Controlled release of C-type natriuretic peptide by microencapsulation dampens proinflammatory effects induced by IL-1 beta in cartilage explants

C-type natriuretic peptide (CNP) exhibits potent anti-inflammatory effects in chondrocytes that have the potential to repair cartilage damage observed in osteoarthritis (OA). However, treatments for OA have been challenging due to poor targeting and delivery of therapeutics. The present study fabric...

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Main Authors: Peake, N.J., Pavlov, A.M., D'Souza, A., Pingguan-Murphy, Belinda, Sukhorukov, G.B., Hobbs, A.J., Chowdhury, T.T.
Format: Article
Published: 2015
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author Peake, N.J.
Pavlov, A.M.
D'Souza, A.
Pingguan-Murphy, Belinda
Sukhorukov, G.B.
Hobbs, A.J.
Chowdhury, T.T.
author_facet Peake, N.J.
Pavlov, A.M.
D'Souza, A.
Pingguan-Murphy, Belinda
Sukhorukov, G.B.
Hobbs, A.J.
Chowdhury, T.T.
author_sort Peake, N.J.
collection UM
description C-type natriuretic peptide (CNP) exhibits potent anti-inflammatory effects in chondrocytes that have the potential to repair cartilage damage observed in osteoarthritis (OA). However, treatments for OA have been challenging due to poor targeting and delivery of therapeutics. The present study fabricated polyelectrolyte microcapsules loaded with CNP and examined whether the layer-by-layer (LbL) approach could have protective effects in cartilage explants treated with the pro-inflammatory cytokine, interleukin-1 beta (IL-1 beta). SEM showed uniform, 2 to 3 mu m spherical microcapsules with morphological characteristic similar to templates loaded with or without CNP. The protein was localized around the external surface of the microcapsules with encapsulation efficiencies >82.9. CNP release profiles were broadly similar following 9 days of culture. The presence of CNP microcapsules did not significantly affect cell viability (80) with DNA values that remained stable throughout the culture conditions. Confocal imaging showed clustering of microcapsules in chondrocytes to natriuretic peptide receptor (Npr) 2 and 3. Treatment of cartilage explants with CNP microcapsules led to concentration-dependent inhibition of NO release in response to IL-1 beta and restoration of matrix synthesis. In summary, we demonstrate controlled delivery of CNP to dampen pro-inflammatory effects induced by IL-1 beta in cartilage explants. The LbL approach has the potential to promote cartilage repair in vivo.
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spelling um.eprints-140502020-02-10T08:38:08Z http://eprints.um.edu.my/14050/ Controlled release of C-type natriuretic peptide by microencapsulation dampens proinflammatory effects induced by IL-1 beta in cartilage explants Peake, N.J. Pavlov, A.M. D'Souza, A. Pingguan-Murphy, Belinda Sukhorukov, G.B. Hobbs, A.J. Chowdhury, T.T. T Technology (General) TA Engineering (General). Civil engineering (General) C-type natriuretic peptide (CNP) exhibits potent anti-inflammatory effects in chondrocytes that have the potential to repair cartilage damage observed in osteoarthritis (OA). However, treatments for OA have been challenging due to poor targeting and delivery of therapeutics. The present study fabricated polyelectrolyte microcapsules loaded with CNP and examined whether the layer-by-layer (LbL) approach could have protective effects in cartilage explants treated with the pro-inflammatory cytokine, interleukin-1 beta (IL-1 beta). SEM showed uniform, 2 to 3 mu m spherical microcapsules with morphological characteristic similar to templates loaded with or without CNP. The protein was localized around the external surface of the microcapsules with encapsulation efficiencies >82.9. CNP release profiles were broadly similar following 9 days of culture. The presence of CNP microcapsules did not significantly affect cell viability (80) with DNA values that remained stable throughout the culture conditions. Confocal imaging showed clustering of microcapsules in chondrocytes to natriuretic peptide receptor (Npr) 2 and 3. Treatment of cartilage explants with CNP microcapsules led to concentration-dependent inhibition of NO release in response to IL-1 beta and restoration of matrix synthesis. In summary, we demonstrate controlled delivery of CNP to dampen pro-inflammatory effects induced by IL-1 beta in cartilage explants. The LbL approach has the potential to promote cartilage repair in vivo. 2015 Article PeerReviewed Peake, N.J. and Pavlov, A.M. and D'Souza, A. and Pingguan-Murphy, Belinda and Sukhorukov, G.B. and Hobbs, A.J. and Chowdhury, T.T. (2015) Controlled release of C-type natriuretic peptide by microencapsulation dampens proinflammatory effects induced by IL-1 beta in cartilage explants. Biomacromolecules, 16 (2). pp. 524-531. ISSN 1525-7797, DOI https://doi.org/10.1021/bm501575w <https://doi.org/10.1021/bm501575w>. http://pubs.acs.org/doi/abs/10.1021/bm501575w 10.1021/bm501575w
spellingShingle T Technology (General)
TA Engineering (General). Civil engineering (General)
Peake, N.J.
Pavlov, A.M.
D'Souza, A.
Pingguan-Murphy, Belinda
Sukhorukov, G.B.
Hobbs, A.J.
Chowdhury, T.T.
Controlled release of C-type natriuretic peptide by microencapsulation dampens proinflammatory effects induced by IL-1 beta in cartilage explants
title Controlled release of C-type natriuretic peptide by microencapsulation dampens proinflammatory effects induced by IL-1 beta in cartilage explants
title_full Controlled release of C-type natriuretic peptide by microencapsulation dampens proinflammatory effects induced by IL-1 beta in cartilage explants
title_fullStr Controlled release of C-type natriuretic peptide by microencapsulation dampens proinflammatory effects induced by IL-1 beta in cartilage explants
title_full_unstemmed Controlled release of C-type natriuretic peptide by microencapsulation dampens proinflammatory effects induced by IL-1 beta in cartilage explants
title_short Controlled release of C-type natriuretic peptide by microencapsulation dampens proinflammatory effects induced by IL-1 beta in cartilage explants
title_sort controlled release of c type natriuretic peptide by microencapsulation dampens proinflammatory effects induced by il 1 beta in cartilage explants
topic T Technology (General)
TA Engineering (General). Civil engineering (General)
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