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Lischer, Kenny
"Acanthaster planci dilaporkan memiliki enzim phospolipase A2 (PLA2) yang memiliki aktivitas antiviral. Sementara itu, penyakit AIDS semakin menyebar yang diakibatkan oleh virus Human Immunodeficiency Virus (HIV). Namun, terdapat resistensi virus HIV terhadap obat yang ada sehingga menurunkan efektivitas yang ada.
Penelitian ini dilakukan untuk mencari alternatif obat terhadap HIV, salah satunya adalah PLA2 ini. Oleh karena itu, penelitian secara umum bertujuan untuk mengobservasi adanya aktivitas antiviral PLA2 terhadap HIV. Dalam penelitian ini digunakan sampel enzim PLA2 berupa CV dan F20 untuk diuji aktivitas dengan degradasi fosfatidikolin dan kemurniannya dengan SDS-PAGE.
Uji aktivitas dilakukan dengan menggunakan sistem in vitro, yaitu kultur virus HIV dengan menggunakan sel PBMC (Peripheral Blood Mononuclear Cells). Sel PBMC diisolasi dari darah orang sehat yang kemudian distimulasi dengan PHA (Phytohaemaglutinin). Sel ini dijadikan feeder untuk memperbanyak virus dari PBMC pasien positif HIV. Sebelum dilakukan uji aktivitas terlebih dahulu dilakukan uji toksisitas dengan LC50.
Hasil uji aktivitas PLA2 didapatkan bahwa F20 memiliki aktivitas spesifik dan tingkat kemurnian 15,66 kali dari CV. Nilai LC50 PLA2 adalah sebesar 1,63799 mg/ml. Sementara itu hasil uji aktivitas antiviral PLA2 secara in vitro menunjukkan hambatan persentase sel yang terinfeksi, dimana untuk kultur HIV yang memiliki rata-rata infeksi 9,718±0,802% menurun setelah ditambahkan dengan PLA2 menjadi hanya 0,299±0,212% infeksi dari jumlah sel.

Acanthaster planci has enzyme, phospolipase A2 (PLA2), which has ability as antiviral agent. AIDS had become big pandemic in the world cause of the spread of Human Immunodeficiency Virus (HIV). Furthermore, HIV had become resistance with current drugs, so it decrease the efectivity of drugs.
This research conduct to obtain the alternative drug for HIV infection, one of them is PLA2. So, the objective of this research was to observe antiviral activity of PLA2 agains HIV. This research using CV and F20 as the sample PLA2 which had been extracted from A. planci. Enzimatic activity will be determine by degradation of phospatidicholin and the purification determine by SDS-PAGE.
Activity test was done in vitro by using PBMC (Peripheral Blood Mononuclear Cells) as feeder to increase HIV population. Meanwhile, toxicity test must be done before by LC50. PLA2 F20 had activity and purity by 15.66 times bigger than CV. LC50 of PLA2 was about 1,63799 mg/ml.
Meanwhile, antiviral activity test of PLA2 in vitro show inhibition of percentage of infected cells. Where, HIV culture shows infected cells about 9,718±0,802%. After Additon of PLA2, infected cells was drop into 0,299±0,212% from the total of cells.
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Depok: Fakultas Teknik Universitas Indonesia, 2013
T35725
UI - Tesis Membership  Universitas Indonesia Library
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Clercq, Erik De
"By focusing on general molecular mechanisms of antiviral drugs rather than therapies for individual viruses, this ready reference provides the critical knowledge needed to develop entirely novel therapeutics and to target new viruses.
It begins with a general discussion of antiviral strategies, followed by a broad survey of known viral targets, such as reverse transcriptases, proteases, neuraminidases, RNA polymerases, helicases and primases, as well as their known inhibitors. The final section contains several cases studies of recent successful antiviral drug development.
Edited by Erik de Clercq, the world authority on small molecule antiviral drugs, who has developed more new antivirals than anyone else.
"
Weinheim: Wiley-VCH Verlag, 2011
e20375713
eBooks  Universitas Indonesia Library
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Galasso, George J.
