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INDONESIA
IDJP (Indonesian Journal of Pharmaceutics)
Published by Universitas Padjadjaran
ISSN : -     EISSN : 25978748     DOI : -
Core Subject :
The Indonesian Journal of Pharmaceutics (IdJP) is an established international journal for pharmaceutical scientists concerned in all fields of pharmaceutical sciences, including pharmaceutical preformulation, formulation, manufacturing technologies, drug delivery systems, biopharmaceutics, and pharmacokinetics for drugs, vaccines and biologicals. IdJP also includes pharmaceutical engineering and industrial pharmacy topics.
Arjuna Subject : -
Articles 5 Documents
 1 
Search results for , issue "Vol 3, Issue 3, Sept - Dec 2021" : 5 Documents clear
Astaxanthin Nanoemulsion Formulation and Evaluation Yanni Dhiani Mardhiani; Deny Puriyani A; Lailatul Fadilah
Indonesian Journal of Pharmaceutics Vol 3, Issue 3, Sept - Dec 2021
Publisher : Universitas Padjadjaran (Unpad)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/idjp.v3i3.36777

Abstract

Astaxanthin has antioxidant activity ten times greater than carotenoids such as -carotene and a hundred times higher than vitamin E. However, its utilization is still limited because its solubility in water is very low which results in low absorption by the skin, resulting in low bioavailability. In this case, to increase the potency of astaxanthin, this research was aimed at the formulation and characterization of astaxanthin nanoemulsions using polysorbate 80 and polyethyleneglycol 400 as a mixture of surfactants with a ratio of 7:1; 8:1 and 9:1 with the method of making a combination of low and high energy emulsification. The data obtained were analyzed using the Kruskal-Wallis test for data on the pH of the preparation and the efficiency of adsorption while the pH test during freeze-thaw stability was analyzed by the Wiloxon test. Based on the test results, it was found that the nanoemulsion preparation with the smix 9:1 formula is the most optimum formula among other formulas, which is to produce preparations with quite good characteristics organoleptically and give a light orange color appearance, clear, distinctive smell with a pH value that meets the SNI standard 16-164399-1996 with pH values ranging from 7.13 to 7.15 and based on the centrifugation test gave stable results and had particle size, polydispersity index and zeta potential values, respectively, 22.9 ± 9.4 nm, 0.435 and -21. ,4 mV and the value of entrapment efficiency ranges from 93.87% to 94.32%. However, the thermodynamic stability is not good enough. This is indicated by the instability of the preparation during the freeze-thaw test with the results of changes in color, transparency and changes in pH.Keywords: Nanoemulsion, Astaxanthin, Polyethyleneglycol 400, Polysorbate 80, Surfactants 
Formulation and Evaluation of instant granules from Ketapang Badak fruit (Ficus lyrata Warb) using wet granulation method as an antioxidant supplement Norisca Aliza Putriana; Efri Mardawati; Yoga Windu Wardhana; Nurul Afifah; Anting Wulandari; Dwi Wahyudha Wira; Nanang Masruchin
Indonesian Journal of Pharmaceutics Vol 3, Issue 3, Sept - Dec 2021
Publisher : Universitas Padjadjaran (Unpad)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/idjp.v3i3.37062

Abstract

Free radicals are naturally produced from the body's metabolic processes, but the excessive amount of free radicals can interfere with human health because they cause oxidative stress. Therefore we need antioxidants that can protect against free radicals. Ficus lyrata W. is one of the antioxidant sources. This study aims to formulate instant granules from the Ethanol extract of Ficus lyrata W. using the wet granulation method. The formula is optimized using the Design Expert with the two-level factorial method. The optimized factors are xanthan gum 0,8-1,5% and PVP 0,5-5%. Granules are evaluated and analyzed using a Design Expert. The results obtained showed that Formula 4 with a combination of xanthan gum 0,8% and PVP 5% is the best formula, which the evaluation result is Loss On Drying (LOD) 3,28%, Flowability 16.043 ± 0.221 (g/s), Angle of Rest 21.77 ± 0.862, no precipitate for15 minutes, pH = 4.7, dispersed in 31 seconds and sedimentation time is 52.213 ± 1.7878 (minutes), the results of the antioxidant activity test of the ethanol extract of Ficus lyrata is 38,27 µg/ml, and instant granules is 145,02 µg/ml.Keywords: Antioxidant, Ficus lyrata W., Instant granules, Design expert
Indonesian Halal Pharmaceutical: Challenges And Market Opportunities Yedi Herdiana; Taofik Rusdiana
Indonesian Journal of Pharmaceutics Vol 3, Issue 3, Sept - Dec 2021
Publisher : Universitas Padjadjaran (Unpad)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/idjp.v3i3.37660

