Thin Layer Chromatography Fingerprinting Research Articles

The evaluation of the antioxidant activity of selected Eryngium species based on thin-layer chromatography fingerprints using chemometric tools

The purpose of the study was to confirm the utility of multivariate technique to predict antioxidant activity of selected Eryngium extracts based on chromatographic data. Five Eryngium species were analyzed using Thin Layer Chromatography (TLC) with silica gel to obtain their fingerprints. The highest relative content of quercitrin (marker) was observed for E. giganteum. The chemical similarity between extracts was evaluated by Principal Component Analysis (PCA) and Hierachical Cluster Analysis (HCA), and the results confirm the similarity between the same three E. planum from various natural sites. The total phenolic content with Folin–Ciocalteu reagent and antioxidant activity with DPPH reagent by spectrophotometry were determined, and the highest content of phenolics (concentration of gallic acid, mg⋅mL−1) was obtained for E. campestre, E. amethystinum and E. planum T. The highest antioxidant activity (concentration of gallic acid and inhibition %) were obtained for E. planum T. and E. amethystinum, while the lowest was obtained for E. planum Dębówka. High value of correlation coefficient between TLC and spectrophotometric data using Partial Least Squares Regression (PLS) confirms the usefulness of statistical method for the predicting the biological activity. In conclusion, the chromatographic and chemometric methods were suitable for prediction of antioxidant activity.

Phytochemical screening and pharmacognostical evaluation of cordia sebestena Linn.

Plants are known as treasures of effective drugs for various ailments from ancient times. Plant metabolites played a protagonist part in the detection and development of novel chemotherapeutic mediators. Therefore, exploring the medicinal importance of plants has become extremely important concerning the evolving ailments of the present times. In the existing investigation, phyto-constituents and antioxidant activity of the plant known as Cordia sebestena Linn. were discovered for their biological importance. Cordia sebestena Linn. is an understudied medicinal plant that belongs to the family Boraginaceae and is commonly known as Aloe wood, geranium tree, and sea trumpet. The investigation objective is to develop the high-performance thin layer chromatography (HPTLC) fingerprint outline of the phytoconstituent of Cordia sebestena Linn, to identify the component of medicinal importance. In the present study, the HPTLC technique for the parting of the active constituents in extracts has been developed via the solvent system toluene: methanol: acetone (16:4:1). This study has provided the biological source which can be an eco-friendly, cost-effective, and better option than the chemically synthesized drugs. In the future, these fingerprinting descriptions will be supportive in further studies like quality regulation of the drug and estimating therapeutic worth.

High performance thin layer chromatography fingerprint on cyano-bonded stationary phase of selected Stachys and Betonica species and their antioxidant activity with chemometric calculations

The methanolic extracts of selected Stachys and Betonica species were analyzed by high performance thin layer chromatography (HPTLC) method using cyano bonded stationary phase and mobile phase consisted of methanol and water 45:55 (v/v) with Natural product reagent derivatization. The HPTLC method was validated (linearity, precision, accuracy, robustness, LOD, LOQ) and the validation results confirm the usefulness of the method used. The obtained images of fingerprint chromatograms presented as numerical data (using the TLC analyzer program) were next processed using Excel and SpecAlign softwares. The phytochemical similarity between analyzed plant extracts was evaluated using the similarity index (Pearson correlation coefficient) and the results were presented as hierarchical cluster analysis dendrograms and as graph for principal component analysis (PCA). The total phenolic content (TPC) by Folin-Ciocalteu method and the antioxidant activity with Ferric Ion Reducing Antioxidant Potential (FRAP) technique were determined for studied extracts using gallic acid as standards in both methods.

