OPTIMASI POLIVINILPIROLIDON DAN CARBOPOL PADA SEDIAAN PATCH DISPERSI PADAT PIROKSIKAM

2018 ◽  
Vol 3 (2) ◽  
pp. 197
Author(s):  
Dwi Nurahmanto ◽  
Friska Wira Sabrina ◽  
Lidya Ameliana

Piroxicam, a non steroidal anti inflammatory drugs (NSAID), is an oxicam derivative which can be used for treatment of various rheumatic diseases, such as rheumatoid arthritis and osteoarthritis. Piroxicam patch is an affective approach evading piroxicam’s side effect such as peptic ulcer and first pass metabolism. One of the patch components is polymer that the function is to control the speed of drug release from the patch. The aims of this study were to determine the optimum formula of a combination of polyvinylpyrolidone (PVP) and Carbopol to % moisture content (MC) and the flux release in solid dispersion piroxicam patch using Simplex Lattice Design. Piroxicam was prepared in the form of a solid dispersion in PEG 4000 to increase its solubility. The design formula of solid dispersion piroxicam patch made with the ratio PVP : Carbopol, that were 1 : 0; 0.5 : 0.5; 0 : 1. The optimum formula was chosen with the ratio PVP : Carbopol, 1: 0, which gave the best result of % MC and flux release. The result of % MC was 6.91% and the result of flux release was 35.543 µg/cm2.menit1/2.

2018 ◽  
Vol 5 (2) ◽  
pp. 80
Author(s):  
Dwi Nurahmanto ◽  
Nurul Shalikha ◽  
Lidya Ameliana

<p align="center"><strong>Abstrak</strong></p><p align="center"> </p><p>Piroksikam merupakan anti inflamasi non steroid (AINS) turunan oksikam yang berkhasiat sebagai analgesik dan antiinflamasi digunakan untuk pengobatan <em>rheumatoid arthritis</em> dan <em>osteoarthritis</em>. Piroksikam menyebabkan masalah pada saluran cerna dan <em>first pass metabolism</em> yang dapat dihindari dengan cara pemberian transdermal <em>patch.</em> Salah satu komponen <em>patch</em> yaitu polimer yang berfungsi untuk mengontrol kecepatan pelepasan obat dari sediaan. Penelitian ini dilakukan untuk menentukan komposisi terbaik dari kombinasi polimer hidroksipropil metilselulosa (HPMC) dan Carbopol terhadap <em>% moisture content</em> (MC) dan <em>flux</em> pelepasan sediaan transdermal <em>patch </em>dispersi padat piroksikam dengan rancangan formula <em>Simplex Lattice Design</em>. Piroksikam dibuat dalam bentuk dispersi padat dengan pembawa PEG 4000 untuk meningkatkan kelarutannya. Rancangan formula <em>patch</em> dispersi padat piroksikam dibuat dengan menggunakan tiga polimer Etil selulosa:HPMC:carbopol dimana yang divariasikan adalah perbandingan HPMC : Carbopol yaitu 1 : 0 ; 0,5 : 0,5 ; 0 : 1. Hasil uji menunjukkan ketiga formula memenuhi persyaratan keseragaman kadar dengan rentang keseragaman 3,735 – 97,349 %. Hasil juga menunjukkan formula 3 menghasilkan patch yang lebih tebal, pH permukaan patch lebih rendah, nilai % moisture content lebih besar dan nilai flux lebih tinggi dibandingkan formula 2 dan formula 3, Formula 3 mempunyai nilai % moisture content yang memenuhi persyaratan