Author/Authors :
Murugesan, Raja Department of Pharmaceutics - JSS College of Pharmacy - JSS Academy of Higher Education & Research, Ooty, India , Sureshkumar, Raman Department of Pharmaceutics - JSS College of Pharmacy - JSS Academy of Higher Education & Research, Ooty, India , Radhakrishnan, Arun Department of Pharmaceutics - JSS College of Pharmacy - JSS Academy of Higher Education & Research, Ooty, India , Jupudi, Srikanth Department of Pharmaceutical Chemistry - JSS College of Pharmacy - JSS Academy of Higher Education & Research, Ooty, India , Chennu, Manisha Department of Pharmacology - JSS College of Pharmacy - JSS Academy of Higher Education & Research, Ooty, India
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.
Keywords :
Prostate cancer , Drug delivery , In silico studies , Carbon nanotubes