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All Journal BIOTROPIA - The Southeast Asian Journal of Tropical Biology Jurnal Kedokteran dan Kesehatan : Publikasi Ilmiah Fakultas Kedokteran Universitas Sriwijaya Jurnal Matematika & Sains Jurnal Sains dan Teknologi Farmasi Jurnal Riset Kimia Acta Pharmaceutica Indonesia JURNAL FARMASI DAN ILMU KEFARMASIAN INDONESIA Science and Technology Indonesia Jurnal Penelitian Sains JSFK (Jurnal Sains Farmasi & Klinis) Jurnal Farmasi Indonesia SRIWIJAYA JOURNAL OF MEDICINE Jurnal Ilmu Kefarmasian Indonesia Majalah Kesehatan Indonesia Jurnal Pengabdian Masyarakat: Humanity and Medicine Journal of Community Development Jurnal Permata Indonesia Pangripta Jurnal Ilmiah Kajian Perencanaan Pembangunan Jurnal Manusia dan Lingkungan
Tri Suciati
Sekolah farmasi - ITB, Jl. Ganesha 10 Bandung
Agriculture, Biological Sciences & Forestry Humanities Biochemistry, Genetics & Molecular Biology Chemical Engineering, Chemistry & Bioengineering Chemistry Computer Science & IT Dentistry Economics, Econometrics & Finance Education Environmental Science Health Professions Immunology & microbiology Materials Science & Nanotechnology Mathematics Medicine & Pharmacology Neuroscience Nursing Physics Public Health Social Sciences Veterinary Other

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FORMULASI DAN KARAKTERISASI SEDIAAN MUKOADHESIF EKSTRAK ETANOL CENTELLA ASIATICA (L.) URB. Suciati, Tri; Prasetya, Dinda; Fidrianny, Irda; Satrialdi, -
Acta Pharmaceutica Indonesia Vol 36, No 3 & 4 (2011)
Publisher : School of Pharmacy Institut Teknologi Bandung

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Abstract

Tujuan penelitian ini adalah untuk mengembangkan dan mengevaluasi sediaanmikrosfer mukoadhesif dari ekstrak etanol Centella asiatica yang diketahui memiliki aktivitas antitukak lambung. Simplisia C. asiatica diekstraksi dengan metode refluks menggunakan etanol. Formulasi mikrosfer dilakukan dengan metode gelasi ionotropik menggunakan natrium alginat yang diinkorporasi dengan ekstrak etanol kental serta kitosan dalam larutan kalsium klorida. Variasi dilakukan terhadap konsentrasi natrium alginat, rasio bobot ekstrak dan natrium alginat, konsentrasi kitosan, dan konsentrasi kalsium klorida. Evaluasi meliputi ukuran dan distribusinya, karakteristik permukaan, efisiensi penjeratan, profil kapasitas mengembang, serta uji mukoadhesi in vitro. Formula optimum diperoleh dengan komposisi 3% natrium alginat, rasio ekstrak-natrium alginat 1:2, 0,5% kitosan, dan 0,5 M kalsium klorida. Mikrosfer yang dihasilkan memiliki distribusi ukuran terbanyak antara 630-710 ?m, efisiensi penjeratan 25,48 ± 1,88%, pertambahan bobot pada uji kapasitas mengembang 40,76 ± 1,51% (t=15 menit), dan kekuatan adhesi 78,67 ± 2,89%.
Formulasi Natrium Ascorbyl Phosphate dalam Mikroemulsi A/M VCO Tri Suciati; Lisa Patricia
Acta Pharmaceutica Indonesia Vol. 37 No. 3 (2012)
Publisher : School of Pharmacy Institut Teknologi Bandung

