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ISOLATION AND STRUCTURE ELUCIDATIONS OF RESVERATROL OLIGOMERS FROM STEM BARK OF Dryobalanops lanceolata Sahidin Sahidin
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (295.396 KB) | DOI: 10.22146/ijc.21549

Abstract

Five resveratrol oligomers which consist of two resveratrol dimers, balanocarpol (1) and ε-viniferin (2), α resveratrol trimer i.e. α-viniferin (3), and two resveratrol tetramers, vaticanol B (4), and hopeaphenol (5) have been isolated from acetone extract of the stem bark of Dryobalanops lanceolata. These compounds were isolated by vacuum liquid chromatography method. Furthermore, the compound structures were determined based on the spectroscopic evidence, including UV, IR, 1-D and 2D NMR spectra, and comparing with those related data reported previously.
RESVERATROL DIMERS FROM STEM BARK OF Hopea gregaria AND THEIR CYTOTOXIC PROPERTIES Sahidin Sahidin; Euis Holisotan Hakim; Yana Maolana Syah; Lia Dewi Juliawaty; Sjamsul Arifin Achmad; Laily Bin Din; Jalifah Latip
Indonesian Journal of Chemistry Vol 8, No 2 (2008)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (266.862 KB) | DOI: 10.22146/ijc.21629

Abstract

Six resveratrol dimers have been isolated from the stem bark of H. gregaria, ampelopsin A (1), balanocarpol (2), ε-viniferin (3), hopeafuran (4), heimiol A (5), and parviflorol (6). The structures of these compounds were determined based on spectroscopic evidence such as UV, IR, 1-D, 2-D NMR and comparison with the reported data. These compound inventions are strengthen conclusion that Hopea tends to produce resveratrol dimers. Biological activity of those compounds against murine leukemia P-388 cells showed that ε-viniferin (3) is the most active compound with IC50 value 5.1 ± 0.3 μg/mL.
Formulasi dan Karakterisasi Ekstrak Etanol Wualae (Etlingera elatior) dalam Sistem Penghantaran Vesikuler Fitofosfolipid Astrid Indalifiany; Sahidin Sahidin; Wahyuni Wahyuni; Mentarry Bafadal; Agung Wibawa Mahatva Yodha; Rina Andryani; La Ode Muhammad Fitrawan; Dian Munasari
Jurnal Mandala Pharmacon Indonesia Vol. 8 No. 1 (2022): Jurnal Mandala Pharmacon Indonesia
Publisher : Program Studi Farmasi Universitas Mandala Waluya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.35311/jmpi.v8i1.152

Abstract

Etlingera elatior (Wualae) termasuk dalam tumbuhan famili zingiberaceae yang memiliki aktivitas antiinflamasi. Namun, bioavailabilitas dan permeabilitas zat aktif yang rendah sehingga diperlukan suatu sistem penghantaran dalam komplek lipid-bahan alam. Sistem yang dikenal dengan fitofosfolipid ini merupakan penghantaran fitokonstituen dalam matriks fosfolipid yang dapat meningkatkan permeabilitas dan bioavailabilitas zat aktif melalui karakteristik ampifilik dan aksi emulsifikasi oleh fosfolipid. Penelitian ini bertujuan untuk melakukan formulasi dan karakterisasi sistem vesikel sehingga diperoleh sistem yang optimum antara ekstrak etanol buah wualae dan fosfatidilkolin yang memiliki karakteristik vesikel terbaik. Preparasi dilakukan    menggunakan    teknik    hidrasi    lapis   tipis dengan adanya variasi komposisi ekstrak dan fosfatidilkolin, yakni 0,5:0,5 (Formula 1); 0,5:1 (Formula 2); 1:0,5 (Formula 3); 1:1 (Formula 4); 1:2 (Formula 5); dan 2:1 (Formula 6). Hasil yang diperoleh adalah komposisi formula optimum antara ekstrak dan fosfatidilkolin yaitu pada F4 dengan komposisi 1:1 dengan karakterisasi meliputi pengamatan morfologi berbentuk bulat (sferis) menggunakan mikroskop optic, efisiensi penjerapan vesikel diperoleh 99,20%, ukuran partikel 898,2 nm dan indeks polidispersitas 0,573 dengan kategori vesikel jenis LUV (Large Unilamellar Vesicle) menggunakan Particel Size Analyzer.
Aktivitas Imunomodulator Ekstrak Etanol Buah Etlingera rubroloba A.D. Poulsen Terhadap Fagositosis Sel Makrofag Pada Tikus Jantan Galur Wistar Fadhliyah Malik; Mentarry Bafadal; Dian Munasari; Rina Andriani; Muh. Ilyas Yusuf; Sahidin Sahidin; Wahyuni Wahyuni; Adryan Fristiohady; Wa Ode Nurfinti
Jurnal Mandala Pharmacon Indonesia Vol. 8 No. 1 (2022): Jurnal Mandala Pharmacon Indonesia
Publisher : Program Studi Farmasi Universitas Mandala Waluya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.35311/jmpi.v8i1.171

