The use of native chemical functional groups presented by wound beds for the covalent attachment of polymeric microcarriers of bioactive factors

Biomaterials

Volumn 34, Issue 2, 2013, Pages 340-352

  Jain, Rishabh ^a   Agarwal, Ankit ^a   Kierski, Patricia R ^b   Schurr, Michael J ^c   Murphy, Christopher J ^d,e   McAnulty, Jonathan F ^b   Abbott, Nicholas L ^a  

^a University of Wisconsin Madison   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

^c UNIVERSITY OF COLORADO   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Diabetic wounds; Dopamine; Maleimide; Microspheres; Raman spectroscopy; Wound healing

Indexed keywords

AMINE GROUPS; ANTI-MICROBIAL AGENT; BIOACTIVE FACTOR; CELL BEHAVIORS; CELLULAR BEHAVIORS; CHEMICAL FUNCTIONAL GROUPS; COVALENT ATTACHMENT; COVALENT BOND FORMATION; DIABETIC MICE; DIABETIC WOUNDS; DOPAMINE; EX-VIVO; GROWTH FACTOR; MALEIMIDES; MICROBEADS; MICROCARRIERS; NON-COVALENT INTERACTION; POLY LACTIC-CO-GLYCOLIC ACID; RAMAN MICROSPECTROSCOPY; SULFHYDRYL; SULFHYDRYL GROUPS; TEMPORAL CONTROLS; TOPOGRAPHICAL CUES; VERSATILE METHODS; WILD TYPES; WOUND CLOSURE; WOUND HEALING;

CHEMICAL BONDS; COPOLYMERS; FUNCTIONAL GROUPS; MAMMALS; MICROSPHERES; PHENOLS; POLYMERS; POLYSTYRENES; RAMAN SPECTROSCOPY; SEDIMENTATION; SURFACE CHEMISTRY;

BIOACTIVITY;

CATECHOL; MALEIMIDE; POLYGLACTIN; POLYSTYRENE; THIOL DERIVATIVE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; COVALENT BOND; DERMIS; DIABETES MELLITUS; EPIDERMIS; EX VIVO STUDY; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; RAMAN SPECTROMETRY; WOUND CLOSURE; WOUND HEALING; WOUND HEALING IMPAIRMENT; ZETA POTENTIAL;

ANIMALS; CATECHOLS; DERMIS; DIABETES MELLITUS, EXPERIMENTAL; DRUG CARRIERS; LACTIC ACID; MALE; MALEIMIDES; MICE; MICROSPHERES; POLYGLYCOLIC ACID; POLYSTYRENES; SPECTRUM ANALYSIS, RAMAN; SWINE; WOUND HEALING;

MUS; SUS;

EID: 84868203325     PISSN: 01429612     EISSN: 18785905     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2012.09.055     Document Type: Article

References (66)