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Abstract

Dilakukan pengembangan formulasi mikroemulsi A/M untuk menghasikan permeasi tertinggi dari Natrium Ascorbyl Phosphate (NAP) sebagai turunan vitamin C yang stabil. Mikroemulsi dibuat dengan menggunakan VCO sebagai basis minyak, gliserin sebagai kosurfaktan, dan kombinasi Tween 80 "“ Span 80 sebagai surfaktan. Hasil mikroemulsi diperoleh pada konsentrasi surfaktan 27,5% dengan rasio Tween 80-Span 80 3:1, konsentrasi kosurfaktan gliserin 30%, dan fasa dalam 15%. Pada pengamatan organoleptik, sediaan mikroemulsi memiliki penampilan jernih kuning tanpa pemisahan fasa setelah dilakukan uji sentrifuga, freeze-thaw, danpenyimpanan 28 hari di suhu ruang dan 40°C. Sediaan memiliki viskositas rata-rata 375 cps dan pH rata-rata 6,80±0,21dengan jumlah rata-rata NAP terdifusi 850,56 μg/cm2 atau sebanyak 75,75% selama 8 jam penentuan in vitro dengan membran kulit ular. Mikroemulsi A/M berpotensi untuk dikembangkan sebagai pembawa NAP dalam kosmetik antikerut.Kata kunci: mikroemulsi, NAP, vitamin C, VCO. Optimization of formulation was done to develop a W/O microemulsion formulation to yield highest diffusion of Natrium Ascorbyl Phosphate (NAP) as the stable form of vitamin C. Microemulsions were made using using VCO as the oil phase, options of ethanol or glycerin as cosurfactant, and combination of Tween 80 and Span 80 as surfactants. Microemulsion was obtained at surfactant concentration of 27.5% with a 3:1 ratio of Tween80-Span80, 30% of glycerin as cosurfactant, and 15% of the inner phase. The organoleptic of preparations had a clear, transparent yellowish appearance without phase separation after centrifugation test, freeze-thaw test, and 28 days of storage at room temperature and 40°C. Preparations had 375 cps of average viscosity and 6.80±0.2 pH with 850.56μg/cm2 or 75.75% of NAP diffused after 8 hoursin vitro testing using snake's skin as the membrane. Microemulsion W/O is potential to be developed as a carrier for NAP in anti-wrinkle cosmetics.Keywords: microemulsion, NAP, vitamin C, VCO.
Optimasi Isolasi dan Karakterisasi Jakalin dari Biji Nangka Tri Suciati; Niknik Widanengsih; Catur Riani; Tutus Gusdinar
Acta Pharmaceutica Indonesia Vol. 37 No. 4 (2012)
Publisher : School of Pharmacy Institut Teknologi Bandung