Abstract

Fungsi sistem imun adalah untuk melindungi tubuh dari benda-benda asing, dimana sistem imun dapat ditingkatkan dengan pemberian imunomodulator. Pendekatan kemotaksonomi Genus Etlingera memungkinkan Etlingera rubroloba A.D. Poulsen memiliki kandungan metabolit sekunder sebagai agen imunomodulator. Penelitian dimaksudkan untuk mengetahui aktivitas imunomodulator ekstrak etanol buah Etlingera rubroloba A.D. Poulsen terhadap fagositosis sel makrofag pada tikus jantan galur wistar. Hewan uji tikus sebanyak dua puluh empat ekor dibagi dalam enam kelompok perlakuan yaitu kontrol negatif (Na-CMC 0,5%), kontrol positif (ekstrak meniran komersial), kontrol normal (tanpa perlakuan), perlakuan dosis 1 (200 mg/kgBB), perlakuan dosis 2 (300 mg/kgBB)  dan  perlakuan dosis 3  (400 mg/kgBB). Perlakuan diberikan selama tujuh hari berturut-turut secara per oral  dan diberikan injeksi bakteri Staphylococcus aureus 0,5 mL secara intraperitonial pada hari kedelapan masing-masing kelompok. Apusan cairan peritoneum digunakan untuk menentukan aktivitas sel makrofag. Hasil penelitian menunjukkan aktivitas fagositosis sel makrofag pada kelompok kontrol negatif, kontrol positif, perlakuan 1, perlakuan 2, perlakuan 3 berturut-turut 36,75 %, 74,25%, 71.75%, 80,50%, 70,75%. Hasil penelitian menunjukkan pemberian ekstrak etanol buah Etlingera rubroloba A.D. Poulsen memiliki aktivitas imunomodulator terhadap fagositosis sel makrofag.
FORMULATION AND PHYSICAL STABILITY TEST OF NANOEMULGEL CONTAINING Petrosia Sp. ETHANOLIC EXTRACT Muhammad Hajrul Malaka; Astrid Indalifiany; Sahidin Sahidin; Adryan Fristiohady; Rina Andriani
Jurnal Farmasi Sains dan Praktis Vol 7 No 3 (2021): Supplementary Issue (The 4th National Pharmacy Conference 2021 Universitas Halu O
Publisher : Universitas Muhammadiyah Magelang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.31603/pharmacy.v7i3.6080

