Pub Date : 2022-03-23DOI: 10.14710/jksa.25.4.137-145
S. Sriatun, Marta Chandra Anikke Putri, Hanifa Zakiyatul Urbach, A. Darmawan, W. Widayat, H. Susanto
Silica-rich sodalite zeolite has been synthesized by ultrasound treatment and hydrothermal temperature variation. This study aimed to determine the effect of ultrasound treatment and hydrothermal temperature variations on the crystallinity, hydrophobicity, and structural properties of silica-rich sodalite zeolite. The synthesis was conducted by reacting a sodium aluminate and sodium silicate solution by varying Si/Al ratios of 20, 30, 40, 60, 80, and 90. The next step was to characterize the product. The product with the best crystallinity was used as a reference to determine the effect of ultrasound and hydrothermal temperature. The reaction gel was treated with and without ultrasound and hydrothermal using autoclave at 100, 150, and 200°C for 24 hours. The last step was the product characterization using XRD, FTIR, and GSA. The XRD showed similarity peaks at 2θ = 14.058°; 24.41°; 31.73°; 34.75°; 42.88°. The best crystallinity was silica-rich sodalite zeolite with a Si/Al ratio of 30. Meanwhile, silica-rich sodalite zeolite peaks were obtained at 2θ = 14.16°, 24.66°, 31.99°, 35.13°, and 43.39° by ultrasound treatment and hydrothermal temperature variation (100, 150, and 200°C). Ultrasound treatment revealed the presence of other peaks besides sodalite at 2θ = 19.05° and 27°, where these peaks were referred to as SAPO-56. In conclusion, the degree of crystallinity increased with increasing temperature, decreasing Si-OH/Si-O-Si showed increased hydrophobic properties. Increasing the hydrothermal temperature of 150 and 200°C with and without ultrasound treatment increased the surface area significantly to 114.137 m2/g and 160.717 m2/g, and the pore volume of sodalite with a Si/Al ratio of 30 to 0.318 cc/g and 0.274 cc/g.
{"title":"Silica-rich Sodalite Synthesis: The Effect of Variations in Ultrasound Treatment and Hydrothermal Temperature","authors":"S. Sriatun, Marta Chandra Anikke Putri, Hanifa Zakiyatul Urbach, A. Darmawan, W. Widayat, H. Susanto","doi":"10.14710/jksa.25.4.137-145","DOIUrl":"https://doi.org/10.14710/jksa.25.4.137-145","url":null,"abstract":"Silica-rich sodalite zeolite has been synthesized by ultrasound treatment and hydrothermal temperature variation. This study aimed to determine the effect of ultrasound treatment and hydrothermal temperature variations on the crystallinity, hydrophobicity, and structural properties of silica-rich sodalite zeolite. The synthesis was conducted by reacting a sodium aluminate and sodium silicate solution by varying Si/Al ratios of 20, 30, 40, 60, 80, and 90. The next step was to characterize the product. The product with the best crystallinity was used as a reference to determine the effect of ultrasound and hydrothermal temperature. The reaction gel was treated with and without ultrasound and hydrothermal using autoclave at 100, 150, and 200°C for 24 hours. The last step was the product characterization using XRD, FTIR, and GSA. The XRD showed similarity peaks at 2θ = 14.058°; 24.41°; 31.73°; 34.75°; 42.88°. The best crystallinity was silica-rich sodalite zeolite with a Si/Al ratio of 30. Meanwhile, silica-rich sodalite zeolite peaks were obtained at 2θ = 14.16°, 24.66°, 31.99°, 35.13°, and 43.39° by ultrasound treatment and hydrothermal temperature variation (100, 150, and 200°C). Ultrasound treatment revealed the presence of other peaks besides sodalite at 2θ = 19.05° and 27°, where these peaks were referred to as SAPO-56. In conclusion, the degree of crystallinity increased with increasing temperature, decreasing Si-OH/Si-O-Si showed increased hydrophobic properties. Increasing the hydrothermal temperature of 150 and 200°C with and without ultrasound treatment increased the surface area significantly to 114.137 m2/g and 160.717 m2/g, and the pore volume of sodalite with a Si/Al ratio of 30 to 0.318 cc/g and 0.274 cc/g.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45416488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-03-23DOI: 10.14710/jksa.25.3.130-136
M. Jufri., R. A. Lusiana, N. Prasetya
