用于去除水中药物的 3D 打印墨盒

IF 4.1 Q1 CHEMISTRY, ANALYTICAL Talanta Open Pub Date : 2024-02-27 DOI:10.1016/j.talo.2024.100299
Ankur Jyoti Thakuria , Purushottam Suryavanshi , Subham Banerjee
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引用次数: 0

摘要

药物进入水体是全世界关注的一个重要问题,在所有近水生态环境中都发现了药物,其浓度往往令人担忧。环境水体中的药物废物已被证明会影响环境平衡,并对人类构成不利风险。在本研究中,我们制作了一种新型系统,其中包含 3D 打印的可持续多孔聚对苯二甲酸乙二酯(PETG)滤芯和 RP-HPLC-DAD 方法,用于去除水样中的非甾体抗炎药(NSAID),如双氯芬酸钠(DS)和吲哚美辛(IND),称为 "滤芯"。该装置是利用本土热熔挤出长丝,以熔融沉积建模(FDM)为媒介的三维打印技术制造的。为了实现 FDM 3D 打印,我们使用 PETG 作为主要材料,聚乙烯醇 (PVA)、Affnisol™ 和 Eudragit®EPO 作为水溶性孔隙形成材料来制造长丝。我们的研究表明,热塑性可回收 PETG 复合材料在去除 PVA、Affnisol™ 和 Eudragit®EPO 后具有微孔特性,能有效地从水溶液中提取这两种药物。通过从水溶液中萃取 DS 和 IND,然后进行 RP-HPLC 分析,证明了当前策略的实用性。两种药物的提取回收率均超过 80%,总体相对标准偏差小于 3%。由于转向使用具有可定制形状、尺寸和化学性质的可持续滤筒,所提出的方法为分析行业的萃取和样品制备带来了一线希望。
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 printed cartridges for the removal of pharmaceuticals from water

The entry of pharmaceuticals into water is a key worldwide concern, with drugs being identified in all near-aqueous ecologies at often worrying concentrations. Pharmaceutical waste in environmental water has been shown to affect environmental equilibrium and pose a risk to humans adversely. In the present study, we fabricated a novel system containing 3D printed sustainable, porous Polyethylene terephthalate glycol (PETG) cartridges and RP-HPLC-DAD methodology to remove non-steroidal anti-inflammatory drugs (NSAIDs) such as diclofenac sodium (DS) and indomethacin (IND) from water samples called “Cartridges.” The device was fabricated using fused deposition modeling (FDM)-mediated 3D printing technology using indigenous hot-melt extruded filaments. To enable FDM 3D printing, the filaments were fabricated using PETG as a primary material and polyvinyl alcohol (PVA), Affnisol™, and Eudragit®EPO as water-soluble pore-forming materials. We showed that the thermoplastic, recyclable PETG composite material, which presents microporous properties after removal of PVA, Affnisol™, and Eudragit®EPO, is effective for extracting both drugs from water solution. The usefulness of the current strategy was demonstrated by the extraction of DS and IND from an aqueous solution followed by RP-HPLC analysis. The% extraction recovery was more than 80 % for both drugs, with an overall relative standard deviation of less than 3 %. The proposed approach can bring a ray of hope in extraction and sample preparation in the analytical industry due to a shift to the use of sustainable cartridges with customizable shapes, sizes, and chemical properties.

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来源期刊
Talanta Open
Talanta Open Chemistry-Analytical Chemistry
CiteScore
5.20
自引率
0.00%
发文量
86
审稿时长
49 days
期刊最新文献
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