Article Per Year (5 Year)
p-Index From 2020 - 2025
2.177
P-Index
This Author published in this journals
All Journal CAKRA KIMIA (Indonesian E-Journal of Applied Chemistry) INDONESIAN JOURNAL OF LEGAL AND FORENSIC SCIENCES Journal Pharmaceutical Science and Application (JPSA) Jurnal Kimia (Journal of Chemistry) METAMORFOSA Journal of Biological Sciences Jurnal Farmasi Udayana Jurnal Farmasi Klinik Indonesia Universa Medicina Acta Pharmaciae Indonesia : Acta Pharm Indo Journal of Health Sciences and Medicine Pharmacy Reports Prosiding Workshop dan Seminar Nasional Farmasi (WSNF)
Ni Made Pitri Susanti
Udayana University
Agriculture, Biological Sciences & Forestry Biochemistry, Genetics & Molecular Biology Chemical Engineering, Chemistry & Bioengineering Chemistry Dentistry Electrical & Electronics Engineering Environmental Science Health Professions Immunology & microbiology Law, Crime, Criminology & Criminal Justice Materials Science & Nanotechnology Medicine & Pharmacology Public Health

Published : 38 Documents Claim Missing Document
Claim Missing Document
Check
Articles

Found 38 Documents
Search

 1   2   3   4 
Pengaruh Pelayanan Kefarmasian Residensial terhadap Ketaatan dan Luaran Klinis Pasien Hipertensi Larasanty, Luh P. F; Meilinayanti, Ni Made L.; Susanti, Ni Made P.; Wirasuta, I Made A.G.
Indonesian Journal of Clinical Pharmacy Vol 4, No 3 (2015)
Publisher : Indonesian Journal of Clinical Pharmacy

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (71.176 KB) | DOI: 10.15416/ijcp.2015.4.3.162

Abstract

Pada era jaminan kesehatan nasional, salah satu target pelayanan kefarmasian residensial adalah pasien hipertensi yang masuk ke dalam kategori kelompok pasien rujuk balik. Penelitian ini bertujuan untuk mengetahui pengaruh pelayanan kefarmasian residensial yang dilakukan apoteker terhadap ketaatan dan luaran klinis pasien hipertensi tanpa penyakit penyerta yang menjalani rawat jalan di Rumah Sakit Umum Daerah Wangaya Kotamadya Denpasar Bali. Desain penelitian ini adalah eksperimental dengan one group pre-post test design. Sebanyak 13 pasien yang memenuhi kriteria inklusi diberikan pelayanan kefarmasian residensial selama 16 kali kunjungan dalam kurun waktu tiga bulan. Skor hasil pengukuran dianalisis menggunakan regresi linier dan Uji Wilcoxon. Pelayanan kefarmasian residensial mampumeningkatkan ketaatan pasien dalam penggunaan obat, pengaturan diet, dan aktivitas fisik dari tingkat baik menjadi tingkat ketaatan tinggi (p=0,001) serta dapat meningkatkan ketaatan pasien terhadap pembatasan konsumsi alkohol dan rokok dari tingkat baik menjadi sangat baik. Pelaksanaan pelayanan kefarmasian dapat memberikan pengaruh dalam perbaikan luaran klinis pasien berupa penurunan tekanan darah sistolik (p=0,000). Pelayanan kefarmasian residensial memiliki pengaruh terhadap peningkatan ketaatan pasien terhadap penggunaan obat, pelaksanaan diet, pelaksanaan aktivitas fisik, serta terhadap pembatasan rokok dan konsumsi alkohol sehingga dapat memperbaiki luaran klinis pasien hipertensi.Kata kunci: Hipertensi, ketaatan pasien, pelayanan kefarmasian residensial, tekanan darahImpact of Pharmaceutical Home Care on Compliances and Clinical Outcomes of Hypertensive PatientsIn the Indonesian health universal coverage system the hypertensive patients that grouped into the refer back patient treatment category, is one target of pharmaceutical home care. The aim of this study was to carried out the impact of pharmaceutical home care on patient compliances and clinical outcomes ofhypertension without compeling indication out-patient on Wangaya General Hospital in the municipality of Denpasar Bali. Design research is an experimental study with one group pre-post test design. The thirteen patients who met the inclusion criteria will be given pharmaceutical home care services for 16 visits over three months period. The complianced levels were scored and statistical analyzed using linear regression and wilcoxon test. The pharmaceutical home care visit could increase the patients adherence to antihypertensive drug administration, increasing diet compliance, and adherence of physical exercise from good adherence to excellent adherence (p value=0,001), Pharmaceutical home care visit could increase patient compliance to restrictions of smoking and alcohol consumption from good adherence to very good adherence. The decreasing of the patient’s systolic blood pressure correlated to the pharmacist home visit (p value=0,000). The pharmaceutical home care has influenced on health behavior of hypertensive patients and the patients concordance to take their medication and introduced better clinical outcome.Keywords: Blood pressure, hypertension, patient compliances, pharmaceutical home care
UJI PENAPISAN DAN PENETAPAN KADAR MORFIN DAN KODEIN DALAM PLASMA MENGGUNAKAN HIGH-PERFORMANCE THIN-LAYER CHROMATOGRAPHY- SPEKTROFOTODENSITOMETRI I Made Agus Gelgel Wirasuta; Dewa Ayu Swastini; Ni Made Pitri Susanti
CAKRA KIMIA (Indonesian E-Journal of Applied Chemistry) Vol 7 No 2 (2019): volume 7, Nomor 2, 2019
Publisher : Magister Program of Applied Chemistry, Udayana University, Bali-INDONESIA

