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All Journal VALENSI JURNAL KIMIA SAINS DAN APLIKASI Pharmaciana: Jurnal Kefarmasian Jurnal Al-Tadzkiyyah E-Dimas: Jurnal Pengabdian kepada Masyarakat Prosiding Penelitian dan Pengabdian kepada Masyarakat Jurnal Kesehatan Bakti Tunas Husada Chimica et Natura Acta ALCHEMY Jurnal Penelitian Kimia JMM (Jurnal Masyarakat Mandiri) Lentera: Jurnal Ilmiah Kependidikan Journal of Pharmacopolium MATAPPA: Jurnal Pengabdian Kepada Masyarakat Martabe : Jurnal Pengabdian Kepada Masyarakat Jurnal Kreativitas PKM Molekul: Jurnal Ilmiah Kimia Jurnal Ilmu Kefarmasian Indonesia Unnes Journal of Mathematics Education Research Pharmacoscript LEARNING : Jurnal Inovasi Penelitian Pendidikan dan Pembelajaran Journal of Educational Sciences Journal of Innovation and Research in Primary Education J-ABDIPAMAS (Jurnal Pengabdian Kepada Masyarakat) Jurnal Pengabdian Pada Masyarakat Journal of Business Management and Economic Development Komunita: Jurnal Pengabdian dan Pemberdayaan Masyarakat Jurnal Pengabdian Masyarakat (Jupemas) Jurnal Kesehatan Bakti Tunas Husada EDUCATIONAL: Jurnal Inovasi Pendidikan dan Pengajaran
Ruswanto, Ruswanto
Department Of Pharmacy, Faculty Of Pharmacy, Universitas Bakti Tunas Husada Tasikmalaya
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Potential of Prenylated Flavonoid Derivatives from Jackfruit Roots (Artocarpus heterophyllus Lam.) as Liver Anticancer Candidates: In Silico Study Richa Mardianingrum; Meylany Sity Rossy Lestary; Nur Aji; Ruswanto Ruswanto
Jurnal Kimia Sains dan Aplikasi Vol 26, No 2 (2023): Volume 26 Issue 2 Year 2023
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.26.2.57-63

Abstract

Hepatocellular carcinoma (HCC), or liver cancer, is the fourth largest cancer in Indonesia, with 21,392 new cases and around 20,920 deaths. One of the standard drugs for liver cancer patients is lenvatinib, but lenvatinib has dangerous side effects such as hypertension. Previous studies reported that jackfruit root extract (Artocarpus heterophyllus Lam.) contains prenylated flavonoid compounds known to have anticancer activity. This study aims to find compounds that have the potential to the anticancer liver from jackfruit root by understanding the interaction between prenylated flavonoid derivative compounds against the VEGFR2 receptor (PDB ID: 3WZE) in silico. The methods include toxicity and pharmacokinetic screening, drug scanning, docking, and molecular dynamics simulation. The toxicity, pharmacokinetic, and drug scans of cycloartocarpesin are better than lenvatinib. The docking cycloartocarpesin compound showed ∆G -8.49 kcal/mol and Ki 0.59967 M lower than lenvatinib by forming the same hydrogen bond at residue Glu885. The molecular dynamics simulation of the cycloartocarpesin compound in the MM-GBSA calculation method resulted in a ∆Gtotal of -56.641 kcal/mol. The cycloartocarpesin compound is predicted to be used as a candidate for liver anticancer drugs because it has better stability and affinity than lenvatinib.
Pemberian Informasi Obat (PIO) Hipertensi dan Pemeriksaan Tekanan Darah di Desa Sirnaputra Kecamatan Cigalontang Tasikmalaya Ruswanto Ruswanto; Gatut Ari Wardani; Tresna Lestari; Heri Herdiana; Sri Asih
Jurnal Kreativitas Pengabdian Kepada Masyarakat (PKM) Vol 6, No 6 (2023): Volume 6 No 6 Juni 2023
Publisher : Universitas Malahayati Lampung

