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Jianjun Guan

Researcher at University of Pittsburgh

Publications -  48
Citations -  5183

Jianjun Guan is an academic researcher from University of Pittsburgh. The author has contributed to research in topics: Grafting & Polycaprolactone. The author has an hindex of 29, co-authored 43 publications receiving 4914 citations. Previous affiliations of Jianjun Guan include Zhejiang University & Ohio State University.

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Preparation and characterization of highly porous, biodegradable polyurethane scaffolds for soft tissue applications

TL;DR: Smooth muscle cells were filtration seeded in the scaffolds and it was shown that both scaffolds supported cell adhesion and growth, with smooth muscle cells growing more extensively in the PEUU scaffold.
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Design and analysis of tissue engineering scaffolds that mimic soft tissue mechanical anisotropy.

TL;DR: This study developed ES-PEUU scaffolds under variable speed conditions and modeled the effects of fiber orientation on the macro-mechanical properties of the scaffold, which will help to provide the basis for rationally designed mechanically anisotropic soft tissue engineered implants.
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Microintegrating smooth muscle cells into a biodegradable, elastomeric fiber matrix.

TL;DR: Electrospraying vascular smooth muscle cells (SMCs) concurrently with electrospinning a biodegradable, elastomeric poly(ester urethane)urea (PEUU) matrix embodies a novel tissue engineering approach that could be applied to fabricate high cell density elastic tissue mimetics, blood vessels or other cardiovascular tissues.
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Synthesis, characterization, and cytocompatibility of elastomeric, biodegradable poly(ester-urethane)ureas based on poly(caprolactone) and putrescine

TL;DR: These biodegradable PEUUs demonstrate potential for future application as cell scaffolds in cardiovascular tissue-engineering or other soft-tissue applications.
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A bilayered elastomeric scaffold for tissue engineering of small diameter vascular grafts.

TL;DR: This approach, combining artery-like mechanical properties and a rapid and efficient cellularization, might contribute to the future clinical translation of TEVGs.