Photoluminescent CdS/dendrimer nanocomposites for fingerprint detection

CdS/dendrimer nanocomposites with a range of concentrations of the photoluminescent semiconductor nanocluster and the dendrimer are prepared in methanol and 1:9 methanol:water solutions. The solutions are utilized for detection of cyanoacrylate ester fumed and unfumed fingerprints on polyethylene and aluminum foil.     

CdSe/TGA与CdS/PAMAM量子点溶液显现胶带粘面油汗手印性能比较研究

目的比较巯基乙酸包覆的硒化镉（CdSe/TGA）和硫化镉/聚酰胺-胺（CdS/PAMAM）量子点溶液显现胶带粘面手印的性能。方法两种材料在显现指纹的过程中,通过比较观察显现时间、显现温度、遗留时间等因素来考察显现效果。结果 CdSe/TGA溶液的荧光强度、显现时间以及材料的稳定性较好;CdS/PAMAM溶液显现的手印纹线流畅,显现细节特征能力强,对陈旧的或微弱的油潜手印的显现效果好。结论两种材料各有所长,对胶带粘面手印有良好的显现效果。     

胺端基型CdS／PAMAM潜在显现指印的应用

目的探索一种新型纳米荧光材料的制备方法及其在潜在指印显现方面的应用前景。方法以聚酰胺-胺（PAMAM）树形分子为模板，原位合成CdS纳米簇。并使用荧光光谱法对产物进行表征：应用这种新型荧光材料对多种客体表面、不同陈旧程度的潜在指印进行显现．并将显现结果与传统荧光染料进行比对。结果该荧光材料在365nm紫外光激发下可以发出很强的可见荧光：与传统的荧光染料相比。-NH2端基型CdS／PA—MAM可以同指印残留物进行靶向结合．其荧光强度高、背景干扰小，指印纹线与客体反差大。结论-NH2端基型CdS／PAMAM可以有效地显出非渗透性客体表面的潜在指EP。     

Photoluminescent semiconductor nanocrystals for fingerprint detection

The concept of utilizing photoluminescent semiconductor nanocrystals for latent fingerprint detection, especially in concert with phase-resolved imaging for background fluorescence suppression, is reduced to practice with CdS nanocrystals that are capped with dioctyl sulfosuccinate. The nanocrystals are dissolved in heptane or hexane and are applied in much the same way as staining with fluorescent dye, on articles that have been pre-fumed with cyanoacrylate ester and also on the sticky side of electrical tape without pre-fuming. Since CdS can form a photoluminescent nanocomposite with dendrimers, a feasibility examination of dendrimer tagging of fingerprints has also been conducted.     

PAMAM G7.0的制备及在非渗透性表面手印显现中的应用

目的探索一种非渗透性表面手印显现的新方法。方法根据现有方法合成第七代聚酰胺-胺（PAMAM G7.0）树形分子材料,并使用荧光光谱法对产物进行荧光测试;将合成材料对多种客体表面、不同遗留时间的手印进行显现,并将显现结果与粉末法和传统的荧光染料法进行比对。结果实验表明该荧光材料在365nm光激发下可以发出较强的可见荧光;与粉末法和传统的荧光染料法相比,PAMAM G7.0可以同手印残留物进行高选择性结合,手印纹线与背景之间的反差大。结论PAMAMG7.0可以有效地显出非渗透性客体表面的手印。     

Evaluation of Nile Red‐Loaded Mesoporous Silica Nanoparticles for Developing Water‐Soaked Fingerprints on Thermal Paper

Nile red has been an alternative reagent for detecting latent fingerprints on wetted substrates. However, the presence of methanol in nile red solution could make injury to handlers and destroy the traces on surfaces, such as texts on thermal papers. A novel small particle reagent formulation constituting of mesoporous silica nanoparticles (MSNs) based on nile red was prepared to overcome the problem. Compared with the conventional reagents Oil Red O or nile red solution, the nile red‐loaded MSNs are highly selective to lipid residues of fingerprints and showed a greater ability to develop clear, sharp, and detailed fingerprints on thermal papers after these were immersed in water. In addition, it can retain texts on the thermal papers well and use only water as a solvent. These suggested that nile red‐loaded MSNs are a safe, efficient, and convenient method to develop latent fingerprints on wide range of substrates of forensic importance.     

