Article Per Year (5 Year)
p-Index From 2021 - 2026
4.842
P-Index
This Author published in this journals
All Journal Jurnal Ilmiah Farmasi Jurnal Farmasi Sains dan Terapan (Journal of Pharmacy Science and Practice) Pharmaciana: Jurnal Kefarmasian Jurnal Farmasi Andalas Jurnal Sains dan Teknologi Farmasi Jurnal Riset Kimia INDONESIAN JOURNAL OF PHARMACY Science and Technology Indonesia JOPS (Journal Of Pharmacy and Science) JSFK (Jurnal Sains Farmasi & Klinis) JFIOnline Jurnal Ilmu Kefarmasian Indonesia Jurnal Farmasi Higea Majalah Farmasetika JPK: Jurnal Proteksi Kesehatan Warta Pengabdian Andalas: Jurnal Ilmiah Pengembangan Dan Penerapan Ipteks Pharmaceutical And Biomedical Sciences Journal (PBSJ) Medical Sains : Jurnal Ilmiah Kefarmasian Journal of Pharmaceutical and Sciences. Medical Sains : Jurnal Ilmiah Kefarmasian Jurnal Farmasi Sains dan Terapan (Journal of Pharmacy Science and Practice)
Erizal Zaini
Departemen Farmasetik, Fakultas Farmasi, Universitas Andalas, Padang 25163
Agriculture, Biological Sciences & Forestry Biochemistry, Genetics & Molecular Biology Chemical Engineering, Chemistry & Bioengineering Chemistry Computer Science & IT Education Environmental Science Health Professions Immunology & microbiology Materials Science & Nanotechnology Medicine & Pharmacology Nursing Physics Public Health Social Sciences Other

Published : 75 Documents Claim Missing Document
Claim Missing Document
Check
Articles

Found 75 Documents
Search

 4   5   6   7   8 
ISOLASI PIPERIN DARI LADA HITAM (Piper nigrum L.) DAN UJI KEMURNIANNYA Octavia, Maria Dona; Zaini, Erizal; Hasmiwati, Hasmiwati; Revila, Gusti
Jurnal Farmasi Higea Vol 16, No 1 (2024)
Publisher : STIFARM Padang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.52689/higea.v16i1.621

Abstract

Piperin merupakan senyawa alkaloid yang terdapat di dalam lada hitam (Piper nigrum L). Pipierin diisolasi dari lada hitam dengan menggunakan metode sokletasi. Penelitian ini bertujuan untuk mendapatkan piperin hasil isolasi yang memiliki kemurnian tinggi. Uji kemurnian dilakukan secara kualitatif dan kuantitatif, meliputi monografi, kelarutan, analisa morfologi dengan menggunakan Scanning Electron Microscopy, KLT, panjang gelombang maksimum piperin, differensial scanning calorimetry (DSC), x-ray difrafraction (XRD), fourier transform-infra red (FT-IR), kromatografi cair kinerja tinggi (KCKT) dan penetapan kadar. Hasil isolasi piperin dibandingkan dengan piperin murni. Hasil rendemen piperin hasil isolasi diperoleh sebesar 2,156%. Hasil morfologi piperin isolasi menunjukkan serbuk kristal berbentuk batang berwarna kuning. Hasil analisis KLT diperoleh nilai Rf 0,314. Hasil Identifikasi ƛserapan maksimum adalah 341,40 nm. Hasil pemeriksaan titik lebur dengan DSC sebesar 132,579 OC. Hasil difraktogram menunjukkan pola difraktogram yang berbeda pada rentang sudut 2Ɵ, namun masih menunjukkan sifat kristal yang sama. Analisis spektrum FT- IR menunjukkan puncak transmitan yang sama pada bilangan gelombang. Hasil KCKT dengan fase gerak asetonitril: air (90:10) menunjukkan pola kromatogram yang sama dengan waktu retensi  adalah 3,967 menit dan memiliki kadar 100,686+2,636. Hasil uji kemurnian piperin isolasi secara kualitatif dan kuantitatif menunjukkan piperin isolasi memiliki kemurnian yang tinggi yang sama dengan piperin murni sebagai pembandingnya.
Pembentukan Kokristal Asam Usnat – N-Methyl-DGlucamine dengan Metode Penguapan Pelarut dan Pengaruhnya terhadap Penurunan Interleukin-8 pada Tikus Inflamasi Fadhila, Muthia; Umar, Salman; Zaini, Erizal
JSFK (Jurnal Sains Farmasi & Klinis) Vol 7 No 1 (2020): J Sains Farm Klin 7(1), April 2020
Publisher : Fakultas Farmasi Universitas Andalas

