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BioMed Research International
Volume 2016 (2016), Article ID 1743472, 7 pages
http://dx.doi.org/10.1155/2016/1743472
Review Article

Microchips in Medicine: Current and Future Applications

Brown University, Providence, RI 02903, USA

Received 17 February 2016; Accepted 4 May 2016

Academic Editor: Fabio Sonvico

Copyright © 2016 Adam E. M. Eltorai et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

With the objective of improving efficacy and morbidity, device manufacturers incorporate chemicals or drugs into medical implants. Using multiple reservoirs of discrete drug doses, microchips represent a new technology capable of on-demand release of various drugs over long periods of time. Herein, we review drug delivery systems, how microchips work, recent investigations, and future applications in various fields of medicine.

1. Introduction of Drug Delivery Systems

As drug therapies become increasingly complex and effective in treating disease, the development of delivery systems has overcome challenges of achieving stable release rates, drug concentrations, and being at a specific site of action [1]. Traditional routes of administration, such as oral capsules or intravenous infusion, encounter problems in maintaining drug concentrations within the therapeutic window, wherein the drug is above a threshold for efficacy but not toxic to the patient. Thus, the design of delivery systems initially focused on attaining a sustained release of drug over a time interval. Much of this work focused on polymers and their material properties that allow for steady-state diffusion of drug out of the polymer or degradation of the polymer itself over time [2, 3]. In addition to sustained release, pulsatile delivery at variable time intervals is necessary for compounds, such as insulin or hormones of the anterior pituitary, for physiological functions that follow either circadian rhythm or a time structure [4, 5].

With advancement in technology, implantable controlled-release systems for drug delivery have emerged as a promising new class of drug formulation to translate pharmacological effect into clinical practice. Implantable drug delivery systems (IDDS) are currently grouped into three classifications: biodegradable/nonbiodegradable implants, implantable pump systems, and the newest atypical class of implants [6]. Biodegradable and nonbiodegradable implants are available as reservoir and matrix systems, which exhibit release kinetics based on system and surrounding parameters [7]. However, these formulations are not suitable for drugs that are unstable in vivo and need to be hermetically sealed, especially since new protein-based drugs become unstable upon water penetration. Some controlled-release microfluidic pumps, valves, and channels have been developed that utilize moving parts such as a pneumatic piston or electroosmotic pumping [8, 9]. However, limitations of drug instability, complexity of fabrication, and breakdown of moving parts hinder clinical translation of microfluidics [10].

As a result, the field of microfabrication demands the need for a new class of controlled-release delivery system of intelligent, programmable microelectronics. Microchips are capable of complex release patterns, simultaneously constant and pulsatile, increased accuracy, and isolation of the drug from the outside environment [11].

2. Overview of Microchips

2.1. Design and Components

Implanted microchips enable on-demand drug release [5, 12, 13]. Solid silicon microchips consist of hundreds of reservoirs filled with up to 1 mL drugs in an aseptic solid, liquid, or gel filing [14, 15]. The multireservoir microchips are hermetically sealed to avoid degradation and subsequently covered by an anode membrane which can be ablated electrothermally to release the reservoir contents [16] (Figures 13).

Figure 1: Microchip fabrication steps [23].
Figure 2: Microchip device schematic [23].
Figure 3: A microchip [24].

Understanding the components of microchips is best done in the context of how microchips are fabricated. Microchips are fabricated using the same well-developed technology as used for microelectronic integrated circuits and microelectromechanical systems (MEMS) [17], processes used to manufacture microdevices such as pressure sensors, accelerometers, flow sensors, inkjet printer heads, and micromirrors for projection [18]. To allow for accurate control of surface microarchitecture, microchips are created using repetitive thin-film deposition, photolithography, and etching (removing) [19].

Leveraging MEMS fabrication technology, the process begins with depositing an insulating or dielectric material on both sides of a substrate surface [20]. The substrate provides structural support to the device. Substrates have been made from ceramics, semiconductors, degradable polyethylene glycol, and most commonly silicon [21, 22]. Then using photolithography the insulating material is photomasked to a light-sensitive chemical resist onto the substrate, to pattern the desired geometric shape, serving as an etching mask. Various etching processes are used to generate the desired reservoir topography on one side of the insulator and substrate. On the yet-interrupted surface, an anode is created by laying electrode over the reservoir opening. The insulating material functions as the cathode. At the base of the to-be reservoir, the insulating material is removed and the reservoirs are filled with the drug solution of choice. Reservoir filling can be accomplished using injection/inkjet printing or spin coating methods. Wafer bonding—a method of hermetically encapsulating MEMS—is then used to cover and seal the reservoir [23].