Phytochemical Investigation of Alysicarpus vaginalis by Gas Chromatography-mass Spectrometry and High-performance Thin-layer Chromatography

Introduction: Alysicarpus vaginalis belongs to the Fabaceae family, commonly known as buffalo clover and one-leaf clover. Alysicarpus vaginalis is medicinally used in disease-related kidney, diuretics, leprosy, pulmonary problems, jaundice, skin problems, respiratory difficulties, and as a hepatoprotective. Alysicarpus vaginalis is a medicinally important plant according to our review of literature on pharmacological activities, modern pharmacological activities, ethnomedicinal surveys, and traditional systems. However, very limited research related to phytochemical investigation by chromatographic techniques was studied. Methods: So, to investigate the phytochemicals of Alysicarpus vaginalis methanol extract by High-performance thin-layer chromatography and gas chromatography-mass spectrometry. Result: Phytochemical screening revealed the presence of steroids, flavonoids, polyphenols, terpenoids, carbohydrates, alkaloids, and tannins. GC-MS revealed, the presence of six out of nine phytochemicals found medicinally important. 4-O-Methylmannose, Undecane, Neophytadiene, 2-amino-5-[(2-carboxy) vinyl]- Imidazole, Lup-20(29)-en-3-one and stigmasterol are some of the important phytochemical useful as anticancer or as anti-inflammatory. A solvent system was developed by thin-layer chromatography, followed by the HPTLC analysis using the mobile phase toluene: methanol: ethyl acetate (7:3:1). High-performance thin-layer chromatography fingerprinting detected total of 8 peaks with Rf value of 0.007, 0.089, 0.142, 0.211, 0.468, 0.585, 0.772, and 0885 at 254nm and total of 9 peaks with Rf value of 0.007, 0.089, 0.140, 0.208, 0.468, 0.661, 0.772, 0887, and 0.940 at 366nm, respectively. Conclusion: Chemoprofiling by sophisticated spectral techniques such as GC-MS and HPTLC fingerprinting can serve as an important tool for quality control of assuring purity, safety, quality, and efficacy of herbal formulation, and herbal extracts from Alysicarpus vaginalis.

Pharmacognostical studies of Eclipta prostrata (Linn.) grown in Sri Lanka

Eclipta prostrata Linn. is an annual herbaceous plant used in traditional medicine, commonly known as “Trailing Eclipta” or False Daisy in English, ‘Keekirindiya’ in Sinhala and ‘Kayyantakara’ in Tamil. The aim of this study was to conduct a detailed pharmacognostical evaluation of E. prostrata found in Sri Lanka. Anatomical, physicochemical, phytochemical studies, and quantification of phyto-constituents were performed as per WHO guidelines. Whole plant was sequentially extracted into solvents with different polarities. Phytochemical screening and Thin Layer Chromatography (TLC) fingerprinting were carried out. Anatomical study and powder microscopy revealed useful diagnostic features. Physicochemical parameters such as moisture content, ash values (total, acid insoluble, water soluble) and extractable matter in water and ethanol were evaluated. Phytochemical screening and TLC fingerprinting revealed the presence of different types of phyto-constituents. Alkaloid, tannin, saponin, total flavonoid and total polyphenol contents were quantified. In conclusion, pharmacognostical study aids in establishing the standardization parameters of E.prostrata found in Sri Lanka.

In-vitro, in-vivo and in-silico anti-inflammatory evaluation of hedychenone and its semisynthetic derivative

Hedychium spicatum is a perennial shrub that is commonly found in the Himalayan region. Thin layer chromatography fingerprint screening of various Hedychium species revealed that only the species Hedychium spicatum possesses hedychenone. Purification and isolation of hedychenone was carried out from methanolic extract of Hedychium spicatum rhizomes powder using column chromatography. After crystallization of enriched fraction, 2.19% of hedychenone crystalline powder was yielded. The physiochemical, pharmacokinetic, and pharmacodynamic evaluation of the active pharmaceutical components was conducted using artificial learning and machine learning (AL/ML) approaches. The results indicate that both medications adhere to Lipinski’s rule of five. The docking study indicated that compound 2 (MBE-10.4 kcal/mol) exhibited a more sub-stantial interaction with the cannabinoid receptor 2 compared to hedychenone (MBE -9.85 kcal/mol). A study was done to assess the physical and chemical stability of hedychenone under biological pH conditions. Furthermore, the administration of both medication concentrations, 100 mg/kg and 200 mg/ kg, effectively inhibits the development of acute paw edema caused by ovalbumin. A preliminary investigation of hedychenone and its synthetic derivative indicated that these compounds have the potential to be utilized as active medicinal ingredients in herbal pharmaceutical preparations.

