曹盼盼, 路常宽. 绿盲蝽交配干扰剂丁酸己酯微囊的制备及田间防治效果[J]. 农药学学报, 2015, 17(4): 492-496. DOI: 10.3969/j.issn.1008-7303.2015.04.17
    引用本文: 曹盼盼, 路常宽. 绿盲蝽交配干扰剂丁酸己酯微囊的制备及田间防治效果[J]. 农药学学报, 2015, 17(4): 492-496. DOI: 10.3969/j.issn.1008-7303.2015.04.17
    Cao Panpan, Lu Changkuan. Preparation and field efficacy of mating interference hexyls butyrate microcapsules of Apolygus lucorum[J]. Chinese Journal of Pesticide Science, 2015, 17(4): 492-496. DOI: 10.3969/j.issn.1008-7303.2015.04.17
    Citation: Cao Panpan, Lu Changkuan. Preparation and field efficacy of mating interference hexyls butyrate microcapsules of Apolygus lucorum[J]. Chinese Journal of Pesticide Science, 2015, 17(4): 492-496. DOI: 10.3969/j.issn.1008-7303.2015.04.17

    绿盲蝽交配干扰剂丁酸己酯微囊的制备及田间防治效果

    Preparation and field efficacy of mating interference hexyls butyrate microcapsules of Apolygus lucorum

    • 摘要: 以乙基纤维素为壁材,丁酸己酯为芯材,采用相分离法制备了绿盲蝽Apolygus lucorum交配干扰剂丁酸己酯微囊。通过正交试验研究了乳化剂700#、聚乙烯醇、乙酸乙酯及控释剂正十二烷4个因素对丁酸己酯微囊形成的影响,得到最佳制备工艺条件。利用生物显微镜对微囊的形态进行了观察,同时测定了在最优条件下制备的丁酸己酯微囊的载药量、包封率和释放速率等指标,并进行了田间药效试验。结果表明:在乙基纤维素3.0 g、丁酸己酯3.0 g、乳化剂700# 1.5 g、聚乙烯醇2.0 g、乙酸乙酯30 mL和正十二烷2.0 g,以及滴加速率为5 mL/min、转速为1 000 r/min条件下制备的丁酸己酯微囊的载药量和包封率分别为21.5%和91.9%,外观较完整,粒径分布较均匀,平均粒径约为301.85 μ m,缓释效果较好(能持续释放35 d以上)。田间试验结果显示,调查期间悬挂丁酸己酯微囊的样区诱捕到绿盲蝽224头,与对照区相比少442头,表明丁酸己酯微囊对绿盲蝽交配具有干扰作用,可明显减少绿盲蝽繁殖的数量。

       

      Abstract: Mating interference hexyls butyrate microcapsules were prepared by phase separating, and ethyl cellulose was used as the shell material. The influence of the dosage of polyvinyl alcohol, the dosage of emulsifiers, the amounts of ethyl acetate and the quantities of release controlling agent n-dodecane was studied through orthogonal tests to obtain the optimum process. The morphology of microcapsules was scanned by biological microscope and the indexes of microcapsules, such as the drug loadings, the covering rate and the release rate, were determined. Finally, the field efficacy of the mating interference microcapsules was determined. The results showed that optimum preparation conditions were as follows: ethyl cellulose 3.0 g, hexyls butyrate 3.0 g, emulsifier 700# 1.5 g, polyvinyl alcohol 2.0 g, ethyl acetate 30 mL and n-dodecane 2.0 g. The drug loading and encapsulation rate of microcapsules prepared under the optimal conditions were 21.5% and 91.9%, respectively. The microcapsules had smooth appearance, uniform distribution of particle sizes and the average particle size was about 301.85 μ m. The releasing property was good and the release time was more than 35 days. The trapping of A.lucorum in control areas(666)was greater than the areas where placed with hexyls butyrate microcapsules(224). Hexyls butyrate microcapsules could interfere with the mating and then reduced the number of A.lucorum.

       

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