设计可行的3d打印工艺生产高效控释农药

Benita C. Yao, Zhining Xu, Jianan Liu, Liang Yang, Jianping Shang, Jingyuan Fan, L. Ouyang, Hua-Jun Shawn Fan
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引用次数: 0

摘要

:溶解度、挥发性、喷雾漂移、径流、光解等多种因素阻碍农药到达所需位置,发挥其全部潜力。在这项研究中,增材制造被用来制造一种可用于熔融沉积建模打印的载药灯丝。最佳打印参数为打印温度(170℃)、温床温度(25℃)、打印速度15 mm/s、长丝直径1.55 mm、层高0.3 mm、喷嘴直径0.4 mm、缩回速度和缩回距离为零。基于pcl的框架为药物包封和低熔融温度提供了支架。后者是维持载药的完整性和化学性质的关键。FTIR证实了复合材料的物理混合性质。XRD分析表明,PCL和模型药物在打印后呈无定形。通过体外溶出度试验实现PCL的控释。在四种动力学模型:零级、一阶、Higuchi模型和Korsmeyer - Peppas模型中,药物溶解和释放的动力学模型符合Korsmeyer - Peppas模型。本研究通过调整释放调节剂的含量和类型,提供了一种可行的农药控释设计,以满足精准防治害虫的需要。该3DP片具有载药量高、载药量可控、释放能力稳定、屏蔽紫外线性能好、生产工艺简单等优点。不需要昂贵的专用设备来生产所需的功能,大大降低了生产成本,简化了生产过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design a Viable 3DP Processing for Producing Effective Controlled-Release Pesticide
: Various factors such as solubility, volatility, spray drift, runoff, and photolysis prevent the pesticides to reach their desired location and realize their full potential. In this study, additive manufacturing is used to create a drug-loaded filament that can be used in Fused deposition modeling printing. The optimal printing parameters are printing temperature (170°C), hotbed temperature (25°C), printing speed 15 mm/s, filament diameter 1.55 mm, layer height 0.3 mm, nozzle diameter 0.4 mm and zero retraction speed and retraction distance. The PCL-based framework provides a scaffold for drug encapsulation and low melting temperature. The latter is the key to maintaining the integrity and chemical properties of the loaded drug. FTIR confirms the physical-mix nature of composite. XRD suggests that PCL and model drug became amorphous after printing. The PCL controlled-release can be realized through in vitro dissolution tests. Among the four kinetic models: the zero-order, first-order, Higuchi model, and Korsmeyer–Peppas model, the kinetic model for dissolution and drug release conforms to the Korsmeyer– Peppas model. This study provides a viable design of controlled-release pesticides by adjusting the release regulator content and type to meet the precision pest-control needs. This 3DP tablet has higher drug loading, controllable drug loading, stable drug release ability, UV shielding performance, and an easy manufacturing process. There is no need for expensive and special equipment to produce the desired functionality, which greatly reduces production costs and simplifies the production process.
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