Modification of montmorillonite by ball-milling method for immobilization and delivery of acetamiprid based on alginate/exfoliated montmorillonite nanocomposite

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• 作者：Huiqiong Yan ; Xiuqiong Chen ; Yuhong Feng ; Fei Xiang ; Jiacheng Li…
• 关键词：Montmorillonite ; Sodium alginate ; Ball ; milling ; Acetamiprid ; Composite beads ; Sustained release
• 刊名：Polymer Bulletin
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：73
• 期：4
• 页码：1185-1206
• 全文大小：1,947 KB
• 参考文献：1.Sopena F, Cavrera A, Maqueda C (2007) Ethylcellulose formulations for controlled release of the herbicide alachlor in a sandy soil. J Agric Food Chem 55:8200–8205CrossRef
  2.Dailey J (2004) Volatilization of alachlor from polymeric formulations. J Agric Food Chem 52:6742–6746CrossRef
  3.Shi H, Zhao G, Liu M, Cao TC (2013) Aptamer-based colorimetric sensing of acetamiprid in soil samples: sensitivity, selectivity and mechanism. J Hazard Mater 260:754–761CrossRef
  4.Li S, Ma X, Jiang Y, Cao X (2014) Acetamiprid removal in waste water by the low-temperature plasma using dielectric barrier discharge. Ecotox Environ Safe 106:146–153CrossRef
  5.Patel ZS, Yamamoto M, Ueda H, Tabata Y, Mikos AG (2008) Biodegradable gelatin microparticles as delivery systems for the controlled release of bone morphogenetic protein-2. Acta Biomater 4(5):1126–1138CrossRef
  6.Dong ZF, Wang Q, Du Y (2006) Alginate/gelatin blend films and their properties for drug controlled release. J Membr Sci 280(1–2):37–44CrossRef
  7.Zhou XF, Liu B, Yu XH, Zha X, Zhang XZ, Chen Y, Wang XY, Jin YH, Wu YJ, Chen Y, Shan YM, Liu JQ, Kong W, Shen JC (2007) Controlled release of PEI/DNA complexes from mannose-bearing chitosan microspheres as a potent delivery system to enhance immune response to HBV DNA vaccine. J Control Release 121(3):200–207CrossRef
  8.Zhang JP, Shan JH, Fan ZM, Yao KD (2011) Preparation and properties of gelatin-chitosan/montmorillonite drug-loaded microspheres. J Wuhan Univ Technol 26(4):628–633CrossRef
  9.Carr MW, Wing RE, Doane WM (1991) Encapsulation of atrazine within a starch matrix by extrusion processing. Cereal Chem 68:262–266
  10.Darvari R, Hasirci V (1996) Pesticide and model drug release from carboxymethyl cellulose microspheres. J Microencapsul 13:9–24CrossRef
  11.Fernandez-Perez M, Gonzalez-Pradas E, Urena-Amate MD, Wilkins RM, Lindup I (1998) Controlled release of imidacloprid from a lignin matrix: water release kinetics and soil mobility study. J Agric Food Chem 46:3828–3834CrossRef
  12.Connick WJ, Bradow JH, Wells W, Steward KK, Van TK (1984) Preparation and evaluation of controlled release formulations of 2,6-dichlorobenzonitrile. J Agric Food Chem 32:1199–1205CrossRef
  13.Pepperman AB, Kuan JW (1993) Slow release formulations of metribuzin based on alginate-kaolin-linseed oil. J Control Release 26:21–30CrossRef
  14.Johnson RM, Pepperman AB (1996) Leaching of alachlor from alginate-encapsulated controlled-release formulations. Pestic Sci 48:157–164CrossRef
  15.Fernandez-Perez M, Villafranca-Sanchez M, Gonzalez-Pradas E, Martınez-Lopez F, Flores-Cespedes F (2000) Controlled release of carbofuran from an alginate–bentonite formulation: water release kinetics and soil mobility. J Agric Food Chem 48:938–943CrossRef
  16.Dong SY (2011) A dual-responsive supramolecular polymer gel formed by crown ether based molecular recognition. Angew Chem Int Edit 123:1945–1949CrossRef
  17.Zohuriaan-Mehr MJ, Pourjavadi A (2003) New polysaccharide-g-polyacrylonitrile copolymers: synthesis and thermal characterization. Polym Adv Technol 14:508–516CrossRef
