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Nanodrug delivery and antimicrobial agents          cytotoxicity. The same conjugates were shown to
            Peptide-polymer conjugates have been shown to       encapsulate a model hydrophobic molecule in the
            be a promising class of amphiphilic biomaterials    hydrophobic core with high  entrapment and
            wherein peptides are used as a  hydrophobic or      loading efficiency. The release was found to be in
            hydrophilic segment facilitating the  process of    a sustained manner with higher degree of release
            molecular self-assembly. Polymers, on the other     under neutral conditions (pH 7.4) advocating the
            hand, are heterogeneous materials with variable     potential of such materials for colonic delivery of
            chain  length,  composition,   hydrophilic  /       drugs.   Our  group has also been working on  to
            hydrophobic in nature. It is envisaged  that        develop polymeric  nanoconjugates as efficient
            combining these two can lead to the formation of    antimicrobials. For confronting the global issue of
            novel biomaterials where the  peptide segment       AMR, development of new classes of biologically
            may confer increased control over the nanoscale     as well as chemically synthesized compounds with
            structural features and toxicity, and the polymer   profound anti-bacterial/microbial activity, is the
            segment  may help in reducing immunogenicity        need of the hour. Such antimicrobials are required
            and prevent enzymatic degradation by acting as a    to kill  the  resistant bacteria  by one or the
            link between  peptide and the external              combination of the mechanisms. Recently, use of
            environment. Modified peptides with more            bactericidal polymers or combination therapy has
            rigidity and  stability  under cellular environment   attracted the attention where two antibiotics are
            can overcome the  concerns associated with the      co-administered or antibiotics along with an
            natural counterparts. Our group has been able to    activity enhancer. Our group has tried to explore
            demonstrate the applications of such biomaterials   the potential of polydopamine-aminoglycoside
            in the area of drug delivery including nucleic acid-  conjugates for this purpose. The  nanosized
            based therapeutics. These amphiphilic  polymer-     conjugates showed excellent biological activity not
            peptide conjugates acquired core-shell type of      only against clinical isolates but also against
            nanostructures  in   aqueous   medium    and        resistant strains without exhibiting cytotoxicity
            transported the nucleic acids inside the cells with   suggesting the promising  potential  of these
            high transfection efficiency without exerting       nanoconjugates.

            Publications
            Ultrashort peptide self-assembly: Front-runners to transport drug and gene cargos. Gupta S, Singh I, Sharma AK, Kumar
            P. Front Bioeng Biotechnol. 2020 May 29;8:504.

            In vitro assessment of core-shell micellar nanostructures of amphiphilic cationic polymer-peptide conjugates as efficient
            gene and drug carriers. Garg C, Priyam A, Kumar P, Sharma AK, Gupta A. J Pharm Sci. 2020 Sep;109(9):2847-2853.
            Biogenic Silver Nanoparticles: Evaluation of Their Biological and Catalytic Potential. Sharma B, Singh I, Bajar S, Gupta S,
            Gautam H, Kumar P. Indian J Microbiol. 2020 Dec;60(4):468-474.

            Supramolecular self-assemblies of engineered polyethylenimines  as  multifunctional  nanostructures  for  DNA
            transportation with excellent antimicrobial activity.  Singh R, Jha D, Gautam HK, Kumar P.  Bioorg Chem. 2021
            Jan;106:104463.Recent  Advances in a Polydopamine-Mediated Antimicrobial  Adhesion  System. Singh  I, Dhawan G,
            Gupta S, Kumar P. Front Microbiol. 2021 Jan 12;11:607099.
















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