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Antimetabolic Syndrome Effect of 70% Ethanol Leaves Extract Ficus carica Linn. in Streptozotocin-Induced and High-Fat Diet Rats 70%乙醇无花果叶提取物的抗代谢综合征作用。链脲佐菌素诱导的高脂饮食大鼠
Pub Date : 2023-05-11 DOI: 10.35814/jifi.v21i1.1399
Rahmatul Qodriah, S. Kumala, Syamsudin Syamsudin, N. D. Yuliana, Vyacheslav Dushenkov, Carrista Carrista
Diabetes and obesity are risk factors for metabolic syndrome. Fig (Ficus carica L.) one of the plants is well known in traditional medicine system for their medicinal and therapeutic potentials. Fig leaves contain flavonoid and triterpenoid compounds which have antimetabolic effect. Streptozotocin is used to make diabetogenic rats to produce hyperglycemia conditions in test animals and high-fat diet to make rats model obesity. This study aimed to test the antidiabetic and antiobesity effect of 70% ethanol extract of fig leaves based on the parameters of measuring blood glucose levels with glucometer and Cholesterol strips. In thisstudy, rats were divided into 6 groups, namely normal, negative, positive control, and 3 control groups at 70%ethanol extract dose level (250, 500, and 600 mg/kgBW) per oral. The measurement results in normal, negative, and positive control dose of 250, 500, 600 mg/kgBW at blood glucose levels were 105.8, 192, 134.2, 161, 157.75, 145.2 mg/dL. The conclusion of the results obtained was that 70% ethanol extract of fig leaves with a dose of 600 mg/kgBW can have an antidiabetic and obesity effect by lowering blood glucose levels as measured using glucometer, cholesterol strips and decreased body weight rats.
糖尿病和肥胖是代谢综合征的危险因素。无花果(Ficus carica L.)是一种在传统医学系统中具有药用和治疗潜力的植物。无花果叶中含有类黄酮和三萜化合物,具有抗代谢作用。用链脲佐菌素使致糖尿病大鼠在实验动物中产生高血糖状态,用高脂肪饮食使大鼠模型肥胖。以血糖仪和胆固醇试纸为指标,研究无花果叶70%乙醇提取物的抗糖尿病和抗肥胖作用。采用70%乙醇提取物剂量水平(250、500、600 mg/kgBW),将大鼠分为正常组、阴性组、阳性对照组和3个对照组。正常、阴性和阳性对照剂量分别为250、500、600 mg/kgBW,血糖水平分别为105.8、192、134.2、161、157.75、145.2 mg/dL。得出的结论是,无花果叶70%乙醇提取物600 mg/kgBW的剂量可以通过降低血糖仪,胆固醇条和体重下降的大鼠的血糖水平来降低糖尿病和肥胖的效果。
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引用次数: 0
Formulation and Antioxidant Activity of Purple Rosella Flower (Hibiscus sabdariffa L.) Combination as Nutraseutical 紫薇花的配方及抗氧化活性研究作为营养品的组合
Pub Date : 2023-05-11 DOI: 10.35814/jifi.v21i1.1395
Intan Permata Sari, Y. Noviani, Ridwan Rachmadi, E. Mumpuni
A nutraceutical is a functional food containing natural components that have the potential for health, especially from medicinal plants. The purple rosela (Hibiscus sabdariffa L.), one of many therapeutic plants that have been effectively transformed into herbal products, is one such example. High quantities of anthocyanin are found in bioactive substances found in rosela flowers. This study aims to formulate and determine the antioxidant activity of purple rosela flower in combination with red ginger and cinnamon bark. Following the liking test, which includes the organoleptic test, and the calculation of shelf life with the Accelerated Shelf-Life Testing (ASLT) method, the brewed tea formulation was kept to determine the total content of phenolate. Antioxidant activity was measured by the DPPH (1,1-diphenyl-2-picrylhidrazyl) method. This study obtained an average result of 0,38±0,05% for the total phenol content of the three formulas. Formula I, II, and III showed antioxidant activity with IC50 values of 21.59 g/mL, 27.13 g/mL, and 20.05 g/mL, respectively. Organoleptic observations that have been observed for 20 days at three different temperatures (4°C, 25°C, and 37°C) in the three formulas indicate no change in color, aroma, or taste, indicating the product remains stable. Based on the score results, the most preferred by panelists was Formula I, with its composition of purple, rose and red ginger.
