Abstract An environmentally safe, simple and robust spectrophotometric method has been developed for determination of H2-receptor antagonists namely: cimetidine (CIM), famotidine (FAM), nizatidine (NIZ), and ranitidine hydrochloride (RAN). The method was depend on the reaction of the studied drugs with N-bromosuccinimide (NBS), environmentally friendly reagent, and the excess NBS was measured by its reaction with phloroglucinol to give a yellow chromogenic product (λmax at 435 nm). The absorption intensity decrease (ΔA) was correlated with drug concentrations in the sample solutions. By using of the optimum conditions, linear calibration curves with good correlation coefficients (0.9958–0.9998) were found between the measured ΔA values and the corresponding drugs concentrations in the range of 12-80 μg mL−1. Limits of detection were in the range 1.31-2.21 μg mL−1. The proposed method was validated and successfully applied for the analysis of the above mentioned drugs in their bulk and pharmaceutical dosage forms with good recoveries (98.5 ± 0.98 to 102.5 ± 0.79%). No interferences were obtained from the common excipients. The proposed method was successfully applied for the analysis of H2RAs in their dosage forms and the results were comparable with that obtained by the official methods.
{"title":"Utility of N-Bromosuccinimide as a Green Chemical Reagent for Determination of H2-Receptor Antagonists in their Pharmaceutical Dosage Forms","authors":"Ahmed I. Hassan","doi":"10.2478/achi-2019-0004","DOIUrl":"https://doi.org/10.2478/achi-2019-0004","url":null,"abstract":"Abstract An environmentally safe, simple and robust spectrophotometric method has been developed for determination of H2-receptor antagonists namely: cimetidine (CIM), famotidine (FAM), nizatidine (NIZ), and ranitidine hydrochloride (RAN). The method was depend on the reaction of the studied drugs with N-bromosuccinimide (NBS), environmentally friendly reagent, and the excess NBS was measured by its reaction with phloroglucinol to give a yellow chromogenic product (λmax at 435 nm). The absorption intensity decrease (ΔA) was correlated with drug concentrations in the sample solutions. By using of the optimum conditions, linear calibration curves with good correlation coefficients (0.9958–0.9998) were found between the measured ΔA values and the corresponding drugs concentrations in the range of 12-80 μg mL−1. Limits of detection were in the range 1.31-2.21 μg mL−1. The proposed method was validated and successfully applied for the analysis of the above mentioned drugs in their bulk and pharmaceutical dosage forms with good recoveries (98.5 ± 0.98 to 102.5 ± 0.79%). No interferences were obtained from the common excipients. The proposed method was successfully applied for the analysis of H2RAs in their dosage forms and the results were comparable with that obtained by the official methods.","PeriodicalId":6958,"journal":{"name":"Acta Chemica Iasi","volume":"49 1","pages":"47 - 64"},"PeriodicalIF":0.5,"publicationDate":"2019-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87446142","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}
Abstract The Co-Zn ferrite (x=0.00) and Nickel doped Co-Zn ferrites (x=0.24) was synthesized by low cost solid state reaction method and characterized by XRD technique. The X-ray diffraction results for the samples showed the formation of single phase cubic spinel. The lattice constant and particle size for Co-Zn ferrite(x=0.00) is found to be 8.3465 Å and 26.72 nm and for Nickel doped (x=0.24) it is 8.3440 Å and 24.21nm. Micro strain (ε), Dislocation density(ρD), Hopping lengths (LA and LB), Bond lengths (A - O and B-O), Ionic radii (rA and rB), Texture coefficients (Thkl) and Standard deviation (σ) are also reported. The particle size is confirmed by scanning electron microscope (SEM). The Williamson-Hall plot and stress-strain plot also employed to understand the mechanical properties of materials.
