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All Journal INDONESIAN JOURNAL OF LEGAL AND FORENSIC SCIENCES Jurnal Kimia (Journal of Chemistry) Buletin Udayana Mengabdi Jurnal Farmasi Udayana Indonesian Journal of Cancer Chemoprevention Indonesian Journal of Pharmaceutical Science and Technology INDONESIAN JOURNAL OF PHARMACY JPSCR : Journal of Pharmaceutical Science and Clinical Research Journal of Health Sciences and Medicine Jurnal Ilmiah Medicamento Pharmacy Reports Prosiding Workshop dan Seminar Nasional Farmasi (WSNF)
Ni Putu Linda Laksmiani
Jurusan Farmasi Fakultas Matematika Dan Ilmu Pengetahuan Alam Universitas Udayana
Biochemistry, Genetics & Molecular Biology Chemical Engineering, Chemistry & Bioengineering Chemistry Computer Science & IT Dentistry Education Environmental Science Health Professions Immunology & microbiology Law, Crime, Criminology & Criminal Justice Materials Science & Nanotechnology Medicine & Pharmacology Public Health

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PENGEMBANGAN METODE REFLUKS UNTUK EKSTRAKSI ANDROGRAFOLID DARI HERBA SAMBILOTO (Andrographis paniculata (Burm.f.) Nees) Laksmiani, N. P. L.; Susanti, N.M.P.; Widjaja, I. N. K.; Rismayanti, A. A. M. I.; Wirasuta IM.A.G.
Jurnal Farmasi Udayana Vol. 4, No. 2, Tahun 2015
Publisher : Departement of Pharmacy, Faculty of Mathematics and Natural Science, Udayana University

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Abstract

Refluks merupakan metode ekstraksi dengan bantuan pemanasan. Faktor yang mempengaruhi proses ekstraksi diantaranya jumlah pelarut dan waktu ekstraksi. Penelitian ini bertujuan mengetahui jumlah pelarut dan waktu ekstraksi andrografolid yang optimum menggunakan metode refluks. Optimasi jumlah pelarut dalam ekstraksi andrografolid menggunakan metode refluks dengan perbandingan jumlah pelarut etanol 96% sebanyak 1:2, 1:3, 1:4, 1:5 dan 1:6. Optimasi waktu ekstraksi dengan variasi waktu 3, 6, 9 dan 12 jam. Penentuan jumlah pelarut dan waktu ekstraksi optimum dilakukan dengan perhitungan kadar andrografolid menggunakan metode KLT-spektrofotodensitometri yang tervalidasi. Fase diam plat silika gel 60 GF254 dielusi dengan campuran pelarut kloroform dan metanol (9:1) v/v kemudian dipindai menggunakan TLC Scanner 3 (CAMAG). Seluruh parameter telah memenuhi persyaratan validasi yaitu rata-rata perolehan kembali 85,68% (80-110%); rentang linieritas dengan r = 0,9938 (r > 0,95); nilai LOD 133,273 ng/µL; nilai LOQ 444,122 ng/µL; presisi <2%; spesifisitas dengan kemurnian puncak >0,99 dan nilai Rs >1,5. Jumlah pelarut optimum yaitu pada perbandingan 1:3 dan waktu ekstraksi optimum yaitu 6 jam.
Uji Sitotoksisitas Ekstrak Etanol Limbah Kulit Buah Naga Merah (Hylocereus polyrhizus) pada Sel Kanker Payudara Secara In Vitro dan In Silico Sarasmita, M.A; Laksmiani, N.P.L
Jurnal Farmasi Udayana Vol. 4, No. 2, Tahun 2015
Publisher : Departement of Pharmacy, Faculty of Mathematics and Natural Science, Udayana University

