提高溶解性的熔融熔融技术:热熔挤出和KinetiSol®技术的比较

IF 2.3 Q3 PHARMACOLOGY & PHARMACY Scientia Pharmaceutica Pub Date : 2022-08-24 DOI:10.3390/scipharm90030051
Srinivas Ajjarapu, Srikanth Banda, Pratap Basim, N. Dudhipala
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引用次数: 2

摘要

口服药物递送的成功候选者需要具有足够的溶解度和溶出率来引发其治疗作用。目前正在进行广泛的研究,通过涉及聚合物和非聚合物方法的许多技术来提高难溶性药物的溶解度。微粉化和纳米晶体等非聚合物方法成功地提高了药物的表观溶解度,但溶解度的维持并不总是可能的。无定形固体分散体(ASD)在聚合物的帮助下提高了溶解度并保持了溶解度,从而提高了生物利用度。喷雾干燥、热熔挤压(HME)和KinetiSol®技术是能够制造ASD的一些技术。在制备ASD的处理挑战和适用性方面,这些技术中的每一种都有自己的优点和缺点。后两种技术在融合和非溶剂技术方面是相似的,以提高溶解度。这篇综述比较了HME和KinetiSol®在机构、设备设计、配方、工艺参数和可扩展性方面的技术。
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Melt Fusion Techniques for Solubility Enhancement: A Comparison of Hot Melt Extrusion and KinetiSol® Technologies
A successful candidate for oral drug delivery needs to possess adequate solubility and dissolution rate to elicit its therapeutic action. Extensive research is being carried out to enhance the solubility of poorly soluble drugs through a number of techniques involving polymeric and non-polymeric approaches. Non-polymeric approaches such as micronization and nanocrystals are successful in improving the apparent solubility of drugs, but the sustenance of solubility is not always possible. Amorphous solid dispersions (ASDs) lead to solubility enhancement as well as the maintenance of solubility with the assistance of polymers, thereby improving bioavailability. Spray drying, hot melt extrusion (HME), and KinetiSol® technologies are some of the techniques capable of manufacturing ASDs. Each of these techniques has its own advantages and disadvantages in terms of processing challenges and applicability in preparing ASDs. The latter two technologies are similar in being fusion and non-solvent techniques to improve solubility. This review compares both HME and KinetiSol® techniques regarding mechanism, equipment design, formulation, and process parameters involved and scalability.
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来源期刊
Scientia Pharmaceutica
Scientia Pharmaceutica Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.60
自引率
4.00%
发文量
67
审稿时长
10 weeks
期刊最新文献
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