新型荧光502粉末与502胶＋荧光染色显现潜在手印的比较

目的对新型荧光502粉末显现非渗透性光滑客体表面潜手印的一步荧光502显现新技术和传统502胶水熏显＋荧光染料染色显现手印技术进行比较研究。方法比较实验研究,对荧光502粉末和502胶水使用同一自动熏显柜先后进行熏显,荧光502粉末熏显结束后直接在蓝光灯下激发进行观察和拍照;502胶水在熏显完成和聚合物完全固化后使用罗丹明6G和BBD溶液进行荧光染色,再进行光致荧光照相。结果一步熏显和二次染色的显现效果基本相同,但两者的显现效果也因检材性质和遗留时间的不同而存在一些差别。结论新型荧光502粉末可以作为一种显现非渗透性光滑客体表面上潜手印的常用方法,尽管新方法对某些客体的显现效果并不好,但对大多数客体来说,其显现效果并不弱于二次染色的方法,并且使用新型荧光502粉末进行一步熏显不会引入有机溶剂,不会引起502聚合物的溶解或造成破坏,确保了纹线及其细节特征不被损坏,也避免了染色后因漂洗不当使手印纹线被冲掉的可能,还不会破坏脱落细胞等生物检材。     

Study of TATP: stability of TATP solutions

Stability of raw TATP (3,3,6,6,9,9-hexamethyl-1,2,4,5,7,8-hexoxonane) samples in solutions of common solvents was studied to highlight problems faced by forensic labs in identification and analysis of organic peroxide samples. The TATP samples were prepared by reaction of acetone and hydrogen peroxide (30%) with the aid of following catalysts: hydrochloric, sulfuric, nitric, perchloric and methanesulfonic acid. Acetone, acetonitrile, methanol and acetonitrile/water solutions of TATP samples were prepared and stored at 50°C. Various degrees of stability were observed for particular combination of catalyst and solvent ranging from totally unstable (catalyst-H(2)SO(4)/any solvent) to very stable (catalyst-HCl/solvent acetonitrile). Purification of crude TATP by re-crystallization results in product stable in all investigated solvents. Stability of solution prepared from re-crystallized DADP (3,3,6,6-tetramethyl-1,2,4,5-tetroxane) was found to be on the same level as the stability of solution of re-crystallized TATP.     

Rapid isolation with Sep-Pak C18 cartridges and capillary gas chromatography of triazine herbicides in human body fluids.

A simple and rapid method, for the isolation of eight triazine herbicides from human serum and urine, using Sep-Pak C18 cartridges is presented. After mixing with distilled water, serum and urine samples containing the herbicides, were loaded on Sep-Pak C18 cartridges and eluted with either chloroform only or chloroform/methanol (9:1). The herbicides were detected by capillary gas chromatography with both flame ionization detection (FID) and nitrogen-phosphorus detection (NPD). Separation of eight triazine herbicides from each other and from impurities was generally satisfactory with the use of a non-polar DB-1 capillary column. Recovery of most compounds was excellent for both chloroform and chloroform/methanol (9:1) as elution solvents. Backgrounds were cleaner and evaporation time was shorter for the chloroform only than for the chloroform/methanol (9:1). The NPD gave sensitivity more than 10-20 times higher than that of FID.     

