25 research outputs found

    ANALISIS TIMBAL (II) DALAM AIR MENGGUNAKAN TEKNIK LIBS DENGAN BANTUAN ADSORBEN POLIURETAN-SELULOSA ASETAT

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    Teknik Laser-Induced Breakdown Spectroscopy (LIBS) tengah marak dikembangkan aplikasinya untuk dapat menganalisis polutan logam berat dalam air. Ini dikarenakan kelebihan yang dimiliki teknik LIBS, seperti proses yang cepat, cara pengoperasian yang mudah, dan tidak memerlukan pre-treatment yang rumit. Namun demikian, ketika laser ditembakkan ke permukaan cairan, plasma yang dihasilkan cenderung kecil dan adanya percikan air yang membuat signal yang terbaca menjadi tidak stabil. Untuk itu, ion logam yang terlarut dalam air terlebih dahulu dikonversi menjadi bentuk solid melalui adsorpsi. Membran poliuretan-selulosa asetat dapat digunakan sebagai adsorben terhadap berbagai macam ion logam, yang mana pada penelitian ini menggunakan Pb2+ sebagai model ion logam berat. Membran poliuretan-selulosa asetat telah dikarakterisasi menggunakan spektroskopi inframerah dan Scanning Electron Microscopy (SEM), menunjukkan adanya modifikasi secara kimia dan morfologi permukaan. Selain itu, penambahan rantai poliuretan pada selulosa asetat juga mempengaruhi sifat fisik dan termalnya. Dalam analisis LIBS, delay time dan energi optimum yang digunakan masing-masing adalah 3000 ns dan 54 mJ. Pengaruh waktu kontak, pH dan konsentrasi awal pada adsorpsi Pb2+ telah diamati dengan teknik LIBS. Kurva kalibrasi yang dihasilkan pada penelitian ini memiliki bentuk kuadratik dengan persamaan y = 0.0036x2 - 0.0035x + 2.4386 dan R2 = 0,996. LOD yang didapatkan relatif lebih rendah dibandingkan dengan penelitian-penelitian sebelumnya. Dengan demikian dapat disimpulkan bahwa membran PUSA dapat diaplikasikan pada analisis kualitatif dan kuantitatif Pb2+ dalam air menggunakan teknik LIBS, dengan keunggulan metode yang lebih praktis dan dapat digunakan secara in-situ

    SINTESIS BUSA POLIURETAN TERMODIFIKASI KITOSAN UNTUK ADSORPSI LOGAM MERKURI

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    Sintesis busa poliuretan termodifikasi kitosan (Chi-PUF) telah dilakukan dan diaplikasikan untuk mengadsorpsi logam merkuri dalam air. Sintesis busa poliuretan memanfaatkan minyak jarak sebagai poliol karena sifatnya yang biodegradable dan harganya yang murah. Untuk meningkatkan sifat fisik busa poliuretan, gliserol ditambahkan dalam bahan poliol sebanyak 20 %. Chi-PUF disintesis dengan variasi komposisi campuran A (minyak jarak dan gliserol), toluen diisosianat (TDI), akuades dan kitosan dengan variasi suhu pre-heating. Sifat fisik dan morfologi Chi-PUF diuji menggunakan spektroskopi fourier transform infra-red FT-IR, scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX) dan differential scanning calorimetry (DSC). Komposisi campuran A : TDI : akuades optimum yang diperoleh adalah 1 : 0,5 : 0,5. Hasil uji adsorpsi pada kondisi optimum ditunjukkan oleh uji adsorpsi pada pH 7 dengan waktu kontak 60 menit. Adsorpsi ion logam Hg (II) oleh Chi-PUF mengikuti model isoterm Fruendlih (R2 = 0,9417). Uji adsorpsi pada tiga sampel air sumur yang mengandung merkuri menunjukkan persen removal tersebar sebanyak 83,049%.Banda Ace

    Distribution of Mercury in Soil, Water, and Vegetable Fern in a Former Gold Mining Area – Evidence from Nagan Raya Regency, Aceh Province, Indonesia

