Scaffolds for Drug Delivery in Tissue Engineering

DOI:

https://doi.org/10.37285/ijpsn.2008.1.2.1

Authors

  • Vikas V. Gaikwad
  • Abasaheb B. Patil
  • Madhuri V. Gaikwad

Abstract

Scaffolds are used for drug delivery in tissue engineering as this system is a highly porous structure to allow tissue growth.  Although several tissues in the body can regenerate, other tissue such as heart muscles and nerves lack regeneration in adults. However, these can be regenerated by supplying the cells generated using tissue engineering from outside. For instance, in many heart diseases, there is need for heart valve transplantation and unfortunately, within 10 years of initial valve replacement, 50–60% of patients will experience prosthesis associated problems requiring reoperation. This could be avoided by transplantation of heart muscle cells that can regenerate. Delivery of these cells to the respective tissues is not an easy task and this could be done with the help of scaffolds. In situ gel forming scaffolds can also be used for the bone and cartilage regeneration. They can be injected anywhere and can take the shape of a tissue defect, avoiding the need for patient specific scaffold prefabrication and they also have other advantages. Scaffolds are prepared by biodegradable material that result in minimal immune and inflammatory response. Some of the very important issues regarding scaffolds as drug delivery systems is reviewed in this article.

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Keywords:

Scaffolds, biodegradable system, injectable scaffolds, heart valve generation scaffold, bone and cartilage regeneration scaffolds

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Published

2008-08-31

How to Cite

1.
V. Gaikwad V, B. Patil A, V. Gaikwad M. Scaffolds for Drug Delivery in Tissue Engineering. Scopus Indexed [Internet]. 2008 Aug. 31 [cited 2024 Nov. 22];1(2):113-2. Available from: https://ijpsnonline.com/index.php/ijpsn/article/view/333

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Section

Review Articles

References

Bhati RS, Mukherjee DP, McCarthy KJ, Rogers SH, Smith DF, Shalaby SW, The growth of chondrocytes into a fibronectin-coated biodegradable scaffold, J. Biomed. Mater. Res. 56: 74-82, (2001).

Chen QZ, Thompson ID, Boccoccini AR, 45S5 Bioglass®-derived glass–ceramic scaffolds for bone tissue engineering, Biomaterials 27: 2414-2425, (2006).

Cortiella J. Nichols JE, Kojima K. Bonassar LJ, Dargon P. Roy AK, Vacant MP, Niles JA, Vacanti CA, Tissue-engineered lung: an in vivo and in vitro comparison of polyglycolic acid and pluronic F-127 hydrogel/osmatic lung progenitor cell constructs to support tissue growth, Tissue Eng. 12: 1213-1225, (2006).

Crompton KE, JD, Goud, Bellamkonda RV, Gengenbach TR, Finkelstein DI, Horne MK, Forsythe JS, Polylysine-functionalised thermoresponsive chitosan hydrogel for neural tissue engineering, Biomaterials 28: 441-449, (2007).

Dang JM, Sun DDN, Shin-Ya Y. Sieber AN, Kostuik JP, Leong KW, Temperature-responsive hydroxybutyl chitosan for the culture of mesenchymal stem cells and intervertebral disk cells, Biomaterials 27: 406-418, (2006).

Davis KA, Burdick JA, Anseth KS, Photoinitiated crosslinked degradable copolymer networks for tissue engineering applications, Biomaterials 24: 2485-2495, (2003).

Gunatillake PA, Adhikari R. Biodegradable synthetic polymers for tissue engineering, Eur. Cells Mater. 5: 1-16, (2003).

Hersel U. Dahmen C. Kessler H. RGDmodified polymers: biomaterials for stimulated cell adhesion and beyond, Biomaterials 24: 4385-4415, (2003).

Hutmacher DW, Scaffolds in tissue engineering bone and cartilage, Biomaterials 21: 2529-2543, (2000)

Kenny SM, Buggy M. Bone cements and fillers: a review, J. Mater. Sci., Mater. Med. 14: 923-938, (2003).

Kim B. Mooney DJ, Engineering smooth muscle tissue with a predefined structure, J. Biomed. Mater. Res. 41: 322-332, (1998).

Kim SH, Nam YS, Lee TS, Park WH, Silk fibroin nanofiber: electrospinning, properties, and structure, Polym. J. 35: 185-190, (2003).

Leach JB, Bivens KA, Patrick CW, Schmidt CE, Photocrosslinked hyaluronic acid hydrogels: natural, biodegradable tissue engineering scaffolds, Biotechnol. Bioeng. 82: 578-589, (2003).

LeGeros RZ, Properties of osteoconductive biomaterials: calcium phosphates, Clin. Orthop. Relat. Res. 395: 81-98, (2002).

Li W. Laurencin CT, Caterson EJ, Tuan RS, Ko FK, Electrospun nanofibrous structure: a novel scaffold for tissue engineering, J. Biomed. Mater. Res. 60: 613-621, (2002).

Li Z. Ramay HR, Hauch KD, Xiao D. Zhang M. Chitosan–alginate hybrid scaffolds for bone tissue engineering, Biomaterials 26: 3919-3928, (2005).

Mao JS, Liu HF, Yin YJ, Yao KD, The properties of chitosan–gelatin membranes and scaffolds modified with hyaluronic acid by different methods, Biomaterials 24: 1621-1629, (2003).

