Radiolabeling and In-Silico Study of 131I-(4-fluorobenzoyl-3-methylthiourea) as Radiopharmaceuticals for Breast Cancer Theranostics

The chemicals produced from thiourea are actively being studied as anticancer possibilities. In complexes with radionuclides like Iodine-131, the 1-(4-Fluorobenzoyl)-3-methyl thiourea is a promising ligand for theragnostic applications. This study aimed to label 1-(4-fluorobenzoyl-3-methylthiourea) with iodine-131 and observe its interaction with breast cancer receptors. The radiolabeling of 131I-(4-fluorobenzoyl-3-methylthiourea) uses the radioiodination method with Chloramine-T, and an in-silico investigation of breast cancer receptors was conducted. According to the results of molecular docking using AutoDockTools, this radiopharmaceutical molecule has the best activity on the HER2 receptor (PDB ID: 3PP0) compared to the native ligand and control positive, with a binding affinity of -6.13 kcal/mol and a Ki value of 32.05 mM. According to the molecular dynamics data using Desmond, the radiopharmaceutical molecule 131I-(4-Fluorobenzoyl-3-methylthiourea) displays good stability starting from the 50ns range. The indirect radioiodination method has successfully labeled 1-(4-Fluorobenzoyl-3-methylthiourea) with iodine-131

Synthesis and Characterization of Low Molecular Weight Irradiated Chitosan in Various Water Levels and Gamma-Ray Doses

Chitosan is a biopolymer derived from marine animal shell waste that exhibits numerous pharmacological activities. However, its high molecular weight limits the application in various fields due to its low solubility. Therefore, this study aims to synthesize low molecular weight chitosan using varying water content and doses of gamma irradiation. To initiate chitosan degradation, H2O (5 and 10 mL) was added, followed by gamma ray irradiation at doses of 5 and 10 kGy. The Molecular Weight (MW) of degraded chitosan was determined using Gel Permeation Chromatography (GPC), while Fourier Transform Infrared Spectroscopy (FTIR) was used to characterize the functional groups and degree of deacetylation of chitosan. The study found that the molecular weight of irradiated chitosan decreased as the irradiation dose and H2O addition increased. The addition of 10 mL of water and gamma irradiation at a dose of 10 kGy has been found to reduce the molecular weight of chitosan to 118 kDa, with a high deacetylation degree of 86.78%. The FTIR analysis showed no significant changes in the functional groups, indicating that gamma irradiation did not affect the structure of chitosan

The Synthesis of Y-zeolite-modified CaCO3-ZnO Nanocomposites as an Antibacterial Agent

The ability of inorganic antibacterial agents like metal oxides and nanoscale inorganic materials to inhibit bacterial growth rates has yet to receive much research attention. In this study, CaCO3-ZnO/Y-zeolite nanocomposites were created utilizing coprecipitation and impregnation techniques with Ca(CH3COO)2, Zn(CH3COO)2 2H2O, Y-zeolite precursors. Physical and chemical characteristics of nanocomposites have been investigated using XRD, FTIR, and SEM-EDX characterizations. The agar-well diffusion method tested the substance for antibacterial activity against gram-positive and gram-negative bacteria. Nanocomposites have a crystal size range of 35.46-36.53 nm and a crystallinity of 35-37 %, according to the results of XRD analysis. The carbonate groups are visible in FTIR data at wave numbers 1433, 875, and 712 cm-1. The Zn-O absorption band was verified at wave numbers 600-400 cm-1. The Y-zeolite absorption bands at wave numbers 1012-997 cm-1 and 745-746 cm-1 were confirmed. The particle morphology is cube-shaped with irregular sizes. The EDX result showed that the composition consists of 35.92 % calcium, 1.68 % zinc, 44.81 % oxygen, and 13.79 % carbon as elements. With the addition of 2.5 % Y-zeolite, the antibacterial activity of nanocomposites showed the best results, with an inhibition zone diameter of 7.62 mm against Escherichia coli and 6.56 mm against Staphylococcus aureus bacteria

