Vacuum Liquid Chromatography Research Articles

In Silico Studies for Multi-Targeting Justicia Secund Phytochemicals Against Ovarian Cancer

ntroduction/Background of study: Ovarian cancer is the fifth leading cause of cancer deaths among women, accounting for more deaths than any other female gynaecological cancer, which includes cervical, uterine, vaginal and vulvar cancers. Current treatment options include surgery, platinum-based chemotherapy, radiation therapy and the use of targeted therapy such as poly ADP-ribose polymerase (PARP inhibitors), as well as immunotherapy. These therapy options, however, are subject to high rates of resistance and many side effects. AIM/ OBJECTIVES: This research aims to study other viable drug targets for ovarian cancer treatment, as well as new phytocompounds that can serve as new drug options using the in-silico approach. Materials/Methods: The ethanolic leaf extract of Justicia secunda was obtained using conventional methods. Liquid Liquid-liquid fractionation was performed with N-hexane, ethyl acetate and butanol solvents to obtain their fractions alongside the aqueous fraction. Vacuum Liquid Chromatography was performed with the N-hexane fraction and gradient mixtures of N-hexane/ethyl acetate and Dichloromethane/Methanol in various ratios to obtain the subfractions. The compounds were identified using Gas Chromatography-Mass Spectrometry (GC-MS). Full pharmacognostic profiling was performed on the J.secunda leaves. The identified compounds were downloaded from Pubchem and subjected to Molecular docking simulations to obtain their binding affinities with the receptors of interest. Drug-likeness and toxicity assessments were performed on frontrunner compounds. Results: After assessment of the frontrunner compounds, four multitargeting J.secunda phytochemicals were identified: Luteolin, Diosmetin, 5H-Quindoline and 10H-Quindoline.

Aktivitas Antioksidan Fraksi Larut Etil Asetat dari Ekstrak Akar Tabar Kedayan (Aristolochia papilifolia Ding Hou)

Kedayan root is a medicinal plant that is traditionally used by the community as medicine, especially as an antidote to poison. This research aimed to determine the antioxidant activity of the ethyl acetate soluble fraction of Tabar Kedayan root extract (Aristolochia papillfolia Ding hou). The fractionation method used is solid-liquid extraction using ethyl acetate solvent to obtain a soluble fraction of ethyl acetate, then vacuum liquid chromatography fractionation using the eluent ratio n-hexane: ethyl acetate and obtain fraction A, fraction B, fraction C, fraction D, fraction E, fraction F. Testing of antioxidant activity using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) method spectrophotometrically. The data obtained was analyzed using linear regression to determine IC50. The results of the C fraction test on the ethyl acetate soluble fraction of Tabar Kedayan roots (A. papillfolia) have antioxidant activity with an IC50 value of 139.11 ppm.

Tephrosin and obovatachalcone with antibacterial activity from Tephrosia vogelii Hook.f

In the search for new antibacterial agents from plants, two known compounds (rotenoid and chalcone) were isolated from Tephrosia vogelii Hook.f. (seeds), namely tephrosin (1), and obovatachalcone (2). The compounds were isolated using vacuum liquid chromatography and radial chromatography. The structures of isolates were determined by 1D and 2D NMR. Both compounds were evaluated for their antibacterial properties against the four pathogenic bacterial strains Staphylococcus aureus S33 R4, Bacillus subtilis subsp. subtilis str. 168, Escherichia coli TISTR 780, and Salmonella typhi Ty 21a, using the microdilution method to determine MIC and MBC. The results showed that tephrosin (1) had moderate antibacterial activity against E. coli with MIC values of 25 μg/mL and MBC values of 100 μg/mL. However, obovatachalcone (2) showed a weak antibacterial activity.

Characterization of Antibiotic Actinomycin D Isolated from Streptomyces parvulus Collected from Marine Sponge of Barrang Lompo Island, Makassar, Indonesia.