营养保健品是一种含有天然成分的功能性食品,具有潜在的健康价值,特别是药用植物。紫色玫瑰(Hibiscus sabdariffa L.)是许多有效转化为草药产品的治疗植物之一,就是这样一个例子。玫瑰花的生物活性物质中含有大量的花青素。本研究旨在制备并测定紫玫瑰花与红姜、桂皮的抗氧化活性。对冲泡后的茶叶进行喜欢度测试,包括感官测试和加速保质期测试(ASLT)法计算保质期,以测定茶叶中酚酸盐的总含量。采用DPPH(1,1-二苯基-2-苦味基hidrazyl)法测定抗氧化活性。本研究得到三种配方的总酚含量平均值为0.38±0.05%。式1、式2、式3具有抗氧化活性,IC50值分别为21.59 g/mL、27.13 g/mL和20.05 g/mL。在3种不同温度(4°C、25°C和37°C)下对3种配方进行了20天的感官观察,结果表明,产品的色、香、味均无变化,产品保持稳定。从评分结果来看,小组成员最喜欢的是f1,它的成分是紫色、玫瑰色和红姜色。
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引用次数: 0
Drug Use Patterns during the COVID-19 Pandemic: A Case Study at Persahabatan General Hospital COVID-19大流行期间的药物使用模式:以Persahabatan总医院为例
Pub Date : 2023-05-09 DOI: 10.35814/jifi.v21i1.1396
Fitri Nurhayati, Dendhi Bagus Andriyanto, Fadhila Putri, Rara Merinda Puspitasari
The COVID-19 pandemic condition has encouraged healthcare practitioners to adapt and constantly work to meet the needs of those who require healthcare, including medication supply. This study aims to provide the drug use patterns prior to and throughout the COVID-19 pandemic. This retrospective descriptive study analyzed the drug use patterns of 10 fast-moving drugs obtained through purposive sampling, as well as all medications listed in COVID-19 guideline therapy at Persahabatan general hospital. The drug use data was derived from the quarterly data from 2019 through the second quarter of 2021. The result showed that there was an increase and variation in the sampled drug usage. The top-ranking classes that have shown an upward trend during the COVID-19 pandemic were Vitamin C 500 mg tablet, Vitamin C 200 mg injection, and Vitamin D3 5000 UI tablet. Meanwhile, non-COVID-19 medicines with reduced use include Cefotaxime 1 g, Cefixime 200 mg, and Docetaxel 20 mg. Therefore, it is necessary to analyze the drug utilization continuously and as frequently as feasible throughout the pandemic and plan in stages. Forecasting demand for medicines is essential for an effective medicinessupply chain, in particular in a pandemic context to avoid shortages or overstock.
