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All Journal Jurnal Tumbuhan Obat Indonesia Journal of Islamic Pharmacy JURNAL FARMASI DAN ILMU KEFARMASIAN INDONESIA Jurnal Farmasi Sains dan Komunitas Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) Journal of Islamic Medicine Jurnal Kesehatan Islam : Islamic Health Journal Jurnal Dunia Farmasi ad-Dawaa : Journal of Pharmaceutical Sciences Borneo Journal Of Pharmascientech Bioscientist : Jurnal Ilmiah Biologi Journal Pharmasci (Journal of Pharmacy and Science) Tri Dharma Mandiri: Diseminasi dan Hilirisasi Riset Kepada Masyarakat (Jurnal Pengabdian Kepada Masyarakat) Jurnal Sintesis: Penelitian Sains, Terapan dan Analisisnya Indonesian Journal of Cancer Jurnal Ilmiah Multidisiplin Indonesia Jurnal Media Akademik (JMA) Borneo Journal of Pharmacy Jurnal Intelek Dan Cendikiawan Nusantara Journal of Social Science and Multidisciplinary Analysis Jurnal Intelek Insan Cendikia Gotong Royong Jurnal Informatika dan Kesehatan International Journal of Contemporary Sciences (IJCS) Jurnal Sains dan Kesehatan Journal Health of Indonesian JES-TM Social and Community Service Journal Abdimas Paspama Service
Faisal Akhmal Muslikh
Magister Ilmu Farmasi, Departemen Ilmu Kefarmasian, Fakultas Farmasi, Universitas Airlangga, Surabaya, Jawa Timur, Indonesia
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Systematic Review: Anti-Osteoporosis Potential Activities Of Phytoestrogen Compounds In Chrysophyllum cainito L., Elaeis guineensis Jacq., Lannea acida Rich., Marsilea crenata Presl., and Medicago sativa L. Burhan Ma'arif; Suryanto Suryanto; Faisal Akhmal Muslikh; Arief Suryadinata; Begum Fauziyah
Jurnal Farmasi Sains dan Komunitas (Journal of Pharmaceutical Sciences and Community) Vol 19, No 1 (2022)
Publisher : Sanata Dharma University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (923.113 KB) | DOI: 10.24071/jpsc.003166

Abstract

Phytoestrogens are compounds from plants that have a structure and function similar to estrogen (17β-estradiol). Phytoestrogens can be found in Chrysophyllum cainito L., Elaeis guineensis Jacq., Lannea acida Rich., Marsilea crenata Presl., and Medicago sativa L. This systematic review aimed to prove that all of these five plants have phytoestrogens which were observed with several instruments, and to assess activities and bone forming mechanisms from these five plants in the female mice (Mus musculus) and female rats (Rattus norvegicus). This systematic review was done by identifying articles in several databases (Google Scholar, PubMed, and Science Direct). The process of selecting the articles used the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines to create a flowchart with inclusion and exclusion study criteria. Meta-synthesis was done to analyze, identify, and interpret all of the data in the articles systematically. 31 articles in total were obtained from the selection process, with 27 articles containing a discussion about chemical compound content and 4 articles describing research results for in vivo testing of the plants that were reviewed. The results showed that these five plants have phytoestrogens and by in vivo testing have the activity in increasing trabecular bone density in the experimental animals.
STUDI IN SILICO PENGHAMBATAN AKTIVASI TLR2 EKSTRAK ETANOL DAUN SEMANGGI (Marsilea crenata Presl.) Burhan Ma'arif; Destiya Argo Pamuji Fihuda; Faisal Akhmal Muslikh; Sadli Syarifuddin; Begum Fauziyah; Dewi Perwito Sari; Mangestuti Agil
Jurnal Tumbuhan Obat Indonesia Vol 15 No 1 (2022): Jurnal Tumbuhan Obat Indonesia
Publisher : Balai Besar Penelitian dan Pengembangan Tanaman Obat dan Obat Tradisional