This study investigated the effects of additional PVA on the physicochemical properties of the chitosan-glutaraldehyde/gelatin bioplastic composite. The best results of the bioplastic film were obtained at a concentration of 3% PVA, with a tensile strength value of 3.3 MPa, flexibility reached 54%, a thickness value of 0.24 mm, percentage of inhibition against E. coli and S. aureus was 21.8% and 8.8% respectively. The FTIR spectrum results showed no change in the wavenumber of the chitosan and gelatin chitosan spectrum with OH, CO, and NH functional groups. The spectrum indicates that only physical interactions occurred. The bioplastics are similar in thermal stability and have slight differences in bioplastic morphological contours. The average thickness of the bioplastics is between 0.20–0.26 mm. Based on the Japanese Industrial Standard (JIS), all bioplastics meet the standard thickness, which is < 0.25 mm, excluding chitosan, which has a thickness of 0.26 mm. The addition of PVA into the bioplastics structure increased the hydrophobicity, pH resistance, and flexibility of bioplastics. Meanwhile, additional PVA decreased biodegradability, only degraded by 60% at eight weeks. Based on these data, not all bioplastics can meet the degradation time criteria set by the international bioplastic standard ASTM D-6002, that bioplastics must be 100% degraded within eight weeks. Bioplastics made from chitosan and chitosan-gelatin have been degraded by 90% for 48 weeks. Based on the antibacterial properties, the inclusion of PVA into the bioplastic structure enhances the antibacterial properties.
{"title":"Effects of Additional Polyvinyl Alcohol (PVA) on the Physiochemical Properties of Chitosan-Glutaraldehyde-Gelatine Bioplastic","authors":"M. Jufri., R. A. Lusiana, N. Prasetya","doi":"10.14710/jksa.25.3.130-136","DOIUrl":"https://doi.org/10.14710/jksa.25.3.130-136","url":null,"abstract":"This study investigated the effects of additional PVA on the physicochemical properties of the chitosan-glutaraldehyde/gelatin bioplastic composite. The best results of the bioplastic film were obtained at a concentration of 3% PVA, with a tensile strength value of 3.3 MPa, flexibility reached 54%, a thickness value of 0.24 mm, percentage of inhibition against E. coli and S. aureus was 21.8% and 8.8% respectively. The FTIR spectrum results showed no change in the wavenumber of the chitosan and gelatin chitosan spectrum with OH, CO, and NH functional groups. The spectrum indicates that only physical interactions occurred. The bioplastics are similar in thermal stability and have slight differences in bioplastic morphological contours. The average thickness of the bioplastics is between 0.20–0.26 mm. Based on the Japanese Industrial Standard (JIS), all bioplastics meet the standard thickness, which is < 0.25 mm, excluding chitosan, which has a thickness of 0.26 mm. The addition of PVA into the bioplastics structure increased the hydrophobicity, pH resistance, and flexibility of bioplastics. Meanwhile, additional PVA decreased biodegradability, only degraded by 60% at eight weeks. Based on these data, not all bioplastics can meet the degradation time criteria set by the international bioplastic standard ASTM D-6002, that bioplastics must be 100% degraded within eight weeks. Bioplastics made from chitosan and chitosan-gelatin have been degraded by 90% for 48 weeks. Based on the antibacterial properties, the inclusion of PVA into the bioplastic structure enhances the antibacterial properties.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44122749","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-03-10DOI: 10.14710/jksa.25.3.108-115
Joana Sugiarto, Zayyani Trianti Fatmasari, Sugiyani Puji Lestari, B. Purwono
Anthocyanins as chemosensory compounds for amines have been tested in this study. Because anthocyanins are sensitive to pH changes, while amines have an alkaline nature, they can cause structural changes in anthocyanins, resulting in changes in the color of anthocyanins. The source of anthocyanins was the Kepok banana bracts (Musa paradisiaca L.), which were extracted using a mixture of ethanol:HCl 0.15% (3:2). The types of anthocyanin compounds were characterized using a UV-Vis spectrophotometer. The anthocyanin content obtained varied from 1.26 mg/100 g to 5.08 mg/100 g. The type of anthocyanin in the Kepok banana bracts was found as a cyanidin-3-rutinoside with maximum absorption at 513 nm at pH 1. The color of anthocyanin extract varied with changes in pH; it turned red in acid and faded in neutral solutions. The green color in the alkaline solution changes to brownish-yellow was associated with anthocyanin degradation. The color change at different pH indicates that banana bracts are regarded as a potential chemosensory compound to detect tuna freshness. The chemosensor was applied to a cellulose-based strip and exhibited a color change that corresponded to the increase in pH and was comparable to the results of the pH meter measurement. The structural changes of anthocyanin before and after the tuna freshness test were identified by the FTIR-ATR, indicating a change in the anthocyanin structure. Tuna freshness began to diminish after being stored for 12 and 24 hours at room temperature, marked by a color change of the paper strip to colorless and blackish gray.