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Abstract

Telah diisolasi jakalin dari biji nangka (Artocarpus heterophyllus) menggunakan metode kromatografi afinitas dengan matriks guar gum yang telah dipaut silang dengan epiklorohidrin, isolasi dilakukan dengan menggunakan pengelusi D-galaktosa. Hasil karakterisasi jakalin menggunakan SDS-PAGE menunjukkan bahwa jakalin memiliki dua pita dengan bobot molekul 14,1 dan 15,5 kDa, antar subunitnya tidak dihubungkan dengan ikatan disulfida. Jakalin yang diisolasi memiliki kemampuan mengaglutinasi eritrosit, kemampuan hemaglutinasi jakalin tidak berkurang setelah diinkubasi pada suhu 20oC dan 30oC, tetapi setelah inkubasi pada suhu 40oC, 50oC, 60oC, 70oC, aktivitasnya turun masing-masing 75%, 87,5%, 93,75% dan 98,4%. Kemampuan hemaglutinasi jakalin tidak berkurang setelah diinkubasi pada pH 5, 6, dan 7, tetapi aktivitasnya turun 75% setelah inkubasi pada pH 2, 3, 4, dan 8, serta turun 96,9% pada pH 9 dan 10. Kemampuan hemaglutinasi jakalin dihambat oleh D-galaktosa dengan kemampuan inhibisi hemaglutinasi sebesar 6,25 mM, aktivitas hemaglutinasi jakalin tidak dihambat oleh D-manosa, D-glukosa, fruktosa, laktosa, arabinosa, maltosa, dan manitol. Diperoleh jakalin dengan perolehan rata-rata sebesar 0,32% b/b dari serbuk kering biji nangka.Kata kunci: Jakalin, lektin, Artocarpus heterophyllus, D-galaktosa.Jacalin from jackfruit (Artocarpus heterophyllus) had been isolated using affinity chromatography method with epichlorohydrin crosslinked guar gum as the matrix, isolation carried out using D-galactose as the eluen. Characterizationjacalin using SDS-PAGE showed that jacalin has two bands with molecular weights 14.1 and 15.5 kDa, intersubunit not connected with disulfide bonds. Jacalin isolates have the ability to haemagglutination erythrocytes, haemagglutination activity of jacalin maintained after incubation at 20oC and 30oC, but the activity decreased at 40, 50, 60, and 70 oC of incubation, which were 75%, 87.5%, 93.75% and 98.4% , respectively. Jacalin hemagglutination ability is not reduced after incubation at pH 5, 6, and 7, but the activity down 75% after incubation at pH 2, 3, 4, and 8, and down 96.9% at pH 9 and 10. The haemagglutination activity of jacalin was inhibited by D-galactose with the capacity inhibition value was 6.25 mM, but it was not inhibited by D-manose, D-glucose, fructose, lactose, arabinose, maltose, and manitol. Average recovery of jacalin is 0.32% w/w of jackfruit dry powder.Keywords: Jacalin, lectin, Artocarpus heterophyllus, D-galactose.
Formulasi Sediaan Emulgel Untuk Penghantaran Transdermal Ketoprofen Sani Ega Priani; Sasanti Tarini Darijanto; Tri Suciati; Maria Immaculata Iwo
Acta Pharmaceutica Indonesia Vol. 38 No. 1 (2013)
Publisher : School of Pharmacy Institut Teknologi Bandung

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Abstract

Ketoprofen adalah obat golongan anti inflamasi non-steroid (AINS) yang banyak digunakan untuk mengobati nyeri dan inflamasi. Penggunaan oral ketoprofen dapat menimbulkan berbagai efek samping sistemik. Pemakaian transdermal diketahui mampu mencapai konsentrasi efektif pada jaringan target, dengan konsentrasi plasma yang lebih rendah dibanding penggunaan oral, sehingga dapat mengurangi resiko efek samping sistemiknya. Penelitian ini bertujuan untuk membuat sediaan emulgel untuk penghantaran transdermal ketoprofen. Propilenglikol 10% dan menthol 3% digunakan sebagai peningkat penetrasi. Sediaan dievaluasi meliputi pengamatan organoleptik, pH, viskositas, serta pengujian stabilitas fisik menggunakan metode sentrifugasi dan freeze thaw. Selanjutnya dilakukan uji difusi in vitro dan uji iritasi kulit dan mata pada kelinci. Sediaan emulgel memenuhi kriteria stabilitas fisik berdasarkan uji sentrifugasi dan freeze thaw. Nilai pH dan viskositas sediaan relatif stabil selama kurun waktu penyimapanan 120 hari pada suhu kamar. Propilenglikol dan mentol dapat meningkatkan difusi perkutan ketoprofen, yang berbeda signifikan dibandingkan emulgel tanpat peningkat penetrasi (p<0,05). Formula emulgel bersifat sedikit mengiritasi kulit dengan nilai indeks iritasi kutan 0,83-1,17 (nilai maksimal 8), tetapi tidak mengiritasi mata.Kata kunci: Ketoprofen, transdermal, emulgel, peningkat penetrasi.AbstractKetoprofen as an non-steroidal anti-inflammatory drugs (NSAIDs) used for pain and inflamation treatment. However, there are some serious adverse effects associated with oral use of NSAIDs. Transdermal route is known to reach effective local concentration with low plasma concentration resulting in reduction systemic adverse effects. The objectives of this study was to formulate emulgel of ketoprofen for transdermal delivery. Ketoprofen emulgel was prepared using 10% of propilene glycol and 3% of menthol as penetrant enhancer. Evaluation of preparation included organoleptic evaluation, pH, viscocity, and physical stability test using centrifugation and freeze thaw method. Skin permeation was evaluated in vitro using spangler membrane and irritation effect test on rabbits. Emulgels were stable after centrifugation and freeze thaw test. The viscosity and pH of preparations were relatively stable during storage at room temperature for 120 days. Propylenglycol and menthol increased diffusion rate of ketoprofen, differ significantly from emulgel without enhancer (p<0.05). Emulgel preparation were slightly irritate to the skin with irritation index 0.83-1.17 (maximum value 8) but was not irritate to the eyes.Keywords: Ketoprofen, transdermal, emulgel, penetrant enhancer
Pengaruh Superoksida Dismutase Rekombinan Staphylococcus equorum Terhadap Viabilitas Sel dan Deposisi Kolagen Pada Sel Fibroblas 3T3 Yang Dipaparkan UVA Ana Indrayati; Sukmadaja Asyarie; Tri Suciati; Debbie Soefie Retnoningrum
Jurnal Farmasi Indonesia Vol 13 No 1 (2016): Jurnal Farmasi Indonesia
Publisher : Fakultas Farmasi Universitas Setia Budi