COVID-19大流行的情况鼓励医疗从业人员适应并不断努力满足需要医疗保健的人的需求,包括药物供应。本研究旨在提供COVID-19大流行之前和整个过程中的药物使用模式。本回顾性描述性研究分析了通过有目的抽样获得的10种速效药物的用药模式,以及佩沙巴坦总医院COVID-19指南治疗中列出的所有药物。药物使用数据来自2019年至2021年第二季度的季度数据。结果表明,样本药物的使用有增加和变化。在新冠肺炎大流行期间,维生素C 500毫克片剂、维生素C 200毫克针剂和维生素D3 5000ui片剂的用量呈上升趋势。同时,减少使用的非covid -19药物包括头孢噻肟1 g、头孢噻肟200 mg和多西他赛20 mg。因此,有必要在整个大流行期间持续和尽可能频繁地分析药物利用情况,并分阶段制定计划。预测药品需求对于有效的药品供应链至关重要,特别是在大流行背景下,以避免短缺或库存过剩。
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引用次数: 0
Comparison of Total Phenolic Content and Antioxidant Activity of Indonesian Propolis Extracted with Various Solvents. 不同溶剂提取的印尼蜂胶总酚含量及抗氧化活性比较。
Pub Date : 2023-05-09 DOI: 10.35814/jifi.v21i1.1400
Diah Kartika Pratami, Nur Elistiani Eksadita, M. Sahlan, Abdul Mun’im, Asep Bayu, Kaysa Faradis Mahira
Propolis is a widely used medicine that may be found in both its pure form and when combined with othernatural ingredients in over-the-counter preparations, cosmetics, and health foods. Some customers develop alcohol sensitivity after using ethanol, which is a common solvent to extract propolis. As propolis solvents, various Natural Deep Eutectic Solvents (NaDES) were examined in this study. Choline chloride, propylene glycol, glycerol, citric acid, and 1,2-propanediol were combined in molar ratios to create some of the NaDES that were employed. Propolis and solvents were used in a kinetic maceration ratio for the extraction process. The Folin-Ciocalteu method was used to measure the total phenolic content (TPC), and the DPPH assay was used to measure antioxidant activity. In ethanol and NaDES solvents, the TPC of propolis extract ranged from 136.52 ± 27.9 to 365.8 ± 20.54 mgGAE/g. The values for antioxidant activity were 45.94 to 183.76 ppm. The propolis extract with the lowest IC50 and the highest TPC content was choline chloride-glycerol (CCG). It was discovered that the optimum NaDES solvent for extracting propolis was CCG-based. NaDES may be a potential solvent for use in Indonesian propolis, both as an extraction medium and as a formulation element.
蜂胶是一种广泛使用的药物,可以在非处方制剂、化妆品和健康食品中以其纯形式和与其他天然成分结合使用时找到。有些客户在使用乙醇后产生酒精敏感性,乙醇是提取蜂胶的常用溶剂。研究了多种天然深共晶溶剂(NaDES)作为蜂胶溶剂。氯化胆碱、丙二醇、甘油、柠檬酸和1,2-丙二醇按摩尔比组合,产生了一些nade。蜂胶和溶剂以动态浸渍比进行萃取。采用Folin-Ciocalteu法测定总酚含量(TPC), DPPH法测定抗氧化活性。在乙醇和NaDES溶剂中,蜂胶提取物的TPC范围为136.52±27.9 ~ 365.8±20.54 mgGAE/g。抗氧化活性为45.94 ~ 183.76 ppm。IC50最低、TPC含量最高的蜂胶提取物为氯化胆碱甘油(CCG)。研究发现,以ccg为基础的NaDES溶剂是提取蜂胶的最佳溶剂。NaDES可能是印尼蜂胶中潜在的溶剂,既可以作为萃取介质,也可以作为配方元素。
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引用次数: 1
Evaluation Anti-Acne Gel Combination of Ethanol Extract of Cayenne Pepper Leaves and Ethanol Extract of Soursop Leaf 辣椒叶乙醇提取物与刺果叶乙醇提取物联合抗痘凝胶的评价
Pub Date : 2023-05-03 DOI: 10.35814/jifi.v21i1.1391
Dimas Setiyono, Deden Mulya Prayoga, Herlan Budi Kusuma, Dina Febrina
Acne is a skin disease that usually occurs near adulthood. Acne is caused by several bacteria namely Staphylococcus epidermidis, Propionibacterium acnes, and Staphylococcus aureus. The alternative acne treatment uses cayenne pepper leaves (Capsicum frutescens L.) and soursop leaves (Annona muricata L.). The research aimed to find out the best formulation and activity of the ethanol extract gel of cayenne pepper leaves combined with the ethanol extract of soursop leaves as an inhibitor for acne-causing bacteria. This research is an experimental research type with 3 formulation designs, each of which was made with concentrations of ethanol extract from cayenne pepper leaves and ethanol extract from soursop leaves, namely F1 (1% and 1%), F2 (3% and 3%), and F3 (5 % and 5%), then tested the physical properties, antibacterial test and physical stability test of the preparation then analyzed the data with one-way ANOVA p-value <0.05. The results showed that the gel preparations were stable in terms of organoleptic, homogeneity, spreadability, adhesion, and viscosity, while there was a change in pH after the physical stability test using the cycling test method. The F2 gel preparation had the best bacterial inhibition, namely Staphylococcus aureus of 10.83 mm. Then the F3 gel preparation best inhibited Staphylococcus epidermidis bacteria by 9.56 mm and Propionibacterium acnes by 10.4 mm.