sebesar 6,613% dan nilai <em>flux</em> pelepasa yang paling bagus sebesar 32,562 µg/cm<sup>2</sup>.menit<sup>1/2</sup>. Hasil penelitian juga menunjukkan formula 1 memiliki keseragaman bobot lebih baik dibandingkan formula 2 dan formula 3. Dapat disimpulkan bahwa komposisi optimum dari kombinasi polimer HPMC dan Carbopol pada sediaan <em>patch</em> dispersi padat piroksikam yaitu formula dengan komposisi polimer HPMC sebanyak 0 mg dan Carbopol sebanyak 75 mg.</p><p> </p><p><strong>Kata kunci</strong><em>:</em><em>     </em>Dispersi padat, <em>patch </em>piroksikam, HPMC, Carbopol</p><p align="center"> </p><p align="center"><strong><em>Optimization of Hydroxypropyl Methylcellulose K-4M</em></strong><strong> <em>and  Carbopol® 940 in</em></strong><strong><em> </em></strong><strong><em>Solid Dispersion Piroxicam Patch</em></strong><strong><em></em></strong></p><p align="center"> </p><p align="center"><strong><em>Abstract</em></strong></p><p><strong> </strong></p><p><em>Piroxicam is a non-steroidal anti-inflammatory (NSA) oxysmic derivative as an analgesic and anti-inflammatory agent used for the treatment of rheumatoid arthritis and osteoarthritis. Piroxicam causes problems in the gastrointestinal tract and first pass metabolism that can be avoided by giving transdermal patches. One of the patch components is a polymer that serves to control the speed of drug release from the preparation. The present study was conducted to determine the best composition of the combination of hydroxypropyl methylcellulose (HPMC) and Carbopol polymers against% moisture content (MC) and fluxes release of the pyroxicam dispersion transdermal patch dispersion with the design of the Simplex Lattice Design formula. Piroxicam is prepared in the form of a solid dispersion with a PEG 4000 carrier to increase its solubility. The design of a pyroxicam solid dispersion patch formulation was prepared using three ethyl cellulose polymers: HPMC: carbopol wherein the HPMC ratio is computed: Carbopol is 1: 0; 0.5: 0.5; 0: 1. The test results show the three formulas meet the requirements of uniformity of the content with a uniformity range of 3.735 - 97.349%. the results also show formula 3 resulting in thicker patches, lower patch pH surfaces, greater moisture content values and higher flux values than formula 2 and formula 3, Formula 3 has a moisture content value of 6.613% the finest fl ux flux of 32,562 μg / cm2.menit1 / 2. The results also show that formula 1 has better weight uniformity than formula 2 and formula 3. It can be concluded that the optimum composition of HPMC and Carbopol polymer combinations in the preparation of piroxicam solid dispersion patch is a formula with HPMC polymer composition as 0 mg and Carbopol as much as 75 mg..</em></p><p><strong><em> </em></strong></p><p><strong><em>Key</em></strong><strong><em> </em></strong><strong><em>words</em></strong><em>: </em><em>     </em><em>solid dispersion, piroxicam patch, HPMC, Carbopol</em></p>


