References
- Sharma, S. K.; Shukla, S. K.; Vaid, D. N. Shellac-Structure, Characteristics & Modification. Def. Sci. J. 1983, 33, 261–271. DOI: https://doi.org/10.14429/dsj.33.6181.
- Ghoshal, S.; Khan, M. A.; Khan, R. A.; Gul-E-Noor, F.; Sarwaruddin Chowdhury, A. M. Study on the Thermo-Mechanical and Biodegradable Properties of Shellac Films Grafted with Acrylic Monomers by Gamma Radiation. J. Polym. Environ. 2010, 18, 216–223. DOI: https://doi.org/10.1007/s10924-010-0182-3.
- Farag, Y.; Leopold, C. S. Physicochemical Properties of Various Shellac Types. Dissolution Technol. 2009, 16, 33–39. [Database] DOI: https://doi.org/10.14227/DT160209P33.
- Kapote, D. N.; Wagner, K. G. Shellac– A Natural Carrier for Colon Targeting of Indomethacin Using Hot Melt Extrusion. Drug Dev. Ind. Pharm. 2021, 47, 748–757. DOI: https://doi.org/10.1080/03639045.2021.1934863.
- Li, K.; Pan, Z.; Guan, C.; Zheng, H.; Li, K.; Zhang, H. A Tough Self-Assembled Natural Oligomer Hydrogel Based on Nano-Size Vesicle Cohesion. RSC Adv. 2016, 6, 33547–33553. DOI: https://doi.org/10.1039/C6RA03720H.
- Kong, L.; Chen, R.; Wang, X.; Zhao, C. X.; Chen, Q.; Hai, M.; Chen, D.; Yang, Z.; Weitz, D. A. Controlled Co-Precipitation of Biocompatible Colorant-Loaded Nanoparticles by Microfluidics for Natural Color Drinks. Lab Chip. 2019, 19, 2089–2095. DOI: https://doi.org/10.1039/c9lc00240e.
- Yuan, Y.; He, N.; Xue, Q.; Guo, Q.; Dong, L.; Haruna, M. H.; Zhang, X.; Li, B.; Li, L. Shellac: A Promising Natural Polymer in the Food Industry. Trends Food Sci. Technol. 2021, 109, 139–153. DOI: https://doi.org/10.1016/j.tifs.2021.01.031.
- Bar, H.; Bianco-Peled, H. The Unique Nanostructure of Shellac Films. Prog. Org. Coat. 2021, 157, 106328. DOI: https://doi.org/10.1016/j.porgcoat.2021.106328.
- Ma, J.; Zhou, Z.; Li, K.; Li, K.; Liu, L.; Zhang, W.; Xu, J.; Tu, X.; Du, L.; Zhang, H. Novel Edible Coating Based on Shellac and Tannic Acid for Prolonging Postharvest Shelf Life and Improving Overall Quality of Mango. Food Chem. 2021, 354, 129510 DOI: https://doi.org/10.1016/j.foodchem.2021.129510.
- Wang, A.; Lin, J.; Zhong, Q. Enteric Rice Protein-Shellac Composite Coating to Enhance the Viability of Probiotic Lactobacillus salivarius NRRL B-30514. Food Hydrocoll. 2021, 113, 106469. DOI: https://doi.org/10.1016/j.foodhyd.2020.106469.
- Ono, K.; Sakai, H.; Tokunaga, S.; Sharmin, T.; Aida, T. M.; Mishima, K. Encapsulation of Lactoferrin for Sustained Release Using Particles from Gas-Saturated Solutions. Processes. 2020, 9, 73. DOI: https://doi.org/10.3390/pr9010073.
- Huang, X.; Gänzle, M.; Zhang, H.; Zhao, M.; Fang, Y.; Nishinari, K. Microencapsulation of Probiotic Lactobacilli with Shellac as Moisture Barrier and to Allow Controlled Release. J. Sci. Food Agric. 2021, 101, 726–734. DOI: https://doi.org/10.1002/jsfa.10685.
