TY - JOUR
T1 - Spray dried hyaluronic acid microparticles for adhesion controlled aggregation and potential stimulation of stem cells
AU - Agnello, Stefano
AU - Fiorica, Calogero
AU - Giammona, Gaetano
AU - Palumbo, Fabio Salvatore
AU - Pitarresi, Giovanna
AU - Puleio, Roberto
AU - Loria, Guido R.
PY - 2017
Y1 - 2017
N2 - Spray-dried microparticles of a derivative of hyaluronic acid (HA) have been engineered to obtain a controlled aggregation with Human Mesenchymal Stem Cells (hMSCs) into 3D constructs. We demonstrated the utility of chemical functionalization of a native constituent of the extracellular matrix to improve processing performances and to control on stem cell adhesion and differentiation. Native hyaluronic acid (HA), cell adhesive peptides (RGD), transforming growth factor β3, dexamethasone are biological agents potentially suitable for chondrogenic stimulation of hMSCS. However unmodified HA suffers of drawbacks in terms of stability and versatility of processing. Functionalization strategies are needed to overcome these drawbacks. In this paper microparticles were produced by spray-drying of an aliphatic and amino functionalized HA derivative. Hydrophobic derivatization of HA allowed the production of microparticles stabilized by physical crosslinking and to load and to control dexamethasone release. The presence of pendant amino groups was exploited to tether cyclic RGD and transforming growth factor β3 via maleimide chemistry; cyRGDC functionalization controlled hMSCs/microparticles aggregation. Chondrogenic potential was preliminary assayed by qualitative immunohistological detection.
AB - Spray-dried microparticles of a derivative of hyaluronic acid (HA) have been engineered to obtain a controlled aggregation with Human Mesenchymal Stem Cells (hMSCs) into 3D constructs. We demonstrated the utility of chemical functionalization of a native constituent of the extracellular matrix to improve processing performances and to control on stem cell adhesion and differentiation. Native hyaluronic acid (HA), cell adhesive peptides (RGD), transforming growth factor β3, dexamethasone are biological agents potentially suitable for chondrogenic stimulation of hMSCS. However unmodified HA suffers of drawbacks in terms of stability and versatility of processing. Functionalization strategies are needed to overcome these drawbacks. In this paper microparticles were produced by spray-drying of an aliphatic and amino functionalized HA derivative. Hydrophobic derivatization of HA allowed the production of microparticles stabilized by physical crosslinking and to load and to control dexamethasone release. The presence of pendant amino groups was exploited to tether cyclic RGD and transforming growth factor β3 via maleimide chemistry; cyRGDC functionalization controlled hMSCs/microparticles aggregation. Chondrogenic potential was preliminary assayed by qualitative immunohistological detection.
KW - Bottom-up approach; Hyaluronic acid; Microparticles; Stem cells; Cell Adhesion; Cell Differentiation; Cells
KW - Cultured; Chondrogenesis; Dexamethasone; Extracellular Matrix; Humans; Hyaluronic Acid; Mesenchymal Stromal Cells; Tissue Engineering; Transforming Growth Factor beta; 3003
KW - Bottom-up approach; Hyaluronic acid; Microparticles; Stem cells; Cell Adhesion; Cell Differentiation; Cells
KW - Cultured; Chondrogenesis; Dexamethasone; Extracellular Matrix; Humans; Hyaluronic Acid; Mesenchymal Stromal Cells; Tissue Engineering; Transforming Growth Factor beta; 3003
UR - http://hdl.handle.net/10447/247274
UR - http://www.elsevier.com/locate/ijpharm
M3 - Article
VL - 519
SP - 332
EP - 342
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
SN - 0378-5173
ER -