Abstract

Petrosia sp. is one of the sponges from the demospongia class that has biological activity as anti-inflammatory, antimalarial, cytotoxic agent, and can be used in nanoemulgel formulation. Nanoemulsion system is thermodynamically stable and produces globule size that can increase the permeability and diffusibility of Petrosia sp. The presence of gelling agent in the nanoemulgel gives the viscosity and spreadability of Petrosia sp nanoemulsion optimally to increase the effectiveness of the active substances on the skin. This study aims to determine the formulation, characterization, and physical stability of nanoemulgel ethanol extract of sponge Petrosia sp. with carbopol 940 as the gel base. Nanoemulsion characterization included transmittance value, particle size, polydispersity index, and type of emulsion formed. The physical stability test of nanoemulgel included centrifugation and freeze thaw tests with organoleptic, pH, viscosity, and dispersibility evaluation. Nanoemulsion of Petrosia sp ethanolic extract with a composition of 1% VCO, 7% Tween-80, and 2% PEG-400 produced an oil-in-water (O/W) nanoemulsion, transmittance value of 94.84%, droplet size of 23.9 nm and particle size distribution of 0.176. The optimum formula for nanoemulgel is F1 with a nanoemulsion concentration of 75 mL and 25 g of gel base produced a clear and transparent nanoemulgel, semi-solid, soft texture, distinctive aroma, pH value of 5, viscosity of 28,000, dispersibility of 5.7 cm and the shape/color did not change after freeze thaw stability test. Based on the data above, it can be concluded that the F1 nanoemulgel formula with carbopol 940 as the base gel produced an optimal nanoemulgel.
ANTIHYPERURICEMIA ACTIVITY OF WUALAE FRUIT (Etlingera elatior Jack R. M. Smith) ETHANOL EXTRACT IN VIVO Asriullah Jabbar; Wahyuni Wahyuni; Mesi Leorita; Muhammad Ilyas Yusuf; Sahidin Sahidin
Jurnal Farmasi Sains dan Praktis Vol 7 No 3 (2021): Supplementary Issue (The 4th National Pharmacy Conference 2021 Universitas Halu O
Publisher : Universitas Muhammadiyah Magelang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.31603/pharmacy.v7i3.6083

Abstract

Plants Etlingera elatior (Wualae) is a family Zingiberaceae of ​​the genus Etlingera which has a large population in the world. The E. elatior plant is widely used empirically in the community to increase endurance and seasoning in fruit. In this study, ethanol extract was used to determine its potential and effectiveness as an antihyperuricemia (in vivo) was tested pharmacologically on Rattus novergicus L. In this study, twenty-four rats were grouped into six groups, namely the ethanol extract of wualae fruit at a dose (100 mg/kgBW, 200 mg/kgBW, 300 mg/kgBW, 400 mg/kgBW), and the negative control group Sodium CMC 0 .5%, and the positive control group used Allopurinol 10 mg/kgBW. Furthermore, To increase the value of uric acid levels, the rats were first induced with 250 mg/kgBW Potassium Oxonate via intraperitoneal (i.p). Furthermore, the preparation according to the treatment was given orally one hour later after the administration of potassium oxonate. At the hour (1, 2, 3), the blood was taken intravenously (i.v) through the rat's tail, and then the uric acid level was analyzed with a photometer. All doses used in this study, namely 100, 200, 300, and 400 mg/kgBW, showed that they could reduce uric acid overall. The effective dose used is the dose (300 mg/kgBW, 400 mg/kgBW). This research can be concluded that the ethanol extract of the fruit of Etlingera elatior (Jack) R.M. Smith (Wualae) has potential as an antihyperuricemia (uric acid) and can be developed as a traditional medicine
ISOLATION AND IDENTIFICATION OF ANTIOXIDANT COMPOUNDS FROM METHANOL EXTRACT OF SAPPAN WOOD (Caesalpinia sappan) Agung Wibawa Mahatva Yodha; Muamar Abdillah; Astrid Indalifiany; Elfahmi Elfahmi; Sahidin Sahidin
Jurnal Farmasi Sains dan Praktis Vol 7 No 3 (2021): Supplementary Issue (The 4th National Pharmacy Conference 2021 Universitas Halu O
Publisher : Universitas Muhammadiyah Magelang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.31603/pharmacy.v7i3.6096

