Mechanically matching the rheological properties of brain tissue for drug-delivery in human glioblastoma models

被引:37
作者
Parkins, Christopher C. [1 ]
McAbee, Joseph H. [2 ,3 ]
Ruff, Lisa [4 ]
Wendler, Astrid [4 ]
Mair, Richard [4 ]
Gilbertson, Richard J. [4 ]
Watts, Colin [2 ,5 ]
Scherman, Oren A. [1 ]
机构
[1] Univ Cambridge, Dept Chem, Melville Lab Polymer Synth, Cambridge CB2 1EW, England
[2] Univ Cambridge, Cambridge Ctr Brain Repair, Dept Clin Neurosci, Cambridge CB2 0PY, England
[3] NCI, Radiat Oncol Branch, NIH, Bethesda, MD 20892 USA
[4] Univ Cambridge, Addenbrookes Hosp, Dept Clin Neurosci, Div Neurosurg, Hills Rd, Cambridge CB2 0QQ, England
[5] Univ Birmingham, Brain Canc Program, Coll Med & Dent Sci, Inst Canc & Genom Sci, Birmingham B15 2TT, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
Glioblastoma; Hydrogel; Cucurbit[8]uril; Drug-delivery; Hyaluronic acid; Rheology; GLIADEL WAFERS; GLIOMA; TUMORS;
D O I
10.1016/j.biomaterials.2021.120919
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Peptide functionalized hyaluronic acid (HA(CF)) cross-linked by cucurbit[8]uril (CB[8]), a new class of drugdelivery reservoirs, is used to enable improved drug bioavailability for glioblastoma tumors in patient-derived xenograft (PDX) models. The mechanical and viscoelastic properties of native human and mouse tissues are measured over 8 h via oscillatory rheology under physiological conditions. Treatment with drug-loaded hydrogels allowed for a significant survival impact of 45 % (55.5-80.5 days). A relationship between the type of PDX tumor formed-a consequence of the heterogeneic nature of GB tumors-and changes in the initial survival is observed owing to greater local pressure from stiffer tumors. These biocompatible and tailorable materials warrant use as drug delivery reservoirs in PDX resection models, where the mechanical properties can be readily adjusted to match the stiffness of local tissue and thus have potential to improve the survival of GB patients.
引用
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页数:7
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