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INDONESIA
Indonesian Journal of Chemistry
ISSN : 14119420     EISSN : 24601578     DOI : -
Indonesian Journal of Chemistry is an International, peer-reviewed, open access journal that publishes original research articles, review articles, as well as short communication in all areas of chemistry including applied chemistry. The journal is accredited by The Ministry of Research, Technology and Higher Education (RISTEKDIKTI) No : 21/E/KPT/2018 (in First Rank) and indexed in Scopus since 2012. Since 2018 (Volume 18), Indonesian Journal of Chemistry publish four issues (numbers) annually (February, May, August and November).
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Articles 25 Documents
Search results for , issue "Vol 23, No 4 (2023)" : 25 Documents clear
Rapid Colorimetric Sensor Based on Gold Nanoparticles Functionalized 4-Amino-3-hydrazino-5-mercapto-1,2,4-triazole for Cortisol Detection in Saliva Sample Hanim Istatik Badi'ah; Ni Nyoman Tri Puspaningsih; Ganden Supriyanto; Nasronudin Nasronudin
Indonesian Journal of Chemistry Vol 23, No 4 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.80874

Abstract

The rapid, simple, and selective colorimetric sensing method of cortisol has been successfully developed using AuNPs modified with 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole (AuNPs-AHMT). The principle of this method is based on the color change from wine red to purple (redshift) when AuNPs-AHMT interacts with cortisol. The hydrogen bonding between the hydroxyl group from cortisol and the amine group from AHMT induces the aggregation of AuNPs. The modification of the AuNPs surface with AHMT aims to increase its stability. The properties of AuNPs and AuNPs-AHMT were characterized by UV-vis spectrophotometer. The interaction between AuNPs-AHMT and cortisol was studied by UV-vis and FTIR spectroscopies. The proposed method was optimized and validated. Au(III) was reduced to AuNPs at an optimum NaBH4 concentration of 1.0 mM. Validation of the proposed method showed good analytical performance with linearity from 1.0–50.0 nM, accuracy 91.07–102.77%, intra-day precision < 2.22% and inter-day precision < 2.17%, detection limit 0.76 nM, quantification limit 2.54 nM, and sensitivity 0.0112 nM/mL. The proposed method also showed good selectivity with the presence of some interferences in the sample. The proposed method was successfully applied for the determination of cortisol in the saliva by the standard addition method with acceptable recovery.
Magnetic Solid Phase Extraction for Determination of Dyes in Food and Water Samples Ruba Fahmi Abbas; Mohammed Jasim Mohammed Hassan; Ahmed Mahdi Rheima
Indonesian Journal of Chemistry Vol 23, No 4 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.80885

Abstract

Recently, magnetic solid-phase extraction (MSPE) is an important technology due to its use in analytical chemistry, biotechnology, and medicinal fields. MSPE shows rapid isolation of target analyte from large volume samples, the huge surface area of magnetic nanoparticles (MNPs), and simplicity in application due to using an external magnetic field instead of using packing column, centrifuge and filter papers. The aim of this review is to evaluate the extraction and determination of dyes in food and water samples by using the MSPE technique.
Physical Properties of Polyvinyl Alcohol/Chitosan Films with the Addition of Anthocyanin Extract from Butterfly Pea for Food Packaging Applications Siti Khanifah; Alda Dwi Karina Legowo; Sholihun Sholihun; Ari Dwi Nugraheni
Indonesian Journal of Chemistry Vol 23, No 4 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.80946