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (535.451 KB)

Abstract

ABSTRAK: Uji skrining dan konfirmasi kandungan morfin dan kodein dalam plasma telah dikembangkan menggunakan high-performance thin-layer chromatography (HPTLC)-Spektrofotodensitometri. Penetapan kadar morfin dan kodein pada plat HPTLC dideteksi pada panjang gelombang 212 nm. Ekstraksi morfin dan kodein dari plasma menggunakan campuran kloroform dan isopropanol, dengan menggunkan metanol atau isopropanol sebagai pengendap protein. Uji konfirmasi dengan teknik di atas belum memberikan hasil yang kurang tajam. Batas dekteksi morfin adalah 48,8 ng dan kodein 70,2 ng. Diperoleh variasi batas deteksi dan batas kuantisasi analit yang sangat besar antar plat HPTLC walaupun memberikan persamaan regrasi yang hampir sama. Kata Kunci: Uji skrining, Konfirmasi, morfin, kodein, HPTLC ABSTRACT: Screening and confirmation test for morphine and codeine by high-performance thin-layer chromatography-densitometry technique has been carried out. The determination test consist of limit detection (LOD) and limit quantification (LOQ) of the analyte using HPTLC scanned on wave length of 212 nm. The morphine and codeine were extracted by liquid-liquid extraction using mixture of chloroform and isopropanol from plasma. The screening and confirmation test based on corrected hRf – value and insitu UV-spectrum of analyte delivered a not convenient result. The LOD of morphine and codeine was 48,8 and 70,2 ng. The determination of opiate by HPTLC-densitometry was obtained a great range of LOD and LOQ between plat of HPTLC, although had a fast equal of linear regression-coefficient.
OPTIMASI METODE PURIFIKASI EKSTRAK DAUN SIRIH HIJAU (Piper betle Linn) YANG MEMILIKI AKTIVITAS ANTIBAKTERI TERHADAP BAKTERI Propionibacterium Acnes W. A. Wijaya; N. L. P. V. Paramita; N. M. P. Susanti
Jurnal Kimia (Journal of Chemistry) Vol. 12 No.1 Januari 2018
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (151.992 KB) | DOI: 10.24843/JCHEM.2018.v12.i01.p07