Pharmacognostic study and preliminary phytochemical investigation of Andrographis paniculata (Burm.f.) Wall. ex Nees

Andrographis paniculata (family –Acanthaceae) is an annual herbaceous plant with branches that grows up to a height of 50-150 cm in moist, shaded areas. Its stem is abruptly quadrangular, heavily branched, and has a delicate texture that is readily broken. It is found in Southeast Asia, tropical and subtropical Asia, and a few other nations like Vietnam, Cambodia, and the Caribbean islands, Indonesia, Laos, Malaysia, Myanmar, Sri Lanka and Thailand etc. It is widely used in different traditional medicinal systems or countries for medicinal purposes by the traditional practitioners, tribes or community as a folklore remedies. The present communication provides a detailed account of the pharmacognostic study carried out on various parts of the Andrographis paniculata. The study includes macroscopy, microscopy, powder microscopic studies, physicochemical tests, preliminary phytochemical screening, development of HPTLC (High Performance Thin Layer Chromatography) fingerprints profile and heavy metal tests. Physicochemical parameters were performed and found average values of three parts (root, stem and leaf) such as root loss on drying at 1050C 4.93% w/w, total ash value 10.16% w/w, acid insoluble ash value 0.21% w/w, alcohol soluble extractive value 13.98% w/w and water soluble extractive value 25.77%w/w. Stem loss on drying at 1050C 6.23% w/w, total ash value 6.88% w/w, acid insoluble ash value 0.25% w/w, alcohol soluble extractive value 18.46% w/w and water soluble extractive value 21.94%w/w and leaf loss on drying at 1050C was found 6.29% w/w, total ash value 7.30% w/w, acid insoluble ash value 0.13% w/w, alcohol soluble extractive value 21.93% w/w and water soluble extractive value 38.68%w/w. HPTLC (High Performance Thin Layer Chromatography) fingerprints profile of methanolic extract was done by using mobile phase toluene: ethyl acetate (7:3). Andrographolide and Ferullic acid standard markers were applied, major spots Rf values with colour were recorded before derivatization at 254nm. Rf values are 0.25 black, leaf, stem and root with Andrographolide standard marker, and 0.20 light black color of stem, and root with Ferullic acid standard marker. Andrographolide is higher present in leaf which was range from 1.51-162 than the stem range1.46-153 and root range 1.45-1.150, while Ferulic acid was higher present in stem range from 0.91-0.96 than root 0.76-0.82 but absent in leaf. Heavy metals i.e Pb, Cd, As, & Hg were tested and found under WHO limits Established parameters can be used as standards for quality control and identification of the plant in herbal compound formulations and also preparation of a monograph of the plant.

Identification of authentic Phyllanthus amarus species in India

The Phyllanthus is a plant used in the traditional Ayurvedic Medicine system and has more than 800 species. These species grow in the same area and there are chances of adulteration of other species and, incorrect identification may also lead to wrong reports. This study was attempted by Enovate Biolife Pvt. Ltd. to identify authentic Phyllanthus amarus. The nine raw material samples were collected from different populations/suppliers from various zones of India for the study. All the samples were analysed using microscopic and macroscopic ID, and by using the High Performance Thin Layer Chromatography (HPTLC) fingerprint method. The samples collected from the Central zone (Lucknow PA-08, Uttar Pradesh) and the Southern zone (Coimbatore PA-05, and Chennai PA-09, Tamil Nadu) of India were found to be authentic P. amarus by the mentioned identification methods.