痤疮是一种皮肤疾病,通常发生在成年期。痤疮是由几种细菌引起的,即表皮葡萄球菌、痤疮丙酸杆菌和金黄色葡萄球菌。另一种治疗痤疮的方法是使用辣椒叶(Capsicum frutescens L.)和番荔枝叶(Annona muricata L.)。本研究旨在找出辣椒叶乙醇提取液与番荔枝叶乙醇提取液联合用于抑制痤疮致病菌的最佳配方及活性。本研究为实验研究型,采用3种配方设计,分别以辣椒叶乙醇提取物和番荔枝叶乙醇提取物的浓度F1(1%和1%)、F2(3%和3%)和F3(5%和5%)配制,分别对制剂进行物理性能、抗菌性能和物理稳定性测试,并用单因素方差分析p值<0.05进行分析。结果表明,凝胶制剂在感官、均匀性、铺展性、粘附性、粘度等方面都是稳定的,而采用循环试验法进行物理稳定性试验后,pH值发生了变化。F2凝胶制剂抑菌效果最佳,对金黄色葡萄球菌的抑菌量为10.83 mm。F3凝胶制剂对表皮葡萄球菌和痤疮丙酸杆菌的抑制效果分别为9.56 mm和10.4 mm。
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引用次数: 0
In Vitro Release Ability of Nanoparticles Poly-Lactic-Co-Glycolic-Acid (PLGA) Gel Containing Pegagan Leaves Ethanolic Extract (Centella asiatica L.) 积雪草叶乙醇提取物聚乳酸凝胶的体外释放性能
Pub Date : 2023-04-30 DOI: 10.20473/jfiki.v10i12023.103-110
Mardiyanto, E. F. Apriani, Pandu Kalingga Jati
Background: Pegagan (Centella asiatica L.) leaves are proven to contain high concentrations of flavonoid compounds as antioxidants. Flavonoids are unstable compounds due to environmental influences such as light, humidity, pH, and oxygen. The stability of pegagan extract was proven to be improved by making the extract into nanoparticle preparations. Objective: This study aims to formulate nanoparticles of pegagan into gel preparations and determine their release ability with the Franz diffusion test using a cellophane membrane compared to pegagan gel not formulated into nanoparticles. Methods: Nanoparticles were made using poly-lactic-co-glycolic acid polymers and then formulated into gels with various concentrations of Carbopol 934, namely 1, 1.5 and 2%. The gel nanoparticles were then subjected to the characterization of the preparation, stability test and release test of the preparation. Results: A concentration of 1% Carbopol 934 provides the best evaluation of gel preparations where the gel produced was homogeneous, pH was around 6.2, viscosity was 3417.12 cPs, spreadability was 5.1 cm, and adhesion was 209.33 seconds. The stability test showed no significant organoleptic and pH changes (p>0.05). The release kinetics model occurs at zero order. F1 has a higher reaction kinetics constant (k) than the other formulations, so drug release occurs faster. Conclusion: The best formula of pegagan (F1) nanoparticle gel was proven to have good physical stability and release ability.