Microorganisms associated with sea sponges have proven to be good natural product resources that are biologically active and pharmaceutically important. This research aimed to identify actinomycetes related to a sponge from Bar-ranglompo Island Makassar and the antibacterial compounds. Identification of actinomycetes was based on molecular characterization of sequence gen16S rRNA. The antibacterial compound was separated using vacuum liquid chromatog-raphy and preparative Thin Layer Chromatography (TLC). The structure determination was done based on spectroscopy 1H-NMR, 13C-NMR, 2D NMR, and mass spectra. Molecular characterization showed that actinomycetes strain BLP 20 had the closest relationship with Streptomyces parvulus and Uncultured Streptomyces sp. with a similarity value of 83%. The results obtained from the characterization of antibacterial compounds based on spectroscopic data indicate that these compounds lead to Actinomycin D. Characterization and identification of Strain 20 / BLP by molecular phylogenetic analysis of 16S rRNA sequences revealed the closest relationship with Uncultured Streptomy-ces sp and S. parvulus with a similarity value of 83 %, which indicated a new species. The structure of the active compound isolated from actinomycetes strain 20 / BLP leads to Actino-mycin D.

Comparative analysis of feature annotation methods for SESI-HRMS in exhaled breath analysis

Secondary electrospray ionization coupled to high-resolution mass spectrometry (SESI-HRMS) is a powerful method for the analysis of exhaled breath in real time. However, feature annotation is challenging due to the flow-injection nature of the technique. To evaluate alternative methods for enhancing feature annotation, a study was conducted where the exhaled breath of sixteen subjects was condensed and analyzed using dynamic headspace vacuum in-trap extraction gas chromatography-mass spectrometry (DHS-V-ITEX-GC–MS) and liquid chromatography coupled to mass spectrometry (LC-MS) using polar and reverse-phase conditions along with a data-independent MS2-acquisition method based on multiple injections. The annotation results obtained from these methods were compared to those from SESI-HRMS. The use of these techniques on breath condensate is unprecedented. The GC–MS method primarily detected compounds of exogenous origin, particularly additives in oral hygiene products like menthol. On the other hand, LC-MS detected a vast number of features, especially with the utilized data-independent acquisition method. Chemical classes to these features were assigned in-silico. In positive ion mode, mostly amino acids and amines were detected, while the largest group in negative ion mode consisted of carboxylic acids. Approximately 25% and 5% of SESI features had a corresponding match with LC-MS and GC–MS. While both GC–MS and LC-MS methods partially overlapped with the SESI features, there was limited overlap of both in the mass-to-charge range from 150 to 200. In conclusion, both GC–MS and LC-MS analysis of breath condensate can serve as supplementary tools for annotating features obtained from SESI-MS. However, to increase confidence in the annotation results, combining these methods with additional on-line fragmentation techniques is recommended.

Chemical constituents of Lasiodiplodia theobromae BPPCA 144, an endophytic fungus, isolated from Aglaia argentea Blume

Endophytic fungi from Aglaia argentea have indicated the prospective to produce secondary metabolites with unique activities, making them promising candidates for anticancer drug development. This study aimed to investigate the secondary metabolites produced by Lasiodiplodia theobromae BPPCA144, isolated from A. argentea. L. theobromae BPPCA144 was found to produce seven compounds: 2-phenylethanol (1), tyrosol (2), 2-(4-hydroxyphenyl)acetic acid (3), (-)-mellein (4), colletopeptide B (5), botryorhodine A (6), and (4R*,6R*)-4-hydroxy-6-n-propyl-1-oxacyclohexan-2-one (7). These compounds were isolated using vacuum liquid and radial chromatography, and their chemical structures were elucidated through 1D-NMR, 2D-NMR analysis, compared with previously reported spectral data. Notably, compounds (5) and (7) were identified as original from L. theobromae. Among the tested compounds, compound (2) exhibited the strongest activity against MCF-7 breast cancer cells. However, compounds (1, 3, 5 and 7) showed insufficient activity against CV-1 cell lines (normal kidney fibroblast cells).