2017 ◽  
Vol 5 (2) ◽  
pp. 80
Author(s):  
Dwi Nurahmanto ◽  
Nurul Shalikha ◽  
Lidya Ameliana

<p align="center"><strong>Abstrak</strong></p><p align="center"> </p><p>Piroksikam merupakan anti inflamasi non steroid (AINS) turunan oksikam yang berkhasiat sebagai analgesik dan antiinflamasi digunakan untuk pengobatan <em>rheumatoid arthritis</em> dan <em>osteoarthritis</em>. Piroksikam menyebabkan masalah pada saluran cerna dan <em>first pass metabolism</em> yang dapat dihindari dengan cara pemberian transdermal <em>patch.</em> Salah satu komponen <em>patch</em> yaitu polimer yang berfungsi untuk mengontrol kecepatan pelepasan obat dari sediaan. Penelitian ini dilakukan untuk menentukan komposisi terbaik dari kombinasi polimer hidroksipropil metilselulosa (HPMC) dan Carbopol terhadap <em>% moisture content</em> (MC) dan <em>flux</em> pelepasan sediaan transdermal <em>patch </em>dispersi padat piroksikam dengan rancangan formula <em>Simplex Lattice Design</em>. Piroksikam dibuat dalam bentuk dispersi padat dengan pembawa PEG 4000 untuk meningkatkan kelarutannya. Rancangan formula <em>patch</em> dispersi padat piroksikam dibuat dengan menggunakan tiga polimer Etil selulosa:HPMC:carbopol dimana yang divariasikan adalah perbandingan HPMC : Carbopol yaitu 1 : 0 ; 0,5 : 0,5 ; 0 : 1. Hasil uji menunjukkan ketiga formula memenuhi persyaratan keseragaman kadar dengan rentang keseragaman 3,735 – 97,349 %. Hasil juga menunjukkan formula 3 menghasilkan patch yang lebih tebal, pH permukaan patch lebih rendah, nilai % moisture content lebih besar dan nilai flux lebih tinggi dibandingkan formula 2 dan formula 3, Formula 3 mempunyai nilai % moisture content yang memenuhi persyaratan sebesar 6,613% dan nilai <em>flux</em> pelepasa yang paling bagus sebesar 32,562 µg/cm<sup>2</sup>.menit<sup>1/2</sup>. Hasil penelitian juga menunjukkan formula 1 memiliki keseragaman bobot lebih baik dibandingkan formula 2 dan formula 3. Dapat disimpulkan bahwa komposisi optimum dari kombinasi polimer HPMC dan Carbopol pada sediaan <em>patch</em> dispersi padat piroksikam yaitu formula dengan komposisi polimer HPMC sebanyak 0 mg dan Carbopol sebanyak 75 mg.</p><p> </p><p><strong>Kata kunci</strong><em>:</em><em>     </em>Dispersi padat, <em>patch </em>piroksikam, HPMC, Carbopol</p><p align="center"> </p><p align="center"><strong><em>Optimization of Hydroxypropyl Methylcellulose K-4M</em></strong><strong> <em>and  Carbopol® 940 in</em></strong><strong><em> </em></strong><strong><em>Solid Dispersion Piroxicam Patch</em></strong><strong><em></em></strong></p><p align="center"> </p><p align="center"><strong><em>Abstract</em></strong></p><p><strong> </strong></p><p><em>Piroxicam is a non-steroidal anti-inflammatory (NSA) oxysmic derivative as an analgesic and anti-inflammatory agent used for the treatment of rheumatoid arthritis and osteoarthritis. Piroxicam causes problems in the gastrointestinal tract and first pass metabolism that can be avoided by giving transdermal patches. One of the patch components is a polymer that serves to control the speed of drug release from the preparation. The present study was conducted to determine the best composition of the combination of hydroxypropyl methylcellulose (HPMC) and Carbopol polymers against% moisture content (MC) and fluxes release of the pyroxicam dispersion transdermal patch dispersion with the design of the Simplex Lattice Design formula. Piroxicam is prepared in the form of a solid dispersion with a PEG 4000 carrier to increase its solubility. The design of a pyroxicam solid dispersion patch formulation was prepared using three ethyl cellulose polymers: HPMC: carbopol wherein the HPMC ratio is computed: Carbopol is 1: 0; 0.5: 0.5; 0: 1. The test results show the three formulas meet the requirements of uniformity of the content with a uniformity range of 3.735 - 97.349%. the results also show formula 3 resulting in thicker patches, lower patch pH surfaces, greater moisture content values and higher flux values than formula 2 and formula 3, Formula 3 has a moisture content value of 6.613% the finest fl ux flux of 32,562 μg / cm2.menit1 / 2. The results also show that formula 1 has better weight uniformity than formula 2 and formula 3. It can be concluded that the optimum composition of HPMC and Carbopol polymer combinations in the preparation of piroxicam solid dispersion patch is a formula with HPMC polymer composition as 0 mg and Carbopol as much as 75 mg..</em></p><p><strong><em> </em></strong></p><p><strong><em>Key</em></strong><strong><em> </em></strong><strong><em>words</em></strong><em>: </em><em>     </em><em>solid dispersion, piroxicam patch, HPMC, Carbopol</em></p>


2021 ◽  
Vol 9 (1) ◽  
pp. 9
Author(s):  
Lusia Oktora Ruma Kumala Sari ◽  
Septi Sudianingsih ◽  
Yudi Wicaksono

Diltiazem HCl is a class of benzodiazepine calcium channel blockers used to treat angina pectoris, arrhythmias, and hypertension. Diltiazem HCl improves first-pass metabolism, a short half time of 3-5 hours, and bioavailability of diltiazem for oral administration of about 40%. Mucoadhesive buccal film diltiazem HCl releases the drug to the buccal mucosa, so the first pass metabolism can be avoided because of its absorption through the venous system that flows from the cheek. This study aimed to study HPMC polymers and polyvinyl pyrrolidone (PVP) polymers on swelling index, residence time, mucoadhesive strength of mucoadhesive buccal film diltiazem HCl, FTIR, and drug release. The prepared film was evaluated for swelling index, mucoadhesive strength, and mucoadhesive residence time. The optimal amount for HPMC was 35 mg, and PVP was 15 mg. The combination of polymers with this amount can produce a swelling index was 3,00, mucoadhesive strength was 41,87 gF, and mucoadhesive residence time was 330,66. FTIR test indicated that there was no interaction between active function clusters of Diltiazem HCl and other excipients. The release of the optimum formula in the 360th minute was about 97.847%, following in the zero-order release model and Higuchi.