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.25077/jsfk.7.1.23-30.2020

Abstract

Pada penetitian ini pembentukan kokristal asam usnat-N-methyl-D-glucamine bertujuan untuk meningkatkan kelarutan dan laju disolusi asam usnat serta uji efektivitasnya dalam kadar IL-8 pada tikus inflamasi. Kokristal asam usnat–N-methyl-D-glucamine dibuat dengan perbandingan 1:1 ekuimola dengan metode penguapan pelarut menggunakan etanol. Karakterisasi sampel dilakukan dengan difraksi sinar-X, Differential Scanning Calorimetry (DSC), Fourier Transform Infrared (FTIR), dan Scanning Electron Microscopy (SEM). Evaluasi kokristal yang dilakukan mencakup uji kelarutan, uji laju disolusi, dan penentuan kadar interleukin-8 (IL-8) pada tikus inflamasi. Uji kelarutan dilakukan menggunakan pelarut air suling bebas CO2 sedangkan uji laju disolusi menggunakan media air suling bebas CO2 0.25% (b/v) sodium lauril sulfat (SLS), kedua larutan uji dianalisis menggunakan spektrofotometer UV-Vis. Pemeriksaan IL-8 tikus inflamasi menggunakan metode ELISA. Hasil karakterisasi difraksi sinar-X menunjukkan profil difraktogram yang berbeda dari komponen penyusun yang mengindikasikan terbentuknya fase kokristal. Hasil termogram DSC menunjukkan adanya puncak endotermik baru yang berbeda dengan kedua komponen penyusun. Spektrum FT-IR menunjukkan terjadinya pergeseran bilangan gelombang pada spektrum kokristal dibandingkan spektrum asam usnat dan N-methyl-D-glucamine. Analisis SEM menunjukkan perubahan morfologi partikel. Kelarutan dan laju disolusi kokristal meningkat secara signifikan (P<0,05) sebanyak 24 kali dan 23 kali dibandingkan dengan senyawa asam usnat murni. Kokristal dapat menurunkan kadar IL-8 pada tikus inflamasi yang setara dengan aktivitas antiinflamasi asetosal (P<0,05). Disimpulkan bahwa koristal asam usnat - N-methyl-D-glucamine dapat meningkatkan kelarutan, laju disolusi, dan menurunkan kadar IL-8 tikus inflamasi.
Pembentukan dan Karakterisasi Multikomponen Kristal Aseklofenak – Asam Suksinat Dengan Metode Solvent Drop Grinding. Jessica, Adhitya; Agustina, Annisa; Fitriani, Lili; Zaini, Erizal
JSFK (Jurnal Sains Farmasi & Klinis) Vol 9 (2022): J Sains Farm Klin 9(suplemen), Desember 2022
Publisher : Fakultas Farmasi Universitas Andalas

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.25077/jsfk.9.sup.138-145.2022

