56 research outputs found

    A 3D-printed microfluidic-enabled hollow microneedle architecture for transdermal drug delivery.

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    Embedding microfluidic architectures with microneedles enables fluid management capabilities that present new degrees of freedom for transdermal drug delivery. To this end, fabrication schemes that can simultaneously create and integrate complex millimeter/centimeter-long microfluidic structures and micrometer-scale microneedle features are necessary. Accordingly, three-dimensional (3D) printing techniques are suitable candidates because they allow the rapid realization of customizable yet intricate microfluidic and microneedle features. However, previously reported 3D-printing approaches utilized costly instrumentation that lacked the desired versatility to print both features in a single step and the throughput to render components within distinct length-scales. Here, for the first time in literature, we devise a fabrication scheme to create hollow microneedles interfaced with microfluidic structures in a single step. Our method utilizes stereolithography 3D-printing and pushes its boundaries (achieving print resolutions below the full width half maximum laser spot size resolution) to create complex architectures with lower cost and higher print speed and throughput than previously reported methods. To demonstrate a potential application, a microfluidic-enabled microneedle architecture was printed to render hydrodynamic mixing and transdermal drug delivery within a single device. The presented architectures can be adopted in future biomedical devices to facilitate new modes of operations for transdermal drug delivery applications such as combinational therapy for preclinical testing of biologic treatments

    Hydrogel‐Enabled Transfer‐Printing of Conducting Polymer Films for Soft Organic Bioelectronics

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    The use of conducting polymers such as poly(3,4‐ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) for the development of soft organic bioelectronic devices, such as organic electrochemical transistors (OECTs), is rapidly increasing. However, directly manipulating conducting polymer thin films on soft substrates remains challenging, which hinders the development of conformable organic bioelectronic devices. A facile transfer‐printing of conducting polymer thin films from conventional rigid substrates to flexible substrates offers an alternative solution. In this work, it is reported that PEDOT:PSS thin films on glass substrates, once mixed with surfactants, can be delaminated with hydrogels and thereafter be transferred to soft substrates without any further treatments. The proposed method allows easy, fast, and reliable transferring of patterned PEDOT:PSS thin films from glass substrates onto various soft substrates, facilitating their application in soft organic bioelectronics. By taking advantage of this method, skin‐attachable tattoo‐OECTs are demonstrated, relevant for conformable, imperceptible, and wearable organic biosensing.The use of hydrogels enables transfer‐printing of poly(3,4‐ethylenedioxythiophene):polystyrene sulfonate thin films from glass substrates onto various soft substrates. Taking advantage of this technique, skin‐attachable organic electrochemical transistors (OECTs) are fabricated on commercially available tattoo paper. Wearable tattoo‐OECTs are further demonstrated with the integration of a wireless readout system.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/154307/1/adfm201906016.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/154307/2/adfm201906016_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/154307/3/adfm201906016-sup-0001-SuppMat.pd

    An Autonomous 3D Biofluid Management and Analysis Lab-on-the-Body Platform for Point-of-Person Biomarker Monitoring Applications

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    Personal biomarker sensors are poised to transform personalized medicine by providing frequent and real-time measures of biomarker molecules, thus catalyzing the transition from point-of-lab and point-of-care testing to near-continuous monitoring at the point-of-person. To realize the full range of possibilities offered by such wearable and mobile sensors, in-situ active microfluid management capabilities are fundamentally required. Previously reported non-invasive wearable and mobile biomarker sensors rely on the in-situ analysis of biofluid samples that are passively collected in absorbent pads or 2D microfluidic housings. The spatial constraints of these platforms and their lack of active control on biofluid inherently limit the efficiency, diversity and frequency of end-point assessments. Here, by devising a suite of programmable electro-fluidic interfaces, integrated within a multi-layer flexible microfluidic device, we demonstrate key biofluid management functionalities, including biofluid flow actuation and compartmentalization, for autonomous lab-on-the-body sample analysis. System-level functionality is achieved by interfacing the microfluidic device with a wireless circuit board. The desired operations are validated on-body through human subject testing. The versatility of these unprecedented lab-on-the-body methodologies enables a wide-ranging complex sample processing and analysis operations that can converge to realize point-of-person monitoring platforms
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