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Abstrak :
Sesoot (G. picrorrhiza Miq.) merupakan sumber daya hayati yang memiliki potensi sitotoksik terhadap sel kanker payudara. Potensi ini memberikan peluang untuk penatalaksanaan kanker payudara melalui permodelan doksorubisin dan kombinasinya dengan sampel herbal. Penelitian ini untuk membuktikan potensi antikanker payudara terhadap sel MCF-7 dan T47D dari daging buah dan kulit buah sesoot (G. picrorrhiza Miq.) yang selanjutnya disebut buah. Telah dilakukan karakterisasi sampel secara kimia dan biomolekuler sehingga menghasilkan sampel terkarakterisasi, GpKar. Sitotoksisitasnya ditentukan dengan metode MTT (3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide) Assay, lalu dilakukan uji kombinasi dengan doksorubisin untuk mendapatkan Combination Index (CI). Pengamatan induksi apoptosis dilakukan dengan metode Double Staining dan ekspresi protein Caspase 3 dengan metode Enzyme-linked Immunosorbent Assay (ELISA). GpKar memiliki LC50 terhadap larva Artemia salina Leach sebesar 21,110 μg/mL (paling kecil di antara 15 sampel lainnya). Pada uji terhadap sel Vero dengan konsentrasi 250 μg/mL hanya mematikan 11,844 %, tetapi mematikan sel T47D 50,825 % dan MCF-7 31,743 %. Kombinasinya dengan doksorubisin menghasilkan efek sinergis dalam mematikan sel MCF-7 pada konsentrasi 0,200 μg/mL doksorubisin dan konsentrasi GpKar maksimal 125,238 μg/mL (1/4 IC50) juga terhadap sel T47D pada konsentrasi 0,200 μg/mL doksorubisin dan konsentrasi GpKar maksimal 61,799 μg/mL (1/4 IC50). GpKar mempengaruhi induksi apoptosis pada konsetrasi 500,951 μg/mL (1 IC50) dengan menghasilkan persentasi kematian sel MCF-7 paling tinggi yaitu 99 % dan terhadap Sel T47D sebesar 91 %, pada konsentrasi 61,799 μg/mL (1/4 IC50) sedangkan terhadap sel Vero dapat menghasilkan persentase kematian paling rendah yaitu 2,100 % pada konsentrasi 132,943 μg/mL (1/4 IC50). Kombinasinya dengan doksorubisin menghasilkan persentase kematian yang lebih rendah akibat induksi apoptosis. GpKar dan kombinasinya dengan doksorubisin mampu meningkatan konsentrasi protein Caspase 3.

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Sesoot (G. picrorrhiza Miq.) is a medicinal plant which has cytotoxic activity against breast cancer cells. This potency provides the opportunity for treatment of breast cancer through doxorubicin modelling and its combination with herb. This study was done to prove the anti-breast cancer potency of the fruit and the hull of sesoot (G. picrorrhiza Miq.) hereinafter referred to as the fruit against MCf-7 cell and T47D cell. Chemical and Biomolecular Characterizations were done to obtain the characterized sample of GpKar. The cytotoxicity effect was determined using the method of MTT (3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide) Assay, and the combination test with doxorubicin resulting the Combination Index (CI). The apoptotic induction was observed using Double Staining Method and the Caspase 3 protein expression was observed using the method of Enzyme-Linked Immunosorbent Assay (ELISA). The LC50 of GpKar against the larvae of the Artemia salina Leach was 21.110 μg/mL (the least among 15 samples). The Gpkar concentration of 250 μg/mL was the least toxic in term of mortality against Vero cell (11.844 %), but toxic in term of mortality against T47D cell (50.825 %) and MCF-7 cell (31.743 %). The combination with doxorubicin resulted in the synergystic effect against MCF-7 cell (0.200 μg/mL doksorubicin with the maximum GpKar concentration of 125.238 μg/mL (1/4 IC50)) and also against T47D cell (0.200 μg/mL doxorubicin with the maximum GpKar concentration of 61.799 μg/mL (1/4 IC50)). GpKar induced the apoptosis at the concentration of 500.951 μg/mL (1 IC50) resulting the mortality percentage of the MCF-7 cell up to 99 % and up to 91 % against T47D cell at the concentration of 61.799 μg/mL (1/4 IC50) of GpKar, whereas the concentration of 132.943 μg/mL (1/4 IC50) of GpKar resulted in the lowest mortality percentage against Vero cell which was 2.100 %. The combination of GpKar with doxorubicin resulted in the lower mortality percentage as the consequence of apoptotic induction. GpKar and its combination with doxorubicin increased the concentration of the Caspase 3 protein.