The effect of lactic acid fermentation on the phytochemical content of fig leaf extracts compared to single solvent and sequential solvents extraction

The aim of this study was to compare the antioxidant, natural products, and polyphenolic profiles of Ficus carica L. leaf extracts obtained with a sequential solvent extraction (n-hexane, dichloromethane, ethyl acetate, and methanol), a single solvent extraction with one of three different solvents (methanol, ethanol and ethyl acetate), and a fermentation assisted extraction. Extracts were assessed by high-performance thin-layer chromatography (HPTLC) fingerprinting pattern (before and after derivatization with DPPH free radical, anisaldehyde-sulfuric acid reagent and ferric chloride) and with ATR-FTIR phytochemical profiling. The results show that sequential solvents extraction may maximise the extraction of natural products, especially polyphenolics. However, the highest antioxidant activity was achieved with a single solvent extraction with ethyl acetate. Furthermore, fermentation assisted extraction further improves extraction of antioxidants when compared to single extraction from nonfermented material. In conclusion, brining and spontaneous lactic acid fermentation of plant material is a highly desirable method for improving the functional properties of extracts due to its low cost and low energy requirements.

Bioactivity assay of Arundina graminifolia (D.Don) Hochr. extracts from diverse plant parts in Thailand: An assay-based investigation

This research involved surveying and collecting 16 samples of Arundina graminifolia from 8 different subpopulation areas. The main objectives were to analyze the preliminary phytochemical fingerprints and biological activity of the crude extracts obtained from various parts of the plant (roots, rhizomes, stems, and leaves). The findings indicated that rhizome extracts generally yielded a higher percentage of crude extract compared to the dry plant weight in comparison to other plant parts. Moreover, the Thin layer chromatography (TLC) fingerprint data revealed distinct compositions for each part of the plant, with rhizomes exhibiting more prevalent bands of compounds than other parts. Regarding antioxidant activity, the root and rhizome crude extracts from various populations displayed stronger inhibitory activity against DPPH, ABTS, and FRAP methods compared to stems and leaves. High total phenolic content was also found to effectively inhibit free radicals. The lipoxygenase inhibition test, which serves as an in vitro anti-inflammatory activity evaluation, demonstrated that most root extracts exhibited higher lipoxygenase inhibitory activity than the rhizome extracts at a concentration of 0.1 mg/mL. The antibacterial activity demonstrated that rhizome extracts from different regions exerted lower MIC and MBC values against all tested bacteria compared to the root extracts. The findings offer valuable information for selecting specific populations of A. graminifolia as potential sources of bioactive compounds for future nutraceutical applications.

Pharmacognostical and Pharmaceutical Analysis of Sthaulyahara Ghana Vati: A Herbal Ayurveda Formulation for Obesity

Abstract Introduction: Sthaulyahara Ghana Vati (SHGV) is a polyherbal formulation, which is indicated in Sthualya (obesity) in Vaidhyasara sangraha. There are few clinical works carried out on this medicine, but no any researchers had evaluated this formulation for its quality control (QC) parameters. Pharmacopeia standards for this formulation are also not available till date. Aim: To evaluate SHGV through pharmacognostical, physiochemical parameters and high-performance thin-layer chromatography (HPTLC) fingerprinting. Materials and Methods: Preauthenticated raw drugs of SHGV were procured, and SHGV was prepared at pharmacy, Institute of Teaching and Research in Ayurveda (ITRA), Jamnagar. Organoleptic parameters and microscopic analysis of SHGV were carried out at the Pharmacognosy Department, ITRA, Jamnagar. Physiochemical analysis and HPTLC of SHGV were carried out at the Pharmaceutical Laboratory, ITRA, Jamnagar. Result: Microscopic features of SHGV were cross-checked with Ayurvedic pharmacopeia of India standards of individual ingredients, and it was found to have characteristics of all ingredients in it. In pharmaceutical parameters, pH value was 6.0, water-soluble extract was 16.2% w/w, methanol-soluble extract was 14.9% w/w, ash value was 11.8% w/w, and loss on drying was 3.9% w/w. HPTLC at 254 and 366 nm showed six and three spots, respectively. Conclusion: This study has generated preliminary data on pharmacognostical, pharmaceutical parameters, and HPTLC. This fingerprinting can be useful for future researchers to reproduce this formulation and to establish QC parameter of SHGV.

