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新型载埃索美拉唑镁双释放微型片多效胶囊:比格犬体内的处方、优化、表征及评价

Novel Esomeprazole Magnesium-Loaded Dual-Release Mini-Tablet Polycap: Formulation, Optimization, Characterization, and In Vivo Evaluation in Beagle Dogs.

作者信息

Kwon Taek Kwan, Kang Ji-Hyun, Na Sang-Beom, Kim Jae Ho, Kim Yong-Il, Kim Dong-Wook, Park Chun-Woong

机构信息

College of Pharmacy, Chungbuk National University, Cheongju 28160, Korea.

Pharmaceutical Research Centre, Hanmi Pharm. Co., Ltd., Hwaseong 18469, Korea.

出版信息

Pharmaceutics. 2022 Jul 5;14(7):1411. doi: 10.3390/pharmaceutics14071411.

DOI:10.3390/pharmaceutics14071411
PMID:35890307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9323828/
Abstract

Esomeprazole magnesium (EMP) is a proton pump inhibitor (PPI) that reduces acid secretion. EMP has a short plasma half-life (approximately 1.3 h); hence, nocturnal acid breakthrough (NAB) frequently occurs, disturbing the patient's nighttime comfort and sleep. We aimed to develop a novel esomeprazole magnesium-loaded dual-release mini-tablet polycap (DR polycap) with a prolonged onset time and improved bioavailability to prevent NAB. The formulation of the EPM mini-tablet core resulted in rapid drug release. The core was coated with an inner coating and an Eudragit L30D-55 aqueous dispersion coating to prepare the first-release mini-tablet. In addition, the core was coated with an inner coating and an aqueous dispersion of Eudragit S100 and Eudragit L100 coating to prepare the second-release mini-tablet. Each mini-tablet type was characterized using an in vitro dissolution test and microscopic examination. After testing, 10 of each mini-tablets were placed together in hard capsules to form DR polycaps. The combination of mini-tablets was optimized via in vitro release testing and in vivo pharmacokinetic studies. The AUC of the DR polycap was similar to that of a comparable commercial product (Nexium); C was lower by approximately 50%, and T was extended by approximately 1.7-fold. In conclusion, DR polycap is an alternative to commercial products with improved NAB and dosing compliance because of its dual-release characteristics.

摘要

埃索美拉唑镁(EMP)是一种质子泵抑制剂(PPI),可减少胃酸分泌。EMP的血浆半衰期较短(约1.3小时);因此,夜间酸突破(NAB)经常发生,影响患者夜间舒适度和睡眠。我们旨在开发一种新型的载有埃索美拉唑镁的双相释放微型片多颗粒胶囊(DR多颗粒胶囊),其起效时间延长且生物利用度提高,以预防NAB。EPM微型片核心制剂导致药物快速释放。核心用内包衣和Eudragit L30D - 55水分散体包衣,以制备速释微型片。此外,核心用内包衣以及Eudragit S100和Eudragit L100的水分散体包衣,以制备缓释微型片。每种微型片类型通过体外溶出试验和显微镜检查进行表征。测试后,将每种10片微型片一起放入硬胶囊中制成DR多颗粒胶囊。通过体外释放测试和体内药代动力学研究对微型片的组合进行优化。DR多颗粒胶囊的AUC与同类市售产品(耐信)相似;Cmax降低约50%,Tmax延长约1.7倍。总之,DR多颗粒胶囊因其双相释放特性,是具有改善的NAB和给药顺应性的市售产品的替代品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/84708ded1c41/pharmaceutics-14-01411-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/ce3b72490363/pharmaceutics-14-01411-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/3609a7a440a2/pharmaceutics-14-01411-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/71544a55ffe5/pharmaceutics-14-01411-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/17cadcfb3b56/pharmaceutics-14-01411-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/64aeb79440a0/pharmaceutics-14-01411-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/e491d27b2cf7/pharmaceutics-14-01411-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/84708ded1c41/pharmaceutics-14-01411-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/ce3b72490363/pharmaceutics-14-01411-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/3609a7a440a2/pharmaceutics-14-01411-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/71544a55ffe5/pharmaceutics-14-01411-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/17cadcfb3b56/pharmaceutics-14-01411-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/64aeb79440a0/pharmaceutics-14-01411-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/e491d27b2cf7/pharmaceutics-14-01411-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c99b/9323828/84708ded1c41/pharmaceutics-14-01411-g007.jpg

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