Soft Injectable Sutures for Dose-Controlled and Continuous Drug Delivery.

Transdermal drug delivery offers a promising alternative to traditional methods such as oral ingestion and hypodermic injection. Hypodermic injections are painful, while oral ingestion requires higher doses due to enzymatic degradation and poor absorption. While microneedles address the pain issue, they are limited to delivering small amounts of drugs and can be impractical due to peeling off with motion and sweat. Herein, this work proposes soft injectables using drug-carrying sutures for painless and localized sustained delivery in the dermis. These sutures can remain in place during delivery and are suitable for all skin types. Surgical sutures can also serve as open capillary microfluidic channels carrying drug from a wearable drug reservoir to enable long-term (weeks to months) transdermal drug delivery. The experiments focus on delivering 5-fluorouracil (5-FU), a cancer drug, and rhodamine B, a drug model. A fixed-length suture of 60 cm delivers 0.43 mg of 5-flurouracil in 15 min. The experiments also demonstrate a continuous drug delivery of rhodamine B for over 8 weeks at a rate of 0.0195 mL h-1 . The results highlight that soft injectable sutures are promising candidates for long-term sustained delivery of varying quantities of drugs over weeks period compared to hypodermic injection, oral ingestion, or microneedles.

A flow through device for simultaneous dielectrophoretic cell trapping and AC electroporation.

Isolation of cells and their transfection in a controlled manner is an integral step in cell biotechnology. Electric field approaches such as dielectrophoresis (DEP) offers a more viable method for targeted immobilization of cells without any labels. For transfection of cells to incorporate exogenous materials, electrical methods such as electroporation, are preferred over chemical and viral delivery methods since they minimally affect cell viability and can target many types. However prior approaches to both methods required multiple excitation sources, an AC source for DEP-based trapping and another DC source for electroporation. In this paper, we present a first of its kind flow through lab-on-chip platform using a single AC excitation source for combined trapping using negative dielectrophoresis (nDEP) and AC electroporation. Use of AC fields for electroporation eliminates the unwanted side effects of electrolysis or joule heating at electrodes compared to DC electroporation. Adjusting the flow rate and the electrical parameters of the incident AC field precisely controls the operation (trap, trap with electroporation and release). The platform has been validated through trapping and simultaneous transfection of HEK-293 embryonic kidney cells with a plasmid vector containing a fluorescent protein tag. Numerical scaling analysis is provided that indicates promise for individual cell trapping and electroporation using low voltage AC fields.

Cost-effective Fabrication of Chitosan Microneedles for Transdermal Drug Delivery.

In this paper we present fabrication of hollow and solid chitosan microneedles using a recently proposed low-cost and cleanroom-free fabrication method called Cross-Over Lines (COL) laser engraving. COL engraving is achieved using a commercial CO2 laser-cutter to create microneedle molds on acrylic sheet. PDMS is then casted on the acrylic sheet microneedle mold to create base PDMS microneedles which are then used to generate other polymeric needles. In this paper, we cast and cure chitosan solution on the base PDMS microneedles which easily detaches from PDMS needles on drying. The resulted microneedles are hollow chitosan microneedles. We also made solid microneedles by silanizing and casting PDMSon-PDMS microneedles. We report promising preliminary results on drug delivery using these hollow and solid chitosan microneedles.

Low-cost metamaterial-on-paper chemical sensor.

We present a disposable low cost paper-based metamaterial for sensing liquids based on their dielectric properties. The sensor is based on resonance shift due to the change in the effective capacitance of each resonator in the metamaterial array. Key novelty in the design is the implementation of metamaterial on low cost and ubiquitous paper substrate. This metamaterial-on-paper sensor is fabricated in a totally cleanroom-free process using wax printing and screen printing. Wax patterning of paper enables creation of microfluidic channels such that liquid analytes can be delivered to each metamaterial unit cell for sensing. Screen printing is used to implement disc shaped resonator unit cells. We demonstrate sensing of liquids: Oil, methanol, glycerol and water each showing an average resonance frequency shift of 1.12 (9.6%), 4.12 (35.4%), 8.76 (75.3%) and 11.63 GHz (100%) around the center frequency of around 94 GHz respectively. Being label-free, this approach can be expanded to sense other liquids based on their dielectric constants.