Abstract

Sappan wood extract (Caesalpinia sappan) provides better antioxidant properties than ascorbic acid. Empirically, Sappan wood is often used as traditional medicine. To support the utilization of Sappan wood, the isolation and identification of active antioxidant compounds from the methanol extract of Sappan wood had been conducted from this study. Extraction was performed with maceration and evaporation methods. The spots of active antioxidant compounds in TLC-DPPH observations were isolated using liquid vacuum chromatography to obtain two pure compounds. The results of the LC-MS/MS identification of the two compounds, respectively, exhibited peak fragmentation of molecular ions at m/z 271.09, 257.15, 167.03, 151.06, 123.12, and 104.06 at the retention time of 6.35 minutes which were translated as Alpinetine and peak fragmentation of molecular ion at m/z 287.09, 177.06, 164.05, 123.04 and 110.04 at a retention time of 5.75. minutes which were translated as 3-Deoxysappanone B. The antioxidant activity quantitatively showed that Alpinetine and 3-Deoxysappanone B were capable of scavenging DPPH radicals with IC50 values ​​of 20.11 M and 15.28 M, respectively.
CYTOTOXIC ACTIVITY OF KASUMBA FLOWER ETHANOL EXTRACT TURATE (Carthamus tinctorius Linn.) AGAINST THE LINE OF CANCER CELLS T47D BREASTS Fadhliyah Malik; Muhammad Hajrul Malaka; Adryan Fristiohady; Wahyuni Wahyuni; Rini Hamsid; Sahidin Sahidin; Annisa Fatinah Gani
Jurnal Farmasi Sains dan Praktis Vol 7 No 3 (2021): Supplementary Issue (The 4th National Pharmacy Conference 2021 Universitas Halu O
Publisher : Universitas Muhammadiyah Magelang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.31603/pharmacy.v7i3.6113

Abstract

Breast cancer is a type of cancer with a high prevalence in the world and causes death in women. Chemotherapy is one type of treatment that is widely used. However, the problems of chemotherapy drugs such as side effects, drug resistance and inadequate efficacy. So, to overcome these problems, many natural ingredients have been explored to find anticancer agents that are expected to have good efficacy with minor side effects. Kasumba turate flowers (Carthamus tinctorius Linn.) is a plant from the Asteraceae tribe which is known to contain secondary metabolites with pharmacological activity as anticancer. This study aims to determine the types of secondary metabolites and the cytotoxic activity of the ethanolic extract of Kasumba turate flower against the T47D breast cancer cell line using the MTT assay method. Kasumba turate flower extract was obtained by maceration using 96% ethanol solvent, so that a concentrated extract with a weight of 107.8 grams was obtained with a yield value of 10.81%. The extract obtained was then subjected to a phytochemical screening test using the tube method and the results are alkaloids, flavonoids, tannins, and terpenoids. In the cytotoxic activity test, the test samples were varied into 7 concentration series, namely 10, 50, 100, 200, 400, 800 and 1000 ppm. The positive control used was 5-Fu. Cytotoxic parameter (IC50 value) was determined using GraphPad Prism and obtained IC50 5-Fu value of 65.88 ppm with active category while IC50 of the test sample was 157.3 with moderately active category as anticancer breast.
ETLINGERA GENUS: PHYTOCHEMICAL SCREENING AND ANTICANCER ACTIVITY Wahyuni Wahyuni; Ajeng Diantini; Mohammad Ghozali; Sahidin Sahidin
Jurnal Farmasi Sains dan Praktis Vol 7 No 3 (2021): Supplementary Issue (The 4th National Pharmacy Conference 2021 Universitas Halu O
Publisher : Universitas Muhammadiyah Magelang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.31603/pharmacy.v7i3.6120

Abstract

Etlingera is one of the plant genera from the Zingiberaceae family and is widely distributed in Asia to the Pacific Islands, with various species ranging from 150 to 200 species. The Etlingera are commonly used as spices, vegetables, and traditional medicines. Many pharmacological activities have been reported from this genus, including antioxidants, antibacterials, cholesterol-lowering, anticancer, and others. The phytochemical content of Etlingera reported are phenolics, diarylheptanoids, flavonoids, steroids, alkaloids, and terpenoids. Eight species from Etlingera, namely Etlingera elatior, E. pavieana, E. brevilabrum, E. pyramidosphaera, E. megalocheilos, E. coccinea, E. fimbriobracteata, and E. corneri are reported provided anticancer activity. This review article aims to review the phytochemical screening from Etlingera genus, and its anticancer activity.
CYTOTOXIC ACTIVITY OF ETHANOL EXTRACT Petrosia sp. IN VITRO AGAINST CANCER CELLS HeLa Mentarry Bafadal; Wa Ode Mutiara; Muhammad Hajrul Malaka; Adryan Fristiohady; Agung W. M. Yodha; Baru Sadarun; Sahidin Sahidin
Jurnal Farmasi Sains dan Praktis Vol 7 No 3 (2021): Supplementary Issue (The 4th National Pharmacy Conference 2021 Universitas Halu O
Publisher : Universitas Muhammadiyah Magelang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.31603/pharmacy.v7i3.6121

