George J Klarmann

Dr. George J Klarmann

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 April 2023 in Bioprinting
Verified
Journal Article
Open access
GKGeorge J Klarmann
George J Klarmann
MPMaria E. Piroli
Maria E. Piroli
JLJoseph R. Loverde
Joseph R. Loverde
ANAndrew F. Nelson
Andrew F. Nelson
ZLZhaozhang Li
Zhaozhang Li
VHVincent B. Ho
Vincent B. Ho

1 December 2021 in Biomaterials and Biosystems
Verified
Journal Article
Open access
GKGeorge J Klarmann
George J Klarmann
JGJoel Gaston
Joel Gaston
VHVincent B. Ho
Vincent B. Ho
• Knee meniscus tears occur with a yearly incidence of nearly 61 per 100,000 people. • Untreated tears lead to progressive osteoarthritis development. • Updates on current state of scaffold and tissue-engineered meniscal replacements. • 3D printing can fabricate meniscal repair devices with patient-specific geometry.

16 March 2023 in Lab on a Chip
Verified
Journal Article
Closed access
PDF file
LLLap Man Lee
Lap Man Lee
GKGeorge J Klarmann
George J Klarmann
DHDustin W. Haithcock
Dustin W. Haithcock
Yi WangYi Wang
Yi Wang
KBKetan H. Bhatt
Ketan H. Bhatt
ELEva Lai
Eva Lai
Combining inertial and deterministic lateral displacement (DLD) microfluidic sorting to isolate mesenchymal stem cells (MSCs) from human adipose tissue for regenerative medicine applications.

3 October 2024 in Life Sciences in Space Research
Verified
Journal Article
Closed access
GKGeorge J Klarmann
George J Klarmann
ARAaron J. Rogers
Aaron J. Rogers
KGKristin H. Gilchrist
Kristin H. Gilchrist
VHVincent B. Ho
Vincent B. Ho

8 August 2024 in Bioengineering
Verified
Journal Article
Open access
PDF file
EWE. Cate Wisdom
E. Cate Wisdom
ALAndrew Lamont
Andrew Lamont
HMHannah Martinez
Hannah Martinez
MRMichael Rockovich
Michael Rockovich
WLWoojin Lee
Woojin Lee
GKGeorge J Klarmann
George J Klarmann
Skin wounds often form scar tissue during healing. Early intervention with tissue-engineered materials and cell therapies may promote scar-free healing. Exosomes and extracellular vesicles (EV) secreted by mesenchymal stromal cells (MSC) are believed to have high regenerative capacity. EV bioactivity is preserved after lyophilization and storage to enable use in remote and typically resource-constrained environments. We developed a bioprinted bandage containing reconstituted EVs that can be fabricated at the point-of-need. An alginate/carboxymethyl cellulose (CMC) biomaterial ink was prepared, and printability and mechanical properties were assessed with rheology and compression testing. Three-dimensional printed constructs were evaluated for Young’s modulus relative to infill density and crosslinking to yield material with stiffness suitable for use as a wound dressing. We purified EVs from human MSC-conditioned media and characterized them with nanoparticle tracking analysis and mass spectroscopy, which gave a peak size of 118 nm and identification of known EV proteins. Fluorescently labeled EVs were mixed to form bio-ink and bioprinted to characterize EV release. EV bandages were bioprinted on both a commercial laboratory bioprinter and a custom ruggedized 3D printer with bioprinting capabilities, and lyophilized EVs, biomaterial ink, and thermoplastic filament were deployed to an austere Arctic environment and bioprinted. This work demonstrates that EVs can be bioprinted with an alginate/CMC hydrogel and released over time when in contact with a skin-like substitute. The technology is suitable for operational medical applications, notably in resource-limited locations, including large-scale natural disasters, humanitarian crises, and combat zones.

28 February 2024 in Bioengineering
Verified
Journal Article
Open access
PDF file
EWE. Cate Wisdom
E. Cate Wisdom
NCNicholas Chartrain
Nicholas Chartrain
KBKelli Blaize-Wise
Kelli Blaize-Wise
GKGeorge J Klarmann
George J Klarmann
KGKristin Gilchrist
Kristin Gilchrist
Vincent HoVincent Ho
Vincent Ho
Medical response to military conflicts, natural disasters, and humanitarian crises are challenged by operational logistics with unreliable supply chains, delayed medical evacuation, and compatibility of the disparate medical equipment and consumables. In these environments, stocks of supplies will become more quickly depleted and the need for equipment parts increases secondary to their higher likelihood for failure from overuse. Additive Manufacturing (AM), or 3D printing, at or closer to the point-of-need provides potential solutions to mitigate these logistics challenges. AM’s ability to tailor the resultant product through computer design enables real-time modification of a product to meet a specific situation. In this study, we deployed two different 3D printers to an arctic locale to demonstrate the utility of 3D printing and bioprinting in austere environments. Deployment of AM solutions in austere environments will likely impact medical care following natural disasters and conflicts with contested logistics. The work presented here furthers the readiness status of AM for use in austere environments to manufacture medical equipment parts and demonstrates its potential use for tissue engineering and advanced medical treatments in remote environments.