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Aboveground biomass, productivity and carbon sequestration in Rhizophora stylosa mangrove forest of Southeast Sulawesi, Indonesia Kangkuso Analuddin; Kadidae La Ode; Muhammad Yasir Haya La Ode; Septiana Andi; Sahidin Idin; Syahrir La; Saban Rahim; Abdul Fajar La Ode; Nadaoka Kazuo
Biodiversitas Journal of Biological Diversity Vol. 21 No. 4 (2020)
Publisher : Society for Indonesian Biodiversity

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.13057/biodiv/d210407

Abstract

Abstract. Analuddin K, Kadidae LO, Haya LOMY, Septiana A, Sahidin I, Syahrir L, Rahim S, Fajar LOA, Nadaoka K. 2020. Aboveground biomass, productivity and carbon sequestration in Rhizophora stylosa mangrove forest of Southeast Sulawesi, Indonesia. Biodiversitas 21: 1316-1325. This study was aimed at analyzing the trends of aboveground biomass (AGB), productivity and carbon sequestration of Rhizophora stylosa Griff. forest in Rawa Aopa Watumohai National Park (RAWNP), Southeast Sulawesi, Indonesia. The DBH was the best predictor for partial and whole AGB of R. stylosa trees. The mean AGB was 562.76 ton ha-1. The yearly biomass increment of living trees, biomass increment of whole stands, standing dead biomass, and litterfall in R. stylosa forest were estimated as 52.87, 50.09, 2.78 and 12.00 ton ha-1, respectively, while its net primary production was about 64.88 ton ha-1 yr-1 indicating higher mangrove productivity. The total carbon stock in R. stylosa forest was 264.50 ton ha-1, while the annual net carbon budget, carbon gain and carbon input in R. stylosa forest was 23.54, 24.85 and 5.64 ton ha-1. However, the total CO2 stored in R. stylosa forest was 969.83 ton ha-1, while the annual of net CO2 uptake, CO2 gained and CO2 input was 86.33, 91.12 and 20.86 ton ha-1. The higher carbon sequestration and CO2 uptake in R. stylosa forest indicate its significant role in the global carbon accumulation and reducing atmospheric CO2.
Growth, biomass, and carotenoids content analysis of Navicula sp. and Chlorella sp. in batch cultures with different salinities HASLIANTI HASLIANTI; SAHIDIN SAHIDIN; ASNANI ASNANI; ADRYAN FRISTIOHADY
Biodiversitas Journal of Biological Diversity Vol. 24 No. 8 (2023)
Publisher : Society for Indonesian Biodiversity

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.13057/biodiv/d240811

Abstract

Abstract. Haslianti, Sahidin, Asnani, Fristiohady A. 2023. Growth, biomass, and carotenoids content analysis of Navicula sp. and Chlorella sp. in batch cultures with different salinities. Biodiversitas 24: 4299-4306. The physiological activity of microalgae is strongly influenced by culture conditions. Therefore, the rebound in this microscopic plant blooming phenomenon varies according to the aquatic environmental parameters, especially the salinity of its medium. This study aimed to analyze the cell density, biomass, and carotenoid content of two types of microalgal cultures isolated from the sea of Southeast Sulawesi. This research was conducted from October 2021 to October 2022. The independent variable in this study was salinity (30, 33, and 36‰), and the dependent variables were the parameters of cell density, biomass, and carotenoids content. This study consisted of 135 unit experiments using a completely randomized design (CRD). The same trend in cell density is observed in the two types of microalgae, where exponential growth occurred from day 2 to day 6 and decreased in growth rate on day 7. The biomass content of the two types observed was relatively the same, ranging from 0.0176-0.0181 g, while the carotenoids content ranged from 12.8294-25.5958 g/mL. The highest carotenoids level was found in the type of Chlorella sp. (25.5958 g/mL) while the lowest was in the type of Navicula sp. (12.8294 g/mL). The data indicate that the salinity parameter (>30?36‰) greatly influences and thus spikes growth in cells due to their biomass and high carotenoid content. The environment parameter also contributes significantly to other physiological parameters (one-way ANOVA, p<0.05).
Chemotaxonomy in the Etlingera Genus from Sulawesi, Indonesia: Design and molecular docking of antioxidant marker RINI HAMSIDI; KARMILAH KARMILAH; NUR SAADAH DAUD; MUHAMMAD HAJRUL MALAKA; AGUNG WIBAWA MAHATVA YODHA; MUSDALIPAH MUSDALIPAH; ARFAN ARFAN; SAHIDIN SAHIDIN
Biodiversitas Journal of Biological Diversity Vol. 25 No. 2 (2024)
Publisher : Society for Indonesian Biodiversity