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33024/jkpm.v6i6.9598

Abstract

ABSTRAK Masalah utama diberbagai negara terkait kesehatan adalah penyakit jantung Dan pembuluh darah. Penderita hipertensi terus meningkat setiap tahunnya. Diperkirakan pada tahun 2025, 1,5 miliar orang akan mengalami tekanan darah tinggi yang diprediksikan terjadi setiap tahun 14,04 juta orang telah meninggal karena tekanan darah tinggi dan komplikasinya. Tujuan kegiatan Pengabdian Masyarakat ini yaitu untuk meningkatkan pengetahuan masyarakat terhadap faktor penyebab dan pencegahan yang berhubungan dengan hipertensi. Penyebaran media informasi obat melalui media dan hasil evaluasi melalui penyebaran kuesioner. Media yang digunakan yaitu brosur mengenai Pemberian Informasi Obat (PIO) dan Komunikasi Informasi Edukasi (KIE). Hasil keseluruhan tingkat pemahaman terhadap materi yang disampaikan lebih dari 94% peserta menjawab sengat paham dalam kuesioner evaluasi kegiatan dan 6% peserta memiliki pemahaman materi menjawab paham. Kegiatan dinilai memiliki dampak yang positif berdasarkan evaluasi jangka pendek terdapat peningkatan pengetahuan dan kemampuan masyarakat Desa Sirnaputra Kec. Cigalontang. Kata Kunci: Hipertensi, PIO, Tekanan Darah  ABSTRACT The main problem in various countries related to health is the heart and blood vessel disease. Patients with hypertension continue to increase every year. It is estimated that in 2025, 1.5 billion people will experience high blood pressure which is predicted to occur every year 14.04 million people have died due to high blood pressure and its complications. The purpose of community service is to increase public knowledge of the causes and prevention factors related to hypertension. Dissemination of drug information media through the media and evaluation results through the dissemination of questionnaires. The media used are brochures regarding the Provision of Drug Information (PIO) and Educational Information Communication (IEC). The results of the overall level of understanding of the material presented were more than 94% of participants answered very well in the activity evaluation questionnaire and 6% of participants had an understanding of the material and answered understanding. The activity is considered to have a positive impact based on a short-term evaluation there is an increase in the knowledge and ability of the people of Sirnaputra Village, Kec. CigalontangKeywords : Hypertension, PIO, Blood Pressure
Kuersetin, Penghambat Uridin 5-Monofosfat Sintase Sebagai Kandidat Anti-kanker Ruswanto Ruswanto; Imam Mustaqim Garna; Lilis Tuslinah; Richa Mardianingrum; Tresna Lestari; Tita Nofianti
ALCHEMY Jurnal Penelitian Kimia Vol 14, No 2 (2018): September
Publisher : UNIVERSITAS SEBELAS MARET (UNS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.20961/alchemy.14.2.14396.236-254