Exploring the Potential of Dacryodes Edulis Leaf Extract as Natural Colourant on Polyamide Fabrics: Extraction, Characterization and Application

There is a growing demand for sustainable and eco-friendly alternatives in the textile industry, particularly in search of natural colourants derived from plants. This research study investigates the extraction and characterization of natural colourant from the leaf of D. edulis and explores its application to polyamide fabrics. Laboratory experiments, such as solvent extraction was performed to obtain the colourant. The extraction process was optimized using Response Surface Methodology-Central Composite Design (RSM). The dye was isolated and characterized using vacuum liquid chromatography, UV-Vis spectrophotometry, high-performance liquid chromatography and Fourier-transform infrared spectroscopy. Physical properties such as light fastness, perspiration fastness, rubbing fastness and wash fastness were assessed to determine the durability and stability of the natural colourant on the fabrics. The results indicated that the optimal conditions for dye extraction are 65.9 ℃ and 2 hours, providing feasible parameters for replication. Examination of the natural dye obtained from the isolated fraction, revealed the presence of carbon-carbon double bonds (C=C), carbonyl (C=O), ester (-COO), aldehyde (CHO) and hydroxyl (-OH) groups; with rutin, isoquercetin and tannic acid as its major compounds. The isolated dye exhibited an absorption peak at 403 nm. The ratings for the treated fabrics varied from fair to good and very good. The light fastness ranged from 4 to 6, perspiration fastness and wash fastness ranged from 2-4, and rubbing fastness ranged from 3-5. On the other hand, the untreated fabrics had ratings, with a range of 2-5 for light fastness, 2-4 for perspiration fastness and wash fastness and 1-4 for rubbing fastness, it was also observed that the colour strength values of mordanted fabrics were deeper than those of the unmordanted fabrics. These results indicate that the dye obtained from D. edulis leaf has considerable potential as a source of natural dyes. These findings contribute valuable insights into the extraction, characterization and application of natural colourants, promoting a shift towards more sustainable and eco-friendly practices in the textile industry.

Two Sesquiterpenes from n-Hexane Fraction of Curcuma soloensis Rhizomes and Their Antimicrobial Activities

Curcuma soloensis is one of the medicinal plants that has the potential to be a source of bioactive compounds. The antimicrobial study of the bioactive compounds from C. soloensis was still limited. This study aimed to isolate the bioactive compounds from C. soloensis rhizomes and to evaluate their potential as antimicrobial agents. C. soloensis rhizome extraction was done using the maceration method with acetone and then fractionated with n-hexane: methanol (1:1). The compounds were separated and purified using vacuum liquid chromatography and radial chromatography. The structure of the isolated compounds was determined using the nuclear magnetic resonance (1H and 13C NMR) spectroscopy analysis and comparison with literature data. Antimicrobial activity assays of the extract, n-hexane fraction, and isolated compounds were carried out by microdilution methods against Escherichia coli, Staphylococcus aureus, Candida albicans, and Malaszezia furfur. Two bioactive compounds from the n-hexane extract of C. soloensis rhizome have been isolated: ar-curcumene and ar-turmerone. Antimicrobial test results on acetone extract, n-hexane fraction, and isolated compounds showed that ar-turmerone had the highest activity against S. aureus with a MIC value of 15.6 μg / mL. In comparison, ar-curcumene showed the same activity against all test microbes with a MIC value of 62.5 μg / mL. This study showed that secondary metabolite compounds of C. soloensis rhizomes have the potential to be developed as antimicrobial agents.

Characterization of antibiofilm compound from marine sponge Stylissa carteri.

The fouling phenomenon grabbed global attention and caused huge economic losses specifically in marine-related industries. Sessile behavior exposed the sponge to the risk of fouling. However, their bodies remained free from foulers, which were attributed to the chemical defense system. The objectives of this study were to determine the antibiofilm activity of the marine sponge, Stylissa carteri, and to characterize the isolated compound involved. The antibiofilm activity of S. carteri methanolic crude extract (MCE) and fractions was tested against biofilm-producing bacteria, Pseudomonas aeruginosa, using two different modes of crystal violet biofilm assays: preventive and detachment. Besides that, the disc-diffusion test was conducted to screen the antibacterial activity against gram-positive and gram-negative bacteria while a cytotoxicity assay was conducted on the HepG2 cell line. Bioassay-guided fractionation was carried out using vacuum liquid chromatography (VLC) and solid phase extraction using a C18 Sep-Pak Cartridge. The crystal compound was isolated and characterized through thin-layer chromatography (TLC), Fourier transform infrared (FTIR) spectroscopy, liquid chromatography-mass spectrometry (LCMS), and nuclear magnetic resonance (NMR) spectroscopy. The S. carteri MCE showed a promising result with a half-maximal inhibitory concentration (IC50) of 20.22μg/mL in the preventive assay, while no IC50 was determined in the detachment assay since all inhibitions < 50%. The S. carteri MCE exhibited broad-spectrum antibacterial activity and displayed a non-cytotoxic effect. Fraction 4 from MCE of S. carteri (IC50 = 2.40μg/mL) reduced the biofilm in the preventive assay at all concentrations and exhibited no antibacterial activity indicating the independence of antibiofilm from antibacterial properties. Based on the data obtained, an alkaloid named debromohymenialdisine (DBH) was identified from Fraction 4 of S. carteri MCE. In conclusion, S. carteri was able to reduce the establishment of the biofilm formed by P. aeruginosa and could serve as a prominent source of natural antifouling agents.

