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Wulan Puji Rahayu
Abstrak :
Kanker paru merupakan penyebab kematian utama di dunia. Nigella sativa merupakan salah satu tanaman yang mempunyai aktivitas sebagai antikanker. Penelitian sebelumnya menunjukkan bahwa ekstrak kloroform N. sativa memiliki efek sitotoksik pada sel T47D. Penelitian ini bertujuan mengetahui aktivitas antiproliferasi ekstrak kloroform biji N. sativa pada hewan uji yang diinduksi DMBA. Tikus betina galur Sprague Dawley dibagi menjadi lima kelompok. Masing-masing kelompok terdiri atas 12 ekor. Kelompok A adalah kontrol DMBA, kelompok B, C, dan D, adalah kelompok perlakuan ekstrak dengan peringkat dosis 250 mg/kgBB, 500 mg/kgBB, dan 750 mg/kgBB, dan kelompok E adalah kelompok kontrol minyak jagung. Aktivitas proliferasi sel diamati dengan pengecatan AgNOR dan pengamatan histopatologi sel menggunakan pengecatan H & E. Niai mAgNOR dianalisis menggunakan uji kolmogorov-dilanjutkan uji satu arah (one way) ANOVA dengan taraf kepercayaan 95% yang diteruskan dengan uji Tukey HSD. Hasil pewarnaan H&E menunjukkan terdapat penurunan kerusakan pada kelompok perlakuan ekstrak dibanding dengan kelompok DMBA. Hasil pewarnaan AgNOR menunjukan terjadi penurunan. Nilai mAgNOR kelompok kontrol DMBA adalah 1,47±0,558, kelompok perlakuan ekstrak dengan tiga peringkat dosis masing-masing adalah 1,44±0,172 untuk dosis 250 mg/kgBB, 1,38±0,140 untuk dosis 500 mg/kgBB dan 1,25±0,164 untuk dosis 750 mg/kgBB dan kelompok kontrol minyak jagung adalah sebesar 0,65±0,050. Hasil penelitian menunjukkan bahwa N. sativa mempunyai potensi untuk dikembangkan sebagai agen kemopreventif pada kanker paru.
Antiproliferative Activity of Black Seed (Nigella sativa) on 7,12-dimethylbenz-[a]antracene (DMBA) Induced Mice Lung Cell. Lung cancer is the leading cause of death in the world. Nigella sativa is a plant that has an anticancer activity. Previous research showed that the chloroform extract of N. sativa have cytotoxic effect on T47D cells. This study aimed to observe the effect of cloroform extract of N. sativa seed (NSS) on mice lung cell after initiation of 7,12-dimethylbenz [a] anthracene. Sprague Dawley strain female rats were divided into five groups. Each group consisted of 12 rats. The experiment consisted of five mice groups, corn oil as a solvent control group, the DMBA dose 20 mg/kgBW p.o. twice a week during five weeks, DMBA+NSS dose 250 mg/kgBW, DMBA+NSS dose 500 mg/kgBW, and DMBA+NSS dose 750 mg/kgBW. Extract which was dissolved into corn oil was administered daily by the oral route 1 week before and during the DMBA induction. At the end of the study, the experimental mice were sacrified and colon organs were collected and then stained with Haematoxylin and Eosin (H&E) and AgNOR method. H&E staining showed there was a decrease damage in the treatment group compare with DMBA group. In AgNOR staining result showed mAgNOR value in DMBA group was 1.47±0.558, in extract group (250, 500 and 750mg/kgBB) was 0.44±0.172, 1.38±0.140 and 1.25±0.164 respectively and in corn oil group was 0.65±0.050. The results showed that N. sativa reduced the damage of colon cells and inhibit colon cell proliferation on mice induced DMBA. This study indicated that N. sativa can be developed into a chemopreventive agent for lung cancer.
Universitas Jenderal Soedirman. Fakultas Kedokteran dan Ilmu-Ilmu Kesehatan, 2012
AJ-Pdf
Artikel Jurnal  Universitas Indonesia Library
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Benjaporn Buranrat
Abstrak :
ABSTRAK
The objective of this research was to investigate the effects of Oroxylum indicum extracts on breast cancer MCF 7 cell proliferation and migration. Four parts of O. indicum, including leaf, bark, pod, and seed, were used. The total phenolic and flavonoid contents were determined to be at high concentrations in the four parts of O. indicum with the seed extract showing the highest levels. For MCF 7 cell death and proliferation, all O. indicum extracts caused stimulating cancer cell death and inhibiting cancer cell proliferation in dose and time dependent manners, surprisingly, the seed extract had the highest effects to inhibit cell proliferation. The IC50 values of cell viability of O. indicum extracts were demonstrated as 161.2 8.63, 286.73 33.01, 149.03 8.81, and 107.06 5.66 mg/mL for leaf, pod, bark, and seed, respectively. Cell counts by crystal violet staining showed that the seed extract stimulated cell death at the lowest concentration. Moreover, all of the O. indicum extracts decreased MCF 7 cell colony formation. Finally, we found that O. indicum extracts could inhibit cancer cell migration in a dose dependent manner. In conclusion, our results showed that the seed extract of O. indicum showed the highest cytotoxic and anti-migratory activity, which was more than in the leaf, pod, and bark, on breast MCF 7 cell cancer and O. indicum can be an anticancer agent for breast cancer patients.
