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Abstrak :
Tumbuhan sukun (Artocarpus altilis) adalah salah satu tumbuhan nangkanangkaan (Artocarpus) dari suku Moraceae yang dikenal baik di Indonesia, merupakan tanaman asli Asia Selatan, Asia Tenggara, New Guinea dan Pasifik Selatan. Dua senyawa berhasil di isolasi dari ekstrak etil asetat daun sukun (Artocarpus altilis) yaitu β-Sitosterol yang berupa kristal jarum berwarna putih mempunyai titik leleh 133-135 ˚C yang memiliki massa molekul 414 dan suatu senyawa JS7 turunan flavonoid berupa padatan kuning cerah dengan massa molekul 404, Senyawa tersebut dapat dipisahkan dengan menggunakan metode ekstraksi secara maserasi, fraksinasi dengan berbagai cara kromatografi, dan pemurnian dengan cara kristalisasi menggunakan sistem dua pelarut. Struktur molekul ditentukan dengan memanfaatkan data fisika dan spektroskopi UV, IR dan 1H dan 13C-NMR. Uji antioksidan menggunakan metode radical scavenger terhadap DPPH menujukkan senyawa turunan flavonoid JS7 kurang aktif sebagai antioksidan dengan IC50 137,00 µg/mL dan uji antikanker menggunakan sel leukemia L-1210 cukup potensial sebagai antikanker dengan IC50 sebesar 5,12 µg/mL. ......Breadfruit (Artocarpus altilis) is one of the Moraceae family well known in Indonesia, is a native plant of South Asia, Southeast Asia, New Guinea and the South Pacific. Two compounds successfully were isolated from the ethyl acetate extract of breadfruit leaves (Artocarpus altilis), there are β-sitosterol (white needle crystals ) with melting point of 133 -135 ˚ C, which has a molecular mass of 414 and one derivative of flavonoid compounds JS7 a bright yellow solid with a molecular mass of 404, these compounds were separated by maceration extraction, fractionation and isolation on chromatography, and purification methods. Crystallization was done by using two solvent systems. The molecular structure were determined by utilizing the physical and spectroscopic data of UV, IR and 1H and 13C-NMR.The isolated compound showed antioxidant activity in DPPH method, JS7 flavonoid derivative compound showed less active as an antioxidant with IC 50 = 137,00 ug / mL and anti-cancer test using L-1210 live cell leukemin a cell exhibited a significant against L1210 cell live with IC50 = 5,12 gram/mL.

Abstrak :
[Buah Manggis (Garcinia mangostana L.) merupakan buah yang banyak tumbuh di negara tropis, di antaranya Indonesia dan Thailand. Bagian kulit (pericarp) Manggis memiliki banyak khasiat, salah satunya sebagai antikanker. Berdasarkan hal tersebut, dilakukan uji sitotoksisitas untuk melihat efek ekstrak kulit buah Manggis terhadap viabilitas sel leukemia MT-2. Untuk membuat ekstrak, pelarut yang digunakan adalah etanol 99%. Ekstrak etanol kulit buah Manggis dibuat dengan menggunakan alat rotary evaporator. Konsentrasi ekstrak dibagi menjadi delapan yakni, 6,25 μg/ml, 12,5 μg/ml, 25 μg/ml, 50 μg/ml, 100 μg/ml, 200 μg/ml, 400 μg/ml, dan 800 μg/ml. Penambahan DMSO dan media kultur digunakan sebagai kontrol. Ekstrak dan kontrol diberikan kepada sel leukemia MT-2 dan dilakukan uji sitotoksisitas dengan menggunakan metode MTT-Assay. Hasil uji sitotoksisitas berupa kepadatan sel yang dinyatakan dengan Optical Density (OD). Data ini diolah sehingga menghasilkan IC50. Nilai IC50 yang didapatkan adalah 1,72 μg/ml yang tergolong sitotoksik kuat. Data penelitian dianalisis menggunakan uji Kruskal-Wallis, dilanjutkan dengan uji post hoc Mann Whitney dan didapatkan hasil perbedaan bermakna pada kelompok kontrol dan kelompok perlakuan dengan konsentrasi 6,25 μg/ml, 12,5 μg/ml, 25 μg/ml, dan 50 μg/ml.;Mangosteen (Garcinia mangostana L.). is a fruit which grows in tropical countries, includes Indonesia and Thailand. Its peel or pericarp has a lot of benefits. One of the benefits is as anticancer. To test the effectiveness of the peel as anticancer, cytotoxicity test should be done. The previous researches haven?t done the test on leukemia MT-2 cells, so this research did this test on leukemia MT-2 cells to know the effect of mangosteen pericarp ethanol extract to the viability of this cancer cell. This research used ethanol 99% for the solvent. Mangosteen pericarp ethanol extract was made by using rotary