{"title":"Synthesis and Characterization of Co0.8-x Nix Zn0.2 Fe2O4 Ferrites by Williamson–Hall and Size–Strain Plot Methods","authors":"R. Kolekar, S. B. Kapatkar, S. Mathad","doi":"10.2478/achi-2019-0006","DOIUrl":"https://doi.org/10.2478/achi-2019-0006","url":null,"abstract":"Abstract The Co-Zn ferrite (x=0.00) and Nickel doped Co-Zn ferrites (x=0.24) was synthesized by low cost solid state reaction method and characterized by XRD technique. The X-ray diffraction results for the samples showed the formation of single phase cubic spinel. The lattice constant and particle size for Co-Zn ferrite(x=0.00) is found to be 8.3465 Å and 26.72 nm and for Nickel doped (x=0.24) it is 8.3440 Å and 24.21nm. Micro strain (ε), Dislocation density(ρD), Hopping lengths (LA and LB), Bond lengths (A - O and B-O), Ionic radii (rA and rB), Texture coefficients (Thkl) and Standard deviation (σ) are also reported. The particle size is confirmed by scanning electron microscope (SEM). The Williamson-Hall plot and stress-strain plot also employed to understand the mechanical properties of materials.","PeriodicalId":6958,"journal":{"name":"Acta Chemica Iasi","volume":"9 1","pages":"73 - 86"},"PeriodicalIF":0.5,"publicationDate":"2019-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76206262","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}
Abstract A large number of drug experiments revealed that there exists strong inherent relation between the drugs molecular structures and the bio-medical and pharmacology characteristics. Due to the effectiveness for pharmaceutical and medical scientists of their ability to grasp the biological and chemical characteristics of new drugs, forgotten topological index was defined to analyze the drug molecular structures. This index is applicable for testing the chemical and pharmacological properties of drug molecular structures that can make up for lack of chemical experiments and can provide a theoretical basis for the manufacturing of drugs which is widely welcomed in developing areas. In this paper, based on the drug molecular structure analysis and vertex dividing technique with respect to their degrees, we present the forgotten topological index of the line graphs of several popular chemical structures which is quite common in drug molecular graphs.
{"title":"Forgotten Topological Index of Line Graphs of Some Chemical Structures in Drugs","authors":"Gul E Mehak, A. A. Bhatti","doi":"10.2478/achi-2018-0012","DOIUrl":"https://doi.org/10.2478/achi-2018-0012","url":null,"abstract":"Abstract A large number of drug experiments revealed that there exists strong inherent relation between the drugs molecular structures and the bio-medical and pharmacology characteristics. Due to the effectiveness for pharmaceutical and medical scientists of their ability to grasp the biological and chemical characteristics of new drugs, forgotten topological index was defined to analyze the drug molecular structures. This index is applicable for testing the chemical and pharmacological properties of drug molecular structures that can make up for lack of chemical experiments and can provide a theoretical basis for the manufacturing of drugs which is widely welcomed in developing areas. In this paper, based on the drug molecular structure analysis and vertex dividing technique with respect to their degrees, we present the forgotten topological index of the line graphs of several popular chemical structures which is quite common in drug molecular graphs.","PeriodicalId":6958,"journal":{"name":"Acta Chemica Iasi","volume":"36 6 1","pages":"181 - 206"},"PeriodicalIF":0.5,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75127641","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}
Kinjal K. Kubavat, Sanman Samova, Hetal Doctor, G. Sindhav, R. Verma
Abstract One of the natural antioxidant flavonols -Quercetin is found in various food products and plants. Its anticancer properties have been proved by in vivo and in vitro experiments; it shows an attempt to examine toxic effects of Bisphenol A in the liver of mice and its alleviation by quercetin. For this inbred Swiss strain male albino mice were orally administered with quercetin (30, 60 and 90 mg/kg body weight/day) along with BPA (240 mg/kg body weight/day) for 45 days. On the completion of the treatment period, animals were sacrificed; organs were isolated and used for biochemical analysis. All these effects were dose-dependent. Co-treatment with quercetin (30, 60 and 90 mg/kg body weight) and BPA (240 mg/kg body weight) alleviates the changes in body weight, absolute and relative organ weights of mice. Biochemical analysis revealed significant (p < 0.05) and dose-dependent reduction in enzymatic antioxidants such as superoxide dismutase, Catalase and glutathione peroxidase and non-enzymatic antioxidants such as Glutathione and Total ascorbic acid content were also observed in Bisphenol A -treated groups as compared to control. The present results revealed that graded doses of BPA caused oxidative damage in the liver of mice, which is mitigated by quercetin.