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22435/jtoi.v15i1.5792

Abstract

Neuroinflamasi dapat menyebabkan Parkinson Disease (PD), dengan salah satu mekanismenya adalah aktivasi berlebih toll-like receptor 2 (TLR2) akibat abnormalitas dan agregasi α-synuclein. Pada penelitian sebelumnya, daun semanggi (Marsilea crenata Presl.) terbukti menghambat progresivitas neuroinflamasi melalui jalur estrogen-receptor (ER) dependent. Penelitian ini bertujuan untuk memprediksi efek antineuroinflamasi daun semanggi pada jalur penghambatan aktivasi TLR2 (3A7B) dengan studi in silico. Senyawa hasil metabolite profiling sekunder dari ekstrak etanol 96% daun semanggi dipreparasi dengan ChemDraw Ultra 12.0, kemudian dilihat sifat farmakokinetik dan farmakodinamiknya dengan webtool SwissADME. Optimasi geometri pada senyawa dilakukan menggunakan Avogadro 1.0.1 dan molecular docking senyawa terhadap reseptor 3A7B dilakukan menggunakan Autodock vina (PyRx 0.8). Tahap visualisasi interaksi dilakukan dengan Biovia Discover Studio 2021, sedangkan nilai toksisitas senyawa dianalisis menggunakan ProTox II online tool. Hasil penelitian menunjukkan terdapat empat senyawa yang memenuhi kriteria farmakokinetik, farmakodinamik, toksisitas, serta mempunyai kemiripan dengan native ligand N-acetyl-D-glucosamine. Oleh karena itu, ekstrak etanol 96% daun semanggi diprediksi memiliki potensi sebagai penghambat progresifitas PD dengan mekanisme antineuroinflamasi.
Development and Challenges of Using Serratiopeptidase Enzymes as Anti-Inflammatory in the Present Era: Literature Review: Pengembangan dan Tantangan Penggunaan Enzim Serratiopeptidase Sebagai Antiinflamasi di Era Masa Kini: Literature Review Faisal Akhmal Muslikh; Sukardiman
Journal Pharmasci (Journal of Pharmacy and Science) Vol. 7 No. 2 (2022): Journal Pharmasci (Journal of Pharmacy and Science)
Publisher : Akademi Farmasi Surabaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.53342/pharmasci.v7i2.283

Abstract

Enzymes are proteins that control and carry out metabolic activities in the body, either directly or indirectly. Enzymes have various advantages over traditional pharmaceuticals in terms of therapeutic efficacy and toxicity. They have great specificity and affinity for their target, minimizing toxicity. Use the terms "Serratiopeptidase enzyme" and "inflammation" to search publications in Google Scholar, Sciencedirect, SAGE journal, and Pubmed databases. According to ten articles, the serratiopeptidase enzyme has been shown to have an anti-inflammatory effect by reducing inflammatory cytokines and adhesion molecules, thereby regulating the movement of inflammatory cells to the site of inflammation, which in clinical trials can reduce swelling of edema and metabolism of scar tissue in the body.
Pharmacological Effects of Glycyrrhiza glabra L. as Antihepatitis and Hepatoprotective for Children Faisal Akhmal Muslikh; Puja Adi Priatna; Wiwied Ekasari
JURNAL FARMASI DAN ILMU KEFARMASIAN INDONESIA Vol. 10 No. 1 (2023): JURNAL FARMASI DAN ILMU KEFARMASIAN INDONESIA
Publisher : Universitas Airlangga

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.20473/jfiki.v10i12023.126-140

Abstract

Background: The incidence of hepatitis in children has grown from the normal number of hepatitis cases since January 2022, and it will continue to rise since the etiology and pathophysiology are unknown. This case is distinct from those caused by the hepatitis A, B, C, D, and E viruses. Glycyrrhiza glabra L. is a medicinal herb that has long been used in medicine to treat respiratory, digestive, and immune system problems, but it is also known to have an inhibitory impact on the virus. Coronavirus-associated acute respiratory syndrome, hepatitis, herpes simplex virus, influenza virus. Objective: This article will look at Glycyrrhiza glabra L.'s antihepatitis and hepatoprotective properties. Methods: The Pubmed, Sage Journal, and Sciencedirect databases were searched using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) standards and the keywords "Glycyrrhiza glabra for hepatitis." The inclusion and exclusion criteria were followed. Results: From the search results, 17 publications were discovered that explain how Glycyrrhiza glabra L. can operate as an antihepatitis agent through anti-inflammatory, antiapoptotic, and hepatoprotective mechanisms. Conclusion: Glycyrrhiza glabra L. can be used as an anti-hepatitis and hepatoprotective in children at doses ranging from 240-480mg/kg/day.
Aktivitas Penyembuhan Luka Formulasi Salep Ekstrak Etanol Daun Kitolod (Isotoma longiflora) pada Mencit (Mus musculus) Faisal Akhmal Muslikh
Jurnal Dunia Farmasi Vol 7, No 2 (2023): Edisi April
Publisher : Program Studi Farmasi, Fakultas Farmasi dan Kesehatan, Institut Kesehatan Helvetia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33085/jdf.v7i2.5425