  18.Yeom CK, Lee KH (1998) Characterization of sodium alginate and poly(vinyl alcohol) blend membranes in pervaporation separation. J Appl Polym Sci 67:949–959CrossRef
  19.Kumbar SG, Aminabhavi TM (2002) Preparation and characterization of interpenetrating network beads of poly(vinyl alcohol)-grafted-poly(acrylamide) with sodium alginate and their controlled release characteristics for cypermethrin pesticide. J Appl Polym Sci 84:552–560CrossRef
  20.Fernández-Pérez M, Flores-Céspedes F, González-Pradas E, Villafranca-Sánchez M, Pérez-García S, Garrido-Herrera FJ (2004) Use of activated bentonites in controlled-release formulations of atrazine. J Agric Food Chem 52:3888–3893CrossRef
  21.Salcedo I, Aguzzi C, Sandri G, Bonferoni MC, Mori M, Cerezo P, Sánchez R, Viseras C, Caramella C (2012) In vitro biocompatibility and mucoadhesion of montmorillonite chitosan nanocomposite: a new drug delivery. Appl Clay Sci 55:131–137CrossRef
  22.Cornejo L, Celis R, Domínguez C, Hermosin MC, Cornejo J (2008) Use of modified montmorillonites to reduce herbicide leaching in sports turf surfaces: laboratory and field experiments. Appl Clay Sci 42:284–291CrossRef
  23.Celis R, Trigo C, Facenda G, Hermosin M, Cornejo J (2007) Selective modification of clay minerals for the adsorption of herbicides widely used in olive groves. J Agric Food Chem 55:6650–6658CrossRef
  24.Cruz-Guzman M, Celis R, Hermosin MC, Koskinen WC, Cornejo J (2005) Adsorption of pesticides from water by functionalized organobentonites. J Agric Food Chem 53:7502–7511CrossRef
  25.Aguzzi C, Capra P, Bonferoni C, Cerezo P, Salcedo I, Sánchez R, Caramella C, Viseras C (2010) Chitosan silicate bionanonanocomposites for colonic delivery of 5-aminosalicylic acid (5-ASA). Appl Clay Sci 50:106–111CrossRef
  26.Chevillard A, Angellier-Coussy H, Guillard V, Gontard N, Gastaldi E (2012) Controlling pesticide release via structuring agropolymer and nanoclays based material. J Hazard Mater 205–206:32–39CrossRef
  27.Zhou LM, Chen H, Jiang XH, Lu F, Zhou YF, Yin WM, Ji XY (2009) Modification of montmorillonite surfaces using a novel class of cationic gemini surfactants. J Colloid Interf Sci 332:16–21CrossRef
  28.Ray SS, Okamoto M (2013) Polymer/layered silicate nanocomposites: a review from preparation to processing. Prog Polym Sci 28:1539–1641
  29.Iliescu RI, Andronescu E, Ghitulica CD, Voicua G, Ficai A, Hoteteu M (2014) Montmorillonite-alginate nanocomposite as a drug delivery system-incorporation and in vitro release of irinotecan. Int J Pharm 463:184–192CrossRef
  30.Jarek F, Reis DM, Mauler RS, Barbosa RV, Kloss JR (2011) Characterization of natural and modified clays to the development of polymeric nanocomposites. Macromol Symp 299(300):124–131CrossRef
  31.Sorrentino A, Tortora M, Vittoria V (2006) Diffusion behavior in polymer–clay nanocomposites. J Polym Sci Pol Phys 44:265–274CrossRef
  32.Choudalakis G, Gotsis AD (2009) Permeability of polymer/clay nanocomposites: a review. Eur Polym J 45:967–984CrossRef
  33.Yan H, Chen X, Wu T, Feng Y, Wang C, Li J, Lin Q (2014) Mechanochemical modification of kaolin surfaces for immobilization and delivery of pesticides in alginate–chitosan composite beads. Polym Bull 71:2923–2944CrossRef
  34.Barret EP, Joyner LG, Halenda PP (1951) The determination of pore volume and area distributions in porous substances. I. Computations from nitrogen isotherms. J Am Chem Soc 73:373–380CrossRef
  35.Rinaudo M (2006) Chitin and chitosan: properties and applications. Prog Polym Sci 31:603–632CrossRef
  36.Zhang WY, Lu LB, Cheng Y, Xu N, Pan LS, Lin Q, Wang YY (2011) Clean and rapid synthesis of double metal cyanide complexes using mechanochemistry. Green Chem 13:2701–2703CrossRef