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (80.827 KB) | DOI: 10.31001/jfi.v13i1.94

Abstract

UVA is the main external factors causing skin aging. UVA increase matrix metalloproteinase (MMP) synthesis that degrade collagen indirectly through reactive oxygen species. Superoksida dismutase (SOD) catalyzes the conversion of superoxide anions to hydrogen peroxide and oxygen. SOD can be used as a cosmetic’s component to prevent skin aging. The objective of this research to determine rSOD S. equorum ability to increase collagen deposition using fibroblast 3T3 against UVA. The research was initiated by the confirmation of E. coli BL21(DE3) carrying pJExpress®414-sod. rSOD was overproduced in E. coli BL21(DE3) by IPTG induction to a final concentration of 1 mM for 4 hours at 37oC. rSOD purification was done using an Ni-NTA affinity column with gradient imidazole concentrations for elution. Various concentrations of rSOD was added to fibroblast 3T3 cell culture after UVA irradiation to determine its role in collagen deposition. The effect of rSOD was analyzed by fibroblast viability using Alamar blue and collagen deposition with picro sirius red. The results showed that fibroblast cell viability exposed with UVA for 45 minutes in the presence of 4, 8, and 16 unit rSOD was not significantly affected, however, the collagen deposition was significantly increased about 3.02%; 20.03% and 35.75% respectively compared to cell without rSOD. This result indicates that rSOD is a good candidate for an anti photoaging agent.
Optimasi Formula Lipid Nanostruktur dengan Pentarget Manosa sebagai Sistem Penghantaran Rifampisin Tri Suciati; Nurani Istiqomah; Benny Permana; Elin Julianti; Marlia Singgih Wibowo; Titah Yudistira; Yani Triyani
JURNAL ILMU KEFARMASIAN INDONESIA Vol 17 No 2 (2019): JIFI
Publisher : Fakultas Farmasi Universitas Pancasila

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1017.477 KB) | DOI: 10.35814/jifi.v17i2.568