Anti-inflammatory and antioxidant activities and the thin layer chromatographic fingerprinting of the fruit pulp and epicarp extracts of D. microcarpum

Anti-inflammatory and antioxidant activities and the thin layer chromatographic fingerprinting of the fruit pulp and epicarp extracts of D. microcarpum

Herbal Emulgel Containing Azadirachta indica (Neem) and Nigella Sativa L. (Black Cumin) Oils in Wound Management: Preclinical Investigations

Abstract Context: In wound management, traditional use of plants has received attention by the scientific community, as traditional medicines are a valuable source of affordable, comprehensive medical care. Azadirachta indica A. Juss (Neem) and Nigella sativa Linn (Black cumin) are well known versatile medicinal plants with wide spectrum of biological activity. Methods: This study was undertaken to evaluate the wound healing activity of neem oil (NO) and black cumin oil (BCO) in rats. The oils were standardized using standard procedures. Gas chromatography mass spectrometry analysis and high performance thin layer chromatography fingerprinting of oils were carried out to identify major phytoconstituents present in the oils. The oils were suitably incorporated in carbopol based emulgel formulation, evaluated for physicochemical parameters and stability. Results: The wound healing potential assessed by the measurement of wound contraction and histopathology studies in excision and burn wound models, demonstrated comparable efficacy with standard nano crystalline silver gel (0.002% w/w). This may be attributed to the presence of phytoconstituents such as nimbidin and thymoquinone present in selected oils. Polyunsaturated fatty acid profile of BCO may be responsible for stimulating the release of vascular endothelial growth factor, which plays a significant role in accelerating wound healing process. Conclusion: Topical carbopol 934 base emulgel containing natural oils such as BCO and NO have been successfully prepared for wound management. However, further studies to establish the mechanistic aspects of wound healing needs to be undertaken.

TLC-fingerprinting and chemometrics for identification of Curcuma xanthorrhiza from different geographical origins in Indonesia

Abstract. Kartini K, Sabatini SS, Haridsa NM, Jayani NIE, Setiawan F, Hadiyat MA. 2023. TLC-fingerprinting and chemometrics for identification of Curcuma xanthorrhiza from different geographical origins in Indonesia. Biodiversitas 24: 6557-6566. Geographical origin is an important parameter that influences the quality of herbal medicine. The fingerprint of herbal plants is expressed as chemical compounds contributing to said quality. Curcuma xanthorrhiza, popular as java turmeric, is extensively used in Indonesian traditional medicine. This study aimed to validate and develop a Thin Layer Chromatography (TLC) fingerprint of C. xanthorrhiza, followed by chemometric techniques to classify C. xanthorrhiza rhizomes from 15 regions in Indonesia. Under selected TLC conditions (i.e., stationary phase: TLC plate Silica gel 60 GF254, mobile phase: dichloromethane, chloroform, and ethanol (10: 10: 1), detection: vanillin-sulfuric acid reagent), C. xanthorrhiza produced five zones of the compound. Extracts were stable both on the TLC plate and in the extract solution during chromatography and within 60 minutes after derivatization. In terms of precision, the chromatogram meets the requirement of intraday precision. Chemometric analysis with Principal Component Analysis (PCA) and Cluster Analysis (CA) showed that the samples of C. xanthorrhiza from 15 regions in Indonesia were grouped into five clusters based on the similarity of the chemical compounds, namely cluster 1 (Tawangmangu, Bangkalan, Kediri, and Surabaya); cluster 2 (Batu, Sragen, Tulungagung, Pasuruan, Blitar, and Lombok Tengah); cluster 3 (Ngawi); cluster 4 (Gresik); and cluster 5 (Bojonegoro, Banyuwangi, and Palangkaraya). The TLC fingerprinting with chemometrics on C. xanthorrhiza rhizome is useful for quality control based on geographic origin and authenticity identification.

