PMID- 33545850 OWN - NLM STAT- MEDLINE DCOM- 20210514 LR - 20210514 IS - 1873-0191 (Electronic) IS - 0928-4931 (Linking) VI - 120 DP - 2021 Jan TI - An injectable and antibacterial calcium phosphate scaffold inhibiting Staphylococcus aureus and supporting stem cells for bone regeneration. PG - 111688 LID - S0928-4931(20)33607-9 [pii] LID - 10.1016/j.msec.2020.111688 [doi] AB - Staphylococcus aureus (S. aureus) is the major pathogen for osteomyelitis, which can lead to bone necrosis and destruction. There has been no report on antibacterial calcium phosphate cement (CPC) against S. aureus. The aims of this study were to: (1) develop novel antibacterial CPC-chitosan-alginate microbead scaffold; (2) investigate mechanical and antibacterial properties of CPC-chitosan-penicillin-alginate scaffold; (3) evaluate the encapsulation and delivery of human umbilical cord mesenchymal stem cells (hUCMSCs). Flexural strength, elastic modulus and work-of-fracture of the CPC-chitosan-penicillin-alginate microbeads scaffold and CPC-chitosan scaffold were evaluated. Penicillin release profile and antibacterial effects on S. aureus were determined. The hUCMSC delivery and release from penicillin-alginate microbeads were investigated. Injectable CPC-chitosan-penicillin-alginate microbeads scaffold was developed for the first time. CPC-chitosan-penicillin-alginate microbeads scaffold had a flexural strength of 3.16 +/- 0.55 MPa, matching that of cancellous bone. With sustained penicillin release, the new scaffold had strong antibacterial effects on S. aureus, with an inhibition zone diameter of 32.2 +/- 2.5 mm, greater than that of penicillin disk control (15.1 +/- 2.0 mm) (p < 0.05). Furthermore, this injectable and antibacterial scaffold had no toxic effects, yielding excellent hUCMSC viability, which was similar to that of CPC control without antibacterial activity (p > 0.05). CPC-chitosan-penicillin-microbeads scaffold had injectability, good strength, strong antibacterial effects, and good biocompatibility to support stem cell viability for osteogenesis. CPC-chitosan-penicillin-microbeads scaffold is promising for dental, craniofacial and orthopedic applications to combat infections and promote bone regeneration. CI - Copyright (c) 2020 Elsevier B.V. All rights reserved. FAU - Wu, Shizhou AU - Wu S AD - Department of Orthopedic Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China; Biomaterials & Tissue Engineering Division, Department of Advanced Oral Sciences and Therapeutics, University of Maryland Dental School, Baltimore, MD 21201, USA. FAU - Lei, Lei AU - Lei L AD - State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan 610041, China. FAU - Bao, Chongyun AU - Bao C AD - State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan 610041, China. FAU - Liu, Jin AU - Liu J AD - Biomaterials & Tissue Engineering Division, Department of Advanced Oral Sciences and Therapeutics, University of Maryland Dental School, Baltimore, MD 21201, USA; Key Laboratory of Shannxi for Craniofacial Precision Medicine Research, Clinical Research Center of Shannxi for Dental and Maxillofacial Diseases, College of Stomatology, Xi'an Jiaotong University, Shannxi 710004, China. FAU - Weir, Michael D AU - Weir MD AD - Biomaterials & Tissue Engineering Division, Department of Advanced Oral Sciences and Therapeutics, University of Maryland Dental School, Baltimore, MD 21201, USA. FAU - Ren, Ke AU - Ren K AD - Department of Neural and Pain Sciences, School of Dentistry, Program in Neuroscience, University of Maryland, Baltimore, MD 21201, USA. FAU - Schneider, Abraham AU - Schneider A AD - Department of Oncology and Diagnostic Sciences, University of Maryland School of Dentistry, Baltimore, USA; Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD 21201, USA. FAU - Oates, Thomas W AU - Oates TW AD - Biomaterials & Tissue Engineering Division, Department of Advanced Oral Sciences and Therapeutics, University of Maryland Dental School, Baltimore, MD 21201, USA. FAU - Liu, Jun AU - Liu J AD - State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan 610041, China. Electronic address: junliu@scu.edu.cn. FAU - Xu, Hockin H K AU - Xu HHK AD - Biomaterials & Tissue Engineering Division, Department of Advanced Oral Sciences and Therapeutics, University of Maryland Dental School, Baltimore, MD 21201, USA; Marlene and Stewart Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD 21201, USA; Center for Stem Cell Biology and Regenerative Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA. Electronic address: hxu@umaryland.edu. LA - eng PT - Journal Article DEP - 20201104 PL - Netherlands TA - Mater Sci Eng C Mater Biol Appl JT - Materials science & engineering. C, Materials for biological applications JID - 101484109 RN - 0 (Anti-Bacterial Agents) RN - 0 (Bone Cements) RN - 0 (Calcium Phosphates) SB - IM MH - Anti-Bacterial Agents/pharmacology MH - Bone Cements/pharmacology MH - Bone Regeneration MH - Calcium Phosphates/pharmacology MH - Cell Differentiation MH - Humans MH - *Mesenchymal Stem Cells MH - Osteogenesis MH - *Staphylococcus aureus MH - Stem Cells MH - Tissue Engineering MH - Tissue Scaffolds OTO - NOTNLM OT - Antibacterial OT - Calcium phosphate scaffold OT - Injectable OT - Penicillin OT - Staphylococcus aureus OT - Stem cells EDAT- 2021/02/07 06:00 MHDA- 2021/05/15 06:00 CRDT- 2021/02/06 01:00 PHST- 2020/09/07 00:00 [received] PHST- 2020/10/26 00:00 [revised] PHST- 2020/10/27 00:00 [accepted] PHST- 2021/02/06 01:00 [entrez] PHST- 2021/02/07 06:00 [pubmed] PHST- 2021/05/15 06:00 [medline] AID - S0928-4931(20)33607-9 [pii] AID - 10.1016/j.msec.2020.111688 [doi] PST - ppublish SO - Mater Sci Eng C Mater Biol Appl. 2021 Jan;120:111688. doi: 10.1016/j.msec.2020.111688. Epub 2020 Nov 4.