Abstract

Limited accumulation of anti-tuberculosis drugs in macrophages become a barrier to the success of latent tuberculosis therapy. The purpose of this study is to develop a D-mannose modified nanoparticle formula as a targeting agent to the mannose receptors to increase the internalization of rifampicin into macrophages. D-mannose was conjugated with chitosan using an amine reducing agent. Chitosan-D-mannose conjugate was characterized using FTIR. Subsequently, the conjugate was adsorbed onto the nanostructured lipid carrier (NLC) electrostatically. The NLC formula consisted of an ethyl acetate solution of solid-liquid lipid blend and rifampicin and an aqueous solution of chitosan-D-mannose conjugate, which were emulsified using polysorbate 80. Solidification of the NLC-chitosan-mannose nanoparticles was carried out by ionotropic gelation and solvent evaporation. The nanoparticle formula was optimized using Box-Behnken design. The formation of chitosan-D-mannose conjugate was shown by the change of the amide band wave number and the Schiff base formation of the FTIR spectra. The optimum formula of nanoparticles had a diameter of 766.1 ± 57.56 nm with a polydispersity index of 0.32 ± 0.02, encapsulation efficiency of 91.54 ± 0.18% and drug loading of 36.62 ± 0.07%. Rifampicin was released from the nanoparticles at pH 5.2 or 7.4 with a similar rate. This D-mannose modified NLC formula has the potential to be further developed as an intracellular antibiotic targeting to macrophages.
Optimasi Nanoemulsi A/M/A Ekstrak Etanol Daun Binahong dan Konjugat AG-Kitosan Menggunakan Desain Box-Behnken Malinda Prihantini; Irda Fidrianny; Tri Suciati
JURNAL ILMU KEFARMASIAN INDONESIA Vol 17 No 2 (2019): JIFI
Publisher : Fakultas Farmasi Universitas Pancasila

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (880.123 KB) | DOI: 10.35814/jifi.v17i2.556

Abstract

Skin premature aging which is characterized by fine wrinkles can be overcome by stimulating collagen production and inhibiting its degradation, and also reducing corneocyte buildup. Madeira vein has been shown to induce collagen production and inhibit its degradation, while glycolic acid increase desquamation. The aim of this research was to optimize W/O/W multiple nanoemulsion formula of Madeira vein-leaves extract in W1 phase and glycolic acid in W2 phase. Glycolic acid was added after conjugated with chitosan to reduce its stinging effect on skin. The W/O/W multiple nanoemulsion was prepared through two emulsification steps: W1/O primary emulsion using high speed homogenizer, and the secondary emulsion using magnetic stirrer. W1/O was optimized including the selection of co surfactant and extract concentration, followed by secondary emulsion optimization using response surface methodology consisted of 2-level factorial and Box-Behnken design. The W1/O consisted of extract, polysorbate 80 as surfactant, PEG 400 as co surfactant and isopropyl myristate as oil phase. The 2-level factorial gave the three significant factors: W1/O sonication time, W1/O concentration, and secondary emulsification stirring time. Box-Behnken optimization for globule size below 400 nm was obtained by 6-10 minutes W1/O sonication time, 12-16% W1/O concentration, and 32-42 minutes stirring time of secondary emulsification.
ENKAPSULASI DAN STABILITAS PIGMEN KAROTENOID DARI Neurospora intermedia N-1 (Encapsulation and the Stability of Carotenoids from Neurospora intermedia N-1) T. Gusdinar; Marlia Singgih; Sri Priatni; AE. Sukmawati; Tri Suciati
Jurnal Manusia dan Lingkungan Vol 18, No 3 (2011): November
Publisher : Pusat Studi Lingkungan Hidup Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/jml.18443

