Synthesis and Properties of Inulin Based Microgels
Source abstract
Abstract
Cross-linked inulin (X-inulin) microparticles were synthesized in reverse micelles using water-in-oil microemulsion polymerization. Linear inulin was crosslinked with divinyl sulfone (DVS) in a sodium bis(2-ethylhexyl) sulfosuccinate (AOT) inverse microemulsion under basic conditions. These particles were demonstrated to be excellent scaffolds for the in situ synthesis of CdS quantum dots (Q-dots). The inulin-based particles were shown to be non-cytotoxic in fibroblast cell culture, and degradable under acidic and basic conditions. Furthermore, gallic acid and caffeine were used as model drugs for loading and release studies from these particles, illustrating their potential as drug carriers with controlled release.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Mesoporous Materials and Catalysis · Quantum Dots Synthesis And Properties · Microbial Metabolites in Food Biotechnology
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (27)
Show source-provided references
1. Castelli · Eur. J. Pharm. Sci. · 2008 · 35 · 7610.1016/j.ejps.2008.06.005 ↗
2. Naskar · Carbohydr. Polym. · 2010 · 81 · 70010.1016/j.carbpol.2010.03.041 ↗
3. Meyer · Food Hydrocolloids · 2011 · 25 · 188110.1016/j.foodhyd.2011.04.012 ↗
4. Greg · Altern. Med. Rev. · 2008 · 13 · 315
5. Nguyen · Appl. Biochem. Biotechnol. · 2009 · 158 · 35210.1007/s12010-009-8596-x ↗
6. Matusek · Eur. Food Res. Technol. · 2009 · 228 · 35510.1007/s00217-008-0941-8 ↗
7. Luo · Adv. Biomed. Eng. · 2011 · 59
8. Muramatsu · J. Biomed. Mater. Res. A · 2004 · 71A · 63510.1002/jbm.a.30197 ↗
9. Wan · J. Biomed. Mater. Res. A · 2007 · 80A · 77610.1002/jbm.a.31025 ↗
10. Link · J. Biomed. Mater. Res. A · 2009 · 90A · 37210.1002/jbm.a.32091 ↗
11. Lee · J. Biomed. Mater. Res. A · 2006 · 76A · 53010.1002/jbm.a.30434 ↗
12. Labhasetwar · Adv. Drug Deliv. Rev. · 1997 · 24 · 6310.1016/S0169-409X(96)00483-8 ↗
13. Sahiner · Mater. Sci. Eng. C · 2014 · 40 · 33610.1016/j.msec.2014.04.028 ↗
14. Sagbas · Carbohydr. Polym. · 2012 · 87 · 271810.1016/j.carbpol.2011.11.064 ↗
15. Mosmann · J. Immunol. Methods · 1983 · 65 · 5510.1016/0022-1759(83)90303-4 ↗
16. Pankove · 1976
17. Božič · Carbohydr. Polym. · 2012 · 87 · 238810.1016/j.carbpol.2011.11.006 ↗
18. Ji · Bioorg. Med. Chem. Lett. · 2006 · 16 · 409510.1016/j.bmcl.2006.04.096 ↗
19. Jung · Meat Sci. · 2010 · 86 · 52010.1016/j.meatsci.2010.06.007 ↗
20. Yen · Food Chem. · 2002 · 79 · 30710.1016/S0308-8146(02)00145-0 ↗
21. Gil-Longo · J. Nutr. Biochem. · 2010 · 21 · 30410.1016/j.jnutbio.2009.01.003 ↗
22. Mahoney · Pharmacol. Biochem. Behav. · 2011 · 99 · 5910.1016/j.pbb.2011.03.024 ↗
23. Tomczak · Prog. Polym. Sci. · 2009 · 34 · 39310.1016/j.progpolymsci.2008.11.004 ↗
24. Sahiner · Prog. Polym. Sci. · 2013 · 38 · 132910.1016/j.progpolymsci.2013.06.004 ↗
25. Boudine · Opt. Mater. · 2004 · 25 · 37310.1016/j.optmat.2003.09.005 ↗
26. Lippens · Phys. Rev. B · 1989 · 15 · 1093510.1103/PhysRevB.39.10935 ↗
27. Colloids Surf