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一次一因子法和析因实验设计用于左旋肉碱微胶囊的配方设计以提高其可制造性。

One Factor at a Time and factorial experimental design for formulation of l-carnitine microcapsules to improve its manufacturability.

作者信息

Hegazy Mahmoud M, Badawi Alia A, El-Nabarawi Mohamed A, Eldegwy Mohammed A, Louis Dina

机构信息

Research and Development Dept., Averreos Pharma, Egypt.

Pharmaceutics and Industrial Pharmacy Dept., Faculty of Pharmacy, Cairo University, Egypt.

出版信息

Heliyon. 2023 Dec 13;10(1):e23637. doi: 10.1016/j.heliyon.2023.e23637. eCollection 2024 Jan 15.

Abstract

l-carnitine is an essential dietary supplement of physiological importance. Handling and manufacture of l-carnitine is difficult due to its hygroscopic nature, resulting in impairing its flow properties, as well as solid dosage form stability. The study aimed at reducing l-carnitine hygroscopicity through its encapsulation within a hydrophobic, pH-insensitive polymer. A solid in oil in oil (s/o/o) emulsion solvent evaporation technique for microencapsulation was adopted to exclude the possibility of water uptake. The polymers used were two ethyl cellulose (EC) grades with different viscosities. The chosen solvent for the polymer was acetone, and liquid paraffin was the dispersion medium in which both the drug and polymer were insoluble. Sixteen formulations were developed, and evaluated to study the formulation parameters as anti-coalescent type, mixing speed, surfactant type and polymer ratio, and viscosity grade. A "One Factor at A Time" (OFAT) design of experiment, and a factorial design were utilized. Study results revealed that successful microencapsulation occurred by using Aerosil 200 (0.1 %) as anti-coalescent, a mixing speed of 1000 rpm, and Ethocel Std 20 at a 3:1 drug-to-polymer ratio. Microcapsule formulation containing l-carnitine base, successfully compressed into tablets, showed acceptable water content, disintegration time, hardness, and dissolution. Moreover, it showed acceptable stability upon storage at 40 °C at 75 % RH for six months compared to l-carnitine tablets prepared by wet granulation.

摘要

左旋肉碱是一种具有重要生理意义的必需膳食补充剂。由于左旋肉碱具有吸湿性,其处理和制造过程较为困难,这会损害其流动性能以及固体剂型的稳定性。该研究旨在通过将左旋肉碱包封在一种疏水性、pH不敏感的聚合物中来降低其吸湿性。采用油包油包固体(s/o/o)乳液溶剂蒸发技术进行微囊化,以排除吸水的可能性。所使用的聚合物是两种不同粘度的乙基纤维素(EC)。聚合物选用的溶剂是丙酮,液体石蜡是药物和聚合物均不溶的分散介质。开发了16种制剂,并对其进行评估以研究制剂参数,如抗聚结类型、混合速度、表面活性剂类型和聚合物比例以及粘度等级。采用了“一次一因素”(OFAT)实验设计和析因设计。研究结果表明,使用气相二氧化硅200(0.1%)作为抗聚结剂、1000转/分钟的混合速度以及药物与聚合物比例为3:1的乙基纤维素标准20时,成功实现了微囊化。含有左旋肉碱碱的微囊制剂成功压制成片剂,其水分含量、崩解时间、硬度和溶出度均符合要求。此外,与湿法制粒制备的左旋肉碱片剂相比,在40°C、75%相对湿度下储存六个月后,该微囊制剂显示出可接受的稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4aa7/10851296/6a9596c0c2c4/ga1.jpg

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