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Preparation and In Vitro–In Vivo Evaluation of Sustained-Release Matrix Pellets of Capsaicin to Enhance the Oral Bioavailability

机译:辣椒素的缓释基质微丸的制备和体内评价以增强口服生物利用度

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摘要

Capsaicin has multiple pharmacological activities including antioxidant, anticancer, and anti-inflammatory activities. However, its clinical application is limited due to its poor aqueous solubility, gastric irritation, and low oral bioavailability. This research was aimed at preparing sustained-release matrix pellets of capsaicin to enhance its oral bioavailability. The pellets comprised of a core of solid-dispersed capsaicin mixed with microcrystalline cellulose (MCC) and hydroxypropyl cellulose (HPMC) and subsequently coating with ethyl cellulose (EC) were obtained by using the technology of extrusion/spheronization. The physicochemical properties of the pellets were evaluated through scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and X-ray diffractometry (XRD). Besides, the in vitro release, in vivo absorption, and in vitro–in vivo correlation were also assessed. More importantly, the relative bioavailability of the sustained-release matrix pellets was studied in fasted rabbits after oral administration using free capsaicin and solid dispersion as references. The oral bioavailability of the matrix pellets and sustained-release matrix pellets of capsaicin was improved approximately 1.98-fold and 5.34-fold, respectively, compared with the free capsaicin. A good level A IVIVC (in vitro–in vivo correlation) was established between the in vitro dissolution and the in vivo absorption of sustained-release matrix pellets. All the results affirmed the remarkable improvement in the oral bioavailability of capsaicin owing to the successful preparation of its sustained-release matrix pellets.
机译:辣椒素具有多种药理活性,包括抗氧化剂,抗癌和抗炎活性。但是,由于其水溶性差,胃刺激性和口服生物利用度低,其临床应用受到了限制。这项研究旨在制备辣椒素的缓释基质药丸,以提高其口服生物利用度。通过使用挤出/滚圆技术,获得了由固体分散的辣椒素核与微晶纤维素(MCC)和羟丙基纤维素(HPMC)混合,然后涂覆乙基纤维素(EC)制成的颗粒。通过扫描电子显微镜(SEM),差示扫描量热法(DSC)和X射线衍射法(XRD)评估颗粒的理化性质。此外,还评估了体外释放,体内吸收以及体外-体内相关性。更重要的是,在口服给药后,以游离辣椒素和固体分散体为参考,研究了禁食兔子中缓释基质药丸的相对生物利用度。与游离辣椒素相比,辣椒素的基质药丸和缓释基质药丸的口服生物利用度分别提高了约1.98倍和5.34倍。在缓释基质药丸的体外溶出度与体内吸收之间建立了良好的A IVIVC(体外-体内相关性)。所有结果都证实,由于成功制备了其持续释放基质药丸,辣椒素的口服生物利用度有了显着提高。

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