evaporator. The extract was adjusted into eight concentrations, which are 6.25 μg/ml, 12.5 μg/ml, 25 μg/ml, 50 μg/ml, 100 μg/ml, 200 μg/ml, 400 μg/ml, and 800 μg/ml. DMSO and culture media were used for the control. Both the extract and the control were given to the leukemia MT-2 cells and were tested for cytotoxicity test. MTT-Assay method was used for the cytotoxicity test. The result of cytotoxicity test is called Optical Density (OD) or the density of the cancer cells which are still ?alive?. This data was processing so that the IC50 can be valued. The IC50 value from this experiment is 1.72 μg/ml which is a very strong cytotoxicity. For data analysis, this research used Kruskal-Wallis Test and was continued by using Post hoc Mann-Whitney Test. From Post hoc Mann-Whitney Test, there are the significant differences between several concentrations. The significant differences can be seen on control group and tested group with concentration 6.25 μg/ml, 12.5 μg/ml, 25 μg/ml, and 50 μg/ml;Mangosteen (Garcinia mangostana L.). is a fruit which grows in tropical countries, includes Indonesia and Thailand. Its peel or pericarp has a lot of benefits. One of the benefits is as anticancer. To test the effectiveness of the peel as anticancer, cytotoxicity test should be done. The previous researches haven?t done the test on leukemia MT-2 cells, so this research did this test on leukemia MT-2 cells to know the effect of mangosteen pericarp ethanol extract to the viability of this cancer cell. This research used ethanol 99% for the solvent. Mangosteen pericarp ethanol extract was made by using rotary evaporator. The extract was adjusted into eight concentrations, which are 6.25 μg/ml, 12.5 μg/ml, 25 μg/ml, 50 μg/ml, 100 μg/ml, 200 μg/ml, 400 μg/ml, and 800 μg/ml. DMSO and culture media were used for the control. Both the extract and the control were given to the leukemia MT-2 cells and were tested for cytotoxicity test. MTT-Assay method was used for the cytotoxicity test. The result of cytotoxicity test is called Optical Density (OD) or the density of the cancer cells which are still ?alive?. This data was processing so that the IC50 can be valued. The IC50 value from this experiment is 1.72 μg/ml which is a very strong cytotoxicity. For data analysis, this research used Kruskal-Wallis Test and was continued by using Post hoc Mann-Whitney Test. From Post hoc Mann-Whitney Test, there are the significant differences between several concentrations. The significant differences can be seen on control group and tested group with concentration 6.25 μg/ml, 12.5 μg/ml, 25 μg/ml, and 50 μg/ml, Mangosteen (Garcinia mangostana L.). is a fruit which grows in tropical countries, includes Indonesia and Thailand. Its peel or pericarp has a lot of benefits. One of the benefits is as anticancer. To test the effectiveness of the peel as anticancer, cytotoxicity test should be done. The previous researches haven’t done the test on leukemia MT-2 cells, so this research did this test on leukemia MT-2 cells to know the effect of mangosteen pericarp ethanol extract to the viability of this cancer cell. This research used ethanol 99% for the solvent. Mangosteen pericarp ethanol extract was made by using rotary evaporator. The extract was adjusted into eight concentrations, which are 6.25 μg/ml, 12.5 μg/ml, 25 μg/ml, 50 μg/ml, 100 μg/ml, 200 μg/ml, 400 μg/ml, and 800 μg/ml. DMSO and culture media were used for the control. Both the extract and the control were given to the leukemia MT-2 cells and were tested for cytotoxicity test. MTT-Assay method was used for the cytotoxicity test. The result of cytotoxicity test is called Optical Density (OD) or the density of the cancer cells which are still ‘alive’. This data was processing so that the IC50 can be valued. The IC50 value from this experiment is 1.72 μg/ml which is a very strong cytotoxicity. For data analysis, this research used Kruskal-Wallis Test and was continued by using Post hoc Mann-Whitney Test. From Post hoc Mann-Whitney Test, there are the significant differences between several concentrations. The significant differences can be seen on control group and tested group with concentration 6.25 μg/ml, 12.5 μg/ml, 25 μg/ml, and 50 μg/ml]