Evaluation of Stability and TLC Fingerprinting of the Artemether Component in Artemether-Lumefantrine Combination Suspension Formulations Available in Nigeria Pharmaceutical Market

Aim: Artemether is the main component of the artemisinin-based combination therapy (ACT), used in the management of malaria infection caused by Plasmodium falciparum. Hence, its stability and conformation to pharmacopeia standards are necessary for use. The study aimed to review the first-order derivative spectrophotometric method for simultaneous estimation of artemether and its derivatives in pure and combined formulations, and their stability profiles, then develop a simple, precise, and fast technique for their rapid physicochemical analysis.
 Methodology: Thin-layer chromatographic (TLC) Fingerprinting principles were used in the analysis. Artemether and its derivatives were spotted on the TLC chromatograms after adding 25 mL of the suspension to a mixture of 100 mL of distilled water and 4 mL of NaOH, extracting the mixture with 60 mL of dichloromethane (DCM), drying, and sonicating the residue with 20 mL of the solvent. It was centrifuged, and the clear supernatant was spotted on the TLC plates.
 Results: The color test results revealed the presence of the artemether compound in the reference standard as well as the six brands of suspensions (A, B, C, D, E, and F) utilized in the study. Artemether melting point was obtained between 86 - 89 °C; within the International Pharmacopeia specified range. The chromatograms of Artemether and derivatives showed Rf values of 0.25 (impurity A), 0.3 (artenimol impurity B), 0.35 (impurity C), 0.4 (α-artemether: impurity D), and 0.55 (artemether).
 Conclusion: The devised method can be applied to the routine quality control analysis of artemether-lumefantrine suspension in addition to existing analytical techniques.

Chemometric Analysis on Fingerprints of Acalypha Indica L Based on the Different Drying Methods

The use of an anting-anting plant (Acalypha indica Linn) as a raw material of herbal medicine requires a standardized process in its production. This research aims to determine the fingerprint pattern of active compounds using a thin-layer chromatography method with specific samples that applied various drying methods, such as direct sunlight drying, greenhouse drying, and oven drying at 50°C. The chemometrics data interpretation with the Principal Component Analysis (PCA) method was applied to analyze the obtained fingerprint patterns to identify the differences among the variations. The separation of active compounds in the anting-anting plant using ultrasonic extraction for 20 minutes with ethyl acetate as the solvent. Consecutively, the thin-layer chromatography fingerprint was investigated by applying a subsequent comparison of mobile phase cyclohexane: toluene: diethylamine by 75:15:10. The result from the TLC plate spots was examined to detect the differences among the fingerprints, with the help of ImageJ and Orange software. The fingerprints with various drying methods resulted in the possession of 11 stains of active compounds. The ImageJ software generated chromatograms with Area Under the Curve (AUC) values, further subjected to chemometrics analysis using PCA. The PCA results showed simple grouping patterns for each variation, with a total principal component (PC) of 86.03% (PC1 = 52.78%, PC2 = 33.25%), indicating the success criteria of PCA chemometrics analysis.

Bioactivities and Phenolic Profiles of Honeys Derived from Plants of the Goldfields, Esperance and Wheatbelt Regions of Western Australia.

