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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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EFFECT OF BENZALDEHYDE EXCESS IN THE SYNTHESIS OF LR-2 AND CYTOTOXIC ACTIVITY OF LR-2 AGAINTS HeLa CELL Ritmaleni, Ritmaleni; Arifin, Muhammad Fajar; Laksmiani, Ni Putu Linda; ., Rumiyati; ., Sismindari
INDONESIAN JOURNAL OF PHARMACY Vol 23 No 1, 2012
Publisher : Faculty of Pharmacy Universitas Gadjah Mada, Yogyakarta, Skip Utara, 55281, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (405.791 KB) | DOI: 10.14499/indonesianjpharm0iss0pp9-17

Abstract

LR-2(4-phenyl-3,4-dihydro-indeno[2’,1’]pyramidine-2(1H)- thione;  Leni  Ritmaleni  2),  which  designed  and  assumed  to  have biologically  activity  as  anticancer,  has  been  successfully synthesized  by  using  the  Biginelli  reaction.  This  research  was aimed  to  investigate  the  effect  of  benzaldehyde  excess  in  the synthesis  of  LR-2  and  to  evaluate  the  cytotoxic  activity  of  LR-2against HeLa cancer cell lines. The synthesis was done by reacting benzaldehyde, 2-indanone and together  with thiourea at one time as  said  as  one  pot  reaction  synthetic  methodology  and  the reaction was acid catalysed. The mole equivalent of benzaldehyde was  in  excess  compare  to  others.  The  effect  of  benzaldehyde  in excess is the higher the mole of benzaldehyde, the lower the yield of  LR-2.  The  cytotoxicity  of  LR-2  was  done  by  using  MTT  method and the LC50 was 268.15 μM.Key words : LR-2, benzaldehyde, cytotoxic, HeLa 
The Prediction of Curcumin Content in the Turmeric Rhizome with Raman Handheld Spectroscopy Wirasuta, I Made Agus Gelgel; Dewi, Cokorda Istri Tirta Rusmala; Laksmiani, Ni Putu Linda; Srinadi, I Gusti Ayu Made; Putra, Deddi Prima
Indonesian Journal of Pharmaceutical Science and Technology Vol 5, No 3 (2018)
Publisher : Indonesian Journal of Pharmaceutical Science and Technology

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (412.832 KB) | DOI: 10.15416/ijpst.v5i3.16315

Abstract

The quality control of herbal medicine should be started from the determination of the active substance at harvest time. The Raman spectrometry has been used for this propose. The aim of this study is to determine the quantification of curcumin in turmeric rhizome (Curcuma longa Linn.) using Raman spectroscopy combined with multivariate analysis of PLS-R that are expected to provide reference method for quality control in turmeric rhizome, especially for raw materials of Herbal drugs. Parameters that can be used for analysis of curcumin levels on turmeric rhizome obtained using intensity of data Raman and the data obtained from the standard method will be processed with multivariate analysis methods PLS-R. The validation value of quantification result using Raman-PLSR is seen from R2 value of 0.957, RMSEC value of 0,199 and p-value of 0.00. The study showed the developed method could be implemented on to determine the prediction quantification of raw material herbal medicine.Keyword : Curcumin,  PLS-R, Turmeric, Raman Spectroscopy
Aktivitas Kuersetin sebagai Antihipertensi secara in silico Utari, Dewa Ayu Pramesti; Anggreni, Ni Putu Ruscita; Putri, Putu Rika Jesika; Laksmiani, Ni Putu Linda
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 Ã… 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.
The Prediction of Curcumin Content in the Turmeric Rhizome with Raman Handheld Spectroscopy I Made Agus Gelgel Wirasuta; Cokorda Istri Tirta Rusmala Dewi; Ni Putu Linda Laksmiani; I Gusti Ayu Made Srinadi; Deddi Prima Putra
Indonesian Journal of Pharmaceutical Science and Technology Vol 5, No 3 (2018)
Publisher : Indonesian Journal of Pharmaceutical Science and Technology