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Abstract

Kanker payudara merupakan salah satu penyakit yang menimbulkan angka kesakitan dan kematian tertinggi. Penderita kanker payudara pada stadium lanjut menggunakan sitostatika yang meningkatkan resiko adverse drug reaction. Buah naga (Hylocereus polyrhizus) mengandung senyawa yang diduga berperan sebagai antioksidan. Kandungan flavonoid dalam kulit buah naga diduga memiliki aktivitas antioksidan yang mampu menurunkan ROS sehingga dapat mencegah kanker. Penelitian ini bertujuan untuk menganalisis aktivitas sitotoksik ekstrak etanol kulit buah naga pada sel kanker payudara MCF-7 secara in vitro dan mengkaji mekanisme molekuler dari komponen aktif ekstrak ethanol kulit buah naga secara in silico dengan protein target PgP, IKK dan HER-2. Uji sitotoksisitas ekstrak ethanol kulit buah naga merah dilakukan dengan metode MTT. IC50 ekstrak kulit buah naga merah diukur terhadap sel MCF-7. Uji docking molekular (in silico) dilakukan dengan preparasi protein, preparasi senyawa uji, validase metode molecular docking dan docking betasianin pada HER-2, Pgp dan IKK. Hasil penelitian menunjukkan ekstrak kulit buah naga memiliki potensi sebagai agen sitotoksik pada sel MCF-7 dengan nilai IC50 387,49 ?g/mL. Potensi sitotoksik dari kulit buah naga merah diperantarai oleh kemampuan betasianin menghambat protein target IkB kinase (IKK) dengan afinitas -6,15 kkal/mol, sehingga NF-?B terinaktivasi dan proliferasi sel MCF-7 dapat terhambat.
OPTIMASI METODE EKSTRAKSI CAIR-CAIR SENYAWA-SENYAWA PADA TABLET EKSTASI DITENTUKAN DENGAN SPEKTROFOTODENSITOMETER Ida Bagus Gde Agung Raditya Eka Putra; Ni Putu Linda Laksmiani; I.N.K. Widjaja
Indonesian Journal of Legal and Forensic Sciences (IJLFS) Vol 5 (2015): Indonesian Journal of Legal and Forensic Sciences
Publisher : Penerbit, sejak 2012 : Asosiasi Ilmu Forensik Indonesia dan UPT Lab. Forensik Sain dan Kriminilogi - Universitas Udayana

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24843/IJLFS.2015.v05.i01.p01

Abstract

A research concerned on liquid-liquid extraction method optimation has been carried out. The optimation was held to choose the extraction solvent and variation of pH. The simulation solution which contained methylendioxy methampethamine, methampethamine, ketamine, and amitryptiline as the internal standard were analyzed by TLC-Spectrophotodensitometry. The extract was spotted on TLC Si 60 G F254 chromatography plate, then eluted by TB mobile phase (cyclohexhane : toluene : dietylamine = 75:15:10). The chromatography plate was scanned at 202 nm. The chromatogram was analyzed based on the ratio between the area under curve (AUC) of the analyte and the AUC of the internal standard. The concentration and the recovery of the extract was determined.The simulation solution was extracted into chloroform and toluene solvent, the best solvent was selected. The selected solvent (chloroform) was used to extract the sample in pH range 10-12. The pH 11.5 was the best condition to extract the sample.The result showed that the optimum liquid-liquid extraction of the compounds on ecstasy was chloroform as the solvent with pH 11.5. This optimum condition give recovery of MDMA (99.192%), MA (98.203%) and ketamine (88.114%).
STUDI PENGARUH BAHAN TAMBAHAN PADA POLA PUNCAK KROMATOGRAM TABLET PARASETAMOL DENGAN TLC-SPEKTROFOTODENSITOMETRI UNTUK DRUG PROFILING Kadek Joni Prayoga; Ni Putu Linda Laksmiani; I Nengah Kadjeng Widjaja
Indonesian Journal of Legal and Forensic Sciences (IJLFS) Vol 5 (2015): Indonesian Journal of Legal and Forensic Sciences
Publisher : Penerbit, sejak 2012 : Asosiasi Ilmu Forensik Indonesia dan UPT Lab. Forensik Sain dan Kriminilogi - Universitas Udayana