{"title":"Chemosensor Strip from Kepok Banana Bracts Extract (Musa paradisiaca L.) for Detection of Tuna Freshness","authors":"Joana Sugiarto, Zayyani Trianti Fatmasari, Sugiyani Puji Lestari, B. Purwono","doi":"10.14710/jksa.25.3.108-115","DOIUrl":"https://doi.org/10.14710/jksa.25.3.108-115","url":null,"abstract":"Anthocyanins as chemosensory compounds for amines have been tested in this study. Because anthocyanins are sensitive to pH changes, while amines have an alkaline nature, they can cause structural changes in anthocyanins, resulting in changes in the color of anthocyanins. The source of anthocyanins was the Kepok banana bracts (Musa paradisiaca L.), which were extracted using a mixture of ethanol:HCl 0.15% (3:2). The types of anthocyanin compounds were characterized using a UV-Vis spectrophotometer. The anthocyanin content obtained varied from 1.26 mg/100 g to 5.08 mg/100 g. The type of anthocyanin in the Kepok banana bracts was found as a cyanidin-3-rutinoside with maximum absorption at 513 nm at pH 1. The color of anthocyanin extract varied with changes in pH; it turned red in acid and faded in neutral solutions. The green color in the alkaline solution changes to brownish-yellow was associated with anthocyanin degradation. The color change at different pH indicates that banana bracts are regarded as a potential chemosensory compound to detect tuna freshness. The chemosensor was applied to a cellulose-based strip and exhibited a color change that corresponded to the increase in pH and was comparable to the results of the pH meter measurement. The structural changes of anthocyanin before and after the tuna freshness test were identified by the FTIR-ATR, indicating a change in the anthocyanin structure. Tuna freshness began to diminish after being stored for 12 and 24 hours at room temperature, marked by a color change of the paper strip to colorless and blackish gray.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45110168","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-03-08DOI: 10.14710/jksa.25.3.87-96
R. Ruswanto, R. Mardianingrum, Arry Yanuar
Cancer is a disease that starts from the uncontrolled growth of abnormal cells in the organs or tissues of the body, which is the second leading cause of death in the world. One of the targets in discovering and developing anticancer drugs is Sirtuin-1. SIRT1 can act as a tumor suppressor or tumor promoter depending on its target in a particular signalling pathway or on particular cancer. This study aimed to study the interaction of a thiourea derivative with SIRT1 (PDB ID:4I5I) through its inhibition of histone deacetylase. Research has been carried out in silico with molecular docking (MGLTools.1.5.6) and molecular dynamics (Desmond 2019) of three thiourea derivatives to the receptor. In addition, pharmacokinetic parameters, toxicity, and selection of Lipinski's Rule of Five were also tested. Molecular docking results showed that compound b ([2-(methylcarbamothioylcarbamoyl)phenyl]benzoate) had the lowest ∆G value of −9.29 kcal/mol with a KI value of 0.156 µM compared to other thiourea derivatives and was proven by molecular dynamics tests for 30 ns and amino acids that play an active role in the interaction include the residue PheA:297. In terms of pharmacokinetics and toxicity, compound b is better than natural ligands. Compound b is predicted to be used as an anticancer candidate through further research.
