Qualitative Screening Analysis Research Articles

Uncertainty Evaluation for Determination of Sibutramine in Health Food by HPLC-MS/MS

High-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was used to determine the content of sibutramine in health foods according to the BJS 201701 standard Determination of Compounds such as Sibutramine in Food. By evaluating each uncertainty component, the influencing factors of the uncertainty were identified and the expanded uncertainty of sibutramine detection in health foods was provided. Using the example of illegal addition of sibutramine to health products, the HPLC-MS/MS method was used for qualitative screening and quantitative analysis of samples. The sources of uncertainty in the quantitative results were analysed, including sample weighing, sample volume determination, standard solution preparation, standard curve fitting and determination of sample repeatability. The synthetic relative standard uncertainty of the measurement results was calculated and the expanded uncertainty was reported. By optimizing the liquid phase conditions, the sample can be detected within 5 min with a linear correlation coefficient of 0.998. When the content of sibutramine in health products was 42.2 mg/kg, the extended uncertainty of the results was 4.56 mg/kg (k = 2) with a 95% confidence interval. Among the various components affecting the results of detection, the uncertainty introduced during the process of preparing the standard solution has the greatest impact on the results. A proper evaluation of the uncertainty, detailed analysis and quantification of the various sources of uncertainty can help to improve the reliability of test results.

Determining the Phytochemical Properties and Antibiogram of Different Chewing Stick Plants on Selected Streptococcal Species Isolated from the Oral Cavity

Chewing sticks are small twigs obtained from plant stems, measuring 12-25cm long and tied in bundles of 5-10. These twigs have been used for oral hygiene for many years, even before the invention of toothpaste, mouthwash, and mouth sprays. This study aims to determine the phytochemical properties and antibiogram of different chewing stick plants on two streptococcal species isolated from the oral cavity. Streptococcus pyogenes and Streptococcus mutans were isolated from oral swabs of patients at Rivers State University Teaching Hospital and identified to the species level. The pure isolates were further tested against the antimicrobial effects of the aqueous and ethanolic extracts of four chewing stick plants: Vernonia amygdalina, Jatropha curcas, Massularia acuminate, and Phyllanthus mullerianus. Qualitative phytochemical screening and quantitative analysis were carried out on the plant stems to determine the presence of antimicrobials. The percentage of antimicrobials present in the plant stems ranged from 33.3% to 66.7%, with Jatropha curcas, Massularia acuminate, and Vernonia amygdalina exhibiting the highest percentages, and Phyllanthus mullerianus the lowest. The antibiogram of the isolates to conventional gram-positive antibiotics was determined by the disc diffusion method. Streptococcus pyogenes showed 75% sensitivity and 25% resistance to the antibiotics, while Streptococcus mutans displayed 50% sensitivity, 16.7% intermediate, and 33.3% resistance to the antibiotics. The investigation found that the ethanolic extract of Massularia acuminate has the highest zone of inhibition of 15.5 ±0.71mm at 100mg/ml, while Phyllanthus mullerianus exhibited the least inhibition at 8 ±0mm. The ethanolic extract of Jatropha curcas and Vernonia amygdalina showed little effect on the test isolates, with a range of 0-9.5±0.71mm. The aqueous extract ranged from 8±5.7 - 9.5±0.71mm at 100mg/ml, with Massulara acuminate exhibiting the highest and the lowest zones of inhibition. This finding indicates that Massularia accuminate has the ability to suppress the growth of dental plaque-forming Streptococcus mutans and Streptococcus pyogenes. Chewing sticks are more affordable and easily accessible, so they could be recommended in community oral health programs.

