Please use this identifier to cite or link to this item: http://ir.buu.ac.th/dspace/handle/1513/1016
Title: DESIGN AND DEVELOPMENT OF A 3D-PRINTED VORTEX TUBE REACTOR FOR INCREASING THE PRODUCTIVITY OF LIPID-BASED NANOPARTICLES VIA FLOW CHEMISTRY
การออกแบบและพัฒนาเครื่องปฏิกิริยาเคมีแบบท่อกระแสวนที่เตรียมด้วยการพิมพ์สามมิติ เพื่อเพิ่มผลิตภาพของอนุภาคไขมันนาโนด้วยเคมีการไหล
Authors: Kittipat Suwanpitak
กิตติภัฎ สุวรรณพิทักษ์
TANIKAN SANGNIM
ธนิกานต์ แสงนิ่ม
Burapha University
TANIKAN SANGNIM
ธนิกานต์ แสงนิ่ม
tanikan@buu.ac.th
tanikan@buu.ac.th
Keywords: อนุภาคไขมันนาโน
คอมพิวเตอร์ช่วยออกแบบ
พลศาสตร์ของไหลเชิงคำนวณ
เคมีการไหลต่อเนื่อง
การพิมพ์สามมิติ
Lipid-based nanoparticles
Computer-aided design
Computational fluid dynamics
Continuous flow chemistry
3D-printing
Issue Date:  12
Publisher: Burapha University
Abstract: Lipid-based nanoparticles are versatile drug delivery systems, composed of lipids, phospholipids, cholesterol, and modified lipids. They efficiently encapsulate hydrophobic and hydrophilic drugs, enhance solubility and stability, and enable controlled drug release and targeted delivery while reducing toxicity due to their biocompatibility and low immunogenicity. However, conventional lipid-based nanoparticle preparation methods like batch synthesis has limitations in terms of nanoparticle properties, productivity, and scalability. To address these challenges, this study focuses on a new design vortex tube reactor fabricated by 3D printing techniques for continuous synthesis via flow chemistry. The optimized reactor, manufactured using polypropylene through fused deposition modeling, exhibits improved mixing and reduced variance compared to conventional approaches. Lipid-based nanoparticles produced in this 3D-printed vortex tube reactor were thoroughly characterized, demonstrating the feasibility of this innovative method. The experimental results showed a reduction in particle size from 192.67 ± 9.40 nm to 166.23 ± 0.98 nm, a decrease in PDI from 0.25 ± 0.01 to 0.17 ± 0.01, an increase in percentage of entrapment efficiency from 49.09 ± 0.65% to 67.75 ± 1.55%, an increase in percentage of loading capacity from 28.99 ± 0.38% to 36.39 ± 0.83%, and a significant boost in productivity from 1.05 ± 0.13 mg/min to 313.4 ± 12.88 mg/min, compared to traditional batch techniques. These tangible improvements underscore the advantages of this novel approach. Paving the way, this study emphasizes the significance of reactor design and flow parameters in continuous flow chemistry for consistent, high-quality large-scale pharmaceutical manufacturing.
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URI: http://ir.buu.ac.th/dspace/handle/1513/1016
Appears in Collections:Faculty of Pharmaceutical Science

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