Abstract

Cervical cancer is one of the highest causes of death in Indonesian women caused by mutations of normal cervical cells turning into abnormal cells. Treatment of cervical cancer causes significant side effects with a relatively long treatment period, so many researchers are exploring various natural ingredients from marine ecosystems as candidates for anticancer drugs. One of them is the sea sponge Petrosia sp. containing various secondary metabolites, one of which is an alkaloid that has a cytotoxic effect on cancer cell lines. This study aims to determine the cytotoxic activity of the ethanol extract of Petrosia sp. in HeLa cervical cancer cells. The ethanol extract of Petrosia sp. obtained by maceration using 96% ethanol and obtained extract as much as 55.9 g and yield value of 2.94%. Cytotoxic activity test was carried out in vitro using the Presto Blue method with varying concentrations of ethanol extract 7.81 ppm; 15.62 ppm; 31.25 ppm; 62.5 ppm; 125 ppm; 250 ppm; 500 ppm; and 1000 ppm. The cytotoxic parameter used was IC50 which was determined using the GraphPad Prism software version 5. The IC50 value of the marine sponge extract Petrosia sp. of 97.20 ppm or 97.20 g/ml with an active category as cervical anticancer. Cervical cancer is one of the highest causes of death in Indonesian women caused by mutations of normal cervical cells turning into abnormal cells. Treatment of cervical cancer causes significant side effects with a relatively long treatment period, so many researchers are exploring various natural ingredients from marine ecosystems as candidates for anticancer drugs. One of them is the sea sponge Petrosia sp. containing various secondary metabolites, one of which is an alkaloid that has a cytotoxic effect on cancer cell lines. This study aims to determine the cytotoxic activity of the ethanol extract of Petrosia sp. in HeLa cervical cancer cells. The ethanol extract of Petrosia sp. obtained by maceration using 96% ethanol and obtained extract as much as 55.9 g and yield value of 2.94%. Cytotoxic activity test was carried out in vitro using the Presto Blue method with varying concentrations of ethanol extract 7.81 ppm; 15.62 ppm; 31.25 ppm; 62.5 ppm; 125 ppm; 250 ppm; 500 ppm; and 1000 ppm. The cytotoxic parameter used was IC50 which was determined using the GraphPad Prism software version 5. The IC50 value of the marine sponge extract Petrosia sp. of 97.20 ppm or 97.20 g/ml with an active category as cervical anticancer.