Pharmacognostic, phytochemical, and chemomicroscopic evaluation of Physalis angulata (L)

Background/Introduction: Since the start of civilization, human culture has used plants to treat illnesses. Many plant samples have been adulterated intentionally or unintentionally during processing or even misidentified during collection. This study aims at authenticating and standardizing of Physalis angulata by carrying out Pharmacognostic evaluation, HPLC and GCMS analysis. Methodology: The dried leaves of Physalis angulata was extracted with 70% ethanol. Phytochemical screening (qualitative and quantitative screening) analysis was carried out on the ethanolic leave extract using standard method, while the chemical compounds were established with HPLC-DAD and GCMS and Pharmacognostic evaluation was carried out on the powdered leave. Results and discussion: Qualitative phytochemical analysis of the leave extract reveals the presence of flavonoids, terpenes, alkaloid, tannins and saponin while carbohydrate, glycosides and resins were absent. Quantitative phytochemical screening shows alkaloid present to be 2.4±0.4% and saponin 2±1.32%. HPLC analysis reveals the presence of quercetin, rutin, catechin and ferulic acid while GCMS reveals the presence of cyclohexene, Palmitic acid, 17-Octadecynoic acid, 1,2-Benzenedicarboxylic acid and Phytol. Total Ash content is (15.23±0.43) %w/w with acid insoluble ash of (1.16 ±0.28) %w/w, water soluble ash of (8.13 ±0.32) %w/w, moisture content (5.67 ±0.14) %w/w, alcohol soluble extractive value of (5.76 ±0.40) %w/w and water-soluble extractive value of (10.96 ±0.35) %w/w. Chemomicroscopic evaluation indicate the presence of lignin, cellulose, tannins, starch, calcium oxalate, oils and protein. Microscopy, fluorescence and organoleptic analysis were also documented. Conclusion: From this study, the presence of valuable phytochemicals has been established from the plant, while HPLC and GCMS revealed the identities of these compounds. Thus, the physico chemical parameters established for Physalis angulata in this study falls within the range approved by WHO (1992) for crude plant and extract.

Phytochemical screening and in vitro anti-inflammatory properties of Jatropha maheshwarii Subram. & Nayar – An endemic plant

The present study was aimed at examining the anti-inflammatory activity of the crude extracts obtained from an endemic plant, Jatropha maheshwarii through employing different assays. The ethanol extract of J. maheshwarii, at a concentration of 500 µg/ml, exhibited a membrane stabilizing effect (78.21 %) on human red blood cells. As regards proteinase inhibitory activity, the ethanol extract showed the higher activity (80.32 %) and the lower by aqueous extract (79.61 %) at a concentration of 500 µg/ml. The protein denaturation inhibition assay showed the higher activity for ethanol (78.26 %) and the lower by aqueous (75.73 %) extracts at a concentration of 500 µg/ml. The anti-inflammatory activity of the plant extracts can be reasoned to the bioactive principles of the plant. On this basis, the phytoconstituents were assayed using preliminary qualitative screening and Gas Chromatography-Mass Spectrometry analyses; phenols, alkaloids, flavonoids, sterols, tannins and cardiac glycosides were detected in the crude extracts. Twenty-two bioactive compounds were identified in the ethanol and aqueous extracts that includes13-docosenamide, (Z)- ((Z)-docos-13-enamide) (15.65 %), 4-propylbenzaldehyde (15.20 %), dibutyl phthalate (dibutyl benzene-1, 2-dicarboxylate) (15.10 %), behenic alcohol (Docosan-1-ol) (14.48 %), gamma-sitosterol (14.45 %), cetyl alcohol (Hexadecane-1-ol) (13.62 %), Tetradecyl trifluoroacetate (Tetradecyl 2, 2, 2-Trifluoroacetate) (11.49 %) and1-pentadecene (Pentadic-1-ene) (11.24 %).

Qualitative and quantitative phytochemical screening and chemical fingerprint analysis of Conocarpus lancifolius plant using HPTLC

Qualitative and quantitative phytochemical screening and chemical fingerprint analysis of Conocarpus lancifolius plant using HPTLC

Multi-pesticide residue screening, identification, and quantification analysis in various fruits and vegetables by UHPLC-Q Exactive HRMS.