The aim of this study was to examine a collection of 79 honeys derived from plants endemic to several Western Australian unique bioregions for bioactivity and physicochemical characteristics. For physicochemical analyses, total phenolic content, high performance thin layer chromatography (HPTLC) fingerprints, pH, Brix, colour and hydrogen peroxide generation were examined. Brix (82.6±1.3) and pH (4.34±0.24) values were within expected ranges, whereas hydrogen peroxide levels determined using an o-dianisidine/horseradish peroxidase assay were relatively low, ranging from 0-244 μM. Antibacterial activity determined by the broth microdilution assay showed that Moort (Eucalyptus platypus) and Yate (Eucalyptus occidentalis) honeys had the highest overall activity with mean minimum inhibitory concentrations of 24.8 % and 25.1 % (w/v) honey, respectively. Yate honey also had the highest overall antioxidant activity (4.38±0.58 mmol Fe2+ /kg of honey), followed by Mallee honeys from various eucalypts, as determined by FRAP (Ferric reducing antioxidant power) and DPPH⋅ (2,2-Diphenyl-1-picrylhydrazyl) assays. This study identified new sources of honeys with potentially useful therapeutic properties from bioregions within Western Australia.

Microscopic characterization, TLC fingerprinting and optimization of total lipid content from Euphorbia neriifolia (L.) using response surface methodology.

Euphorbia neriifolia (EN) is a medicinal plant used to treat a variety of ailments in traditional systems. Despite numerous studies on pharmacological activities, no information was available on the microscopic study of this plant. This is the first study that has been attempted to fill this need by performing the light and field emission scanning electron microscopy (FESEM) of leaf, stem, and latex. The powder microscopy of several organs (leaves, stem, and bark) and exudate (latex) of EN was carried out using safranine, fast green, phloroglucinol, and other standard solutions at different magnifications. The chemical fingerprinting of petroleum ether extract was accomplished by using thin layer chromatography. The optimization of total lipid content from the EN leaf under ultrasound-assisted extraction (UAE) and soxhlet extraction (SE) procedure was determined using response surface methodology (RSM). The studied factors that affect the lipid content were: solvent ratio, extraction temperature, and extraction time. Several notable characteristics observed in the leaf of EN are amphistomatic leaves with anticlinical cell walls, anomocytic stomata, spongy mesophyll cells, elongated palisade cells, angular collenchyma, and U-shaped vascular bundle. The plano-convex midrib is covered by polygonal to oval-shaped cuticles and contains anomocytic stomata. The circular petiole has no trichomes and contains laticifers, crystals, and idioblasts. The circular stem was observed with trichomes, hypodermis, collenchyma, parenchymatous cells, central pith, pentagonal stellar region, cambium, and 2-4 times more xylem that of phloem. All of the powdered plant parts and exudate under study contained trichomes, xylem vessels, wood fibers, cork cells, starch grains, calcium oxalate crystals, idioblasts, lignified cork, tannin content, stone cells, and oil globules. The blackish-green colored petroleum ether extract with semi-solid consistency showed the greatest percent (%) yield of 4% in the latex of EN. The thin layer chromatography (TLC) examination of petroleum ether extract of EN leaf produced a maximum 6 spots with Rf values of 0.16, 0.58, 0.62, 0.73, and 0.96 in the mobile phase of petroleum ether-acetone (8:2). In terms of optimization, the dark green colored UAE extract with semi-sticky consistency showed highest % yield of 4.5% whereas the yellowish green colored SE extract of sticky consistency showed the highest % yield of 4.9%. The findings showed that there were not many differences in the total lipid content between UAE (0.16%) and SE (0.11%). However, the best optimum condition for lipid content extraction analysis was obtained as follows: solvent ratio (PE:HE) 50:50, extraction temperature 50°C, extraction time 45 min for UAE, and solvent ratio (PE:HE) 60:40, extraction temperature 45°C, and extraction time of 24 h for SE. Hence, this study signifies the various noteworthy microscopic features along with the presence of different phytocompounds through TLC and best optimized condition for the extraction of lipids from different parts of EN. As no previous study has been reported, the outcomes obtained from the current study prove to be beneficial in the identification of species, quality control, and detection of any adulteration from the laboratory and commercial samples of EN. RESEARCH HIGHLIGHTS: The percent yield was found to be maximum in latex extract (4%). The leaf pet ether extract was separated into 6 bands with different Rf values. The extracted compounds from Euphorbia neriifolia leaves were categorized into non-polar heat tolerant. The highest total lipid yield (0.1119) was obtained at solvent ratios 60:40 of PE:HE (petroleum ether: petroleum hexane).