Co-Authors ,, Suryani A.A. Ketut Agung Cahyawan W Abdi Nipangeran Abdul Fajar La Ode Abdul Karim Abdul Khoir HS Abdulkadir Kamaluddin Achmad, SA Ade Dedi Rohayana Adriatman Rasak ADRYAN FRISTIOHADY Adryan Fristiohadi Adryan Fristiohady Adryan Fristiohady Adryan Fristiohady Adryan Fristiohady Adryan Fristiohady Adryan Fristiohady Adryan Fristiohady Adryan Fristiohady Adryan Fristiohady Adryan Fristiohady Adryan Fristiohady Adryan Fristiohady Adryan Fristiyohadi Agung Wibawa Mahatva Yodha Agustina Agustina Ahmad Nursodiq Ahmad Zaeni Ajeng Diantini, Ajeng Alyza Zaulya Amalia Alfitrianingrum Amalia, Riezki Amaliah Amaliah Amaliah, Wa Ode Fitri Amir Tajrid Ananda, M Aflahmuna Anas Subarnas Andi Septiana Andini Sundowo Andini Sundowo Andini Sundowo Andini Sundowo Andini Sundowo Andriani, Rina Andryani Ningsih Angriani Fusvita Annisa Fatinah Gani Arba, Muh. Arba, Muhammad ARDIANSYAH ARDIANSYAH Ardiansyah Ardiansyah Arfan Arfan Arfan Arfan Arfan ARFAN ARFAN Ari Sartinah Ari Sartinah, Ari Aries Saifudin Arif Rahman Hakim Asasutjarit, Rathapon Asman Sadino Asman Sadino Asman Sadino ASMAN SADINO, ASMAN Asmawati Asmawati ASNANI ASNANI Asniar Pascayantri Asniar Pascayantri Asnita Hafsani Aspadiah, Vica Asriullah Jabbar Asriullah Jabbar Asriullah Jabbar Asriullah Jabbar Asriullah Jabbar Asrul Sani Asrul Sani, Asrul Asrun Budiatma Astri Alawia Astrid Indalifiany Atasya, Fretiniar Ayu Wulandari Badia, Esti Bafadal, Mentarry Baru Sadarun Baru Sadarun Baru Sadarun Baru Sadarun Baso, La Bonni Rubak Budikafa, Muhammad Jefriyanto Cicilia, Retno Daud, Nur Saadah Dayatriana Muthalib Dewi Puspita Dewiyanti Madu Dian Munasari Diasty Nuraisya Din, LB Dzaky Aulia Rahman EH Hakim Elfahmi Elfahmi, Elfahmi Euis H. Hakim Euis Holisotan Hakim Euis Holisotan Hakim Euis Julaeha Fadeli Ehsan Hanafi Fadhliyah Malik Fahria Nadiryati Sadimantara Fahria Nadiryati Sadimantara Fahriah Nadiryati Sadimantara Faisal Faisal Fajri Fitra Amalia FANNY RAHMADHANI .N Fathan Ramadhan Fatima, Nur Fauzia Azzahra, Fauzia Fauziah, Yulianti Febrianti, Sari Firasmi Sangadji Firdayanti Firdayanti Firdayanti, Firdayanti Firman Oktivendra Fitrawan, La Ode Muhammad Fitrawan, La Ode Muhammad Fredy Talebong Frely Cristiadzi Fawaz Fristiohady Adryan Fristiohady, Adryan Galih, Olga Grasiana Eka E.Y.G Gunawan, Syahrul Gusti Ray Sadimantara Gusti Ray Sadimantara Gusti Ray Sadimantara Hadad, Nur Diana Haera, Evi Hadrawati Hair, La Hajah Ningsih Inta Hakim, EH Hakini, EuisH Halik, Halik Hamsah, Hamsah Handayani, Lili Sri HANIFAH, SYIFA Hariana Haristan, Haristan Harnita, Wa Ode Hartina Hartina Haruna, Lidya A. Haruna, Lidya Agriningsih HASLIANTI HASLIANTI Hasnawati Hasnawati Hasnawati Hasriani H Japar Hastiar, Arfiani Helmia, Wa Ode Nia Hendra Febriansyah Hendrawan Tulungi, Wahyu Hikmayani I W. Sutapa Ibnu Nurrahman, Pandu Idhul Ade Rikit Fitra Idrus, Loly Subhiaty Ilhan Fauzan Ilma Sarimustaqiyma Rianse Ilyas Y, Muhammad Ilyas Y., Muhammad Imam Yahya Imran Imran Imran Indalifiany, Astrid Intan Permata Putri Iren Meylani Irnawati Irnawati Irnawati Irnawati Irnawati