背景:积雪草(Centella asiatica L.)叶被证明含有高浓度的黄酮类化合物作为抗氧化剂。黄酮类化合物是一种不稳定的化合物,受光照、湿度、pH值和氧气等环境影响。pegagan提取物的稳定性已被证明通过将提取物制成纳米颗粒制剂来提高。目的:本研究旨在将聚乙二醇纳米颗粒配制成凝胶制剂,并使用玻璃纸膜进行Franz扩散试验,与未配制成纳米颗粒的聚乙二醇凝胶相比,测定其释放能力。方法:用聚乳酸-乙醇酸聚合物制备纳米颗粒,然后将其配制成不同浓度的Carbopol 934凝胶,即1%、1.5%和2%。然后对凝胶纳米粒子进行制剂的表征、稳定性测试和释放测试。结果:1%Carbopol 934的浓度提供了凝胶制剂的最佳评价,其中产生的凝胶是均匀的,pH约为6.2,粘度为3417.12cPs,铺展性为5.1cm,粘附力为209.33秒。稳定性试验表明,在感官和pH值方面没有显著变化(p>0.05)。释放动力学模型为零级。F1具有比其他制剂更高的反应动力学常数(k),因此药物释放发生得更快。结论:筛选出的聚乙二醇(F1)纳米粒子凝胶具有良好的物理稳定性和释放性能。
{"title":"In Vitro Release Ability of Nanoparticles Poly-Lactic-Co-Glycolic-Acid (PLGA) Gel Containing Pegagan Leaves Ethanolic Extract (Centella asiatica L.)","authors":"Mardiyanto, E. F. Apriani, Pandu Kalingga Jati","doi":"10.20473/jfiki.v10i12023.103-110","DOIUrl":"https://doi.org/10.20473/jfiki.v10i12023.103-110","url":null,"abstract":"Background: Pegagan (Centella asiatica L.) leaves are proven to contain high concentrations of flavonoid compounds as antioxidants. Flavonoids are unstable compounds due to environmental influences such as light, humidity, pH, and oxygen. The stability of pegagan extract was proven to be improved by making the extract into nanoparticle preparations. Objective: This study aims to formulate nanoparticles of pegagan into gel preparations and determine their release ability with the Franz diffusion test using a cellophane membrane compared to pegagan gel not formulated into nanoparticles. Methods: Nanoparticles were made using poly-lactic-co-glycolic acid polymers and then formulated into gels with various concentrations of Carbopol 934, namely 1, 1.5 and 2%. The gel nanoparticles were then subjected to the characterization of the preparation, stability test and release test of the preparation. Results: A concentration of 1% Carbopol 934 provides the best evaluation of gel preparations where the gel produced was homogeneous, pH was around 6.2, viscosity was 3417.12 cPs, spreadability was 5.1 cm, and adhesion was 209.33 seconds. The stability test showed no significant organoleptic and pH changes (p>0.05). The release kinetics model occurs at zero order. F1 has a higher reaction kinetics constant (k) than the other formulations, so drug release occurs faster. Conclusion: The best formula of pegagan (F1) nanoparticle gel was proven to have good physical stability and release ability.","PeriodicalId":17684,"journal":{"name":"JURNAL FARMASI DAN ILMU KEFARMASIAN INDONESIA","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42446330","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Molecular Docking of Bicycloproline Derivative Synthetic Compounds on Envelope Protein: Anti-SARS-CoV-2 Drug Discovery 双环脯氨酸衍生物合成化合物与包膜蛋白的分子对接:抗sars - cov -2药物的发现
Pub Date : 2023-04-30 DOI: 10.20473/jfiki.v10i12023.11-21
Syaiful Prayogi, B. A. Dhiani, A. Djalil
Background: Although a SARS-CoV-2 vaccine is readily available, new cases of COVID-19 are still occurring. New drug discovery is needed to treat COVID-19. Protein E is one of the potential targets. Two synthetic compounds of bicycloproline derivatives have the potential to be developed. Objective: This study aimed to estimate the interaction of bicycloproline compounds to protein E in-silico. Methods: There were two bicycloproline-derived compounds, MI-09 and MI-30, used in docking. Remdesivir was used as a reference