New York: Raven press, 1984
616.9 Gal a
Buku Teks SO  Universitas Indonesia Library
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Risza Hartawan
"Latar Belakang: Penyakit avian influenza subtipe H5N1 Asian lineage yang mulai mewabah di kawasan Asia, Afrika dan Eropa sejak tahun 1997 selain menimbulkan kerugian ekonomi yang sangat signifikan juga mengancam aspek kesehatan manusia dimana sejumlah korban meninggal dunia karena infeksi virus yang bersifat zoonosis. Penanganan penyakit dilakukan dengan antiviral yang berbasis neuraminidase inhibitor. Permasalahan timbul sebagai akibat mutasi beberapa strain virus menjadi resisten terhadap antiviral yang ada. Penelitian ini bertujuan untuk melakukan desain antiviral alternatif berbasis siRNA terhadap gen nucleoprotein yang lebih sesuai terhadap virus avian influenza subtipe H5N1 yang bersirkulasi di Indonesia. Metode: Desain siRNA dilakukan secara in silico dengan program siDirect 2.0 berdasarkan 210 sekuen gen nucleoprotein virus H5N1 yang bersirkulasi di Indonesia. Dua kandidat siRNA-NP672 dan siRNA-NP1433 dipilih berdasarkan kajian bioinformatik. Selanjutnya, kedua kandidat siRNA-NP tersebut ditantang secara in vitro pada sel Mabin-Darby canine kidney (MDCK) terhadap virus H5N1 asal Indonesia clade 2.1.3 dan 2.3.2 dengan menggunakan siRNA-NP1496 sebagai pembanding. Paramater yang diamati adalah produksi virus dan ekspresi gen virus. Terakhir, analisa mutasi gen nucleoprotein virus H5N1 dilakukan untuk melihat paparan siRNA-NP secara berulang kali. Hasil: Kandidat siRNA-NP672 memberikan efek penurunan infeksi virus H5N1 yang lebih baik dalam menurunkan tingkat infeksi virus HPAI subtipe H5N1 baik clade 2.1.3 dan 2.3.2 secara in vitro pada sel MDCK yang dicerminkan dengan titer produksi virus dibandingkan dua desain lainnya yaitu siRNA-NP1433 dan siRNA-NP1496. Pemberian siRNA-NP672 juga memberikan efek peredaman yang lebih tinggi dan konsisten terhadap ekspresi gen-gen virus, antara lain nucleoprotein, polymerase acidic, hemagglutinin, neuraminidase, Matrix, dan non-structural. Hasil kajian bioinformatik terhadap struktur sekunder dan tersier RNA gen nucleoprotein menunjukkan bahwa target siRNA-NP672 lebih berinteraksi karena memiliki bagian bebas (loop) yang lebih banyak dibandingkan dua kandidat siRNA-NP lainnya. Selanjutnya, paparan siRNA-NP tidak memicu terjadinya mutasi gen target pada virus H5N1 baik clade 2.1.3 dan clade 2.3.2 setelah 3 kali paparan. Kesimpulan: Desain siRNA-NP672 menunjukkan prospek yang lebih baik dalam menurunkan tingkat infeksi virus avian influenza subtipe H5N1 baik clade 2.1.3 dan clade 2.3.2.