Bael (Aegle marmelos L. Correa) fruit extracts encapsulated alginate nanoparticles as a potential dietary supplement with improved bioactivities.

Nanoencapsulated bael fruit (Aegle marmelos L. Correa (Family: Rutaceae)) extracts reveal novel prospects in the development of dietary supplements with improved biological activities in the field of the food industry. The main objectives of this study were to prepare and characterize aqueous, ethanol, 50% ethanol, and 50% acetone extracts of bael fruit encapsulated alginate nanoparticles and investigate the effect of encapsulation on in vitro release of polyphenols, antidiabetic, antioxidant, and anti-inflammatory activities, and their stability. Bael fruit extracts encapsulated alginate nanoparticles were prepared using the ionic gelation method. Characterization, in vitro release profiles of polyphenols, determination of antidiabetic, anti-inflammatory, antioxidant activity, and accelerated stability were conducted. The results of the characterization confirmed the successful encapsulation of extracts of bael fruit in the alginate matrix. The aqueous extract of bael fruit encapsulated alginate nanoparticles exhibited a more controlled slow-release profile, accounting for 21.82%±1.17% and 48.14%±0.52% of polyphenols at solutions of pH 1.2 and pH 6.8, respectively. In general, the results of the bioactivity assessment suggested that nanoencapsulation could facilitate the enhancement of its antidiabetic, antioxidant, and anti-inflammatory properties. The results of thermogravimetric analysis and thin layer chromatography fingerprint showed the stability of aqueous bael fruit extract encapsulated alginate nanoparticles at 27 and 4°C over a month. In summary, the results of this study revealed the potency of nanoencapsulated aqueous extract of bael fruit to develop a dietary supplement with improved antidiabetic, antioxidant, and anti-inflammatory activities. PRACTICAL APPLICATION: The encapsulation of bael fruit extracts into a nanocarrier enhances bioactivities and promotes the controlled release of bioactive compounds. This could be useful in the future food industry, based on scientifically proven data, and inspire the market by means of the development of dietary supplements. Overall, the results would facilitate the formulation of novel commercially elegant nanoencapsulated dietary supplements with improved potential to manage a healthy life.

Establishment of Thin Layer Chromatographic Fingerprints for the Quality Control of Chanthalila Preparation, A Thai Traditional Antipyretic Medicine

Objective: This study aimed to develop thin layer chromatographic (TLC) fingerprints to control the quality of Chanthalila preparation (CP).Material and Methods: Twelve batches of reference CP were prepared from various sources and used as reference batches (CP1 to CP12). Artemisinin, atractylodin, eurycomanone, imperatorin and loureirin A were used as markers. The common and characteristic bands were assigned using the reference TLC fingerprints and applied to assess the qualitative parameters used in the identification and chemical profiling of eight commercial CPs.Results: The reference TLC fingerprints were established on a silica gel GF254 plate with two mobile phase systems, System A and System B. In System A, atractylodin, imperatorin, and loureirin A were assigned as characteristic bands along with 10-12 common bands under Ultraviolet (UV) 254 nm, UV 366 nanometer (nm), and derivatization. In System B, 6 common bands were observed under UV 254 nm, while 11 fluorescent bands were detected under UV 366 nm. Eurycomanone and artemisinin were not found in any reference CP batches, which revealed the TLC method had poor sensitivity. The TLC patterns of commercial CPs were markedly different from those of the reference fingerprints. Most commercial products failed to meet the specification criteria because only imperatorin appeared in the chromatogram.Conclusion: TLC fingerprinting is a fast and efficient method that can be employed in the quality control of CP. It enables the revelation of the quality of the raw materials in the chromatograms, which can be useful to manufacturers to evaluate their supplier sources. However, the sensitivity of this method for determining some markers was quite low.