2.2. Controlled Release

Microreservoir release is achieved by applying a voltage between the thin, metallic (e.g., copper or gold) anode membrane and a cathode to electrochemically dissolve the reservoir cover. This electrical potential can be activated wirelessly, external to the body, or secondary to metabolic changes in the host. The control circuitry can be integrated into the microchips. This circuitry includes a timer, demultiplexer, microprocessor, and input source (e.g., biosensor) [11]. Such controlled drug delivery can release drugs over months, on a preset or as needed schedule [24, 25].

3. Current Applications: Recent Studies and Patents

A survey of recent microchip developments, notable patents, and clinically relevant applications can inform about the position of microchips in medicine today, as well as motivating areas of further study. In 1998, the US Patent “Microchip Drug Delivery Devices” was awarded to Santini Jr. et al., which first outlined the parameters of a multireservoir microchip system with an active release system [26]. In 1999, Santini Jr. et al. debuted the first electrochemically activated drug delivery microchip [12]. In their device, release from individually dosed reservoirs is activated by applying an electric potential between the cathode and the anode—a thin gold membrane covering the specific reservoir to be deployed [12]. An extensive number of further advancements, notably including (but not limited to) refined fabrication methods [27], microchip flexibility for ophthalmic use and improved versatility [22], methods of operation [28], and details of wireless data and power transfer [29], have since been discovered and patented by the group.

Building on these studies, initial in vitro release studies determined whether microchip technology could achieve controlled release of a chosen therapeutic agent, with regular pulses of drug expulsion into the experimental system (Figure 4) [5]. Various molecular masses of PLGA copolymer (PLGA 4.4, 11, 28, or 64) were chosen as the reservoir membrane material of choice, with a 50 : 50 ratio of lactic acid and glycolic acid [5]. As seen with 3H-heparin release below, a consistent stepwise release of the drug was observed—correlating with each of the microchip reservoir membranes degrading and opening [5]. Similar results were achieved with 14C-dextran, 125I-HGH, and a combination of dextran and heparin. These findings provided evidence that controllable and pulsatile drug release from microchips was achievable in vitro, catalyzing in vivo experimental models. A 2007 study investigated the canine pharmacokinetic profiles of leuprolide—a polypeptide therapeutic indicated for prostate cancer and endometriosis treatment—when delivered in vivo via microchip reservoirs compared to subcutaneous injection [13]. The authors concluded that the pharmacokinetics of the two delivery methods were indeed comparable, yet the microchip method offered greater control over serum drug concentration [13]. Interestingly, the fibrous capsule that formed around the implant was found to not significantly affect the pharmacokinetic parameters of the drug—a notable consideration for human in vivo use, where bioadhesion to foreign material (conducive to equipment malfunction, altered performance, infection, etc.) is well documented.

Figure 4: Each symbol represents the testing of a single device. Each device was loaded with four drug reservoirs. For all drugs utilized, “the release times of the chemicals from the reservoirs increased as the molecular mass of the reservoir membrane polymers was increased” [5].
3.1. Brain Cancer

The first investigation of polymer microchip in vivo efficacy for brain cancer therapy provided evidence that microchips, paired with the correct application and therapeutic agents, could be clinically implemented. Varying doses of 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU), a brain cancer chemotherapeutic, were loaded onto microchips and subsequently implanted into the flank of rats, where gliosarcomas had been introduced (Figure 5) [30]. The microchip-mediated BCNU effect on tumor size was compared to the standard of care, BCNU delivery from homogenous polymer wafers [30]. By measuring the concurrent tumor size with treatment, the authors concluded that the microchip BCNU release matched the efficacy of the polymer wafer in a dose-dependent manner [30]. As seen in Figure 5, the BCNU chip achieved comparable suppression of tumor volume. Applications within chronic conditions such as brain cancer, in which continuous and controllable local drug delivery to a difficult-to-access anatomical location is desired, indicate promising emerging fields for microchip technology.