Chemical Constituents of the Artemisia ciniformis Aerial Parts Grown in the Northeast of Iran and Their Chemotaxonomic Significance

Background: The Artemisia genus is one of the largest genera of the Asteraceae family, with various traditional and modern reported uses. Within this group, Artemisia ciniformis (Dermane Talaei) is an endemic plant of Iran with antioxidant, antimalarial, anticancer, cytoprotective, and neuroprotective properties. Due to these potential benefits, further phytochemical research needs to be conducted to understand its chemotaxonomic and pharmaceutical effects. Objectives: The main purpose of this study is to investigate the dichloromethane fraction of A. ciniformis from Iran for phytochemical and chemotaxonomic aspects. Methods: Artemisia ciniformis aerial parts were collected, dried, and extracted by the maceration method using dichloromethane after defatting. The prepared extract was subjected to chromatographic techniques, including column chromatography, vacuum liquid chromatography, and HPLC, to isolate purified compounds, which were identified using spectroscopic analyses such as NMR and EI-MS. Results: Two tetrahydrofuran-type sesquiterpenoids: (1) hydroxydavanone and (2) arteincultone; two acetophenone derivatives; (3) xanthoxylin and (4) 2,4-dihydroxy-6-methoxy acetophenone; and a flavonoid, (5) jaceosidin, were isolated. Additionally, a polymethoxylated flavone was obtained in small amounts, and its structure was tentatively assigned as (6) 5,6-dihydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-7-methoxy-4H-chromen-4-one (Ciniformon). Conclusions: Artemisia ciniformis is a rich source of phytochemicals from various categories, such as sesquiterpenes and phenolic compounds, that can be used in systematic studies and medicinal research to treat human disorders by discovering new biologically active as well as lead compounds.

Synthesis of silver nanoparticles from coffee parasite leaf extract (Scurrulla ferruginea (Roxb. ex Jack) Danser) and potential activity as an antioxidant and anticancer

This study aim is to know the results of the synthesis of silver nanoparticles from quercetin and Scurrula ferruginea (Roxb. Ex Jack) danser as well as its potential as an antioxidant and anticancer. The solvent used in the maceration extraction method in this research is the polar solvent methanol. Isolation and purification of thick extract compounds from coffee parasite leaves were carried out using liquid vacuum chromatography (CVC) and gravity column chromatography (GCC) methods. Silver (Ag) nanoparticle is made with the stirrer method at a speed of 1500 rpm for 60 minutes at a temperature of 70o C. Silver nanoparticle solution was produced and then characterized using FTIR (Fourier Transform Infra Red) and PSA (Particles Size Analyzer). PSA results analysis using extract coffee parasite size 214 nm particles, whereas using flavonoid isolate quercetin confirmed size 29 nm. FTIR showed that there was a stretching vibration of the OH group at a wave number of 3229.25 cm-1, the C=O function at the wave number 1637.87 cm-1, and the CO functional group at the wave number 1016.31 cm-1. Antioxidant test using the DPPH method was carried out in silver nanoparticle solution using extract Scurrula ferruginea (Roxb. Ex Jack) danser and with quercetin obtained an IC50 value of around 115.4 and 114.9 this result describes as moderate level of antioxidants. Even though the nanoparticle anticancer test was very weak, overall, the synthesis of silver nanoparticles using flavonoid isolates was better than using extracts from coffee parasite leaves.