Abstract

Kanker adalah pembentukan jaringan baru yang abnormal dan bersifat ganas. Efek toksisitas yang ditimbulkan pada setiap senyawa obat antikanker selalu menjadi problem dalam pengobatan kanker dengan cara kemoterapi, maka dari itu perlu dicari alternatife lain untuk mengatasi kanker. Kuersetin telah diketahui mempunyai aktivitas sitotoksik pada sel kanker tapi belum diketahui mekanisme kerjanya. Pada penelitian ini telah dilakukan penelitiaan in silico untuk mengetahui target reseptor dari senyawa kuersetin melalui identifikasi target reseptor melalui http://lilab.ecust.edu.cn/pharmmapper/ dan studi interaksi melalui metode docking. Hasil menunjukkan bahwa kuersetin memiliki aktivitas pada target reseptor proto-onkogen protein-tirosin kinase dan uridin 5-monofosfat sintase. Berdasarkan nilai energi bebas (∆G) dari hasil docking dapat disimpulkan kuersetin memiliki aktivitas terbaik pada protein target uridin 5-monofosfat sintase dengan nilai energi binding affinity sebesar -8,28617 kkal/mol dan berinteraksi dengan residu asam amino yang sesuai dengan active site dari protein target reseptor uridin 5-monofosfat sintase yaitu membentuk 2 ikatan hidrogen dengan residu Tyr 432 dan Gly 450 dan kontak bagian hidrofobik dengan residu Asn 312, Met 371, pro 417.Quersetine: Uridine 5-Monophosphate Synthase Inhibitor as Anticancer Candidate. Cancer is the abnormal formation of new tissue and malignant. Toxicity effects inflicted on any anti-cancer drug compounds has always been a problem in the treatment of cancer by chemotherapy, therefore it is necessary to find other alternatives to treat cancer. Quercetin has been known to have cytotoxic activity on cancer cells but unknown mechanism of action. This study has been conducted in silico to determine the receptor target of the quercetin compound through the identification of target receptors by http://lilab.ecust.edu.cn/pharmmapper/ and interaction studies through docking methods. The results showed that the quercetin has activity on the receptor target proto-oncogene protein-tyrosine kinase and uridine 5- monophosphate synthase. Based on free energy value (ΔG) of the docking results we can conclude the quercetin has the best activity of the receptor target uridine 5- monophosphate synthase with a binding affinity energy value of -8.28617 kcal/mol and interacts with the amino acid residues to the active site of the receptor target 5-uridine monophosphate synthase which form two hydrogen bonds with Tyr 432 and Gly 450 and the hydrophobic contact with Asn 312, Met 371, and pro 417.
Penyuluhan Pengetahuan tentang Narkoba pada Penggiat Anti-narkoba di Kota Tasikmalaya Ira Rahmiyani; Ruswanto Ruswanto; Saeful Amin; Nur Rahayuningsih; Ilham Alifiar; Nurlaili Dwi Hidayati; Muharam Priatna; Tresna Lestari; Tita Nofianti; Anisa Pebiansyah; Anna Yuliana; Mochamad Fathurohman; Vera Nurviana; Citra Dewi Salasanti; Anindita Tri Kusuma Pratita
E-Dimas: Jurnal Pengabdian kepada Masyarakat Vol 14, No 2 (2023): E-DIMAS
Publisher : Universitas PGRI Semarang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.26877/e-dimas.v14i2.11433

Abstract

Masih maraknya penyalahgunaan narkoba di masyarakat yang akan berpengaruh terhadap perkembangan dan kemajuan bangsa Indonesia di masa depan maka perlu adanya pengetahuan dan pemahaman tentang narkoba. Karena ini, diperlukan kegiatan-kegiatan yang mendukung pada peningkatan dan pencegahan penyalahgunaan narkoba. Maka dosen dan mahasiswa Fakultas Farmasi Universitas Bakti Tunas Husada bekerja sama dengan Badan Narkotika Nasional dalam kegiatan pengabdian masyarakat. Peserta pengabdian masyarakat adalah para penggiat anti-narkoba di Kota Tasikmalaya. Metode yang dilakukan adalah penyuluhan dan pembagian kuesioner pengetahuan tentang narkoba. Hasil pengabdian masyarakat dapat berjalan dengan lancar dan adanya pemahaman peserta pengabdian masyarakat tentang narkoba.
Antibacterial Activity of Streptococcus mutans from Saga Herbaceous Plant (Abrus precatorius): In Silico Study Richa Mardianingrum; Neta Ekayanti Suganda; Srie Rezeki Nur Endah; Ruswanto Ruswanto
ALCHEMY Jurnal Penelitian Kimia Vol 19, No 2 (2023): September
Publisher : UNIVERSITAS SEBELAS MARET (UNS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.20961/alchemy.19.2.67780.177-189

Abstract

Antibacterial is a substance that can inhibit growth or can even kill bacteria that cause infection. One of them is infection with Streptococcus mutans bacteria that cause damage to teeth, such as dental caries. Dental caries is a disease that affects many adults and children, permanently damaging the tooth layer and forming small holes in the teeth. The purpose of this study was to find active compounds from the herb Saga plant (Abrus precatorius), which has the potential to be antibacterial of S. mutans in silico. The methods used are pharmacokinetics and toxicity screening, Lipinski's Rule of Five, as well as simulations of molecular docking and molecular dynamics. The Abruquinone D (-6.43) and Abruquinone F (-7.08) were predicted to have stable interactions and be similar to amoxicillin (-7.69) and native ligand (-8.56 kcal/mol) based on the results of screening and molecular docking simulations of active compounds from Saga herbaceous (Abrus precatorius) against deoxycytidylate deaminase receptors. Molecular dynamics findings confirmed by MMGBSA methods that Abruquinone D (-41.3876 kcal/mol) had a lower energy value than Abruquinone F (-24.8521 kcal/mol). It can be inferred that Abruquinone D has a higher potential as an antibiotic (S. mutans) than Abruquinone F.
Bioinformatics Studies of Flavonoid Derivatives Compound from Saga Rambat Leaves as an Antipyretic Candidate Neni Sri Gunarti; Ruswanto Ruswanto; Elsa Oktavia Angelica; Himyatul Hidayah
Jurnal Kimia Sains dan Aplikasi Vol 26, No 12 (2023): Volume 26 Issue 12 Year 2023
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.26.12.466-476