Introduction: Avian influenza disease outbreak of subtype H5N1 Asian lineage that has spread in Asia, Africa, and European continental since 1997 caused massive economic drawbacks as well as a zoonotic threat where numerous deaths related to viral infection. The treatment of viral infection has been done with antiviral based on neuraminidase inhibitors. However, mutation of numerous virus strains has been confirmed that may lead to resistance against current antivirals. This study's objective was to design an alternative antiviral based on siRNA targeting nucleoprotein gene that is more suitable for the avian influenza viruses subtype H5N1 circulating in Indonesia. Methods: The siRNA design was accomplished in silico using the siDirect 2.0 program based on 210 nucleoprotein gene sequences of H5N1 viruses circulating in Indonesia. Two siRNA candidates (siRNA-NP672 and siRNA-NP1433) were chosen based on bioinformatic analyses. Subsequently, these siRNA-NP candidates were challenged in vitro in Mabin-Darby canine kidney cell culture against the Indonesian H5N1 both clade 2.1.3 and clade 2.3.2 using siRNA-NP1496 as a comparison. The parameters analyzed within the study are including virus production and viral gene expression level. Finally, mutation analysis was performed to evaluate the effect of three serial siRNA-NP exposures to the target gene of the H5N1 viruses. Results: The siRNA-NP672 provides a better reduction of the H5N1 viral infection, especially on viral production titer for both clade 2.1.3 and clade 2.3.2 compared to the two other siRNA candidates, including siRNA-NP1433 and siRNA-NP1496. The siRNANP672 also provides a better and more consistent reduction of viral gene expression levels, including nucleoprotein, polymerase acidic, hemagglutinin, neuraminidase, Matrix, dan non-structural. This finding was confirmed by bioinformatic analyses of the siRNA-NP672 biding site in the secondary and tertiary structure of the nucleoprotein gene which has more free parts (loop) compared to the two other siRNA-NP candidates. Subsequently, three serial exposures of siRNA-NP do not induce any mutation on the target site of the nucleoprotein gene of the H5N1 virus both clade 2.1.3 and 2.3.2. Conclusion: The design of siRNA-NP672 provides a better prospect to reduce the Indonesian avian influenza virus subtype H5N1 infection for both clade 2.1.3 and 2.3.2."
Jakarta: Fakultas Kedokteran Universitas Indonesia, 2022
D-pdf
UI - Disertasi Membership  Universitas Indonesia Library
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Kartika Laksmi H
"[DENV merupakan sebuah virus yang penularannya melalui vektor nyamuk, yaitu Aedes aegypti. Virus ini terdiri dari 4 tipe, yaitu DENV-1, DENV-2, DENV-3, dan DENV-4. Infeksi DENV banyak terjadi pada negara dengan iklim tropis, diantaranya seperti Karibia, Asia Tenggara, serta Pasifik Barat. Indonesia termasuk salah satu negara dengan endemis infeksi DENV di seluruh wilayahnya. Hingga saat ini, tatalaksana yang diberikan untuk pasien dengan infeksi DENV masih berupa tatalaksana suportif dikarenakan belum ditemukan obat yang efektif untuk mengobati keempat tipe DENV. Ekstrak daun Shorea spp. disinyalir memiliki kemampuan untuk menginhibisi DENV sehingga dapat digunakan sebagai antiviral. Pada penelitian ini, sel Huh7It-1diinfeksikan dengan DENV dan diberikan ekstrak Shorea spp. dengan berbagai konsentrasi. Efektifitas ekstrak diteliti dengan menggunakan konsentrasi 320 μg/ml, 160 μg/ml, 80 μg/ml, 40 μg/ml, 20 μg/ml, dan 10 μg/ml. Efek inhibisi diuji menggunakan metode Focus Assay. Sedangkan efek sitotoksik diuji menggunakan metode MTT Assay. Pada penelitian ini didapatkan nilai sitotoksik (CC50) ekstrak terhadap sel dan nilai inhibisi (IC50) ekstrak terhadap DENV, yaitu nilainya sebesar 150,85 μg/ml dan 23,22 μg/ml. Berdasarkan nilai IC50 dan CC50, didapatkan nilai Selectivity Index (SI) sebesar 6,496. Hal ini menunjukkan bahwa ekstrak daun Shorea spp. memiliki efek inhibisi terhadap DENV dan dapat dikembangkan sebagai antiviral terhadap DENV di masa mendatang.;DENV is a virus transmitted through mosquito vectors, named Aedes aegypti. This virus consists of four types, which is DENV-1, DENV-2, DENV-3 and DENV-4. DENV infection are more prevalent in countries