Producing High-Dose Liqui-Tablet (Ketoprofen 100 mg) for Enhanced Drug Release Using Novel Liqui-Mass Technology

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Matthew Lam, Ali Nokhodchi
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引用次数: 5

Abstract

Purpose

Liqui-Tablet is a dosage form derived from Liqui-Mass technology. It has proven to be a promising approach to improve drug dissolution rate of poorly water-soluble drugs. So far, Liqui-Tablet is feasible for low-dose drugs. In this study, an attempt was made to produce high-dose Liqui-Tablet, whilst maintaining ideal physicochemical properties for ease of manufacturing.

Methods

Liqui-Tablets containing 100 mg of ketoprofen were produced using various liquid vehicles including PEG 200, Span 80, Kolliphor EL, PG, and Tween 85. Investigations that were carried out included saturation solubility test, dissolution test, tomographic study, and typical quality control tests for assessing flowability, particle size distribution, friability, and tablet hardness.

Results

The weight of these Liqui-Tablets was acceptable for swallowing (483.8 mg), and the saturation solubility test showed PEG 200 to be the most suitable liquid vehicle (493 mg/mL). Tests investigating physicochemical properties such as flowability, particle size distribution, friability, and tablet hardness have shown no issue concerning quality control and manufacturability. The drug release test of the best formulation has shown extremely rapid drug release at pH 7.4 (100% after 5 min). At pH 1.2 the drug release was reasonable considering the formulation was yet to be optimized.

Conclusion

Despite the high amount of API and liquid vehicle, it is possible to produce a high-dose dosage form with acceptable size and weight for swallowing using the novel Liqui-Mass technology. This has the potential to diversify the technology by removing the restriction of high dose drug that has been seen in liquisolid technology.

利用新型液质技术生产高剂量酮洛芬液体片剂(100mg)以促进药物释放
目的:液体质片是液体质技术的一种剂型。它已被证明是提高低水溶性药物溶出率的一种很有前途的方法。到目前为止,液体片剂对于小剂量药物是可行的。本研究尝试在保持理想理化性质的前提下,生产大剂量的液体片剂,以方便生产。方法采用PEG 200、Span 80、Kolliphor EL、PG、Tween 85等不同的液体载体制备酮洛芬片。进行的调查包括饱和溶解度测试、溶解测试、层析研究和典型的质量控制测试,以评估流动性、粒度分布、脆性和片剂硬度。结果两种药液片的重量(483.8 mg)均可接受,饱和溶解度试验表明PEG 200为最合适的载液剂(493 mg/mL)。对流动性、粒度分布、易碎性和片剂硬度等理化性质的测试表明,在质量控制和可制造性方面没有问题。最佳配方的释药试验表明,在pH 7.4时释药极快(5 min后释药100%)。考虑到配方尚待优化,在pH为1.2时药物释放是合理的。结论尽管原料药和液体载体用量大,但采用新型液质技术可生产出可接受大小和重量的大剂量剂型。这有可能通过消除在液体固体技术中看到的高剂量药物的限制来使技术多样化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pharmaceutical Innovation
Journal of Pharmaceutical Innovation PHARMACOLOGY & PHARMACY-
CiteScore
3.70
自引率
3.80%
发文量
90
审稿时长
>12 weeks
期刊介绍: The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories: Materials science, Product design, Process design, optimization, automation and control, Facilities; Information management, Regulatory policy and strategy, Supply chain developments , Education and professional development, Journal of Pharmaceutical Innovation publishes four issues a year.
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