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24843/IJLFS.2015.v01.i01.p04

Abstract

The study of chromatogram peak pattern by influence of excipient in paracetamol tablet with TLC- Spectrophotodensitometry method for drug profiling has been done. Sample (6 kind of paracetamol tabletsfrom different factory) and reference compounds were analyzed with TB (cyclohexane : toluene:diethylamine = 75:15:10) and TAEA (toluene : acetone : ethanol: ammonia = 45:45:7:3) as mobile phase andAl-TLC Si 60 G F254 as stationary phase.The initial step was non analyte peak reduction on Al-TLC plate with washing method, drying time and temperature variation. Sample was extracted with 1 ml chloroform and Na2CO3 buffer pH 10 and spotted onAL-TLC plate. First, sample extract from same factory was spotted on one plate, continued by sample extractfrom 6 different factories on one plate which is replicated five fold on each plate that different. Plate was eluted and scanned at 210 nm. Chromatogram was analyzed by cosine and cluster function. C95 value thatwas calculated from sample was used as a parameter to determine the influence of excipient towardchromatogram peak pattern.The result of this research showed that each tablet from same factory gave C95 value near 100 if calculated with cosine function (96 - 98,7 for TB and 78 - 83 for TAEA), whereas if all tablets from 6different factories was used, the excipient from each tablet will give C95 value alteration (63 for TB and 68 for TAEA). Cluster analysis will divide sample into 3 different groups for TB and 1 group for TAEA.
STUDI TINGKAT PENYALAHGUNAAN NARKOBA PADA PELAJAR SLTA (SMA/SMK) DI KABUPATEN TABANAN Ni Putu Linda Laksmiani; Ni Putu Eka Sulastini
Indonesian Journal of Legal and Forensic Sciences (IJLFS) Vol 4 (2014): Indonesian Journal of Legal and Forensic Sciences
Publisher : Penerbit, sejak 2012 : Asosiasi Ilmu Forensik Indonesia dan UPT Lab. Forensik Sain dan Kriminilogi - Universitas Udayana

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Abstract

The level of drug abuse and drug knowledge among senior high school students in Tabanan regency has been assessed. A simple random sampling method was used to select the students. Under 90% confidence level was obtained 270 students, who involved in this study. The students were asked to answer the questionnaire to find out their knowledge of drug abuse effects. They also followed a urine screen test using rapid EMIT-test for the amphetamine, methamphetamine, opiate, cocaine, cannabis and benzodiazepine. More than 95% of students had a bad level knowledge of drug abuse effect. We found out a positive correlation between frequency students to access drug information online and attending drug-abuser prevention course to their knowledge. Base on screen test was found out just one student positive to benzodiazepine.
Skrining dan Determinasi Senyawa Golongan Opiat pada Sampel Urin dengan Teknik Immunoassay dan KLT-Spektrofotodensitometri Ni Putu Diah Kusuma Dewi; Ni Wayan Intan Indayanti; I Komang Niko Sanjaya; Anak Agung Intan Kharisma Dewi; Ni Putu Linda Laksmiani
Indonesian Journal of Legal and Forensic Sciences (IJLFS) Vol 9 No 2 (2019): Indonesian Journal of Legal and Forensic Sciences
Publisher : Penerbit, sejak 2012 : Asosiasi Ilmu Forensik Indonesia dan UPT Lab. Forensik Sain dan Kriminilogi - Universitas Udayana

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24843/IJLFS.2019.v09.i02.p03