  37.Bhattacharyya KG, Gupta SS (2008) Adsorption of a few heavy metals on natural and modified kaolinite and montmorillonite: a review. Adv Colloid Interfac 140:114–131CrossRef
  38.Joshia GV, Kevadiya BD, Patel HA, Bajaj HC, Jasra RV (2009) Montmorillonite as a drug delivery system: intercalation and in vitro release of timolol maleate. Int J Pharm 374:53–57CrossRef
  39.Singh B, Sharma DK, Gupta A (2009) Controlled release of the fungicide thiram from starch–alginate–clay based formulation. Appl Clay Sci 45:76–82CrossRef
  40.Galimberti M, Coombs M, Cipolletti V, Spatola A, Guerra G, Lostritto A, Giannini L, Pandini S, Riccò T (2014) Delaminated and intercalated organically modified montmorillonite in poly(1,4-cis-isoprene) matrix. Indications of counterintuitive dynamic-mechanical behavior. Appl Clay Sci 97–98:8–16CrossRef
  41.Gao M, Zhu PX (2012) A starch/milled-montmorillonite nanocomposite for warp sizing. Starch Starke 64:97–104CrossRef
  42.Sánchez-Soto PJ, Jiménez de Haro MC, Pérez-Maqueda LA, Pérez-Rodríguez IVJ (2000) Effects of dry grinding on the structural changes of kaolinite powders. J Am Ceram Soc 83:1649–1657CrossRef
  43.Yi CL, Yang YQ, Zhu Y, Liu N, Liu XY, Luo J, Jiang M (2012) Self-assembly and Emulsification of poly{[styrene-alt-maleic acid]-co-[styrene-alt-(N-3,4-dihydroxy phenylethyl-maleamic acid)]}. Langmuir 28:9211–9222CrossRef
  44.Sing KSW, Everett DH, Haul RAW, Moscou L, Pierotti RA, Rouquerol J, Siemieniewska T (1985) Reporting physisorption data for gas/solid systems with special reference to the determination of surface area and porosity. Pure Appl Chem 57:603–619CrossRef
  45.Kuroda Y, Ito K, Itabashi K, Kuroda K (2011) One-step exfoliation of kaolinites and their transformation into nanoscrolls. Langmuir 27(5):2028–2035CrossRef
  46.Hua S, Ma H, Li X, Yang H, Wang A (2010) pH-sensitive sodium alginate/poly(vinyl alcohol) hydrogel beads prepared by combined Ca2+ crosslinking and freeze-thawing cycles for controlled release of diclofenac sodium. Int J Biol Macromol 46:517–523CrossRef
  47.Ghaemi N, Madaeni SS, Alizadeh A, Rajabi H, Daraei P (2011) Preparation, characterization and performance of polyethersulfone/organically modified montmorillonite nanocomposite membranes in removal of pesticides. J Membr Sci 382:135–147CrossRef
  48.Ito E, Yip KW, Katz D, Fonseca SB, Hediey DW, Chow S, Xu GW, Wood TE, Bastianutto C, Schimmer AD, Kelley SO, Liu FF (2009) Potential use of cetrimonium bromide as an apoptosis-promoting anticancer agent for head and neck cancer. Mol Pharmacol 76:969–983CrossRef
  49.Onyido I, ShaAto R, Nnamonu LA (2012) Environmentally friendly formulations of trifluralin based on alginate modified starch. J Environ Prot Ecol 3:1085–1093CrossRef
  50.Talukder R, Fassihi R (2004) Gastroretentive delivery systems: hollow beads. Drug Dev Ind Pharm 30(4):405–412CrossRef
  51.Pongjanyakul T, Suksri H (2009) Alginate-magnesium aluminium silicate films for buccal delivery of nicotine. Colloid Surface B 74(1):103–113CrossRef
  52.Kevadiya BD, Joshi GV, Mody HM, Bajaj HC (2011) Biopolymer–clay hydrogel composites as drug carrier: host–guest intercalation and in vitro release study of lidocaine hydrochloride. Appl Clay Sci 52:364–367CrossRef
  53.Kevadiya BD, Joshi GV, Patel HA, Ingole PG, Mody HM, Bajaj HC (2010) Montmorillonite-alginate nanocomposites as a drug delivery system: intercalation and in vitro release of vitamin B1 and vitamin B6. J Biomater Appl 25(2):161–177CrossRef
  54.Kevadiya BD, Joshi GV, Bajaj HC (2010) Layered bio-nanocomposites as carrier for procainamide. Int J Pharm 388(1):280–286CrossRef
  55.Ritger PL, Peppas NA (1987) A simple equation for description solute release. J Control Release 5:23–36CrossRef
  