Abstract

This research is backed by the frequent use of herbal plants in the community, one of which is the saga (Abrus precatory L.), which is used to reduce body temperature in the Tirtajaya District, Karawang Regency. Saga leaves contain several secondary metabolites with potential antipyretics, one of which is flavonoids. The study aimed to determine the inhibitory activity of flavonoid compounds of saga leaves as inhibitors of COX-2 receptors and IL-1 receptors that reduce fever. The methods used were pharmacokinetic and toxicity studies, molecular docking, and molecular dynamic simulation. The outcomes of molecular docking experiments with seven flavonoid-derived compounds from saga leaves targeting cyclooxygenase-2 (4PH9) receptors revealed that isohemiphloin compounds exhibited the most favorable Gibbs free energy (ΔG) at -7.08 kcal/mol. In the case of interleukin-1 (5R85), cirsimaritin compounds displayed the lowest Gibbs free energy (ΔG) at -7.78 kcal/mol. The analysis of drug screening results indicates that the best compound adheres to four of the five Lipinski rules. Furthermore, the predictions for pharmacokinetics and toxicity are fairly good, as the best compound demonstrates a favorable pharmacokinetic profile and is determined to be non-toxic. These findings collectively suggest that the isohemiphloin compound from saga leaves may be a promising candidate for developing an antipyretic drug, particularly due to its predicted interaction with the cyclooxygenase-2 (4PH9) receptor.
Synthesis and Computational Study of Bis-(1-(3-Chlorobenzoyl)-3-Phenylthiourea) Cobalt (III) as Anticancer Candidate Ruswanto Ruswanto; Nisa Uswatun Khasanah; Gatut Ari Wardani; Richa Mardianingrum
Jurnal Kimia Sains dan Aplikasi Vol 26, No 7 (2023): Volume 26 Issue 7 Year 2023
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.26.7.238-248

Abstract

Cancer is a disease characterized by cells forming abnormally so that a buildup can cause lumps. Drug compounds used for anticancer treatment by chemotherapy become a severe problem because they have dangerous side effects and can affect patient’s quality of life. This study aims to discover new drug compounds with lowered toxicity effects. This was achieved by modifying their structures through synthesis, characterization, and estimating the interactions of the synthesized compounds with specific target receptors, utilizing a docking method. The result obtained was a synthesis yield of 36.2%. The characterization of complex compounds was characterized by the presence of a maximum wavelength of 273 nm and a molecular weight of 652 g/mmol, indicating the absorption of Co-O and Co-S at respective wavenumbers of 498 cm-1 and 604 cm- 1. The docking results showed that the Bis-(1-(3-Chlorobenzoyl)-3-Phenylthiourea) Cobalt (III) complex had the best activity on human estrogen receptor alpha (hER alpha) with a binding affinity value of - 9.40 kcal/mol and an inhibition constant of 0.129 M, which was lower than the comparison compound (cisplatin) and had a better pharmacokinetic profile than cisplatin. This study shows that the Bis-(1-(3-Chlorobenzoyl)-3-Phenylthiourea) Cobalt (III) complex is predicted to have potential as an anticancer candidate.
MOLECULAR DOCKING EMPAT TURUNAN ISONICOTINOHYDRAZIDE PADA MYCOBACTERIUM TUBERCULOSIS ENOYL-ACYL CARRIER PROTEIN REDUCTASE (InhA) Ruswanto Ruswanto
Jurnal Kesehatan Bakti Tunas Husada: Jurnal Ilmu-ilmu Keperawatan, Analis Kesehatan dan Farmasi Vol 13, No 1 (2015)
Publisher : LPPM Universitas Bakti Tunas Husada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.36465/jkbth.v13i1.25