with tropical climates, such as the Caribbean, Southeast Asia, and the Western Pacific. Indonesia is one of the country with endemic DENV infection founded in the entire region. Until now, the treatment which is given to patients with DENV infection is still in the form of supportive treatment, because effective drugs to treat the four types of DENV has not been discovered yet. Leaf extract of Shorea spp. allegedly has the ability to inhibit DENV which acts as an antiviral. In this study, Huh7lt cell was infected with DENV and was given Shorea spp. extracts in various concentrations from 320 μg/ml, 160 μg/ml, 80 μg/ml, 40 μg/ml, 20 μg/ml, and 10 μg/ml. Inhibitory effect was tested by using focus assay, while cytotoxic effect was tested by using MTT assay. In this study, the extract's cytotoxic value (CC50) against cell and inhibition values (IC50) against DENV was determined, with the results 150.85 μg/ml and 23.22 μg/ml. Based on value of IC50 dan CC50, Selectivity Inde x (SI) score was 6,496. This indicates that the leaf extract of Shorea spp. has inhibitory effects against DENV and could be developed as an antiviral againsts DENV in the future;DENV is a virus transmitted through mosquito vectors, named Aedes aegypti. This virus consists of four types, which is DENV-1, DENV-2, DENV-3 and DENV-4. DENV infection are more prevalent in countries with tropical climates, such as the Caribbean, Southeast Asia, and the Western Pacific. Indonesia is one of the country with endemic DENV infection founded in the entire region. Until now, the treatment which is given to patients with DENV infection is still in the form of supportive treatment, because effective drugs to treat the four types of DENV has not been discovered yet. Leaf extract of Shorea spp. allegedly has the ability to inhibit DENV which acts as an antiviral. In this study, Huh7lt cell was infected with DENV and was given Shorea spp. extracts in various concentrations from 320 μg/ml, 160 μg/ml, 80 μg/ml, 40 μg/ml, 20 μg/ml, and 10 μg/ml. Inhibitory effect was tested by using focus assay, while cytotoxic effect was tested by using MTT assay. In this study, the extract's cytotoxic value (CC50) against cell and inhibition values (IC50) against DENV was determined, with the results 150.85 μg/ml and 23.22 μg/ml. Based on value of IC50 dan CC50, Selectivity Inde x (SI) score was 6,496. This indicates that the leaf extract of Shorea spp. has inhibitory effects against DENV and could be developed as an antiviral againsts DENV in the future, DENV is a virus transmitted through mosquito vectors, named Aedes aegypti. This virus consists of four types, which is DENV-1, DENV-2, DENV-3 and DENV-4. DENV infection are more prevalent in countries with tropical climates, such as the Caribbean, Southeast Asia, and the Western Pacific. Indonesia is one of the country with endemic DENV infection founded in the entire region. Until now, the treatment which is given to patients with DENV infection is still in the form of supportive treatment, because effective drugs to treat the four types of DENV has not been discovered yet. Leaf extract of Shorea spp. allegedly has the ability to inhibit DENV which acts as an antiviral. In this study, Huh7lt cell was infected with DENV and was given Shorea spp. extracts in various concentrations from 320 μg/ml, 160 μg/ml, 80 μg/ml, 40 μg/ml, 20 μg/ml, and 10 μg/ml. Inhibitory effect was tested by using focus assay, while cytotoxic effect was tested by using MTT assay. In this study, the extract's cytotoxic value (CC50) against cell and inhibition values (IC50) against DENV was determined, with the results 150.85 μg/ml and 23.22 μg/ml. Based on value of IC50 dan CC50, Selectivity Inde x (SI) score was 6,496. This indicates that the leaf extract of Shorea spp. has inhibitory effects against DENV and could be developed as an antiviral againsts DENV in the future]"
[;Fakultas Kedokteran Universitas Indonesia, Fakultas Kedokteran Universitas Indonesia], 2015
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UI - Skripsi Membership  Universitas Indonesia Library
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Chinta Novianti Mufara
"ABSTRAK