Abstract

Opiates are a class of substances, both natural and semisynthetic that have the ability to relieve pain (analgesics), put to sleep (hypnotics), and cause feelings of joy (euphoric). Repeated use will lead to tolerance (immunity to substances) and dependence. Therefore opiate class compounds besides can be used in medicine, are also very vulnerable to abuse. So that we need a method to detect the presence of opiates in biological specimens, one of which is in the urine. In this study, testing of simulated samples that have been added with certain narcotic compounds. The process of screening of compounds in the urine can be done using the immunoassay technique with a strip test. The test results showed positive for opiates. Confirmation test using TLC Spectrophotodensitometry in the TE mobile phase system (ethyl acetate: methanol: ammonia 85: 10: 5% v/v/v) and the mobile phase TAE (methanol 100% v / v) shows the confirmation of the content of opiate compounds in urine samples simulation is morphine. The next step is the determination test with TLC Spectrophotodensitometry in the TE motion system (ethyl acetate: methanol: ammonia 85: 10: 5% v/v/v) using six series solutions with different concentrations (100, 300, 500, 700, 900, and 1100 ng / µL). The resulting correlation coefficient is 0.9762, LOD is 493.24 ng, and LOQ is 1494.66 ng. In the simulation urine sample morphine levels were 25.55 ?g / mL, 17.56 25.55 ?g / mL, and 14.96 25.55 ?g / mL at three replications. Opiates are a class of substances, both natural and semisynthetic that have the ability to relieve pain (analgesics), put to sleep (hypnotics), and cause feelings of joy (euphoric). Repeated use will lead to tolerance (immunity to substances) and dependence. Therefore opiate class compounds besides can be used in medicine, are also very vulnerable to abuse. So that we need a method to detect the presence of opiates in biological specimens, one of which is in the urine. In this study, testing of simulated samples that have been added with certain narcotic compounds. The process of screening of compounds in the urine can be done using the immunoassay technique with a strip test. The test results showed positive for opiates. Confirmation test using TLC Spectrophotodensitometry in the TE mobile phase system (ethyl acetate: methanol: ammonia 85: 10: 5% v/v/v) and the mobile phase TAE (methanol 100% v / v) shows the confirmation of the content of opiate compounds in urine samples simulation is morphine. The next step is the determination test with TLC Spectrophotodensitometry in the TE motion system (ethyl acetate: methanol: ammonia 85: 10: 5% v/v/v) using six series solutions with different concentrations (100, 300, 500, 700, 900, and 1100 ng / µL). The resulting correlation coefficient is 0.9762, LOD is 493.24 ng, and LOQ is 1494.66 ng. In the simulation urine sample morphine levels were 25.55 ?g / mL, 17.56 25.55 ?g / mL, and 14.96 25.55 ?g / mL at three replications.
Ethyl Acetate Fraction of Caesalpinia sappan L. Enhances Cisplatin’s Cytotoxicity on HeLa Cells via G1 and S Arrest through p53 Expression Ulfatul Husnaa; Ni Putu Linda Laksmiani; Ratna Asmah Susidarti; Edy Meiyanto
Indonesian Journal of Cancer Chemoprevention Vol 8, No 2 (2017)
Publisher : Indonesian Society for Cancer Chemoprevention

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14499/indonesianjcanchemoprev8iss2pp51-60