- Kraisit, P.; Limmatvapirat, S.; Nunthanid, J.; Sriamornsak, P.; Luangtana-Anan, M. Nanoparticle Formation by Using Shellac and Chitosan for a Protein Delivery System. Pharm. Dev. Technol. 2013, 18, 686–693. DOI: https://doi.org/10.3109/10837450.2012.685657.
- Sun, C.; Xu, C.; Mao, L.; Wang, D.; Yang, J.; Gao, Y. Preparation, Characterization and Stability of Curcumin-Loaded Zein-Shellac Composite Colloidal Particles. Food Chem. 2017, 228, 656–667. DOI: https://doi.org/10.1016/j.foodchem.2017.02.001.
- Sedaghat, D. A.; Muhammad, D. R. A.; Stevens, C. V.; Dewettinck, K.; Van der Meeren, P. Fabrication and Characterization of Quercetin Loaded Almond Gum-Shellac Nanoparticles Prepared by Antisolvent Precipitation. Food Hydrocoll. 2018, 83, 190–201. DOI: https://doi.org/10.1016/j.foodhyd.2018.04.050.
- Chen, S.; Xu, C.; Mao, L.; Liu, F.; Sun, C.; Dai, L.; Gao, Y. Fabrication and Characterization of Binary Composite Nanoparticles between Zein and Shellac by Anti-Solvent Co-Precipitation. Food Bioprod. Process. 2018, 107, 88–96. DOI: https://doi.org/10.1016/j.fbp.2017.11.003.
- Sedaghat Doost, A.; Kassozi, V.; Grootaert, C.; Claeys, M.; Dewettinck, K.; Van Camp, J.; Van der Meeren, P. Self-Assembly, Functionality, and In-Vitro Properties of Quercetin Loaded Nanoparticles Based on Shellac-Almond Gum Biological Macromolecules. Int. J. Biol. Macromol. 2019, 129, 1024–1033. DOI: https://doi.org/10.1016/j.ijbiomac.2019.02.071.
- Prawatborisut, M.; Seidi, F.; Yiamsawas, D.; Crespy, D. Pegylation of Shellac-Based Nanocarriers for Enhanced Colloidal Stability. Colloids Surf B Biointerf. 2019, 183, 110434. DOI: https://doi.org/10.1016/j.colsurfb.2019.110434.
- Yuan, Y.; Zhang, X.; Pan, Z.; Xue, Q.; Wu, Y.; Li, Y.; Li, B.; Li, L. Improving the Properties of Chitosan Films by Incorporating Shellac Nanoparticles. Food Hydrocoll. 2021, 110, 106164. DOI: https://doi.org/10.1016/j.foodhyd.2020.106164.
- Muhammad, D. R. A.; Sedaghat Doost, A.; Gupta, V.; bin Sintang, M. D.; Van de Walle, D.; Van der Meeren, P.; Dewettinck, K. Stability and Functionality of Xanthan Gum–Shellac Nanoparticles for the Encapsulation of Cinnamon Bark Extract. Food Hydrocoll. 2020, 100, 105377. DOI: https://doi.org/10.1016/j.foodhyd.2019.105377.
- Baby, T.; Liu, Y.; Yang, G.; Chen, D.; Zhao, C. X. Microfluidic Synthesis of Curcumin Loaded Polymer Nanoparticles with Tunable Drug Loading and pH-Triggered Release. J. Colloid Interface Sci. 2021, 594, 474–484. DOI: https://doi.org/10.1016/j.jcis.2021.03.035.
- Barik, A.; Patnaik, T.; Parhi, P.; Swain, S. K.; Dey, R. K. Synthesis and Characterization of New Shellac–Hydroxypropylmethylcellulose Composite for Pharmaceutical Applications. Polym. Bull. 2017, 74, 3467–3485. DOI: https://doi.org/10.1007/s00289-017-1903-8.
- Dey, R. K.; Tiwary, G. S.; Patnaik, T.; Jha, U. Shellac-Polyamidoamine: Design of a New Polymeric Carrier Material for Controlled Release Application. J. Appl. Polym. Sci. 2012, 125, 2626–2635. DOI: https://doi.org/10.1002/app.36411.
