Improving the Solubility and Bioavailability of Progesterone Cocrystals with Selected Carboxylic Acids

Progesterone (PROG) is a natural steroid hormone with low solubility and high permeability that belongs to biopharmaceutics classification system class II. In this study, novel pharmaceutical cocrystals of PROG were successfully prepared by solvent evaporation or a liquid-assisted grinding process a...

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Main Authors: Jing Xiong (Author), Dezhong Xu (Author), Hui Zhang (Author), Yan Shi (Author), Xiangxiang Wu (Author), Sicen Wang (Author)
Format: Book
Published: MDPI AG, 2024-06-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Jing Xiong  |e author 
700 1 0 |a Dezhong Xu  |e author 
700 1 0 |a Hui Zhang  |e author 
700 1 0 |a Yan Shi  |e author 
700 1 0 |a Xiangxiang Wu  |e author 
700 1 0 |a Sicen Wang  |e author 
245 0 0 |a Improving the Solubility and Bioavailability of Progesterone Cocrystals with Selected Carboxylic Acids 
260 |b MDPI AG,   |c 2024-06-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics16060816 
500 |a 1999-4923 
520 |a Progesterone (PROG) is a natural steroid hormone with low solubility and high permeability that belongs to biopharmaceutics classification system class II. In this study, novel pharmaceutical cocrystals of PROG were successfully prepared by solvent evaporation or a liquid-assisted grinding process aimed at enhancing its solubility and bioavailability. The cocrystal formers selected based on crystal engineering principles were carboxylic acids, namely, 4-formylbenzeneboronic acid (BBA), isophthalic acid (IPA), and 3-nitrophthalic acid (NPA). The cocrystal structures were characterized using multiple techniques. Single-crystal X-ray diffraction results showed that the carbonyl group, acting as a hydrogen bond acceptor, was pivotal in the cocrystal network formation, with C-H···O interactions further stabilizing the crystals. The cocrystals exhibited improved solubility and dissolution profiles in vitro, with no significant changes in hygroscopicity. The parallel artificial membrane permeability assay (PAMPA) models indicated that the cocrystals retained PROG's high permeability. Pharmacokinetic studies in Sprague-Dawley rats revealed that all cocrystals increased PROG exposure, with AUC<sub>(0~∞)</sub> values for PROG-BBA, PROG-IPA, and PROG-NPA being 742.59, 1201.72 and 442.67 h·ng·mL<sup>−1</sup>, respectively. These values are substantially higher compared to free PROG, which had an AUC<sub>(0~∞)</sub> of 301.48 h·ng·mL<sup>−1</sup>. Notably, PROG-IPA provided the highest AUC improvement, indicating a significant enhancement in bioavailability. Collectively, the study concludes that the cocrystal approach is a valuable strategy for optimizing the physicochemical properties and oral bioavailability of PROG, with potential implications for the development of other poor water-soluble drugs. 
546 |a EN 
690 |a pharmaceutical cocrystal 
690 |a crystal engineering 
690 |a solubility 
690 |a permeability 
690 |a oral bioavailability 
690 |a progesterone 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 16, Iss 6, p 816 (2024) 
787 0 |n https://www.mdpi.com/1999-4923/16/6/816 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/8a55b0f0f13d461c86c85a89ae77ac19  |z Connect to this object online.