FORMULATION AND STABILITY EVALUATION OF ANTI-OBESITY NUTRACEUITCAL BLEND OF WHITE KIDNEY BEAN EXTRACT (PHASEOLUS VULGARIS L.), PROPOLIS ETHANOLIC EXTRACT AND CRPIC3

Q2 Pharmacology, Toxicology and Pharmaceutics
Doaa Salah ELDIN ABDELFATTAH, Mervat A Fouad, Aliaa N Elmeshad, M. EL-NABARAWI, S. F. Elhabal
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Abstract

Objective: This study aimed to formulate and evaluate the stability profile of an anti-obesity nutraceutical combination in different dosage forms. Methods: Active and inactive ingredients were formulated into pharmaceutical dosage forms. The quality parameters of the dosage forms were determined, followed by accelerated stability testing (40±2 °C and 75±5% Relative Humidity (RH)) for 180 d was completed to evaluate their physical, chemical and microbiological attributes throughout the storage period. Results: Pre-formulation parameters of the powder blend of active and inactive ingredients for each dosage form showed a satisfactory flowability with Hausner's ratio falling between 1.16 and 1.18, average angle of repose between 22.29° and 22.90° and acceptable compressibility with Carr’s index below 25%. Tablets assessments were acceptable with a mean friability value of 0.21±0.03%, hardness of 4.12±0.09 kg/cm2. The average disintegration time of 5 min 10 sec for tablets and 4 min and 30 sec for capsules. The accelerated stability study revealed that tablet dosage forms are stable for longer period that can reach up to 180 d (24 mo real-time), while sachets and capsules are stable for a period of 135 d (18 mo real-time). Conclusion: The anti-obesity blend of White Kidney Bean Extract (WKBE), Propolis Ethanolic Extract (PEE) and CrPic3 can be successfully formulated in acceptable and convenient dosage forms that can be stable for 18-24 mo.
白芸豆提取物(Phaseolus vulgaris L.)、蜂胶乙醇提取物和 Crpic3 的抗肥胖营养混合物的配方和稳定性评价
研究目的本研究旨在配制和评估不同剂型的抗肥胖营养保健品组合的稳定性:方法:将活性成分和非活性成分配制成药物剂型。方法:将活性成分和非活性成分配制成药物剂型,测定剂型的质量参数,然后进行 180 天的加速稳定性测试(40±2 °C,75±5% 相对湿度),以评估其在整个储存期间的物理、化学和微生物属性:每种剂型的活性和非活性成分混合粉末的预制参数都显示出令人满意的流动性,豪斯纳比率介于 1.16 和 1.18 之间,平均倾角介于 22.29 和 22.90 之间,可压缩性可接受,卡尔指数低于 25%。片剂的评估结果是合格的,平均易碎率为 0.21±0.03%,硬度为 4.12±0.09kg/cm2。片剂的平均崩解时间为 5 分 10 秒,胶囊的平均崩解时间为 4 分 30 秒。加速稳定性研究表明,片剂的稳定期较长,可达 180 天(24 个月实时),而袋装和胶囊的稳定期为 135 天(18 个月实时):结论:白芸豆提取物(WKBE)、蜂胶乙醇提取物(PEE)和CrPic3的抗肥胖混合物可成功配制成可接受性和方便的剂型,并可在18-24个月内保持稳定。
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来源期刊
International Journal of Applied Pharmaceutics
International Journal of Applied Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
1.40
自引率
0.00%
发文量
219
期刊介绍: International Journal of Applied Pharmaceutics (Int J App Pharm) is a peer-reviewed, bimonthly (onward March 2017) open access journal devoted to the excellence and research in the pure pharmaceutics. This Journal publishes original research work that contributes significantly to further the scientific knowledge in conventional dosage forms, formulation development and characterization, controlled and novel drug delivery, biopharmaceutics, pharmacokinetics, molecular drug design, polymer-based drug delivery, nanotechnology, nanocarrier based drug delivery, novel routes and modes of delivery; responsive delivery systems, prodrug design, development and characterization of the targeted drug delivery systems, ligand carrier interactions etc. However, the other areas which are related to the pharmaceutics are also entertained includes physical pharmacy and API (active pharmaceutical ingredients) analysis. The Journal publishes original research work either as a Original Article or as a Short Communication. Review Articles on a current topic in the said fields are also considered for publication in the Journal.
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