- Limmatvapirat, S.; Panchapornpon, D.; Limmatvapirat, C.; Nunthanid, J.; Luangtana-Anan, M.; Puttipipatkhachorn, S. Formation of Shellac Succinate Having Improved Enteric Film Properties through Dry Media Reaction. Eur. J. Pharm. Biopharm. 2008, 70, 335–344. DOI: https://doi.org/10.1016/j.ejpb.2008.03.002.
- Panchapornpon, D.; Limmatvapirat, C.; Luangtana-Anan, M.; Nunthanid, J.; Sriamornsak, P.; Limmatvapirat, S. Fabrication of Thermally Stabilized Shellac through Solid State Reaction with Phthalic Anhydride. Mater. Lett 2011, 65, 1241–1244. DOI: https://doi.org/10.1016/j.matlet.2011.01.068.
- Bar, H.; Bianco-Peled, H. Modification of Shellac Coating Using Jeffamine® for Enhanced Mechanical Properties and Stability. Prog. Org. Coat. 2020, 141, 105559. DOI: https://doi.org/10.1016/j.porgcoat.2020.105559.
- Wang, J.; Chen, L.; He, Y. Preparation of Environmental Friendly Coatings Based on Natural Shellac Modified by Diamine and Its Applications for Copper Protection. Prog. Org. Coat. 2008, 62, 307–312. DOI: https://doi.org/10.1016/j.porgcoat.2008.01.006.
- Weththimuni, M. L.; Milanese, C.; Licchelli, M.; Malagodi, M. Improving the Protective Properties of Shellac-Based Varnishes by Functionalized Nanoparticles. Coatings. 2021, 11, 419. DOI: https://doi.org/10.3390/coatings11040419.
- Walkey, C. D.; Olsen, J. B.; Guo, H.; Emili, A.; Chan, W. C. W. Nanoparticle Size and Surface Chemistry Determine Serum Protein Adsorption and Macrophage Uptake. J. Am. Chem. Soc. 2012, 134, 2139–2147. DOI: https://doi.org/10.1021/ja2084338.
- Schöttler, S.; Becker, G.; Winzen, S.; Steinbach, T.; Mohr, K.; Landfester, K.; Mailänder, V.; Wurm, F. R. Protein Adsorption is Required for Stealth Effect of Poly(Ethylene Glycol)- and Poly(Phosphoester)-Coated Nanocarriers. Nat. Nanotechnol. 2016, 11, 372–377. DOI: https://doi.org/10.1038/nnano.2015.330.
- Bertrand, N.; Grenier, P.; Mahmoudi, M.; Lima, E. M.; Appel, E. A.; Dormont, F.; Lim, J. M.; Karnik, R.; Langer, R.; Farokhzad, O. C. Mechanistic Understanding of In Vivo Protein Corona Formation on Polymeric Nanoparticles and Impact on Pharmacokinetics. Nat. Commun. 2017, 8, 777 DOI: https://doi.org/10.1038/s41467-017-00600-w.
- Miceli, E.; Kuropka, B.; Rosenauer, C.; Blanco, E. R. O.; Theune, L. E.; Kar, M.; Weise, C.; Morsbach, S.; Freund, C.; Calderón, M. Understanding the Elusive Protein Corona of Thermoresponsive Nanogels. Nanomedicine (Lond). 2018, 13, 2657–2667. DOI: https://doi.org/10.2217/nnm-2018-0217.
- Zhang, Y.; Cai, J.; Li, C.; Wei, J.; Liu, Z.; Xue, W. Effects of Thermosensitive Poly(N-Isopropylacrylamide) on Blood Coagulation. J. Mater. Chem. B. 2016, 4, 3733–3749. DOI: https://doi.org/10.1039/c6tb00823b.
- Nagase, K.; Yamato, M.; Kanazawa, H.; Okano, T. Poly(N-Isopropylacrylamide)-Based Thermoresponsive Surfaces Provide New Types of Biomedical Applications. Biomaterials. 2018, 153, 27–48. DOI: https://doi.org/10.1016/j.biomaterials.2017.10.026.