Matthews JA, Wnek GE, Simpson DG, Bowlin GL, Electrospinning of collasgen nanofibers, Biomacromolecules 3: 232-238, (2002).

Ma Z. Gao C. Gong Y. Shen J. Cartilage tissue engineering PLLA scaffold with surface immobilized collagen and basic fibroblast growth factor, Biomaterials 26: 1253-1259, (2005).

Mikos AG, Sarakinos G. Leite SM, Vacanti JP, Langer R. Laminated three-dimensional biodegradable foams for use in tissue engineering, Biomaterials 14: 323-330, (1993).

Mooney DJ, Baldwin DF, Suh NP, Vacanti JP, Langer R. Novel approach to fabricate porous sponges of poly (D, L-lactic-co-glycolic acid) without the use of organic solvents, Biomaterials 17: 1417-1422, (1996).

Nam YS, Park TG, Biodegradable polymeric microcellular foams by modified thermally induced phase separation method, Biomaterials 20: 1783-1790, (1999).

Nam YS, Yoon JJ, Park TG, A novel fabrication method for macroporous scaffolds using gas foaming salt as porogen additive, J. Biomed. Mater. Res. (Appl. Biomater.) 53: 1-7, (2000).

Nettles DL, Elder SH, Gilbert JA, Potential use of chitosan as a cell scaffold material for cartilage tissue engineering, Tissue Eng. 8: 1009-1016, (2002).

Noh, Lee JW, Chondrogenic differentiation of human mesenchymal stem cells using a thermosensitive poly (N-isopropylacrylamide) and water-soluble chitosan copolymer, Biomaterials 25: 5743-5751, (2004).

Nuttelman CR, Mortisen DJ, Henry SM, Anseth KS, Attachment of fibronectin to poly (vinyl alcohol) hydrogels promotes NIH3T3 cell adhesion, proliferation, and migration, J. Biomed. Mater. Res. 57: 217-223, (2001).

Padera R. Venkataraman G. Berry D. Godavarti R. Sasisekharan R. FGF-2/fibroblast growth factor receptor/heparin-like glycosaminoglycan interactions: a compensation model for FGF-2 signaling, FASEB J. 13: 677-1687, (1999).

Park TG, Perfusion culture of hepatocytes within galactose-derivatized biodegradable poly (lactide-co-glycolide) scaffolds prepared by gas foaming of effervescent salts, J. Biomed. Mater. Res. 59: 127-135, (2002).

Perets A. Baruch Y. Weisbuch F. Shoshany G. Neufeld GS, Cohen, Enhancing the vascularization of three-dimensional porous alginate scaffolds by incorporating controlled release basic fibroblast growth factor microspheres, J. Biomed. Mater. Res. 65A: 489-497, (2003).

Peter SJ, Miller MJ, Yasko AW, Yaszemski MJ, Mikos AG, Polymer concepts in tissue engineering, J. Biomed. Mater. Res. (Appl. Biomater.) 43: 422-427, (1998).

Pieper JS, Hafmans T. Wachem PB, van, Luyn MJA, van, Brouwer LA, Veerkamp JH, Kuppevelt TH, van, Loading of collagen–heparan sulfate matrices with bFGF promotes angiogenesis and tissue generation in rats, J. Biomed. Mater. Res. 62: 185-194, (2002).

Rowley JA, Madlambayan G. Mooney DJ, Alginate hydrogels as synthetic extracellular matrix materials, Biomaterials 20: 45-53, (1999).

Sakiyama-Elbert SE, Hubbell JA, Development of fibrin derivatives for controlled release of heparin-binding growth factors, J. Control. Release 65: 389-402, (2000).

Stabenfeldt SE, García AJ, LaPlaca MC, Thermoreversible lamininfunctionalized hydrogel for neural tissue engineering, J. Biomed. Mater. Res. A 77A: 718-725, (2006).

Temenoff JS, Shin H. Conway DE, Engel PS, Mikos AG, In vitro cytotoxicity of redox radical initiators for cross-linking of oligo (poly (ethylene glycol) fumarate) macromers, Biomacromolecules 4: 1605-1613, (2003).

Thomas MV, Puleo DA, Al-Sabbagh M. Bioactive glass three decades on, J. Long-Term Eff. Med. Implants 15 (6): 585-597, (2005).

Thompson LD, Pantoliano MW, Springer BA, Energetic characterization of the basic fibroblast growth factor–heparin interaction: identification of the heparin binding domain, Biochemistry 33: 3831-3840, (1994).

Yang S. Leong K. Du Z. Chua C. The design of scaffolds for use in tissue engineering. Part II. Rapid prototyping techniques, Tissue Eng. 8: 1-11, (2002).

Yoo HS, Lee EA, Yoon JJ, Park TG, Hyaluronic acid modified biodegradable scaffolds for cartilage tissue engineering, Biomaterials 26: 1925-1933, (2005).

Whang K. Thomas CH, Healy KE, A novel method to fabricate bioabsorbable scaffolds, Polymer 36: 837-842, (1995).

Wissink MJB, Beernink R. Poot AA, Engbers GHM, Beugeling T. Aken WG, van, Feijen J. Improved endothelialization of vascular grafts by local release of growth factor from heparinized collagen matrices, J. Control. Release 64: 103-114, (2000).

Zhong J. Greenspan DC, Processing and properties of sol–gel bioactive glasses, J. Biomed. Mater. Res., B Appl. Biomater. 53: 694-701, (2000).