Abstract

Pendahuluan: Kitolod (Isotoma longiflora) merupakan tanaman yang memiliki manfaat untuk mengobati luka. Kitolod mengandung beberapa senyawa seperti flavonoid, saponin, dan tanin yang berperan penting dalam proses penyembuhan luka. Tujuan: Penelitian ini bertujuan untuk mengetahui aktivitas formula salep ekstrak etanol 70% daun kitolod terhadap penyembuhan luka sayat pada mencit BALB/c. Metode: Penelitian ini diawali dengan preparasi formula salep ekstrak etanol 70% daun kitolod, kemudian dilakukan uji in vivo dilakukan dengan membuat sayatan pada punggung mencit menggunakan scalpel dengan panjang 2 cm dan kedalaman 0,2 cm. Mencit diberi perlakuan formula salep ekstrak etanol daun kitolod dengan konsentrasi 12,5%, 25%, 50%, serta betadine untuk kontrol positif. Perlakuan diberikan pada hari ke-1 sampai hari ke-10, dan diamati kemajuan penyembuhannya setiap 2 hari sekali dengan mengukur panjang luka sayatan pada mencit menggunakan penggaris, dan hasilnya dianalisis menggunakan software IBM SPSS Statistic 24. Hasil: Formula salep ekstrak etanol daun kitolod konsentrasi 25% menunjukkan penyembuhan luka sayat paling cepat dengan menunjukkan penurunan intensitas warna atau eritema pada sayatan dibandingkan dengan formula salep ekstrak etanol daun kitolod konsentrasi lainnya 12,5% dan 50%. Kesimpulan: Dapat disimpulkan bahwa formula salep ekstrak etanol 70% daun kitolod memiliki aktivitas penyembuhan luka pada mencit.
SENYAWA FITOESTROGEN UNTUK POTENSI TERAPI PENYAKIT NEURODEGENERATIF TERHADAP RESEPTOR TLR2: PENDEKATAN IN SILICO Faisal Akhmal Muslikh; Rizki Rahmadi Pratama; Marisca Evalina Gondokesumo
Jurnal Kesehatan Islam : Islamic Health Journal Vol. 12 No. 1 (2023): Jurnal Kesehatan Islam : Islamic Health Journal
Publisher : Publikasi oleh Fakultas Kedokteran Universitas Islam Malang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33474/jki.v12i1.19860

Abstract

ABSTRAK Latar belakang: Toll-like receptor (TLRs) secara umum diekspresikan dalam sistem saraf pusat (SSP) dan memainkan peran penting dalam keberlangsungan hidup sel baik sel neuron, mikroglia, astrosit, dan oligodendrosit. TLR2 merupakan salah satu kelompok TLR yang banyak diteliti dan dikaitkan dengan penyakit neurodegenerative karena dapat menimbulkan kondisi pro-inflamasi dalam SSP. Senyawa fitoestrogen mampu menggantikan peran estrogen dalam menjaga homeostasis tubuh termasuk pada SSP. Penelitian ini bertujuan untuk mengetahui peran senyawa fitoestrogen dalam menghambat aktivasi TLR2 (6NIG) yang dapat menyebabkan penyakit neurodegenerative. Metode: Metode yang digunakan adalah molecular docking dengan AutoDockTools 1.5.6 program. Prediksi sifat farmakokinetik dan farmakodinamik dilakukan menggunakan SwissADME, sedangkan toksisitas menggunakan pkCSM dan ProTox II. Hasil dan Pembahasan: Hasil docking menggunakan protein 6NIG menunjukkan bahwa senyawa α-amyrin dan β-amyrin memiliki potensi terbaik dalam pengikatan dibandingkan dengan 17β-estradiol yang merupakan kontrol positif. Secara uji farmakokinetik dan farmakodinamik menunjukkan bahwa kedua senyawa tersebut memiliki permeabilitas yang baik, lipofilitas yang kuat sehingga mampu menembus membrane sel, dan tidak bersifat toksik. Kesimpulan: senyawa memiliki potensi untuk terapi penyakit neurodegenerative terhadap reseptor TLR2 (6NIG). Kata Kunci: ADMET; in silico; neurodegenerative; senyawa fitoestrogen; TLR2.
Studi In Silico Senyawa Flavonoid dalam Mengambat RNA-dependent RNA polymerase (RdRp) sebagai Antivirus COVID-19 Faisal Akhmal Muslikh; Rizki Rahmadi Pratama; Burhan Ma'arif; Neny Purwitasari
Journal of Islamic Pharmacy Vol 8, No 1 (2023): J. Islamic Pharm.
Publisher : Universitas Islam Negeri Maulana Malik Ibrahim Malang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.18860/jip.v8i1.21722