Abstract

Composites of polyvinyl alcohol (PVA) and chitosan (CH) polymers, with the addition of anthocyanin (AN) obtained from the butterfly pea flower, were prepared using drop-casting. The composites were made by adding different concentrations of 5–40% anthocyanin with 5 wt.% PVA and 2 wt.% CH solutions (weight ratio of PVA/CH is 80:20). These polymers solution was mixed at 80 °C and dried using the drop-casting method at 25 °C for 48 h. The composites were characterized using a scanning electron microscope (SEM), Fourier-transform infrared (FTIR), ultraviolet-visible (UV–vis spectroscopy), contact angle, antibacterial properties, and food packaging applications. The morphology obtained using an SEM showed that the PVA/CH surface with AN and glycerol was smoother than that of PVA/CH. The increased absorption at a wavelength of 650–700 nm from UV-vis spectroscopy confirmed the success addition of AN. The contact angles of PVA/CH/AN and PVA/CH/GS/AN films were 15°–66°, which showed that the films were hydrophilic. The simple antibacterial test with Escherichia coli and Staphylococcus aureus showed 16 mm inhibition zone by adding AN. The test results of these characteristics show the potential for using PVA/CH/AN and PVA/CH/GS/AN composite film to be used as an excellent development food packaging material.
Synthesis of Calix[4]resorcinarene Derivatives as Antimalarial Agents through Heme Polymerization Inhibition Assay Rizky Riyami Putri; Harno Dwi Pranowo; Yehezkiel Steven Kurniawan; Hana Anisa Fatimi; Jumina Jumina
Indonesian Journal of Chemistry Vol 23, No 4 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.81452

Abstract

Malaria is an endemic disease in tropical countries, including Indonesia, with a high annual mortality rate. Because of that, serious attention shall be given to find new antimalarial agents that are highly active for medical treatment. In this work, we designed and synthesized three calix[4]resorcinarene derivatives and evaluated them as antimalarial agents through in vitro heme polymerization inhibitory assay. The calix[4]resorcinarenes were prepared from resorcinol and corresponding aldehyde derivatives in ethanol media through a cyclo-condensation reaction. The calix[4]resorcinarene products were obtained in 31.1–85.1% yield. The synthesized compounds were subjected to structure elucidation using spectroscopy techniques. The antimalarial activity of calix[4]resorcinarene with aromatic substituent (IC50 = 0.198 mg/mL) was higher than the aliphatic ones (IC50 = 0.282–0.814 mg/mL). It was found that all calix[4]resorcinarenes in this work exhibited stronger antimalarial activity than chloroquine diphosphate as the positive control (IC50 = 1.157 mg/mL). The calix[4]resorcinarenes could interact with hydrogen bonding, thus inhibiting the heme polymerization process. These findings demonstrate that calix[4]resorcinarene derivatives are potential antimalarial agents to be developed for effective medical treatment in the near future.
Synthesis, Characterization, and Magnetic Properties of Iron(II) Complex with 2,6-Bis(pyrazol-3-yl)pyridine Ligand and Tetracyanonickelate Anion Fitriani Fitriani; Irma Mulyani; Djulia Onggo; Kristian Handoyo Sugiyarto; Ashis Bhattacharjee; Hiroki Akutsu; Anas Santria
Indonesian Journal of Chemistry Vol 23, No 4 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.81625

Abstract

The complex containing iron(II), 2,6-bis(pyrazol-3-yl)pyridine (3-bpp) as ligand, and tetracyanonickelate as counter anion has been synthesized and characterized. The characterization data suggest the corresponding formula of [Fe(3-bpp)2][Ni(CN)4]·4H2O. Meanwhile, the SEM–EDX analysis image confirms the existence of all elements contained in the complex except the hydrogen atom. The infrared spectra exhibit vibration bands of the functional groups of 3-bpp ligand and [Ni(CN)4]−1 anion. From magnetic property measurement, the complex's molar magnetic susceptibility (XMT) value is 2.65 emu mol−1 K at 300 K, which contains about 75% high-spin state of the Fe(II) complex. Upon lowering the temperature, the XMT value gradually decreases around 1.37 emu mol−1 K at 13 K. It decreases sharply to about 0.73 emu mol−1 K at 2 K. These values reveal that Fe(II) complex is in the low-spin (LS) state. As a result, the complex exhibited spin-crossover characteristics of gradual transition without thermal hysteresis, and the transition temperature occurred below room temperature with a transition temperature (T1/2) close to 140 K. The spin crossover property of the complex is supported by a thermochromic reversible color change from red-brown at room temperature to dark brown on cooling in liquid nitrogen associated with the high-spin to low-spin transition.
Utilization of Lignin and Lignosulfonate from Oil Palm Empty Fruit Bunches as Filler in PVDF Proton Exchange Membrane Fuel Cell Nala Ridhwanul Mu&#039;izzah; Pinka Zuhdiana Hapsari; Nabila Putri Aulia; Dian Wahyu Tri Wulansari; Fauziyah Azhari; Edi Pramono
Indonesian Journal of Chemistry Vol 23, No 4 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.81750

