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利用两亲性聚合物开发多菌灵控释纳米制剂及其对立枯丝核菌的生物药效评价

Development of controlled release nanoformulations of carbendazim employing amphiphilic polymers and their bioefficacy evaluation against Rhizoctonia solani.

作者信息

Koli Pushpendra, Singh Braj B, Shakil Najam A, Kumar Jitendra, Kamil Deeba

机构信息

a Division of Agricultural Chemicals, Indian Agricultural Research Institute , New Delhi , India.

出版信息

J Environ Sci Health B. 2015;50(9):674-81. doi: 10.1080/03601234.2015.1038961.

DOI:10.1080/03601234.2015.1038961
PMID:26079342
Abstract

Controlled release nanoformulations of carbendazim (Methyl 1H-benzimidazol-2-ylcarbamate), a systemic fungicide, have been prepared using laboratory synthesized poly(ethylene glycols) (PEGs)-based functionalized amphiphilic copolymers. The release kinetics of carbendazim from developed controlled release (CR) formulations was studied and compared with that of the commercially available 50% Wettable Powder (WP). Further, the bioefficacy evaluation of developed formulations was done against plant pathogenic fungi Rhizoctonia solani by the poison food technique method. The release of maximum amount of carbendazim from developed formulations was dependent on the molecular weight of PEGs and was found to increase with increasing molecular weights. The range of carbendazim release was found to be between 10th to 35th day as compared to commercial formulation which was up to 7th day. The diffusion exponent (n value) of carbendazim in water ranged from 0.37 to 0.52 in the tested formulations. The half-release (t1/2) values ranged between 9.47 and 24.20 days, and the period of optimum availability (POA) of carbendazim ranged from 9.15 to 26.63 days. Also, ED50 values of the developed formulations vary from 0.40 to 0.74 mg L(-1). These formulations can be used to optimize the release of carbendazim to achieve disease control for the desired period depending on the matrix of the polymer used.

摘要

多菌灵(甲基1H-苯并咪唑-2-基氨基甲酸酯)是一种内吸性杀菌剂,已使用实验室合成的基于聚乙二醇(PEG)的功能化两亲共聚物制备了其控释纳米制剂。研究了多菌灵从所开发的控释(CR)制剂中的释放动力学,并与市售50%可湿性粉剂(WP)进行了比较。此外,通过毒饵技术方法对所开发制剂针对植物病原真菌立枯丝核菌进行了生物有效性评价。多菌灵从所开发制剂中的最大释放量取决于PEG的分子量,并且发现随着分子量的增加而增加。与商业制剂在第7天之前释放相比,多菌灵的释放范围在第10天至第35天之间。在所测试的制剂中,多菌灵在水中的扩散指数(n值)范围为0.37至0.52。半衰期(t1/2)值在9.47至24.20天之间,多菌灵的最佳有效期限(POA)范围为9.15至26.63天。此外,所开发制剂的半数致死剂量(ED50)值在0.40至0.74 mg L(-1)之间变化。这些制剂可用于优化多菌灵的释放,以根据所用聚合物的基质在所需时间段内实现病害控制。

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