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Adv Pharm Bull. 2022;12(3): 509-514.
doi: 10.34172/apb.2022.053
PMID: 35935048
PMCID: PMC9348525
Scopus ID: 85140415991
  Abstract View: 842
  PDF Download: 430
  Full Text View: 259

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Multiwalled Carbon Nanotubes as Nanomaterial Tool in the Management of Prostate Cancer: A Possible Nanoformulation Approach

Raja Murugesan 1 ORCID logo, Raman Sureshkumar 1* ORCID logo, Arun Radhakrishnan 1, Srikanth Jupudi 2, Manisha Chennu 3

1 Department of Pharmaceutics, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Ooty, India.
2 Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Ooty, India.
3 Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Ooty, India.
*Corresponding Author: Corresponding Author: Raman Sureshkumar, Email: , Email: sureshcoonoor@jssuni.edu.in

Abstract

Prostate cancer (PCa) is one of the leading diseases in men all over the world caused due to over-expression of prostate-specific membrane antigen (PSMA). Currently, the detection and targeting of PCa is one of the major challenges in the prostate gland. Therefore, Bruton tyrosine kinase inhibitor molecules like ibrutinib (Ibr) loaded with nanomaterials like multiwalled carbon nanotubes (MWCNTs), which has good physico-chemical properties may be the best regimen to treat PCa. In this strategy, the chemically modified MWCNTs have excellent ‘Biosensing’ properties makes it easy for detecting PCa without fluorescent agent and thus targets particular site of PCa. In the present study, Ibr/MWCNTs conjugated with T30 oligonucleotide may selectively target and inhibit PSMA thereby reduce the over-expression in PCa. Hence, the proposed formulation design can extensively reduce the dosage regimen without any toxic effect. Additionally, the present hypothesis also revealed the binding mode of Ibr in the catalytic pocket of PSMA by in silico method. Therefore, we presume that if this hypothesis proves correct, it becomes an additional novel tool and one of the conceivable therapeutic options in treating PCa.
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Submitted: 02 Nov 2020
Revision: 10 Apr 2021
Accepted: 27 Sep 2021
ePublished: 29 Sep 2021
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