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (412.832 KB) | DOI: 10.24198/ijpst.v5i3.16315

Abstract

The quality control of herbal medicine should be started from the determination of the active substance at harvest time. The Raman spectrometry has been used for this propose. The aim of this study is to determine the quantification of curcumin in turmeric rhizome (Curcuma longa Linn.) using Raman spectroscopy combined with multivariate analysis of PLS-R that are expected to provide reference method for quality control in turmeric rhizome, especially for raw materials of Herbal drugs. Parameters that can be used for analysis of curcumin levels on turmeric rhizome obtained using intensity of data Raman and the data obtained from the standard method will be processed with multivariate analysis methods PLS-R. The validation value of quantification result using Raman-PLSR is seen from R2 value of 0.957, RMSEC value of 0,199 and p-value of 0.00. The study showed the developed method could be implemented on to determine the prediction quantification of raw material herbal medicine.Keyword : Curcumin,  PLS-R, Turmeric, Raman Spectroscopy
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
PENETAPAN RHODAMIN B PADA SAMPEL LIPSTIK DENGAN MENGGUNAKAN KLT-SPEKTROFOTODENSITOMETRI N.N.A.S. Devi; N.P.M.P.P. Winarni; I.P. Priyasana; G.A.D. Mayagita; V. Rahmadinha; K.M. Limba; A.A.I.K. Dewi; I K.N. Sanjaya; N.P.L. Laksmiani
Jurnal Kimia (Journal of Chemistry) Vol.14 No.1 Januari 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 | Full PDF (99.374 KB) | DOI: 10.24843/JCHEM.2020.v14.i01.p13

Abstract

Lipsticks are widely used by women to beautify themselves. Among the various colors that make lipstick more interesting, red color lipstick is the most demanded one. Rhodamine B is a synthetic dye that banned for use and certified as a hazardous material according to Minister of Health of Indonesian Republic No. 376/Menkes/Per/1990 because it causes liver damage, kidney and lymph glands damage, followed with organ enlargement. The aim of this study is to identify Rhodamine B in lipsticks in the market. Samples were taken from 3 shops in Denpasar City and Badung Regency. Samples were soaked with amonia solution with using wool yarn to extract the rhodamine B dye and identification using TLC plate silica gel GF254 withn-butanol: ethyl acetate: amonia (1322:5.2:6.5) as mobile phase then detected with UV light 254 and 366 nm. Identification by spectrophotodensitometry where the TLC plate was observed in the TLC Analyzer to observe the AUC in each spot formed. The AUC obtained from the instrument illustrates the concentration of the analyte in each bottle. The result shows that 3 examined samples doesn’t contain rhodamine B. Keywords: Rhodamin B, Lipstik, TLC, Spectrophotodensitometry
OPTIMASI METODE EKSTRAKSI KUERSETIN DARI DAUN KELOR (Moringa oleifera L.) N. P. L. Laksmiani; I W. A. Widiantara; K. D. Adnyani; A. B. S. Pawarrangan
Jurnal Kimia (Journal of Chemistry) Vol.14 No.1 Januari 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 | Full PDF (596.65 KB) | DOI: 10.24843/JCHEM.2020.v14.i01.p04

