Evaluation of an improved Giemsa staining technique for blood borne parasite in thick and thin blood film from dogs

Many a times the use of rapid diagnostic tests for blood borne parasites like trypanosomiasis and Babesiosis is increasingly being used, but the gold standard for its detection is still the use of microscopy both as reference and confirmatory diagnosis. To determine the effectiveness of the adjusted stock giemsa staining technique over the conventional methods. Venous Blood samples were collected from 10 dogs in EDTA and then used for the simultaneous preparation of two thin and thick smear slides, one stained according to Giemsa 1:20 dilution for 30 mins while the other was stained using the Stock Solution for 30seconds the diluted with buffered saline for 20seconds and rinsed. Fixation of the thin smear was done in a covered staining jar containing anhydrous methanol for 1 to 2 min, after which the slides were air-dried. From the result obtained from 10 dogs blood samples gotten from the veterinary clinic, the adjusted giemsa staining technique showed a positive differentiation when compared to the 1:20 dilution, a total of 7 blood samples tested positive for blood borne parasites, Trypanosoma evansi, Babesiosis cani and Heart worm. The highest percentage occurrence was T.evansi (40%), Babesiosis cani(20%) and Heart worm (10%).The adjusted Giemsa staining technique serves as a fast, easy and less complex alternative to the 1:20 dilution, where the solution has to be diluted from the stock solution and then stained, although the only disadvantage to this technique would be easy contamination of the stock solution, but the advantages here is that it saves time, quicker result output and better differentiation microscopically.

Microfabrication of VO2 Thin Films via a Photosensitive Sol-Gel Method

VO2 films are widely used in photoelectric switches, smart glasses, storage media, and terahertz communications. In these applications, microfabrication technology is a very important process for producing microdevices or even improving film properties. In this paper, a novel photoetching microfabrication method is proposed for VO2 thin films. First, a VO2 precursor sol with ultraviolet photosensitivity was prepared using vanadyl acetylacetonate as the raw material and anhydrous methanol as the solvent. The dip-coated VO2 gel film can be directly subjected to photolithography processing without coating additional photoresist by using the photosensitive sol. A fine pattern on the VO2 film with good phase-transition performance can be obtained after annealing in a nitrogen atmosphere at 550 °C for 1 h. This method can be used to prepare grating, microarray, and various other fine patterns with the remarkable advantages of a low cost and simplified process, and the as-obtained material performances are unaffected using the method. It is a potential alternative method for optics, electronics, and magnetics devices based on VO2 thin films.

Liver Protection Mechanism and Absorption Promotion Technology of Silybin Based on Intelligent Medical Analysis

With the continuous popularization of smart medicine, the protective effect of silibinin in the liver has attracted much attention. This study mainly explores the liver protection mechanism and absorption promotion technology of silybin based on intelligent medical analysis. Refining of silibinin: accurately weigh 1.0 g of silibinin in a three-necked flask; gradually add 50 mL of anhydrous methanol, reflux and filter the precipitated solid; and weigh it after drying. ICR male mice were taken as experimental subjects and randomly divided into groups of 10 each. The mice in the normal group and the model group were given intragastrically with 0.5% CMC-Na solution; the mice in the silibinin group were given intragastrically with SB/CMC-Na suspension; the mice in the remaining groups were given low, medium, and high-dose suspensions to their stomachs, and silibinin 23 acylate/CMC-Na suspension was administered at a dose of 10 mL/kg for 7 consecutive days. After that, the mice were fasted for 12 hours. After 6 hours of fasting (18 hours after modeling), the blood cells from their orbits were taken, placed in a 37°C water bath for 30 minutes, and centrifuged at 4000 rpm for 10 minutes, and then the serum was taken; the activity equivalent of AST and ALT in serum was measured; serum determination Medium AST and ALT vitality. The mice were killed by decapitation, fresh liver tissue was immediately collected, and part of it was frozen in liquid nitrogen for the RT-PCR test. The hepatocyte expansion and death were observed using a transmission electron microscope, and the oncosis index (OI) was calculated. Another part of the liver tissue was fixed in 4% paraformaldehyde solution, embedded in paraffin, dehydrated, and sliced at 4 μm. Some sections were stained with conventional HE, and the pathological changes of liver cells were observed under light microscope; some sections were subjected to immunohistochemistry. Only one mouse died when 240 mg/kg of silibinin was given 10 minutes after the model was modeled. However, when 240 mg/kg silibinin was given to the mice 20 minutes after modeling, the mortality rate of the mice rose to 50%, and the therapeutic effect was significantly weakened. This research is helpful to advance the research of silybin in liver protection.