Abstract

Cisplatin (cisp) is the first line chemotherapeutic agent for several cancer diseases which can cause significant side effects and cellular resistance. Combination-chemotherapy treatment (co-chemotherapy) was reported to be able to reduce cisp effects. Therefore, this study was carried out to investigate the cytotoxic activity of ethyl acetate fraction of C. sappan (EFC) in combination with cisp by observing apoptosis induction and cell cycle profile. Cytotoxic activity was evaluated by MTT assay. Cell cycle and apoptosis analysis were performed using flow cytometry and p53 expression was analyzed using immunocytochemistry. EFC performed cytotoxic effect on HeLa cells by showing morphological changes such as cell shrinkage, rounding and decreasing of cells viability in concentration dependent manner, giving IC50 value of 65 μg/mL. Combination of EFC and cisp in low concentration decreased cell viability into 36.86%. Further assay indicated that this combination caused redistribution of cell cycle arrest in G1 and S phases through p53 stabilization in nucleus. However, that mechanism was not followed by apoptosis. These results provide evidence to support EFC development as the enhancer of cisp effect, by improving its cytotoxicity on HeLa cells. EFC increases HeLa cells sensitivity to cisp through G1 and S cells’ arrest depending on p53 expression. Key words: co-chemotherapy, EFC, cervix cancer HeLa cells, p53, G1 and S arrest.         
Brazilein Increased Cytotoxic Activity of Doxorubicin on MCF-7/DOX Cells Ni Putu Linda Laksmiani; Ratna Asmah Susidarti; Edy Meiyanto
Indonesian Journal of Cancer Chemoprevention Vol 6, No 2 (2015)
Publisher : Indonesian Society for Cancer Chemoprevention

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14499/indonesianjcanchemoprev6iss2pp58-63

Abstract

Brazilein is a compound obtained in a large amount from the dried heartwood of Secang (Caesalpinia sappan L.). Brazilein has strong cytotoxic effect in several cancer cell lines. This research was designed to evaluate the cytotoxic effect of brazilein and its combination with a chemotherapy agent, doxorubicin on MCF-7/DOX breast cancer cells. In the cytotoxicity assay, MCF-7/DOX cells were cultured in the presence of brazilein solely and in combination with doxorubicin for 24 hours and cell viability was evaluated by using MTT assay. MTT assay showed a dose-dependent inhibition of cell proliferation with IC50 value of 37 µM. Brazilein increased doxorubicin’s cytotoxic activity on MCF-7/DOX cells. Both of single treatment with different concentration of brazilein 12.5 and 25 mM or doxorubicin 0.8 and 1 mM gave cell viability percentage above 80%, but combination of them led to decrease the cell viability percentage significantly. Based on this research, it can be concluded that brazilein is potential to be developed as a co-chemotherapy agent on breast cancer cell that have been resistant to doxorubicin. Futher study must be held to evaluate its molecular mechanism.Keywords : brazilein, doxorubicin, MCF-7/DOX, cytotoxic. 
Optimization Of Isolation Method Of Carrageenan From Kappaphycuss Alvarezii Doty Using Factorial Experimental Design Ketut Widyani Astuti; Ni Putu Ayu Dewi Wijayanti; I Gusti Ngurah Agung Dewantara Putra; Ni Putu Linda Laksmiani
Journal of Health Sciences and Medicine Vol 1 No 2 (2017): JHSM (September 2017)
Publisher : Institute for Research and Community Services Udayana University

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Abstract

Kappaphycus alvarezii Doty is a species of red algae ( Rhodophyceae) producing kappa carrageenan. The value of carrageenan will increase if it is able to form thermoreversible gels. The quality of carrageenan is determined by the isolation method which includes several stages, namely soaking, extraction, purification, and drying. This study aims to obtain an optimum isolation method of carrageenan from seaweed Kappaphycus alvarezii Doty using the factorial experimental design software, Design Expert Version.7.0.0. with the characteristics that meet the standards set by FAO. The seaweed was collected from the sea in Nusa Lembongan, Bali Province. The carrageenan isolation method was optimized by varying three factors, namely the concentration of NaOH (4% and 8%), extraction time (0.5 hour and 3 hours), and precipitation time (0.25 hour and 0.5 hour) in order to obtain 8 formulae which then went through an evaluation of the physical and chemical characteristics of the carrageenan. The physical and chemical characteristics include the yield, viscosity, sulfate content, and ash content, analyzed using Design Expert Version 7.0.0 program to determine the optimum method of isolation. The analysis showed that the optimum method of carrageenan isolation was using NaOH with a concentration of 4.40%, the extraction time of 2.16 hours and the precipitation time of 0.29 hour. The physical and chemical characteristics of carrageenan with the optimum isolation method include the yield of 25.73%, the viscosity of 11.92 cPs, sulfate content of 31.95% and the ash content of 26.16% which have met the standards set by FAO.
Aktivitas Kuersetin sebagai Antihipertensi secara in silico Dewa Ayu Pramesti Utari; Ni Putu Ruscita Anggreni; Putu Rika Jesika Putri; Ni Putu Linda Laksmiani
Jurnal Ilmiah Medicamento Vol 7 No 1 (2021): Jurnal Ilmiah Medicamento
Publisher : Fakultas Farmasi Universitas Mahasaraswati Denpasar