{"title":"Computational Studies of Thiourea Derivatives as Anticancer Candidates through Inhibition of Sirtuin-1 (SIRT1)","authors":"R. Ruswanto, R. Mardianingrum, Arry Yanuar","doi":"10.14710/jksa.25.3.87-96","DOIUrl":"https://doi.org/10.14710/jksa.25.3.87-96","url":null,"abstract":"Cancer is a disease that starts from the uncontrolled growth of abnormal cells in the organs or tissues of the body, which is the second leading cause of death in the world. One of the targets in discovering and developing anticancer drugs is Sirtuin-1. SIRT1 can act as a tumor suppressor or tumor promoter depending on its target in a particular signalling pathway or on particular cancer. This study aimed to study the interaction of a thiourea derivative with SIRT1 (PDB ID:4I5I) through its inhibition of histone deacetylase. Research has been carried out in silico with molecular docking (MGLTools.1.5.6) and molecular dynamics (Desmond 2019) of three thiourea derivatives to the receptor. In addition, pharmacokinetic parameters, toxicity, and selection of Lipinski's Rule of Five were also tested. Molecular docking results showed that compound b ([2-(methylcarbamothioylcarbamoyl)phenyl]benzoate) had the lowest ∆G value of −9.29 kcal/mol with a KI value of 0.156 µM compared to other thiourea derivatives and was proven by molecular dynamics tests for 30 ns and amino acids that play an active role in the interaction include the residue PheA:297. In terms of pharmacokinetics and toxicity, compound b is better than natural ligands. Compound b is predicted to be used as an anticancer candidate through further research.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46311511","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-03-08DOI: 10.14710/jksa.25.3.97-107
Zatta Yumni Ihdhar Syarafina, M. Safithri, M. Bintang, Rini Kurniasih
Alzheimer’s is a progressive and neurodegenerative disease that mainly affects people aged 65 years and older. The pathophysiology of Alzheimer’s is possibly related to the depletion of the neurotransmitter acetylcholine (ACh) due to beta-amyloid plaques and neurofibrillary tangles. Secondary metabolites found in cinnamon bark (Cinnamomum burmannii) have the potential as anticholinesterases to treat Alzheimer’s symptoms. This study aimed to identify the potency of bioactive compounds from cinnamon bark as AChE inhibitors in silico through analysis of binding energy, inhibition constants, and types of interactions. The research was conducted by screening virtually 60 test ligands using the PyRx program and molecular docking using the Autodock Tools program. The results of the ligand-receptor interaction analysis showed that 12 of the 15 tested ligands had potential as AChE inhibitors. Epicatechin and medioresinol are the ligands with the best potential for AChE inhibition with affinity close to the natural ligand or donepezil. Epicatechin has a binding energy of −10.0 kcal/mol and inhibition constant of 0.0459 M, with four hydrogen bonds and seven hydrophobic bonds. Meanwhile, medioresinol has −9.9 kcal/mol binding energy and inhibition constant of 0.0543 M, with one hydrogen bond and thirteen hydrophobic bonds.
