京尼平与茚三酮显现手印方法的比较研究

目的对京尼平与茚三酮两种手印显现方法进行综合评价。方法用两种方法显现不同遗留客体上不同遗留时间的手印,并对显现效果、显出手印的稳定性及纸张字迹油墨扩散等现象进行考察。结果京尼平与茚三酮有着相似的的显现原理、适用范围和熏显条件,但在显现效果、显出手印稳定性、试剂成本和安全性能方面存在差异。结论京尼平相比茚三酮方法更安全、绿色环保、显出的手印稳定性更强。     

京尼平序列显现手印方法研究

目的考察京尼平溶液显现手印的灵敏度,并探索DFO→京尼平→茚三酮方法联用显现纸张上潜在手印的效果。方法通过使用京尼平溶液对同一手印样本进行一次、两次和三次浸泡处理,考察浸泡次数是否会影响显现效果;通过对京尼平→茚三酮、茚三酮→京尼平,京尼平→DFO和DFO→京尼平方法的组合设计方案与每种方法的单独使用进行比较研究,考察序列显现方法对显出手印的影响。结果单用京尼平溶液对同一样本进行多次浸泡在自然光和荧光模式下都不会明显增强手印的显现效果,DFO方法先于京尼平、京尼平先于茚三酮使用都能起到增强手印纹线的效果。结论京尼平方法显现手印灵敏度较高,DFO→京尼平→茚三酮方法联用可以进一步提高手印的显出率。     

茚三酮固体介质法显现不同纸张表面潜指纹

茚三酮是显现渗透性客体上潜在汗液手印的最常用方法之一,采用微量物证提取纸和茚三酮溶液有机结合制作的茚三酮固体介质可以有效避免客体表面背景着色,不容易引起纸张油墨扩散,另外避免使用的溶剂易燃。能够更便捷的显现现场指纹,并且能够突破茚三酮只能显现渗透性客体的局限,拓宽茚三酮显现客体的范围,在热敏纸上潜指纹的显现方面有独特的应用优势。     

纸张上手印的DFO-茚三酮-物理显影液系列显现方法研究

目的 提高纸张上手印显现率.方法 采用DFO-茚三酮-物理显影液系列显现法,比较每一显现步骤的指印显现率.结果 每一显现步骤均能提高手印显现率.结论 DFO-茚三酮-物理显影液系列显现法有效提高纸张上手印的显现率.     

三种β-取代茚三酮的合成及显现汗潜手印的研究

本文基于傅克酰基化取代反应合成了三种茚三酮类似物：β-甲氧基茚三酮、β-硝基茚三酮、β-甲基茚三酮,比较并研究相同配方下三种β-取代茚三酮在不同纸张上显现汗潜手印的效果,并分别与茚三酮进行比较,分析其优劣。结果显示,三种β-取代茚三酮的显现液基本可显示不同纸张上的新鲜指纹,但β-硝基茚三酮对于陈旧指纹的显现效果较差,且显现液本身为棕褐色,显示出的指纹纹线为黑褐色,故视觉感官上稍劣于其他两者;β-甲氧基茚三酮和β-甲基茚三酮的效果均与茚三酮相当,灵敏度略高于茚三酮,显色后的稳定性高于茚三酮。研究表明,β-位取代基的变化能够改变茚三酮类化合物显现手印的效果,给电子基团的修饰能够提高该类化合物的手印显现性能,化合物本身的荧光性能与实际的指纹显现效果并不直接相关。     

纸张上潜在手印三种前处理方法对DNA检验的影响

目的通过比较常见纸张上潜在手印盲提法与显现后精准提取法的接触DNA检出率,探讨常见纸张上接触DNA前处理的优选方案。方法比较五种常见纸张上使用盲提法和显现潜在手印(茚二酮显现法、茚三酮熏显法)后精准提取法采集的接触DNA样本检出率。结果粗糙日历纸盲提的接触DNA检出率为17.8%,通过茚二酮法和茚三酮法显现的潜在手印所提取的DNA检出率分别为75.6%、77.8%;光滑日历纸三种方法所提取的接触DNA检出率为4.4%、11.1%、11.1%;A4复印纸三种方法接触DNA检出率为20%、37.8%、66.7%;牛皮纸三种方法接触DNA检出率为20%、68.9%、64.4%;快递纸袋的三种方法接触DNA检出率为2.2%、6.7%、46.7%。结论不同纸张上潜在手印经显现后接触DNA检出率不同,通过茚二酮或茚三酮显示潜在手印后精准提取DNA的前处理方法相较于盲提法的接触DNA检出率高。实战中可应用此类方法同时获得手印与DNA分型,以有效提高证据力。     

硝酸银、茚三酮、DFO法显现纸张上指印的效果比较

目的为有效的提高纸张上汗潜手印的显现率。方法根据汗潜手印的显现原理,针对不同的纸张,分别运用硝酸银、茚三酮与DFO（1,8-二氮芴-9-酮）3种显现方法进行了实验,并对实验结果进行了分析比较。重点分析了这3种方法在显现不同纸张、不同遗留时间、不同汗液量的汗潜手印时的效果及其适用范围。结果为改善渗透性客体上的汗潜手印显现效果,提供科学的依据。     