Abstract

Pada akhir tahun 2019, muncul coronavirus disease 2019 (COVID-19) yang disebabkan oleh severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), yang menjadi ancaman serius bagi kesehatan masyarakat global sampai saat ini. Seiring berjalannya waktu, pengembangan obat repurposing telah menjadi metode yang efektif. Flavonoid, sejenis senyawa, telah dikenal memiliki sifat antivirus. Oleh karena itu, tujuan dari penelitian ini adalah untuk mengidentifikasi lima senyawa flavonoid (Genistein, Daidzein, Glycitein, Formonoetin, dan Biochanin A) yang sudah dikenal memiliki berbagai manfaat farmakologi dalam menghambat aktivitas RdRp SARS-CoV-2. Untuk melakukan analisis, metode molecular docking digunakan dengan menggunakan software AutoDockTools 1.5.6. Prediksi sifat farmakokinetik dan farmakodinamik dilakukan dengan menggunakan SwissADME, sedangkan untuk mengevaluasi toksisitas, digunakan ProTox II. Hasil molecular docking menunjukkan bahwa kelima senyawa flavonoid memiliki hasil yang lebih baik dibandingkan dengan senyawa kontrol positif remdesivir. Selain itu, hasil prediksi sifat farmakokinetik, farmakodinamik, dan toksisitas menunjukkan bahwa Biochanin A, Glycitein, Genistein, dan Formonoetin memiliki potensi terbaik untuk dikembangkan sebagai obat antivirus COVID-19 dengan kemampuan mengikat reseptor RdRp dengan PDB id. 6M71.
Metabolite Profiling of the Environmental-Controlled Growth of Marsilea crenata Presl. and Its In Vitro and In Silico Antineuroinflammatory Properties Burhan Ma'arif; Faisal Akhmal Muslikh; Dilla Amalia; Anisah Mahardiani; Luthfi Achmad Muchlasi; Pramudita Riwanti; Maximus Markus Taek; Hening Laswati; Mangestuti Agil
Borneo Journal of Pharmacy Vol. 5 No. 3 (2022): Borneo Journal of Pharmacy
Publisher : Institute for Research and Community Services Universitas Muhammadiyah Palangkaraya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33084/bjop.v5i3.3262