- Prawatborisut, M.; Jiang, S.; Oberländer, J.; Mailänder, V.; Crespy, D.; Landfester, K. Modulating Protein Corona and Materials–Cell Interactions with Temperature‐Responsive Materials. Adv. Funct. Materials. 2021, 2106353. DOI: https://doi.org/10.1002/adfm.202106353.
- Jeon, S. I.; Lee, J. H.; Andrade, J. D.; De Gennes, P. G. Protein—Surface Interactions in the Presence of Polyethylene Oxide: I. Simplified Theory. J. Colloid Interface Sci. 1991, 142, 149–158. DOI: https://doi.org/10.1016/0021-9797(91)90043-8.
- Satulovsky, J.; Carignano, M. A.; Szleifer, I. Kinetic and Thermodynamic Control of Protein Adsorption. Proc. Natl. Acad. Sci. U S A. 2000, 97, 9037–9041. DOI: https://doi.org/10.1073/pnas.150236197.
- Yang, S. T.; Liu, Y.; Wang, Y. W.; Cao, A. Biosafety and Bioapplication of Nanomaterials by Designing Protein-Nanoparticle Interactions. Small 2013, 9, 1635–1653. DOI: https://doi.org/10.1002/smll.201201492.
- Sun, G.; Lin, X.; Wang, Z.; Feng, Y.; Xu, D.; Shen, L. Pegylated Inulin as Long-Circulating Pharmaceutical Carrier. J. Biomater. Sci. Polym. Ed. 2011, 22, 429–441. DOI: https://doi.org/10.1163/092050610X487729.
- Lin, X.; Wang, S.; Jiang, Y.; Wang, Z. J.; Sun, G. L.; Xu, D. S.; Feng, Y.; Shen, L. Poly(Ethylene Glycol)-Radix Ophiopogonis Polysaccharide Conjugates: Preparation, Characterization, Pharmacokinetics and In Vitro Bioactivity. Eur. J. Pharm. Biopharm. 2010, 76, 230–237. DOI: https://doi.org/10.1016/j.ejpb.2010.07.003.
- Huh, K. M.; Ooya, T.; Lee, W. K.; Sasaki, S.; Kwon, I. C.; Jeong, S. Y.; Yui, N. Supramolecular-Structured Hydrogels Showing a Reversible Phase Transition by Inclusion Complexation between Poly(Ethylene Glycol) Grafted Dextran and a-Cyclodextrin. Macromolecules 2001, 34, 8657–8662. DOI: https://doi.org/10.1021/ma0106649..
- Vacondio, F.; Bassi, M.; Silva, C.; Castelli, R.; Carmi, C.; Scalvini, L.; Lodola, A.; Vivo, V.; Flammini, L.; Barocelli, E.; et al. Amino Acid Derivatives as Palmitoylethanolamide Prodrugs: Synthesis, In Vitro Metabolism and In Vivo Plasma Profile in Rats. PLoS One. 2015, 10, e0128699 DOI: https://doi.org/10.1371/journal.pone.0128699.
- Kulkarni, A. S.; Tapase, S. R.; Kodam, K. M.; Shinde, V. S. Thermoresponsive Pluronic Based Microgels for Controlled Release of Curcumin against Breast Cancer Cell Line. Colloids Surf B Biointerfaces 2021, 205, 111834 DOI: https://doi.org/10.1016/j.colsurfb.2021.111834.
- Coessens, V.; Schacht, E. H.; Domurado, D. Synthesis and In Vitro Stability of Macromolecular Prodrugs of Norfloxacin. J. Control. Release 1997, 47, 283–291. DOI: https://doi.org/10.1016/S0168-3659(97)01655-6.
- Vázquez, G.; Alvarez, E.; Navaza, J. M. Surface Tension of Alcohol Water + Water from 20 to 50 Oc. J. Chem. Eng. Data 1995, 40, 611–614. DOI: https://doi.org/10.1021/je00019a016.
- Agency for Toxic Substances and Disease Registry (ATSDR). Toxicological profile for nitrophenols: 2-nitrophenol, 4-nitrophenol; U.S. Department of Health and Human Services, Public Health Service: Atlanta, GA, 1992; p 104.