Amino Acids Isolation from α-keratin of Javanese Goat (Capra hircus) Hair and Garut Sheep (Ovis aries) Hair Waste Using Acid Hydrolysis Method as BCAA Supplement

Javanese goat and Garut sheep hair contain α-keratin, a protein that can be broken by hydrolysis to produce simpler amino acids. Feather waste generates millions of tons of α-keratin biomass originating from animal slaughterhouses, thereby raising health concerns. The utilization of acid hydrolysis is considered to be more cost-effective compared to enzymatic hydrolysis, and it provides a broader range of amino acid cleavage sites compared to enzymes, which exhibit specific cleavage. This study aimed to isolate amino acids from Javanese goat and Garut sheep hair through acid hydrolysis. The methods included hair sample preparation, acid hydrolysis used 6 M HCL at 110°C, reflux isolation, amino acid separation based on isoelectric pH 4.9 –5.4, functional groups analysis using FTIR, and analysis of amino acid content by HPLC methods. The results showed that the yield produced after isolation on Javanese goat hair samples was 0.92% and Garut sheep hair 0.32%, respectively. The FTIR spectrum showed amino acid functional groups in both samples, including carboxyl (COOH), amine (C-N primer), (C-S disulfide), and amide I (-CONH2). Successful breakdown of α-keratin proteins into simpler amino acids was achieved for Javanese goat and Garut sheep hair. Amino acid analysis of Javanese goat hair isolates revealed the presence of aspartic acid, threonine, serine, glutamate, proline, glycine, alanine, valine, methionine, isoleucine, leucine, tyrosine, phenylalanine, histidine, lysine, and arginine amino acids, respectively. The highest content was isoleucine at 0.60% w/w. In conclusion, the isolated amino acids from Javanese goat hair can be used as a halal supplement that serves as nutrition in the body

Hybrid CaO/ZnFe2O4 Modified with Al2O3 as a Green Catalyst for Biodiesel Production from Waste Cooking Oil

In this work, biodiesel was produced from waste cooking oil (WCO) via a green catalyst of CaO-ZnFe2O4 modified Al2O3. The catalyst was characterized using Fourier-transform infrared spectroscopy (FTIR), X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy dispersive x-ray (EDX), SEM-mapping, Brunauer-Emmett-Teller (BET), transmission electron microscopy (TEM) analyses. The catalyst performance was studied in the transesterification reaction of WCO conversion to biodiesel. The catalytic activity increased with the combination of nanoparticles effect and support catalysts obtained biodiesel yield of nano-Al2O3, nano-CaO, ZnFe2O4, CaO-ZnFe2O4, and CaO-ZnFe2O4/Al2O3 is 36.86%, 67.16%, 74.83%, 86.54%, and 93.41%, respectively. The best biodiesel yield was 93.41% with a mass ratio of Al2O3 to CaO-ZnFe2O4 (2:1). The physicochemical properties (acid number, density, kinematic viscosity, flash point, and cetane number) of biodiesel under the optimal conditions agreed with the ASTM standard. These results show that the developed nanocomposite has great potential to reduce biodiesel production costs because derived from WCO. In conclusion, CaO-ZnFe2O4 modified Al2O3 as a catalyst has a high potential for biodiesel production on a large scale

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

Anticancer Activities of Bromelain Hydrolysate of Soy Protein Against Breast Cancer Cells MCF-7

Soybeans contain proteins that have the potential to produce anticancer bioactive peptides. This study aims to determine the anticancer activity of soy protein hydrolysate against MCF-7 breast cancer cells. Soybean protein hydrolyzed by bromelain enzyme 0.5% (w/v) at the optimum temperature and pH for protein hydrolysis using the Bergmeyer and Grassl method. The degree of hydrolysis value of protein hydrolysate was determined by the Alder-Niesen method and the protein profile was analyzed by SDS-PAGE. The hydrolysate with the best degree of hydrolysis value was analyzed for anticancer activity against MCF-7 breast cancer cells by the Presto Blue assay method, and fractionation of protein hydrolysates by gel filtration chromatography (Sephadex G-15). The molecular weight of the peptide was characterized by LCMS/MS. Soy protein hydrolysis using 0.5% (w/v) bromelain enzyme was optimum at 65 ºC and pH 7.0 for 4 hours, with a hydrolysis degree value of 20.57%. The SDS-PAGE analysis showed that the protein hydrolysates had quite thick protein bands in the range of <35 kDa with an IC50 value of 70.37 mg/mL. Based on the LCMS/MS results, the peptide from fractionation has a molecular weight of 5.133 kDa