水溶性碲化镉量子点溶液显现血潜指纹

目的建立巯基丁二酸修饰的水溶性碲化镉量子点溶液（MSA/CdTe QDs）显现多种客体表面的血潜指纹的方法。方法利用量子点对人体血液成分的特异性标识作用,365nm紫外光激发使其荧光显像。结果 MSA/CdTe溶液显现时间显著短于文献报导的同类方法;显现效果和灵敏度优于显现血潜指纹常用试剂四甲基联苯胺和氨基黑10B。结论水溶性MSA/CdTe溶液适于显现多种客体表面的血潜指纹,效果优异。     

The effect of metal salt treatment on the photoluminescence of DFO-treated fingerprints

Ninhydrin developed fingerprints can be enhanced by treatment with a zinc or cadmium salt. The resulting fingerprint luminescence has been attributed to the induced coplanarity of the bicyclic indanedione rings of Ruhemann's purple due to complexation with the metal ions. This paper explores whether this effect also occurs in the 1,8-diaza-9-fluorenone (DFO)-amino acid adduct (1), formed from the reaction of DFO with amino acids. Molecular modeling studies of (1) indicate a relatively small out-of-plane angle of 24 degrees. 1H NMR studies indicate (1) is asymmetric about the C2 axis in contrast to what has been previously reported. Little, if any, enhancement of luminescence was observed with Zn, Cd, Ru or Eu treated DFO developed latent fingerprints. This lack of enhancement was also borne out by solution luminescence studies. Given this lack of enhancement of luminescence, solutions of (1) and the four metal ions above were analyzed by electrospray mass spectrometry (ESMS). This indicated the formation of predominantly 1:1 complexes of (1) with both Zn and Cd, and the 2:1 complex with ruthenium. No evidence of a Eu complex was found by ESMS.     

用Sep—Pak C18固相萃取柱快速提取净化氨基甲酸酯类农药

本文介绍了一种应用Sep—Pak C_(18)固相萃取柱从各类生物检材中快速提取净化9种氨基甲酸酯类农药的方法,并用大口径毛细管气相色谱进行分析。9种药物包括:速灭威、叶蝉散、灭多虫、灭除威、灭杀威、残杀威、巴沙、呋喃丹、西维因。萃取前,水基质检材用蒸馏水稀释;脏器检材加0.4N高氯酸溶液。用3ml氯仿/异丙醇(9:1)洗脱药物。水基质检材的回收率(尿、血浆、全血)在80—100％之间;脏器检材的回收率(肝、肾、脑)在66—100％之间。Sep—Pak C_(18)小柱用于尿和血浆样品时可反复使用。     

Cadmium-free quantum dots in aqueous solution: Potential for fingermark detection,synthesis and an application to the detection of fingermarks in blood on non-porous surfaces

The use of quantum dots (QDs) in the area of fingermark detection is currently receiving a lot of attention in the forensic literature. Most of the research efforts have been devoted to cadmium telluride (CdTe) quantum dots often applied as powders to the surfaces of interests.Both the use of cadmium and the nano size of these particles raise important issues in terms of health and safety. This paper proposes to replace CdTe QDs by zinc sulphide QDs doped with copper (ZnS:Cu) to address these issues. Zinc sulphide–copper doped QDs were successfully synthesized, characterized in terms of size and optical properties and optimized to be applied for the detection of impressions left in blood, where CdTe QDs proved to be efficient. Effectiveness of detection was assessed in comparison with CdTe QDs and Acid Yellow 7 (AY7, an effective blood reagent), using two series of depletive blood fingermarks from four donors prepared on four non-porous substrates, i.e. glass, transparent polypropylene, black polyethylene and aluminium foil. The marks were cut in half and processed separately with both reagents, leading to two comparison series (ZnS:Cu vs. CdTe, and ZnS:Cu vs. AY7). ZnS:Cu proved to be better than AY7 and at least as efficient as CdTe on most substrates. Consequently, copper-doped ZnS QDs constitute a valid substitute for cadmium-based QDs to detect blood marks on non-porous substrates and offer a safer alternative for routine use.     