- Won, C.-Y. Synthesis of Heterobifunctional Poly(Ethylene Glycol)Containing an Acryloyl Group at One End and Anisocyanate Group at the Other End. Polym. Bull 2004, 52, 109–115. DOI: https://doi.org/10.1007/s00289-004-0264-2.
- Ragelle, H.; Riva, R.; Vandermeulen, G.; Naeye, B.; Pourcelle, V.; Le Duff, C. S.; D'Haese, C.; Nysten, B.; Braeckmans, K.; De Smedt, S. C.; et al. Chitosan Nanoparticles for SiRNA Delivery: Optimizing Formulation to Increase Stability and Efficiency. J. Control. Release 2014, 176, 54–63. DOI: https://doi.org/10.1016/j.jconrel.2013.12.026.
- Kang, B.; Okwieka, P.; Schöttler, S.; Winzen, S.; Langhanki, J.; Mohr, K.; Opatz, T.; Mäilander, V.; Landfester, K.; Wurm, F. R. Carbohydrate-Based Nanocarriers Exhibiting Specific Cell Targeting with Minimum Influence from the Protein Corona. Angew. Chem. Int. Ed. Engl. 2015, 54, 7436–7440. DOI: https://doi.org/10.1002/anie.201502398.
- Mai, C.; Elder, T. Wood: Chemically Modified. In Reference Module in Materials Science and Materials Engineering; Elsevier: 2016; pp 1–6. DOI: https://doi.org/10.1016/B978-0-12-803581-8.03537-2.
- Tamburini, D.; Dyer, J.; Bonaduce, I. Bonaduce, I. The Characterisation of Shellac Resin by Flow Injection and Liquid Chromatography Coupled with Electrospray Ionisation and Mass Spectrometry. Sci. Rep. 2017, 7, 14784 DOI: https://doi.org/10.1038/s41598-017-14907-7.
- Kanamaru, M.; Takata, T.; Endo, T. A Novel Polymerization of Bis(N-Acyl Isocyanate)s and Dicarboxylic Acids-Synthesis of Poly(N-Acylamide)s. Macromolecules 1995, 28, 7979–7982. DOI: https://doi.org/10.1021/ma00128a002.
- Fan, L.; Chen, H.; Hao, Z.; Tan, Z. Cellulose-Based Macroinitiator for Crosslinked Poly(Butyl Methacrylate-co-Pentaerythritol Triacrylate) Oil-Absorbing Materials by SET-LRP. J. Polym. Sci. A Polym. Chem. 2013, 51, 457–462. DOI: https://doi.org/10.1002/pola.26404.
- Wang, Z.; Zhang, Y.; Jiang, F.; Fang, H.; Wang, Z. Synthesis and Characterization of Designed Cellulose-graft-Polyisoprene Copolymers. Polym. Chem. 2014, 5, 3379–3388. DOI: https://doi.org/10.1039/c3py01574b.
- Kapishon, V.; Whitney, R. A.; Champagne, P.; Cunningham, M. F.; Neufeld, R. J. Polymerization Induced Self-Assembly of Alginate Based Amphiphilic Graft Copolymers Synthesized by Single Electron Transfer Living Radical Polymerization. Biomacromolecules 2015, 16, 2040–2048. DOI: https://doi.org/10.1021/acs.biomac.5b00470.
- El Tahlawy, K.; Hudson, S. M. Synthesis of a Well-Defined Chitosan Graft Poly(Methoxy Polyethyleneglycol Methacrylate) by Atom Transfer Radical Polymerization. J. Appl. Polym. Sci. 2003, 89, 901–912. DOI: https://doi.org/10.1002/app.12001.
- Kim, Y. S.; Kadla, J. F. Preparation of a Thermoresponsive Lignin-Based Biomaterial through Atom Transfer Radical Polymerization. Biomacromolecules 2010, 11, 981–988. DOI: https://doi.org/10.1021/bm901455p.
- Kim, D. J.; Heo, J.; Kim, K. S.; Choi, I. S. Formation of Thermoresponsive Poly(N-Isopropylacrylamide)/Dextran Particles by Atom Transfer Radical Polymerization. Macromol. Rapid Commun. 2003, 24, 517–521. DOI: https://doi.org/10.1002/marc.200390076.