Abstrak :
Kanker adalah penyakit yang disebabkan oleh sel abnormal yang berkembang secara tidak terkontrol. Dua jenis penyakit kanker dengan insidensi yang cukup tinggi di Indonesia adalah kanker payudara dan kanker kolon. Beberapa tata laksana yang dilakukan untuk penyakit kanker adalah terapi radiasi, kemoterapi, terapi hormon dan juga pembedahan. Patah tulang (Euphorbia tirucalli) merupakan spesies tanaman yang memiliki berbagai efek baik terhadap Kesehatan. Patah tulang terbukti memiliki efek anti inflamasi, antivirus dan juga keperluan analgesik. Selain itu, beberapa penelitian menunjukkan bahwa daun patah tulang juga bermanfaat sebagai antikanker. Penelitian ini bertujuan untuk mengetahui aktivitas sitotoksisitas daun patah tulang (Euphorbia tirucalli) terhadap sel kanker kolon HT-29 dan kanker payudara MCF-7.Euphorbia tirucalli yang sudah di ekstraksi menggunakan metode maserasi aktivitas sitotoksiknya sebagai inhibitor pertumbuhan sel kanker kolorektal HT-29 dan payudara MCF-7 secara in vitro dengan metode MTT assay. Ekstrak etanol Euphorbia tirucalli memiliki aktivitas sitotoksik moderat terhadap sel kanker payudara MCF-7 dan sel kanker kolorektal HT-29 dengan nilai IC50 masing-masing sebesar 33,88 μg/mL dan 34,86 μg/mL. Ekstrak heksana Euphorbia tirucalli juga menunjukkan aktivitas sitotoksik yang lemah terhadap sel kanker payudara MCF-7 dan sel kanker kolorektal HT-29 dengan nilai IC50 masing-masing sebesar 631,5 μg/mL dan 919,13 μg/mL. Euphorbia tirucalli menunjukkan aktivitas sitotoksik terhadap sel kanker kolon HT-29 dan sel kanker payudara MCF-7......Cancer is a type of disease involving uncontrolled growth of abnormal cells. Two types of cancer that have a high incidence rate are colon cancer and breast cancer. There are various treatment options such as radiation therapy, chemotherapy, hormone therapy, and surgery. Despite that, an exploration on finding new treatment options has been done such as using substances that are found in plants. Pencil cactus (Euphorbia tirucalli) is known as a medicinal plant that has anti inflammation effect, antivirus, used for analgesic, and also anticancer. Based on previous research, Euphorbia tirucalli has an anticancer activity.This study aims to determine cytotoxicity of the Euphorbia tirucalli against HT-29 colon cancer cells and MCF-7 breast cancer cells.Euphorbia tirucalli has been extracted by maceration method using ethyl acetate, n-hexane and ethanol solvent. Each extract was evaluated in vitro its cytotoxic activity against colon HT-29 and breast MCF-7 cancer cells using MTT assay method.Ethanol extract of Euphorbia tirucalli showed moderate cytotoxic effect against breast MCF-7 and colon HT-29 cancer cells with IC50 of 33.88 μg/mL and 34.86 μg/mL, respectively. N-hexane extract of Euphorbia tirucalli showed weak cytotoxic effect against breast cancer and colon cancer with IC50 value respectively at 631.5 μg/mL dan 919.13 μg/mL. Euphorbia tirucalli shows cytotoxic activity towards and colon cancer cell line HT-29 and breast cancer cell line MCF-7

Abstrak :
ABSTRAK
Breast cancer is the second leading cause of cancer death and the most common form of cancer affecting women worldwide. The search for natural products for cancer therapy is an area of great interest. The main aim of this study was to determine the cytotoxic effects and the mechanisms of cell death of the crude extracts from mangrove plant, Avecennia alba on human breast carcinoma cell line, MCF-7. Diethyl ether, butanol and methanol extracts were prepared from the leaves of Avecennia alba. cytotoxicity study using MTS assay demonstrated that all the three extracts produced dose-dependent inhibition on MCF-7 cell growth, albeit at different levels. Diethyl ether extracts produced the most potent cytotoxicity, followed by butanol and methanol extracts with IC50 values of 25.1, 27.1 and 28.9 µg/mL, respectively, after 72 h incubation. The DeadEndTM Colorimetric Apoptosis Detection System suggested that all the three extracts exerted cytotoxicity on MCF-7 cells via apoptosis. TLC proling demonstrated the presence of phenolic and alkaloid compounds in methanol, diethyl ether and butanol extracts which may be responsible for mediating the cytototoxicity. the methanol, diethyl ether and butanol extracts of Avecennia alba may contain potential compounds to be developed as anti-cancer agents against breast cancer.