Figure 5: In comparison to the standard of care (inserted polymeric containing wafers containing the chemotherapeutic BCNU) microchip-mediated BCNU release achieved comparable levels of tumor volume suppression in the flank of rats [30].
3.2. Osteopenia and Osteoporosis

In 2012, Farra et al. investigated the human in vivo pharmacokinetics of human parathyroid hormone, hPTH(1-34), released from microchip devices in eight female patients with osteopenia or osteoporosis (Figure 6) [25]. Release from the devices was activated 8 weeks after implantation, to allow for formation of a tissue capsule [25]. The pharmacokinetic profiles of the parathyroid hormone released were found to be reproducible day-to-day by device and bioequivalent in comparison to injections of FORSTEO, the on-the-market hPTH(1-34) treatment [25]. Biomarkers of skeletal response and bone formation closely paralleled PK findings, and total biocompatibility, safety, and patient satisfaction were also documented [25].

Figure 6: Biocompatibility of the implant was demonstrated, with normal immune responses and wound healing markers observed in six of seven implants. In addition, the release kinetics of the drug (along with its efficacy) were not impaired despite tissue capsule formation around implant [25].
3.3. Abdominal Implantation

A concern of implementing microchips for drug release is the development of a tissue capsule around the microchip device, which could alter the release kinetics of the bioactive agent and decrease efficacy. Based on serum samples, the investigators demonstrated that release kinetics were comparable to injections. Taking into consideration the potential deleterious effects or immune responses from the implant itself, the investigators subjected the microchip (and tissue capsule) to histology testing upon removal from the abdominal cavity (photo of microchip and tissue capsule is shown in Figure 6). Six of the seven capsules demonstrated normal wound healing responses, with healthy levels of inflammatory cells. The seventh capsule histology sample indicated an elevated level of macrophages but was still within normal limits [25]. These findings helped to further assuage concerns regarding the viability of microchip usage in humans.

In summary, the largest drawback to the study was found to be overall equipment functionality. One of the eight implanted devices failed to release any drug and was thus excluded from analysis [25]. Despite this malfunction, this landmark study demonstrated the convenient and efficacious application of microchips in medicine, as an alternative to treatment with multiple regular injections.

4. Future Applications

The widespread application of microchip technology has the potential to be transformative to the modern healthcare system. Therapeutic processes will be changed, billions of dollars worth of unnecessary expenses will be avoided, and the quality of life of patient populations will increase.

While human studies involving microchips have been limited to treating a few specific diseases, advancements will allow expansion of this technology into a larger range of therapeutic areas. Drugs with dose delivery systems which would otherwise be considered difficult or undesirable could take place in passive manners. Treatments for diseases such as diabetes and hypertension where dose titrations are necessary could be revolutionized to create automated therapy regimens that are safer and more efficacious. When used in conjunction with implants, this controlled-release technology will decrease the likelihood of foreign body responses and rejection, therefore lowering the probability of inflammation and pain, allowing the body to heal faster after surgery. Applications of microchips could be extended to create artificial glands. Regulations of hormones in the body associated with dysfunctional glands could aid in both controlling current disease states and preventing the onset of other hormone prompted disorders.

Microchip delivery systems will aid in the treatments for diseases that classically include a lower rate of compliance (mental disorders, some cancer therapeutics, long-term antibiotics, etc.) or potential for abuse. An expansion in patient compliance will save billions in healthcare expenses every year through the reductions in hospital stays, doctor visits, and failures to follow prescriptions. Drug abuse could be better regulated for patients who receive schedules II and III classified treatments. Patients with addiction prior to implantation could be weaned off of their medication until they receive the intended set of benefits.

With advances in microchip technology itself, as well as trials demonstrating pulsatile release, stable drug pharmacokinetics, and utility and efficacy in treating disease states, microchip applicability is on the rise. Further research is required to establish clinical settings in which a drug (or health condition) requires local release, pulsatile control, and/or decreased compliance burden. Since the anode membrane is ablated electrothermally, the fate of the degraded byproducts on drug release, compatibility, and toxicity requires additional investigation in vivo.

Diabetes serves as the primary cause of death for 69,071 Americans every year, making it one of the top ten killers in the US. While still in development stages, microchip technology will have a large impact on the diabetes treatment landscape, saving the lives of hundreds of thousands of people. Current diabetes treatments are largely limited by delivery methods. Oral therapies offer a low bioavailability and relatively delayed impact. While liquid insulin (in the form of pumps or syringes) has a high bioavailability and fast entrance into the systemic circulation, patients are often deterred from considering it as a therapy option because of the need for self-injection. Furthermore, error in treatment occurs frequently with both methods of insulin therapy when patients give themselves the wrong dosage or forget to test their blood.

