cover
Contact Name
Masruri
Contact Email
masruri@ub.ac.id
Phone
+62341-575838
Journal Mail Official
jpacr@ub.ac.id
Editorial Address
Departemen Kimia, Fakultas MIPA, Universitas Brawijaya, Jl. Veteran 65145 Malang
Location
Kota malang,
Jawa timur
INDONESIA
The Journal of Pure and Applied Chemistry Research
Published by Universitas Brawijaya
ISSN : 23024690     EISSN : 25410733     DOI : http://dx.doi.org/10.21776/ub.jpacr
The Journal of Pure and Applied Chemistry Research focuses in publishing research articles in the field of Chemistry and Applied Chemistry. The target is in exploring, investigating, and developing chemicals sources from local and/or Indonesian to increase the value. Scope of the journal is organic chemistry, analytical chemistry, inorganic chemistry, biochemistry, and physical chemistry. Included the topic also organic chemistry natural product, theoretical and computational chemistry.
Articles 6 Documents
Search results for , issue "Vol. 13 No. 1 (2024): Edition January-April 2024" : 6 Documents clear
Syntheses, Characterization, Antioxidant Activity, and Toxicity Evaluation of Schiff Base Derivates from O-Vanillin Hanapi, Ahmad; Ningsih, Rachmawati; Nafiah, Sri Ani; Nadhiroh, Ainun; Oktavianti, Fatin
The Journal of Pure and Applied Chemistry Research Vol. 13 No. 1 (2024): Edition January-April 2024
Publisher : Chemistry Department, The University of Brawijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.21776/ub.jpacr.2024.013.01.3321

Abstract

Three Schiff bases (1a, 1b, and 1c) have been prepared from the reaction of o-vanillin with primary amine (aniline, p-toluidine, and p-anisidine). Schiff base derivates from o-vanillin were synthesized using the grinding method for 20 minutes. Physical properties were observed based on color, melting point, and solubility. Synthesis products were also characterized using FTIR, GCMS, 1H-NMR, and 13C-NMR. The antioxidant activity of the Schiff base was tested using DPPH. While the toxicity test uses the BSLT method. The result of this synthesis and characterization Schiff base (1a, 1b, and 1c) showed that the Schiff base compound was formed into 2-methoxy-6 (phenyliminomethyl) phenol; 2-methoxy-6- (((4-methylphenyl) imino) methyl) phenol; and 2-methoxy-6-(((4-methoxyphenyl) imino) methyl) phenol. The result of NMR analysis, on 1H-NMR spectrum showed the shift chemical at 8,5-8,6 ppm which indicates the typical peak of proton (-HC=N-). Meanwhile, the 13C-NMR spectrum shown the shift chemical at 160-162 ppm which indicates the typical peak of carbon (-C=N-). The result of antioxidant activity showed that all Schiff base was antioxidant quite low ability with value of EC50 is 106.2-196.4 ppm. Meanwhile, the result of toxicity test showed that all Schiff base was anticancer with an LC50 value of 9.99-22.29 ppm.
Evaluation of Bioactive Compounds, Release Profiles, and Toxicity Test from Microcapsules Containing R. tuberosa L. Extracts Utilizing Gum Arabic Almayda, Nabila; Roosdiana, Anna; MASRURI, Masruri; Safitri, Anna
The Journal of Pure and Applied Chemistry Research Vol. 13 No. 1 (2024): Edition January-April 2024
Publisher : Chemistry Department, The University of Brawijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.21776/ub.jpacr.2024.013.01.3336

Abstract

This study is essential to analyze the toxicity and release of bioactive compounds in R. tuberosa L. extract microcapsules coated with gum Arabic and to provide information on the use of microcapsules as a drug delivery system with controlled release of active ingredients. Investigations focused on the effect of pH and timing on discharge kinetics, as well as toxicity evaluation. The release of active ingredients from microcapsules was carried out in medium variations, namely pH 2.2 and pH 7.4, with release durations of 30, 60-, 90-, 120-, and 150-min. Bioactive compounds were released by 59.23% at pH 2.2 and 58.21% at pH 7.4 within 150 min. The BSLT (brine shrimp lethal toxicity) assay was used using brine shrimp larvae (Artemia salina L.), resulting in a non-toxic classification as evidenced by an LC50 value of 5729 μg/mL. Microcapsules in optimum conditions were then characterized using FTIR (Fourier-Transform Infrared) and SEM (scanning electron microscopy) instruments. The FTIR analysis showed variations in functional groups in R. tuberosa L. extracts, gum Arabic, and microcapsules. Furthermore, the SEM examination highlighted the morphology of microcapsules that were mostly spherical.
Immobilization of Cutinase from Fussarium oxysporum into Sea Sand Matrix for Catalytic Degradation of Polyethylene Terephthalate (PET) Prameswari, Tira P. K.; Sutrisno, Sutrisno; Roosdiana, Anna
The Journal of Pure and Applied Chemistry Research Vol. 13 No. 1 (2024): Edition January-April 2024
Publisher : Chemistry Department, The University of Brawijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.21776/ub.jpacr.2024.013.01.3325