Abstract

Aseklofenak merupakan obat golongan antiinflamasi nonsteroid (OAINS) yang mempunyai efek farmakologi utama sebagai antiinflamasi dan analgesik, turunan asam fenil asetat. Namun, aseklofenak memiliki kelarutan yang rendah sehingga mempengaruhi bioavaibilitasnya. Penelitian ini bertujuan untuk memperbaiki laju disolusi aseklofenak melalui pembentukan multikomponen kristal dengan metode pembuatan solvent drop grinding dan asam suksinat sebagai koformer. Multikomponen kristal yang terbentuk dikarakterisasi menggunakan instrumen Powder X-ray Diffractor (PXRD), Differential Scanning Calorimeter (DSC), Fourier Transform Infrared (FT-IR) spectrometer, dan Scanning Electron Microscope (SEM). Aseklofenak yang terlarut dan terdisolusi ditentukan dengan spektrofotometer UV-Vis. Hasil karakterisasi dari multikomponen kristal: penurunan intensitas puncak pada difraktogram, penurunan titik lebur dan nilai entalpi peleburan pada  termogram, pergeseran yang tidak signifikan pada bilangan gelombang spektrum spektroskopi FT-IR, dan habit kristal baru pada hasil SEM. Hasil uji disolusi aseklofenak murni, campuran fisik dan multikomponen kristal aseklofenak-asam suksinat dalam medium dapar fosfat pH 6,8 dengan sodium lauril sulfat 0,1 % pada menit ke-60 secara berturut-turut adalah 8,43 %, 26,60 % dan 34,14 %. Dari hasil penelitian ini dapat disimpulkan bahwa multikomponen kristal aseklofenak - asam suksinat yang terbentuk merupakan tipe campuran eutektik dan dapat meningkatkan laju disolusi aseklofenak 4,09 kali dibandingkan aseklofenak murni.
Pembentukan dan Karakterisasi Dispersi Padat Kandesartan Sileksetil-HPMC dengan Teknik Solvent Co-Evaporation Jessica, Adhitya; Sari, Elvita; Yenti, Revi; Zaini, Erizal
JSFK (Jurnal Sains Farmasi & Klinis) Vol 10 No 1 (2023): J Sains Farm Klin 10(1), April 2023
Publisher : Fakultas Farmasi Universitas Andalas

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.25077/jsfk.10.1.71-77.2023

Abstract

Candesartan cilexetil (CC) merupakan agen antihipertensi yang sangat efektif tetapi memiliki kelarutan yang buruk sehingga bioavailabilitasnya terbatas. Penelitian ini bertujuan untuk meningkatkan CC terdisolusi melalui pembuatan dispersi padat dengan hidroxypropylmethylcellulose (HPMC). Dispersi padat CC-HPMC dibuat menjadi 3 formula, yaitu 2:1, 1:1 dan 1:2 (b/b) menggunakan metode solvent co-evaporation. CC tunggal, campuran fisik dan dispersi padat yang terbentuk kemudian dikarakterisasi secara fisikokimia dan pengaruh variasi konsentrasi HPMC diselidiki terhadap laju disolusi. Hasil PXRD menunjukkan penurunan intensitas puncak pada dispersi padat. Analisis termal dengan DSC memperlihatkan titik leleh yang lebih rendah pada dispersi padat. Morfologi dispersi padat menggambarkan bentuk yang berbeda dibandingkan dengan CC tunggal dan campuran fisik. Spektrum inframerah menunjukkan sedikit pergeseran pada bilangan gelombang gugus fungsi tetapi tidak terbentuk gugus fungsi baru. Disolusi dispersi padat meningkat secara signifikan, hasil uji disolusi setelah 60 menit masing-masing untuk CC tunggal, campuran fisik, dispersi padat F1, F2, dan F3 adalah 32,46 ± 0,26; 67,76 ± 0,07; 61,22 ± 0,20; 71,74 ± 0,20; dan 78,58 ± 020 (μg/ml). Kesimpulannya, sistem dispersi padat CC-HPMC mampu memodifikasi sifat fisikokimia dan meningkatkan disolusi hingga 2,42 kali CC tunggal. Selain itu, peningkatan konsentrasi HPMC berdampak positif pada peningkatan CC yang terdisolusi.
Enhancing the Solubility and Dissolution Rate of Tenoxicam through Co-Amorphous Formation with Meglumine by a Solvent Dropped Grinding Method Fitriani, Lili; Arif, Zhafira; Hasanah, Uswatul; Zaini, Erizal
Science and Technology Indonesia Vol. 10 No. 1 (2025): January
Publisher : Research Center of Inorganic Materials and Coordination Complexes, FMIPA Universitas Sriwijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.26554/sti.2025.10.1.131-138