{"title":"Hepatoprotective Effect of Quercetin on Bisphenol A-Induced Toxicity","authors":"Kinjal K. Kubavat, Sanman Samova, Hetal Doctor, G. Sindhav, R. Verma","doi":"10.2478/achi-2018-0013","DOIUrl":"https://doi.org/10.2478/achi-2018-0013","url":null,"abstract":"Abstract One of the natural antioxidant flavonols -Quercetin is found in various food products and plants. Its anticancer properties have been proved by in vivo and in vitro experiments; it shows an attempt to examine toxic effects of Bisphenol A in the liver of mice and its alleviation by quercetin. For this inbred Swiss strain male albino mice were orally administered with quercetin (30, 60 and 90 mg/kg body weight/day) along with BPA (240 mg/kg body weight/day) for 45 days. On the completion of the treatment period, animals were sacrificed; organs were isolated and used for biochemical analysis. All these effects were dose-dependent. Co-treatment with quercetin (30, 60 and 90 mg/kg body weight) and BPA (240 mg/kg body weight) alleviates the changes in body weight, absolute and relative organ weights of mice. Biochemical analysis revealed significant (p < 0.05) and dose-dependent reduction in enzymatic antioxidants such as superoxide dismutase, Catalase and glutathione peroxidase and non-enzymatic antioxidants such as Glutathione and Total ascorbic acid content were also observed in Bisphenol A -treated groups as compared to control. The present results revealed that graded doses of BPA caused oxidative damage in the liver of mice, which is mitigated by quercetin.","PeriodicalId":6958,"journal":{"name":"Acta Chemica Iasi","volume":"59 1","pages":"207 - 220"},"PeriodicalIF":0.5,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73654936","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}
Abstract The first Zagreb index (occurred in an approximate formula of total π-electron energy, communicated in 1972) and the second Zagreb index (appeared in 1975, within the study of molecular branching) are among the most studied topological indices. Recently, three modified versions of the Zagreb indices were proposed independently in [A. Ali, N. Trinajstić, A novel/old modification of the first Zagreb index, arXiv:1705.10430 [math.CO], 2017] and [A. M. Naji, N. D. Soner, I. Gutman, On leap Zagreb indices of graphs, Commun. Comb. Optim., 2017, 2, 99–117], which were named as the Zagreb connection indices and the leap Zagreb indices, respectively. In this paper, we derive formulas for calculating these modified versions of the Zagreb indices of four well known nanostructures.
第一个萨格勒布指数(出现于1972年的总π电子能量近似公式中)和第二个萨格勒布指数(出现于1975年的分子分支研究中)是目前研究最多的拓扑指数。最近，在[A]中分别提出了三个修改版本的Zagreb指数。[3]陈志强，张志强，张志强。一种基于数学模型的Zagreb指数[j] .中国科学:自然科学版。[c]， 2017。M. Naji, N. D. Soner, I. Gutman，图的跳跃萨格勒布指数，公共。梳子。Optim。[j]， 2017, 2, 99-117]，分别命名为萨格勒布连接指数和飞跃萨格勒布指数。在本文中，我们推导了计算四种已知纳米结构的这些修正版本的萨格勒布指数的公式。
{"title":"Zagreb Connection Indices of Some Nanostructures","authors":"Saba Manzoor, N. Fatima, A. A. Bhatti, Akbar Ali","doi":"10.2478/achi-2018-0011","DOIUrl":"https://doi.org/10.2478/achi-2018-0011","url":null,"abstract":"Abstract The first Zagreb index (occurred in an approximate formula of total π-electron energy, communicated in 1972) and the second Zagreb index (appeared in 1975, within the study of molecular branching) are among the most studied topological indices. Recently, three modified versions of the Zagreb indices were proposed independently in [A. Ali, N. Trinajstić, A novel/old modification of the first Zagreb index, arXiv:1705.10430 [math.CO], 2017] and [A. M. Naji, N. D. Soner, I. Gutman, On leap Zagreb indices of graphs, Commun. Comb. Optim., 2017, 2, 99–117], which were named as the Zagreb connection indices and the leap Zagreb indices, respectively. In this paper, we derive formulas for calculating these modified versions of the Zagreb indices of four well known nanostructures.","PeriodicalId":6958,"journal":{"name":"Acta Chemica Iasi","volume":"1 1","pages":"169 - 180"},"PeriodicalIF":0.5,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90046597","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}
Abstract The synthesis of 4-(2-hydroxyaryl)-5-methyl-1,3-dithiol-2-thiones has been accomplished by the reaction of the corresponding 4-(2-hydroxyaryl)-5-methyl-1,3-dithiol-2-ylium perchlorates with sodium sulfide nonahydrate in ethanol at room temperature. The newly obtained derivatives were characterized by NMR and MS spectrometry and IR spectroscopy.