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    The mercury contamination associated with the former intense illegal gold mining activities is suspected in the watershed of Krueng Cot Satu, Nagan Raya Regency, Aceh Province, Indonesia. The aim of this study was to evaluate the mercury contamination residue in the water, soil, and vegetable fern (Pityrogramma calometanos (L)) The samples were collected from locations in the already closed artisanal gold mining sites. The sampling locations were purposively determined by considering their closeness to the previous gold mining activities sites. The content of mercury was analyzed using flow injection for atomic spectroscopy – atomic absorption spectroscopy. The method used was validated by linearity, Limit of Detection (LoD), Limit of Quantification (LoQ), Relative Standard Deviation (RSD), and recovery. The validation test showed that this method is well linear, sensitive, accurate, and precise with a correlation coefficient, LoD, LoQ, RSD and recovery of 0.9999, 0.0477 μg/L, 0.1447 μg/L, 2.96% and 95–105%, respectively. Herein, it was found that the concentrations of mercury contents in the water samples were below the detectable range. However, a high range of mercury concentration of 0.236 – 0.328 μg/g was found in soil, with the highest concentration obtained in the sample collected from the riverbank. The fern sample collected near the riverbank contained mercury in all its parts and concentrated in the root (0.408 μg/g in the leaves, 0.276 μg/g – stalks, and 9.994 μg/g – roots). Meanwhile, the absence of mercury contamination was obtained in the leaves and stalks of the fern samples collected far from the riverbank. The roots, however, were detected with mercury contamination with the highest concentration reaching 27.660 μg/g. Despite its disappearance in the water, mercury contamination residue from the former artisanal gold mining activities still could be traced in the soil and heavy metal accumulating plant – P. calometanos (L)

    Heavy Metals in the Water, Sediment, and Fish Harvested from the Krueng Sabee River Aceh Province, Indonesia

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    The pollution of rivers from human activities such as housing, markets, workshops, transportation, land cultivation, and industry has become an issue. The increasing contribution of heavy metals to pollution in rivers has a direct effect on the metal bioaccumulation in fish. Therefore, this study aimed to examine the concentrations of Cd, Cu, and Pb in the waters, sediment, and fish harvested from the Krueng Sabee River, Aceh Province, Indonesia. Furthermore, the water, sediment, and fish samples were collected from six locations representing the upstream and downstream regions of the river. Cd, Cu, and Pb were analyzed using Atomic Absorption Spectrophotometry (AAS). The results showed that Cd, Cu, and Pb were not detected in the water, while the concentration of Cd in the sediments ranges between 0.0544 to 0.2683 mg kg-1, Cu ranges between 4.4149 to 14.8160 mg kg-1, and Pb ranges between 0.9186–15.4954 mg kg-1. Therefore, Cd, Cu, and Pb in the water and sediment were below the quality standard, but these heavy metals in the fish sample met the threshold limit. The highest Cd concentration was reported in Tor soro (5.5591 mg kg-1), and the highest concentration of Cu was reported in Mugil cephalus (6.7021 mg kg-1), while the higher Pb concentration was reported in Cyclocheilichthys Apogon (0.0279 mg kg-1)

    Extracts from Phyllanthus emblica L stem barks ameliorate blood glucose level and pancreatic and hepatic injuries in streptozotocin-induced diabetic rats

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    Phyllanthus emblica L is a promising medicinal plant for antidiabetic therapy but current research has not explored its stem bark potential as an antidiabetic agent despite the fact that the stem bark contains rich antioxidants. Herein, we aimed to investigate the antidiabetic potential of P. emblica stem barks in vivo. The dried simplicial powder of the stem barks was macerated sequentially using n-hexane, ethyl acetate, and methanol. The extracts were administered orally to streptozotocin (STZ)-induced diabetic rats, where the blood glucose levels were monitored every week. Histopathological analyses were performed for the pancreas and liver. The results revealed that ethyl acetate extract from P. emblica stem barks could lower the fasting blood glucose levels three weeks post-STZ injection (140.3 ± 38.99 versus 270.0 ± 50.51; p = 0.0375). Significant improvement on pancreas and liver histopathology at p < 0.05 was found in the group receiving P. emblica extracts. The IC50 of the ethyl acetate extract against DPPH free radical was 4.67 ± 1.2 mg/g, with total flavonoids, phenolics, and tannins content of 65.54 ± 0.11 QE mg/g, 35.72 ± 0.5 mg GAE/g, and 134.69 ± 0.7 mg TAE/g, respectively. Taken altogether, the ethyl acetate extract from P. emblica stem barks is potential as an antidiabetic drug candidate

