Ian Gaudet

Ian Gaudet

San Jose, California, United States
5K followers 500+ connections

About

Cell therapy translation, development, and manufacturing leader.

Specialties: Team…

Activity

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Experience

  • Galapagos Graphic

    Galapagos

    Morgan Hill, California, United States

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    San Jose, California, United States

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    Mountain View, CA

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    Mountain View, CA

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    Piscataway, NJ

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Education

Publications

  • Methacrylation Induces Rapid, Temperature-Dependent, Reversible Self-Assembly of Type-I Collagen

    Langmuir

    Type-I collagen self-assembles into a fibrillar gel at physiological temperature and pH to provide a cell-adhesive, supportive, structural network. As such, it is an attractive, popular scaffold for in vitro evaluations of cellular behavior and for tissue engineering applications. In this study, type-I collagen is modified to introduce methacrylate groups on the free amines of the lysine residues to create collagen methacrylamide (CMA). CMA retains the properties of collagen such as…

    Type-I collagen self-assembles into a fibrillar gel at physiological temperature and pH to provide a cell-adhesive, supportive, structural network. As such, it is an attractive, popular scaffold for in vitro evaluations of cellular behavior and for tissue engineering applications. In this study, type-I collagen is modified to introduce methacrylate groups on the free amines of the lysine residues to create collagen methacrylamide (CMA). CMA retains the properties of collagen such as self-assembly, biodegradability, and natural bioactivity but is also photoactive and can be rapidly cross-linked or functionalized with acrylated molecules when irradiated with ultraviolet light in the presence of a photoinitiator. CMA also demonstrates unique temperature-dependent behavior. For natural type-I collagen, the overall structure of the fiber network remains largely static over time scales of a few hours upon heating and cooling at temperatures below its denaturation point. CMA, however, is rapidly thermoreversible and will oscillate between a liquid macromer suspension and a semisolid fibrillar hydrogel when the temperature is modulated between 10 and 37 °C. Using a series of mechanical, scattering, and spectroscopic methods, we demonstrate that structural reversibility is manifest across multiple scales from the protein topology of the triple helix up through the rheological properties of the CMA hydrogel. Electron microscopy imaging of CMA after various stages of heating and cooling shows that the canonical collagen-like D-periodic banding ultrastructure of the fibers is preserved. A rapidly thermoreversible collagen-based hydrogel is expected to have wide utility in tissue engineering and drug delivery applications as a biofunctional, biocompatible material. Thermal reversibility also makes CMA a powerful model for studying the complex process of hierarchical collagen self-assembly.

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  • Characterization of methacrylated type-I collagen as a dynamic, photoactive hydrogel

    Biointerphases

    Type-I collagen is an attractive scaffold material for tissue engineering due to its ability to self-assemble into a fibrillar hydrogel, its innate support of tissue cells through bioactive adhesion sites, and its biodegradability. However, a lack of control of material properties has hampered its utility as a scaffold. We have modified collagen via the addition of methacrylate groups to create collagen methacrylamide (CMA) using a synthesis reaction that allows retention of fundamental…

    Type-I collagen is an attractive scaffold material for tissue engineering due to its ability to self-assemble into a fibrillar hydrogel, its innate support of tissue cells through bioactive adhesion sites, and its biodegradability. However, a lack of control of material properties has hampered its utility as a scaffold. We have modified collagen via the addition of methacrylate groups to create collagen methacrylamide (CMA) using a synthesis reaction that allows retention of fundamental characteristics of native collagen, including spontaneous fibrillar self-assembly and enzymatic biodegradability. This method allows for a rapid, five-fold increase in storage modulus upon irradiation with 365 nm light. Fibrillar diameter of CMA was not significantly different from native collagen. Collagenolytic degradability of uncrosslinked CMA was minimally reduced, while photocrosslinked CMA was significantly more resistant to degradation. Live/Dead staining demonstrated that a large majority (71%) of encapsulated mesenchymal stem cells remained viable 24 h after photocrosslinking, which further increased to 81% after 72 h. This material represents a novel platform for creating mechanically heterogeneous environments.

    Other authors
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Patents

  • Process for the synthesis of methacrylate-derivatized type-1 collagen and derivatives thereof

    Issued USPTO 08658711

    Methods for synthesizing a methacrylate-derivatized type-I collagen in which methacrylic acid is reacted with a carboxylic acid activating reagent in the presence of a carbodiimide to form a methacrylic acid with an activated carboxylic acid group, which is then reacted with free amino groups on type-I collagen to form a collagen methacrylamide. Methacrylate-derivatized collagen, cross-linked collagens formed therefrom and products containing the cross-linked collagen are also disclosed.

    Other inventors
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Courses

  • Bioengineering Design

    BENG 186C

  • Bioengineering Laboratory

    BENG 172

  • Bioengineering Mass Transport

    BENG 103B

  • Bioengineering Physiology

    BENG 140 A&B

  • Biomaterials and Biomechanics

    16125582

  • Biomechanics

    MAE 112A&B

  • Biomedical Electronics

    BENG 122B

  • Biosignal Processing

    16125571

  • Biosystems and Control

    BENG 122A

  • Cell and Tissue Engineering

    BENG 166A

  • Clinical Practicum

    16125628

  • Computational Methods

    MAE 107

  • Computer-Aided Design

    MAE 150

  • Continuum Mechanics

    BENG 110

  • Critical Writing

    MCWP 50

  • Ethical Scientific Conduct

    16115556

  • Fluid Mechanics

    CENG 101A

  • Fortran for Engineers

    AMES 10

  • Journal Club

    16125601

  • Kinetics Thermodynamics and Transport

    16125573

  • Linear Algebra

    MATH 20F

  • Linear Circuits

    MAE 140

  • Mammalian Physiology

    16125581

  • Mechanics I: Statics

    AMES 121A

  • Mechanics II: Dynamics

    AMES 121B

  • Methods in Applied Mathematics

    16642527

  • Molecular Biology and Biochemistry

    16115511

  • Molecular Physical Chemistry

    BENG 130

  • Neural Injury and Repair

    16963632

  • Polymer Science and Engineering

    16155551

  • Principles of Bioinstrumentation

    BENG 186B

  • Principles of Biomaterials

    BENG 186A

  • Stem Cell Biology and Engineering

    16125586

  • Vector Calculus

    MATH 20E

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