1. Sweitzer S.M., Fann S.A., Borg T.K., Baynes J.W., Yost M.J. What is the future of diabetic wound care?. Diabetes Educator 2006, 32:197-210.
2. Werner S., Grose R. Regulation of wound healing by growth factors and cytokines. Physiol Rev 2003, 83:835-870.
3. Biggs M.J.P., Richards R.G., Dalby M.J. Nanotopographical modification: a regulator of cellular function through focal adhesions. Nanomed Nanotechnol 2010, 6:619-633.
4. Liliensiek S.J., Wood J.A., Yong J.A., Auerbach R., Nealey P.F., Murphy C.J. Modulation of human vascular endothelial cell behaviors by nanotopographic cues. Biomaterials 2010, 31:5418-5426.
5. Pot S.A., Liliensiek S.J., Myrna K.E., Bentley E., Jester J.V., Nealey P.F., et al. Nanoscale topography-induced modulation of fundamental cell behaviors of rabbit corneal keratocytes, fibroblasts, and myofibroblasts. Invest Ophthalmol Vis Sci 2010, 51:1373-1381.
6. Hinz B. The myofibroblast: paradigm for a mechanically active cell. J Biomech 2010, 43:146-155.
7. Chien S., Li S., Shiu Y.T., Li Y.S. Molecular basis of mechanical modulation of endothelial cell migration. Front Biosci 2005, 10:1985-2000.
8. Baker E.L., Zaman M.H. The biomechanical integrin. J Biomech 2010, 43:38-44.
9. Senet P., Vicaut E., Beneton N., Debure C., Lok C., Chosidow O. Topical treatment of hypertensive leg ulcers with platelet-derived growth factor-BB: a randomized controlled trial. Arch Dermatol 2011, 147:926-930.
10. Landsman A., Agnew P., Parish L., Joseph R., Galiano R.D. Diabetic foot ulcers treated with becaplermin and theragauze a moisture-controlling smart dressing: a randomized, multicenter, prospective analysis. J Am Podiat Med Assoc 2010, 100:155-160.
11. Bello Y.M., Phillips T.J. Recent advances in wound healing. J Am Med Assoc 2000, 283:716-718.
12. Schultz G.S., Sibbald R.G., Falanga V., Ayello E.A., Dowsett C., Harding K., et al. Wound bed preparation: a systematic approach to wound management. Wound Repair Regen 2003, 11:S1-S28.
13. Falanga V., Grinnell F., Gilchrest B., Maddox Y.T., Moshell A. Workshop on the pathogenesis of chronic wounds. J Invest Dermatol 1994, 102:125-127.
14. Dworniczek E., Nawrot U., Seniuk A., Wlodarczyk K., Bialynicki-Birula R. The in vitro Effect of a silver-containing dressing on biofilm development. Adv Clin Exp Med 2009, 18:277-281.
15. Mooney E.K., Lippitt C., Friedman J. Plastic Surg Ed Fdn DC. Silver dressings. Plast Reconstr Surg 2006, 117:666-669.
16. Atiyeh B.S., Costagliola M., Hayek S.N., Dibo S.A. Effect of silver on burn wound infection control and healing: review of the literature. Burns 2007, 33:139-148.
17. Dunn K., Edwards-Jones V. The role of Acticoat (TM) with nanocrystalline silver in the management of burns. Burns 2004, 30:S1-S9.
18. Lee K., Silva E.A., Mooney D.J. Growth factor delivery-based tissue engineering: general approaches and a review of recent developments. J Roy Soc Interface 2011, 8:153-170.
19. Richardson T.P., Peters M.C., Ennett A.B., Mooney D.J. Polymeric system for dual growth factor delivery. Nat Biotechnol 2001, 19:1029-1034.
20. Jaklenec A., Hinckfuss A., Bilgen B., Ciombor D.M., Aaron R., Mathiowitz E. Sequential release of bioactive IGF-I and TGF-beta(1) from PLGA microsphere-based scaffolds. Biomaterials 2008, 29:1518-1525.
21. DeFail A.J., Chu C.R., Izzo N., Marra K.G. Controlled release of bioactive TGF-beta(1) from microspheres embedded within biodegradable hydrogels. Biomaterials 2006, 27:1579-1585.
22. Chen F.M., Zhao Y.M., Sun H.H., Jin T., Wang Q.T., Zhou W., et al. Novel glycidyl methacrylated dextran (Dex-GMA)/gelatin hydrogel scaffolds containing microspheres loaded with bone morphogenetic proteins: formulation and characteristics. J Control Release 2007, 118:65-77.