Abstract

Moringa plants is very abundant in Indonesia. Moringa leaves are a source of polyphenol compounds, namely flavonoids. One of the main flavonoids found in Moringa leaves is quercetin. To be able to increase the concentration of quercetin from moringa plants, extraction is necessary. This study aims to determine the most optimal extraction method in extracting quercetin from Moringa leaves. Optimization of quersein extraction methods from Moringa leaves was carried out using maceration, soxhletation, and reflux methods. The solvent used was methanol acidified with 1,2 N HCl. Determination of the concentration of quercetin in the extract used a validated TLC-densitometry method. The highest rendement obtained from the maceration extraction method was 24.08 % w/w. Extraction by reflux and sochletation methods yielded rendement of 23.44 % w/w and 10.12 % w/w respectively. Qualitative analysis of quercetin in the extract was carried out by comparing its Rf value with the standard quercetin which is 0,4. The quercetin level of the extract from maceration extraction was the highest, which was 24.45 % w/w. Extraction using the soxhletation method obtained quercetin as much as 20.95 % w/w. Keywords: quercetin, Moringa oleifera leaves, extraction method, optimization
STUDI POTENSI SIANIDIN DAN PEONIDIN DARI UBI JALAR UNGU (ipomoea batatas L.) SEBAGAI AGEN DEPIGMENTASI SECARA IN SILICO N. P.L. Laksmiani; I G.P. Putra; I P.W. I P. W. Nugraha; I W. Suwartawan; N. K.S. Ani
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 (598.749 KB) | DOI: 10.24843/JCHEM.2019.v13.i01.p06

Abstract

Hyperpigmentation is caused by enhancement of melanin production that causes skin darkening. Purple sweet potato is one of the plants that is potentially developed as skin depigmentation agent because it contains anthocyanin. The most common types of anthocyanins in purple sweet potato are cyanidin and peonidin which are in vitro proven to be used as skin lightening. The objective of this study is to determine the potential of cyanidin and peonidin as skin depigmentation agent against target protein D-Dopachrome taumerase through in silico molecular docking method. The research steps include the preparation of target protein using Chimera 1.10.1 program, optimization of cyanidine and peonidin 3D structures using Hyperchem 8 program, validation of molecular docking method, and docking of cyanidine and peonidine on target protein using Autodock 4.2 program. The bond energy between cyanidin and peonidin with the target protein D-Dopachrome taumerase are -7.75 kcal / mol and -8.38 kcal / mol. The cyanidin and peonidin bond values ??are smaller than the native ligand, suggesting that the bond between the test compound (cyanidin and peonidin) with the target protein are stronger and more stable than the native ligand, so that the affinity of the test compound was greater than the native ligand. This suggests that the cyanidin and peonidin compounds in purple sweet potato have potential as a depigmentation agent by inhibiting D-Dopachrome taumerase protein.
AKTIVITAS AGEN PENCERAH KULIT DARI KATEKIN SECARA IN SILICO N. K. M. Giantari; I W. I. Prayoga; 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 (294.076 KB) | DOI: 10.24843/JCHEM.2019.v13.i02.p12

Abstract

Darkening of the skin results from excessive production of melanin in the skin caused by an increase in tyrosinase related protein 1 enzyme activity. Catechins are flavonoid compounds which contain antioxidants. This study aims to determine the affinity and mechanism of catechins as skin lightening agents by inhibiting tyrosinase related protein 1 target proteins in silico using molecular docking methods. The study was carried out exploratively with the stages of preparing a database of 3D structures of catechins and tyrosinase related protein 1, optimization of 3D structure of catechins, protein preparation, validation of molecular docking methods, and docking of catechins in tyrosinase related protein 1. Docking results are assessed from the bonding energy and hydrogen bonds formed between catechins and proteins. The smaller the bond energy value, the stronger the bond between the catechins and proteins. The results showed that catechins had activity as skin lightening agents because they were able to inhibit the tyrosinase related protein 1 with a bond energy value of -6,35 Kcal/mol. The energy value of the catechin bond with the tyrosinase related protein 1 is smaller than the tyrosinase related protein 1 with its native ligand. This shows that catechins have greater potential and affinity in inhibiting the tyrosinase related protein 1 enzyme with hydrogen bonds on amino acid residues, namely ARG374. Based on the results obtained, catechins have activity as skin lightening agents with the mechanism of inhibiting the tyrosinase related protein 1 enzyme so that the amount of eumelanin formed is less and the skin becomes brighter. Key words: catechins, skin lightening, tyrosinase related protein 1, in silico, molecular docking
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