Abstract

ABSTRAKNeurospora sp merupakan spesies fungi yang dilaporkan menghasilkan pigmen karotenoid, yaitu metabolit sekunder yang termasuk kelompok pigmen yang berwarna kuning, jingga atau merah jingga. Pada penelitian ini telah dilakukan enkapsulasi pigmen karotenoid Neurospora intermedia N-1 menggunakan kopolimer gelatin-maltodekstrin. Suspensi dari campuran ekstrak karotenoid dengan kopolimer gelatin-maltodekstrin, dikeringkan dengan alat spray drier sehingga diperoleh serbuk karotenoid GME (gelatin-maltodekstrin-ekstrak) dan diuji stabilitasnya terhadap pengaruh penyimpanan RH 20-30%, selama 5 minggu. Hasil enkapsulasi ekstrak karotenoid diperoleh serbuk GME dengan nilai EY (encapsulation yields) ± 48%. Mikroenkapsulasi ekstrak karotenoid tersebut dapat meningkatkan kelarutannya dalam air dan stabil pada kondisi RH 20-30%, stabilitas menurun mulai pada minggu ke 3. Analisis KCKT terhadap serbuk GME menunjukkan penurunan kandungan β-karoten sekitar 30%, setelah penyimpanan 5 minggu. Analisis SEM terhadap serbuk GME menunjukkan partikel yang berbentuk bulat dan berlekuk di permukaan dengan ukuran ±1 µm.ABSTRACTNeurospora sp, a species of fungi was reported containing the carotenoid pigments, the secondary metabolite of the  yellow, orange or red-orange pigments group. On this research, the carotenoid pigments of Neurospora intermedia N-1 has been encapsulated by a copolymer of gelatin-maltodextrins. The encapsulated products were dried by a spray drier and the carotenoid powder was determined its stability to the storage influence at RH 20-30%,  for 5 weeks. Encapsulation product of carotenoids extract obtained the  GME powder with EY value± 48%. Microencapsulation of this extract was increased the water solubility and  stable at RH 20-30% condition,   the stability was decreased start at the third week. HPLC analysis of GME powder showed the decreasing of β-carotene about 30%, after storage for 5 weeks. SEM analysis of GME powder showed the globular shape and dents on the surface of particles, with size ±1 µm.
Konsumsi sayur dan buah dalam upaya mencegah penyakit tidak menular Kurniati, Ardesy Melizah; Tamzil, Nia Savitri; Dalilah, Dalilah; Prasasty, Gita Dwi; Suciati, Tri; Muhammad, Fadhil; Fitrianti, Fitrianti
Jurnal Pengabdian Masyarakat: Humanity and Medicine Vol 3 No 2 (2022): Jurnal Pengabdian Masyarakat: Humanity and Medicine
Publisher : Fakultas Kedokteran Universitas Sriwijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.32539/Hummed.V3I2.82

Abstract

Hypertension and obesity are one of the risk factors for the increasing number of non-communicable diseases. In Indonesia, in 2018 there was an increase in cases of non-communicable diseases where there were five diseases that were included as the largest cause of death. There were heart disease, cancer, and diabetes. Some of the risk factors that cause an increase in cases of non-communicable diseases include high consumption of sugar/salt/fat, smoking habits, lack of physical activity, and lack of consumption of fruits and vegetables. This study aims to determine the picture of body mass index and blood pressure as well as the portion of fruit and vegetable consumption in the community in Kelurahan 20 Ilir D-IV Palembang. In this study, there were 33 respondents consisting of 10 men and 23 women, with an age range of 23-76 years. A total of 18 respondents (54.5%) were overweight, and as many as 13 (39.4%) and 12 (36.4%) respondents had 1st degree of hypertension and pre-hypertension respectively. Of the average portions of vegetable and fruit consumption in 1 meal, as many as 15 (45.4%) and 10 (30.3%) respondents consumed less vegetables and fruits. This study shows that there were people that consume fruits and vegetable in fewer portions and have overweight and 1st degree hypertension.
Skrining kesehatan mental terhadap mahasiswa baru Fakultas Kedokteran Karim, Fatmawati; Suciati, Tri; Amalia, Ella; Ikhsan, Diyaz Syauki; Aini, Syarifah
Jurnal Pengabdian Masyarakat: Humanity and Medicine Vol 4 No 2 (2023): Jurnal Pengabdian Masyarakat: Humanity and Medicine
Publisher : Fakultas Kedokteran Universitas Sriwijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.32539/Hummed.V4I2.113