Abstract

Cutinase is an enzyme that can be used as a catalyst in the hydrolysis reaction of polyethylene terephthalate (PET) waste into terephthalic acid and ethylene glycol. Generally, cutinase has low stability in its free form. Therefore, to increase cutinase stability, cutinase needs to be immobilized. In this study, cutinase was immobilized into a sea sand matrix by adsorption technique. The purpose of this study was to determine the optimum conditions of PET hydrolysis (pH, temperature, and incubation time), and to study the ability of immobilized cutinase for catalytic degradation of PET. The results show that immobilized cutinase has optimum conditions at pH 8, temperature of 50 °C, and incubation time of 24 hrs. Moreover, the immobilized cutinase can be used for up to three cycles with a residual activity percentage of 66.2% and an activity value of 23.224 nmol. g-1. min-1. The total enzyme activity of immobilized cutinase after being used in three cycles was 89.99 nmol. g-1. min-1 or 28.6% of its free enzyme activity.
Particle Processing of Acetaminophen using Cooling and Anti-solvent Crystallization Methods Kurniawansyah, Firman; Ahmad, Fathanudin; Widagda, Indra Cahya; Idzati, Eka Maulana; Ni'mah, Hikmatun; Mahfud, Mahfud
The Journal of Pure and Applied Chemistry Research Vol. 13 No. 1 (2024): Edition January-April 2024
Publisher : Chemistry Department, The University of Brawijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.21776/ub.jpacr.2024.013.01.3326

Abstract

Several crystallization strategies are being implemented to enhance the solubility of acetaminophen, also known as paracetamol. Therefore, this study aimed to determine the effectiveness of the cooling and anti-solvent crystallization on the properties of acetaminophen. The results showed that the anti-solvent recrystallization produced achieved an impressive yield of up to 41.40%, while the cooling method yielded approximately 2–9%. Through FTIR, XRD, and DSC analysis on the samples, it was discovered that these methods had minimum effects on the molecular and thermal properties of the compound. Furthermore, the methods did not alter the crystallinity of acetaminophen, with crystal form I dominating the products. In addition, processing using the cooling and anti-solvent effectively reduced particle size of acetaminophen from 68.60 μm to 26.92 μm and 28.25 µm, respectively. In conclusion, the solubility of paracetamol in aqueous solutions experienced a significant enhancement. In the unprocessed samples, it measured 0.0107 gram/ml, while the recrystallized samples had an improved range of 0.0123 to 0.0167 g/ml.
Determination of Erucamide Slip Additive in Polypropylene Masterbatch: Comparison of Soxhlet and Dissolution-Precipitation Method Purwaningtyas, Eka Listari; Wahyuni, Debby; Yanuar Ramadhan, Muhammad; Veni Susanti, Silfi; Naufal Ariesta, Muhammad; Aulia Agustina, Laily; Febriani, Rakhma
The Journal of Pure and Applied Chemistry Research Vol. 13 No. 1 (2024): Edition January-April 2024
Publisher : Chemistry Department, The University of Brawijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.21776/ub.jpacr.2024.013.01.3342

Abstract

Erucamide is a long-chain carboxylic acid amide used as a slip agent in plastic films. In this research, the slip additive in polypropylene masterbatch with 6% erucamide content was extracted by comparing two methods which are dissolution-precipitation and the Soxhlet method. The variant of sonication times in the dissolution-precipitation method and extractor-solvents in the Soxhlet method were done to determine the optimum parameter in each method. The examination of slip additive content in each extraction method used the KBr Disk-FTIR and the weight loss of sample analysis. The form of the sample, which was in the granule and powder form was also studied. Based on the result, the dissolution-precipitation method with 3 minutes of sonication times and the use of ethyl acetate as extractor solvent in the Soxhlet method gave a closer result for additive content in the masterbatch. The powder form of the sample also gave better results than the granule form for the extraction of erucamide. The Soxhlet method in the powder form showed comparable results with the dissolution-precipitation method by KBr Disk-FTIR analysis and higher results by weight loss analysis. By comparing the two methods of extraction, the Soxhlet method showed more robustness and efficiency for extraction of erucamide additive in polypropylene masterbatch than the dissolution-precipitation method.
Phytochemical screening, investigation of the antisalmonella, antishigella, and antioxidant properties of the leaves of Rauvolfia vomitoria Afzel Kpadonou-Kpoviessi, Bénédicta; Noudamadjo, Amandine; Goueti, Basile; Atchade, Bardieu; Djouonzo Toukam, Paul; Gbenou, Joachim; Glinma, Bienvenu; Dossou Sika KPOVIESSI, Salomé
The Journal of Pure and Applied Chemistry Research Vol. 13 No. 1 (2024): Edition January-April 2024
Publisher : Chemistry Department, The University of Brawijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.21776/ub.jpacr.2024.013.01.3328

Abstract

Rauvolfia vomitoria is a plant acclimatized in Benin - Africa that people use to treat several illnesses such as malaria, cough, typhoid fever, madness, toothache, diabetes, and nausea. The most used organs are leaves, stems, and roots. Thus, the purpose of this work is to contribute to the valorization of R. vomitoria by chemical and biological studies of this plant. Phytochemical analyses of the powder extracts were performed and revealed the presence of alkaloids, tannins, flavonoids, anthocyanins, saponins, terpenes, coumarins, mucilages, reducing compounds, free anthracene derivatives, bound anthracene derivatives (O-glycosides and C-glycosides) with absence of leuco-anthocyanins, quinone derivatives, steroids and cardiotonic glycosids. Evaluation of antisalmonella and antishigella properties of ethanol-water (70:30; V/V) and ethanolic extracts of R. vomitoria leaves showed minimum inhibitory concentrations (MIC) greater than 2000 µg.mL-1 against Salmonella and Shigella strains. The ethanolic extract was the most active by ABTS and FRAP methods and had very good antioxidant activity at scavenging concentration (SC50) equal to 138,62 µg.mL-1 and 185,99 µg.mL-1 respectively

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