ALD/ALE 2022 Session AA1-TuM2: ALD for Medical Applications

Tuesday, June 28, 2022 10:45 AM in Room Auditorium

Tuesday Morning

Session Abstract Book
(288KB, May 7, 2022)
Time Period TuM2 Sessions | Abstract Timeline | Topic AA Sessions | Time Periods | Topics | ALD/ALE 2022 Schedule

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11:00 AM AA1-TuM2-2 Plasma-assisted ALD of IrO2 for Neuroelectronic Applications
Valerio Di Palma, Andrea Pianalto (University of Milano Bicocca, Department of Materials Science); Michele Perego, Graziella Tallarida (CNR-IMM, Unit of Agrate Brianza); Marco Fanciulli (University of Milano Bicocca, Department of Materials Science. CNR-IMM, Unit of Agrate Brianza)
Investigation in-vitro of neural networks is fundamental for the development of strategies to study neurological diseases such as Alzheimer’s. Large arrays of microelectrodes (MEAs), planar or micro/nanostructured, are commonly used to stimulate neurons and record their response to external stimuli. MEAs materials are selected to perform charge transfer towards the cells medium efficiently and in a reversible way. IrO2 has attracted attention in the field because of its pseudo-capacitive behavior, along with its stability and non-toxicity. In parallel atomic layer deposition (ALD) is confirmed as an efficient tool for the conformal functionalization of micro/nanostructured MEAs, with a good control of the thickness and of the physical properties of the film.
In this work we report on the ALD growth of IrO2 thin films and their physical/chemical characterization. The functional properties relevant for neuroelectronic applications, have been addressed with electrochemical measurements. We propose a new plasma-assisted ALD process, using (EtCp)Ir(CHD) as precursor and a mix of Ar/O2 plasma as reactant. The process exhibits a linear growth, with a growth per cycle of about 0.3 Å at 150°C. In-situ spectroscopic ellipsometry shows the typical step-like behavior, i.e. the thickness increases during precursor absorption and then it decreases, because of the ligands removal, during the O2 plasma step.
XRD analysis exhibits the characteristic peaks reported in the literature for the rutile phase of IrO2. Furthermore, XPS confirms the presence of Ir in the oxidation state of +4, characterized by the chemical shift of the Ir 4f7/2 component to 61.7 ± 0.1 eV. AFM characterization shows that ALD prepared IrO2 is smooth and conformal to the substrate. On smooth Al2O3 substrates, IrO2 RMS roughness is 0.7 ± 0.3 nm for a 24 nm thick layer. The chemical characterization via TOF-SIMS indicates that carbon content in the film is below the detection limit, indicating the good quality of the ALD prepared IrO2.
Electrochemical characterization of the IrO2/electrolyte interface was performed by impedance spectroscopy (EIS), cyclic voltammetry (CV) and voltage transient (VT) measurements, using a phosphate buffer solution (PBS) as electrolyte. The EIS results indicate that the interaction IrO2/PBS is purely capacitive, with no faradaic contribution involved in the charge transfer mechanism. In addition, CV measurements confirm that the faradaic contribution is negligible within the range from -0.8 to +0.8 V vs. Ag/AgCl. The charge injection capacity for ALD prepared IrO2 thin films determined by VT measurements is 1.40 mC, in line with the literature.
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11:15 AM AA1-TuM2-3 Atomic Layer Deposition (Ald) on 5-Aminosalicylic Acid for Delayed and Targeted Drug Release Treatment of Inflammatory Bowel Disease
Jaynlynn Sosa, Parag Banerjee (University of Central Florida)

The incidence of chronic diseases continues to increase worldwide. Exploring new treatment alternatives for chronically ill patients has therefore been an active field of research. To improve patient compliance and reduce harsh side effects, delayed drug release systems have been developed. However, the techniques currently used to coat pharmaceuticals still face limitations in specific site targeting, loading efficiency, and pH tunability when administered orally. To overcome these challenges, we demonstrate the potential of using atomic layer deposition (ALD) as a technique to coat 5-Aminosalicylic acid (5-ASA)—a pharmaceutical drug to treat inflammatory bowel disease—to control the release of 5-ASA throughout the gastrointestinal tract.

5-ASA drug release was investigated by coating 7 mm pellets with 300, 150, and 75 cycles of ALD Al2O3. All pellets were made using a hydraulic pellet press and were then coated using an ALD Fiji Veeco® system at a deposition temperature of 120oC to avoid the decomposition of the organic material. To understand the dissolution rate of the coated pellets, we performed kinetic studies using a UV-1800 Shimadzu spectrometer by monitoring the 5-ASA UV signal at 298 nm. Each pellet was analysed for extended periods of time (< 20,000 seconds) in acidic media with various pH’s to track dissolution rates. Successful coating on the 5-ASA powders was further characterized by high resolution transmission electron microscopy (TEM) and energy dispersive x-ray spectroscopy (EDX).

Through our investigation, we show ALD’s potential in coating 5-ASA as a proof-of concept to achieve delayed and controlled drug release that is tunable based on the ALD coating thickness/chemistry. Our research seeks to promote further research and interdisciplinary collaboration between ALD and pharmaceutical researchers to discover new pathways for personalized treatment for patients who suffer from chronic illnesses.

11:30 AM AA1-TuM2-4 Atomic Layer Deposition Enables Dimensionless, Biocompatible Encasings for Medical Implants Pro-Longing Their Lifetime
Juhani Taskinen, Riina Ritasalo, Marko Pudas, Tom Blomberg, Mikko Matvejeff (Picosun Oy)

All kinds of medical devices – various types of implants and wearables - must withstand the corrosive environment of salts, temperature variations, electrical stress, and pollutants, inside and outside the human body, for prolonged periods of time. Hermetic sealing of the device to protect it from the outside environment when used in contact with the human body, (and further to protect the body from the device) is a key step to enable a longer service lifetime, better patient safety, and lower number of replacement surgeries.

To make a robust protective sealing for the medical device, the film properties must fulfill many criteria. First and foremost, the film material needs to be non-toxic for human cells, i.e., biocompatible. Secondly, the film needs to function as an extremely good diffusion barrier against the ions and molecules present in body fluids, while also blocking any leaks (ion or molecular) from the device into the body. In addition, the adhesion of the film to the device surface needs to be high enough that delamination of the film will not occur.

Since Intel introduced ALD HfO2-based high-k into their mass production line in mid-2000’s1, ALD has been a gold standard coating method in various electronics industries, and it is now doing the same in the medical field. A key benefit of an ALD coating is that it is one of the very few ways to make a barrier that leaves no surface of the device “visible” to the surroundings, making the device “invisible” to human body fluids and the immune system. Without an immune response, ALD coated device lasts longer than devices that are coated through other methods. At the same time the ALD coatings are virtually dimensionless, e.g., enabling miniaturization of all MEMS devices and improving surface activity on orthopedic implants.

The advantages of ALD over other deposition techniques makes it a powerful method for applications where sensitive substrate materials combined with extreme demands on coating quality and temperature / chemical resistance are needed, such as those often seen in the medical applications.

We will present applications and use cases of ALD in the medical field.

Keywords:

Electronics, encasing, biocompatible, medical devices, electronic implants, implants, immunology

Ref. [1] K. Mistry et al., Electron Devices Meeting 2007, IEDM 2007, IEEE International (2007), pp. 247-250.

Session Abstract Book
(288KB, May 7, 2022)
Time Period TuM2 Sessions | Abstract Timeline | Topic AA Sessions | Time Periods | Topics | ALD/ALE 2022 Schedule