{"title":"In Silico Screening of Cinnamon (Cinnamomum burmannii) Bioactive Compounds as Acetylcholinesterase Inhibitors","authors":"Zatta Yumni Ihdhar Syarafina, M. Safithri, M. Bintang, Rini Kurniasih","doi":"10.14710/jksa.25.3.97-107","DOIUrl":"https://doi.org/10.14710/jksa.25.3.97-107","url":null,"abstract":"Alzheimer’s is a progressive and neurodegenerative disease that mainly affects people aged 65 years and older. The pathophysiology of Alzheimer’s is possibly related to the depletion of the neurotransmitter acetylcholine (ACh) due to beta-amyloid plaques and neurofibrillary tangles. Secondary metabolites found in cinnamon bark (Cinnamomum burmannii) have the potential as anticholinesterases to treat Alzheimer’s symptoms. This study aimed to identify the potency of bioactive compounds from cinnamon bark as AChE inhibitors in silico through analysis of binding energy, inhibition constants, and types of interactions. The research was conducted by screening virtually 60 test ligands using the PyRx program and molecular docking using the Autodock Tools program. The results of the ligand-receptor interaction analysis showed that 12 of the 15 tested ligands had potential as AChE inhibitors. Epicatechin and medioresinol are the ligands with the best potential for AChE inhibition with affinity close to the natural ligand or donepezil. Epicatechin has a binding energy of −10.0 kcal/mol and inhibition constant of 0.0459 M, with four hydrogen bonds and seven hydrophobic bonds. Meanwhile, medioresinol has −9.9 kcal/mol binding energy and inhibition constant of 0.0543 M, with one hydrogen bond and thirteen hydrophobic bonds.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44840174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-02-26DOI: 10.14710/jksa.25.2.49-55
Lidwina Angelica Soetantijo, Hendrik Oktendy Lintang, Mitha Ayu Pratama Handojo, T. H. Brotosudarmo
The headspace solid phase microextraction (HS-SPME) technique has been recognized as a reliable technique for characterizing the aroma profile of Arabica coffee beans. The amount and content of the detected volatile compounds depend on the volatile analyte extraction process with HS-SPME, namely the adsorption and desorption processes. However, the optimal extraction time in applying coffee volatile compounds is still limited. This research aimed to obtain the optimum adsorption and desorption time in analyzing volatile compounds in brewed Java Arabica coffee. The adsorption time was optimized for 20 to 60 minutes with 5 minutes desorption time. The desorption time was optimized from 5 to 45 minutes with a 20 minutes of adsorption time. There are 14 volatile compounds with a peak area percentage of more than 2% from adsorption and desorption optimization. The optimal adsorption time was 50 minutes, where there were 5 of 7 compounds with the most significant area, such as 2-furfural (29%), 2-acetyl furan (3%), 2-furfuryl acetate (6%), 5-methyl furfural (12%), and 2-furfuryl alcohol (14%). Meanwhile, the most optimal desorption time was 5 minutes which detected 12 compounds, while the other desorption time only detected eight compounds. Furfuryl formate (2%), pyridine (12%), and 2-furfuryl alcohol (14%) had a higher peak area than the other compounds at a desorption time of 5 minutes. The results showed the same number of volatile compounds at each adsorption time. In conclusion, the adsorption time did not affect the number of compounds detected as in the optimization of desorption time. Adsorption and desorption time is crucial in analyzing volatile compounds from coffee using the HS-SPME/GC-MS technique.
{"title":"Optimization of Adsorption and Desorption Time in the Extraction of Volatile Compounds in Brewed Java Arabica Coffee Using the HS-SPME/GC-MS Technique","authors":"Lidwina Angelica Soetantijo, Hendrik Oktendy Lintang, Mitha Ayu Pratama Handojo, T. H. Brotosudarmo","doi":"10.14710/jksa.25.2.49-55","DOIUrl":"https://doi.org/10.14710/jksa.25.2.49-55","url":null,"abstract":"The headspace solid phase microextraction (HS-SPME) technique has been recognized as a reliable technique for characterizing the aroma profile of Arabica coffee beans. The amount and content of the detected volatile compounds depend on the volatile analyte extraction process with HS-SPME, namely the adsorption and desorption processes. However, the optimal extraction time in applying coffee volatile compounds is still limited. This research aimed to obtain the optimum adsorption and desorption time in analyzing volatile compounds in brewed Java Arabica coffee. The adsorption time was optimized for 20 to 60 minutes with 5 minutes desorption time. The desorption time was optimized from 5 to 45 minutes with a 20 minutes of adsorption time. There are 14 volatile compounds with a peak area percentage of more than 2% from adsorption and desorption optimization. The optimal adsorption time was 50 minutes, where there were 5 of 7 compounds with the most significant area, such as 2-furfural (29%), 2-acetyl furan (3%), 2-furfuryl acetate (6%), 5-methyl furfural (12%), and 2-furfuryl alcohol (14%). Meanwhile, the most optimal desorption time was 5 minutes which detected 12 compounds, while the other desorption time only detected eight compounds. Furfuryl formate (2%), pyridine (12%), and 2-furfuryl alcohol (14%) had a higher peak area than the other compounds at a desorption time of 5 minutes. The results showed the same number of volatile compounds at each adsorption time. In conclusion, the adsorption time did not affect the number of compounds detected as in the optimization of desorption time. Adsorption and desorption time is crucial in analyzing volatile compounds from coffee using the HS-SPME/GC-MS technique.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44699114","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-02-25DOI: 10.14710/jksa.25.3.116-122