Irnawati Irnawati Irnawati Irnawati Irvan Anwar Izzati, Emy J Latip Jabbar, Asriullah Jalifah Latip Jalifah Latip Jamili Jamili Japar, Hasriani H. Juliawaty, LD Juliawaty, Lia D Jumadil Jumriani Jumriani Junli Hong Kadidae La Ode Kamaluddin Kamaluddin Kangkuso Analuddin Kangkuso Analuddin, Kangkuso Kardin, Laode Karimu, Laila Qodriyah Karmilah, Karmilah Khansa Rafida Triaqilah Kholilah, Aulia Kirana, Rezky Marwah Kuncoro, Shienny L. O. A. N. Ramadhan La Ode Ahmad La Ode MJ Purnama La Ode Muh. Fitrawan La Ode Muh. Julian Purnama La Ode Muhammad Andi Zulbayu La Ode Muhammad Julian Purnama La Ode Muhammad Julian Purnama La Ode Muhammad Julian Purnama La OMJ. Permana Laily Bin Din Laily Bin Din Laode Muhamad Mbuyang Nadia Latip, J LB Din LD Juliawaty Lia D. Juliawaty Lia Dewi Juliawaty Lidya Agriningsih Haruna Lidya Agriningsih Haruna Loly Subhiaty Idrus Loly Subhiaty Idrus Lubis, Adryan Fristiohady M. Hajrul Malaka Malaka, Muh. Hajrul Malaka, Muhammad Hajrul Malaka, Muhammad Hajrul Manggau Marianti Mangurana, Wa Ode Intiyani Mardikasari, Sandra Aulia Marianti A Manggau Marianti A. Manggau Marianti, Manggau Martiani Martiani Maryani Masrika, Nur Upik En Maulana Anwar Mawaddah, Nur Ainul Mega Fatimah Rosana Mentarri Bafadal Mesi Leorita Mesi Leorita Mesi Leorita, Mesi Mini Bekti Ningsih Mirawanti G, Wa Ode Mirda Mirda Mirdayani, Eli Mochammad Imron Awalludin Mohammad Ghozali Muamar Abdillah Mubarak Mubarak Mugiarno, Dita Oktavianti Muh. Arba Muh. Ilyas Yusuf Muhamad Handoyo Sahumena Muhamad Handoyo Sahumena Muhammad Alim Marhadi Muhammad Arba Muhammad Arba Muhammad Azhar Muhammad H Malaka MUHAMMAD HAJRUL MALAKA Muhammad Hajrul Malaka Muhammad Hajrul Malaka Muhammad Hajrul Malaka Muhammad Hajrul Malaka Muhammad Hajrul Malaka Muhammad Hajrul Malaka Muhammad Hajrul Malaka Muhammad Hajrul Malaka Muhammad Hajrul Malaka Muhammad Hajrul Malaka Muhammad Ilyas Muhammad Ilyas Y Muhammad Ilyas Y Muhammad Ilyas Y Muhammad Ilyas Yusuf Muhammad Ilyas Yusuf Muhammad Ilyas Yusuf Muhammad Ilyas Yusuf Muhammad Ilyas Yusuf Muhammad Ilyas Yusuf Muhammad Israwan Azis Muhammad Isrul Muhammad Ramadhan Muhammad Ramli Muhammad Rifky Wahyu Alfatih Muhammad Yasir Haya La Ode Muhammad, Taher Muktiarni, Muktiarni Mursanti, Wa Ode Indah Arum Musadar Mappasomba Musdalifa Musdalifa Musdalipah MUSDALIPAH MUSDALIPAH Mustakim Muzuni, Muzuni N. Nohong Nadaoka Kazuo Nadhifatul Aslikah Nasir Nasir Nasir Nasrudin NASRUDIN Nasrudin Nasrudin Nasution, Ali Napiah Nazira, Arni Neneng Andriani Joko Ni Kadek Ayu Berlian Nirwati Rusli Nofriani, Andi Nohong Nohong Nohong, Nohong Nordin Hj Lajis Nubzatussaniyyah, Nunu Nugroho, Ariel Dwiyanto Nunuk Hariani Soekamto Nur Aisyah Abdullah Nur Fadhillah Sahari Sahari Nur Illiyyin Akib Nur Indri Rahayu Nur Salma Nur Syifa Rahmatika Nur