Abstrak :
Objective: Garcinia xanthochymus extract has been reported to have several pharmacological properties. This study was conducted to evaluate cytotoxic and anti-inflammatory activities of G. xanthochymus extracts on cell lines. Methods: The roots and stem barks of plant were extracted using maceration method with n-hexane, dichloromethane and methanol, successively. Cytotoxic activity of the extracts was tested against MCF-7 breast adenocarcinoma using MTT assay. Anti-inflammatory study was evaluated using RAW 264.7 mouse macrophage cells. The nitric oxide production in LPS-stimulated cells was measured using Griess reagent. Results: The results of cytotoxic and anti- inflammatory study showed that dichloromethane and n-hexane extracts of root and stem bark exhibited cytotoxic activity in dose-dependent manner. Meanwhile, for anti-inflammatory study, all root extracts together with stem bark dichloromethane and n-hexane extracts reduce NO production in LPS-stimulated cells in dose dependent manner. Conclusions: This finding indicated that G. xanthochymus extracts might become interesting candidate for treatment of cancer and inflammation.;

Abstrak :
Tamarindus indica (tamarind) is an established traditional medicine. Pulpa tamarindorum includes vitamin C, protein, fat, glucose, citric acid, etc. Citric acid is a root canal irrigant and vitamin C an antioxidant. This study aimed to elucidate the cytotoxicity of 5% tamarind extract as a root canal irrigant to the cell line BHK-21. Eighteen cultures of cell line BHK-21 were divided into 2 groups. Sterile aquabidest was placed on the group 1 cultures (as control), and 5% tamarind extract was on the group 2, for 2.5 minutes each, and then the percentage of the living and dead cells were counted. The collected data were statistically analyzed by using independent t test to 0.05 limit of significance. The results showed 1% of dead cells in group 1 and 22% in group 2, and that there was a significant difference between the effect of 5% tamarind extract and that of sterile aquabidest (p<0.05). It was concluded that 5% tamarind extract is cytotoxic to the cell line BHK-21.

Abstrak :
Objective: Garcinia xanthochymus extract has been reported to have several pharmacological properties. This study was conducted to evaluate cytotoxic and anti-inflammatory activities of G. xanthochymus extracts on cell lines. Methods: The roots and stem barks of plant were extracted using maceration method with n-hexane, dichloromethane and methanol, successively. Cytotoxic activity of the extracts was tested against MCF-7 breast adenocarcinoma using MTT assay. Anti-inflammatory study was evaluated using RAW 264.7 mouse macrophage cells. The nitric oxide production in LPS-stimulated cells was measured using Griess reagent. Results: The results of cytotoxic and antiinflammatory study showed that dichloromethane and n-hexane extracts of root and stem bark exhibited cytotoxic activity in dose-dependent manner. Meanwhile, for anti-inflammatory study, all root extracts together with stem bark dichloromethane and n-hexane extracts reduce NO production in LPS-stimulated cells in dose dependent manner. Conclusions: This finding indicated that G. xanthochymus extracts might become interesting candidate for treatment of cancer and inflammation.

