Synthesis and characterization of curcumin loaded PLA—Hyperbranched polyglycerol electrospun blend for wound dressing applications
Tài liệu tham khảo
Eming, 2007, Regulation of angiogenesis: wound healing as a model, Prog. Histochem. Cytochem., 42, 115, 10.1016/j.proghi.2007.06.001
Harper, 2014, The physiology of wound healing, Surgery, 32, 445
Kulac, 2013, The effects of topical treatment with curcumin on burn wound healing in rats, J. Mol. Histol., 44, 83, 10.1007/s10735-012-9452-9
Ammon, 1991, Pharmacology of Curcuma longa, Planta Med., 57, 1, 10.1055/s-2006-960004
Cheng, 2001, Phase I clinical trial of curcumin, a chemopreventive agent, in patients with high-risk or pre-malignant lesions, Anticancer Res., 21, 2895
Williams, 2007, Inflammatory mechanisms of diabetic complications, Curr. Diab. Rep., 7, 242, 10.1007/s11892-007-0038-y
Liang, 2008, Synthesis and anti-inflammatory activities of mono-carbonyl analogues of curcumin, Bioorg. Med. Chem. Lett., 18, 1525, 10.1016/j.bmcl.2007.12.068
Karri, 2016, Curcumin loaded chitosan nanoparticles impregnated into collagen-alginate scaffolds for diabetic wound healing, Int. J. Biol. Macromol., 10.1016/j.ijbiomac.2016.05.038
Merrell, 2009, Curcumin-loaded poly (ε-caprolactone) nanofibres: diabetic wound dressing with anti-oxidant and anti-inflammatory properties, Clin. Exp. Pharmacol. Physiol., 36, 1149, 10.1111/j.1440-1681.2009.05216.x
Ireson, 2002, Metabolism of the cancer chemopreventive agent curcumin in human and rat intestine, Cancer Epidemiol. Biomark. Prev., 11, 105
Kaminaga, 2003, Production of unnatural glucosides of curcumin with drastically enhanced water solubility by cell suspension cultures of Catharanthus roseus, FEBS Lett., 555, 311, 10.1016/S0014-5793(03)01265-1
Greiner, 2007, Electrospinning: a fascinating method for the preparation of ultrathin fibers, Angew. Chem. Int. Ed., 46, 5670, 10.1002/anie.200604646
Langer, 2004, Designing materials for biology and medicine, Nature, 428, 487, 10.1038/nature02388
Luten, 2008, Biodegradable polymers as non-viral carriers for plasmid DNA delivery, J. Control. Release, 126, 97, 10.1016/j.jconrel.2007.10.028
Li, 2002, Electrospun nanofibrous structure: a novel scaffold for tissue engineering, J. Biomed. Mater. Res., 60, 613, 10.1002/jbm.10167
Santoro, 2016, Poly (lactic acid) nanofibrous scaffolds for tissue engineering, Adv. Drug Deliv. Rev., 10.1016/j.addr.2016.04.019
Tyler, 2016, Polylactic acid (PLA) controlled delivery carriers for biomedical applications, Adv. Drug Deliv. Rev., 10.1016/j.addr.2016.06.018
Chen, 2012, Preparation and blood compatibility of electrospun PLA/curcumin composite membranes, Fibers Polym., 13, 1254, 10.1007/s12221-012-1254-x
Nguyen, 2013, Characteristics of curcumin-loaded poly (lactic acid) nanofibers for wound healing, J. Mater. Sci., 48, 7125, 10.1007/s10853-013-7527-y
Imran Ul-Haq, 2012, Influence of architecture of high molecular weight linear and branched polyglycerols on their biocompatibility and biodistribution, Biomaterials, 33, 9135, 10.1016/j.biomaterials.2012.09.007
Kainthan, 2007, In vivo biological evaluation of high molecular weight hyperbranched polyglycerols, Biomaterials, 28, 4779, 10.1016/j.biomaterials.2007.07.046
Kainthan, 2008, Hydrophobically derivatized hyperbranched polyglycerol as a human serum albumin substitute, Biomaterials, 29, 1693, 10.1016/j.biomaterials.2007.11.030
Kainthan, 2006, Biocompatibility testing of branched and linear polyglycidol, Biomacromolecules, 7, 703, 10.1021/bm0504882
Yeh, 2008, Self-assembled monothiol-terminated hyperbranched polyglycerols on a gold surface: a comparative study on the structure, morphology, and protein adsorption characteristics with linear poly (ethylene glycol) s, Langmuir, 24, 4907, 10.1021/la702867t
Vargas, 2010, Hyperbranched polyglycerol electrospun nanofibers for wound dressing applications, Acta Biomater., 6, 1069, 10.1016/j.actbio.2009.09.018
Chen, 2013, Electrospun poly (l-lactide)/poly (ε-caprolactone) blend nanofibrous scaffold: characterization and biocompatibility with human adipose-derived stem cells, PLoS One, 8