Cytotoxic Potential of Compounds Isolated from Non-Polar Fractions of Sungkai Plant Leaves (Peronema canescens Jack) Against Artemia salina Leach Larvae

The sungkai plant (Peronema canescens Jack), belonging to the Lamiaceae family, is a plant that is traditionally used as medicine, including toothache, malaria, and fever medicine. In this research, isolation was carried out with vacuum liquid chromatography (VLC), solid and liquid fractions were obtained. The solid fraction was further separated using column chromatography to obtain the isolated compound as a white solid (amorphous) weighing 10 mg (melting point 140˚C-142˚C). The results of the UV spectrum data show that there are no conjugated double bonds. The results of the IR spectrum show the presence of C-H groups at wave numbers 2921,49 cm-1 and 2856,94 cm-1, C=O groups at wave numbers, C=C groups at wave numbers 1641,51 cm-1, and dimethyl germinal which is characteristic of triterpenoid compounds at wave numbers 1456.68 cm-1 and 1372.41 cm-1. Meanwhile, the isolated oil was analyzed for chemical components using GC-MS. It was discovered that there were 83 chemical compound components contained therein with 4 main compound components, namely pentadecanoic acid (16.65%), 9,12-octadecanoic acid (16.12%), propyl palmitate (7.89%), and hexadecenoic acid, methyl ester (5.59%). A cytotoxic test was carried out on both fractions using the Brine Shrimp Lethality Test (BSLT) method. The results showed that the isolated compound was non-toxic with an LC50 value of 190214.2807 mg/L and the isolated oil was very toxic with an LC50 value of 34.2452 mg/L.

Karakterisasi Struktur Kumarin pada Akar Tumbuhan Langsat (Lansium domesticum Corr.)

Lansium plants produce not only terpenoids as the main constituent but also contain phenolics on the basis of phytochemical analysis. Unfortunately, there are still limited information about phenolic structures from this plants. This study was conducted to identify one of phenolic structures from chloroform fraction of Lansium domesticum root. The chloroform fraction was fractionated and purified by chromatographic techniques such as vacuum liquid chromatography (VLC) and column chromatography (CC) to obtain a coumarin. Additionally, the coumarin structure was characterized by 1H-NMR. The isolated coumarin showed a positive result for the phenolic test with FeCl3 5%. The 1H-NMR spectrum of isolated coumarin revealed chemical shifts at δH 7,60 (1H, d, J = 9,5 Hz), 6,92 (1H, s), 6,84 (1H, s), 6,27 (1H, d, J = 9,5 Hz), 6,14 (1H, s), and 3,95 (3H, s). Based on those results and comparison with literature data, it can be concluded that the isolated coumarin is iso-scopoletin (1)

Anti-lipase Activity of Kemuning (Murraya paniculata) Leaves Extract and Its Fractions

Kemuning (Murraya paniculata) belongs to the Rutaceae family, it grows a lot in tropical areas such as Indonesia. Traditionally, Kemuning leaves are used for weight loss preparations and are believed to contain compounds that can inhibit pancreatic lipase, including flavonoids. This study aimed to reveal the antilipase activity of Kemuning leaves extract and its fractions. The extraction of Kemuning leaves was carried out by maceration with 70% ethanol as solvent. The vacuum liquid chromatography method was used to separate the secondary metabolites in the extract with the stationary phase of silica gel and the eluent mixture of n-hexane, ethyl acetate, and methanol in a gradient manner. Meanwhile, the antilipase activity was tested by colorimetric method, with p-nitrophenyl butyrate as a substrate and orlistat as a positive control. The extract obtained was 19.94% of the weight of the simplicia. The separated extract was collected in 20 flasks and then combined based on the Rf value of the spots observed on thin layer chromatography (TLC) producing 8 fractions (fractions A-H). The percentage yields of fractions A-H were 1.20, 1.33, 1.80, 3.92, 3.57, 4.20, 16.85, and 14.47%, respectively. Antilipase activity was indicated by IC50 values, which were 17.603 ± 1.660 and 108.554 ± 1.660 µg/mL for orlistat and extract, respectively. The antilipase activities of fractions A-H were 130.19 ± 2.90, 119.52 ± 1.95, 96.95 ± 1.81, 91.65 ± 0.78, 95.30 ± 1.46, 114.76 ± 2.87, 127.07 ± 3.56, and 134,04 ± 3.16 µg/mL, respectively. Based on these results, it can be concluded that the extract and its fractions exhibit very strong antilipase activity. Keywords: Murraya paniculata; extract; fraction; antilipase