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.36733/medicamento.v7i1.1504

Abstract

Hipertensi merupakan salah satu penyakit tidak menular yang memiliki prevalensi tinggi. Hipertensi disebabkan oleh terbentuknya Angiotensin II dari proses konversi dekapeptida inaktif Angiotensin I oleh angiotensin converting enzyme (ACE) yang akan menyebabkan penyempitan pembuluh darah. Selain itu, hipertensi juga dikaitkan dengan meningkatnya pembentukan reactive oxygen species (ROS). Pengembangan senyawa obat sebagai antihipertensi diperlukan untuk meningkatkan keberhasilan terapi yang belum adekuat. Sebagai salah satu senyawa bahan alam, kuersetin dipilih karena memiliki aktivitas sebagai ACE inhibitor yang diketahui dengan melakukan uji in silico terhadap induksi ACE. Analisis data dilakukan dengan melihat energi ikatan yang dihasilkan dan ikatan yang terbentuk antara senyawa dengan residu asam amino pada protein. Hasil penelitian ini menunjukkan bahwa senyawa kuersetin berpotensi mengatasi hipertensi. Validasi metode menunjukkan konformasi 7 memiliki nilai RMSD yaitu 2,86 Å dan energi ikatan antara protein target (ACE) dengan native ligan-nya yaitu -4.66 kkal/mol. Sedangkan nilai energi ikatan yang diperoleh antara senyawa uji kuersetin dan protein target yaitu -6,32 kkal/mol dimana ikatan hidrogen yang terbentuk menghasilkan residu asam amino ALA356, HIS383, ALA356, TYR523, dan GLU411 berturut-turut melalui gugus O-H, HE2-O, HN-O, HH-O, dan OE1-H. Nilai energi ikatan yang didapat menunjukkan bahwa senyawa uji kuersetin memiliki aktivitas farmakologi sebagai sebagai ACE inhibitor karena energi ikatannya lebih negatif dibandingkan dengan native ligand protein target yaitu lisinopril. Hal ini menunjukkan bahwa kuersetin dapat membentuk ikatan yang lebih stabil dibandingkan dengan lisinopril. Sehingga kuersetin berpotensi dalam pengembangan terapi hipertensi yang berperan sebagai ACE inhibitor.
Co-Authors A. A.W. Lestari A. B. S. Pawarrangan A.A. Bagus Yoga Saputra A.A.I.K. Dewi Adhyaksa, I Nyoman Mahesa Praba Adiluhur M. A. Anak Agung Intan Kharisma Dewi Andika Prayoga Andini, Kadek Lia Anggreni, Ni Ketut Sri Anggreni, Ni Putu Ruscita Anjani, Ni Luh Ari Krisma Arifin, Muhammad Fajar Arimbawa I.B.S. Cahyani, Ni Ketut Nitya Cokorda Istri Sri Arisanti Cokorda Istri Tirta Rusmala Dewi Coky N. W. C. D.M. Nita Pratiwi Deddi Prima Putra Dewa Ayu Pramesti Utari Dewa Ayu Swastini Dewantari A. A. I. S. H Dewi L. R. Dewi Puspita Apsari Dewi, Cokorda Istri Tirta Rusmala Dewi, Komang