Journal
INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 606, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.ijpharm.2021.120894
Keywords
Sinomenine; NSAID( 2); Co-amorhous Systems Solubility Sustained Release Rheumatoid arthiris combination theraphy
Categories
Funding
- National Natural Science Foundation of China [81473123, 21874148]
- Chinese Ministry of Education 111 Project [BP0820034]
- Hunan Provincial Innovation Foundation for Postgraduate [CX20200276]
- Guangdong Basic and Applied Basic Research Foundation [2019A1515110336]
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This study prepared co-amorphous systems of SIN with three NSAIDs to achieve combination therapy for RA, improving drug solubility and controlled release. Analysis using techniques like FTIR showed that the co-amorphous systems exist in salt form and exhibit excellent physicochemical stability.
Rheumatoid arthritis (RA) is a chronic autoimmune joint disorder that affects about 1% of the world population and may lead to severe disability and comorbidity. Despite breakthroughs in past decades to understand its pathogenesis and the development of transforming disease-modifying antirheumatic drugs, the symptoms of many patients are not substantially improved. Sinomenine (SIN), a natural alkaloid with poor solubility, has been used to treat RA in China for years because of its unique immunoregulative activity. However, its commercial hydrochloride form has a short half-time, which may cause huge fluctuations of blood drug concentration leading to severe adverse reactions. In this study, co-amorphous systems of SIN with three nonsteroidal antiinflammatory drugs (NSAIDs), including indomethacin, naproxen, and sulindac, were prepared for the combination therapy, as well as the improvement of its aqueous solubility and controlled release. Each co-amorphous sample was characterized by powder X-ray diffraction (PXRD), temperature-modulated differential scanning calorimetry (mDSC), and Fourier transform infrared spectroscopy (FTIR). The CO2- and N+-H stretching vibration in the three co-amorphous samples appears in FTIR spectra, suggesting the formation of salts between SIN and NSAIDs. SIN also exhibits sustained release rates in all three co-amorphous samples. These coamorphous systems show excellent physicochemical stability because no recrystallization was observed at 25 degrees C and 75% relative humidity (RH) after four months. Our study suggests that SIN-NSAIDs co-amorphous systems represent an affordable and promising treatment against RA.
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