Investigating the feasibility of utilizing &lt;i&gt;Pennisetum purpureum&lt;/i&gt; leaves waste as a sustainable dye: Extraction, characterization and application on textile

This study investigated the potential of Pennisetum purpureum (Elephant grass) leaves waste as a source of natural dyes. The objective was to extract, characterize and apply the natural dyes on textile fabrics. Elephant grass was chosen due to its abundant availability as agricultural waste, making it an environmentally sustainable alternative to synthetic dyes. The extraction process involved maceration, followed by filtration to obtain the dye extract. The dye components were isolated using vacuum liquid chromatography and then characterized using analytical tools such as UV-Visible Spectrophotometry, High-Performance Liquid Chromatography (HPLC) and Fourier-Transform Infrared Spectroscopy (FTIR) to identify the presence of specific compounds responsible for the dyeing potential. The perspiration fastness, rubbing fastness, light fastness and wash fastness properties were assessed to evaluate the durability and suitability of the natural dyes. The UV-Visible spectrum, HPLC and FTIR analysis confirmed the presence of chromophores such as conjugated systems, and provided information about chemical components namely rutin, quercetin, senecionine, hyoscyamine and tannic acid present in the dye, as well as the types of bond present in the molecules including C-H, O-H, C=O and C-O groups, which are characteristics of natural dyes. The dyed textile fabrics demonstrated somewhat fair to good with a rating of 3-7 for perspiration fastness, light fastness, rubbing fastness and wash fastness, indicating the potential of the natural dye for practical applications. The findings can inspire further research and development in utilizing agricultural waste for natural dye production, promoting sustainable practices in textile manufacturing.

Isolation of New Asiatic Acid derivative from Centella asiatica (L.) Urban as Antioxidant

Centella asiatica (L.) Urban is known to have a pharmacological effect as an antioxidant. Indonesian research on gotu kola, especially the ethyl acetate fraction it produces, is rarely carried out. Previous research stated that kaempferol and quercetin which isolated from the ethyl acetate fraction of Centella asiatica herb had antioxidant activity with respective IC50 values of 16.50 and 21.61 μg/mL, so this study aimed to get other compounds from the ethyl acetate fraction which has antioxidant activity. The purposes of this study were to isolate, identify, and examine the free radical scavenging activity of DPPH from the ethyl acetate fraction of gotu kola (C.asiatica (L.) Urban) herb. Isolation of the ethyl acetate fraction was carried out from 70% ethanol extract of Centella asiatica plant using vacuum liquid chromatography and gravity column chromatography afforded a new asiatic acid derivative. Elucidation of a new compound based on UV-Vis, FT-IR, LC-MS/MS, 1D-NMR and 2D-NMR to get 11-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-10-((3,4,5-trihydroxytetrahydrofuran-2-yl)oxy )-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid and it had moderate antioxidant activity with IC50 of 106.99 ± 1.76 µg/mL. The pure isolate obtained is suspected to be a new compound derived from asiatic acid.

β-Sitosterol and ferulic acid from the hexane extract of Bryophyllum pinnatum stems

This study aims at the isolation and characterization of bioactive constituents from the stem of Bryophyllum pinnatum in n-hexane extract. Spectroscopic and chromatographic methods were used. The isolation was conducted through vacuum Liquid Chromatography (VLC) in the polarity gradient of solvent systems, Thin Layer Chromatography (TLC) was used to confirm their purity, and purification was carried out using gel filtration chromatography (GFC). Characterization of the isolated compounds was carried out using Nuclear Magnetic Resonance Spectroscopy. Experimental data of active compounds was in agreement with NMR data of β-Sitosterol and ferulic acid available in the literature, Elemental analysis showed that percentages of C, H and O in the isolated compounds conformed with calculated values of those in β-Sitosterol and ferulic acid. Isolation and characterization of β-Sitosterol and ferulic acid was reported for the first time, from the stem of Bryophyllum pinnatum n-hexane extract.