碘熏显现热敏纸上的汗潜手印

热敏纸作为一种特殊的客体,其传统显现普通纸张汗潜手印的显现方法,如(硝酸银显现法、茚三酮溶液法、DFO法等) ,都不能有效显现热敏纸上的汗潜手印。热敏纸遇到有机溶剂,药膜面上会产生黑色污染背景,影响指纹显现,甚至使整个膜面变黑,上面的手印消失。直接加热法显现热敏纸潜手印时,显现温度难以掌握,易污染检材,只能显现热敏纸膜面上的手印,背面的手印没法解决,对有效显现热敏纸上的手印有很大的局限。而碘熏法能克服上述不足,有效的显现热敏纸上的潜手印,此方法操作简便,显现效果较好,不仅能显现新鲜手印,还能显现保存较好的热敏纸上的…     

饱和银氨溶液显现纸张上手印的研究

在犯罪现场中,经常涉及到各种纸张上手印的显现。以往多是利用硝酸银溶液及茚三酮溶液进行显现。硝酸银曝光不易控制,且硝酸银溶液与茚三酮溶液显出的手印往往出现断断续续的现象。饱和银氨溶液基本上克服了以上缺点,而且显现速度明显高于前两者。 1 显现原理 人体汗液中含有大量水份、部分无机盐以及少量有机物质。银氨溶液中含有银氨铬离子Ag(NO_3)_2~ ,它与卤离子发生反应生成卤化银,卤化银极易被感光,在光照     

茚三酮、硝酸银显现热敏纸上汗液手印

由于热敏纸在商业、金融、医疗、交通等各领域上的广泛使用，办案中经常会遇到此类纸张上的手印显现和提取问题。因为多数热敏纸遇极性有机溶剂和高温会变色，破坏检材无法显现手印，近年来有不少关于显现热敏纸上的汗液手印的新方法出现，如茚三酮真空熏显法、氨基化合物漂洗法和红油O显现法等，但是这些方法使用的药品价格较贵，对操作过程和仪器要求较高，不便于推。笔者采用传统的茚三酮和硝酸银显现方法，对彩票、超市收银纸、火车票、     

Fingerprint reagents with dual action: color and fluorescence

We define "dual fingerprint reagents" as chemical formulations that produce with latent fingerprints in one stage impressions that are both colored and fluorescent. Solutions containing ninhydrin and group IIb metal salts appear to be true dual reagents. Application of these formulations to latent fingerprints on paper is as efficient as the two-step process beginning with ninhydrin and followed by treatment with metal salt. In the color mode, fingerprint detectability with the two ninhydrin-metal salt reagents (one with zinc chloride and the other with cadmium chloride) is comparable with that of ninhydrin itself, in spite of the difference in color. The sensitivity is significantly higher in the fluorescence mode. To view the latent impressions the exhibits are treated with ninhydrin-metal salt reagents and observed under white light illumination and under fluorescence conditions. Cooling to liquid nitrogen temperature enhances the fluorescence considerably. In the shorter wavelength domain, ninhydrin-metal salt reagents exhibit higher sensitivity than the recently reported dual reagent, genipin. The latter is advantageous, however, in the longer wavelength domain, on paper items with strong self-fluorescence, such as brown wrapping paper or paper printed with fluorescent ink. Upon reduction of the ninhydrin concentration 10-fold, ninhydrin-metal salt formulations become purely fluorogenic reagents; no color is noticed but the fluorescence is as intense as with concentrated solutions. Working at lower concentrations is an advantage from ecological and economical viewpoints.     

Improvement in Latent Fingerprint Detection on Thermal Paper Using a One‐Step Ninhydrin Treatment with Polyvinylpyrrolidones (PVP)

Abstract: Most thermosensitive surfaces of thermal paper turn black when they come into contact with polar organic solvents such as are used in ninhydrin petroleum benzin solution. This dark staining reduces the contrast between the developed fingerprint and the background to such an extent that the identification process becomes very difficult. Integrating polyvinylpyrrolidones (PVP) into a ninhydrin solution prevents the black staining, and the developed fingerprints appear in clear contrast to the background. The new ninhydrin solution containing PVP is successful compared to the two‐step ninhydrin–acetone washing method for thermal paper which is popular in Germany.     

Chemical development of latent fingerprints: 1,2-indanedione has come of age

The performance of 1,2-indanedione as a latent fingerprint reagent on some types of paper was found to exceed that of DFO, the leading fluorogenic fingerprint reagent. It even exceeds the performance of the sequence, DFO, followed by ninhydrin. No new prints could be observed when ninhydrin was applied after indanedione. On a large number of actual exhibits (used checks) indanedione developed 46% more identifiable prints than the sequence DFO-ninhydrin. A standard procedure for fingerprint development by indanedione is proposed. Best results are obtained with a 0.2% indanedione solution in HFE7100 solvent containing 7% ethyl acetate, but no acetic acid. It can be recommended to start using 1,2-indanedione, which is already commercially available, in actual fingerprint casework.     

