| Literature DB >> 34199739 |
Marco Chaud1,2, Eliana B Souto3,4, Aleksandra Zielinska5, Patricia Severino6, Fernando Batain1, Jose Oliveira-Junior2,7, Thais Alves1.
Abstract
Nanopesticides are nanostructures with two to three dimensions between 1 to 200 nm, used to carry agrochemical ingredients (AcI). Because of their unique properties, the loading of AcI into nanoparticles offers benefits when compared to free pesticides. However, with the fast development of new engineered nanoparticles for pests' control, a new type of environmental waste is being produced. This paper describes the nanopesticides sources, the harmful environmental and health effects arising from pesticide exposure. The potential ameliorative impact of nanoparticles on agricultural productivity and ecosystem challenges are extensively discussed. Strategies for controlled release and stimuli-responsive systems for slow, sustained, and targeted AcI and genetic material delivery are reported. Special attention to different nanoparticles source, the environmental behavior of nanopesticides in the crop setting, and the most recent advancements and nanopesticides representative research from experimental results are revised. This review also addresses some issues and concerns in developing, formulating and toxicity pesticide products for environmentally friendly and sustainable agriculture.Entities:
Keywords: agricultural productivity; agrochemical ingredients; controlled release; environmental risk; nanopesticides; pesticides; stimuli-responsive nanoparticles; toxicological risk
Year: 2021 PMID: 34199739 PMCID: PMC8230079 DOI: 10.3390/toxics9060131
Source DB: PubMed Journal: Toxics ISSN: 2305-6304
Chemical and physical systems as carrier agents in nanopesticides formulation.
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| Hybrid materials | (CNT-g-PCA) | Zineb | [ |
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| Peptide-polymer | Trypsin-PEG | Modulating oostatic factor | [ |
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| Hallow sphere | Calcium-alginate | Cypermethrin | [ |
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| Polyelectrolyte complex | Clay-gelatine | MCPA | [ |
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| Metallic nanoparticles | Cu—TM | Thiophanate methyl | [ |
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| Coprecipitation | Polyelectrolytic interaction. | Trichlorfon | [ |
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| Mixed micelles | mPEG13–b–PLGA5–3 | Pyrethrin | [ |
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| Hybrid materials | mPEG-PLGA | Metolachlor | [ |
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| Grafted-NP. | 4-ethylortho-Silicate ATP-biochar colloidal silica | Benzoylurea-Fe2O3 Glyphosate | [ |
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| Polymeric emulsion | Poly(alkylene-oxide] alkanol | Glyphosate acid | [ |
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| Polymeric coating | Cellulose ester/ PEG/Inorganic salt | Diazinon | [ |
ATP (attapulgite); CNT-g-PCA (carbon nanotube-polycaprolactone); mPEG13–b–PLGA5–3 (monomethoxy (polyethylene glycol)13-poly(D, L-Lactide-co-glycolide); NP (nanoparticle); MCPA (4-chloro-2-methylphenoxy-acetic acid); PC (phosphatidyl choline) PEG (polyethylene-glycol); pGPMA (guanidine-propyl methacrylamide polymers); PLGA (poly-lactic-glycolic acid); dsRNA (double-stranded RNA).
Innovative nanomaterials for stimuli-responsive release.
| Mechanism/Nanomaterials | Pros Effect | Cons Effect | Refs. |
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| Continuously release, utilization efficiency | Slow insect toxicity non-target | [ |
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| Safe | High costs | [ |
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| Controlled release, reducing the loss, increased efficiency, biosensor, fast action, high availability | Random control | [ |
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| Biosensor; water uptake | Rise of ROS and cell death | [ |
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| Decrease bacterial resistance | Non-target | [ |
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| Increase bioavailability decrease leaching/drift. Catalytic reduction. Biosensor | Low environmental stability | [ |
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| Multifunctional. Overcome multidrug resistance | Low chemical stability | [ |
Figure 1Schematic illustration of light-responsive system for modified pesticide release.
Figure 2Schematic illustration for dual stimuli-responsive and diffusion release profile.
Figure 3Schematic illustration of self-assembly reaction between cationic copolymer and dsRNA (double-stranded RNA) to prepare a cationic polyplex system as pesticide reservoir pH-sensitive.
Figure 4Schematic illustration of the sol-gel interaction pH-responsive and anchoring the 3-(triethoxysilyl) propane-1-Amine (3-TEP-1A) molecule on the inner pore surface of the modified mesoporous silica nanoparticles (MSN).
Figure 5Structural form and composition of the micelle, nanoemulsion droplet and liposome formulations. The tail of the surfactant forms the hydrophobic core of the micelle. Nanoemulsion water-in-oil stabilized by surfactant surround lipid core. Liposome lipid bilayer and aqueous core.
Figure 6Structural form of Pickering emulsion and release mechanisms passive and stimuli-responsive.