Abstract

Propionibacterium acnes merupakan bakteri utama penyebab jerawat, dimana dilaporkan dalam suatu penelitian bahwa persentase ditemukannya bakteri P. acnes pada lesi jerawat sebesar 78,8%. Daun sirih hijau telah banyak dilaporkan memiliki aktivitas sebagai antibakteri. Kemampuan antibakteri daun sirih hijau disebabkan karena adanya senyawa golongan fenol yang terdiri dari kavikol, hydroxychavicol, chavibetol, estragol, eugenol, carvacrol dan golongan senyawa seskuiterpen. Penelitian ini bertujuan untuk mengetahui metode optimum yang menghasilkan aktivitas antibakteri terhadap bakteri P. acnes dari enam fraksi yang diperoleh. Metode purifikasi yang digunakan untuk mendapatkan ke-6 fraksi tersebut adalah LLE dengan penggunaan pelarut polar etanol-air yang tidak bercampur dengan pelarut heksan, kloroform dan dietileter. Ke-6 fraksi uji tersebut selanjutnya diuji aktivitas antibakterinya dengan metode difusi disk dan dilanjutkan dengan metode tambahan yaitu KLT bioautografi kontak. Analisis data yang dilakukan secara deskriptif terhadap nilai diameter zona hambat dengan mengkategorikannya berdasarkan CLSI dan terhadap hasil skrining fitokimia. Dari hasil penelitian ini diperoleh hanya dua fraksi yaitu fraksi n-heksan dan fraksi dietileter yang mampu menghambat pertumbuhan bakteri P. acnes dengan nilai diameter zona hambat sebesar 8 mm dan 9 mm. Metode purifikasi ekstrak daun sirih hijau yang merupakan gabungan metode maserasi dan LLE yang dilakukan belum optimal karena dilihat dari 6 fraksi yaitu fraksi etanol-air (FEA I), etanol-air (FEA II), etanol-air (FEA III), kloroform, dietil eter dan fraksi n- belum mampu menghambat pertumbuhan bakteri P. acnes dimana ke-6 fraksi tersebut termasuk dalam kategori resistant.
MOLECULAR MODELING OF CATIONIC PORPHYRINS AS LIGAD OF RADIOPHARMACEUTICAL KIT Ni Made Pitri Susanti; Rahmana E. Kartasasmita; Amir Musadad; Daryono H. Tjahjono
Jurnal Kimia (Journal of Chemistry) Vol. 5, No. 1 Januari 2011
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (536.172 KB)

Abstract

Cationic porphyrins and their interactions with DNA have become an important concern due to its role as a photosensitizer in photodynamic therapy for cancer treatment. However, this therapy technique has the disadvantage, i.e. its inability to document photographically the fluorescence observed endoscopically. The present research aims to observe the change in molecular level of cationic porphyrins which labeled by radionuclides emitting ? particle and ? radiation. Molecular models of 5,10,15,20-tetrakis-[3.4-bis (carboxymetylenoxy) imidazoliumyl] porphyrin (T3,4BCImP), 5,10,15,20-tetrakis-[3,4-bis (carboxymetylenoxy) pirazoliumyl] porphyrin (T3,4BCPzP) and its complexes which labeled by Tc and Re radionuclides were optimized and calulated by density functional theory methods (DFT). Atomic charges were calculated with natural population analysis/NPA method. The calculation result showed that Tc-T3,4BCPzP has the highest photosensitivity and the strongest affinity to DNA. Carboxylate groups of meso-subtituent of porhyrins lead to label cationic porphyrins by Tc and Re as radiopharmaceutical ligand candidates .
MOLECULAR DOCKING LIKOPEN SEBAGAI ANTIOSTEOPOROSIS SECARA IN SILICO N. M.P. Susanti; D. P.D. Saputra; P. L. Hendrayati; I. P.D.N. I. P. D. N. Parahyangan; G. A.K. Amarawati
Jurnal Kimia (Journal of Chemistry) Vol.13 No.1 Januari 2019
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (334.668 KB) | DOI: 10.24843/JCHEM.2019.v13.i01.p05