Abstract

A study on the polyvinylidene fluoride (PVDF) membrane using lignin and lignosulfonate oil palm empty fruit bunch (OPEFB) fillers have been carried out. This study aims to determine the additional effect of lignin and lignosulfonate on PVDF membrane. Lignin sulfonation has a good result proven by Fourier transform infrared spectra with a peak at 1192 cm−1 which indicates sulfonate group. The sulfonation degree was increased by 8.9% for lignosulfonate. The membrane was prepared by the phase inversion method. Data present that all the membranes have an asymmetric structure with finger-like and sponge-like pores. Good thermal stability indicated by thermal gravimetric analysis showed degradation at 432 °C. The mechanical properties of the membrane decrease with the addition of filler. From the X-ray diffraction, peaks appeared at 18.39°, 21.35°, and 23.75° for all the membranes indicating of α and β phases. Lignin and lignosulfonate increased membrane hydrophilicity and water uptake. The presence of the sulfonate group increases the ionic exchange capacity and ionic conductivity up to 2.78 mmol/g and 9.95 × 10−5 S/cm, respectively, for 5% lignosulfonate addition. Thus, PVDF/lignosulfonate has the potential as a polymer electrolyte membrane.
Improved Mucoadhesive Properties of Repaglinide-Loaded Nanoparticles: Mathematical Modelling through Machine Learning-Based Approach Nader Ibrahim Namazi
Indonesian Journal of Chemistry Vol 23, No 4 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.82031

Abstract

This research work aims to develop a modified repaglinide-loaded chitosan-ethyl cellulose nanoparticles (RPG-ECSNPs) as a novel sustained-release dosage form with improved mucoadhesive properties using an emulsification solvent-evaporation technique. The RPG-ECSNPs with different particle sizes were prepared from various polymers containing ethyl cellulose (EC) as the internal phase and chitosan (CS) as the external phase, and the use of surfactants, including Tween 80 and poloxamer 188 as emulsifiers. In vitro drug release, drug loading amount, and entrapment efficiency have been influenced by changes in the concentrations of CS and EC. The mean droplet size and zeta potential of RPG-ECSNPs were 213 ± 8.5 nm and 16.4 ± 2.4 mV, respectively. The optimized formulation's entrapment efficiency was 66 ± 2.3%, and drug loading was 7.9 ± 1.65%. The release profile was significantly higher in PBS (90%) than in diluted hydrochloric acid (30%) during 24 h of the study. The mucoadhesive function of the particles was examined in vitro using part of rat intestines. The highest adhesive % was observed for the chitosan-coated NPs. No adhesive properties were noticed for chitosan-free NPs (P-value > 0.05). This indicated that ECSNPs can be successfully utilized for sustained and controlled drug delivery of RPG through the GIT.
Synthesis and Antidiabetic Evaluation of N’-Benzylidenebenzohydrazide Derivatives by In Silico Studies Yusuf Syaril Alam; Pratiwi Pudjiastuti; Saipul Maulana; Nur Rahmayanti Afifah; Fahimah Martak; Arif Fadlan; Tutik Sri Wahyuni; Syukri Arief
Indonesian Journal of Chemistry Vol 23, No 4 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.82073