Abstract

Good mental health is needed to support the smooth learning process. Students have different learning patterns from high schools, so they must be able to adapt to the learning process. New student’s mental health screening is needed to be detected earlier. Medical Faculty (FK) Unsri has undergraduate programs (PS) such as Medical Education (PSPD), Dentistry (PSKG), Nursing (PSIK) and Psychology (PS Psychology). The educational process in FK, which is different from other faculties, can affect students' mental health. Academic and non academic problems encountered during the educational process, hinder students in their education. The aims was to determine mental health such as mental emotional disorders, the saturation and learning motivation of new undergraduate students at FK Unsri. There were 444 of 513 new students (86.54%) who were involved in this mental health screening, which PSKG (96%), PSPD (94.74%), PSIK (86.07%) and PS Psychology (47.83 %). Screening the saturation level using the Boredom Proness Scale (BPS) found that 7 (1.58%) new students were in category 4 who needed more attention from academic supervisors. Screening for mental-emotional disorders is carried out using the Self-Reporting Questionnaire (SRQ), in which 34.23% of new students have mental-emotional disorders. While the SMMS was only conducted for PSPD and PSKG students, it was found that 83.01% of students had good motivation, while 16.99% had less motivation. The results of this screening are quantitative in nature, which can be used as input and initial data for academic supervisors so that the student education process can run well.
Co-Authors Adipputra, Ricky Fajar Adnindya, Msy Rulan AE. Sukmawati AE. Sukmawati, AE. Afifah, Ervi Aminatun Ana Indrayati Angga Saputra Ardesy Melizah Kurniati Arinta, Yukko Benny Permana Cita, Juang Arwafa Dalilah Dalilah Darijanto, Sasanti Tarini DEBBIE SOEFIE RETNONINGRUM Dwi Ratnaningsih, Dwi Dwiani, R. R. Sarlita Elin Julianti Ella Amalia, Ella Fauziah, Arsy Fith Khaira Nursal Fitrianti Fitrianti, Fitrianti Gita Dwi Prasasty Gunawarman Gusdinar, Tutus Hasbi, Alfian HENI RACHMAWATI Herlina Herlina Ilyah Abdullah, Nour Indri Seta Septadina Irda Fidrianny Iwo, Maria Immaculata Januar, M. Anis Jo Suherman Julianti, Elin Karim, Fatmawati Khairunnisa Khairunnisa Legiran Legiran Lili Fitriani Lisa Patricia Lusiana Darsono Mahardika Putri, Sima Asmara Dewa Marya Malahayati, Putri Maria Immaculata Iwo Maria Immaculata Iwo Marlia Singgih Marlia Singgih Marlia Singgih Wibowo Mohamad, Che Wan Sharifah Robiah Muhammad, Fadhil Munir, Ryaas Mishbachul Niknik Widanengsih Nirwan Syarif, Nirwan Nugraha, Yuda Prasetya Nurani Istiqomah Odiesta, Muhammad Ramadhan Patricia, Lisa Prasetya, Dinda Prihantini, Malinda Rahmana Emran Kartasasmita Rahmatullah, Nurul Ilmi Rahmatullah, Nurul Ilmi Rasyid, Riana Sari Puspita Resmiyani, Ubbadah Riani, Catur Rizal Rizal Sani Ega Priani Sari, Mona Sasanti Tarini Darijanto Sasanti Tarini Darijanto, Sasanti Tarini Satrialdi, - Satrialdi, Satrialdi Sima Asmara Dewa Marya Mahardika Putri Solihah, Indah Sri Priatni Sri Priatni Sudiati, Titi Sujilah, Ajeng Rana Wulan Sukmadaja Asyarie Sumirtapura, Yeyet Cahyati Susanto, Eriwan Syarifah Aini Syauki Ikhsan, Diyaz T. Gusdinar T. Gusdinar, T. Titah Yudistira Tjandrawati Mozef Tutus Gusdinar WAHYU WIDOWATI Wardiansah Wardiansah, Wardiansah Widanengsih, Niknik Yani Triyani Yessie Widya Sari Yusril Yusuf