A general strategy for qualitative screening and quantitative analysis of 403 pesticides in various fruits and vegetables was developed using ultrahigh-performance liquid chromatography (UHPLC) in conjunction with a Thermo Q Exactive Focus high-resolution mass spectrometer, relying on an executable compound database comprised of the exacted mass of precursor ions, retention times, and fragment ions. Taking advantage of the powerful separation capacity of UHPLC, an Orbitrap analyzer with high sensitivity in full scan mode and elevated mass resolution of product ions in the MS/MS mode, eight pairs of isomers and fifty-seven groups of isobaric compounds were selectively identified. The method was then systematically assessed and validated for eight fruits and vegetables, in terms of screening detection limit (SDL), matrix effects, recovery, and precision over 400 pesticides. The results showed that the SDLs of 68.0-84.4% for the pesticides were less than or equal to 10 μg kg-1 in the representative matrices, recoveries in the range of 60-120% accounting for 48.6-84.4% of all the targets at three lower fortified levels of 5, 20, and 50 μg kg-1 with a precision of less than 20% while the range of overall average recoveries for the majority of the pesticides were from 82.4% to 105.1% in the as-selected matrices with RSDs between 3.9% and 7.7%. Using this method, screening data from a survey of pesticide residues in 68 practical samples across 32 different matrix types provides scientific data for the inspection and supervision of pesticide residue safety of fruits and vegetables.

Validation of the Chemical Constituents of Crude Leaf Extract of <i>Datura discolor</i> with Qualitative Phytochemical Screening and GC-MS Analysis

Validation of the Chemical Constituents of Crude Leaf Extract of <i>Datura discolor</i> with Qualitative Phytochemical Screening and GC-MS Analysis

Phytoconstituents of Terminalia catappa linn fruits extract exhibit promising antidiabetic activities against α-amylase and α-glucosidase in vitro and in silico

Terminalia Catappa fruits are recognized for their use in diabetes treatment, yet the mechanism by which they inhibit diabetes-related enzymes remain largely undefined. This study aimed to elucidate the therapeutic potential and interactions of T. catappa fruit extract through in vitro and in silico approaches. The compounds from T. catappa fruit were extracted using microwave-assisted extraction techniques, followed by qualitative phytochemical screening and quantitative analysis via GC-MS. The physicochemical properties were evaluated according to the Lipinski rule and ADMET criteria. Antidiabetic analyses, both in vitro and in silico, were performed on the secondary metabolites found in T. catappa fruit, targeting α-amylase and α-glucosidase enzymes. The methanol and ethyl acetate extracts of T. catappa fruit contained alkaloids, flavonoids, saponins, steroids, and terpenoids. These extracts inhibited α-glucosidase and α-amylase in a dose-dependent manner, with the methanol extract of T. catappa showing significantly higher inhibitory activity than pure acarbose (by two- and five-fold, respectively) and the ethyl acetate extract. Furthermore, the antioxidant activity of the methanolic extract was seven times greater than that of the ethyl acetate extract. Molecular docking studies supported these findings, revealing that the ΔG values of gibberellic acid, rescinnamine, and digoxin were comparable to those of acarbose. Notably, digoxin has higher ΔG values against α-amylase than acarbose, while gibberellic acid, rescinnamine, and nerolidol showed ΔG values similar to acarbose. Gibberellic acid, unique to the methanol extract, demonstrated high ΔG values, suggesting its significant role in the extract's enhanced glucosidase and amylase inhibitory activities. This study identifies specific compounds (digitoxin, rescinnamine, gibberellic acid, and nerolidol) and proposes the potential of multi-target drugs in diabetes treatment. Understanding these phytochemical constituents and their effects on diabetes-involved enzymes could benefit individuals with type 2 diabetes, particularly those at higher risk of complications.

Standardization of Hibiscus rosa-sinensis Flower by HPTLC, HPLC and AAS

Hibiscus rosa-sinesis, a well-known flowering plant in India, is used to worship Lord Ganesha. It is a member of the Malvaceae family. It is used in traditional medicine in many tropical countries to treat wounds, inflammation, fever, diabetes, infections, hair loss, and gastric ulcers. Therapeutic benefits of Hibiscus rosa-sinesis are attributed to flavonoids, tannins, terpenoids, saponins, and alkaloids. Hibiscus rosa-sinesis flowers are a good source of flavonoids, which are important components of herbal and Ayurvedic preparations. The goal of this study was to standardize the flower extract through qualitative phytochemical screening and quantitative HPTLC analysis of quercetin, an active biomarker. The result of the HPTLC analysis was compared to those obtained using HPLC. HPTLC found that the extract contained 0.33% quercetin, while HPLC found that it contained 0.37% quercetin. Further, heavy metals and trace elements were measured using atomic absorption spectroscopy (AAS). Results showed that cadmium, lead, arsenic, copper, chromium, and mercury levels (in ppm±SEM) were within acceptable limits: cadmium (0.018±0.050), lead (0.630±0.025), arsenic (0.041±0.014), copper (2.605±0.045), chromium (0.450±0.025), and mercury (0.023±0.006). This method allows standardization of plant material for raw material and finished product testing, ensuring better efficacy and safety.

