2016
DOI: 10.1016/j.reactfunctpolym.2016.07.006
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Synthesis and characterization of imidacloprid microspheres for controlled drug release study

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Cited by 14 publications
(10 citation statements)
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“…As shown in Figure 3, three major bands (2950-3700, 1600-1810 and 1000-1350 cm -1 ) and some fingerprint bands (500-1000 cm -1 ) appeared in the spectra of the two layers, plus a few extra bands (~1560 and 1050 cm -1 ) in the shape-memory layer. These major bands were composite due to the multi-component composition in the reactor, spectroscopically corresponding to the stretching vibration of O-H (N-H), C=O and C-N (C-C) bonds and their rotation/bending in the two layers [26,27], plus extra S=O bands [28] in the shape-memory layer. These absorption bands involved in the two layers may be ascribed to the constituent monomers (i.e., 2-acrylamido-2-methylpropane-sulfonic acid and 2-nonenoic acid in the first layer and acrylamide in the second layer) which all included O-H (N-H), C=O, and C-N (C-C) bonds.…”
Section: Results and Discussion 31 Ftir Tem Eds And Spr Analysesmentioning
confidence: 99%
“…As shown in Figure 3, three major bands (2950-3700, 1600-1810 and 1000-1350 cm -1 ) and some fingerprint bands (500-1000 cm -1 ) appeared in the spectra of the two layers, plus a few extra bands (~1560 and 1050 cm -1 ) in the shape-memory layer. These major bands were composite due to the multi-component composition in the reactor, spectroscopically corresponding to the stretching vibration of O-H (N-H), C=O and C-N (C-C) bonds and their rotation/bending in the two layers [26,27], plus extra S=O bands [28] in the shape-memory layer. These absorption bands involved in the two layers may be ascribed to the constituent monomers (i.e., 2-acrylamido-2-methylpropane-sulfonic acid and 2-nonenoic acid in the first layer and acrylamide in the second layer) which all included O-H (N-H), C=O, and C-N (C-C) bonds.…”
Section: Results and Discussion 31 Ftir Tem Eds And Spr Analysesmentioning
confidence: 99%
“…The schematic diagram of the preparation process of the proposed composite nanoparticles is shown in Figure . The composite nanoparticles were prepared using the W/O/W solvent evaporation technique. , The 24-EBL (28 mg) was dissolved in acetone (4 mL) and water (3 mL) as the internal water phase. Polymers (RS 32.5 mg/RL 7.5 mg and PHA 112.5 mg) and IMI (150 mg) were dissolved in 5 mL of dichloromethane to form a polymer solution as the oil phase.…”
Section: Methodsmentioning
confidence: 99%
“…32 The particle size distribution (Figure 2d) conforms to the normal distribution, with an average particle size of 502.03 ± 114.85 nm. Compared with IMI-controlled release formulation 11,12,20,33 and 24-EBL-controlled release formulation, 34,35 the size of the composite nanoparticles was even smaller than that of some single pesticide nanoparticles.…”
Section: Morphology and Size Distribution Of Thementioning
confidence: 96%
“…This nanoparticle can effectively improve the prognosis of pancreatic cancer by overcoming chemotherapy resistance and reducing systemic toxicity. Meanwhile, drug carriers of PPC with other modifications have also been reported, which are normally prepared by electrospinning, melt blending and emulsification and solvent evaporation [ 14 , 123 , 124 ]. An example is given in Figure 7 b. Li and co-workers fabricated PPC-loaded imidacloprid microspheres by emulsion solvent evaporation [ 14 ].…”
Section: Biomedical Applications Of Ppcmentioning
confidence: 99%
“…At present, PPC has been extensively used in food packaging [ 7 , 8 ], battery manufacturing [ 9 , 10 ], agricultural mulch films [ 11 ] and cushioning foams [ 12 ], etc. In addition, owing to its good biocompatibility and non-toxic degradation products, PPC also holds significant promise for biomedical applications, such as drug carriers [ 13 , 14 ], tissue engineering scaffolds [ 15 , 16 ] and medical dressings [ 17 ].…”
Section: Introductionmentioning
confidence: 99%