2020 ◽  
Vol 17 (1) ◽  
pp. 31-44
Author(s):  
Ikhwan Yuda Kusuma ◽  
Rani Prabandari

Piroxicam solubility in water is very small this cause problem in the process of absorption so that it’s required an optimal formula to establish the physical properties of tablet quality for piroxicam tablets. The purpose of this research was creating formulas with the optimal combination of excipients lactose, Avicel pH 101, and piroxicam amprotab to obtain tablets with good physical properties and disolution. Seven piroxicam tablet formulas were made with a combination of lactose, avicel PH-101, and Amprotab on 2 batches. Method for making tablets piroxicam was established by direct compression. Tests included were the physical properties of piroxicam tablets tablets weight uniformity, uniformity of size, hardness, brittleness, disintegration test, as well as dissolution test, and content uniformity. Based on the simplex lattice design method, lactose is a dominant factor to improved the uniformity of tablet’s concentartions. Interaction of two components avicel PH-101 and amprotab is a dominant factor to reduced vulnerability. Interaction of three components lactose, avicel PH-101 and amprotab is a dominant factor to lowered the value coefisien variation of weight uniformity, increased hardness, decreased the disintegration, and improved dissolution of tablets. Selection of the optimum formula was determined by the method of simplex lattice design through diagrams superimposed contour plots and contour plots for obtaining the optimal proportions of each ingredient as follows: lactose (85,154–100%), avicel PH-101 (0–12,437%), and amprotab (0–5,425%).


2021 ◽  
Vol 8 (2) ◽  
pp. 145
Author(s):  
Yeyen Dwi Iryani ◽  
Ika Yuni Astuti ◽  
Diniatik Diniatik

Ekstrak kulit buah manggis (Garcinia mangostana L) mengandung senyawa xanton yang memiliki aktivitas farmakologis dimana salah satu turunan xanton  α-mangostin bekerja sebagai antioksidan. Penelitian ini bertujuan untuk mengetahui etanol yang menghasilkan ekstrak dengan jumlah xanton tertinggi, menguji aktivitas antioksidan dan tabir surya dari ekstrak terpurifikasi serta mengoptimasi formula sediaan losion tabir surya dari ekstrak terpurifikasi kulit manggis.Optimasi formula losion dilakukan menggunakan software Design Expert® versi 11 dengan kombinasi ekstrak terpurifikasi, asam stearat dan trietanolamin. 14 formula losion dievaluasi nilai SPF, pH dan viskositasnya untuk penentuan formula optimum. Formula optimum selanjutnya diuji nilai SPF, ph dan viskositas untuk membandingkan prediksi software dan hasil percobaan. Selain itu dilakukan uji daya sebar, daya lekat serta stabilitas mekanis terhadap formula optimum. Hasil penelitian menunjukkan kandungan xanton dalam ekstrak etanol 50% sebesar 20,42%, ekstrak etanol 70 % sebesar 29,88% dan ekstrak etanol 96% sebesar 64,57%. Ekstrak terpurifikasi kulit buah manggis memiliki aktivitas antioksidan dengan nilai IC50 sebesar 5,53 dan nilai AAI 14,46 serta memiliki nilai SPF 8,94 pada konsentrasi 50 µg/ml. Formula optimum yang diperoleh memiliki nilai SPF 7,49 ± 0,0297, kekentalan 21.166,666 cp ± 10,41 serta pH 6,490 ± 0,0404, daya sebar 7,833333 ± 0,15, daya lekat 2,03 ± 0,01.


2019 ◽  
Vol 1 (3) ◽  
pp. 225-237
Author(s):  
Dwi Saryanti ◽  
Iwan Setiawan ◽  
Romadona Ayu Safitri

Banana kepok peel has flavonoid compounds used as antioxidants. The aim of this research is to get optimum formula of cream by combination of stearic acid and trietanolamin on good physical propertie of cream. Cream was made with stearic acid 15% minimum concentration and maximum concentration 17%, triethanolamine with minimum concentration 2% and maximum concentration 4%. The optimization of the formula was using the simplex lattice design method with parameters are pH, viscosity, spreadability, adhesion and protection. The optimum cream formula on the combination of stearic acid 16.7 grams and triethanolamine 2.3 grams. Verification results of optimal formula cream for pH got 6.1, viscosity 237.47, adhesion 12.32, power spread 18.11, protection 14.98 which showed no significant difference in the test, and has good stability.