Formaldehyde Analysis in Non-Aqueous Methanol Solutions by Infrared Spectroscopy and Electrospray Ionization

We present the analysis of formaldehyde (HCHO) in anhydrous methanol (CH3OH) as a case study to quantify HCHO in non-aqueous samples. At higher concentrations (C > 0.07 M), we detect a product of HCHO, methoxy methanol (MM, CH3OCH2OH), by Fourier transform infrared spectroscopy, FTIR. Formaldehyde reacts with CH3OH, CD3OH, and CD3OD as shown by FTIR with a characteristic spectral feature around 1,195 cm−1 for CH3OH used for the qualitative detection of MM, a formaldehyde derivative in neat methanol. Ab initio calculations support this assignment. The extinction coefficient for 1,195 cm−1 is in the order of 1.4 × 102 M−1cm−1, which makes the detection limit by FTIR in the order of 0.07 M. For lower concentrations, we performed the quantitative analysis of non-aqueous samples by derivatization with dinitrophenylhydrazine (DNPH). The derivatization uses an aqueous H2SO4 solution to yield the formaldehyde derivatized hydrazone. Ba(OH)2 removes sulfate ions from the derivatized samples and a final extraction with isobutyl acetate to yield a 1:1 methanol: isobutyl acetate solvent for injection for electrospray ionization (ESI). The ESI analysis gave a linear calibration curve for concentrations from 10 to 200 µM with a time-of-flight analyzer (TOF). The detection and quantification limits are 7.8 and 26 μM, respectively, for a linear correlation with R2 > 0.99. We propose that the formaldehyde in CH3OH is in equilibrium with the MM species, without evidence of HCHO in solution. In the presence of water, the peaks for MM become less resolved, as expected from the well-known equilibria of HCHO that favors the formation of methylene glycol and polymeric species. Our results show that HCHO, in methanol does not exist in the aldehyde form as the main chemical species. Still, HCHO is in equilibrium between the production of MM and the formation of hydrated species in the presence of water. We demonstrate the ESI-MS analysis of HCHO from a non-aqueous TiO2 suspension in methanol. Detection of HCHO after illumination of the colloid indicates that methanol photooxidation yields formaldehyde in equilibrium with the solvent.

Light-triggered hydrogen production from anhydrous alkaline methanol on a multi-layer device

Hydrogen production from methanol has attracted substantial interest because of the clean combustion of hydrogen and the convenience of methanol in storage and transportation. However, it requires high-temperature and high-pressure conditions to reform methanol with water to hydrogen with high turnover frequency (TOF, e.g. 104 moles of hydrogen per mole of Pt per hour). Here we show that hydrogen can be produced from anhydrous alkaline methanol with a remarkable TOF of 1.8×106 moles of hydrogen per mole of Pt per hour on a light-triggered multi-layer system under mild conditions. The performance is attributed to the use of anhydrous methanol as both the proton source and the hole scavenger in alkaline conditions. In contrast to a slurry system, we show that the proposed multi-layer system avoids particle aggregation, and it leads to the effective utilization of methanol, light and Pt active sites. This notable performance steps forward to the practical light-triggered hydrogen generation.

CO2-based hydrogen storage – hydrogen liberation from methanol/water mixtures and from anhydrous methanol

New strategies for the reforming of methanol under mild conditions on the basis of heterogeneous and molecular catalysts have raised the hopes and expectations on this fuel. This contribution will focus on the progress achieved in the production of hydrogen from aqueous and anhydrous methanol with molecular and heterogeneous catalysts. The report entails thermal approaches, as well as light-triggered dehydrogenation reactions. A comparison of the efficiency and mechanistic aspects will be made and principles of catalytic pathways operating in biological systems will be also addressed.

Synthesis and antiproliferative activity of flavonoid triazolyl glycosides

Sixteen flavonoid triazolyl glycosides4–19were synthesized in good yieldsviaCu(I)-catalyzed azide-alkyne cycloadditions of terminal alkynes of flavonoids1–3with acetylated sugar azides followed by deacetylation with sodium methoxide in anhydrous methanol. The antiproliferative activity of the synthesized compounds against three human cancer cell lines (Hela, HCC1954 and SK-OV-3)in vitrowas evaluated. Flavonoids1,2and flavonoid triazolyl glycosides7,12,17exhibit potent antiproliferative activity against these cancer cell lines.