Page 47 - ITU Journal Future and evolving technologies Volume 2 (2021), Issue 3 – Internet of Bio-Nano Things for health applications
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ITU Journal on Future and Evolving Technologies, Volume 2 (2021), Issue 3




          overview of transmitter and receiver nano‑systems has  drugs  can  be  delivered  to  the  malignant  cell  while  min‑
          been provided in [17]. A survey related to transmitter and  imizing  the  drug  delivery  to  healthy  cells.  Fig.  3  shows
          receiver architectures has been published in [18], where  the  static  nano‑machines  bound  to  the  endothelial  cells.
          some of the modulation, coding, and detection techniques  However,  the  signaling  molecules  reach  the  receiver  via
          have been discussed. In addition to these techniques, a  drift and diffusion inside the blood vessel.  This case can
          Graphene‑based transmitter and bio‑Field Effect Transis‑  be found in the application of blood viscosity monitoring
          tor (bio‑FET)‑based receiver have been described to real‑  [9]  and  other  health  monitoring  applications.  In  Fig.  4
          ize the MC based systems.                            the  nano‑machines  and  the  signaling  molecules  are  mo‑
                                                               bile  and  follow  Brownian  motion  (free  diffusion).  This
          A cooperative drug delivery system was discussed in [19]  scenario can arise in the TDD application within the Ex‑
          where multiple mobile nano‑machines communicate and
                                                               tracellular Fluid (ECF) [25] as the movement of transmit‑
          deliver drugs in cooperative manner. More speci ically,
                                                               ter/receiver within ECF is governed by free diffusion. Fig.
          the leader nano‑machines sense the presence of a tar‑
                                                               5 shows that the nano‑machines and signaling molecules
          get and release the attractant molecules in the environ‑
                                                               are  mobile  under  the  in luence  of  drift  and  diffusion  in‑
          ment. The follower nano‑machines subsequently sense
                                                               side  the  blood  vessel.  Mobile  nano‑machines  inside  the
          the attractant molecules and move towards the target
                                                               blood vessels can be used for early detection of biomark‑
          for releasing drugs. Channel modeling for an MC‑based
                                                               ers released by cancer cells in the blood vessels [15]. This
          system considering different types of transmitters (e.g.,  is also a health monitoring application.
          point, volume and ion channel based), and receivers (e.g.,
          passive, fully absorbing and reactive) has been studied  Also, different types of MC systems have been proposed in
          in [20]. A survey on biological building blocks for MC  the literature in which the simplest case considers a single
          has been presented in [21] where the transmitter and  transmitter and receiver. An example of a single transmit‑
          receiver for different types of signaling particles (i.e.,  ter and receiver communicating in a  low‑based channel
          cations, neurotransmitters, and phosphopeptides) have  is shown in Fig.  6.  A wearable device with a transmitter
          been described. This work also discussed the biologi‑  and receiver is implanted over human skin for monitoring
          cal approach for Inter‑Symbol Interference (ISI) mitiga‑  the  blood  viscosity.  The  transmitter  releases  molecules
          tion. Further, a survey on modulation techniques for  through  a  needle  and  these  molecules  pass  through  the
          molecular communication has been presented in [22].  blood vessel.  On the other hand,  the statistics of the re‑
          In [22], the modulation techniques have been classi ied  ceived signal are monitored at the receiver since the diffu‑
          as concentration‑based, type‑based, release‑time‑based,  sion coef icient of the released molecules varies with vis‑
          spatial techniques and higher order modulations. More‑  cosity of blood which in turn change the statistics of the
          over, the metrics used for evaluating the performance of  received signal. This setup can be useful for detecting the
          modulation schemes are also presented therein.       hyper‑viscosity syndrome [9].

          In contrast to these existing survey papers, this survey  This  simple  case  is  further  extended  for  the  Multiple‑
          paper comprehensively focuses only on the transmission  Input  Multiple‑Output  (MIMO)  scenario  to  enhance  the
          and detection techniques present in the existing litera‑  data rate by dividing the bit stream among multiple trans‑
          ture under different channel conditions. It is worth not‑  mit  antennas.  As  shown  in  Fig.  7,  these  MIMO‑MC  sys‑
          ing that the modeling of the channel is different for differ‑  tems can also be used for improving the rate of drug de‑
          ent applications. Therefore, this paper also classi ies the  livery by using multiple transmitters and receivers. Here a
          transmission and detection techniques based on the ap‑  transmitter (e.g., controller nano‑machine) can sense the
          plications. Broadly we discuss four different scenarios as  amount of drug required over the cell surface and sends a
          shown in Fig. 1: (i) static nano‑machines communicating  signal to the receiver for drug delivery [26].  The receiver
          in pure‑diffusive channel without drift or  low, (ii) static  carrying  drug  molecules  can  deliver  the  drug  molecules
          nano‑machines under a  low‑induced diffusive channel  at the cell surface after receiving the signaling molecules
          which experiences diffusion as well as drift, (iii) mobile  from the transmitter.  This process can be faster if more
          nano‑machines under a pure‑diffusive channel, and (iv)  than one transmitter and receiver are used for drug deliv‑
          mobile nano‑machines under the  low‑induced diffusive  ery.  Further,  note  that  in  diffusion‑based  MC,  the  range
          channel. Further, we discuss the transmission and de‑  of communication is limited due to the loss of molecules
          tection for relay‑assisted‑based MC systems, cooperative  caused by the random Brownian motion. Therefore, to in‑
          or distributed‑detection‑based MC systems, MIMO‑based  crease the range of communication, an intermediate relay
          MC systems, and machine‑learning‑based MC systems un‑  node is introduced in between the transmitter and the re‑
          der all four possible scenarios described above.     ceiver.
          The  irst static transmitter and receiver scenario is shown  On  the  other  hand,  cooperative  or  distributed  detection
          in Fig. 2, where nano‑machines reach the cell surface re‑  is  proposed  mostly  for  abnormality  detection  problems,
          ceptor and can communicate over the cell surface. Such  where multiple receivers send their individual decision to
          a con iguration of nano‑machines is present in the ap‑  a  Fusion  Center  (FC)  to  make  a  global  decision.
          plication of TDD over a cell surface [23], [24]. Here the





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