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通过熔融沉积成型3D打印机制造零级缓释漂浮片。

Fabrication of Zero-Order Sustained-Release Floating Tablets via Fused Depositing Modeling 3D Printer.

作者信息

Kimura Shin-Ichiro, Ishikawa Taichi, Iwao Yasunori, Itai Shigeru, Kondo Hiromu

机构信息

Department of Pharmaceutical Engineering and Drug Delivery Science, School of Pharmaceutical Sciences, University of Shizuoka.

出版信息

Chem Pharm Bull (Tokyo). 2019;67(9):992-999. doi: 10.1248/cpb.c19-00290.

DOI:10.1248/cpb.c19-00290
PMID:31474738
Abstract

A three-dimensional (3D) printer is a powerful tool that can be used to enhance personalized medicine. A fused deposition modeling (FDM) 3D printer can fabricate 3D objects with different internal structures that provides the opportunity to introduce one or more specific functionalities. In this study, zero-order sustained-release floating tablet was fabricated using FDM 3D printer. Filaments comprising poorly water-soluble weak base drug, itraconazole (ITZ) and polymers (hydroxypropyl cellulose and polyvinylpyrrolidone) were prepared, and tablets with a hollow structure and different outside shell thicknesses were fabricated. In the 3D printed tablets, ITZ existed as an amorphous state and its solubility improved markedly. As the outside shell thickness of the tablet increased, drug release was delayed and floating time was prolonged. In the tablets with 0.5 mm of the upper and bottom layer thickness and 1.5 mm of the side layer thickness, holes were not formed in the tablets during the dissolution test, and the tablets floated for a long period (540 min) and showed nearly zero-order drug release for 720 min. These findings may be useful for improving the bioavailability of several drugs by effective absorption from the upper small intestine, with floating gastric retention system.

摘要

三维(3D)打印机是一种强大的工具,可用于增强个性化医疗。熔融沉积建模(FDM)3D打印机能够制造具有不同内部结构的3D物体,这为引入一种或多种特定功能提供了机会。在本研究中,使用FDM 3D打印机制造了零级缓释漂浮片。制备了包含难溶性弱碱性药物伊曲康唑(ITZ)和聚合物(羟丙基纤维素和聚乙烯吡咯烷酮)的细丝,并制造了具有中空结构和不同外壳厚度的片剂。在3D打印片剂中,ITZ以无定形状态存在,其溶解度显著提高。随着片剂外壳厚度的增加,药物释放延迟,漂浮时间延长。在上层和底层厚度为0.5毫米、侧层厚度为1.5毫米的片剂中,溶出试验期间片剂未形成孔洞,片剂长时间漂浮(540分钟),并在720分钟内显示出近零级药物释放。这些发现可能有助于通过漂浮胃滞留系统从十二指肠有效吸收来提高几种药物的生物利用度。

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