reality with the development of a confocal X-ray fluorescence microscope. Stereoview elemental X-ray imaging can provide unique views of materials that flat two-dimensional images cannot achieve. Spectral imaging offers chemical imaging capability, moving MXRF into a higher level of information content. The future is bright for MXRF as a materials characterization tool.

The dried spot technique is an effective method for elemental analysis. However, the current technology, using microliter volume spots, suffers from lack of repeatability and long sample preparation times. In this study, a new nanoliter dried spot sample preparation method was developed and tested. Drying time, drying pattern and detection limits were compared between spots formed from microliter- and nanoliter-sized droplets. This new nanoliter deposition method reproducibly produced uniform spots. The sample throughput was increased significantly with nanoliter droplet drying times ranging from only seconds to minutes. The minimum detectable concentrations for the nanoliter spots were in the ppb range with the ability to detect picogram-level masses. This new sample preparation method has the potential for use in situations where sample availability is limited. Furthermore, nanoliter dried spots are smaller in diameter than the exciting x-ray beam in micro-XRF and conventional XRF instrumentation. This allows faster drying nanoliter droplet microarrays to be used in situations where microliter droplets are primarily used. Published in 2004 John Wiley & Sons, Ltd.

A new tool was developed for separation and elemental detection by interfacing a simple capillary electrophoresis (CE) apparatus, constructed using a thin-walled fused-silica capillary, with a benchtop energy-dispersive micro X-ray fluorescence (MXRF) system. X-ray excitation and detection of the separated analytes was done using an EDAX Eagle II micro X-ray fluorescence system equipped with a polycapillary Rh target excitation source and a SiLi detector. It was demonstrated that this prototype system could be used for the separation and detection of species containing two different metals from one another, specifically Cu and Co. Free Co could also be separated from Co bound to cyanocobalamin (vitamin B-12). Two organic compounds were also separated from one another, a large biological protein, ferritin, from a small biological organic, cyanocobalamin. Preliminary average detection limits obtained on this system were on the order of 10(-)(4) M and compared favorably to those reported for the similar technique of CE-synchrotron XRF. CEMXRF allows for nondestructive, simultaneous, on-line, benchtop elemental analysis for chemical speciation applications.

A novel ion-exchange system was developed by tethering a small, monofunctional metal ligand, 3-mercaptopropionic acid (MPA), through thiol linkages onto a glass substrate overlaid with gold, using electroless deposition of Au onto 100 mesh controlled pore glass (CPG) particles. Two different CPG glass pore sizes of 22.6 and 104.9 nm were used in an attempt to optimize Au deposition and ligand coverage. It was found that the Au was present on both of the substrates as a nonuniform deposit, possibly existing as small multilayer islands, throughout the CPG particles. The deposit also did not fill the intricate CPG pore network. Au-CPG is a reasonable substrate for the support of small metal binding ligands such as the monofunctional MPA. Typical metal binding capacities were in the range of 7–24 μmol metal/g column, with the smaller pore system binding approximately twice as much metal as the larger pore system due to increased surface area and fractional ligand coverage. The immobilized binding systems were also found to remain chemically and structurally stable in pH environments ranging from pH∼9 to

Two biologically based ligands, cysteine (Cys) and poly- l -cysteine (PLCys), were coupled with Carbopack-X, a commercially available porous carbon surface after acid activation, through simple cross-linking techniques. The resulting Cys-X and PLCys-X systems are effective for metal binding with capacities in the range of 1–25 μmol metal/g column, depending on the metal tested. Both columns demonstrate similar selectivity for the soft and moderately soft acid metals such as Cd 2+ , Cu + , and Pb 2+ , probably as a result of the soft basic character of the thiol ligand side chains, and exhibit minimal binding of the harder groups IA and IIA metals. Even though PLCys-X and Cys-X displayed similar strong and weak binding characteristics, the PLCys-X system contained stronger binding sites than those possessed by Cys-X. The strongest site displayed by Cys-X has a binding constant of 1×10 9 , with the ability to compete for metal with moderately strong ligands such as ethylenediamine. However, the strongest PLCys-X site possessed a binding constant of about 10 13 , with the ability to compete for metals bound by very strong ligands such as EDTA. Both systems gave quantitative release of bound metals upon exposure to acid. Exposing the thiol-rich ligands to chemical reducing or oxidizing environments altered the metal binding characteristics of both columns, with at least a 50% decrease in metal binding on the oxidized columns due to thiol binding sites because of disulfide bond formation.