Kepatuhan sangat dibutuhkan dalam terapi antiretroviral. Kepatuhan yang tinggi dalam terapi antiretroviral dapat menurunkan risiko retensi obat, angka kesakitan bahkan angka kematian.Tujuan penelitian ini untuk mengetahui faktor-faktor yang mempengaruhi kepatuhan ODHA dalam menjalani terapi antiretroviral di Rumah Sakit Persiapan Kabupaten Kaimana. Tehnik pengambilan sampel penelitian ini yaitu consecutive sampling. Analisa data menggunakan uji chi square, serta analisa multivariat dengan regresi logistik. Hasil penelitan dengan 81 responden didapatkan sebagian besar responden memiliki kepatuhan rendah 74,1 . Faktor yang berpengaruh secara signifikan terhadap kepatuhan yaitu pengetahuan tentang HIV OR 10,748, p = 0,001 , lamanya terdiagnosis HIV OR 0,173, p = 0,018 , konsumsi alkohol 1-2 gelas/hari OR 0,184, p = 0,033 konsumsi alkohol >2 gelas/hari OR 0,077, p = 0,027 konsumsi alkohol 0-1 gelas/hari p = 0,040 . Kesimpulan: semakin baik pengetahuan ODHA mengenai HIV maka semakin patuh dalam terapi antiretroviral, semakin banyak konsumsi alkohol dan semakin lama terdiagnosis HIV maka semakin rendah tingkat kepatuhan. Hasil penelitian ini diharapkan dapat bermanfaat bagi upaya peningkatan pelayanan terapi antiretroviral dengan meningkatkan pengetahuan ODHA mengenai HIV. Kata kunci: kepatuhan, ART, pengetahuan HIV, lama terdiagnosis HIV, alkohol, kabupaten kaimana.

ABSTRACT
Name Chinta Novianti MufaraStudy program NursingTitle Factors affecting antiretroviral therapy in people living with HIV in Hospital of Kaimana District Province of Papua Barat Adherence is crucial concern for people undertaking antiretroviral regimen. A high adherence to antiretroviral treatment may lower the risk of drug retention, morbidity, or even mortality rate. This study aimed to identify factors affecting adherence of people living with HIV AIDS to antiretroviral therapy in Kaimana hospital. This quantitative study used descriptive correlational design with cross sectional approach. Consecutive sampling was applied in this study with total sample of 81 respondents. The data were analyzed by using chi square analysis and multivariate analysis with logistic regression. The result suggested a low adherence to the regimen by majority of respondents 74.1 . The most significant factors affecting the adherence were knowledge on HIV OR 10,748, p 0,001 , time since diagnosed with HIV OR 0,173, p 0,018 , alcohol consumption 1 2 glasses day OR 0,184, p 0,033 , alcohol consumption more than 2 glasses day OR 0,077, p 0,027 , alcohol consumption 0 1 glass day p 0,040 . Conclusion the better knowledge of people with HIV AIDS on their own condition, the higher their adherence to ART therapy would be the higher alcohol consumption and longer time since HIV, the lower their adherence to the regimen would be. The study result was suggested for improvement in providing antiretroviral regimen with increase knowledge of people living with HIV AIDS on their own condition. Key words adherence, ART, knowledge on HIV, time since HIV, alcohol, Kaimana District."
2017
S67514
UI - Skripsi Membership  Universitas Indonesia Library
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Juanita L T Samban
"ABSTRAK
Infeksi dengue memiliki prevalensi yang tinggi di dunia, dengan spektrum penyakit yang luas yaitu Demam Dengue, Demam Berdarah Dengue, dan Sindrom Syok Dengue. Namun, tatalaksana yang ada tidak bersifat spesifik. Sudah banyak penelitian yang dilakukan untuk mencari vaksin dan antivirus dengue. Salah satu yang sudah terbukti memiliki efek antivirus dengue adalah senyawa turunan asam galat yaitu propil galat dan etil galat. Penelitian eksperimental ini bertujuan untuk mengetahui efek antivirus campuran propil galat dan etil galat terhadap virus dengue serotipe 2 pada sel Huh7it-1. Efek sitotoksisitas senyawa terhadap sel diuji dengan metode 3- 4,5-dimethylthiazol-2-yl -2,5-diphenyltetrazolium bromide assay. Nilai yang didapat digunakan untuk mencari nilai konsentrasi toksik 50 . Efek inhibisi senyawa terhadap replikasi virus diuji dengan metode focus assay. Nilai yang didapat digunakan untuk mencari nilai konsentrasi hambat 50 . Dari hasil penelitian didapatkan nilai CC50 = 117.942 mg/ml, IC50 = 4.455 mg/ml, dan SI = 26.474. Campuran propil galat dan etil galat memiliki efek antivirus terhadap DENV-2 dan cukup selektif.

