为了给药,通过桌面容器光聚合(立体光刻)技术3D打印纳米复合药丸。

IF 3.2 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING 3D printing in medicine Pub Date : 2022-01-17 DOI:10.1186/s41205-022-00130-2
Peeyush Kumar Sharma, Dinesh Choudhury, Vivek Yadav, U S N Murty, Subham Banerjee
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引用次数: 13

摘要

背景:桌面还原聚合工艺或立体光版印刷是开发多功能纳米复合材料的理想方法,其中传统的固体剂型被用作药物负载纳米载体的兼容管理的储存器。方法:在本研究中,开发了一种纳米复合药物递送系统,即一种经批准的营养保健品小檗碱的水凝胶纳米颗粒包埋在大容器光聚合单体中,用于药物递送应用。为了制备纳米复合药物递送系统/药丸,选择了一种生物相容性的容器光聚合树脂作为最佳基质,能够有效地从立体光刻介导的3D打印纳米复合药丸中递送小檗碱。结果:获得的数据反映了小檗碱负载水凝胶纳米颗粒的高效形成,平均粒径为95.05±4.50 nm,但负载较低。立体光刻辅助制作的单块体具有高保真度(与计算机辅助设计一致),并通过傅里叶变换红外光谱确定了光交联。在立体光刻过程中,水凝胶纳米颗粒被包裹在药片内,这是电子显微镜所证明的。纳米复合丸在酸性环境中溶胀较大,4 h后小檗碱释放速度较快,为50.39±3.44%。总体结果表明,在胃肠道运输时间内释放最大,排出的药丸。结论:我们打算证明通过桌面还原聚合工艺制造3D打印纳米复合药丸用于药物递送应用的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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3D printing of nanocomposite pills through desktop vat photopolymerization (stereolithography) for drug delivery reasons.

Background: The desktop vat polymerization process or stereolithography printing is an ideal approach to develop multifunctional nanocomposites wherein a conventional solid dosage form is used as a reservoir for compliant administration of drug-loaded nanocarriers.

Methods: In this study, a nanocomposite drug delivery system, that is, hydrogel nanoparticles of an approved nutraceutical, berberine entrapped within vat photopolymerized monoliths, was developed for drug delivery applications. For the fabrication of the nanocomposite drug delivery systems/pills, a biocompatible vat photopolymerized resin was selected as an optimum matrix capable of efficiently delivering berberine from stereolithography mediated 3D printed nanocomposite pill.

Results: The obtained data reflected the efficient formation of berberine-loaded hydrogel nanoparticles with a mean particle diameter of 95.05 ± 4.50 nm but low loading. Stereolithography-assisted fabrication of monoliths was achieved with high fidelity (in agreement with computer-aided design), and photo-crosslinking was ascertained through Fourier-transform infrared spectroscopy. The hydrogel nanoparticles were entrapped within the pills during the stereolithography process, as evidenced by electron microscopy. The nanocomposite pills showed a higher swelling in an acidic environment and consequently faster berberine release of 50.39 ± 3.44% after 4 h. The overall results suggested maximal release within the gastrointestinal transit duration and excretion of the exhausted pills.

Conclusions: We intended to demonstrate the feasibility of making 3D printed nanocomposite pills achieved through the desktop vat polymerization process for drug delivery applications.

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