Abstract

This study was aimed to evaluate the metabolite contents and antineuroinflammatory potential of Marsilea crenata Presl. grown under a controlled environmental condition. The antineuroinflammatory test has been carried out in vitro using ethanolic extract of M. crenata leaves on HMC3 microglia cells. An in silico approach was applied to predict the active compounds of the extract. The HMC3 microglia cells were induced with IFNγ to create prolonged inflammatory conditions and then treated with 96% ethanolic extract of the M. crenata leaves of 62.5, 125, and 250 μg/mL. The expression of MHC II was analyzed using the ICC method with the CLSM instrument. Metabolites of the extract were profiled using UPLC-QToF-MS/MS instrument and MassLynx 4.1 software. In silico evaluation was conducted with molecular docking on 3OLS protein using PyRx 0.8 software, and physicochemical properties of the compounds were analyzed using SwissADME webtool. The ethanolic extract of M. crenata leaves could reduce the MHC II expression in HMC3 microglia cells in all concentrations with the values 97.458, 139.574, and 82.128 AU. The result of metabolite profiling found 79 compounds in the extract. In silico evaluation showed that 19 compounds gave agonist interaction toward 3OLS, and three met all parameters of physicochemical analysis. The ethanolic extract of the environmental-controlled growth of M. crenata leaves antineuroinflammatory activity on HMC3 microglia cells. The extract was predicted to contain some phytoestrogen compounds which act as 3OLS agonists.
In Silico Molecular Docking and ADMET Analysis for Drug Development of Phytoestrogens Compound with Its Evaluation of Neurodegenerative Diseases Faisal Akhmal Muslikh; Reyhan Rahma Samudra; Burhan Ma’arif; Zulvikar Syambani Ulhaq; Suko Hardjono; Mangestuti Agil
Borneo Journal of Pharmacy Vol. 5 No. 4 (2022): Borneo Journal of Pharmacy
Publisher : Institute for Research and Community Services Universitas Muhammadiyah Palangkaraya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33084/bjop.v5i4.3801

Abstract

Neurodegenerative disease is one of the problems faced by postmenopausal women due to estrogen deficiency. Phytoestrogen compounds can be used as an alternative treatment for diseases caused by estrogen deficiency by binding to their receptors through the estrogen receptor (ER) dependent pathway. With in silico studies, this study aims to predict how phytoestrogen compounds will stop neurons from dying by using the dependent ER pathway. Genistein, daidzein, glycitein, formononetin, biochanin A, equol, pinoresinol, 4-methoxypinoresinol, eudesmin, α-amyrin, and β-amyrin compounds were prepared with ChemDraw Ultra 12.0. Then their pharmacokinetic and pharmacodynamic properties were examined using SwissADME. Geometry optimization of the compound was performed using Avogadro 1.0.1, and molecular docking of the compound to the ERα (1A52) and ERβ (5TOA) receptors was performed using AutoDock vina (PyRx 0.8). The interaction visualization stage was carried out with Biovia Discover Studio 2021, while the toxicity values of the compounds were analyzed using pkCSM and ProTox II. The results showed that the equol compound met the pharmacokinetic, pharmacodynamic, toxicity criteria, and had similarities with the native ligand 17β-estradiol. Equol compound inhibits neurodegeneration via an ER-dependent pathway by binding to ERα (1A52) and ERβ (5TOA) receptors.
Studi In Silico Senyawa Flavonoid dalam Mengambat RNA-dependent RNA polymerase (RdRp) sebagai Antivirus COVID-19 Muslikh, Faisal Akhmal; Pratama, Rizki Rahmadi; Ma'arif, Burhan; Purwitasari, Neny
Journal of Islamic Pharmacy Vol 8, No 1 (2023): J. Islamic Pharm.
Publisher : Universitas Islam Negeri Maulana Malik Ibrahim Malang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.18860/jip.v8i1.21722

