Preparation of adriamycin gelatin microsphere-loaded decellularized periosteum that is cytotoxic to human osteosarcoma cells.
Chuan ChenJianghui DongHong ChenXin WangJin MeiLiping WangCory J XianPublished in: Journal of cellular physiology (2018)
The purpose of this study was to develop a novel approach to treat bone osteosarcoma using a multipurpose scaffold aiming for local drug delivery. The slowly releasing microspheres was designed to deliver the chemotherapy drug adriamycin (ADM) and a decellularized (D) periosteum scaffold (which is known to be able to promote bone regeneration) was used to carry these microspheres. D-periosteum was obtained by physical and chemical decellularization. Histological results showed that the cellular components were effectively removed. The D-periosteum showed an excellent cytocompatibility and the ability to promote adhesion and growth of fibroblasts. Two kinds of slowly releasing microspheres, adriamycin gelatin microspheres (ADM-GMS) and adriamycin poly (dl-lactide-co-glycolide) gelatin microspheres (ADM-PLGA-GMS), were prepared and anchored to D-periosteum, resulting in two types of drug-releasing regenerative scaffolds. The effectiveness of these two scaffolds in killing human osteosarcoma cells was tested by evaluating cell viability overtime of the cancer cells cultured with the scaffolds. In summary, a gelatin/decellularized periosteum-based biologic scaffold material was designed aiming for local delivery of chemotherapy drugs for osteosarcoma, with the results showing ability of the scaffolds in sustaining release of the cancer drug and in suppressing growth of the cancer cells in vitro.
Keyphrases
- tissue engineering
- bone regeneration
- drug delivery
- molecularly imprinted
- endothelial cells
- induced apoptosis
- cell cycle arrest
- randomized controlled trial
- signaling pathway
- rheumatoid arthritis
- induced pluripotent stem cells
- physical activity
- cancer therapy
- systematic review
- mental health
- oxidative stress
- drug induced
- locally advanced
- adverse drug
- endoplasmic reticulum stress
- extracellular matrix
- radiation therapy
- stem cells
- cell death
- solid phase extraction
- high resolution
- cell proliferation
- postmenopausal women
- mass spectrometry
- cell therapy
- young adults
- cell migration
- lymph node metastasis