{"title":"Synthesis of 4-(2-Hydroxyaryl)-5-Methyl-1,3-Dithiol-2-Thiones","authors":"L. Bahrin","doi":"10.2478/achi-2018-0021","DOIUrl":"https://doi.org/10.2478/achi-2018-0021","url":null,"abstract":"Abstract The synthesis of 4-(2-hydroxyaryl)-5-methyl-1,3-dithiol-2-thiones has been accomplished by the reaction of the corresponding 4-(2-hydroxyaryl)-5-methyl-1,3-dithiol-2-ylium perchlorates with sodium sulfide nonahydrate in ethanol at room temperature. The newly obtained derivatives were characterized by NMR and MS spectrometry and IR spectroscopy.","PeriodicalId":6958,"journal":{"name":"Acta Chemica Iasi","volume":"21 1","pages":"351 - 358"},"PeriodicalIF":0.5,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77861749","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}
M. Belalia, Meriem Bendjelloul, A. Aziz, E. Elandaloussi
Abstract This paper reports the synthesis and characterization of an efficient anionic olive stone waste-based material as new ion-exchanger adsorbent. The olive stone waste was subjected to an alkaline pretreatment in order to enhance their reactivity towards maleic anhydride. The maleate-derived material MOS was characterized by FTIR, 13C NMR, TGA and DSC. The resulting sodium form of material NaMOS was subjected to batch experiments in order to evaluate its cadmium and lead removal efficiency. Adsorption experimental data showed a uniform and rapid process. Both Langmuir and Freundlich isotherm models were found to fit adequately the equilibrium isotherm data. The sorption capacities reached 240.96 mg Cd g−1 and 127.38 mg Pb g−1. The thermodynamic parameters showed that the process was exothermic and the adsorption occurred spontaneously. The desorption experiments show a quantitative recovery of the metal ions from NaMOS material.
摘要本文报道了一种高效阴离子橄榄石废基材料的合成和表征。对橄榄石废渣进行碱性预处理，以提高其对马来酸酐的反应性。采用FTIR、13C NMR、TGA和DSC对马来酸衍生物MOS进行了表征。为了评价其对镉和铅的去除效果，对所得到的钠形式的材料NaMOS进行了批量实验。吸附实验数据表明，吸附过程均匀、快速。发现Langmuir和Freundlich等温线模型都能充分拟合平衡等温线数据。吸附量为240.96 mg Cd g−1和127.38 mg Pb g−1。热力学参数表明，该过程为放热过程，吸附是自发进行的。解吸实验表明，从NaMOS材料中可以定量回收金属离子。
{"title":"Surface Modification of Olive Stone Waste for Enhanced Sorption Properties of Cadmium and Lead Ions","authors":"M. Belalia, Meriem Bendjelloul, A. Aziz, E. Elandaloussi","doi":"10.2478/achi-2018-0018","DOIUrl":"https://doi.org/10.2478/achi-2018-0018","url":null,"abstract":"Abstract This paper reports the synthesis and characterization of an efficient anionic olive stone waste-based material as new ion-exchanger adsorbent. The olive stone waste was subjected to an alkaline pretreatment in order to enhance their reactivity towards maleic anhydride. The maleate-derived material MOS was characterized by FTIR, 13C NMR, TGA and DSC. The resulting sodium form of material NaMOS was subjected to batch experiments in order to evaluate its cadmium and lead removal efficiency. Adsorption experimental data showed a uniform and rapid process. Both Langmuir and Freundlich isotherm models were found to fit adequately the equilibrium isotherm data. The sorption capacities reached 240.96 mg Cd g−1 and 127.38 mg Pb g−1. The thermodynamic parameters showed that the process was exothermic and the adsorption occurred spontaneously. The desorption experiments show a quantitative recovery of the metal ions from NaMOS material.","PeriodicalId":6958,"journal":{"name":"Acta Chemica Iasi","volume":"1 1","pages":"281 - 306"},"PeriodicalIF":0.5,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85167399","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}
Abstract The study deals with the exploration of the possibilities to control the morphology of cinnamyl-imine-chitosan hydrogels in view of their bio-application. Three series of hydrogels were synthetized from chitosan of three different molecular weights and cinnamaldehyde, varying the molar ratio between the amine groups on chitosan and aldehyde functional groups. The hydrogel morphology has been monitored by scanning electron microscopy. The variation of the hydrogel morphology as a function of chitosan molecular weight, crosslinking degree, and incubation conditions has been monitored. It was concluded that there are multiple possibilities of tuning the morphology of these hydrogels in function of the targeted application.