Abstract

Tenoxicam is a non-steroidal anti-inflammatory drug (NSAID), one of the oxicam group. It is categorized as Biopharmaceutical Classification System class II, as its low solubility and high permeability. The aims of this research were to enhance the solubility and dissolution rate of tenoxicam by its modification into a co-amorphous phase with meglumine at a molar 1:1 ratio. The co amorphous form of tenoxicam-meglumine was prepared by a solvent drop grinding method, and characterized by thermal analysis using differential scanning calorimetry (DSC), solid phase by powder X-ray diffraction (PXRD), identification of functional group by Fourier-transform infrared (FT-IR) spectroscopy, and morphology by polarized light microscopy (PLM) and scanning electron microscopy (SEM). The solubility test was conducted in water, whereas the dissolution test was performed in 0.1 N HCl solution and water. The DSC thermogram demonstrated a decrease in the endothermic peak of the co-amorphous tenoxicam-meglumine. The PXRD diffractogram revealed a reduction in the peak intensity of the X-ray diffraction, which formed a halo pattern. The FT-IR spectroscopy analysis indicated the formation of the co-amorphous system. The co-amorphous of tenoxicam-meglumine solubility’s increased by 42.71-fold as compared to intact tenoxicam. The co-amorphous tenoxicam meglumine exhibited a dissolution rate of 92.71% and 100% in 0.1 N HCl and distilled water, respectively, after 60 minutes, and resulting in separate increases in dissolution efficiency by 3.05 and 9.12-times in 0.1 N HCl and distilled water. In summary, the formation of the co-amorphous phase of tenoxicam and meglumine successfully enhanced the solubility and dissolution of tenoxicam.
Ticagrelor Solubility and Dissolution Rate Enhancement Using Mesoporous Silica SBA-15 Hasanah, Uswatul; Rizky, Fattihatul; Mohd Amin, Mohd Cairul Iqbal; Zaini, Erizal
Science and Technology Indonesia Vol. 10 No. 2 (2025): April
Publisher : Research Center of Inorganic Materials and Coordination Complexes, FMIPA Universitas Sriwijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.26554/sti.2025.10.2.598-604

Abstract

Ticagrelor is a triazolopyrimidine antiplatelet agent with poor water solubility. Ticagrelor was incorporated into mesoporous silica SBA15 in this study to evaluate its physical stability and improve its solubility and dissolution rate. TEOS was employed as a silica precursor and Pluronic P123 as a template to synthesize SBA-15. Ticagrelor was loaded into SBA-15 at a mass ratio of 1:1. Physicochemical characterization was conducted using nitrogen adsorption-desorption isotherm analysis, powder X-ray diffraction (PXRD), differential scanning calorimetry (DSC), fourier-transform infrared spectroscopy (FT-IR), and scanning electron microscopy (SEM). Ticagrelor solubility and dissolution were tested using distilled water as the medium. To evaluate the physical stability, Ticagrelor-SBA-15 was stored in a climatic chamber at 75% RH and 40°C for a month and analyzed using PXRD. Physicochemical characterization indicated efficient adsorption of ticagrelor into the SBA-15 pores, resulting in an amorphous form of solid material. Meanwhile, solubility and dissolution rate testing showed respective increases of 1.33 times and 1.74 times with significant differences (p<0.05) while maintaining its physical stability after storage for one month. Based on this study, it can be concluded that the incorporation of  mesoporous SBA-15 significantly enhances ticagrelor’s solubility and dissolution rate while maintaining stability.
Enhancing Gambir's Economic Value from Processing to Bath Soap Raw Materials: Community Service Program Uswatul Hasanah; Nova Syafni; Adhitya Jessica; Erizal Zaini; Rini Agustin
Warta Pengabdian Andalas Vol 31 No 2 (2024)
Publisher : Lembaga Penelitian dan Pengabdian kepada Masyarakat (LPPM) Universitas Andalas

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.25077/jwa.31.2.277-284.2024

Abstract

Gambir, an extract derived from the leaves and branches of the gambir plant, holds significant potential for enhancing the local economy and its benefits as a cosmetics product. Jorong Balai Tampuak Pinang, Nagari Simpang Kapuak, Kecamatan Mungka, was one of the areas producing traditional gambir in Lima Puluh Kota district, West Sumatra, Indonesia. This community service initiative aimed to augment the economic value of gambir from its processing to raw materials of bath soap. The initiative began with an educational session for training participants, outlining the advantages of gambir in skincare and how to incorporate it into bath soap formulations. Following the learning session, participants actively produced gambir-contained bath soap utilizing the provided formula. The activity received favorable feedback from participants who appreciated enhancing knowledge and skills. The outcomes of this endeavor underscore the substantial potential of developing body care products utilizing gambir as a primary ingredient. Participant testimonials underscore the need to conduct similar community engagement activities to harness Gambir's further utilization of other personal care products. The collaboration between the pharmacy study program and the local community has opened new avenues for local economic development and sustainable growth, significantly impacting the local population's well-being in the region.
Body Mist-Making Training and Socialization of Cosmetic Product Registration and Marketing Authorization to Youth Organisations in Kerinci Nova Syafni; Try Andy Sahputra; Saafrida Saafrida; Uswatul Hasanah; Rini Agustin; Rahmi Yosmar; Friardi Ismed; Erizal Zaini
Warta Pengabdian Andalas Vol 31 No 2 (2024)
Publisher : Lembaga Penelitian dan Pengabdian kepada Masyarakat (LPPM) Universitas Andalas