Abstract

Osteoporosis is a degenerative disease due to the reduction of mass or bone tissue so that the bones become brittle. One of the causes of the fragility of bone is the formation of free radicals due to oxidative stress by reactive oxygen species (ROS). ROS can stimulate bone resorption. Lycopene is a compound contained in tomatoes found in large quantities. Lycopene is known to have strong antioxidant activity. The purpose of this research is to know the activity of lycopene as antiosteopotosis from tomato fruit through antioxidant mechanism using molecular docking method in silico. The stages of this research are preparation of 3D lycopene structure database and SOD and GPx protein, protein preparation using Chimera 1.10.1 application, optimization of lycopene 3D structure using HyperChem 8 application, and validation of molecular docking and lycopene docking methods on the proteins using Autodock application 4.2. The results showed that lycopene was able to interact with SOD and GPx proteins shown by negative bond energy, ie -0.75 and -1,61 kcal mol respectively. These interactions show that lycopene can neutralize free radicals by inducing SOD and GPx proteins so that oxidative stress triggering the bone resorption which as one of the causes of osteoporosis can be prevented
MOLECULAR DOCKING TERPINEN-4-OL SEBAGAI ANTIINFLAMASI PADA ATEROSKLEROSIS SECARA IN SILICO N. M. P. Susanti; N. P. L. Laksmiani; N. K. M. Noviyanti; K. M. Arianti; I K. Duantara
Jurnal Kimia (Journal of Chemistry) Vol.13 No.2 Juli 2019
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (589.307 KB) | DOI: 10.24843/JCHEM.2019.v13.i02.p16

Abstract

Atherosclerosis is a chronic inflammatory disease that begins with endothelial dysfunction, it caused fat accumulation and plaque growth in the inner arteries walls. Endothelial dysfunction will activate the Mitogen Activated Protein Kinase (MAPK) pathway involving ERK1, ERK2, JNK1, JNK2, and p38MAPK proteins, as well as the Nuclear Factor Kappa B (NF-kB) pathway involving IKK proteins. Terpinen-4-ol is constituent found in the bangle rhizome. The purpose of this study were to determine the affinity and mechanisms of terpinen-4-ol against ERK1, ERK2, JNK1, JNK2, and p38MAPK proteins as anti-inflammatory in atherosclerosis performed using molecular docking method. The study was conducted exploratively with several steps such as preparation and optimization of terpinen-4-ol structure, preparation of 3D ERK1, ERK2, JNK1, JNK2, and p38MAPK proteins, validation method of molecular docking, and docking terpinen-4-ol in these proteins. The docking result are assessed from the binding energy and hydrogen bonds formed between terpinen-4-ol and proteins. The smaller value of binding energy terpinen-4-ol with target proteins showed the complex that form more stable. The result showed that terpinen-4-ol and has activity in inhibiting the inflammatory process because it is able to disturb ERK1, ERK2, JNK1, JNK2, and p38MAPK proteins with respective bond energy values -5,12; -5,24; -5,08; -5,88; and -4,99 Kcal/mol. The molecular mechanism in inhibiting the activity of ERK1, ERK2, JNK1, JNK2, and p38MAPK proteins is through the formation of hydrogen bonds in these proteins. These results show that terpinen-4-ol have the potential to inhibit inflammatory process and the formation of atherosclerotic plaque can be obstructed. Keywords : atherosclerosis, terpinen-4-ol, molecular docking, in silico
SENYAWA KUERSETIN SEBAGAI AGEN ANTIKANKER KOLOREKTAL SECARA IN SILICO P. V. P. Putri; N. M. P. Susanti; N. P. L. Laksmiani
Jurnal Kimia (Journal of Chemistry) Vol.13 No.2 Juli 2019
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (356.858 KB) | DOI: 10.24843/JCHEM.2019.v13.i02.p07

Abstract

Colorectal cancer is a third rank malignant cancer in Indonesia, generally caused by the diet of the Indonesian people who have change with the consumption of food with high fat and low in fiber, also due to the production of carcinogenic substances from the breakdown of fat. In the condition of colorectal cancer there is overexpression of COX-2 and inhibition of Caspase-3 which causes the increase of cancer cells survival and causes inhibition of apoptosis mechanism. Quercetin is one of flavonoid which known have activity as an antitumor and tested in vitro can induce apoptosis on WiDr colorectal cancer cells . The purpose of this study was to determine the affinity and mechanism of quercetin compounds on COX-2 and Caspase-3 target proteins as colorectal anticancer by in silico with molecular docking. The study was conducted exploratively with the stages of preparing a database of 3D quercetin structures, as well as COX-2 and Caspase-3 proteins, optimization of 3D quercetin structure, protein preparation, molecular docking method validation, and quercetin docking on these proteins. Docking results were assessed from the binding energy and hydrogen bonds that formed between quercetin with proteins. The smaller binding energy value, the stronger the bond between quercetin and proteins is. The results showed that quercetin had an activity as a colorectal anticancer because it was able to inhibit COX-2 and induce Caspase-3 with binding energy values of -9.54 and -4.59. These results showed that quercetin has the potential to induce apoptosis in colorectal cancer. Keywords: colorectal cancer, quercetin, caspase-3, in silico
AKTIVITAS ANTIHIPERPIGMENTASI LIKOPEN SECARA IN SILICO M. D. Widyastuti; N. K. M. Noviyanti; I K. N. S. Sanjaya; N. M. P. Susanti
Jurnal Kimia (Journal of Chemistry) Vol. 14, No. 2 Juli 2020
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24843/JCHEM.2020.v14.i02.p01