Abstrak :
Prevalensi kanker payudara pada tahun 2020 menduduki peringkat pertama di dunia maupun di Indonesia. Pencarian obat antikanker menggunakan metode komputasi dinilai lebih efektif dan selektif. Asam galat dan turunannya (ester dan amida) merupakan senyawa yang memiliki aktivitas biologis seperti antikanker. Tujuan dari studi ini adalah melakukan analisis secara in-siliko dan in-vitro terhadap senyawa turunan asam galat (N-Alkil galamida) sebagai agen apoptosis sel kanker payudara MCF7. Sebelas senyawa N-Alkil galamida yang telah disintesis dilakukan studi in-siliko meliputi, interaksi protein-protein, interaksi obat-protein, analisis ADMET dan pemodelan molekuler. Tiga senyawa terbaik berdasarkan studi in-siliko diuji aktivitas sitotoksisitasnya pada sel MCF7 menggunakan metode MTT dan analisis apoptosis menggunakan annexin V-FITC/PI dengan flow cytometry. Protein target terpilih, yaitu JUN, AKT1, CASP3 dan CASP7. Senyawa N-Oktil galamida, N-Ters-Butil galamida dan N-Isoamil galamida merupakan tiga senyawa terbaik. Senyawa asam galat dan turunannya, secara analisis prediksi ADMET termasuk dalam kategori aman sebagai kandidat obat. Aktivitas sitotoksik ketiga senyawa tersebut dinyatakan dengan nilai IC50 berturut-turut adalah 205.2 ± 0,44 μM, 372.6 ± 4,09 μM, dan 441.7 ± 1,41 μM. Aktivitas apoptosis mencapai 55 hingga 56% dibandingkan dengan kontrol sel. Senyawa N-Oktil galamida, N-Ters-Butil galamida dan N-Isoamil galamida berpotensi sebagai agen apoptosis pada sel kanker payudara MCF7. ......The prevalence of breast cancer in 2020 is ranked first in the world and in Indonesia. Searching for anticancer drugs using computational methods is considered more effective and selective. Gallic acid and its derivatives (esters and amides) are compounds that have biological activities such as anticancer. In this study, N-Alkyl gallamides were analyzed in-vitro and in-silico for their potential to act as apoptotic agents for MCF7 breast cancer cells. In-silico investigations on eleven N-alkyl gallamide compounds, including protein-protein interactions, drug-protein interactions, ADMET analysis, and molecular modelling, have been conducted. The three best compounds based on in-silico studies were tested for cytotoxicity activity on MCF7 cells using the MTT assay and apoptosis analysis using annexin V-FITC/PI with flow cytometry. Selected target proteins, namely JUN, AKT1, CASP3 and CASP7. According to ADMET study, gallic acid and their derivatives are safe as therapeutic candidates. The cytotoxic activities of the three compounds were expressed by IC50 values of 205.2 ± 0.44 μM, 372.6 ± 4.09 μM, and 441.7 ± 1.41 μM, respectively. Apoptotic activity reached 55 to 56% compared to control cells. The N-Octyl gallamide, N-Ters-Butyl gallamide and N-Isoamil gallamide compounds have the potential as apoptotic agents in MCF7 cells.