{"title":"Cinnamyl-Imine-Chitosan Hydrogels. Morphology Control","authors":"A. Craciun","doi":"10.2478/achi-2018-0014","DOIUrl":"https://doi.org/10.2478/achi-2018-0014","url":null,"abstract":"Abstract The study deals with the exploration of the possibilities to control the morphology of cinnamyl-imine-chitosan hydrogels in view of their bio-application. Three series of hydrogels were synthetized from chitosan of three different molecular weights and cinnamaldehyde, varying the molar ratio between the amine groups on chitosan and aldehyde functional groups. The hydrogel morphology has been monitored by scanning electron microscopy. The variation of the hydrogel morphology as a function of chitosan molecular weight, crosslinking degree, and incubation conditions has been monitored. It was concluded that there are multiple possibilities of tuning the morphology of these hydrogels in function of the targeted application.","PeriodicalId":6958,"journal":{"name":"Acta Chemica Iasi","volume":"93 1","pages":"221 - 232"},"PeriodicalIF":0.5,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84238654","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}
R. Bharamagoudar, A. S. Patil, S. Mathad, V. Kumbar, L. B. Kankanawadi
Abstract The main objective of the manuscript is the structural analysis, magnetic investigation and antimicrobial activity of Mn1−xZnxFe2O4 with stoichiometry (x = 0, 0.25, 0.5, 0.75, and 1.0). The Mn-Zn nanoferrites were synthesized by self propagating high-temperature synthesis using a mixture of fuels. The synthesized Mn-Zn nanoferrites were characterized by X-ray diffraction (XRD) that confirms cubic crystal structure with lattice constant in the range 8.372-8.432Ao. It is observed that saturation magnetization (Ms), remanence magnetization (Mr) and magneton number (Mr/Ms) decreased gradually with the increasing of Zn2+ concentration. The decrease in the saturation magnetization may be explained as, the Zn2+ concentration increases, the relative number of ferric ions on the A sites diminishes and this reduces the A–B interaction. Further, the synthesized Mn-Zn nanoferrites were tested for antibacterial activities against two-gram positive strains (Staphylococcus aureus ATCC No–12598, Lactobacillus amylovorus ATCC No– 12598), gram-negative strains E.coli ATCC No – 25922, Pseudomonas- ATCC No- 25619) and one fungal strain (C.albicans -ATCC No – 2091).
{"title":"Magnetic and Antibacterial Studies of Nanoferrites Prepared by Self Propagating High-Temperature Synthesis Route","authors":"R. Bharamagoudar, A. S. Patil, S. Mathad, V. Kumbar, L. B. Kankanawadi","doi":"10.2478/achi-2018-0016","DOIUrl":"https://doi.org/10.2478/achi-2018-0016","url":null,"abstract":"Abstract The main objective of the manuscript is the structural analysis, magnetic investigation and antimicrobial activity of Mn1−xZnxFe2O4 with stoichiometry (x = 0, 0.25, 0.5, 0.75, and 1.0). The Mn-Zn nanoferrites were synthesized by self propagating high-temperature synthesis using a mixture of fuels. The synthesized Mn-Zn nanoferrites were characterized by X-ray diffraction (XRD) that confirms cubic crystal structure with lattice constant in the range 8.372-8.432Ao. It is observed that saturation magnetization (Ms), remanence magnetization (Mr) and magneton number (Mr/Ms) decreased gradually with the increasing of Zn2+ concentration. The decrease in the saturation magnetization may be explained as, the Zn2+ concentration increases, the relative number of ferric ions on the A sites diminishes and this reduces the A–B interaction. Further, the synthesized Mn-Zn nanoferrites were tested for antibacterial activities against two-gram positive strains (Staphylococcus aureus ATCC No–12598, Lactobacillus amylovorus ATCC No– 12598), gram-negative strains E.coli ATCC No – 25922, Pseudomonas- ATCC No- 25619) and one fungal strain (C.albicans -ATCC No – 2091).","PeriodicalId":6958,"journal":{"name":"Acta Chemica Iasi","volume":"52 1","pages":"249 - 262"},"PeriodicalIF":0.5,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91143806","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}
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