4.7 Article

Sustained Release of Co-Amorphous Matrine-Type Alkaloids and Resveratrol with Anti-COVID-19 Potential

Journal

PHARMACEUTICS
Volume 14, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics14030603

Keywords

co-amorphous systems; sustained-release; COVID-19; matrine-type alkaloids; resveratrol

Funding

  1. National Natural Science Foundation of China [82173688]
  2. Chinese Ministry of Education 111 Project [BP0820034]
  3. Guangdong Basic and Applied Basic Research Foundation [2019A1515110336]
  4. Science and Technology Innovation Program of Hunan Province [2021RC4067]
  5. Hunan Provincial Natural Science Foundation of China [2021JJ30791]

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The natural alkaloids matrine, oxymatrine, and sophoridine have been used for the treatment of COVID-19, but their short half-lives and rapid elimination present challenges for effectiveness. This study explores using resveratrol as a co-former to create co-amorphous systems that improve therapeutic index. The co-amorphous systems demonstrated sustained release behavior and excellent physicochemical stability, suggesting a promising approach for repurposing these drugs against COVID-19.
Matrine (MAR), oxymatrine (OMAR), and sophoridine (SPD) are natural alkaloids with varying biological activities; matrine was recently used for the treatment of coronavirus disease 2019 (COVID-19). However, the short half-lives and rapid elimination of these matrine-type alkaloids would lead to low oral bioavailability and serious side effects. Herein, resveratrol (RES) was selected as a co-former to prepare their co-amorphous systems to improve the therapeutic index. The formation of co-amorphous MAR-RES, OMAR-RES, and SPD-RES was established through powder X-ray diffraction and modulated temperature differential scanning calorimetry. Furthermore, Fourier transform infrared spectroscopy and NMR studies revealed the strong molecular interactions between resveratrol and these alkaloids, especially OMAR-RES. Matrine, oxymatrine, and sophoridine in the co-amorphous systems showed sustained release behaviors in the dissolution experiments, due to the recrystallization of resveratrol on the surface of co-amorphous drugs. The three co-amorphous systems exhibited excellent physicochemical stability under high relative humidity conditions. Our study not only showed that minor structural changes of active pharmaceutical ingredients may have distinct molecular interactions with the co-former, but also discovered a new type of sustained release mechanism for co-amorphous drugs. This promising co-amorphous drug approach may present a unique opportunity for repurposing these very promising drugs against COVID-19.

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