Construction of a high-level market model to forecast the future sales for a company that utilizes microchip technology begins with a measure of the size of the patient population and current statistics regarding treatment options. From these projections, estimates of conversion rates, pricing, and raw peak sales are determined (Table 1). Raw peak sales were calculated for the year 2035, which would be reasonable if preclinical trials were currently underway. This estimate was used for the sake of modeling potential sales since no date is known for the start of research into its application in the diabetes field. Though the technology already has evidence supporting its efficacy, its modeled early stage in development and the large number of competitors in the insulin market yield both a low probability of success and a low market share. With these numbers handicapping the sales projections, Company X would still be near $1 billion in peak sales, giving the application of microchip technology in the field of diabetes a blockbuster status.

Table 1: Market model, insulin for types 1 and 2 diabetes. Diabetes statistics providing estimates for population sizes were collected from the American diabetes association [31].

While the financial modeling in Table 1 is used in the context of one specific industry, microchip technology can be utilized in a number of different facets of the modern healthcare system. As a disruptive technology, microchips would produce analyses that would yield similar degrees of impacts on their respective industries.

Competing Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

  1. R. Langer, “Drug delivery and targeting,” Nature, vol. 392, no. 6679, supplement, pp. 5–10, 1998. View at Google Scholar · View at Scopus
  2. W. B. Liechty, D. R. Kryscio, B. V. Slaughter, and N. A. Peppas, “Polymers for drug delivery systems,” Annual Review of Chemical and Biomolecular Engineering, vol. 1, pp. 149–173, 2010. View at Publisher · View at Google Scholar · View at Scopus
  3. L. E. Kalantzi, E. Karavas, E. X. Koutris, and D. N. Bikiaris, “Recent advances in oral pulsatile drug delivery,” Recent Patents on Drug Delivery and Formulation, vol. 3, no. 1, pp. 49–63, 2009. View at Publisher · View at Google Scholar · View at Scopus
  4. A. Kikuchi and T. Okano, “Pulsatile drug release control using hydrogels,” Advanced Drug Delivery Reviews, vol. 54, no. 1, pp. 53–77, 2002. View at Publisher · View at Google Scholar · View at Scopus
  5. A. C. Richards Grayson, I. S. Choi, B. M. Tyler et al., “Multi-pulse drug delivery from a resorbable polymeric microchip device,” Nature Materials, vol. 2, no. 11, pp. 767–772, 2003. View at Publisher · View at Google Scholar · View at Scopus
  6. A. K. Dash and G. C. Cudworth II, “Therapeutic applications of implantable drug delivery systems,” Journal of Pharmacological and Toxicological Methods, vol. 40, no. 1, pp. 1–12, 1998. View at Publisher · View at Google Scholar · View at Scopus
  7. N. Rajgor, M. Patel, and V. H. Bhaskar, “Implantable drug delivery systems: an overview,” Systematic Reviews in Pharmacy, vol. 2, no. 2, pp. 91–95, 2011. View at Publisher · View at Google Scholar · View at Scopus
  8. S. Sharma, A. J. Nijdam, P. M. Sinha et al., “Controlled-release microchips,” Expert Opinion on Drug Delivery, vol. 3, no. 3, pp. 379–394, 2006. View at Publisher · View at Google Scholar · View at Scopus
  9. J. T. Santini, A. C. Richards, R. A. Scheidt, M. J. Cima, and R. S. Langer, “Microchip technology in drug delivery,” Annals of Medicine, vol. 32, no. 6, pp. 377–379, 2000. View at Publisher · View at Google Scholar · View at Scopus
  10. P. Woias, “Micropumps—past, progress and future prospects,” Sensors and Actuators B: Chemical, vol. 105, no. 1, pp. 28–38, 2005. View at Publisher · View at Google Scholar · View at Scopus
  11. J. T. Santini Jr., A. C. Richards, R. Scheidt, M. J. Cima, and R. Langer, “Microchips as controlled drug-delivery devices,” Angewandte Chemie—International Edition, vol. 39, no. 14, pp. 2396–2407, 2000. View at Publisher · View at Google Scholar · View at Scopus
  12. J. T. Santini Jr., M. J. Cima, and R. Langer, “A controlled-release microchip,” Nature, vol. 397, no. 6717, pp. 335–338, 1999. View at Publisher · View at Google Scholar · View at Scopus
