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Development of controlled release formulations of imidacloprid employing novel nano-ranged amphiphilic polymers

机译:使用新型纳米级两亲性聚合物开发吡虫啉控释制剂

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Amphiphilic copolymers, synthesized from poly (ethylene glycols) and various aliphatic diacids, which self assemble into nano-micellar aggregates in aqueous media, were used to develop controlled release (CR) formulations of imidacloprid [l-(6 chloro-3-pyridinyl methyl)-N- nitro imidazolidin-2- ylideneamine] using encapsulation technique. High solubilisation power and low critical micelle concentration (CMC) of these amphiphilic polymers may increase the efficacy of formulations. Formulations were characterised by Infrared (IR) spectroscopy, Dynamic Light Scattering (DLS) and Transmission Electron Microscope (TEM). Encapsulation efficiency, loading capacity and stability after accelerated storage test of the developed formulations were checked. The kinetics of imidacloprid release in water from the different formulations was studied. Release from the commercial formulation was faster than the CR formulations. The diffusion exponent (n value) of imidacloprid, in water ranged from 0.22 to 0.37 in the tested formulations. While the time taken for release of 50 % of imidacloprid ranged from 2.32 to 9.31 days for the CR formulations. The developed CR formulations can be used for efficient pest management in different crops.
机译:由聚乙二醇和各种脂肪族二酸合成的两亲共聚物,可在水性介质中自组装成纳米胶束聚集体,用于开发吡虫啉[1-(6氯-3-吡啶基甲基)的控释(CR)配方。 )-N-硝基咪唑烷基-2-亚苄基胺]采用包封技术。这些两亲性聚合物的高溶解能力和低临界胶束浓度(CMC)可能会提高制剂的功效。通过红外(IR)光谱,动态光散射(DLS)和透射电子显微镜(TEM)表征制剂。在开发的制剂的加速储存测试后,检查了包封效率,负载能力和稳定性。研究了吡虫啉在不同配方水中的释放动力学。从商业制剂中释放比CR制剂更快。在测试制剂中吡虫啉在水中的扩散指数(n值)为0.22至0.37。对于CR制剂,释放50%吡虫啉所需的时间为2.32至9.31天。研发的CR配方可用于不同作物的有效害虫管理。

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