Dian Merta Sari Dewi, Ni Kadek Diah Parwati Diarini A. S. Dwivayana, I Kadek Diva E.I. Setyawan Edy Meiyanto Febyani, Putu Dewi Fitriari, Diah Mawarni G. A. K. Amarawati G.A.D. Mayagita H. Prabowo I G.P. Putra I Gusti Ayu Made Srinadi I Gusti Ngurah Agung Dewantara Putra I K. Duantara I K. N. Sanjaya I K.N. Sanjaya I Ketut Gede Gilang Gama Harta I Komang Niko Sanjaya I Made Agus Gelgel Wirasuta I N.K. Widjaja I Nengah Kadjeng Widjaja I P.W. I P. W. Nugraha I P.Y. Astara Putra I W. A. Widiantara I W. I. Prayoga I W. Suwartawan I.G.A. Januarta I.G.N.A.D. Putra I.K. Subagia I.N.K. Widjaja I.P. Priyasana Ida Bagus Gde Agung Raditya Eka Putra K. D. Adnyani K. D. Adnyani K. M. Arianti K. R. Reynaldi K.M. Limba K.R Suciptha K.W. Astuti Kadek Joni Prayoga Ketut Widyani Astuti Ketut Yuantarisa Kartika Putri Krisnayana, I Gede Bayu L. W. E. Lestari L.P.F. Larasanty M. A. P. P. Rashid M. B. O. Rastini M. D. Widyastuti M. I. Widiastari Mahaswari, Anak Agung Istri Rani Mirayanti, Ni Putu Dinda N. K. M. Giantari N. K. M. Giantari N. K. M. Noviyanti N. K.S. Ani N. L. P. V. Paramita N.K. Cornelia Ayu Trisna N.N.A.S. Devi N.P.A.D. Wijayanti N.P.M.P.P. Winarni N.PA.D. Wijayanti Ni Kadek Warditiani Ni Luh Ari Krisma Anjani Ni Luh Putu Cintya Pramesti Ni Made Ary Sarasmita Ni Made Pitri Susanti Ni Made Rita Wiantini Ni Putu Ayu Dewi Wijayanti Ni Putu Diah Kusuma Dewi Ni Putu Eka Leliqia Ni Putu Eka Sulastini Ni Putu Ruscita Anggreni Ni Wayan Intan Indayanti Nyunda, Ricky Putra Banyim Oka M. P. A. I. A. Siaka P. V. P. Putri P.D. Wilantari P.P. Pramita Dewi Pande Made Nova Armita Sari, Pande Made Nova Pradnyana Putra Pradnyana, I Gusti Ngurah Agung Pradnyaswari, G. A. Desya Pramesti, Ni Luh Putu Cintya Pratama, I Putu Ari Anggara Catur Pujasari, Luh Wayan Sita Purnama, I.G.P.P Putra, I Made Harimbawa Putra, Komang Dian Aditya Putra, Made Ferdio Amarta Putri, Ketut Yuantarisa Kartika Putri, Lucienne Agatha Larasati Nugraha Putri, Putu Rika Jesika Putri, Wahyu Nadi Eka Putu Rika Jesika Putri Rashid, M.A.P.P Ratna Asmah Susidarti Rismayanti, A. A. M. I. Ritmaleni, Ritmaleni Rumiyati, Rumiyati Saputra, Made Agus Widiana Sari, Ida Ayu Yadnyaningtias Permata Sasi Ani Silawarti, Putu Ayu Karunia Sismindari . Sonia Sonia Suastika, I.G.A. Sunariyani, P. E. A. Suryadewi, Kadek Dinda Ulfatul Husnaa Utari, Dewa Ayu Pramesti V. Rahmadinha Wayan Suwartawan Wiantini, Ni Made Rita Widjaja, I. N. K. Widjaja, I. N. K.. Winarti, N.W. Wiratama Nugraha Yan Ramona Yudiastra, I.K. Yustiantara, Putu Sanna