23. Schmidt C.E., Dai J.W., Lauffenburger D.A., Sheetz M.P., Horwitz A.F. Integrin-cytoskeletal interactions in neuronal growth cones. J Neurosci 1995, 15:3400-3407.
24. Saperia D., Glassberg E., Lyons R.F., Abergel R.P., Baneux P., Castel J.C., et al. Demonstration of elevated type-I and type-III procollagen messenger-RNA levels in cutaneous wounds treated with Helium-Neon laser - proposed mechanism for enhanced wound-healing. Biochem Biophys Res Commun 1986, 138:1123-1128.
25. Ashcroft G.S., Kielty C.M., Horan M.A., Ferguson M.W.J. Age-related changes in the temporal and spatial distributions of fibrillin and elastin mRNAs and proteins in acute cutaneous wounds of healthy humans. J Pathol 1997, 183:80-89.
26. Grinnell F., Billingham R.E., Burgess L. Distribution of fibronectin during wound-healing in vivo. J Invest Dermatol 1981, 76:181-189.
27. Nguyen B.P., Ryan M.C., Gil S.G., Carter W.G. Deposition of laminin 5 in epidermal wounds regulates integrin signaling and adhesion. Curr Opin Cell Biol 2000, 12:554-562.
28. Houghton A.M., Mouded M., Shapiro S.D. Consequences of elastolysis. Extracellular matrix degradation 2011, 217-249. Springer-Verlag Inc., Berlin. W.C. Parks, R.P. Mecham (Eds.).
29. Prockop D.J., Kivirikko K.I. Collagens - molecular-biology, diseases, and potentials for therapy. Ann Rev Biochem 1995, 64:403-434.
30. Puccinelli T.J., Bertics P.J., Masters K.S. Regulation of keratinocyte signaling and function via changes in epidermal growth factor presentation. Acta Biomater 2010, 6:3415-3425.
31. Stefonek-Puccinelli T.J., Masters K.S. Co-immobilization of gradient-patterned growth factors for directed cell migration. Ann Biomed Eng 2008, 36:2121-2133.
32. Ashcroft G.S., Yang X., Glick A.B., Weinstein M., Letterio J.J., Mizel D.E., et al. Mice lacking Smad3 show accelerated wound healing and an impaired local inflammatory response. Nat Cell Biol 1999, 1:260-266.
33. Greenhalgh D.G., Sprugel K.H., Murray M.J., Ross R. PDGF and FGF stimulate wound-healing in the genetically diabetic mouse. Am J Pathol 1990, 136:1235-1246.
34. Sullivan T.P., Eaglstein W.H., Davis S.C., Mertz P. The pig as a model for human wound healing. Wound Repair Regen 2001, 9:66-76.
35. Reisner L.A., Cao A., Pandya A.K. An integrated software system for processing, analyzing, and classifying Raman spectra. Chemometr Intell Lab 2011, 105:83-90.
36. Guthrie K.M., Agarwal A., Tackes D.S., Johnson K.W., Abbott N.L., Murphy C.J., et al. Antibacterial efficacy of silver-impregnated polyelectrolyte multilayers immobilized on a biological dressing in a murine wound infection model. Ann Surg 2012, 256(2):371-377.
37. Lee H., Dellatore S.M., Miller W.M., Messersmith P.B. Mussel-inspired surface chemistry for multifunctional coatings. Science 2007, 318:426-430.
38. Lee H., Rho J., Messersmith P.B. Facile conjugation of biomolecules onto surfaces via mussel adhesive protein inspired coatings. Adv Mater 2009, 21:431-434.
39. Lee H., Lee B.P., Messersmith P.B. A reversible wet/dry adhesive inspired by mussels and geckos. Nature 2007, 448:338-344.
40. Gademann K., Kobylinska J., Wach J.Y., Woods T.M. Surface modifications based on the cyanobacterial siderophore anachelin: from structure to functional biomaterials design. Biometals 2009, 22:595-604.
41. Waite J.H. Surface chemistry - mussel power. Nat Mater 2008, 7:8-9.
42. Schweigert N., Zehnder A.J.B., Eggen R.I.L. Chemical properties of catechols and their molecular modes of toxic action in cells, from microorganisms to mammals. Environ Microbiol 2001, 3:81-91.
43. Land E.J., Ramsden C.A., Riley P.A. Quinone chemistry and melanogenesis. Quinones and quinone enzymes, Pt A 2004, Academic Press Inc, San Diego, pp. 88-109.
44. Stefonek T.J., Masters K.S. Immobilized gradients of epidermal growth factor promote accelerated and directed keratinocyte migration. Wound Repair Regen 2007, 15:847-855.