Synthesis of Zr/La-BTC Bimetallic Metal-Organic Framework (MOF) for Oleic Acid Esterification

Biodiesel plays an essential role in renewable energy as an alternative fuel to tackle the challenges of global warming, environmental degradation, and alternative fossil fuels. Oleic acid can be converted into biodiesel by the esterification process, which employs heterogeneous catalysts such as metal-organic frameworks (MOF). In this study, Zr/La-BTC MOFs were used as different kinds of catalysts to change oleic acid into biodiesel. The characterization results of Zr-BTC, La-BTC, and Zr/La-BTC using FTIR and XRD show that the MOF has been successfully formed. The crystallite sizes for La-BTC, and Zr/La-BTC MOFs are 15.7407 nm and 39.0392 nm, respectively. The surface area of Zr-BTC, La-BTC, and Zr/La-BTC MOFs are 167.101 m2/g, 12.328 m2/g, and 4.764 m2/g. The morphology of Zr-BTC MOF using SEM is irregular, La-BTC is rod-shaped crystal, and Zr/La-BTC is like a knot bond with a narrow waist. The most optimal reaction was obtained at a 5% (w/w) catalyst dosage of total oleic acid and methanol (1:60 mol), 65 °C, and a reaction time of 4 hours, producing 78.11% oleic acid conversion. GC-MS analysis identified that the biodiesel contains oleic acid, palmitic acid, methyl oleate, and methyl palmitate

Garciniaxanthone E and 12b-Hydroxy-des-D-garcigerrin A from The Tree Bark Garcinia dulcis and their Inhibitory Properties against Receptor Tyrosine Kinases

Two xanthone derivatives, garciniaxanthone E (1) and 12b-Hydroxy-des-D-garcigerrin A (2) have been isolated from ethyl acetate extract of the tree bark of Garcinia dulcis. The Ultraviolet (UV), Infrared (IR), Nuclear Magnetic Resonance (NMR), and Mass Spectrometry (MS) data analysis elucidated the structure of the isolated compounds. This study represents the first evaluation of compounds 1 and 2 in terms of their efficacy against receptor tyrosine kinases. The results showed that compound 1 exhibited weak activity with 12% inhibition against Insulin Receptor (InsR), while compound 2 showed moderate activity with 29% inhibition against epidermal growth factor receptor (EGFR). A molecular docking study targeting EGFR-TK suggests that the hydroxyl group at C-4 on compound 2 can be demolished to raise the inhibitory activity in future research

Dealumination Effect on ZSM-5 as a Bimetal Fe-Co Support for The Oxidative Desulfurization Process Catalyst

Petroleum fuel is still the main energy source today but causes environmental problems such as SOx gas emissions. The Oxidative Desulfurization (ODS) method removes sulfur from fuel under mild conditions. ZSM-5 is a catalyst framework considered promising in the ODS process but the small pores cause a steric barrier. The hydrophobic, mesoporous Fe-Co/ZSM-5Hierarchy catalyst was designed using the dealumination method with steam treatment to overcome the steric barrier and biphasic hindrances which are problems in this ODS process. The Fe-Co/ZSM-5Hierarchy catalyst is effective for the ODS process at a temperature of 45 °C, 45 min, the amount of catalyst used is 0.2 g, oxidant at an O/S ratio of 2, and without mass transfer agents. The embedded Fe-Co ratio shows effective mass activity by providing a TOF number of 205 h-1 on the Fe-Co(5)/ZSM-5 Hierarchy and 157 h-1 on the Fe-Co(15)/ZSM-5 Hierarchy catalyst