A new efficient sample pooling procedure for qualitative screening analysis. Application to the detection of salmonella spp and nut allergen by PCR

Foodborne pathogens and allergens are a major concern for public health that determines food safety policy, and their screening could be improved using pooled samples.The purpose of this paper is to propose a cost-effective and accurate pooling strategy for the unambiguous identification of foodborne pathogens and allergens, enabling laboratories to redouble testing capacity while saving time and making optimal use of resources.Although a variety of pooling algorithms have been used in different fields, the strategy suggested here is a logical analysis of sample pooling aimed at qualitative analytical screening problems. It involves, on the one hand, a design matrix to make the pooled samples, which is a supersaturated-based design, particularly, a half-fraction of a Plackett-Burman. On the other hand, a logical (non-algebraic) modeling of the problem, as well as a logical procedure for the identification of the original positive samples, is included.Regarding the efficiency of the proposal, it is higher than that of other pooling algorithms, with an expected number of tests per individual sample ranging between 0.10, for a prevalence below 1%, and 0.59, for a prevalence above 10%. In terms of accuracy, the pooling sensitivity reaches 0.9697 for a sensitivity of the analytical test about 0.99, while pooling specificity ranges from 0.9872 to 0.9999, provided that the sensitivity and specificity of the analytical test are equal to or greater than 0.90.This pooling strategy has been applied to the detection of salmonella spp and nut allergen with complete identification of the contaminated samples. Furthermore, based on the EU reported food samples contaminated with salmonella, a comprehensive comparison between individual sampling and the applied pooling strategy has been conducted. For the specific case of salmonella, detailed calculations have been made on the expected efficiency gains induced by this pooling methodology for different types of food samples monitored in the EU.

Determination of 26 bisphenols in dust by ultra performance liquid chromatography-tandem mass spectrometry