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.25077/jwa.31.2.336-342.2024

Abstract

Indonesia is an important country that produces essential oils that are widely used in fragrance cosmetic products. The use of local essential oils for cosmetics needs to be introduced to the youth generation with the aim that they do not just become consumers. Youth organisations in Kerinci have many activities to improve their skills and abilities for a better future. Collaboration between the university and the youth organisation was achieved by providing training on doing cosmetic product training on making cosmetic products. The product uses essential oils called body mist. Nowadays, the youth still know very little about the manufacturing process of cosmetics products. To provide further benefits, this community service activity collaborated with BBPOM in Padang, West Sumatra, to explain cosmetic safety and the registration process of cosmetic products. With this series topic in this training and outreach-related cosmetics, it is hoped that it can increase business ideas for young people who are members of the Sakti Alam Kerinci Organisation.
Amine-Functionalized Mesoporous Silica SBA-15 for Enhanced Solubility and Release Rate of Gliclazide Sayyidina, Fasqina; Gumala, Azhoma; Zaini, Erizal; Hanifa, Dini; Hasanah, Uswatul
Science and Technology Indonesia Vol. 10 No. 3 (2025): July
Publisher : Research Center of Inorganic Materials and Coordination Complexes, FMIPA Universitas Sriwijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.26554/sti.2025.10.3.963-971

Abstract

Gliclazide (GLI), a sulfonylurea-class antidiabetic drug, exhibits poor aqueous solubility, limiting its bioavailability. This study aimed to enhance gliclazide’s solubility and dissolution rate by adsorbing it into mesoporous silica SBA-15 and amine-functionalized SBA-15 (SBA-15-A). SBA-15 was synthesized using Pluronic® P123 as a template and tetraethyl orthosilicate (TEOS) as the silica precursor, while 3-aminopropyltriethoxysilane (APTES) was used to introduce amine functional groups. Gliclazide was loaded into SBA-15 and SBA-15-A at a 1:3 mass ratio. The materials (GLI, SBA-15, SBA-15-A, GLI-SBA, and GLI-SBA-A) were characterized using nitrogen adsorption-desorption isotherms, differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and powder X-ray diffraction (PXRD). Characterization revealed that the pore diameters of SBA-15 and SBA-15-A were 6.079 nm and 5.483 nm, respectively. FT-IR confirmed the interaction between gliclazide and the mesoporous carriers. SEM and TEM analysis showed crystalline gliclazide and rod-shaped morphologies for the mesopores samples. DSC and PXRD results indicated that most of the gliclazide had been converted to an amorphous form. Solubility testing over 24 hours showed that GLI-SBA and GLI-SBA-A improved gliclazide solubility by 1.375- and 2.334-fold, respectively, compared to pure gliclazide. Dissolution testing in distilled water revealed a 6.033-fold and 3.887-fold increase in the release rate at 5 minutes for GLI-SBA and GLI-SBA-A, respectively. Both solubility and release rate improvements were statistically significant (p <0.05). These findings suggest that amine functionalization of SBA-15 effectively enhances the solubility and dissolution rate of gliclazide.
Pembentukan dan karakterisasi kristal cair aceklofenak untuk sistem penghantaran transdermal Agustin, Rini; Mutiara Zulkarnaini; Zaini, Erizal
JSFK (Jurnal Sains Farmasi & Klinis) Vol 12 No 1 (2025): J Sains Farm Klin 12(1), April 2025
Publisher : Fakultas Farmasi Universitas Andalas