Gunn, 2010, Polyblend nanofibers for biomedical applications: perspectives and challenges, Trends Biotechnol., 28, 189, 10.1016/j.tibtech.2009.12.006
Kim, 2004, Incorporation and controlled release of a hydrophilic antibiotic using poly (lactide-co-glycolide)-based electrospun nanofibrous scaffolds, J. Control. Release, 98, 47, 10.1016/j.jconrel.2004.04.009
Taepaiboon, 2006, Drug-loaded electrospun mats of poly (vinyl alcohol) fibres and their release characteristics of four model drugs, Nanotechnology, 17, 2317, 10.1088/0957-4484/17/9/041
Wu, 2005, Immobilization of cellulase in nanofibrous PVA membranes by electrospinning, J. Membr. Sci., 250, 167, 10.1016/j.memsci.2004.10.024
Kontogiannopoulos, 2011, Electrospun fiber mats containing shikonin and derivatives with potential biomedical applications, Int. J. Pharm., 409, 216, 10.1016/j.ijpharm.2011.02.004
Pappuru, 2013, Group IV complexes containing the benzotriazole phenoxide ligand as catalysts for the ring-opening polymerization of lactides, epoxides and as precatalysts for the polymerization of ethylene, Dalton Trans., 42, 16412, 10.1039/c3dt52065j
Sunder, 1999, Controlled synthesis of hyperbranched polyglycerols by ring-opening multibranching polymerization, Macromolecules, 32, 4240, 10.1021/ma990090w
Kim, 2006, Electrospinning biomedical nanocomposite fibers of hydroxyapatite/poly (lactic acid) for bone regeneration, J. Biomed. Mater. Res. A, 79, 643, 10.1002/jbm.a.30866
Thangaraju, 2012, Fabrication of electrospun poly l-lactide and curcumin loaded poly l-lactide nanofibers for drug delivery, Fibers Polym., 13, 823, 10.1007/s12221-012-0823-3
Vaz, 2005, Design of scaffolds for blood vessel tissue engineering using a multi-layering electrospinning technique, Acta Biomater., 1, 575, 10.1016/j.actbio.2005.06.006
Benhabbour, 2008, Cell adhesion and proliferation on hydrophilic dendritically modified surfaces, Biomaterials, 29, 4177, 10.1016/j.biomaterials.2008.07.016
Liang, 2007, In vitro scratch assay: a convenient and inexpensive method for analysis of cell migration in vitro, Nat. Protoc., 2, 329, 10.1038/nprot.2007.30
Atala, 2011
Ushikusa, 1990, Pyrolysis behaviors and thermostability of polyglycerols and polyglycerol fatty acid esters, J. Jpn. Oil Chem. Soc., 39, 314, 10.5650/jos1956.39.5_314
Wang, 2013, One-pot reaction for the large-scale synthesis of hyperbranched polyglycerol-grafted Fe3O4 nanoparticles, Dalton Trans., 42, 13642, 10.1039/c3dt51532j
Hazra, 2014, Hydrophobic hydration driven self-assembly of curcumin in water: similarities to nucleation and growth under large metastability, and an analysis of water dynamics at heterogeneous surfaces, J. Chem. Phys., 141, 10.1063/1.4895539
Moghaddam, 2009, The combination effect of curcumin with different antibiotics against Staphylococcus aureus, Int. J. Green Pharm., 3, 141, 10.4103/0973-8258.54906
Packiavathy, 2014, Inhibition of biofilm development of uropathogens by curcumin–an anti-quorum sensing agent from Curcuma longa, Food Chem., 148, 453, 10.1016/j.foodchem.2012.08.002
Deng, 2014, The effect of hyperbranched polyglycerol coatings on drug delivery using degradable polymer nanoparticles, Biomaterials, 35, 6595, 10.1016/j.biomaterials.2014.04.038
Durgaprasad, 2011, Effect of a topical curcumin preparation (BIOCURCUMAX) on burn wound healing in rats, J. Pharm. Biomed. Sci., 8, 1
Bainbridge, 2013, Wound healing and the role of fibroblasts, J. Wound Care, 22
Baum, 2005, Normal cutaneous wound healing: clinical correlation with cellular and molecular events, Dermatol. Surg., 31, 674, 10.1097/00042728-200506000-00011
Mohanty, 2012, Sustained wound healing activity of curcumin loaded oleic acid based polymeric bandage in a rat model, Mol. Pharm., 9, 2801, 10.1021/mp300075u
Sidhu, 1999, Curcumin enhances wound healing in streptozotocin induced diabetic rats and genetically diabetic mice, Wound Repair Regen., 7, 362, 10.1046/j.1524-475X.1999.00362.x
Scharstuhl, 2009, Curcumin-induced fibroblast apoptosis and in vitro wound contraction are regulated by antioxidants and heme oxygenase: implications for scar formation, J. Cell. Mol. Med., 13, 712, 10.1111/j.1582-4934.2008.00339.x