Bisphenol A (BPA) is one of the most widely produced compounds in the world and was listed as a substance of very high concern by the European Chemicals Agency in 2016. Because of its toxicity, many countries and regions, including China, have banned BPA addition in feeding-bottles. And the European Union (EU) has banned BPA use in other food contact materials and thermal paper. Restrictions on BPA have contributed to the widespread use of alternatives. As the toxicity of BPA alternatives continues to be revealed, the alternatives of BPA alternatives are being developing. As the most extensive alternative for BPA, bisphenol S (BPS) was proven to have estrogen-disrupting effects and developmental toxicity of the neuroendocrine system. Therefore, BPS alternatives are used in thermal paper. In this study, alternatives to both BPA and BPS are collectively referred to as bisphenols (BPs). As a pooling matrix of many indoor chemicals, dust is an important pathway for human exposure to BPs. BPA and its alternatives are routinely detected in dust. As BPS alternatives have been detected in recycled paper and sludge, it is also very important to detected in dust. However, common analytical methods for BPs have low sensitivity and contain few BPS alternatives. Therefore, a high-throughput, high-accuracy, and high-sensitivity method must be established for the determination of BPs in dust; this will lay the foundation for subsequent studies on the environmental behavior and exposure risk of BPs. In this study, an ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed for the simultaneous determination of 26 variations of BPs in dust. UPLC-MS/MS parameters of the variations were optimized to compare the separation effect and response intensity in different columns and mobile phases. The influence of the extraction solvent and solid phase extraction (SPE) on the extraction efficiency and purification effect of target compounds were optimized by using the isotopic internal standard method, and the 26 variations of BPs in dust was quantitatively analyzed. Finally, the dust samples were extracted by using 3 mL of acetonitrile and 3 mL of a 50% methanol aqueous solution in an ultrasound bath. The combined extract was further purified by using an Oasis HLB cartridge (60 mg/3 mL). The cartridge was then washed with a 40% methanol aqueous solution (0.5 mL) and eluted with methanol (2 mL). The target compounds were separated on a CORTECS® UPLC® C18 column (100 mm×2.1 mm, 1.6 μm), with methanol and 1 mmol/L ammonium fluoride solution as mobile phases and a flow rate of 0.3 mL/min. Electrospray ionization (ESI) was applied in the positive, negative, and multiple reaction monitoring (MRM) modes for the mass scan. Under optimized conditions, the linear ranges of the 26 targets behaved well linearly in their respective ranges with correlation coefficients (r2)>0.999. The limits of detection (LODs) and limits of quantification (LOQs) were assessed using signal-to-noise (S/N) ratios of 3 and 10, respectively. The LODs and LOQs of the method were 0.01-0.75 μg/kg and 0.02-2.50 μg/kg, respectively. The accuracy of the method was evaluated by conducting a recovery test at three spiked levels: LOQ, two times the LOQ, and 10 times the LOQ, with the average recoveries ranging from 83.7% to 114.9%. The precision of the method was evaluated by using the relative standard deviation (RSD). The intra-day RSDs and inter-day RSDs were 0.86%-9.79% (n=6) and 5.16%-19.5% (n=6), respectively. The established method was used to determine 11 dust samples. Fifteen BPs were detected at a detection rate of 9.1%-100.0%. The detection rate for BPA, BPS, bisphenol F (BPF), 4-hydroxy-4'-isopropoxydiphenylsulfone (BPSIP), and diphenyl sulfone (DPS) was 100.0%. BPSIP, 4-allyloxy-4'-hydroxydiphenyl sulfone (BPS-MAE), and bis-(3-allyl-4-hydroxyphenyl) sulfone (TGSA) were first detected in Chinese dust, whereas 4-benzyloxy-4'-hydroxydiphenyl sulfone (BPS-MPE), 4-hydroxybenzoic acid benzyl (PHBB), and DPS were first detected in dust samples worldwide. This method is simple, rapid, and sensitive, and is suitable for the qualitative screening and quantitative analysis of the 26 BPs in dust samples.

English

Euphorbia ingens is a woody, succulent tree with ethnomedicinal applications; however, its chemical constituents are not well documented. This study determined the phytochemical profile of Euphorbia ingens dichloromethane-methanol root bark extract. Following sample collection and preparation, extraction was done using the cold percolation technique. This was followed by qualitative phytochemical screening and gas chromatography-mass spectrometry (GC-MS) analysis. This study reports relative high abundance of phenols, tannins and saponins with moderate and low levels of flavonoids and terpenoids respectively in E. ingens dichloromethane-methanol root bark extract. However, alkaloids, quinones and sterols were not identified in this study. Additionally, 14 phytocompounds were identified through GC-MS analysis, including undecane; copaene; 3,4-altrosan; 9, 12, 15-octadecatrienoic acid; hexadecanoic acid; 1,2-benzenedicarboxylic acid; lanosterol; androst-2-en-17-one; lanosterol; 2-Bornanol; octadecanoic acid; squalene; 6-Pentylidene-4,5-secoandrostane-4,17.beta.-diol, and ethyl trans-4a, cis-4b, trans-8a, cis-10a-perhydro-trans-2,4a,8a-trimethyl-8-oxophenanthrene-2-carbothiolate. These phytocompounds have been documented to have diverse pharmacological activities from antimicrobial, antioxidant, anticancer, hypercholesterolemic and anti-inflammatory activities. Therefore, it was assumed in this study that these phytocompounds could be responsible for documented E. ingens pharmacological activities. Thus, the results of this study could support to some extent the ethnomedical uses of E. ingens. However, further biological investigations to validate the reported ethnobotanical uses of E. ingens are required. Key words: Euphorbia ingens, phytocompounds, ethnomedical, pharmacological potential, biological activity.