ABSTRACT
Dengue infection have a serious prevalence in worldwide with a broad spectrum of disease from dengue fever, dengue hemorrhagic fever, and dengue shock syndrome. Otherwise, the nowadays treatment seems not specific for the dengue itself. There were a lot of study to search for the vaccine and the antivirus. One of the successful study that contained a significant effect of dengue antivirus is a chemical compound from gallate acid named propyl gallate and ethyl gallate. This experimental study aim to know the antivirus effect from the mixture of propyl gallate and ethyl gallate to the dengue virus serotype 2 in Huh7it 1 cells. Cytotoxicity effect of the mixture to the cells tested by 3 4,5 dimethylthiazol 2 yl 2,5 diphenyltetrazolium bromide assay technique. Obtained results can be used to search for the half cytotoxic concentration. The inhibition effect from this mixture to the viral replication processes tested by focus assay technique. Obtained results can be used to search for the half inhibitory concentration. From this study, the value of CC50 is 117.942 g mL, meanwhile the value of IC50 is 4.455 g mL with the SI value is 26.474. The mixture of propyl gallate and ethyl gallate have an antivirus effect to DENV 2 strain which are quite selective."
2017
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UI - Skripsi Membership  Universitas Indonesia Library
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Syifa Salsabila
"ABSTRAK
Demam dengue masih memiliki angka insidensi tinggi terutama di Indonesia. Sampai saat ini, belum ditemukan terapi antivirus dengue. Penelitian untuk mendapatkan antivirus dengue dari sumber herbal sudah banyak dilakukan. Salah satu tanaman yang berpotensi sebagai antivirus dengue adalah Calophyllum nodosum yang diketahui memiliki aktivitas antimikroba. Penelitian ini menguji efek antiviral fraksi butanol Calophyllum nodosum terhadap aktivitas virus dengue tipe 2 dengan sel Huh-7-it sebagai sel host secara in vitro dan konsentrasi inhibisi minimal. Efek antiviral dinilai dengan nilai konsentrasi inhibitorik 50 IC50 dan konsentrasi sitotoksik 50 CC50 . Nilai IC50 menilai efek inhibisi ekstrak dan didapatkan dari hasil focus assay dengan menggunakan konsentrasi ekstrak 80, 40, 20, 10, 5, dan 2,5 g/mL Nilai CC50 menunjukkan efek sitotoksik ekstrak dan dihasilkan dari MTT assay dengan menggunakan konsentrasi 640, 320, 160, 80, 40, 20, dan 10 g/mL Perbandingan IC50 dan CC50 menghasilkan indeks selektivitas SI . Hasil IC50 adalah 5.6 g/mL dan hasil CC50 adalah 1181 g/mL sehingga didapatkan SI 210.9. Konsentrasi inhibisi minimal adalah 2.5 g/mL. Analisis statistic menunjukkan perbedaan bermakna antara kelompok control dengan kelompok perlakuan pada focus assay dan MTT assay. Dapat disimpulkan bahwa fraksi butanol Calophyllum nodosum memiliki efek antiviral tinggi dibandingkan efek sitotoksiknya.