Abstrak :
Remdesivir antivirus berspektrum luas digunakan pada pengobatan covid-19. Struktur hidroksipropil-β-siklodekstrin seperti kerucut yang terpotong dapat meningkatkan kelarutan dan ambilan serapan seluler obat yang sukar larut dalam air. Penelitian ini bertujuan memperoleh kompleks inklusi RDV-HPβCD yang stabil baik secara fisika maupun kimia sehingga dapat meningkatkan pengambilan seluler dan tidak toksik terhadap sel Vero. Kompleks inklusi RDV-HPβCD disintesis dengan metode penguapan pelarut, kompleks yang terbentuk dikarakterisasi dengan serangkaian evaluasi. Kemudian dilakukan evaluasi pelepasan obat dan uji stabilitas. Selanjutnya, mikroskop fluoresensi digunakan untuk mengevaluasi serapan seluler dan uji 3-(4,5-dimetitiazol-2-il)-2,5-difeniltetrazolium bromida (MTT) digunakan dalam studi sitotoksisitas. Baik kompleks inklusi maupun remdesivir menunjukkan puncak serapan maksimum pada 246 nm. Kompleks inklusi memiliki ukuran partikel 1609 ± 189,96 nm dengan potensial zeta -20,13 ± 2,08 mV. Spektrum inframerah yang bergeser, puncak XRD yang luas, dan puncak termogram DSC yang luas pada 72,93 °C menunjukkan keberhasilan pembentukan kompleks inklusi RDV-HPβCD. Kompleks inklusi dan remdesivir memperlihatkan nilai %KV yang tidak lebih dari 2% menandakan bahwa sampel tetap stabil selama 24 jam pengamatan. Pengamatan ambilan serapan seluler kompleks inklusi RDV-HPβCD-FITC menunjukkan intensitas yang lebih baik di dalam sel Vero daripada remdesivir-FITC. Lebih lanjut, kompleks Inklusi menunjukkan viabilitas sel yang lebih tinggi daripada remdesivir murni pada konsentrasi tertentu. ......The broad-spectrum antiviral remdesivir is used in the treatment of COVID-19. The truncated cone-like structure of hydroxypropyl-β-cyclodextrin can increase the solubility and cellular uptake of poorly soluble drugs. This study aimed to obtain the RDV-HPβCD inclusion complex which is physically and chemically stable thus it can increase cellular uptake and not toxic to Vero cells. The RDV-HPβCD inclusion complex was synthesized by solvent evaporation method, the inclusion complex was characterized by some evaluations. The dissolution test and stability test were evaluated, fluorescence microscopy was used to locate cellular uptake and the 3-(4,5-dimetitiazole-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was used in the cytotoxicity study. Both the inclusion complex and remdesivir showed a maximum absorption peak at 246 nm. The inclusion complex had a particle size of 1609 ± 189.96 nm with a zeta potential of -20.13 ± 2.08 mV. The shifting spectrum, broad XRD peak, and broad DSC thermogram peak at 72.93 °C indicated the successful formation of the inclusion complex. The inclusion complex and remdesivir %CV values ​​not more than 2% indicated that the sample remained stable for 24 hours of observation. Cellular uptake of the RDV-HPβCD-FITC inclusion complex showed better intensity in Vero cells than pure remdesivir-FITC. Furthermore, the inclusion complex showed higher cell viability than pure remdesivir at certain concentrations.

Abstrak :
Paduan biner Mg-Gd memiliki potensi sebagai material implan yang mudah larut dalam tubuh. Penambahan sedikit gadolinium dapat memperbaiki sifat mekanik dan laju korosi sehingga memenuhi syarat sebagai material implan yang sesuai dengan kondisi tubuh. Penelitian ini bertujuan untuk merancang paduan Mg-1,6Gd sebagai material implan yang mudah larut yang memiliki sifatsifat mekanik yang baik dan laju korosi terkontrol setelah diproses termomekanik. Paduan tersebut diproses melalui ekstrusi panas dan canai panas dalam rentang temperatur 300-550°C dengn variasi reduksi ketebalan. Sampel diekstrusi panas dengan kecepatan 1 mm/s dengan ratio ekstrusi 30dan sampel canai panas dengan reduksi 30% dan 95%, kecepatan 10 m/min. Proses canai dilakukan dengan dua metode yaitu canai searah dan canai silang. Canai searah dilakukan searah dengan putaran rol, sesuai dengan reduksi dan canai silang membentuk sudut 90° dari setiap tahap rol. Pada rol reduksi 30% dilakukan sekali rol, sementara rol reduksi 95% searah dilakukan