Abstract

Mycobacterium tuberculosis enoil-ACP reduktase (InhA) adalah target yang menarik untuk pengembangan obat baru terhadap TBC. InhA adalah target pertama obat isoniazid untuk pengobatan infeksi tuberkulosis. Senyawa yang secara langsung bekerja pada InhA,  tidak memerlukan aktivasi oleh mikobakteri katalase-peroksidase katG adalah kandidat yang menjanjikan untuk mengobati infeksi yang disebabkan oleh strain yang resisten terhadap isoniazid (Luckner, 2010). Baru-baru ini, telah dilakukan studi interaksidan toksisitas beberapa senyawa turunan isoniazid (isonicotinohydrazide) dengan InhA dengan metode molecular docking. Semua senyawa di-docking-an menggunakan aplikasi ArgusLab 4.0.1. Proses docking yang dilakukan dengan memilih metode ArgusDock. Validasi docking dengan nilai Root Mean Square Deviation (RMSD) yang diperoleh 1,9457. Analisis hasil docking menunjukkan bahwa senyawa 2,5-Dimethyl-2H-pyrazole-3-carboxylic acid N'-(pyridine-4-carbonyl)-hydrazide (senyawa 4) dapat diprediksi memiliki interaksi yang paling baik daripada senyawa pembanding isoniazid. Dari hasil penelitian ini dapat disimpulkan bahwa senyawa (4) memiliki aktivitas penghambatan terhadap reseptor InhA. Hasil uji toksisitas menggunakan program ECOSAR (Ecological Structure Activity Relationships) semua senyawa turunan isonicotinohydrazide memiliki nilai LC50 dan EC50 > 100 mg/ L sehingga termasuk dalam kategori rendah karena > 100 mg/ L. Kata kunci  : Docking, isoniazid, InhA,  toksisitas.
DESAIN DAN STUDI INTERAKSI SENYAWA N'-(3,5-DINITROBENZOYL)-ISONICOTINOHYDRAZIDE PADA MYCOBACTERIUM TUBERCULOSIS ENOYL-ACYL CARRIER PROTEIN REDUCTASE (INHA) Ruswanto Ruswanto
Jurnal Kesehatan Bakti Tunas Husada: Jurnal Ilmu-ilmu Keperawatan, Analis Kesehatan dan Farmasi Vol 12, No 1 (2014)
Publisher : LPPM Universitas Bakti Tunas Husada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.36465/jkbth.v12i1.79

Abstract

Pada penelitian ini dilakukan proses docking dari senyawa N'-(3,5-dinitrobenzoyl)-isonicotinohydrazide terhadap reseptor Mycobactarium Tuberculosis Enoyl-Acyl carrier Protein Reductase (INHA). Kode reseptor yang digunakan adalah 2H7I, 2H7L dan 2X23 yang di download dari situs protein data bank (PDB). Tujuan penelitian ini untuk mengetahui interaksi dan toksisitas senyawa N'-(3,5-dinitrobenzoyl)-isonicotinohydrazide  terhadap reseptor INHA. Semua senyawa di-docking-an menggunakan aplikasi ArgusLab 4.0.1. Proses docking yang dilakukan dengan memilih metode ArgusDock. Validasi docking dengan nilai Root Mean Square Deviation (RMSD) yang diperoleh < 2. Analisis hasil docking menunjukkan bahwa senyawa N'-(3,5-dinitrobenzoyl)-isonicotinohydrazide dapat diprediksi memiliki interaksi yang lebih baik daripada senyawa pembanding isoniazid. Dari hasil penelitian ini dapat disimpulkan bahwa senyawa N'-(3,5-dinitrobenzoyl)-isonicotinohydrazide memiliki aktivitas penghambatan terhadap reseptor INHA. Hasil uji toksisitas menggunakan program ECOSAR (Ecological Structure Activity Relationships) senyawa N'-(3,5-dinitrobenzoyl)-isonicotinohydrazide memiliki nilai LC50 dan EC50 > 100 mg/ L sehingga termasuk dalam kategori rendah karena > 100 mg/ L. Sedang dari uji toksisitas menggunakan program Toxtree menunjukan bahwa senyawa N'-(3,5-dinitrobenzoyl)-isonicotinohydrazide termasuk dalam kategori 3 (High Class) sehingga tidak terjamin keamanannya tetapi tidak bersifat karsinogenik genotoksik dan nongenotoksik
SINTESIS SENYAWA 1-(4-HEPHTILBENZOIL-3-METILTIOUREA) DAN UJI SITOTOKSISITAS TERHADAP SEL T47D SEBAGAI KANDIDAT ANTIKANKER Ruswanto Ruswanto; Asep Nugraha
Jurnal Kesehatan Bakti Tunas Husada: Jurnal Ilmu-ilmu Keperawatan, Analis Kesehatan dan Farmasi Vol 14, No 1 (2015)
Publisher : LPPM Universitas Bakti Tunas Husada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.36465/jkbth.v14i1.123