ligand. The crystal structure of the E protein was created using homology modeling, while the test compound was drawn using the Marvin Sketch. MOE 2022.02 and BDS 2021 were used for docking and visualization processes. Results: The pentamer of the SARS-CoV-2 E protein obtained a clash score (1.06); poor rotatomer (0.00%); favored rotamers (98.11%); Ramachandran favored (96.43%); Ramachandran outlier (1.78%); Rama Z-score (-1.08); and mol probity (1.04). Research shows promising inhibition potential of the MI-09 and MI-30. The MI-30 has the best binding energy of -10.3326 kcal/mol. Conclusion: The docking results show that MI-30 has potency as an inhibitor of protein E and can be developed in treating COVID-19. Further research is needed to confirm the result by in vitro and in vivo studies.
背景:尽管SARS-CoV-2疫苗很容易获得,但新冠肺炎的新病例仍在发生。治疗新冠肺炎需要新的药物发现。蛋白质E是潜在的靶标之一。双环丙烷衍生物的两种合成化合物具有开发潜力。目的:本研究旨在评估双环脯氨酸化合物与蛋白质E在硅胶中的相互作用。方法:将两个双环脯氨酸衍生的化合物MI-09和MI-30用于对接。瑞德西韦被用作参考配体。E蛋白的晶体结构是使用同源性建模创建的,而测试化合物是使用Marvin Sketch绘制的。MOE 2022.02和BDS 2021用于对接和可视化过程。结果:严重急性呼吸系统综合征冠状病毒2型E蛋白的五聚体获得了碰撞分数(1.06);旋转不良(0.00%);偏爱轮调异构体(98.11%);Ramachandran青睐(96.43%);Ramachandran异常值(1.78%);Rama Z评分(-1.08);研究表明MI-09和MI-30具有良好的抑制潜力。MI-30的结合能最好,为-10.3326 kcal/mol。结论:对接结果表明,MI-30具有E蛋白抑制剂的作用,可用于治疗新冠肺炎。需要进一步的研究来通过体外和体内研究来证实这一结果。
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引用次数: 0
Effect of Different Lipid Ratios on Physicochemical Stability and Drug Release of Nanostructured Lipid Carriers Loaded Coenzyme Q10 不同脂质比例对辅酶Q10纳米结构脂质载体的物理化学稳定性和药物释放的影响
Pub Date : 2023-04-30 DOI: 10.20473/jfiki.v10i12023.44-53
Abdulloh Suyuti, Esti Hendradi, Tutiek Purwanti
Background: For treatment or skin care via topical route, Coenzyme Q10 needs to permeate the epidermis which it is practically insoluble in water and a high molecular weight that make it difficult to penetrate the skin. Nanostructured Lipid Carriers (NLC) is chosen because of its ability to dissolve and solve the problem of low skin permeation. The type and ratio of solid and liquid lipids used in NLC affect the physicochemical characteristics, thus affecting the release profile and system stability. Objective: This study aimed to determine the effect of various ratios of Compritol 888 ATO as solid lipid and Miglyol 812 as liquid lipid on the physicochemical stability and Coenzyme Q10 release profile of NLC system. Methods: NLC was prepared using High Shear Homogenization method with three different lipid ratios. The ratio of Compritol 888 ATO : Miglyol 812 was 70:30, 80:20, and 90:10, respectively. NLC was evaluated for drug release and stability parameters including organoleptic, particle size, polydispersity index (PI), pH, viscosity, assay, and entrapment efficiency. Results: The stability test result for 90 days showed increments in the particle size and viscosity, whereas for assay and entrapment efficiency were decreased. The release test results showed no significant difference in the release parameters of the three tested formulas. Conclusion: During stability evaluation, NLC-CoQ10 systems did not significantly change pH and PI values, but statistically significantly changed particle size, viscosity, assay, and entrapment efficiency. The different in lipid ratios used in the formulas did not show significantly different results for release parameters.