Ninhydrin Thiohemiketals: Basic Research Towards Improved Fingermark Detection Techniques Employing Nano‐Technology*

Abstract: In the first part of a comprehensive research project towards more efficient application of nano‐technology to fingerprint visualization, we investigated the possibility of more selective binding of gold nanoparticles (NP) to fingerprint material. We synthesized derivatives of ninhydrin and 1,2‐indanedione containing loosely bound thiol groups. In particular: thiohemiketals (THK) of ninhydrin, and thioketals of 1,2‐indanedione were prepared and tested as potential fingerprint reagents. By reacting ninhydrin with various thiols we were able to produce a series of novel THK, bearing the SR group always at C2. Ninhydrin THK reacted with amino acids to produce the expected Ruhemann’s purple, and they also developed latent fingermarks on paper in a similar manner to ninhydrin. Ketals and thioketals derived from 1,2‐indanedione reacted neither with amino acids nor with latent fingermarks. In the second part of the research, the thiols which are formed on the ridges as byproducts of the reaction with amino acids will be tested for their potential as stabilizers for gold NP that will become covalently bound to the fingerprint ridges.     

Dual fingerprint reagents with enhanced sensitivity: 5-methoxy- and 5-methylthioninhydrin

"Dual fingerprint reagents" are chemical formulations which produce with latent fingerprints in a single step, impressions that are both colored and fluorescent. Pre-mixed solutions of the two commercially available ninhydrin analogues, 5-methoxyninhydrin (MN) and 5-methylthioninhydrin (MTN) with zinc or cadmium salts, are true dual reagents. They are much more sensitive than the parent dual reagent, ninhydrin/ZnCl(2). The main advantage of the new formulations is that they can be used at room temperature, with no need to cool the sample to liquid nitrogen temperature. At 0.05% concentration, which is 10-fold lower than the common ninhydrin working solution, MTN/ZnCl(2) is as sensitive as DFO in the fluorescence mode and considerably more sensitive in the color mode. MTN is also slightly cheaper than DFO.     

Reagents for the chemical development of latent fingerprints: scope and limitations of benzo[f]ninhydrin in comparison to ninhydrin

Benzo[f]ninhydrin was compared to ninhydrin for fingerprint development on paper. Overall, the performance of ninhydrin on exhibits was slightly better than that of benzo[f]ninhydrin. The significant advantages of the benzo[f]ninhydrin over ninhydrin were the much stronger fluorescence it gave after treatment with zinc salts and a slightly quicker reaction under ambient conditions. This fluorescence is, however, similar to that obtained with other reagents, such as DFO or ninhydrin analogs. These advantages apparently are not sufficient to justify regular usage of benzo[f]ninhydrin, especially when one considers its low solubility and high cost.     

Genipin, a novel fingerprint reagent with colorimetric and fluorogenic activity, part II: optimization, scope and limitations

Genipin, a hydrolytic product of geniposide extracted from gardenia fruit, was thoroughly studied as a potential fingerprint reagent, and optimal conditions for fingerprint development have been determined. Latent fingerprints on paper items that have been treated with a non-ink running formulation containing 0.17% of the reagent, showed up as both colored and fluorescent images. On brown wrapping paper and on papers with highly luminescent backgrounds, genipin developed more visible and clearer prints than did classical reagents such as ninhydrin or DFO. Another potential advantage of genipin is that it is totally harmless and an environmentally friendly reagent.     

茚三酮显现汗潜指印的三种操作方法对DNA检测的影响

目的探讨并比较茚三酮显现汗潜指印的3种操作方法,即溶液浸泡法、涂抹法和喷雾法对后续DNA检测带来的影响。方法取16名志愿者的指印分4组,分为茚三酮浸泡法、涂抹法和喷雾法以及空白组,然后提取DlNA进行定量和STR分型检测。结果3种操作方法都会减少汗潜指印DNA的量,喷雾法的损失量最大,浸泡法和涂抹法结果比较接近。结论现场可疑指印检材,应根据检验需要决定指印显现和DNA提取的先后顺序。     

Evaluation of some oxygen, sulfur, and selenium substituted ninhydrin analogues, nitrophenylninhydrin and benzo[f]furoninhydrin

Six ninhydrin analogues containing oxygen, sulfur, and selenium substituents at the C-5 position, 5-(4-nitrophenyl)ninhydrin, and benzo[f]furoninhydrin were evaluated as fingerprint development reagents. The analogues all showed good fingerprint color development but were not superior to ninhydrin in this respect. The benzo[f]furoninhydrin complex was strongly luminescent at room temperature following zinc complexation, while the remaining analogues required cooling to -196 degrees C to produce optimum luminescence. The benzo[f]furo, nitrophenyl, and methyl selenide analogues showed the best potential as fingerprint reagents with the benzo[f]furo analogue comparing favorably with DFO.