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- 1 Kai P. Yuet
- 1.1 Education
- 1.2 Past Research
- 1.3 Current Contact Info
Kai P. Yuet
California Institute of Technology, Pasadena, CA
1st Year Chemical Engineering PhD Candidate
Massachusetts Institute of Technology, Cambridge, MA
S.B. in Chemical-Biological Engineering, 2009
S.B. in Biology, 2009
Dynamics of Biopolymers and Complex Fluids Group (2008-2009)
Microfluidic Synthesis and Self-Assembly of Hydrogel Particles
Over the past decade, advances in three-dimensional hydrogels have generated microstructures that successfully simulate cellular microenvironment with regards to optimal mechanical behavior and growth factor and nutrient delivery. Despite their promise in many tissue engineering and regenerative medicine applications, hydrogel technology falls short of reconstructing the intricacies of physiological structures such as organs or blood vessels. The Doyle Lab has previously combined microfluidics and photo-mask lithography and has shown that this technique called “stop-flow lithography” (SFL) is efficacious in high-throughput synthesis of geometrically and chemically anisotropic microstructures. We hypothesize that SFL-derived microstructures can act as essential building blocks for precisely engineering complex hydrogels with novel architecture.
- Panda P, Yuet KP, Hatton TA, and Doyle PS. Tuning curvature in flow lithography: a new class of concave/convex particles. Langmuir. 2009 May 19;25(10):5986-92. DOI:10.1021/la8042445 |
Nanoparticle-Mediated Delivery of siRNAs for Cancer Therapy
Targeted therapies have the benefits of lower toxicity and an improved therapeutic ratio. Recently, RNAi/small interfering RNAs (siRNA), a new class of therapeutic, have generated much enthusiasm in their application to diseases, especially cancer. However, the generation of an optimal in vivo carrier is required in order for siRNAs to develop into a viable therapeutic. We are currently developing an siRNA delivery system for prostate cancer therapy that utilizes multifunctional polymeric nanoparticles to encapsulate and protect siRNAs from non-specific nuclease degradation and deliver siRNAs specifically to targets using aptamers, oligonucleotides that fold into unique confirmations and bind to proteins with great affinity.
- Chan JM, Zhang L, Yuet KP, Liao G, Rhee JW, Langer R, and Farokhzad OC. PLGA-lecithin-PEG core-shell nanoparticles for controlled drug delivery. Biomaterials. 2009 Mar;30(8):1627-34. DOI:10.1016/j.biomaterials.2008.12.013 |
- Wang AZ, Bagalkot V, Vasilliou CC, Gu F, Alexis F, Zhang L, Shaikh M, Yuet K, Cima MJ, Langer R, Kantoff PW, Bander NH, Jon S, and Farokhzad OC. Superparamagnetic iron oxide nanoparticle-aptamer bioconjugates for combined prostate cancer imaging and therapy. ChemMedChem. 2008 Sep;3(9):1311-5. DOI:10.1002/cmdc.200800091 |
Massachusetts General Hospital (2006)
Alternative pre-mRNA Splicing
Splicing is the removal of non-coding regions of DNA, introns, from precursor messenger RNA (pre-mRNA)/heterogeneous nuclear RNA (hnRNA) in order to produce mature mRNAs for protein translation in eukaryotic cells and enables 3'-end processing, mRNA export, localization, and nonsense-mediated decay. Because alternative splicing substantially accounts for human proteome diversity, it is a desirable target relevant to many diseases. I am using Myocyte Enhancer Factor 2 (MEF2) genes as prototypes to study alternative splicing by developing an in vivo reporter of MEF2 splicing events that could be used to identify and evaluate cis-elements, factors, and signaling mechanisms that control splicing of these genes.
High-temperature superconducting tapes based on Yttrium Barium Copper Oxide (YBCO) coated conductors have the potential to transform the fields of electric power and high-energy physics. With YBCO conductor tapes nearing commercialization, there is a substantial need to characterize and optimize long-length coated conductors with higher current densities, longer tape length, and improved pinning properties. We are developing several position-dependent continuous critical measurement systems for studying tapes produced by various deposition methods.
Current Contact Info
Kai P. Yuet
MIT Department of Chemical Engineering
77 Massachusetts Avenue
Cambridge, MA 02139
kpyuet [at] MIT.edu
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