Phytochemicals, proximate composition, minerals and volatile oil analysis of Zanthoxylum acanthopodium DC. fruits

Background: The use of herbal plants is adopted as a traditional medicine because of their minimal side effects. Most plants have bioactive ingredients and nutritional content that can potentially be used as treatments. One plant that has the potential to be a source of modern medicine is Zanthoxylum acanthopodium DC. Historically the use of traditional medicine as a treatment has enjoyed a good sense of trust among the public. The purpose of this study was to perform a qualitative phytochemical screening and proximate analysis of samples of Zanthoxylum acanthopodium DC. Methods: Used in this study were the phytochemical screening test using the thin-layer chromatography method and the proximate analysis using the AOAC method, which included measuring the ash, water, carbohydrate, total fat, protein, and crude fiber content of the samples. Hydrodistillation was used to isolate volatile oil from the sample, which was then identified using gas chromatography-mass spectrometry. The research method used is experimental. Results: From the test, it was found that the phytochemical content of Zanthoxylum acanthopodium DC is alkaloids, flavonoids, tannins, saponins, glycosides, steroids, and triterpenoids. Proximate analysis obtained ash content of 6.19%, water content of 6.35%, carbohydrates of 35.4%, total fat of 2.46%, protein of 16.2%, and crude fiber of 33.4%. Mineral test results prove that Zanthoxylum acanthopodium DC contains Pb (<0.07 mg/Kg), Cd (<0.03 mg/Kg), As (<0.03 mg/Kg), Hg (0.0011 mg/Kg), Mn (43.1 mg/Kg), K (321 mg/Kg), Ca (0.22 mg/Kg), Mg (198 mg/Kg), Fe (52.1 mg/Kg), and Na (23.6 mg/Kg). The highest content of essential oil in Zanthoxylum acanthopodium DC is geranyl acetate, with a concentration of 24.26%. Conclusions: This study concludes that the research findings of Zanthoxylum acanthopodium DC indicate that the phytochemical, mineral, and volatile oil content of the sample is strongly related to its potential to be developed as food and medicine.

Chromolaena odorata Linn leaf extract - Geothermal versus nongeothermal: Phytochemical, antioxidant, and cytotoxicity screenings.

Chromolaena odorata Linn, a popular yet underutilized ethnomedicinal plant, is hypothesized to possess higher bioactive phytoconstituents when it grows in geothermal areas. In this study, the comparison of ethanolic extract from geothermal and nongeothermal C. odorata leaves was carried out based on the phytochemical profile, antioxidant activity, and cytotoxicity. The leaf extracts were produced from a maceration using ethanol 96%, where the products were identified using reagents and gas chromatography-mass spectrometry (GC-MS). Antioxidant activities of both samples were measured based on their 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging activities. Cytotoxicity was determined by brine shrimp lethality test using Artemia salina. Phenols were found to be more abundant in geothermal sample based on the qualitative screening and GC-MS analysis (i.e. higher relative abundance of phytol - 3.97%). DPPH antioxidant was higher in geothermal sample than in nongeothermal sample (median inhibitory concentration =13.04 ± 3.35 mg/L vs. 41.09 ± 4.13 mg/L, respectively). Geothermal sample was noncytotoxic (median lethal concentration [LC50] =2139.30 mg/L), whereas the nongeothermal sample had low cytotoxicity (LC50 = 491.48 mg/L). Taken altogether, geothermal C. odorata leaves contain higher bioactive compounds with potent antioxidant activities.

Qualitative phytochemical screening and FTIR spectroscopic analysis of Thalictrum dalzelli hook leaf extract

Qualitative phytochemical screening and FTIR spectroscopic analysis of Thalictrum dalzelli hook leaf extract

Qualitative and Quantitative Phytochemical Screening and GC-MS Analysis of Avicennia marina Leaf Extracts

Qualitative and Quantitative Phytochemical Screening and GC-MS Analysis of Avicennia marina Leaf Extracts

Qualitative phytochemical screening and ftir spectroscopic analysis of mitracarpus hirtus leaf extracts

The present study aim is to analyze the phytochemicals present in Mitracarpus hirtus leaf extracts by using Qualitative phytochemical analysis, Fourier-transform infrared spectroscopy (FTIR). The leaf extracts were prepared using three different solvents. The phytochemical analysis Fourier transform infrared spectroscopy (FTIR) analysis were performed using standard methods. The FTIR spectroscopic studies revealed different characteristic peak values with various functional groups present in the compounds of respective extracts. The FT-IR analysis shows the presence of different functional groups such as alcohols, phenols, alkanes, carboxylic acids, aldehydes, ketones, alkenes, primary amines, aromatics, esters, ethers, alkyl halides and aliphatic amine compounds, which showed major compounds present in the leaf extracts. The present study generated the FTIR spectrum profile for the medicinally important plant Mitracarpus hirtus. The present study provides evidences that different extracts of Mitracarpus hirtus leaf is useful to cure many serious diseases which remained still problematic and for further isolation of bioactive compounds from the plant which could be of interest for the development of the new drug.