Abstract

Telah dilakukan sintesis senyawa 1-(4-heptilbenzoil-3-metiltiourea) dari reaksi asilasi antara N-metiltiourea dengan 4-heptilbenzoil klorida dalam pelarut tetrahidrofuran dengan modifikasi metode Schotten Baumann menggunakan refluks selama 8 jam dalam suasana basa. Persentase perolehan kembali hasil sintesis adalah 30,16 %. Kemurnian hasil sintesis ditunjukkan dengan adanya noda tunggal pada KLT dan jarak lebur yang sempit. Identifikasi struktur senyawa hasil sintesis dilakukan dengan menggunakan spektrofotometri Ultraviolet, spektrofotometri Infra Merah, dan spektrometri Resonansi Magent Inti Proton (RMI) yang menandakan bahwa senyawa hasil sintesis merupakan senyawa 1-(4-heptilbenzoil-3-metiltiourea) sesuai dengan perkiraan. Uji sitotoksisitas dilakukan dengan menggunakan metode MTT (3-(4,5-dimetiltiazol-2-il)-2,5-difenil tetrazolium bromid). Dari uji in vitro diperoleh IC50 dari senyawa 1-(4-heptil benzoil-3-metiltiourea) terhadap sel T47D sebesar 27,9 μg/mL. Hasil penelitian menunjukkan bahwa senyawa 1-(4-heptilbenzoil-3-metiltiourea) memiliki potensi sebagai kandidat antikanker. Kata kunci : sintesis, 1-(4-heptilbenzoil-3-metiltiourea), sitotoksisitas, MTT.
Co-Authors A.A. Ketut Agung Cahyawan W Aas Nuraisah Aas Nuraisah Aas Nuraisah Abdul Hakim Agus Susanti Aguslina Kirtishanti Ahmad Tantowi Jaohari Ai Teni Siti Robi`ah Aimi Ratnasari Aimi Ratnasari, Aimi Albie, Fadhlan Adtya Alicia Nadira Alifia Nurfadhilah S Anggi Agustira Anindita Tri Kusuma , Pratita Anindita Tri Kusuma Pratita Anindita Tri Kusuma Pratita Anindita Tri Kusuma Pratita Anindita Tri Kusuma Pratita Anindita Tri Kusuma Pratita Anisa Pebiansyah Anjuni, Dhea Putri Anna Yuliana, Anna Annazalia Rustandi Putri Annisa Pebiansyah Annisa Pebiansyah Aprillia, Ade Yeni Arry Yanuar Asep Nugraha Ayudia, Sukma Billah, Tazkia Hasna Citra Dewi Salasanti Citra Dewi Salasanti Deden Makbuloh Deliani Deliani Deliaz, Mochamad Fajar Delis Susilawati Desri Lestari Dewi Dewi Dewi, Nida Puspa Dewi, Rika Zahara Diana Sri Zustika Dini Febianeu Ditha Rizqi Aulia Utami Dudi Nurmalik Dwijanto Dwijanto, Dwijanto Elsa Oktavia Angelica Elsi Eryanti Fadilah, Refi Tazhqiyatul FAJAR SETIAWAN Fajar Setiawan Fanisa Riadhiani Fathurohman, Mochamad Fauziah, Mina Febby, Pratama Feri Sandria Firiani, Yuli Firman Gustaman Fujiyanti, Melia Gatut Ari Wardani Gina Maya Lestari Gina Septiani Agustien Gina Yulias Triyani Ginna Sri Nuryani Gustaman, Firman Hasanah, Melati Nur Aini Hendy Suhendy Herdiana, Yana Heri Herdiana Heru Juabdin Sada Hery Wibowo, Hery Himyatul Hidayah Holis Abdul Holik, Holis