ABSTRACT
Dengue fever still has a high incidence rate especially in Indonesia. Until now, there is no dengue antiviral therapy found. Researches to develop dengue antiviral from herbal sources had been done. One of the potential plants as dengue antiviral is Calophyllum nodosum which is known to have antimicrobial activity. This research evaluated the antiviral effects of butanol fraction of Calophyllum nodosum on DENV 2 activity with Huh 7 it cells as host cells in vitro and also evaluated minimal inhibitory concentration. Antiviral effects were assessed with 50 inhibitory concentration IC50 and 50 cytotoxic concentration CC50 values. The value of IC50 showed the effect of extract inhibition and is obtained from the focus assay results using the extract concentrations of 80, 40, 20, 10, 5, and 2.5 g mL. The CC50 value showed the effect of cytotoxic extract and resulted from MTT assay using concentrations of 640, 320 , 160, 80, 40, 20, and 10 g mL. Ratio of CC50 and IC50 is the selectivity index SI . The value of IC50 is 5.6 g mL and the value of CC50 is 1181 g mL and resulted in SI 210.9. The minimum inhibitory concentration is 2.5 g mL. Statistical analysis showed significant differences between control group and treatment group on focus assay and MTT assay. It can be concluded that the butanol fraction of Calophyllum nodosum has a high antiviral effect compared to its cytotoxic effects"
2017
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UI - Skripsi Membership  Universitas Indonesia Library
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Susilawati Sabri
"ABSTRAK
Demam berdarah dengue DBD merupakan salah satu penyakit infeksi yang prevalensinya masih tinggi di Indonesia. Peningkatan insidensi DBD terjadi secara luas pada dekade terakhir ini. Pada tahun 2016, WHO telah mengumumkan vaksin untuk DBD pertama kalinya. Namun, masih dilaporkan kasus infeksi virus dengue DENV. Manajemen klinis berdasarkan dari terapi suportif. Karena, belum ada pengobatan antiviral yang spesifik untuk mengatasi penyakit DBD. Penelitian ini dilakukan secara eksperimental menggunakan ekstrak batang Calophyllum canum dan Sel Huh7it-1 untuk menguji infektivitas dan viabilitas sel terhadap DENV-2 dengan metode Focus Assay dan MTT 3- 4,5- dimetiltiazol-2-il -2,5-difeniltetrazolium bromid assay. Hasil yang didapatkan yaitu nilai 50 Inhibitory Concentration IC50, 50 Cytotoxic Concentration CC50, dan Indeks Selektivitas IS dari uji ekstrak Calophyllum canum fraksi butanol sebesar 12,01 g/mL, 152,91 g/mL, dan 12,73 secara berturut-turut. Ekstrak Calophyllum canum fraksi butanol memiliki potensi sebagai antiviral terhadap DENV-2.

ABSTRACT
Dengue hemorrhagic fever DHF is one of the infectious disease that has prevalence is still high in Indonesia. Increased incidence of DHF occurred widely in the last decade. In 2016, WHO has announced the vaccine for DHF for the first time. However, there is still reported cases of dengue virus infection DENV. Clinical management is based on supportive therapy. Because, there is no specific antiviral treatment for dengue disease. This study was conducted experimentally using extracts of Calophyllum canum and Huh7it 1 cell to examined the infectivity and viability of cells against DENV 2 by Focus Assay and MTT 3 4,5 dimetiltiazol 2 il 2,5 difeniltetrazolium bromid assay methods. The results obtained are 50 Inhibitory Concentration IC50, 50 Cytotoxic Concentration CC50, and Selectivity Index SI values from Calophyllum canum extracts of butanol fraction of 12.01 g mL, 152.91 g mL, and 12.73, respectively. Calophyllum canum extract of butanol fraction has potency as an antiviral against DENV 2."
