| Literature DB >> 27748576 |
Silvia Panzavolta1, Paola Torricelli2, Sonia Casolari1, Annapaola Parrilli2, Sofia Amadori1, Milena Fini2, Adriana Bigi1.
Abstract
The systemic administration of bisphosphonates (BPs) for the treatment of metabolic diseases characterized by abnormal bone loss suffers from several adverse side effects, which can be reduced by implementation of alternative modes of administration. In this work, glutaraldehyde cross-linked gelatin scaffolds are proposed as delivery systems of calcium alendronate monohydrate (CaAL•H2 O). The 3D highly porous scaffolds display a relevant interconnected porosity (>94%), independently from CaAL•H2 O content (0, 3, and 6 wt%). At variance, pore size varies with composition. The relative increase of the number of smaller pores on increasing BP content is in agreement with the parallel significant increase of the compressive modulus and collapse strength. The scaffolds exhibit a sustained CaAL•H2 O release profile, and a significant amount of the drug is retained in the scaffolds even after 14 d. In vitro tests are carried out using cocultures of osteoblast (OB) and osteoclast (OC). The evaluation of differentiation markers is performed both on the supernatants of cell culture and by means of quantitative polymerase chain reaction. The results indicate that BP containing scaffolds support osteoblast proliferation and differentiation, whereas they inhibit osteoclast viability and activity, displaying a promising beneficial role on bone repair processes.Entities:
Keywords: bisphosphonates; drug delivery systems; gelatin scaffolds; mechanical properties
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Year: 2016 PMID: 27748576 DOI: 10.1002/mabi.201600272
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979