    Once-Weekly Somapacitan as an Alternative Management of Growth Hormone Deficiency in Prepubertal Children: A Systematic Review and Meta-Analysis of Randomized Controlled Trial

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    Growth hormone treatment has effectively restored normal growth in children with growth hormone deficiency (GHD); however, it poses challenges in compliance with a daily growth hormone injection regimen, leading to low adherence and persistence rates. Once-weekly Somapacitan is a potential alternative for treating children with GHD. This study aimed to evaluate the efficacy, safety, and adherence of once-weekly subcutaneous Somapacitan compared to daily growth hormone injection in prepubertal children with GHD. A search for the published records was carried out on 17 October 2023 utilizing the searching feature available on PubMed, Embase, and Scopus. Primary study outcomes included (1) efficacy, measured by height velocity (HV), standard deviation score (SDs), height SDs, insulin-like growth factor-SDs (IGF-I SDs), and bone age vs. chronological age ratio (BA vs. CA); (2) safety, assessed through adverse events and injection site reactions; and (3) adherence, determined by the percentage of the sample completing treatments. Secondary outcomes evaluated disease burden scores, divided into three subgroup domains: emotional well-being, physical functional, and social well-being scores. We retrieved 6 studies that were eligible for the systematic review (417 versus 186 for intervention and control, respectively). Only 2 of the total included studies were eligible for pooled analysis (175 versus 82 for intervention and control, respectively). The efficacy profile of Somapacitan was similar to daily growth hormones, indicated by HV (mean difference (MD = 0.04; p = 0.96), HV SDs (MD = −0.71; p = 0.09), height SDs (MD = 0.11; p = 0.69), IGF-I SDs (MD = 0.06; p = 0.70), and CA vs. BA (MD = 0.67; p = 0.70)), demonstrated similar and non-inferior outcomes. Treatment adherence is 3 times higher in the Somapacitan group as compared to control (OR = 3.02; p = 0.03) with adherence rates reaching 95% and 88% for Somapacitan and Norditropin®, respectively. The disease burden measurement is similar in Somapacitan and daily growth hormones (MD = −0.62; p = 0.83), as indicated by the Growth Hormone Deficiency–Child Impact Measure. In almost all outcomes, the level of confidence is strong. The confidence level in the data is generally strong, but for CA vs. BA and the subgroup of severe adverse events with heterogeneity >50%, the confidence level is moderate. Although the efficacy and safety profiles of Somapacitan were found to be similar to those of daily growth hormones, a reduced frequency of once-weekly Somapacitan injections led to increased adherence. PROSPERO registration: CRD42023473209

    Antiproliferative Activity of Triterpenoid and Steroid Compounds from Ethyl Acetate Extract of Calotropis gigantea Root Bark against P388 Murine Leukemia Cell Lines

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    Calotropis gigantea has been known to produce bioactive secondary metabolites with antiproliferative activities against cancer cells. Herein, we extracted the secondary metabolites using ethyl acetate from its root bark and further tested its antiproliferative activities against P388 murine leukemia cell lines. The subfractions from the ethyl acetate extract was obtained from Vacuum Liquid Column Chromatography (VLCC), and followed by Gravity Column Chromatography (GCC). The subfraction C2 and D1 were identified to contain triterpenoids and steroids with the most potent cytotoxicity against Brine Shrimp Lethality Test (BSLT). A 3-(4,5-dimethylthiazol-2-yl) -2-5 diphenyl tetrazolium bromide (MTT) assay suggested that ethyl acetate extract has the highest antiproliferative activities against P388 murine leukemia cell lines (IC50 = 21.79 μg/mL), as opposed to subfraction C2 (IC50 = 50.64 µg/mL) and subfraction D1 (IC50 = 49.33 µg/mL). The compound identified in subfraction C2 and D1 are taraxerol acetate and calotropone, respectively. Though taraxerol acetate and calotropone were active in inhibiting the leukemic cell lines, their IC50s were lower than the ethyl acetate extract, which is probably due to the synergism of the secondary metabolites
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