Abstract

Two new of N’-benzylidenebenzohydrazide (NBB) derivatives were successfully synthesized and yielded 50–58%. FTIR, ESI-MS, 1H-NMR and 13C-NMR were used to investigate the characteristic of NBB derivates. The structure and relationship of NBB derivatives into α-glucosidase and α-amylase as good targets for diabetes treatment were evaluated using in silico screening. Molecular Mechanics-Poisson Boltzmann/Generalized Born Surface Area (MM-PB/GBSA) was used to calculate the free binding energy (ΔGbind (MM-GBSA)) of NBB to α-glucosidase and α-amylase receptors showed that the results of −0.45 and −20.79 kcal/mol respectively. In the ortho position, NBB derivatives exhibited electron donating groups (EDG like -OCH3, -OH and -Cl with binding free energies of −21.94, −6.71 and 21.94, respectively, and acarbose, a native ligand energy of 32.62 kcal/mol. In addition, the binding free energy of N-2-(-OCH3, -OH and -Cl)-NBB to the α-amylase receptor showed the number of −39.33, −43.96, −42.81, respectively and −46.51 kcal/mol in comparing with a native ligand. As a result, it was found that all the NBB derivatives were able to interact with several amino acids in the α-glucosidase cavity as well as the native ones, including Ala281, Asp282, and Asp616.  NBB and native ligand showed similar interaction between α-amylase with Gly110 amino acid residue.
Synthesis of ZnO Nanoparticle and Utilized as a Drug Carrier to Treat Leukemia Areej Ali Jarullah; Nidhal Meteab Khamees; Taghreed Mohy Al-Deen Musa
Indonesian Journal of Chemistry Vol 23, No 4 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.82208

Abstract

This study includes two parts, and the first was the preparation of the Zn(II)complex by reacting N-[4-(5-{(Z)-[(5-oxo-2-sulfanyl-4,5-dihydro-1H-imidazol-1-yl)imino]methyl}furan-2-yl)phenyl]acetamide with ZnCl2. The complex was characterized by using microscopic analysis such as UV-Vis spectrum, LC-MS, FTIR spectrophotometer, measurements of conductivity, magnetic susceptibility, and atomic absorption. The second part was the preparation of the ZnO nanoparticles by dissolving the Zn(II) complex in HNO3 and HCl and its use as a drug transporter to treat leukemia. FSEM, TEM, and XRD were examined for the characterization of ZnO nanoparticles that will be used in the synthesis of most medicines and drugs in the future.
Performance Assessment: Influence of Sorbate-Sorbent Interphase Using Magnetite Modified Graphene Oxide to Improve Wastewater Treatment Olayinka Oluwaseun Oluwasina; Mochamad Zakki Fahmi; Olugbenga Oludayo Oluwasina
Indonesian Journal of Chemistry Vol 23, No 4 (2023)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.82454

Abstract

The adsorption of brilliant green onto magnetite-graphene oxide nanoparticles (MGONPs) from an aqueous solution was explored via batch experiments. The adsorption properties of MGONPs were carried out under various experimental conditions related to pH, contact time, adsorbent dose, temperature, and initial adsorbate concentration. The adsorption capacity of MGONPs and optimum pH were 54.57 mg g−1 and 6, respectively. Equilibrium was attained after 30 min, and the adsorption kinetics data best fitted the pseudo-second-order. The Freundlich isotherm best fits the equilibrium. Acetone was able to desorb the dye from the loaded adsorbent. Additionally, the newly developed adsorption attributes effective surface area (eSBET) and dimensionless preferential adsorption (qp) were more accurate than the conventional specific surface area (SBET). The adsorption capacity provides information about the sorbate-sorbent interface (q). The relevance and accuracy of the new parameters for future adsorption system design by correlation analysis were validated. This study confirms the successful modification of MGONPs for the sorption of the cationic dye brilliant green.

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