背景:对于通过局部途径进行的治疗或皮肤护理,辅酶Q10需要渗透到表皮中,它实际上不溶于水,而且分子量高,难以渗透到皮肤中。选择纳米结构脂质载体(NLC)是因为它能够溶解并解决皮肤渗透性低的问题。NLC中使用的固体和液体脂质的类型和比例影响物理化学特性,从而影响释放特性和系统稳定性。目的:本研究旨在确定不同比例的固体脂质形式的Compitol 888 ATO和液体脂质形式的Miglyol 812对NLC系统理化稳定性和辅酶Q10释放谱的影响。方法:采用高剪切均化法制备三种不同脂质比例的NLC。Compritol 888 ATO与Miglyol 812的比例分别为70:30、80:20和90:10。评估NLC的药物释放和稳定性参数,包括感官、粒度、多分散指数(PI)、pH、粘度、测定和包封效率。结果:90天的稳定性测试结果显示颗粒大小和粘度增加,而测定和包封效率降低。释放试验结果显示,三种试验配方的释放参数没有显著差异。结论:在稳定性评估过程中,NLC-CoQ10体系没有显著改变pH和PI值,但在统计学上显著改变了颗粒大小、粘度、含量和包封率。配方中使用的不同脂质比例没有显示出释放参数的显著不同结果。
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引用次数: 1
Optimasi CMC-Na dan Gliserin dalam Sediaan Gel Ekstrak Lidah Buaya secara Simplex Lattice Design
Pub Date : 2023-04-30 DOI: 10.35814/jifi.v21i1.1226
Martina Indah Anita, Agatha Budi Susiana Lestari
Lidah buaya (Aloe barbandesis Mill.) merupakan tanaman yang mempunyai banyak manfaat salah satunya sebagai antibakteri. Ekstrak lidah buaya terbukti memiliki aktivitas sebagai antibakteri. Ekstrak lidah buaya dicoba untuk diformulasikan dalam bentuk sediaan gel karena kelebihan dari sediaan gel seperti mudah diaplikasikan pada kulit, tidak lengket dan mudah dicuci dengan air sehingga mempermudah dalam penggunaannya. Penelitian ini merupakan penelitian eksperimental murni yang bertujuan untuk mendapatkan komposisi CMC-Na sebagai gelling agent dan gliserin sebagai humektan yang optimal sehingga menghasilkan sifat fisik dan stabilitas fisik sediaan gel yang baik menggunakan metode optimasi Simplex Lattice Design. Hasil respon daya sebar, viskositas, pergeseran viskositas, dan pergeseran daya sebar digunakan untuk menentukan formula optimum. Data hasil uji dianalisis dengan ANOVA satu arah menggunakan Software Design Expert. Berdasarkan hasil penelitian, ditemukan formula optimum yaitu pada formula 1, 2, dan 3 dengan konsentrasi CMC-Na dan gliserin secara berturut-turut yaitu 1,500 g dan 1,750 g; 1,563 g dan 1,688 g; dan 1,625. Selain itu, formula 1, 2, dan 3 memenuhi parameter sifat fisik dan stabilitas fisik gel.