- Lindqvist, J.; Nyström, D.; Östmark, E.; Antoni, P.; Carlmark, A.; Johansson, M.; Hult, A.; Malmström, E. Intelligent Dual-Responsive Cellulose Surfaces via Surface-Initiated ATRP. Biomacromolecules 2008, 9, 2139–2145. DOI: https://doi.org/10.1021/bm800193n.
- Alosmanov, R.; Wolski, K.; Zapotoczny, S. Grafting of Thermosensitive Poly(N-Isopropylacrylamide) from Wet Bacterial Cellulose Sheets to Improve Its Swelling-Drying Ability. Cellulose 2017, 24, 285–293. DOI: https://doi.org/10.1007/s10570-016-1120-x.
- Wang, L.; Wu, Y.; Men, Y.; Shen, J.; Liu, Z. Thermal-Sensitive Starch-g-Pnipam Prepared by Cu(0) Catalyzed SET-LRP at Molecular Level. RSC Adv. 2015, 5, 70758–70765. DOI: https://doi.org/10.1039/C5RA14765D.
- Seeliger, F.; Matyjaszewski, K. Temperature Effect on Activation Rate Constants in ATRP: New Mechanistic Insights into the Activation Process. Macromolecules 2009, 42, 6050–6055. DOI: https://doi.org/10.1021/ma9010507.
- Liu, Y.; Klep, V.; Zdyrko, B.; Luzinov, I. Polymer Grafting via ATRP Initiated from Macroinitiator Synthesized on Surface. Langmuir. 2004, 20, 6710–6718. DOI: https://doi.org/10.1021/la049465j.
- Wang, L.; Shen, J.; Men, Y.; Wu, Y.; Peng, Q.; Wang, X.; Yang, R.; Mahmood, K.; Liu, Z. Corn Starch-Based Graft Copolymers Prepared via ATRP at the Molecular Level. Polym. Chem. 2015, 6, 3480–3488. DOI: https://doi.org/10.1039/C5PY00184F.
- Lee, L.-T.; Cabane, B. Effects of Surfactants on Thermally Collapsed Poly(N-Isopropylacrylamide) Macromolecules. Macromolecules 1997, 30, 6559–6566. DOI: https://doi.org/10.1021/ma9704469.
- Zhang, Q.; Weber, C.; Schubert, U. S.; Hoogenboom, R. Thermoresponsive Polymers with Lower Critical Solution Temperature: From Fundamental Aspects and Measuring Techniques to Recommended Turbidimetry Conditions. Mater. Horiz. 2017, 4, 109–116. DOI: https://doi.org/10.1039/C7MH00016B.
- Boutris, C.; Chatzi, E. G.; Kiparissides, C. Characterization of the LCST Behaviour of Aqueous Poly(N-Isopropylacrylamide) Solutions by Thermal and Cloud Point Techniques. Polymer 1997, 38, 2567–2570. DOI: https://doi.org/10.1016/S0032-3861(97)01024-0.
- Docter, D.; Distler, U.; Storck, W.; Kuharev, J.; Wünsch, D.; Hahlbrock, A.; Knauer, S. K.; Tenzer, S.; Stauber, R. H. Quantitative Profiling of the Protein Coronas That Form around Nanoparticles. Nat. Protoc. 2014, 9, 2030–2044. DOI: https://doi.org/10.1038/nprot.2014.139.
- Partikel, K.; Korte, R.; Mulac, D.; Humpf, H. U.; Langer, K. Serum Type and Concentration Both Affect the Protein-Corona Composition of PLGA Nanoparticles. Beilstein J Nanotechnol. 2019, 10, 1002–1015. DOI: https://doi.org/10.3762/bjnano.10.101.
- Zheng, X.; Baker, H.; Hancock, W. S.; Fawaz, F.; McCaman, M.; Pungor, E. Proteomic Analysis for the Assessment of Different Lots of Fetal Bovine Serum as a Raw Material for Cell Culture. Part IV. Application of Proteomics to the Manufacture of Biological Drugs. Biotechnol. Prog. 2006, 22, 1294–1300. DOI: https://doi.org/10.1021/bp060121o.