N. Saridewi, Adelian Risa Adinda, S. Nurbayti
The ability of cotton fabrics to absorb water creates several problems, such as providing an environment for bacterial growth. Antibacterial properties of textiles can be conducted by coating with nanoparticles with antibacterial activity. This study aimed to synthesize ZnO via green process nanoparticles using avocado seed extract (Persea americana), then characterize and evaluate its antibacterial activity on cotton fabrics. This research began with extracting avocado seed powder with distilled water. Then the avocado seed extract was mixed with Zn(CH3COO)2.2H2O and heated in a water bath at 70°C. The mixture was stirred while NaOH was added until the mixture reached pH 7, 8, and 9. The FTIR measurement of the avocado seed extract showed the presence of free hydroxyl and amino groups that act as reducing agents, capping agents, and stabilizers in the synthesis of ZnO nanoparticles. The XRD pattern of synthesized ZnO nanoparticles was hexagonal. The SEM results showed that the morphology of ZnO nanoparticles was spherical, with a particle size of 19.965 nm. Antibacterial activity was carried out on the cotton cloth coated with ZnO nanoparticles, resulting in an inhibition zone of 1.8 cm against E. coli and 1.97 cm against S. aureus bacteria. This study result indicated that ZnO nanoparticles have antibacterial activity by producing inhibition against E. coli and S. aureus.
{"title":"Characterization and Antibacterial Activity Test of Green Synthetic ZnO Nanoparticles Using Avocado (Persea americana) Seed Extract","authors":"N. Saridewi, Adelian Risa Adinda, S. Nurbayti","doi":"10.14710/jksa.25.3.116-122","DOIUrl":"https://doi.org/10.14710/jksa.25.3.116-122","url":null,"abstract":"The ability of cotton fabrics to absorb water creates several problems, such as providing an environment for bacterial growth. Antibacterial properties of textiles can be conducted by coating with nanoparticles with antibacterial activity. This study aimed to synthesize ZnO via green process nanoparticles using avocado seed extract (Persea americana), then characterize and evaluate its antibacterial activity on cotton fabrics. This research began with extracting avocado seed powder with distilled water. Then the avocado seed extract was mixed with Zn(CH3COO)2.2H2O and heated in a water bath at 70°C. The mixture was stirred while NaOH was added until the mixture reached pH 7, 8, and 9. The FTIR measurement of the avocado seed extract showed the presence of free hydroxyl and amino groups that act as reducing agents, capping agents, and stabilizers in the synthesis of ZnO nanoparticles. The XRD pattern of synthesized ZnO nanoparticles was hexagonal. The SEM results showed that the morphology of ZnO nanoparticles was spherical, with a particle size of 19.965 nm. Antibacterial activity was carried out on the cotton cloth coated with ZnO nanoparticles, resulting in an inhibition zone of 1.8 cm against E. coli and 1.97 cm against S. aureus bacteria. This study result indicated that ZnO nanoparticles have antibacterial activity by producing inhibition against E. coli and S. aureus.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41367544","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-02-24DOI: 10.14710/jksa.25.3.123-129
Dwi Rahmasari Fatmawati, Danny Nur Wahyu Hidayat, Diah Kartika Sari, Rizky Riyami Putri, J. Jumina, Y. S. Kurniawan
Cancer therapy through conventional chemotherapy has been widely applied; however, one of the main disadvantages of chemotherapy is the non-selective targeting of cancer cells which causes various adverse side effects. The development of drug delivery agents that are more selective and effective in cancer therapy needs to be performed so that the drugs have a therapeutic effect and minimize side effects. In this study, the compound C-phenylcalyx[4]resorcinarene epoxide (CFKRE) has acted as a drug delivery agent because it can form host complex interactions with ligands. The CFKRE compound was synthesized through two reaction steps: the condensation and alkylation reactions of the epoxide. The structure was analyzed using FTIR, 1H-, and 13C-NMR spectrophotometers and then tested for in vitro cytotoxicity using the MTT assay. The results showed that 70% yield of CFKRE was obtained. Molecular docking analysis of CFKRE compounds against PDGFR and EGFR proteins showed high binding energy compared to conventional chemotherapeutic agents. Molecular dynamic studies showed that CFKRE compounds could form a host-ligand complex with a −350.4 kcal/mol binding energy. Cytotoxic assay of CFKRE compound against MCF-7 breast cancer cells and Vero cells gave IC50 values of 4.04 and 29.59 μg/mL, respectively. These results indicated that CFKRE compounds are not toxic and have the potential to be utilized as new candidates for drug delivery agents.