Abstract

Pada akhir tahun 2019, muncul coronavirus disease 2019 (COVID-19) yang disebabkan oleh severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), yang menjadi ancaman serius bagi kesehatan masyarakat global sampai saat ini. Seiring berjalannya waktu, pengembangan obat repurposing telah menjadi metode yang efektif. Flavonoid, sejenis senyawa, telah dikenal memiliki sifat antivirus. Oleh karena itu, tujuan dari penelitian ini adalah untuk mengidentifikasi lima senyawa flavonoid (Genistein, Daidzein, Glycitein, Formonoetin, dan Biochanin A) yang sudah dikenal memiliki berbagai manfaat farmakologi dalam menghambat aktivitas RdRp SARS-CoV-2. Untuk melakukan analisis, metode molecular docking digunakan dengan menggunakan software AutoDockTools 1.5.6. Prediksi sifat farmakokinetik dan farmakodinamik dilakukan dengan menggunakan SwissADME, sedangkan untuk mengevaluasi toksisitas, digunakan ProTox II. Hasil molecular docking menunjukkan bahwa kelima senyawa flavonoid memiliki hasil yang lebih baik dibandingkan dengan senyawa kontrol positif remdesivir. Selain itu, hasil prediksi sifat farmakokinetik, farmakodinamik, dan toksisitas menunjukkan bahwa Biochanin A, Glycitein, Genistein, dan Formonoetin memiliki potensi terbaik untuk dikembangkan sebagai obat antivirus COVID-19 dengan kemampuan mengikat reseptor RdRp dengan PDB id. 6M71.
Co-Authors Abd Rofiq Adifa, Wildan Hanifatul Aditama, Agnis Agnis Pondineka Ria Aditama Al-Hasyimi, Said Muhammad Alrayan, Reza Andhiarto, Yanu Anis Akhwan Dhafin Anis Akhwan Dhafin Anisah Mahardiani Ardianto, Nanda Arief Suryadinata Asri Wido Mukti Asrizal Azis Asti Rahayu Aszari, Efendi H. Azis, Asrizal Azzahra, Azizah Bambang Widjaja Basuki, Dewy Begum Fauziyah Begum Fauziyah Besan, Emma Jayanti Binar Asrining Dhiani Burhan Ma'arif Burhan Ma'arif Burhan Ma'arif Burhan Ma'arif Burhan Ma’arif Burhan Ma’arif Burhan Ma’arif Candra Arifin, Candra Chandra Arifin Charliandri Saputra Wahab Choiroh, Afifahtul Dafin, Anis Akhwan Della, Desi Mujiastuti Destiya Argo Pamuji Fihuda Dewi Retno Puspitosari Dilla Amalia Dyah Aryantini, Dyah Eka Nur Fatmawati Elsa Mahardika Putri Ema Tri Wulan Emma Jayanti Besan Eryani, Mikhania Christiningtyas Evi Kurniawati, Evi Fadilla, Rahma Nur Farida, Agustini Febriana, Laela Fendy Prasetyawan Fidia Rizkiah Inayatilah Fihuda, Destiya Argo Pamuji Firdaus, Natasya Octavia Putri Firsta Roisatul Islamiyah Fita Sari, Fita Fricananta, Salma Salsabila Galih Satrio Putra Ginanjar Putri Nastiti Hakim, Adiyansyah Lukman Hasniah Hasniah Hening Laswati Putra Husnul Khotimah Ilhawa Zahra Imanda'ar, Pavitra Meilina Isma Oktadiana Ivan Junius Mesak Izza Nailia Shirvi Kamelin, Badira Kurniawan Hidayat Perdana Putra Kusumawardani, Arine Giovani Lalong, Paulus Risan F. Latarissa, Nayla Annida Luthfi Achmad Muchlasi Luthfi, Fitrati Hasanah M. Wahyu Ariawan Ma'arif, Burhan Ma’arif, Burhan Mangestuti Agil Marisca Evalina Gondokesumo Marisca Evalina Gondokesumo, Marisca Evalina Maximus M Taek Ma’arif, Burhan Mildawati, Ratna Muhammad Alviyan Shutiawan Muhammad Nurul Fadel Muzayanah, Arifatul Nahdhia, Nadhifatun Nanda Ardianto Novia Maulina Nugroho, Septiawan Nurwijayanti Octavian Ashido Nababan Oktadiana, Isma Prameswari, Fadila A. Pramudita Riwanti Priyantri, Risma Virgian Puja Adi Priatna Purbosari, Ira Purwitasari, Neny Putri, Elsa Mahardika Raharjo, Susilo Margining Ratna Mildawati Reyhan Rahma Samudra Reza, Putri Firdaus Shafiera Rina Andayani, Rina Rofiq, Abd Rosa Juwita Hesturini Sadli Syarifuddin Salmasfattah, Novyananda Sari, Dewi Perwito Sawjana, Oashiva H. Septianto, Andre Sukardiman Suko Hardjono Suryanto Suryanto Suryanto Suryanto Suryanto Susilawati, Delis Sya'adah, Puri Zumrotul Taek, Maximus M. Taek, Maximus Markus Tanaya Jati Dharma Dewi Tasya, Pradiva Julias Wahyuni, Ela Weka Sidha Bhagawan Werdiningsih, Wiwik Winayah, Mesri Ananta Wisnu Haryo Widyoko Wiwied Ekasari Wulan, Ema Tri Yuneka Sarisitiana Yuneka Saristiana Yunita Dian Permatasari Zenmas, Syendriva Zeptyan Zulvikar Syambani Ulhaq