Pathum Thani: Thammasat University, 2018
607 STA 23:4 (2018)
Artikel Jurnal  Universitas Indonesia Library
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Muhammad Sahlan
Abstrak :
[ABSTRAK Tanaman sambiloto (Andrographis Paniculata Nees ) memiliki banyak manfaat dalam pengobatan, salah satunya sebagai obat antikanker. Liposom merupakan salah satu perkembangan dari sistem penghantaran obat yang telah diteliti dapat digunakan sebagai pembawa obat-obat, protein, dan zat?zat molekuler lain. Penelitian ini bertujuan untuk mengembangkan obat dengan bahan dasar ekstrak herba sambiloto yang dienkapsulasi liposom dan diuji aktivitas antiproliferasinya terhadap sel kanker payudara T47D. Metode yang digunakan dalam pembuatan liposom ini adalah metode hidrasi lapis tipis. Pengecilan ukuran partikel dilakukan dengan cara ekstrusi. Evaluasi yang dilakukan dalam penelitian ini adalah distribusi ukuran partikel dan zeta potensial dengan alat DLS, efisiensi penjerapan dengan alat dialisis, morfologi ukuran dengan alat TEM. Uji antiproliferasi sel kanker menggunakan metode MTT. Hasil yang diperoleh pada TEM yang menggambarkan model liposom OLV dengan ukuran ±50 nm; distribusi ukuran partikel liposom sebesar 452,5 dan 43,82 nm serta zeta potensial sebesar -11,3 mV; efisiensi penjerapan sebesar 61,63 %. IC50 dari liposom ekstrak dan larutan ekstrak berturut-turut adalah 11,997 ppm dan 27,488 ppm. Hasil ini menunjukkan bahwa enkapsulasi ekstrak herba sambiloto dengan liposom memberikan pengaruh terhadap aktivitas antiproliferasi sel kanker payudara T47D.
ABSTRACT ;A Sambiloto?s Plant (Andrographis paniculata Nees) has many benefits in the medicals treatment, one of them as an anticancer drug. Liposomes are one of the development of drug delivery systems that have been studied can be used as carriers of drugs, proteins, and other molecular substances. This research aims to develop drugs with a basis of extract of bitter herbs are encapsulated with liposomes for comparison their antiproliferation activity against T47D breast cancer cells. The method which used in the manufacture of liposomes is thin layer hydration method. Reduction of particle size liposomes is done by extrusion. Evaluations were performed in this study is the particle size distribution and zeta potential by DLS, entrapment efficiency by dialisis, morphology size by TEM. Antiproliferation cancer cells test using MTT method. Results obtained at the TEM depicting the model OLV liposomes with a size of about ±50 nm; liposome particle size distribution of 441 and 45.3 nm, and zeta potential of -11.3 mV; The entrapment efficiency of 61.69%. Showed IC50 of liposomes extract and extract solution are respectively 11,997 ppm and 27,488 ppm. This result showed that the extract of bitter herbs encapsulation with liposomes give effect to the antiploriferative activity of T47D breast cancer cells. ;A Sambiloto?s Plant (Andrographis paniculata Nees) has many benefits in the medicals treatment, one of them as an anticancer drug. Liposomes are one of the development of drug delivery systems that have been studied can be used as carriers of drugs, proteins, and other molecular substances. This research aims to develop drugs with a basis of extract of bitter herbs are encapsulated with liposomes for comparison their antiproliferation activity against T47D breast cancer cells. The method which used in the manufacture of liposomes is thin layer hydration method. Reduction of particle size liposomes is done by extrusion. Evaluations were performed in this study is the particle size distribution and zeta potential by DLS, entrapment efficiency by dialisis, morphology size by TEM. Antiproliferation cancer cells test using MTT method. Results obtained at the TEM depicting the model OLV liposomes with a size of about ±50 nm; liposome particle size distribution of 441 and 45.3 nm, and zeta potential of -11.3 mV; The entrapment efficiency of 61.69%. Showed IC50 of liposomes extract and extract solution are respectively 11,997 ppm and 27,488 ppm. This result showed that the extract of bitter herbs encapsulation with liposomes give effect to the antiploriferative activity of T47D breast cancer cells. , A Sambiloto’s Plant (Andrographis paniculata Nees) has many benefits in the medicals treatment, one of them as an anticancer drug. Liposomes are one of the development of drug delivery systems that have been studied can be used as carriers of drugs, proteins, and other molecular substances. This research aims to develop drugs with a basis of extract of bitter herbs are encapsulated with liposomes for comparison their antiproliferation activity against T47D breast cancer cells. The method which used in the manufacture of liposomes is thin layer hydration method. Reduction of particle size liposomes is done by extrusion. Evaluations were performed in this study is the particle size distribution and zeta potential by DLS, entrapment efficiency by dialisis, morphology size by TEM. Antiproliferation cancer cells test using MTT method. Results obtained at the TEM depicting the model OLV liposomes with a size of about ±50 nm; liposome particle size distribution of 441 and 45.3 nm, and zeta potential of -11.3 mV; The entrapment efficiency of 61.69%. Showed IC50 of liposomes extract and extract solution are respectively 11,997 ppm and 27,488 ppm. This result showed that the extract of bitter herbs encapsulation with liposomes give effect to the antiploriferative activity of T47D breast cancer cells. ]
2015
S59380
UI - Skripsi Membership  Universitas Indonesia Library