Poly-L-aspartic acid (PLAsp), a biopolymer, and a similar synthetic polymer, poly-acrylic acid (PAA), each consisting of approximately 50 repeating Asp and acrylic acid monomers, respectively, were immobilized onto controlled pore glass (CPG) and evaluated for use as metal ion-exchange materials. Both polymers achieve metal complexation primarily through their repeating carboxylate side groups resulting in a similar binding trend for the metals tested (Ca(2+), Cd(2+), Co(2+), Cu(2+), Mg(2+), Mn(2+), Na(+), Ni(2+), Pb(2+)), with metal binding capacities ranging from

A novel ion-exchange column for metal chelation was developed employing stacked gold TEM grids from Polysciences Inc. as a support for the immobilization of poly(l-aspartic acid) (PLAsp) using self...

Poly-l-aspartic acid (PLAsp), which consists of ca. 50 Asp residues in a linear polypeptide, has been immobilized on controlled pore glass (CPG) and evaluated for its selectivity and binding strength in the complexation of metal ions from aqueous solutions. The carboxylate side chain of Asp (pKa = 5.4 ± 0.2) is thought to be primarily responsible for chelation of the target metals. Of the several metals evaluated, Eu3+, Ce3+, La3+, Cu2+, and Pb2+ exhibited good binding capacities. Quantitative determination of single-element capacities were determined for Cu2+ (12 ± 1 μmol/g PLAsp-CPG) and La3+ (7.1 ± 0.3 μmol/g PLAsp-CPG). Isotherms were constructed from breakthrough curves using a flow injection system. These curves were used to evaluate the effective site capacity and formation constants. A combination of moderate and strong binding sites for Pb2+ was detected, while moderate binding of Cd2+ was observed with a minimal number of strong binding sites. Several cations showed little to no binding by PLAsp...

A powerful high-throughput screening technique is described for the rapid screening of bead-based libraries for catalyst discovery and molecular recognition. Micro-X-ray fluorescence (MXRF) screens materials for elemental composition with mesoscale analysis. This method is nondestructive and requires minimal sample preparation and no special tags for analysis, and the screening time is dependent on the desired sensitivity. The speed, sensitivity, and simplicity of MXRF as a high-throughput screening technique were applied to screen bead-based libraries of oligopeptides for phosphate hydrolysis catalysts and molecular recognition of selective receptors for the degradation products and analogues of chemical warfare agents. This paper demonstrates the analytical or HTS capability of MXRF for combinatorial screening. It is meant only to show the capabilities of MXRF and is not meant as an exhaustive study of the catalyst and molecular recognition systems presented.

Micro X-ray fluorescence is used as a high-throughput screening method for combinatorial applications. These include chemical weapon degradation products, catalytic phosphate hydrolysis and radiologic dispersion device metals. In each application the intrinsic elemental signature was utilized to identify the lead hits for the combinatorial screening in locating peptide sequences exhibiting the desired binding characteristics. In addition to being nondestructive, rapid and non-perturbing to the binding event, this method can be used to quantify the amount of target material.

Near-field scanning optical microscopy and tapping mode, liquid cell atomic force microscopy were used to study the conformational changes in simple short-chain silica-immobilized biopolymer, poly(L-cysteine) (PLCys), as the polymer was exposed to reducing, metal-rich, and acidic environments, respectively, to simulate on-line metal preconcentration. In a reducing environment (0.01 M dithiothreitol in pH 7.0 ammonium acetate buffer), the PLCys features resembled islands on the surface of the glass, 36 +/- 7 nm in height and 251 +/- 60 nm in diameter. Upon exposure to metal (Cd2+ buffered at pH 7.0), the PLCys islands broke up into smaller metal binding clusters whose features were lower in height, 22 +/- 5 nm, and diameter, 213 +/- 53 nm. Exposure to 0.01 M HCl used for metal stripping resulted in protonation of the polymer chains and further reduction in the polymer height to 12 +/- 5 nm. These changes in molecular structure have given new insight into the mechanisms involved to achieve strong binding as well as rapid, quantitative release of bound metals to flexible short-chain synthetic biopolymers.

Micro-x-ray fluorescence (MXRF) is a useful characterization tool for high-throughput screening of combinatorial libraries. Due to the increasing threat of use of chemical warfare (CW) agents both in military actions and against civilians by terrorist extremists, there is a strong push to improve existing methods and develop means for the detection of a broad spectrum of CW agents in a minimal amount of time to increase national security. This paper describes a combinatorial high-throughput screening technique for CW receptor discovery to aid in sensor development. MXRF can screen materials for elemental composition at the mesoscale level (tens to hundreds of micrometers). The key aspect of this work is the use of commercial MXRF instrumentation coupled with the inherent heteroatom elements within the target molecules of the combinatorial reaction to provide rapid and specific identification of lead species. The method is demonstrated by screening an 11-mer oligopeptide library for selective binding of the degradation products of the nerve agent VX. The identified oligopeptides can be used as selective molecular receptors for sensor development. The MXRF screening method is nondestructive, requires minimal sample preparation or special tags for analysis, and the screening time depends on the desired sensitivity.