Heavy metals cause considerable environmental pollution due to their extent and non-degradability in the environment. Analysis and trace levels of arsenic, lead, mercury, and cadmium as the most toxic heavy metals show that they can cause various hazards in humans' health. To achieve rapid, high-sensitivity methods for analyzing ultra-trace amounts of heavy metals in different environmental and biological samples, novel biosensors have been designed with the participation of strategies applied in nanotechnology. This review attempted to investigate the novel, sensitive, efficient, cost-benefit, point of care, and userfriendly biosensors designed to detect these heavy metals based on functional mechanisms. The study's search strategies included examining the primary databases from 2015 onwards and various keywords focusing on heavy metal biosensors' performance and toxicity mechanisms. The use of aptamers and whole cells as two important bio-functional nanomaterials is remarkable in heavy metal diagnostic biosensors' bioreceptor design. The application of hybridized nanomaterials containing a specific physicochemical function in the presence of a suitable transducer can improve the sensing performance to achieve an integrated detection system. Our study showed that in addition to both labeled and label-free detection strategies, a wide range of nanoparticles and nanocomposites were used to modify the biosensor surface platform in the detection of heavy metals. The detection limit and linear dynamic range as an essential characteristic of superior biosensors for the primary toxic metals are studied. Furthermore, the perspectives and challenges facing the design of heavy metal biosensors are outlined. The development of novel biosensors and the application of nanotechnology, especially in real samples, face challenges such as the capability to simultaneously detect multiple heavy metals, the interference process in complex matrices, the efficiency and stability of nanomaterials implemented in various laboratory conditions.
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MLN Med Coll, Dept Pharm, Prayagraj, Uttar Pradesh, IndiaMLN Med Coll, Dept Pharm, Prayagraj, Uttar Pradesh, India
Yadav, Sarita K. K.
Yadav, Rahul Deo
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MLN Med Coll, Dept Pharm, Prayagraj, Uttar Pradesh, IndiaMLN Med Coll, Dept Pharm, Prayagraj, Uttar Pradesh, India
Yadav, Rahul Deo
Tabassum, Heena
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Dr DY Patil Vidyapeeth, Dr D Y Patil Biotechnol & Bioinformat Inst, Pune, Maharashtra, IndiaMLN Med Coll, Dept Pharm, Prayagraj, Uttar Pradesh, India
Tabassum, Heena
Arya, Malti
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Chandra Shekhar Singh Coll Pharm, Dept Pharmaceut, Kaushambi, Uttar Pradesh, IndiaMLN Med Coll, Dept Pharm, Prayagraj, Uttar Pradesh, India
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Univ Sains Malaysia, Sch Med Sci, Human Genome Ctr, Kelantan 16150, Kubang Kerian, MalaysiaUniv Malaysia Kelantan, Fac Agrobased Ind, Jeli 17600, Kelantan, Malaysia
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Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30322 USA
Emory Univ, Atlanta, GA 30322 USA
Shanghai Jiao Tong Univ, State Key Lab Oncogenes & Related Genes, Renji Hosp,Inst Mol Med, Shanghai Key Lab Nucle Acid Chem & Nanomed,Sch Me, Shanghai 200127, Peoples R ChinaGeorgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30322 USA
Shen, Luyao
Wang, Pengfei
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Shanghai Jiao Tong Univ, State Key Lab Oncogenes & Related Genes, Renji Hosp,Inst Mol Med, Shanghai Key Lab Nucle Acid Chem & Nanomed,Sch Me, Shanghai 200127, Peoples R ChinaGeorgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30322 USA
Wang, Pengfei
Ke, Yonggang
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Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30322 USA
Emory Univ, Atlanta, GA 30322 USAGeorgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30322 USA