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.13057/biodiv/d250202

Abstract

Abstract. Hamsidi R, Karmilah, Daud NS, Malaka MH, Yodha AWM, Musdalipah, Arfan, Sahidin. 2024. Chemotaxonomy in the Etlingera Genus from Sulawesi, Indonesia: Design and molecular docking of antioxidant marker. Biodiversitas 25: 449-457. Etlingera is one of the important genera in the Zingiberaceae family because of its potential uses. Several studies have been conducted on the Genus Etlingera as nutraceuticals and drugs. Recently new species have been found in the Sulawesi Region, Indonesia, namely E. canaria A.D.Poulsen and E. echinulate A.D.Poulsen. Based on literature review through sciencedirect and springer link, both species unknown for their chemical and pharmacological content, so it is necessary to continue to reveal the deeper potential. The fruits of E. calophrys (K.Schum.) A.D.Poulsen, E. canaria and E. echinulate were extracted with methanol by maceration method. The chemical content of each extract was analyzed using a Liquid Chromatography Mass Spectrometer (LCMS). Antioxidant activity was tested based on the 1,1-Diphenyl-2-Picrylhydrazyl (DPPH) method. The ability as an antioxidant is proven by the molecular interactions of marker compounds in inhibiting xanthine oxidase. The secondary metabolites contained in the fruit extracts of E. calophrys, E. canaria and E. echinulate are E-p-Coumatic acid, 1,5-Dimethyl citrate, Trimethyl citrate, Crocetin, Tanshinone IIA, Ethinyl Estradiol, Yakuchinone B, Anisalacetone, Yakuchinone A, Nobilin, ?-Estradiol, Momor-cerebroside I, Spinasterone, 12-Hydroxy-methyl abietate, Spinasterol, 2,3-Dihydroxypropyl oleate, 11-Octadecenoate acid methyl ester, Stigmastan-3,6-dione, b-Sitosterol- 3-O-b-D-glucopyranoside, Trilaurin, 28-O-Hexahydrophthalate and Fasciculol C. Yakuchinone A and Yakuchinone B are chemotaxonomic marker compounds identified in all species. The antioxidant properties of each extract of 42.27±0.53, 46.59±0.81 and 35.66±0.73 mg/L have been proven by the molecular interactions of the marker compounds in their ability to act as xanthine oxidase inhibitors. The compounds Yakuchinone A and Yakuchinone B are thought to be responsible for the pharmacological activity of the species E. calophrys, E. canaria and E. echinulate. Yakuchinone A and Yakuchinone B are marker compounds because they are distributed in all samples.
Antioxidant and Anti-Breast Cancer Potentials of the Hydrophilic Fraction from Soft Coral Nepthea sp.: In Vitro and In Silico Assessment Sahidin Sahidin; Baru Sadarun; Marianti A Manggau; Adryan Fristiohady; Dzaky Aulia Rahman; Agung Wibawa Mahatva Yodha; Arfan Arfan; Andini Sundowo; Sofa Fajriah
Molekul Vol 21 No 2 (2026)
Publisher : Universitas Jenderal Soedirman

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.20884/1.jm.2026.21.2.19418

Abstract

ABSTRACT. Soft corals of the genus Nepthea are recognized as rich sources of marine bioactive compounds, yet their hydrophilic metabolites remain poorly explored. This study characterized the hydrophilic fraction of Nepthea sp. and assessed its antioxidant and anti–breast cancer activities through in vitro and in silico approaches. Ethyl acetate extract (EAE) of Nepthea sp. was fractionated into six subfractions (F1–F6), with F5–F6 representing hydrophilic fractions. Phytochemical screening, TPC, TFC, and LC–MS/MS analyses were conducted alongside antioxidant (DPPH, ABTS), cytotoxicity (MTT, MCF-7), and molecular docking assays against xanthine oxidase (XO) and estrogen receptor alpha (ERα). Phytochemical profiling revealed alkaloids, phenolics, flavonoids, saponins, and terpenoids, with F5 exhibiting the highest TPC (73.11 mg GAE/g) and TFC (2.20 mg QE/g). LC–MS/MS identified rengyolester and piperolactam-C9:1(8E) in F5 and isosalsoline and 3-tert-butyl-4-methoxyphenol in F6. F5 demonstrated stronger antioxidant (DPPH IC₅₀ = 67.39 mg/L; ABTS IC₅₀ = 54.12 mg/L) and cytotoxic (MTT IC₅₀ = 42.68 mg/L) activities than F6. Docking analysis supported these results: rengyolester and piperolactam-C9:1(8E) showed strong affinities toward XO (−8.4, −8.7 kcal/mol) and ERα (−7.6, −7.4 kcal/mol), forming interactions with key residues (Phe914, Phe1009, Glu353, Leu525) similar to reference ligands. The hydrophilic fraction particularly F5 contains multifunctional metabolites exhibiting both antioxidant and anticancer properties. The synergistic role of phenolic and terpenoid constituents highlights Nepthea sp. as a promising marine source of bioactive therapeutic leads. Keywords: Antioxidant, breast cancer, hydrophilic fraction, molecular docking, Nepthea sp.
Antidepressant Potential of Etlingera Calophrys in Mice Tail Suspension Test and Forced Swim Test Ni Kadek Ayu Berlian; Ruslin Ruslin; Asriullah Jabbar; Irnawati Irnawati; Adryan Fristiohady; Sahidin Sahidin
Indonesian Journal of Global Health Research Vol. 8 No. 4 (2026): Indonesian Journal of Global Health Research
Publisher : GLOBAL HEALTH SCIENCE GROUP