Abstract

The halal food market has grown worldwide, including the shift from food to other products, including halal pharmaceuticals (HPC).  The growth followed by the abundance of literature has been on halal, especially pharmaceuticals. Muslim consumers need halal certification (HCT) on medicines to ensure that they do not consume or use products or services that are not halal. The government must guarantee to Muslim consumers that consumer goods or services circulating in the community are truly halal. The halal label itself will increase consumer confidence, expand the reach of the global halal food market, and increase the marketability of products in the market. Indonesia, which is predominantly Muslim, is considered a long extension in implementing HP until 2034. Different attitudes are shown by several countries with large non-Muslim majority populations but are very concerned about the implementation of HPC. The accelerated growth of knowledge of halalness, impact social media, will push the industry to implement HPC. In this review, we will discuss critical players in implementing HPC, including the ingredients that have been widely used but still doubt their halalness and what they are used for in the pharmaceutical industry. This knowledge is essential for industry and researchers to build safer alternative materials.Keywords: Halal, Indonesia,  Muslim, Halal Pharmaceutical, Halal Certification. 
Preparation of organic-solvent free liposome of Piper albi Linn extract in solution and powder form Eri Amalia; Iyan Sopyan; Norisca Aliza Putriana; Sriwidodo Sriwidodo; Anas Subarnas
Indonesian Journal of Pharmaceutics Vol 3, Issue 3, Sept - Dec 2021
Publisher : Universitas Padjadjaran (Unpad)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/idjp.v3i3.38335

Abstract

Piperine is bioactive alkaloid extracted from white pepper (Piper albi Linn) with several beneficial pharmacological activities. It is also known to enhance the bioavailability of several limited solubilities of other compounds such as curcumin and resveratrol. Nevertheless, due to its poorly water-soluble character, piperine and extract of white pepper are less applied among other plant extracts. Therefore, our research focussed on the engineering of white pepper extract standardized to piperine in liposome solution and liposome powder for further preparation of various pharmaceutical dosage forms.Our research in preparation of extracted white pepper in liposome delivery system successfully prepared spheric liposome solution with 98.92%±1.17% and an average size of 398.7 nm. The liposome was also successfully prepared in dry powder form with sucrose as a carrier for liposome protection. The rehydration is successfully forming a spheric shape with a similar profile to the initial liposome solution. This research paves the way for scalable white pepper extract liposome preparation without the utilization of toxic organic solvent, to produce the commercial solvent-free product in the future.Keywords: Piperine, Piper albi Linn, liposome, extract, organic solvent-free, drug delivery system, spray dry 
Ophthalmic release of in situ gel Ciprofloxacin HCl based on combination of Hypromellose and HPC Yoga Windhu Wardhana; Wieke Budiati; Rizky Dwi Oktavia; Kalista Tritama Widyanti; Insan Sunan Kurniawansyah; Yedi Herdiana
Indonesian Journal of Pharmaceutics Vol 3, Issue 3, Sept - Dec 2021
Publisher : Universitas Padjadjaran (Unpad)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/idjp.v3i3.36140

Abstract

The development for ophthalmic delivery was purposed to achieve optimum drug loading for ocular therapeutic benefits. An adequate dose of the drug is needed to absorb in the conjunctival sac to take effect. In situ gel preparation was expected to provide these needs with the polymer aid that makes the droplets suddenly coagulate in the eye area to maintain the drug dose. The in situ gel dosage form is desired to overcome the poor bioavailability of conventional ciprofloxacin HCl eye drops on the market. Thus, this work was studied using two cellulose polymers such as hydroxyl propyl cellulose (HPC) and hydroxypropyl methylcellulose (HMPC) as a gelling forming agent.  The effect of the in situ ophthalmic quality of the gel due to the two individual polymers separately and their combined use was investigated. The in situ gel quality includes the ability of gel-forming under the influence of varying temperature and stirring frequency difference (as a rheological study) was tested together with the drug release model model. Other ophthalmic preparation quality parameters such as clarity, pH measurement, drug content determination, sterility, and antibacterial activity have been evaluated. However, overall in situ gel formulation developed was of better quality compared to the conventional one. Consideration of the choice of cellulose derivative polymer type is seen to affect the quality of controlled release kinetics models.Keywords: Ophthalmic gel, Ciprofloxacin HCl, HPMC, HPC, Drug release kinetics 

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