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Posted: Nov 13, 2015
Researchers design and patent graphene biosensors
(Nanowerk News) The Moscow Institute of Physics and Technology (MIPT) is patenting biosensor chips based on graphene, graphene oxide and carbon nanotubes that will improve the analysis of biochemical reactions and accelerate the development of novel drugs.
The US Patent Office has recently published the patent application (US 2015/0301039), which was filed by the MIPT in May this year and is titled Biological Sensor and a Method of the Production of Biological Sensor. In Russia, this development is already protected by the patent No. 2527699 with a priority date of February 20, 2013. The key feature of the sensor is the use of a linking layer for biomolecule immobilization comprising a thin film of graphene or graphene oxide.
The first biosensor chips based on graphene and its derivatives were presented by the MIPT at the Open Innovations 2015 Forum and Technology Show (28 Oct. - 1 Nov., 2015, Moscow, Russia).
Graphene is the first truly two-dimensional crystal, which was obtained experimentally and investigated regarding its unique chemical and physical properties. In 2010, two MIPT alumni, Andre Geim and Konstantin Novoselov were awarded the Nobel Prize in Physics “for ground-breaking experiments regarding the two-dimensional material graphene”. There has now been a considerable increase in the number of research studies aimed at finding commercial applications for graphene and other two-dimensional materials. One of the most promising applications for graphene is thought to be biomedical technologies, which is what researchers from the Laboratory of Nanooptics and Plasmonics at the MIPT’s Center of Excellence for Nanoscale Optoelectronics are currently investigating.
Label-free biosensors are relatively new in biochemical and pharmaceutical laboratories, and have made work much easier. The sensors enable researchers to detect low concentrations of biologically significant molecular substances (RNA, DNA, proteins, including antibodies and antigens, viruses and bacteria) and study their chemical properties. Unlike other biochemical methods, fluorescent or radioactive labels are not needed for these biosensors, which makes it easier to conduct an experiment, and also reduces the likelihood of erroneous data due to the effects that labels have on biochemical reactions.
The main applications of this technology are in pharmaceutical and scientific research, medical diagnostics, food quality control and the detection of toxins. Label-free biosensors have already proven themselves as a method of obtaining the most reliable data on pharmacokinetics and pharmacodynamics of drugs in pre-clinical studies.
The advantages of this method are explained by the fact that the kinetics of the biochemical reactions of the ligand (active substance) with different targets can be observed in real time, which allows researchers to obtain more accurate data about the reaction rates, which was not previously possible. The data obtained gives information about the efficacy of a drug and also its toxicity, if the targets are “healthy” cells or their parts, which the drug, ideally, should not affect.
Most label-free biosensors are based on the use of surface plasmon resonance (SPR) spectroscopy. The “resonance” parameters depend on the surface properties to such an extent that even trace amounts of “foreign” substances can significantly affect them. Biosensors are able to detect a trillionth of a gram of a detectable substance in an area of one square millimetre.
Commercial devices of this type are sold in a format similar to “razor blade” business model, which includes an instrument and highly expensive consumables. The instrument is the biosensor itself, comprising optics, microfluidics and electronics. The consumables for biosensors are sensor chips comprised of a glass substrate, thin gold film and a linking layer for the adsorption of biomolecules.
Sensor chips currently use two types of linking layer technology that were developed more than 20 years ago and are based either on a layer of self-assembled thiol molecules, or a layer of hydrogel (usually carboxymethyl dextran). The profit that companies have received from the sale of biosensors and consumables is evenly distributed at a ratio of 50:50.
The authors of the patent, Aleksey Arsenin and Yury Stebunov, are proposing an alternative to existing sensor chips for biosensors based on surface plasmon resonance. Under certain conditions, the use of graphene or graphene oxide as a linking layer between metal film and a biological layer comprised of molecule targets is able to significantly improve the sensitivity of biodetection. The graphene sensor chips were tested on Biacore™ T200 (General Electric Company) and BiOptix 104sa biosensors.
Schematic cross-sectional view of the graphene biosensor chip from US Patent Application No. 2015/0301039 (Oct 2015).
The use of graphene oxide sensor chips to analyse DNA hybridization reactions is described in detail in a recent paper by the authors in the American Chemical Society’s journal ACS Applied Materials & Interfaces ("Highly Sensitive and Selective Sensor Chips with Graphene-Oxide Linking Layer"). In addition to a higher level of sensitivity than similar commercial products, the proposed sensor chips possess the required property of biospecificity and can be used multiple times, which greatly reduces the costs of conducting biochemical studies using the chips.
The use of graphene increases the sensitivity of analyses conducted using SPR spectroscopy more than ten times, which will revolutionize the field of pharmaceutical biodetection. The application of biosensors is currently limited to analysing biological products based on large molecules, whilst more than half of the drugs produced each year have a low molecular weight (no more than a few hundred Daltons). Immobilization of drug targets on the surface of a graphene chip will enable scientists to test the interaction between targets and small molecules.
An example of this could be the development of drugs that act on receptors coupled with G-proteins (GPCRs), which are currently the targets for 40% of drugs on the market. Pharmaceutical studies of drugs acting on GPCRs are not currently conducted using SPR due to the insufficient sensitivity of the method. It is therefore expected that the use of graphene biosensors in pharmaceutical studies will help to accelerate the development of drugs and overcome dangerous diseases that cannot be treated with the drugs currently on the pharmaceutical market.
The authors are continuing to work to improve their development and expect that for certain reactions, biosensor chips based on the new carbon materials will provide a level of sensitivity that is dozens or hundreds of times higher than similar commercial products currently on the market. They are also considering the possibility of commercializing graphene chips. In 2014 alone, approximately 10 billion US dollars were spent on pre-clinical studies. According to estimates, the annual market for biosensor chips is worth a total of approximately 300 million US dollars. The excellent properties of graphene biosensor chips will enable them to compete strongly with existing types of chips – up to one third of the entire market.
Source: Moscow Institute of Physics and Technology