multi pass (40%, 40 %, 15% setiap tahap) dan rol reduksi 95% silang dilakukan 23,75% setiap tahap. Paduan Mg-1,6Gd membentuk senyawa intermetallik (Mg5Gd) menyebar di dalam dan dibatas butir untuk semua proses termomekanik. Ekstrusi menghasilkan ukuran butir terkecil dibanding kedua proses canai yaitu mencapai 14um dengan kekerasan 48,7 HVN. Kekuatan tarik dan luluh juga dihasilkan paling tinggi pada proses ini yaitu 232 MPa dan 142 MPa. Sementara proses canai hanya memilki ukuran butir dalam rentang 50-400 um, namun kekerasan rata-rata proses canai lebih tinggi dari ekstrusi yaitu 40-66 HVN. Canai searah 95% menghasilkan kekuatan tarik dan luluh lebih tinggi dari canai 30% yaitu adalah 197 MPa, 157 MPa dan keuletan 26 %. Pada awal perendaman paduan Mg-1,6Gd memiliki laju korosi yang tinggi untuk kedua larutan (SBF dan Ringers). Selanjutnya pada perendaman lama (14 hari) laju korosi cenderung menurun, dikarenakan telah terbentuk lapisan pasif. Ekstrusi menghasilkan laju korosi yang tertinggi dibanding canai yaitu 4.4 mmpy setelah imersi 3 hari dalam larutan Ringers. Melalui polarisasi, canai 95% menghasilkan laju korosi tertinggi (5,7 mmpy). Pengujian sitotoksisitas untuk ketiga proses termomekanik menunjukkan sampel ini tidak menghasilkan toksin karena ratarata hasil % viabilitas diatas viabilitas kontrol (75%). Paduan Mg-1,6Gd setelah proses termomekanik mampu memiliki sifat-sifat mekanik yang baik, laju korosi terkontrol dan tidak toksik untuk digunakan sebagai material implan mampu luruh sesuai kondisi tubuh.

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Binary Mg-Gd alloys have been the potential as biodegradable implant materials. The small addition of element Gd could improve the mechanical properties and corrosion rate that the alloy can be used as implant materials for the body condition. This study aims to design the Mg-1.6Gd alloy as degradable implant that it has good mechanical properties and corrosion rate after thermomechanical process. The Mg-1,6Gd alloys is processed by the hot extrusion and the severely hot rolled in the temperature range 300-550°C with the different reduction. The samples were hot extruded with a speed of 1 mm/s, a ratio of 30 and a hot rolled with a reduction of 30% and 95% and a speed of 10 m/min. The rolling process is done by two methods: Unidirectional rolling (UR) and cross-rolling (CR). UR is carried out in the direction of rotation of the rolland CR formed an angle of 90 from each stage of the roll. The roll of 30% reduction is done only one roll, while the UR of 95% reductionis done multi pass (40%, 40%, 15% each stage) and the CR of 95% reduction is done at 23.75% per stage.The Mg-1.6Gd alloys forms intermetallic compounds (Mg5Gd) and spread inside and grain boundaries for all thermomechanical processes. The hot extrusion resulted the smallest grain size compared to both the rolling process, which the grain size of 14 um and the hardness of 48.7HVN. The highest strength and yield are 232 MPa and 142 MPa for this the extrusion process.The hot rolled samples have the grain size of 50-130um but the average hardness of the this process is higher than that of 40-66 HVN. The hot rolled with the 95% reduction has the higher tensile strength and yield strength than the 30 % reduction, were 197 MPa and 157 MPa, respectively, while the ductility is 26 %.The highest corrotion rate occur on the short time for the both solutions. Furthermore, in the long immersion (14 days) the corrosion rate tends to decrease, because it formed a passive layer. Extrusion process produced the highest corrosion rate of 4.4 mmpy after 3 days of imersion in the Ringer's solution. The hot rolled of the 95% reduction resulted the high corrosion rate of 5,7 mmpy on the polarization test. The cytotoxicity test for all three thermomechanical processes showed the sample have no cytotoxicity because the % viability result was above viability control (75%). The Mg-1.6Gd alloy after thermomechanical process produced good mechanical properties, corrosion rate and no toxins to be used as degradable implant for the body condition.