Rapid isolation of some antiepileptic hydantoins and their analogues with Sep-Pak C18 cartridges and capillary gas chromatography with splitless injection

A simple and rapid method for isolation of seven antiepileptics (2 hydantoin, 2 oxazolidin, and 3 suximide derivatives) from urine and plasma is presented. Urine and plasma (1 ml) samples containing seven antiepileptics were mixed with distilled water (4 ml), and the sample solution was poured into a pretreated Sep-Pak C18 cartridge; this was washed with water and chloroform/methanol was passed through it to elute the antiepileptics. The eluate was mixed with isoamyl acetate and evaporated under a stream of N2. The drugs were detected by gas chromatography with fused silica capillary columns, splitless injection and flame ionization detection. Separation of the seven antiepileptics from each other and from impurities was satisfactory with the use of an SPB-1 capillary column. The detection limit for the seven antiepileptics with the present method was 0.1-1.0 microgram/ml urine or plasma. The recovery of the drugs from urine and plasma was more than 70% and 50%, respectively.     

The application of infrared chemical imaging to the detection and enhancement of latent fingerprints: method optimization and further findings

Fourier transform infrared (FTIR) chemical imaging allows the collection of fingerprint images from backgrounds that have traditionally posed problems for conventional fingerprint detection methods. In this work, the suitability of this technique for the imaging of fingerprints on a wider range of difficult surfaces (including polymer banknotes, various types of paper, and aluminum drink cans) has been tested. For each new surface, a systematic methodology was employed to optimize settings such as spectral resolution, number of scans, and pixel aggregation in order to reduce collection time and file-size without compromising spatial resolution and the quality of the final fingerprint image. The imaging of cyanoacrylate-fumed fingerprints on polymer banknotes has been improved, with shorter collection times for larger image areas. One-month-old fingerprints on polymer banknotes have been successfully fumed and imaged. It was also found that FTIR chemical imaging gives high quality images of cyanoacrylate-fumed fingerprints on aluminum drink cans, regardless of the printed background. Although visible and UV light sources do not yield fingerprint images of the same quality on difficult, nonporous backgrounds, in many cases they can be used to locate a fingerprint prior to higher quality imaging by the FTIR technique. Attempts to acquire FTIR images of fingerprints on paper-based porous surfaces that had been treated with established reagents such as ninhydrin were all unsuccessful due to the swamping effect of the cellulose constituents of the paper.     

Detection of latent fingerprints by the use of silver nitrate

Silver nitrate has been an established agent for the detection of latent fingerprints for some 120 years, and it was one of the few reagents suitable for use on porous surfaces until ninhydrin was introduced in forensics. The method is based on the reaction of silver ions with chlorides in the fingerprints, which are visualized in brown, violet or black. The literature describes many variations of the procedure, but the information provided is often vague and imprecise. The purpose of this study was to show whether this method can also be used on modern types of paper and how it should be applied. The results of the tests showed that silver nitrate solutions do work also on modern papers, but that they cannot be recommended as a standard, because the appearance of the prints and the paper background can strongly change in the course of time. The findings also do not justify the use of methanol-containing silver nitrate solutions in contrast to the variations based on water. For reasons of occupational safety, methanol, which is classified as poisonous, should not be used. The silver nitrate method may be taken into consideration, however, e.g. after the application of ninhydin, if there are hints that the potential fingerprints are not too old, have not been affected by moisture and if there are clues that the perpetrator perspired strongly while causing the prints.     

直接耐晒黄ARL显现加层油手印的研究

目的建立显现渗透性较强客体上加层油手印的一种优化配方。方法利用单因素实验法对直接耐晒黄ARL显现液中的4种成分的用量分别进行筛选，得到一种最佳配比，再通过时效性实验，观察油手印的不同遗留时间对显现效果的影响。结果实验得到优化配方是，4mL0．59／5直接耐晒黄ARL液＋4mL甲醇＋1．6mL氯化锌溶液，充分搅拌后加入0．6mLSD-8去油灵。结论该配方显现出的纹线清晰，直接耐晒黄ARL显现液对不同客体上的新鲜、较陈旧加层油手印都有较好的显现效果。     