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.25077/jsfk.12.1.81-91.2025

Abstract

Aceclofenac is a phenylacetic acid derivative classified as a nonsteroidal anti-inflammatory drug (NSAID) used to relieve pain caused by inflammation. It has potential for topical application through a transdermal delivery system. One promising approach is the use of liquid crystals as carriers in transdermal dosage forms. This study aims to develop a simple liquid crystal cream formulation for aceclofenac, using glyceryl monostearate as a mesogen and Pluronic as a stabilizer. The aceclofenac liquid crystal cream was characterized using Polarized Light Microscopy (PLM), Attenuated Total Reflectance-Fourier Transform Infrared Spectroscopy (ATR-FTIR), and Differential Scanning Calorimetry (DSC). Evaluations included drug release, permeation, viscosity, flow properties, zeta potential, and freeze-thaw stability. The optimal formulation consisted of oil: glyceryl monostearate–Pluronic P123: water in a 5:15:80% ratio. PLM results showed birefringence and a lamellar phase texture. FTIR analysis confirmed no new chemical bonds, while DSC indicated a reduced melting point and increased enthalpy of fusion. The release and permeation of aceclofenac after 6 hours were 27.849 ± 0.5479 µg/cm² and 21.093 ± 0.5761 µg/cm², respectively—higher than non-liquid crystal preparations. The cream exhibited thixotropic flow behavior, a zeta potential of -50.8 mV, and remained stable after six freeze-thaw cycles. In coclusion, Aceclofenac can be formulated into a liquid crystal cream with glyceryl monostearate as a mesogen, showing a birefringent lamellar phase that enhances its release and permeation
Co-Authors -, Salman Adhitya Jessica Agusri Boestari Agustina, Annisa Akmal Djamaan Amri Bakhtiar Andarifera, Alya Zahira Annisa Agustina Aprilianti, Hizra Dwi Arif, Zhafira Asiska Permata Dewi Asiska Permata Dewi Asiska Permatadewi Auzal Halim Auzal Halim Azzahra, Cindy Maynia Ben, Elfi Sahlan Deni Anggraini Deni Noviza Dhea Sultana Lutfiyah DINI HANIFA, DINI Dwi Setyawan Ellyza Nasrul Elpa Giovana Zola Elsa Badriyya Elvi Rahma Yulisman Elvita Sari Fadhila, Muthia Fauzi Saputra Fifi Harmely Friardi Ismed Gaesari, Sherly Rahmah Gaesari, Sherly Rahmah Gumala, Azhoma Habibie Deswilyaz Ghiffari Hansen Nasif Haq AH, Ahdi Dinil Hasmiwati Helen Sonita Henny Lucida Hulwa Salsabila Ihsan, Ikhwanul Ima Kurniati Irna Kurniati Jessica, Adhitya Kiki Rizky Wirza Kurniati, Irna Lili Fitriani Mai Efdi Maria Dona Octavia Melanny Ika Sulistyowaty Melisa Melisa Melzi Octaviani Mohd Amin, Mohd Cairul Iqbal Muhammad Taher Muthia Fadhila Mutiara Zulkarnaini Najmi Hilaliyati Netty Novitasari Nova Syafni Novica Sari Prameswari, Putu Pradnya Mimba Raden Joko Kuncoroningrat Susilo Rahmadasmi, Nola Rahmadevi Rahmi Nofita Rahmi Yosmar Rahmi Yosmar Resva Meinisasti Revila, Gusti Reza Safitri Rifka Naura Rini Agustin Rini Agustin Rizky, Fattihatul Rosaini, Henni Rose Intan Perma Sari Rustini Rustini Rustini Rustini S, Agnes Saafrida Saafrida Saafrida Saafrida Saafrida Salman - Salman - Salman Salman Salman Umar Sari, Elvita Sayyidina, Fasqina Simbolon, Clara Alverina Sundani N. Soewandhi Sundani N. Soewandhi, Sundani N. Syofyan Syofyan SYUKRAN HAMDENI Syukriati Chaira Tahta Amrillah Trisfa Augia Try Andy Sahputra Try Andy Sahputra Usman, Hendrizal Uswatul Hasanah Uswatul Hasanah, Uswatul Verlia Nisrina Putri Vike Zulia Putri Vina Oktavia Yeni Novita Sari Yeyet C. Sumirtapura Yufri Aldi Yuliza, Sukma Yuska Noviyanty Zahara Gayo Zidan, Sabry A. H. Zulhadjri Zulhadjri