Syifa Rahmatika Nur Syifa Rahmatika Nur Syifa Rahmatika Nurcahyani, Fitria Nurhikma Nurhikma Nurhikma Nurkhalis Bintang Astiasal Nurpajriani, Nurpajriani Nurramadhani A. Sida Nurull Hikmah Ode, Muhammad Fajrin Parawansah Parawansah Parawansah Parrung, Arsyani Pascayantri, Asniar Paulina Taba Pauzan Haryono Poko, Feny Riskiana Poko, Feny Rizkia Purnama, La O. M. J. Purnama, La Ode Muh. Julian Purnama, La Ode Muhammad Julian Pusmarani, Jastria Puspita Sari Putri, Natalia Christiani Putri, Olivia Dicha Raden Arfan Rifqiawan Raden Maya Febrianti Rahangga, Dewa Gede Oka Rahman, Sudarman RAHMAT MULIADI, RAHMAT Rahmatika, Nur S. Ramadhan, LOAN Ramadhani, Rizky Barkah Rathapon Asasutjarit Rathapon Asasutjarit Reymon, Reymon RH. Fitri Faradilla Riezki Amalia Rilla Dwi Anjasari Mangidi Rina Andriani Rina Andriani Rina Andriani Rina Andryani Rina Maryanti RINI HAMSIDI Rini Hamsid Rini Hamsidi Roihan Ramadhan, Muhammad Romadhon Haris Alfian Ruslan Ruslin Ruslin Ruslin Ruslin Ruslin Ruslin, Ruslin Rustam HN, Muhammad S. J. Suprapto SA Achmad Saban Rahim Sabarwati, Hadijah Sadimantara, Gusti Ray SADIMANTARA, I GUSTI RAY Saharuddin Sahputra, Adi Salsabila, Syefira Saputri, Ulan Mulyani Saranani, Muhammad Aqsal Azriel Fajar Saripuddin Saripuddin Saripuddin Saripuddin Saripuddin Sariyana, S Sasmita, Wa Ode Indri Selfyana Austin Tee Septiana Andi Sernita Setiawan, La Ode Roni Setiawan, La Ode Wawan Setiawan, Muhammad Azdar Sewan Theeramunkong Shiddiq, Asep Mohamad I Siti Helmyati Siti Rahmawati Ondjo Siti Suriyani Kapa Siti Syafika Sitti Mardiana Sitti Rahmawati Sitti Raodah Nurul Jannah Sitti Raodah Nurul Jannah Sjamsul A. Achmad Sjamsul Arifin Achmad Sjamsul Arifin Achmad Sofa Fajriah Sofa Fajriah Sofa Fajriah Solo, Dian Munasari Sri Hutami Lety Grashella Srimuliana Suaib, S Sulsiah Sulsiah Sunandar Ihsan Supangat Supangat Suryani Suryani Syah, YM Syahrir La Syarif, Aiman Syarul Nataqain Baharum Syarul Nataqain Baharum Syukur, Novita Sari Taher Muhammad Tanzil, Dwi Lestari Khaulani Tatik Handayani, Tatik Thamrin Azis Tian Amalia Halik Tien Tien Titin Syafiransyah Trinovitasari, Nita Trisnaputri, Dian Rahmaniar Ubaidillah W Wahyuni, W W. O. N. Haryanti W. Wahyuni WA KUASA Wa Ode Erna Fitriani Wa Ode Ida Fitriah Wa Ode Jumiati Nur Wa Ode Mutiara Wa Ode Norma Wa Ode Nurfinti Wa Ode Nurfinti Wa Ode Salma Wa Ode Siti Zubaydah Wa Ode Sitti Zubaydah Wa OIL. Kalimin WAHYUNI Wahyuni Wahyuni wahyuni wahyuni Wirasmanto, Bayu Wirhamsah Al-Ramadan Wiwik Rusdin wiwin Wiwin Y, Muhammad Ilyas Yamin Yamin Yana M Syah Yana M. Syah Yana Maolana Syah Yayan Sopyan Yerin Tri Agustina YM Syah Yuliansyah Yuliansyah Yulianti, Sri Samrina Yuliastri, Wa Ode Yunarzat, Ersyanda Yuni Elsa Hadisaputri Yusnaini Yusnaini Zubaydah, Wa Ode Sitti Zulbayu, La Ode Muhammad Andi