Abstract

Hiperpigmentasi disebabkan oleh terakumulasinya melanin yang berlebihan pada kulit sehingga terjadi penggelapan kulit. Hiperpigmentasi ini salah satu penyebab orang kurang percaya diri, sehingga produk kosmetik dipasaran menawarkan solusi antihiperpigmentasi. Senyawa yang umum digunakan pada produk antihiperpigmentasi adalah hidrokuinon Permasalahan penggunaan hidrokuinon terletak pada efek samping yang ditimbulkan yaitu okronosis, genotoksisitas, dan karsinogenik. Tujuan penelitian ini untuk mengetahui potensi likopen sebagai antihiperpigmentasi secara in silico dengan mekanisme penghambatan tirosinase dibandingkan dengan hidrokuinon. Metode yang digunakan adalah molecular docing. Analisis data dilakukan dengan membandingkan energi ikatan yang diperoleh dari likopen dan hidroquinone yang di-docking-kan dengan tirosinase. Energi ikatan dari kedua senyawa tersebut dengan tirosinase secara berturut-turut adalah -5,18 dan -4,22. Nilai energi ikatan tirosinase lebih rendah dibandingkan dengan hidrokuinon. Perbandingan energi ikatan dari likopen dan hidroquinone menunjukkan bahwa likopen merupakan senyawa yang memiliki potensi sebagai inhibitor tirosinase secara in silico dengan aktivitas yang lebih tinggi dibandingkan dengan hidrokuinon. Kata kunci: Hiperpigmentasi, Hidrokuinon, Likopen, In Silico
AKTIVITAS ANTI-RHEUMATOID ARTHRITIS DARI BRAZILIN DAN BRAZILEIN SECARA IN SILICO G. A. K. Amarawati; N. M. P. Susanti; N. P. L. Laksmiani
Jurnal Kimia (Journal of Chemistry) Vol.13 No.2 Juli 2019
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (373.5 KB) | DOI: 10.24843/JCHEM.2019.v13.i02.p05

Abstract

Rheumatoid arthritis is an autoimmune disease that occur by inflammation chronic which persist as a permanent symptom. That inflammatory process caused joint destruction. Production of pro-inflammatory sytokin such as Tumor Necrosis Factor Alpha (TNF-?) stimulate an autoimmunity. Active TNF-? plays a role in the occurrence of chronic inflammation, in which the formation of active TNF-? is regulated by TNF-? Converting Enzyme (TACE). Brazilin and brazilein are known to have anti-inflammatory activity and immunommodulator potentially as anti-rheumatoid arthritis. The purpose of this study were to determine the affinity and mechanisms of brazilin and brazilein against TACE proteins as anti-rheumatoid arthritis perfomed using molecular docking method. The study was conducted exploratively with several steps such as databases preparation of 3D structures brazilin, brazilein, TACE protein, optimization of brazilin and brazilein 3D structures, protein preparation, molecular docking method validation, and docking brazilin and brazilein in these proteins. The docking results are assessed from the binding energy and hydrogen bonds formed between brazilin and brazilein in proteins. The smaller value to the binding energy, will made the bond between brazilin and brazilein with proteins will be stronger and more stable. The results showed that brazilin and brazilein have activities as anti-rheumatoid arthritis because they are able to inhibit TACE proteins with respective bond energy values -7,24 for brazilin and – 7,59 kcal/mol for brazilein. These results show that brazilin and brazilein have the potential to inhibit inflammatory process and joint destruction in rheumatoid arthritis. Keywords : brazilin, brazilein, in silico, rheumatoid arthritis
IDENTIFIKASI SENYAWA GOLONGAN FENOL DARI EKSTRAK ETANOL DAUN SIRIH HIJAU (PIPER BETLE LINN.) DENGAN METODE KLT-SPEKTROFOTODENSITOMETRI Ni Made Pitri Susanti; Luh Putu Mirah Kusuma Dewi; Harlina Setiawati Manurung; I Made Agus Gelgel Wirasuta
Metamorfosa: Journal of Biological Sciences Vol 4 No 1 (2017)
Publisher : Prodi Magister Ilmu Biologi, Fakultas MIPA, Universitas Udayana