芦荟是一种用途广泛的植物,有抗菌作用。芦荟提取物被证明具有抗菌活性。芦荟提取物被试图以剂凝胶的形式重新定义,因为剂凝胶的好处可以很容易地应用于皮肤,它是不粘性的,容易用水清洗,使它更容易使用。这是一项纯粹的实验研究,目的是将cmcna的agent gelling和甘油的最佳量组成为最优求,从而利用简单的简单着色度设计产生良好的生理性能和生理稳定性。散热响应、粘度、粘度移位和舒张作用的结果用于确定最佳公式。测试数据是使用设计专家软件进行方向分析的。根据这项研究,在公式1、2和3中发现的最佳公式是cmcna和甘油的浓度为1500克和1750克;1563克和1688克;和1,625。此外,公式1、2和3符合凝胶的物理性质和物理稳定性参数。
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引用次数: 0
Characteristics and Physical Stability of Nanoemulsion as a Vehicle for Anti-Aging Cosmetics: A Systematic Review 纳米乳液作为抗衰老化妆品载体的特性和物理稳定性:系统综述
Pub Date : 2023-04-30 DOI: 10.20473/jfiki.v10i12023.62-85
Eva Syariefah Rachman, Widji Soeratri, Tristiana Erawati M
Background: Skin aging can be overcome by applying anti-aging cosmetics. Many active ingredients that have anti-aging potential are derived from plants, and these materials must be delivered with a sound skin delivery system, namely nanoemulsion. The characteristics of nanoemulsion are closely related to physical stability. Objective: This study aims to conduct a systematic review of in vivo and in vitro study designs to examine the characteristics and physical stability of nanoemulsions used in topical anti-aging cosmetics. Methods: A systematic literature review based on the PRISMA statement was used to review the articles regarding nanoemulsions’ characteristics and physical stability. The article search was accessed from an internet search database: Scopus, Pubmed, and Web of Science, published between January 2012 and June 2022. Results: Of the 244 articles, 44 were found to be related to the characteristics and physical stability of nanoemulsions in anti-aging cosmetics. These showed that active ingredients with antioxidant activity, filter UV rays, moisturizing agents, and cell-repairing agents are delivered by a nanoemulsion system with various types and ratios of surfactants, cosurfactants, and oil phases. Tween 80, Span 80, Transcutol HP, and Caprylic/capric triglyceride are the most widely used nanoemulsion compositions. Conclusion: The type and composition of the oil phase, surfactant, and cosurfactant affect the characteristics of the nanoemulsion (droplet size, polydispersity index, viscosity, zeta potential) and the physical stability of the nanoemulsion so that it can deliver active ingredients that have the potential as anti-aging well.
背景:皮肤老化可以通过使用抗衰老化妆品来克服。许多具有抗衰老潜力的活性成分来源于植物,这些物质必须通过健全的皮肤输送系统,即纳米乳液来输送。纳米乳的特性与其物理稳定性密切相关。目的:本研究旨在对用于局部抗衰老化妆品的纳米乳液的体内和体外研究设计进行系统综述,以考察纳米乳液的特性和物理稳定性。方法:采用基于PRISMA语句的系统文献综述,对纳米乳的特性和物理稳定性进行综述。文章搜索从互联网搜索数据库Scopus, Pubmed和Web of Science访问,发表于2012年1月至2022年6月。结果:244篇文献中,有44篇与纳米乳液抗衰老化妆品的特性及物理稳定性有关。这些结果表明,纳米乳液体系中含有不同类型和比例的表面活性剂、助表面活性剂和油相,可以传递具有抗氧化活性、过滤紫外线、保湿剂和细胞修复剂的活性成分。Tween 80、Span 80、Transcutol HP和Caprylic/capric甘油三酯是最广泛使用的纳米乳液组合物。结论:油相、表面活性剂和助表面活性剂的类型和组成影响纳米乳的粒径、多分散性指数、粘度、zeta电位等特性和物理稳定性,从而使纳米乳能够输送具有抗衰老潜力的活性成分。
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JURNAL FARMASI DAN ILMU KEFARMASIAN INDONESIA
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