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37287/ijghr.v8i4.1967

Abstract

Depression is a mood disorder characterized by feelings of sadness, loss of interest, and decreased activity, and is associated with neurotransmitter imbalance and oxidative stress. The use of conventional antidepressant drugs still has limitations so that alternatives from natural ingredients such as Etlingera calophrys are needed which are known to contain potential bioactive compounds. This study aims to determine the antidepressant potential of methanol extract of Etlingera calophrys rhizome in mice (Mus musculus) using the Tail Suspension Test (TST) and Forced Swim Test (FST) methods. This study used the Chronic Mild Stress (CMS) model in mice which were divided into several treatment groups, namely normal control, negative control, positive control (amitriptyline 25 mg/kgBW), and extracts with doses of 100, 200, and 300 mg/kgBW. The parameters observed were the duration of immobility in the TST and FST tests. Data were analyzed using One Way ANOVA followed by the Tukey HSD test. Phytochemical screening results showed the presence of alkaloids, flavonoids, tannins, saponins, and terpenoids. In vivo tests showed that all doses of the extract were able to reduce the duration of immobility compared to the negative control, with a dose of 300 mg/kgBW providing the most significant effect and approaching the positive control (p < 0.05). The methanol extract of Etlingera calophrys rhizome has significant antidepressant activity, with a dose of 300 mg/kgBW being the most effective dose. These findings indicate that the methanolic extract of Etlingera calophrys rhizome exhibits significant antidepressant activity, which may be attributed to the synergistic effects of its bioactive compounds through modulation of monoaminergic neurotransmission and antioxidant mechanisms. In conclusion, Etlingera calophrys rhizome has promising potential as a natural antidepressant candidate, warranting further investigation at the molecular and clinical levels.
Antidepressant Activity of Etlingera Rubroloba Rhizome Extract using Tail Suspension and Forced Swimming Tests Nur Fadhillah Sahari Sahari; Sahidin Sahidin; Wahyuni Wahyuni; Adryan Fristiohady; Asriullah Jabbar; Ari Sartinah
Indonesian Journal of Global Health Research Vol. 8 No. 4 (2026): Indonesian Journal of Global Health Research
Publisher : GLOBAL HEALTH SCIENCE GROUP

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37287/ijghr.v8i4.1979

Abstract

Epression is a mental health disorder characterized by mood changes, loss of interest, and physiological disturbances, which are associated with dysfunction of the monoaminergic system in the brain. The limitations of conventional therapies have prompted the exploration of natural sources, including plants from the Zingiberaceae family, which are known to be rich in bioactive metabolites with neuropharmacological potential. Etlingera rubroloba is one of Indonesia’s endemic plants with potential as an antidepressant agent; however, scientific studies on it remain limited. This study aims to evaluate the antidepressant activity of Etlingera rubroloba rhizome extract and to identify its secondary metabolites that may play a role in this effect. Extraction was performed via maceration using methanol, followed by phytochemical screening using tube assays. Antidepressant activity was tested in vivo on mice induced with Chronic Mild Stress (CMS), using the Tail Suspension Test (TST) and Forced Swimming Test (FST). The observed parameter was immobility time. Data were analyzed using a One-Way ANOVA test with a significance level of p < 0.05. Results: Phytochemical screening results indicated the presence of alkaloids, flavonoids, tannins, saponins, and terpenoids in the extract. Antidepressant activity tests showed that E. rubroloba rhizome extract significantly reduced immobility time in the TST and FST (p < 0.05) compared to the negative control. This effect was dose-dependent, with a dose of 300 mg/kg body weight providing the most optimal activity and comparable to the positive control (amitriptyline). Etlingera rubroloba rhizome extract possesses significant antidepressant activity and has potential for development as a natural antidepressant agent. This effect is thought to involve multimodal mechanisms, including the modulation of monoamine neurotransmitters, increased neuroplasticity, as well as the antioxidant and anti-inflammatory activities of its secondary metabolites.
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 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