{"title":"Potential of C-Phenylcalix[4]Resorcinarene Epoxide Compound as Drug Delivery Agent in Breast Cancer Cells MCF-7","authors":"Dwi Rahmasari Fatmawati, Danny Nur Wahyu Hidayat, Diah Kartika Sari, Rizky Riyami Putri, J. Jumina, Y. S. Kurniawan","doi":"10.14710/jksa.25.3.123-129","DOIUrl":"https://doi.org/10.14710/jksa.25.3.123-129","url":null,"abstract":"Cancer therapy through conventional chemotherapy has been widely applied; however, one of the main disadvantages of chemotherapy is the non-selective targeting of cancer cells which causes various adverse side effects. The development of drug delivery agents that are more selective and effective in cancer therapy needs to be performed so that the drugs have a therapeutic effect and minimize side effects. In this study, the compound C-phenylcalyx[4]resorcinarene epoxide (CFKRE) has acted as a drug delivery agent because it can form host complex interactions with ligands. The CFKRE compound was synthesized through two reaction steps: the condensation and alkylation reactions of the epoxide. The structure was analyzed using FTIR, 1H-, and 13C-NMR spectrophotometers and then tested for in vitro cytotoxicity using the MTT assay. The results showed that 70% yield of CFKRE was obtained. Molecular docking analysis of CFKRE compounds against PDGFR and EGFR proteins showed high binding energy compared to conventional chemotherapeutic agents. Molecular dynamic studies showed that CFKRE compounds could form a host-ligand complex with a −350.4 kcal/mol binding energy. Cytotoxic assay of CFKRE compound against MCF-7 breast cancer cells and Vero cells gave IC50 values of 4.04 and 29.59 μg/mL, respectively. These results indicated that CFKRE compounds are not toxic and have the potential to be utilized as new candidates for drug delivery agents.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44057936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Supported bimetallic palladium-tin catalyst on gamma-alumina (γ-Al2O3) (denoted as Pd–Sn(3.0)/γ-Al2O3; Pd = 5%wt and Pd/Sn molar ratio is 3.0) has been synthesized via the hydrothermal method at a temperature of 423 K for 24 h and reduced with H2 at 673 K for 3 h. The XRD patterns of the samples showed typical diffraction peaks of support γ-Al2O3, metallic Pd, Sn, and Pd–Sn alloy phases. Diffraction peaks of metallic Pd were observed at 2θ = 39.8°; 46.6°; and 68.0°, which can be attributed to the Pd(111), Pd(200), and Pd(220), respectively, while the diffraction peaks at 2θ = 39.8° and 41.0° can be attributed to Pd2Sn and Pd3Sn2, respectively, which may overlap with the Pd(111) species. The ammonia desorption and pyridine adsorption profiles showed Lewis and Brönsted acid sites. The specific surface area (SBET) of Pd–Sn(3.0)/γ-Al2O3 catalyst was 117.83 m2/g which is dominated by a micropore structure. The highest conversion of stearic acid was 99.1% with a yield of 1-octadecanol 43.2% was obtained at temperature 513 K, initial H2 pressure of 2.0 MPa, a reaction time of 13 h, and in 2-propanol/water (4.0:1.0 v/v) solvent.