Bioassay-directed isolation of two novel antimicrobial coumarin and flavanone from Acanthus montanus

Abstract This work is geared towards extraction, isolation and characterization of phytocompounds from the ethyl acetate extract of Acanthus montanus root. The ethyl acetate extract was obtained through sequential maceration using a nonpolar solvent first before introducing ethyl acetate. The extract was subjected to vacuum liquid chromatography (VLC) for fractionation and phytocompounds were purified through column chromatography. Characterization was done employing infrared spectroscopy (IR) and nuclear magnetic spectroscopy (NMR). The phytocompounds were isolated and characterized as 6,7-dihydroxy-4-methoxycoumarin and 2ʹ-acetoxy-4ʹ,5-dihydroxy-6ʹ-methoxy-3-(2ʹʹ-hydroxy-6ʹʹ-oxanyl)-8-(2ʹʹʹ-hydroxy-4ʹʹʹ-oxanyl)flavanone named Acanthusin G with percentage yield of 0.7% and 1.16% respectively. 6,7-dihydroxy-4-methoxycoumarin and Acanthusin G indicated good antimicrobial activities at 200 µg/ml with zone of inhibition range of 18 - 36 mm against fifteen pathogens using agar well diffusion method.

ISOLATION AND CHARACTERIZATION OF FLAVONOID DERIVATIVE OF ETHYL ACETATE EXTRACT FROM BAUHINIA LATISILIQUA STEM BARK AND ITS ACTIVITY AS ANTIOXIDANT

Various bioactivities on natural compounds, the antioxidant potency can provide a broad spectrum in their utilization and development into medicinal raw material. One of the plants that have potency for antioxidant activity is the Kemerakan sapenit (Bauhinia latisilqua) plant. The study aimed to isolate, characterize, and determine the antioxidant activity of a compound isolated in the ethyl acetate extract of the stem bark of B. latisilqua. This research includes extraction, fractionation, purification, and elucidation of secondary metabolite structure as well as testing its antioxidant activity. Extraction was carried out by maceration technique, fractionation, and purification using liquid vacuum chromatography and gravitation column chromatography. The elucidation of the structural compound was determined by analysis of the UV, IR, and NMR spectra. The antioxidant test was performed using the DPPH method. Based on the analysis of the spectral data, the isolated compound was catechin, a derivative of flavan-3-ol. Antioxidant test on catechin compound showed a strong antioxidant with an IC50 value of 35.01 µg /mL (IC50 for positive control, ascorbic acid, of 42.94 µg /mL).

Potential of purple eggplant skin fraction (Solanum Melongena Var. Serpentinum L.) as an in vitro sunscreen

Sunscreen is a product that is used as skin protection against sun exposure. The skin of purple eggplant is known to contain secondary metabolites which are used as sunscreens. This study aims to determine the activity of sunscreen fraction of the purple eggplant (Solanum melongena var. serpentinum L.) in vitro. Testing of sunscreen activity was carried out by calculating the value of SPF (Sun Protection Factor), %TE (Percent Transmission of Erythema) and %TP (Percent Transmission of Pigmentation) using the UV-Vis Spectrophotometry method. The purple eggplant skin fractionation method is by using LVC (Liquid Vacuum Chromatography). The results of the fractionation were identified using phytochemical screening and combined TLC. The fraction results were tested for SPF (Sun Protection Factor), %TE and %TP values. The results showed that the extract yield was 26.33%. The fractions used are fraction 9; 10; 11; and 12 which showed the same stain after being evaporated, which was a brownish yellow stain with a yield of 21,24%. The purple eggplant skin fraction (Solanum melongena var. serpentinum L.) has SPF, %TE and %TP values with optimal protection at a concentration of 400 ppm with each value obtained being 19; 1.35 and 9.79. The results of the statistical test of the purple eggplant skin fraction showed that the data were normally distributed but not homogeneous. The results of the homogeneity test for each concentration of results showed that the data were not significantly different.