45. Wu C.W., Yarbrough L.R., Wu F.Y.H. N-(1-pyrene)maleimide - fluorescent cross-linking reagent. Biochemistry-US 1976, 15:2863-2868.
46. Yoshitake S., Yamada Y., Ishikawa E., Masseyeff R. Conjugation of glucose-oxidase from Aspergillus-niger and rabbit antibodies using N-hydroxysuccinimide ester of N-(4-carboxycyclohexylmethyl)-maleimide. Eur J Biochem 1979, 101:395-399.
47. Hermanson G.T. The chemistry of reactive groups. Bioconjugate techniques 2008, Academic Press, London, UK, pp. 183-4. 2nd ed.
48. Valko M., Leibfritz D., Moncol J., Cronin M.T.D., Mazur M., Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell B 2007, 39:44-84.
49. Sen C.K. Redox signaling and the emerging therapeutic potential of thiol antioxidants. Biochem Pharmacol 1998, 55:1747-1758.
50. Caspers P.J., Lucassen G.W., Wolthuis R., Bruining H.A., Puppels G.J. In vitro and in vivo Raman spectroscopy of human skin. Biospectroscopy 1998, 4:S31-S39.
51. Greve T.M., Andersen K.B., Nielsen O.F. ATR-FTIR, FT-NIR and near-FT-Raman spectroscopic studies of molecular composition in human skin in vivo and pig ear skin in vitro. Spectrosc Int J 2008, 22:437-457.
52. Krafft C. Vibrational spectroscopic imaging of soft tissue. Infrared and Raman spectroscopic imaging 2009, 113-147. Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany. R. Salzer, H.W. Siesler (Eds.).
53. Barry B.W., Edwards H.G.M., Williams A.C. Fourier-transform Raman and infrared vibrational study of human skin - assignment of spectral bands. J Raman Spectrosc 1992, 23:641-645.
54. Naito S., Min Y.K., Sugata K., Osanai O., Kitahara T., Hiruma H., et al. In vivo measurement of human dermis by 1064 nm-excited fiber Raman spectroscopy. Skin Res Technol 2008, 14:18-25.
55. Edwards H. Spectra-structure correlations in Raman spectroscopy. Handbook of vibrational spectroscopy 2002, 1838-1871. John Wiley and Sons. J. Chalmers, P. Griffiths (Eds.).
56. Gniadecka M., Nielsen O.F., Christensen D.H., Wulf H.C. Structure of water, proteins, and lipids in intact human skin, hair, and nail. J Invest Dermatol 1998, 110:393-398.
57. Baraga J.J., Feld M.S., Rava R.P. Insitu optical histochemistry of human artery using near-infrared Fourier-transform Raman-spectroscopy. Proc Natl Acad Sci USA 1992, 89:3473-3477.
58. Frushour B.G., Koenig J.L. Raman-scattering of collagen, gelatin, and elastin. Biopolymers 1975, 14:379-391.
59. Debelle L., Alix A.J.P., Jacob M.P., Huvenne J.P., Berjot M., Sombret B., et al. Bovine elastin and kappa-elastin secondary structure determination by optical spectroscopies. J Biol Chem 1995, 270:26099-26103.
60. Crane N.J., Brown T.S., Evans K.N., Hawksworth J.S., Hussey S., Tadaki D.K., et al. Monitoring the healing of combat wounds using Raman spectroscopic mapping. Wound Repair Regen 2010, 18:409-416.
61. McKittrick P.T., Katon J.E. Infrared and Raman group frequencies of cyclic imides. Appl Spectrosc 1990, 44:812-817.
62. Coleman D.L. Diabetes-obesity syndromes in mice. Diabetes 1982, 31:1-6.
63. Brownlee M. Advanced protein glycosylation in diabetes and aging. Annu Rev Med 1995, 46:223-234.
64. Werner S., Breeden M., Hubner G., Greenhalgh D.G., Longaker M.T. Induction of keratinocyte growth-factor expression is reduced and delayed during wound-healing in the genetically diabetic mouse. J Invest Dermatol 1994, 103:469-473.
65. Uehara Y., Fisher J.M., Rabinovitz M. Showdomycin and its reactive moiety, maleimide - a comparison in selective toxicity and mechanism of action in vitro. Biochem Pharmacol 1980, 29:2199-2204.
66. Galiano R.D., Michaels J., Dobryansky M., Levine J.P., Gurtner G.C. Quantitative and reproducible murine model of excisional wound healing. Wound Repair Regen 2004, 12:485-492.