  13. J. H. Prescott, S. Lipka, S. Baldwin et al., “Chronic, programmed polypeptide delivery from an implanted, multireservoir microchip device,” Nature Biotechnology, vol. 24, no. 4, pp. 437–438, 2006. View at Publisher · View at Google Scholar · View at Scopus
  14. J. H. Prescott, T. J. Krieger, S. Lipka, and M. A. Staples, “Dosage form development, in vitro release kinetics, and in vitro-in vivo correlation for leuprolide released from an implantable multi-reservoir array,” Pharmaceutical Research, vol. 24, no. 7, pp. 1252–1261, 2007. View at Publisher · View at Google Scholar · View at Scopus
  15. E. R. Proos, J. H. Prescott, and M. A. Staples, “Long-term stability and in vitro release of hPTH(1-34) from a multi-reservoir array,” Pharmaceutical Research, vol. 25, no. 6, pp. 1387–1395, 2008. View at Publisher · View at Google Scholar · View at Scopus
  16. J. M. Maloney, S. A. Uhland, B. F. Polito, N. F. Sheppard Jr., C. M. Pelta, and J. T. Santini Jr., “Electrothermally activated microchips for implantable drug delivery and biosensing,” Journal of Controlled Release, vol. 109, no. 1-3, pp. 244–255, 2005. View at Publisher · View at Google Scholar · View at Scopus
  17. S. Sant, S. L. Tao, O. Z. Fisher, Q. Xu, N. A. Peppas, and A. Khademhosseini, “Microfabrication technologies for oral drug delivery,” Advanced Drug Delivery Reviews, vol. 64, no. 6, pp. 496–507, 2012. View at Publisher · View at Google Scholar · View at Scopus
  18. J. Z. Hilt and N. A. Peppas, “Microfabricated drug delivery devices,” International Journal of Pharmaceutics, vol. 306, no. 1-2, pp. 15–23, 2005. View at Publisher · View at Google Scholar · View at Scopus
  19. S. L. Tao and T. A. Desai, “Microfabricated drug delivery systems: from particles to pores,” Advanced Drug Delivery Reviews, vol. 55, no. 3, pp. 315–328, 2003. View at Publisher · View at Google Scholar · View at Scopus
  20. M. J. Cima, R. S. Langer, and J. T. Santini Jr., “Massachusetts Institute of Technology, assignee. Fabrication of microchip drug delivery device,” US Patent US6123861, Sept 2000.
  21. K. E. Uhrich, S. M. Cannizzaro, R. S. Langer, and K. M. Shakesheff, “Polymeric systems for controlled drug release,” Chemical Reviews, vol. 99, no. 11, pp. 3181–3198, 1999. View at Publisher · View at Google Scholar · View at Scopus
  22. J. T. Santini Jr., M. J. Cima, and R. S. Langer, “Flexible microchip devices for ophthalmic and other applications,” MicroCHIPS Inc., Assignee, US Patent US6976982 B2, 2005.
  23. K. B. Sutradhar and C. D. Sumi, “Implantable microchip: the futuristic controlled drug delivery system,” Drug Delivery, vol. 23, no. 1, pp. 1–11, 2014. View at Publisher · View at Google Scholar
  24. Microchips Biotech, “Technology,” http://microchipsbiotech.com/.
  25. R. Farra, N. F. Sheppard Jr., L. McCabe et al., “First-in-human testing of a wirelessly controlled drug delivery microchip,” Science Translational Medicine, vol. 4, no. 122, Article ID 122ra21, 2012. View at Publisher · View at Google Scholar · View at Scopus
  26. J. T. Santini Jr., M. J. Cima, and R. S. Langer, “Microchip drug delivery devices,” US Patent US5797898, 1998.
  27. M. J. Cima, R. S. Langer, and J. T. Santini Jr., “Massachusetts Institute of Technology, assignee. Fabrication of microchip drug delivery device,” US Patent US6123861, 2000.
  28. J. T. Santini Jr., M. J. Cima, and R. S. Langer, “Massachusetts Institute of Technology, assignee. Method for operating microchip reservoir devices,” US Patent US7901397B2, 2011.
  29. N. F. Sheppard Jr., J. T. Santini Jr., S. J. Herman, M. J. Cima, R. S. Langer, and D. Ausiello, “Microchip reservoir devices using wireless transmission of power and data,” MicroCHIPS Inc., Assignee, US Patent US7226442 B2, 2007.
  30. G. Y. Kim, B. M. Tyler, M. M. Tupper et al., “Resorbable polymer microchips releasing BCNU inhibit tumor growth in the rat 9L flank model,” Journal of Controlled Release, vol. 123, no. 2, pp. 172–178, 2007. View at Publisher · View at Google Scholar · View at Scopus
  31. American Diabetes Association, Fast Facts: Data and Statistics about Diabetes, American Diabetes Association, Alexandria, Va, USA, 2015.