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24843/metamorfosa.2017.v04.i01.p16

Abstract

Phenol compound in Piper betle leaves has several pharmacology activities such as antibacteria, antifungi and antioxidant. The pharmacology activities of a herbal drug are influenced by the phytochemistry content, so in order to do a quality determination that provides phytochemistry profile and consistent pharmacology activities, a standardization is required. Fingerprint is the main standard to perform quality control for herbal drug. TLC-spectrophotodensitometry was used as the method in order to provide fingerprint profile of phenol compound. In this experiment, Piper betle leaves samples were extracted by reflux method using ethanol 96% as the solvent. Identification of phenol compound was done using TLC-spectrophotodensitometry with Silica gel 60 F254 as the stationary phase, toluena: ethyl acetate (93:7 v/v) as the mobile phase, FeCl3 and Folin-Ciocalteau as the reagent. The fingerprint profile of phenol compund was shown in Rf value 0,19; 0,42; and 0,62. Positive results of phenol compound are black spot on FeCl3 colour test and dark blue spot  on Folin-Ciocalteau colour test. Maximum wavelength of phenol compound was 283 nm.
Co-Authors Adhyaksa, I Nyoman Mahesa Praba Amir Musadad Anjani, Ni Luh Ari Krisma Bhadreswara, I Gede Rheza Wisnu C. Juwianti D. P.D. Saputra Daryono H. Tjahjono Dewa Ayu Swastini Dewi K. A. S. Dewi, A.A.R.P. Dewi, Luh Putu Mirah Kusuma Dewi, N. M. A. P. Diajeng Putri Dwinda Saputra Febriani, Ni Kadek Dwi G. A. K. Amarawati G. A.K. Amarawati Harlina Setiawati Manurung I Dewa Ayu Inten Dwi Primayanti, I Dewa Ayu Inten Dwi I K. Duantara I K. N. S. Sanjaya I Made Agus Gelgel Wirasuta I N.K. Widjaja I. N. T. Wisesa I. P.D.N. I. P. D. N. Parahyangan K. G. Gityarani K. M. Arianti Khatija Taher Ali L. P. M. K. Dewi Laksmiani, Ni Made Linda Luh Gede Winda Kusuma Dewi Luh Putu Febryana Larasanty Luh Putu Mirah Kusuma Dewi M. D. Widyastuti M. Primantara Made Gede Praditya Putra Meilinayanti, Ni Made L. Milawati Milawati N. K. M. Noviyanti N. K. M. Noviyanti N. L. P. V. Paramita Ni Kadek Dwi Candra Sasmita Yanti Ni Kadek Warditian Ni Kadek Warditiani Ni Putu Arista Dewi Ni Putu Linda Laksmiani Nyunda, Ricky Putra Banyim Oka M. P. L. Hendrayati P. V. P. Putri P.P.K. Vedawati P.R. Satriari Pinangkaan, C. Pradnyana, I Gusti Ngurah Agung Pramesti, Ni Luh Putu Cintya Primadewi C. Putri, Ketut Yuantarisa Kartika Putri, Lucienne Agatha Larasati Nugraha Putu Ayu Asri Damayanti Putu Oka Samirana Rahmana E. Kartasasmita Rismayanti, A. A. M. I. Riswana, I Kadek Rizki Sri Laksemi, Dewa Ayu Agus Sunariyani, P. E. A. Surudarma, I Wayan W. A. Wijaya Wiantini, Ni Made Rita Widhiastuti, K.A.P. Widjaja I N.K. Widjaja, I N. K Widjaja, I. N. K.