2016 ◽  
Vol 1 (1) ◽  
Author(s):  
Youstiana Dwi Rusita

Abstract: Dewa Leaves, Lozenges, Simplex Lattice Design. Dewa is an Indonesian traditional medicinal plants are efficacious among others to the tonsils. Dewa leaf extract can be prepared as lozenges because it is more practical and effective than the traditional way in the form of infusion. This study aimed to get the optimum formula mannitol - sucrose using the simplex lattice design that has more value than triall error. Dewa leaf aqueous extract obtained by maceration leaf powder dewa with 70% ethanol and then evaporated to obtain a thick extract is dried with aerosil. This study is based on the method simplex lattice design with two components, namely FI (100% mannitol), F II (100% sucrose), F III (50% mannitol: 50% sucrose). The method used in the manufacture of leaf extract lozenges Dewa was wet granulation using the binder PVP. The granules tested flow rate, compactibility and granules ditablet to test the taste responses. Of the value of the response characteristics of the granules obtained the largest total selected as the optimum formula. Furthermore ditablet and tested physical properties which include uniformity of weight, hardness and friability of tablets. Data of physical properties of the granules suction of the optimum formula theoretically and statistically tested using the t test (T-test). The results showed that the optimum formula derived from a mixture of mannitol 70% - sucrosa 30%. From the results of the t test (T-test) and compactibility flow rate did not different significantly betwen theoretical experiment. To test the taste responses acceptable 98% of respondents. Dewa leaf extract lozenges optimum formula produced meets the physical properties of the tablet.


2018 ◽  
Vol 6 (1) ◽  
pp. 11
Author(s):  
Baiq Wahyudyati Karnia Qisti ◽  
Dwi Nurahmanto ◽  
Viddy Agustian Rosyidi

Ibuprofen is a non-steroid anti inflammatory drug (NSAID) used for rheumatoid arthritis treatment. In this study, formulation, evaluation, and optimization of ibuprofen gel formula were conducted in order to determine the best ibuprofen penetration rate through the rats skin using propylene glycol and ethanol as penetration enhancers and to find out the optimum formula to get the best penetration rate with simplex lattice design method. Evaluations included organoleptic, pH, viscosity, gel dispersive, assay of gel formulations, and ibuprofen penetration rate assay. Penetration rate was determined by paddle type dissolution and the samples were analyzed by spectrophotometry UV-Vis. The results of ibuprofen penetration rate assay were analyzed and optimized using design expert trial version 10. The results of ibuprofen penetration rate were F1 1.524 ± 0.121 µg/cm2.minute; F2 1.945 ± 0.0104 µg/cm2.minute; and F3 1.173 ± 0.216 µg/cm2.minute. Penetration rate optimization resulted in one optimum solution formula which was 18.000% propylene glycol and 12.000% ethanol with a maximum flux of 1.957 ug/cm2.minute and desirability 1. It can be concluded that the best ibuprofen penetration rate was F2 with flux 1.945 ± 0.0104 µg/cm2.minute with 15% propylene glycol and 15% ethanol.   Keywords: gel, ibuprofen, propylene glycol, ethanol, simplex lattice design  


2020 ◽  
Vol 8 (3) ◽  
pp. 139
Author(s):  
Desy Diana Sari ◽  
Lidya Ameliana ◽  
Dwi Nurahmanto

Ultraviolet (UV) radiation is the main cause of sunburn and skin cancer. The adverse effects of UV radiation are solved by sunscreen as protection for longer outdoors. In this study, optimization of glycolic acid and citric acid in sunscreen cream combination of titanium dioxide, avobenzone, and octyl methoxycinnamate were investigated using simplex lattice design method. The sunscreen cream evaluation includes physicochemical testing (organoleptic, homogeneity, emulsion type, spreadability, viscosity, and pH) and sunscreen effectiveness (SPF, % erythema transmission, and % pigmentation transmission). The value of physicochemical testing are 5,96 cm - 6,3 cm of  spreadability testing; 83,33 dPa.s – 108,33 dPa.s of viscosity testing; 4,06 – 4,67 of pH testing. The value of sunscreen effectiveness are 9,79 – 13,35 of SPF testing; 4,55x10-06 - 0,15x10-06% of % erythema transmission; 5,77 – 7,16 % of % pigmentation transmission. The optimum formula was obtained by combining glycolic acid 2% and citric acid 0% with a desirability value of 0,649.


2021 ◽  
Vol 6 (1) ◽  
pp. 21-28
Author(s):  
Joko Santoso ◽  
◽  
Heru Nurcahyo

Handsanitizer gel is composed of various additives such as geling agents, humectants and neutralizing / stabilizing agents. This material is certainly a basic ingredient that will affect the shape and quality of the preparation. Carbopol is very good when used, so that low levels can provide a significant viscosity response. Eleven hand sanitizer gel formulas with variations of carbomer, aloe vera and TEA were tested for their physical properties including organoleptic, homogeneity test, pH test, spreadability and adhesion test . The optimum formula is obtained by using the Simplex Lattice Design method, then the results are analyzed using an expert design software. The optimum formula for oleum citri hand sanitizer gel contains 0.944 with carbomer 0 (0.5%), aloe vera 0.471 (5.239%) and TEA 0.529 (0.576%). The t test results obtained showed insignificant differences between the response of the physical properties of the experiment results and the prediction software.


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