首页> 外文期刊>Journal of Environmental Science and Health. Part B >Eco-friendly PEG-based controlled release nano-formulations of Mancozeb: Synthesis and bioefficacy evaluation against phytopathogenic fungi Alternaria solani and Sclerotium rolfsii
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Eco-friendly PEG-based controlled release nano-formulations of Mancozeb: Synthesis and bioefficacy evaluation against phytopathogenic fungi Alternaria solani and Sclerotium rolfsii

机译:基于生态友好的PEG的Mancozeb控释纳米制剂:对抗植物病原真菌Solnaria solani和Sclerotium rolfsii的合成和生物功效评估

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摘要

Controlled release (CR) nano-formulations of Mancozeb (manganese-zinc double salt of N,N-bisdithiocarbamic acid), a protective fungicide, have been prepared using laboratory-synthesized poly (ethylene glycols) (PEGs)-based functionalized amphiphilic copolymers without using any surfactants or external additives. The release kinetics of the developed Mancozeb CR formulations were studied and compared with that of commercially available 42% suspension concentrate and 75% wettable powder. Maximum amount of Mancozeb was released on 42nd day for PEG-600 and octyl chain, PEG-1000 and octyl chain, and PEG-600 and hexadecyl chain, on 35th day for PEG-1000 and hexadecyl chain, on 28th day for PEG-1500 and octyl chain, PEG-2000 and octyl chain, PEG-1500 and hexadecyl chain, and PEG-2000 and hexadecyl chain in comparison to both commercial formulations (15th day). The diffusion exponent (n value) of Mancozeb in water ranged from 0.42 to 0.62 in tested formulations. The half-release (t_(1/2)) values ranged from 1735 to 35.14 days, and the period of optimum availability of Mancozeb ranged from 18.54 to 35.42 days. Further, the in vitro bioefficacy evaluation of developed formulations was done ' against plant pathogenic fungi Altemaria solani and Sclerotium rolfsii by poison food technique. Effective dose for 50% inhibition in mgL~(-1) (Ep_(50)) values of developed formulations varied from 1.31 to 2.79 mg L~(-1) for A sotani, and 1.60 to 3.14 mg L~(-1) for S. rolfsii. The present methodology is simple, economical, and eco-friendly for the development of environment-friendly CR formulations of Mancozeb. These formulations can be used to optimize the release of Mancozeb to achieve disease control for the desired period depending upon the matrix of the polymer used. Importantly, the maximum amount of active ingredient remains available for a reasonable period after application. In addition, the developed CR formulations were found to be suitable for fungicidal applications, allowing use of Mancozeb in lower doses.
机译:使用实验室合成的基于聚乙二醇(PEG)的功能性两亲共聚物制备了Mancozeb(N,N-双二硫代氨基甲酸的锰锌复盐)(一种保护性杀菌剂)的控释(CR)纳米制剂。使用任何表面活性剂或外部添加剂。研究了开发的Mancozeb CR配方的释放动力学,并将其与市售的42%悬浮剂和75%可湿性粉剂进行了比较。 PEG-600和辛基链,PEG-1000和辛基链以及PEG-600和十六烷基链的第42天释放出最大的Mancozeb,PEG-1000和十六烷基链的第35天释放出,PEG-1500的28天释放出最大量与两种市售制剂相比(第15天),它们分别是辛基链,PEG-2000和辛基链,PEG-1500和十六烷基链以及PEG-2000和十六烷基链。在测试制剂中,Mancozeb在水中的扩散指数(n值)为0.42至0.62。半释放(t_(1/2))值的范围从1735天到35.14天,Mancozeb的最佳可得时间范围从18.54天到35.42天。此外,通过有毒食品技术对植物病原性真菌Altemaria solani和Sclerotium rolfsii进行了开发制剂的体外生物功效评价。所开发制剂的mgL〜(-1)(Ep_(50))值对50%抑制的有效剂量,对于Sotani而言在1.31至2.79 mg L〜(-1)之间,而在1.60至3.14 mg L〜(-1)之间变化罗非鱼。本方法简单,经济且对环境友好,可用于开发Mancozeb的环保CR配方。这些制剂可用于优化Mancozeb的释放,以根据所用聚合物的基质在所需时期内控制疾病。重要的是,在施用后的一段合理时间内,仍可保持最大量的活性成分。此外,已发现开发的CR制剂适用于杀真菌应用,允许以较低的剂量使用Mancozeb。

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