Diagnosis of chronic alcohol consumption. Hair analysis for ethyl-glucuronide

This paper describes a procedure for the detection and quantification of ethyl-glucuronide (EtG) in hair samples. During method development the efficacy of extraction of EtG from hair was compared in four extraction methods: (a) methanol; (b) methanol:water (1:1); (c) water; and (d) water:trifluoroacetic acid (9:1). In addition, three derivatizing agents were compared as well: N,O-bistrimethylsilyl-trifluoroacetamide (BSTFA): trimethylchlorosilane (TMCS) (99:1), pentafluoropropionic anhydride (PFPA) and heptafluorobutyric anhydride (HFBA). Water was found to be the best extracting solvent and PFPA the best derivatizing agent. Both provided the highest recoveries, with cleaner extracts and more stable derivatives. The final method is as follows: about 100mg of hair are sequentially washed with water and acetone. The decontaminated sample is finely cut with scissors, then the deuterated internal standard (EtG-d5) and 2 mL of water are added. After sonication for 2 h, the sample is maintained at room temperature overnight. Derivatization is performed with PFPA. Derivatives are injected into a GC-MS system in the electronic impact mode. The method shows linearity over the range of concentrations from 0.050 to 5 ng/mg. Detection and quantification limits are 0.025 and 0.050 ng/mg, respectively. Mean recoveries for the three studied concentrations (low, medium and high) are higher than 87%. The coefficients of variation in intra- and inter-assay precision are always lower than 7%. The method is being routinely applied in our lab for the diagnosis of chronic alcohol consumption.     

A case of death after ingestion of an agrochemical spreading agent

An agrochemical spreading agent was found near the slightly decomposed corpse of a deceased female. The appearance of the stomach contents suggested that ingestion of a surfactant had occurred before death. The spreading agent was found to contain nonionic nonylphenol ethoxylates (NPEO(n)) and anionic sulfonated naphthalene-formaldehyde condensates (SNFC(n)). A solid phase extraction cartridge containing a mixed reversed phase-weak anion exchange sorbent (Oasis WAX, Waters) was used to successfully extract both NPEO(n) and SNFC(n) from the blood. The cartridge was preconditioned with methanol and acetic acid (AcOH). After the dilute blood sample was applied to the cartridge, it was washed with AcOH, and then NPEO(n) and SNFC(n) were eluted with methanol/dichloromethane (7:3, v/v) and 5% NH(3)/80% methanol, respectively. The concentrations of NPEO(n=2-9) and SNFC(n=0) in the blood sample were 7.7μg/mL and 1.8mg/mL, respectively. It is possible that postmortem changes increased the concentration of SNFC(n=0) monomer by breaking down the polymer. However, the behavior of these compounds in the human body is unclear and further case studies are needed to investigate this result.     

A novel chitosan/tripolyphosphate/L‐lysine conjugates for latent fingerprints detection and enhancement

Most chemical and physical methods employed in visualizing latent marks have shown detrimental effects on human health and, therefore, some research groups have directed their attention to the utilization of various (bio)polymers with the aforementioned purpose. Although chitosan is widely used in medicine, pharmacy, food, and drug delivery systems, there are very few studies that address this biopolymer utilization in forensic applications, such as the detection of latent fingerprints. We used chitosan crosslinked with sodium tripolyphosphate and conjugated with L‐lysine to enhance the visualization of latent fingerprints, due to its ability to interact with fingerprint sweat residues. These conjugates were prepared using different (w/w) amounts of chitosan and tripolyphosphate (6/1; 4/1; 1/1; 1/4; and 1/6), and those with the most promising results (i.e., 6/1 formulation) were investigated in detail. Fourier transform infrared (FT‐IR) spectroscopy confirmed interactions between components of the systems. Optical microscopy and scanning electron microscope (SEM) analysis showed that prepared powder formulations were uniform in size and confirmed that chitosan/tripolyphosphate/lysine conjugates bind easily to the sweat and lipid residues present in the latent fingerprints. The testing of prepared conjugates demonstrated the potential of these systems as bio‐based powder substitution for commercially available powders.