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dc.contributor.advisorSuwarso, Edy
dc.contributor.advisorNasution, Pandapotan
dc.contributor.authorWastuti, Sri
dc.date.accessioned2018-02-27T03:23:34Z
dc.date.available2018-02-27T03:23:34Z
dc.date.issued2015
dc.identifier.urihttp://repositori.usu.ac.id/handle/123456789/485
dc.description.abstractTumbuhan inggir-inggir (Solanum sanitwongsei Craib.) dari keluarga Solanaceae yang dikenal dengan nama terung Siam (Jawa), digunakan sebagai obat nyeri haid, obat kencing manis, obat tekanan darah tinggi, dan buahnya digunakan sebagai obat kanker serviks secara turun temurun. Penelitian ini bertujuan untuk mengetahui efek sitotoksik dari ekstrak dan fraksi buah inggiringgir, selektivitas indeks, siklus sel, apoptosis dan peningkatan ekspresi protein p-53 pada sel kanker serviks (hela). Ekstrak etanol diperoleh secara maserasi dari buah inggir-inggir dengan pelarut etanol 96%, selanjutnya difraksinasi dengan pelarut n-heksan dan etilasetat menghasilkan fraksi n-heksan, fraksi etilasetat dan fraksi air (sisa). Ekstrak etanol buah inggir-inggir, fraksi n-heksan buah inggir-inggir, fraksi etilasetat buah inggir-inggir dan Fraksi air buah inggir-inggir diuapkan dengan bantuan rotary evaporator dan dikeringkan dengan freeze dryer. Simplisia dan ekstrak etanol dilakukan karakterisasi dan skrining fitokimia, sedangkan pada fraksi juga dilakukan skrining fitokimia. Selanjutnya ekstrak dan fraksi dilakukan uji sitotoksik terhadap sel hela menggunakan metode MTT (Microculture Tetrazolium Technique). Fraksi yang paling aktif dilanjutkan untuk uji selektivitas indeks, mekanisme penghambatan siklus sel, apoptosis dengan metode flowsitometri dan efek peningkatan ekspresi protein p-53 pada sel hela dengan metode imunositokimia. Hasil karakterisasi simplisia dan ekstrak etanol buah inggir-inggir diperoleh kadar air berturut-turut 7,32%; 4,97%; kadar sari larut air 18,75%; 12,57%; kadar sari larut etanol 15,65%; 59,71%; kadar abu total 3,86%; 0,47% serta kadar abu yang tidak larut asam 0,43%; 0,08%. Hasil skrining fitokimia simplisia dan ekstrak diperoleh golongan alkaloid, flavonoid, glikosida, saponin, tanin dan triterpenoid/ steroid. Skrining fitokimia fraksi n-heksan positif steroid/triterpenoid, skrining fitokimia fraksi etil asetat positif alkaloid, flavonoid, glikosida, saponin dan tanin, skrining fitokimia fraksi air positif glikosida dan saponin. Hasil pengujian sitotoksik larutan uji terhadap sel hela memberikan nilai IC50 ekstrak etanol buah inggir-inggir sebesar 178,194 μg/ml, fraksi n-heksan buah inggir-inggir 812,954 μg/ml, fraksi etilasetat buah inggir-inggir 85,489 μg/ml dan fraksi air buah inggir-inggir 241,580 μg/ml. Fraksi etiasetat buah inggir-inggir merupakan fraksi yang paling aktif dengan nilai Selektivitas indeks 4,05 menunjukkan selektif terhadap sel hela. Fraksi etilasetat buah inggir-inggir dengan konsentrasi 1X IC50 menghambat siklus sel pada fase G2-M, konsentrasi 2X IC50 menghambat siklus sel pada fase sub G1, sedangkan pengujian apoptosis menunjukkan mekanisme apoptosis dikarenakan terjadi peningkatan ekspresi protein p-53 pada sel hela.en_US
dc.description.abstractInggir-inggir (Solanum sanitwongsei Craib.) of the family Solanaceae which is also known as Terung Siam (Java), has been used traditionally for menstrual pain medication, diabetes, high blood pressure medication, and also used for curing cervical cancer. The aim of this study was to determine the cytotoxic effect; the selectivity index, cell cycle inhibition, apoptosis mechanism and the enhancement of the expression of p-53 protein by of ethanolic extract and fractions of inggir-inggir on HeLa cells. The ethanolic extract was prepared by maceration of the inggir-inggir fruits using 96% ethanol , then fractionated using n-hexane and ethylacetate solvent. n-hexane fraction, ethyl acetate fraction and aqueous fraction (residue). All fractions were evaporated on freeze dryer and were subjects to characterization and phytochemical. Simplicia and were subjects to phytochemical screening also were done on fractions of inggir-inggir. Furthermore, extracts and fractions were tested for cytotoxic activity in HeLa cells using MTT (Tetrazolium microculture Technique) method. The most active fraction was subjected to selectivity index test, cell cycle inhibition, apoptosis mechanism with flowcytometric method and the increase in the expression of p-53 in HeLa cells by immunocytochemistry method was observed. The characterization results gave water content 7.32% and 4.97%; watersoluble extract 18.75% and 12.57%; ethanol-soluble extract content 15.65% and 59.71%; total ash content 3.86% and 0.47% and acidic insoluble ash 0.43% and 0.08%. Phytochemical screening of simplex and ethanolic extract showed the presence of alkaloid; flavonoid; glycoside; saponin; tannin and steroids/triterpenoids. n-hexane fraction gave possitive results for the presence of steroids/triterpenoids; ethylacetate fraction was positive for alkaloid; flavonoid; glycoside; saponin; and tannin. The aqueous fraction was positive for flavonoid; glycoside and saponin. The cytotoxic activity test of the sample test solution on HeLa cells gave IC50 value of ethanolic extract 178.194 μg/ml; n-hexane fraction 812.954 μg/ml, ethylacetate fraction was 85.489 μg/ml and aqueous fraction was 241.580 μg/ml. Ethylacetate fraction is the most active fraction with SI value of 4.05, which means that the sample has selective toxicity against HeLa cells. it can inhibit cell cycle at the G2-M phase with IC50 concentration, while double IC50 concentration, can inhibit cell cycle at sub-G1 phase. Based on apoptosis testing, it was showed that apoptotic mechanism is increasing the expression of p-53 protein on HeLa cells.en_US
dc.language.isoiden_US
dc.subjectBuah Inggir-Inggiren_US
dc.subjectHelaen_US
dc.subjectSitotoksiken_US
dc.subjectSelektivitas Indeksen_US
dc.subjectApoptosisen_US
dc.subjectp-53en_US
dc.titleAktivitas Anti Kanker Ekstrak Etanol Dan Fraksi Buah Inggir-Inggir (Solanum Sanitwongsei C.) Pada Sel Kanker Serviksen_US
dc.typeThesisen_US
dc.identifier.nimNIM127014010en_US
dc.identifier.submitterNurhusnah Siregar
dc.description.typeTesis Magisteren_US


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