2017
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UI - Skripsi Membership  Universitas Indonesia Library
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Abritho Zaifar
"ABSTRACT
Virus Dengue (DENV) adalah salah satu penyakit virus dengan transmisi oleh nyamuk dan telah menyebar ke negara negara yang sebelumnya tidak pernah ada kejadian infeksi DENV. Walaupun demikian, belum ada obat antivirus berlisensi yang efektif. Salah satu agen alami yang diduga memiliki sifat anti virus terhadap
DENV adalah asam galat yang telah terbukti memiliki sifat antivirus terhadap Herpes Simplex Virus 1 (HSV 1). Tujuan dari penelitian ini adalah untuk mempelajari toksisitas dan efektifitas amyl galat sebagai antivirus untuk DENV secara in vitro. Huh 7it-1 sel diinfeksikan dengan DENV 2 NGC strain yang telah diberi perlakuan dengan amyl galat pada konsentrasi 80 μg/ mL, 40 μg/ mL, 20 μg/
mL, 10 μg/ mL, 5 μg/ mL, dan 2.5 μg/ mL. Viabilitas sel setelah diberi perlakuan dengan amyl galat kemudian diukur dengan MTT assay menggunakan spektrofotometer, sementara inhibisi virus oleh amyl galat diukur dengan menggunakan focus assay. Untuk menguji validitas dan perbedaan yang signifikan data uji statistik Kruskal Wallis dilakukan kepada setiap variabel dan uji Mann- Whitney juga digunakan untuk membandingkan hasil dengan kontrol negatif. Nilai CC50, IC50, dan SI dari penelitian adalah >80 ug/mL, 6 ug/mL, dan >13.333. Viabilitas sel setelah diberi amyl galat dengan konsentrasi 2.5 mg/mL tidak berbeda secara bermakna dengan control (P>0.05) akan tetapi pada konsentrasi ≥ 5 ug/mL ada perbedaan yang bermakna dengan kontrol (P<0.05). Hambatan infektivitas pada perlakuan amyl galat dengan konsentrasi 2.5 ug/mL, 5 ug/mL tidak berbeda secara bermakna dengan kontrol (P>0.05) namun pada konsentrasi ≥ 10 ug/mL ada perbedaan bermakna dengan control (P<0.05). Amyl galat mempunyai selektivitas yang signifikan terhadap sel yang terinfeksi DENV (SI>10) dan dapat disimpulkan bahwa amyl galat mempunyai potensi untuk dipakai sebagai obat anti virus melawan DENV, namun kajian dan percobaan lebih lanjut masih diperlukan.

ABSTRACT
Dengue virus (DENV) is a viral disease transmitted by mosquitoes and has spread to countries where there has never been a DENV infection. However, there are no effective antiviral drugs available. One of the natural agents suspected of having anti-virus properties is against DENV is gallic acid which has been proven to have antiviral properties against Herpes Simplex Virus 1 (HSV 1). The aim of this research is to study the toxicity and effectiveness of amyl galat as an antiviral for DENV in vitro. Huh 7it-1 cells were infected with DENV 2 NGC strains that had been treated with amyl error at concentrations of 80 μg / mL, 40 μg / mL, 20 μg /
mL, 10 μg / mL, 5 μg / mL, and 2.5 μg / mL. Cell viability after being treated with amyl error was then measured by MTT assay using a spectrophotometer, while viral inhibition by amyl error was measured using focus assay. To test the validity and significant differences Kruskal Wallis statistical test data was performed on each variable and the Mann-Whitney test was also used to compare results with negative controls. Score CC50, IC50, and SI of the study were > 80 μg / mL, 6 μg / mL, and > 13,333. Cell viability after being given amyl error with a concentration of 2.5 mg / mL was not significantly different from control (P > 0.05) but at a concentration of ≥ 5 ug / mL there was a significant difference with control (P < 0.05). Barriers to infectivity in the treatment of amyl galat with a concentration of 2.5 μg / mL, 5 μg / mL did not differ significantly with control (P > 0.05) but at concentrations ≥ 10 ug / mL there were significant differences with control (P < 0.05). Amyl error has a significant selectivity to cells infected with DENV (SI > 10) and can be concluded
that amyl error has the potential to be used as an antiviral drug against DENV, but further studies and trials are still needed."
2017
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UI - Skripsi Membership  Universitas Indonesia Library
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