Abdul Ibnu Hajar Ikram, Nur Kusaira Khairul Ilham Alifiar Ilham Alifiar Ilham Alifiar Ilham Nurfadilah, Asopari Imam Mustaqim Garna Indah Cantika Ira Rahmiyani Irawan, Rudy Isti Daruwati Kamiel Roesman Bachtiar Khoerunisa, Widia Salsabila Korry Novitriani, Korry Kristiana, Wiwin Leli Siti Zaqiah Lestari, Gina Maya Lilis Tuslinah Lilis Tuslinah Lilis Tuslinah Lilis Tuslinah Lilis Tuslinah, Lilis Lina Rahmawati Rizkuloh Lusi Nurdianti, Lusi M. Faturohman Mardhiah Mardhiah Mardhiah Mardhiah Mardianingrum Richa Melia Fujiyanti Meylany Sity Rossy Lestary Mina Fauziah Mitha Anggitha Moch. Zainuddin, Moch. Mochamad Fajar Deliaz Mochamad Fathurahman Mochamad Fathurohman Mochamad Fathurohman Muhammad Ismail Muharam Priatna Muharam Priatna Muharam Priatna Nadira, Alicia Naser Fahmi Muhamad Nasipah, Anis Neni Sri Gunarti Neta Ekayanti Suganda Nida Puspa Dewi Nisa Uswatun Khasanah Nofianti, Tita Nofianti, Tita Nofriyaldi, Ali Nugraha, Asep Nugraha, Hafizh Maulana Nur Aji Nur Laeli Dwi Hidayati Nur Laili Dwi Hidayati Nur Rahayuningsih Nur Rahayuningsih Nur Rahayuningsih, Nur Nur, Rahayuningsih Nurlaili Dwi Hidayati Nurlita, Putri Nurmalik, Dudi Nurmalik, Dudi NURUL AZIZAH Nurul Kamilah Nurul Kamilah Oktaviani Ayu Saputri Oktaviani, Widya Paras Layna Safa Pebiansyah, Anisa Pertiwi, Nur Ihsani Pikri Adit Praditya R Pratama, Febby Pratita, Anindita Tri Kusuma Putri Pratiwi Rachman, Dineu Septy Ulfiatur Rahmawati Rahmawati Raja Ramadiansyah Ramadan, Fajar Renadi, Sedin Riadhiani, Fanisa Richa Mardianingrum Richa, Mardianingrum Rika Zahara Dewi Rissa Putri Aulia Yulianto Rivaldi Muhsin Roswandi, Wemfi Riska Saeful Amin Safa, Paras Layna Saputri, Oktaviani Ayu Sarah, Ai Sarwatiningsih, Yunia Sa’idy, Sa’idy Septian, Ade Dwi Setiawati, Wina Aprilia Shal Nurdinda Fauziah Silvi Novitasari, Silvi Sindi Lestari Siswandono, Siswandono Sri Asih Sri Mulyani Srie Rezeki Nur Endah Srie Rezeki Nur Endah Sucipto Sucipto Sukma Ayudia SUPRIADI, HENY Surya Amal Susanti Susanti Susanti Susanti SUSILAWATI , BETI Taufik Hidayat Tiara Permata Sari Tifa Nofianti Tira Mutiara Utami Tita Nofianti Tita Nofianti Tita Nofianti Tita Nofianti Tita Nofianti Tita Nofianti Tita Nofianti Tita Nofianti, Tita Tresna Lestari Tresna Lestari, Tresna Tuslinah, Lilis Tuslinah, Lilis Ummy, Mardiana Vera Nurviana Vera Nurviana Veronika Yulianti Susilo Wahdah, Lestari Wahyuni, Wini Wemfi Riska Roswandi Widya Oktaviani Wildan Rizki Asilmi Wina Aprilia Setiawati Winda Trisna Wulandari Winda Trisna Wulandari Wini Wahyuni Wiwin Kristiana Yana Herdiana Yulia Salmini Yundari, Yundari YUSNITA, ERNI