Targeted Redox Balancing through Pulmonary Nanomedicine Delivery Reverses Oxidative Stress Induced Lung Inflammation

Author:

Ghosh Ria12,Das Monojit34,Mondal Susmita2,Banerjee Amrita5,Roy Lopamudra6,Das Anjan Kumar7,Pal Debasish4ORCID,Bhattacharya Siddhartha Sankar4,Bhattacharyya Maitree1,Pal Samir Kumar2

Affiliation:

1. Department of Biochemistry University of Calcutta 35, Ballygunge Circular Rd Kolkata 700019 India

2. Department of Chemical and Biological Sciences S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake Kolkata 700 106 India

3. Department of Zoology Vidyasagar University, Rangamati Midnapore 721102 India

4. Department of Zoology Uluberia College University of Calcutta, Uluberia Howrah 711315 India

5. Department of Physics Jadavpur University 188, Raja S.C. Mallick Rd Kolkata 700032 India

6. Department of Applied Optics and Photonics University of Calcutta 92, Acharya Prafulla Chandra Rd, Machuabazar Kolkata 700009 India

7. Department of Pathology Coochbehar Government Medical College and Hospital, Kotwali Coochbehar 736101 India

Abstract

AbstractNon‐invasive delivery of drugs is important for the reversal of respiratory diseases essentially by‐passing metabolic pathways and targeting large surface area of drug absorption. Here, we study the inhalation of a redox nano medicine namely citrate functionalized Mn3O4 (C−Mn3O4) duly encapsulated in droplet evaporated aerosols for the balancing of oxidative stress generated by the exposure of Chromium (VI) ion, a potential lung carcinogenic agent. Our optical spectroscopic in‐vitro experiments demonstrates the efficacy of redox balancing of the encapsulated nanoparticles (NP) for the maintenance of a homeostatic condition. The formation of Cr‐NP complex as an excretion of the heavy metal is also demonstrated through optical spectroscopic and high resolution transmission optical microscopy (HRTEM). Our studies confirm the oxidative stress mitigation activity of the Cr‐NP complex. A detailed immunological assay followed by histopathological studies and assessment of mitochondrial parameters in pre‐clinical mice model with chromium (Cr) induced lung inflammation establishes the mechanism of drug action to be redox‐buffering. Thus, localised delivery of C−Mn3O4 NPs in the respiratory tract via aerosols can act as an effective nanotherapeutic agent against oxidative stress induced lung inflammation.

Publisher

Wiley

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