Qualitative Phytochemical Screening and GC-MS analysis of (Eleusine coracana (L.)

Qualitative Phytochemical Screening and GC-MS analysis of (Eleusine coracana (L.)

Screening of risky substances in sea cucumbers based on gas chromatography-orbitrap high-resolution mass spectrometry

建立了一种基于改良QuEChERs的样品前处理新方法,并通过气相色谱-静电场轨道阱高分辨质谱(GC-Orbitrap HRMS)对海参样品中的有机氯农药类(OCPs)、多环芳烃类(PAHs)、酞酸酯类(PAEs)、多氯联苯类(PCBs)及其他农药类(ACs)等10大类289种具有健康风险的有机污染物进行了高通量高精准的定性鉴别和定量分析。通过将传统的QuEChERs方法与柱净化方法结合,提出了一种基于改良QuEChERs的简便生物样品制备新方法,经弗洛里硅土(Florisil)柱净化后脂含量降低了99.9%,显著减少了基质效应对分析结果的干扰,可在高分辨质谱(6万分辨率)全扫描模式下对289种目标化合物同时进行高精准定性筛查和定量分析。该方法定量限约0.56~57.8 pg/g,线性范围约6个数量级,回收率范围为40%~120%。由于Q Exactive GC-Orbitrap HRMS具备较高的质量分辨率和灵敏度,因此对目标化合物的定量限显著优于常规的色谱和质谱分析方法,常规方法无法检出的超痕量有机污染物利用该研究开发的方法可进行精准定量。基于此高覆盖度多目标分析方法对养殖场采集的海参样品进行分析,共从海参体内检出100种有机污染物,其中PAHs、ACs、PAEs、OCPs类检出总含量相对高于其他类污染物,总含量均值分别为157.8、153.2、64.4和46.4 ng/g dw。9-氯芴、5-氯苊、3-甲基胆蒽等多种新污染物首次在海参样品中检出,但含量都非常低。该方法简单高效,定量限低,线性范围宽,结果准确。此高覆盖度多目标分析方法可广泛应用于各种水产品中风险物质的广谱筛查和精准定量,为食品安全和绿色养殖提供技术支撑。

Morphology, Storage Behavior, Dormancy, Germination Pattern and Chemical Composition of Tabernaemontana pandacaqui Lam. Seeds

Background: Seed characteristics of Tabernaemontana pandacaqui Lam., an indigenous medicinal plant species from the Philippines, were investigated to help identify appropriate conservation strategies. Methods: Mature seeds were tested for viability at different dormancy-breaking treatments and storage conditions. Seeds were also characterized morphologically and the seedling developmental pattern was established using the Biologische Bundesanstalt, Bundessortenamt and CHemische Industrie (BBCH) scale. We also determined the preliminary chemical composition through qualitative phytochemical screening and proximate analysis. Result: Seeds of T. pandacaqui are obovate in shape with a 1000-seed weight of 20.99±0.62 g at 4.7% moisture content. Removal of the aril from the fresh seeds improved germination from 30%±0.98 to 84%±0.71 and shortened the time to seedling emergence from 45 days to 4 days after sowing. The seeds can tolerate drying to 4.7% moisture content and storage at -10°C for 3 months; thus, they have orthodox storage behavior. The germination pattern is epigeal phanerocotylar type, wherein the foliaceous cotyledons are raised (BBCH 09) and unfolded above the soil surface (BBCH 10). The seedling then develops an ovate to elliptic-shaped first true pair of leaves (BBCH 12) completing the germination process. The pre-dried seeds also have a high oil content of 28.7407±0.09316% with a strong presence of alkaloids and saponins. This indicates that the seed is amenable to ex-situ conservation through seedbanking, but its viability must be monitored in shorter intervals due to its high oil content.