{"title":"Catalytic hydrogenation of stearic acid to 1-octadecanol using supported bimetallic Pd–Sn(3.0)/γ–Al2O3 catalyst","authors":"Atina Sabila Azzahra, Elisa Hayati, Rodiansono Rodiansono","doi":"10.14710/jksa.25.2.71-78","DOIUrl":"https://doi.org/10.14710/jksa.25.2.71-78","url":null,"abstract":"Supported bimetallic palladium-tin catalyst on gamma-alumina (γ-Al2O3) (denoted as Pd–Sn(3.0)/γ-Al2O3; Pd = 5%wt and Pd/Sn molar ratio is 3.0) has been synthesized via the hydrothermal method at a temperature of 423 K for 24 h and reduced with H2 at 673 K for 3 h. The XRD patterns of the samples showed typical diffraction peaks of support γ-Al2O3, metallic Pd, Sn, and Pd–Sn alloy phases. Diffraction peaks of metallic Pd were observed at 2θ = 39.8°; 46.6°; and 68.0°, which can be attributed to the Pd(111), Pd(200), and Pd(220), respectively, while the diffraction peaks at 2θ = 39.8° and 41.0° can be attributed to Pd2Sn and Pd3Sn2, respectively, which may overlap with the Pd(111) species. The ammonia desorption and pyridine adsorption profiles showed Lewis and Brönsted acid sites. The specific surface area (SBET) of Pd–Sn(3.0)/γ-Al2O3 catalyst was 117.83 m2/g which is dominated by a micropore structure. The highest conversion of stearic acid was 99.1% with a yield of 1-octadecanol 43.2% was obtained at temperature 513 K, initial H2 pressure of 2.0 MPa, a reaction time of 13 h, and in 2-propanol/water (4.0:1.0 v/v) solvent.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48115888","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-02-24DOI: 10.14710/jksa.25.2.63-70
L. Kadidae, R. Ruslin, T. Azis, L. Aba, L. A. Kadir
The synthesis of a dansyl cyclen-based compound as a potential chemical sensor has been carried out. The initial study of its fluorescent properties has also been conducted. This study aims to synthesize a cyclen-based compound comprising three identical pendant arms and another different arm carrying a dansyl fluorophore. Producing these heterogenous pendant arms, a-three pendant arm cyclen 9 was reacted with dansyl aziridine 10. The synthesis products were characterized using 1H NMR, 13C NMR, IR, and elemental analysis. In addition, a Fluorescent Spectrophotometer has been used to assess the fluorescent intensity changes of the synthetic ligand in a range of pH 2–13 and when it was titrated with some metal ions. Based on the results of characterization with 13C NMR for compound 2 and additional characterization with IR and elemental analysis for its hydrochloric form 11, it is wisely said that the proposed compound has been successfully synthesized, giving 66% yield as viscous brown oil 2. Moreover, the fluorescent property showed that the higher the pH employed, the higher the fluorescent intensity observed. Meanwhile, the addition of some cationic metals revealed that cadmium (II) gave the highest increase in the fluorescent intensities among other cationic metals.
{"title":"Synthesis of Dansyl Cyclen and Preliminary Study of Its Fluorescent Properties","authors":"L. Kadidae, R. Ruslin, T. Azis, L. Aba, L. A. Kadir","doi":"10.14710/jksa.25.2.63-70","DOIUrl":"https://doi.org/10.14710/jksa.25.2.63-70","url":null,"abstract":"The synthesis of a dansyl cyclen-based compound as a potential chemical sensor has been carried out. The initial study of its fluorescent properties has also been conducted. This study aims to synthesize a cyclen-based compound comprising three identical pendant arms and another different arm carrying a dansyl fluorophore. Producing these heterogenous pendant arms, a-three pendant arm cyclen 9 was reacted with dansyl aziridine 10. The synthesis products were characterized using 1H NMR, 13C NMR, IR, and elemental analysis. In addition, a Fluorescent Spectrophotometer has been used to assess the fluorescent intensity changes of the synthetic ligand in a range of pH 2–13 and when it was titrated with some metal ions. Based on the results of characterization with 13C NMR for compound 2 and additional characterization with IR and elemental analysis for its hydrochloric form 11, it is wisely said that the proposed compound has been successfully synthesized, giving 66% yield as viscous brown oil 2. Moreover, the fluorescent property showed that the higher the pH employed, the higher the fluorescent intensity observed. Meanwhile, the addition of some cationic metals revealed that cadmium (II) gave the highest increase in the fluorescent intensities among other cationic metals.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43662648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
京公网安备 11010802042870号
京ICP备2023020795号-1
扫码关注我们
求助内容：
应助结果提醒方式：