• 作者单位：Huiqiong Yan (1)
  Xiuqiong Chen (1)
  Yuhong Feng (2)
  Fei Xiang (2)
  Jiacheng Li (2)
  Zaifeng Shi (1)
  Xianghui Wang (1)
  Qiang Lin (1)
  
  1. College of Chemistry and Chemical Engineering, Hainan Normal University, 571100, Haikou, Hainan, People’s Republic of China
  2. Key Laboratory of Ministry of Education for Application Technology of Chemical Materials in Hainan Superior Resources, College of Materials and Chemical Engineering, Hainan University, 570228, Haikou, People’s Republic of China
  
• 刊物类别：Chemistry and Materials Science
• 刊物主题：Chemistry
  Polymer Sciences
  Characterization and Evaluation Materials
  Soft Matter and Complex Fluids
  Physical Chemistry
  
• 出版者：Springer Berlin / Heidelberg
• ISSN：1436-2449

文摘

The objective of this study was to develop a sustained drug release system based on alginate/exfoliated montmorillonite nanocomposite for acetamiprid, a neonicotinoid insecticide, to improve its sustained release performance. Montmorillonite (MMT) was modified with cetyl trimethyl ammonium bromide (CTAB) using a ball-milling method. Then, acetamiprid was immobilized into the modified MMT layers through freeze-drying technology. Subsequently, the drug-loaded alginate-exfoliated MMT composite beads were prepared by dropwise addition of the mixture of the drug-loaded modified MMT and the alginate solution into the calcium chloride and chitosan blended solutions. The structure and surface morphology of the modified MMT and composite materials were determined by the means of Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS), BET-specific surface area measurements, thermogravimetric analysis (TGA) and scanning electron microscopy (SEM) analysis. The experiments on immobilization and release of acetamiprid were performed to examine the effect of the modified MMT on the properties of the composite beads. Experimental results showed the intercalation of CTAB into MMT has been successfully achieved during the ball-milling process, which was beneficial to the formation of exfoliated MMT nanocomposites in alginate matrix. The intensive force supplied during the superfine pulverization of the ball-milling process was effective to increase the modified MMT’s specific surface areas and decrease its particle size, consequently improving the drug-loading rate (DL) and encapsulation efficiency (EE) of the composite beads. The alginate/exfoliated MMT nanocomposite formulation exhibited a slow and sustained release property, which was demonstrated as a promising carrier material to promote the efficient use of organic pesticide, and thereby reduce environmental pollution.