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      International Journal of Nanomedicine (submit here)

      This international, peer-reviewed Open Access journal by Dove Medical Press focuses on the application of nanotechnology in diagnostics, therapeutics, and drug delivery systems throughout the biomedical field. Sign up for email alerts here.

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      A Novel Para-Amino Salicylic Acid Magnesium Layered Hydroxide Nanocomposite Anti-Tuberculosis Drug Delivery System with Enhanced in vitro Therapeutic and Anti-Inflammatory Properties

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          Abstract

          Introduction

          Mycobacterium tuberculosis infections are associated with severe local inflammatory reactions, which may be life-threatening and lead to tuberculosis pathogenesis and associated complications. Inorganic nanolayers have been vastly exploited for biomedical applications (especially in drug delivery) because of their biocompatible and biodegradable nature with the ability to release a drug in a sustained manner. Herein, we report a new nanodelivery system of inorganic nanolayers based on magnesium layered hydroxides (MgLH) and a successfully intercalated anti-tuberculosis drug para-aminosalicylic acid (PAS).

          Methods

          The designed anti-tuberculosis nanodelivery composite, MgLH-PAS, was prepared by a novel co-precipitation method using MgNO 3 as well MgO as starting materials.

          Results

          The designed nano-formulation, PAS-MgLH, showed good antimycobacterial and antimicrobial activities with significant synergistic anti-inflammatory effects on the suppression of lipopolysaccharide (LPS) stimulated inflammatory mediators in RAW 264.7 macrophages. The designed nano-formulation was also found to be biocompatible with human normal lung cells (MRC-5) and 3T3 fibroblast cells. Furthermore, the in vitro release of PAS from PAS-MgLH was found to be sustained in human body simulated phosphate buffer saline (PBS) solutions of pH 7.4 and pH 4.8.

          Discussion

          The results of the present study are highly encouraging for further in vivo studies. This new nanodelivery system, MgLH, can be exploited in the delivery of other drugs and in numerous other biomedical applications as well.

          Most cited references68

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          Inflammatory responses and inflammation-associated diseases in organs

          Inflammation is a biological response of the immune system that can be triggered by a variety of factors, including pathogens, damaged cells and toxic compounds. These factors may induce acute and/or chronic inflammatory responses in the heart, pancreas, liver, kidney, lung, brain, intestinal tract and reproductive system, potentially leading to tissue damage or disease. Both infectious and non-infectious agents and cell damage activate inflammatory cells and trigger inflammatory signaling pathways, most commonly the NF-κB, MAPK, and JAK-STAT pathways. Here, we review inflammatory responses within organs, focusing on the etiology of inflammation, inflammatory response mechanisms, resolution of inflammation, and organ-specific inflammatory responses.
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            Hydrotalcite-type anionic clays: Preparation, properties and applications.

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              Innate immunity in tuberculosis: host defense vs pathogen evasion

              The major innate immune cell types involved in tuberculosis (TB) infection are macrophages, dendritic cells (DCs), neutrophils and natural killer (NK) cells. These immune cells recognize the TB-causing pathogen Mycobacterium tuberculosis (Mtb) through various pattern recognition receptors (PRRs), including but not limited to Toll-like receptors (TLRs), Nod-like receptors (NLRs) and C-type lectin receptors (CLRs). Upon infection by Mtb, the host orchestrates multiple signaling cascades via the PRRs to launch a variety of innate immune defense functions such as phagocytosis, autophagy, apoptosis and inflammasome activation. In contrast, Mtb utilizes numerous exquisite strategies to evade or circumvent host innate immunity. Here we discuss recent research on major host innate immune cells, PRR signaling, and the cellular functions involved in Mtb infection, with a specific focus on the host’s innate immune defense and Mtb immune evasion. A better understanding of the molecular mechanisms underlying host–pathogen interactions could provide a rational basis for the development of effective anti-TB therapeutics.
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                Author and article information

                Journal
                Int J Nanomedicine
                Int J Nanomedicine
                ijn
                International Journal of Nanomedicine
                Dove
                1176-9114
                1178-2013
                15 October 2021
                2021
                : 16
                : 7035-7050
                Affiliations
                [1 ]Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology (ITMA), Universiti Putra Malaysia , Serdang, Selangor, Malaysia
                [2 ]Department of Management Sciences and Technology, The Begum Nusrat Bhutto Women University Sukkur , Sukkur, Sindh, 65170, Pakistan
                [3 ]Laboratory for Vaccine and Immunotherapeutics, Institute of Biosciences, University Putra Malaysia , Serdang, Selangor, 43400, Malaysia
                [4 ]Muthayammal Centre for Advanced Research, Muthayammal College of Arts and Science , Namakkal, Tamil Nadu, 637408, India
                [5 ]Zoonosis Science Center, Department of Microbiology and Immunology, Uppsala University , Uppsala, Sweden
                [6 ]Department of Human Anatomy, Faculty of Medicine and Health Science, Universiti Putra Malaysia , Serdang, Selangor, Malaysia
                [7 ]Department of Chemical Engineering, Northeastern University , Boston, MA, USA
                Author notes
                Correspondence: Mohd Zobir Hussein Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology, (ITMA), Universiti Putra Malaysia , Serdang, Selangor, Malaysia Tel +60 397698092 Email mzobir@upm.edu.my
                Author information
                http://orcid.org/0000-0002-1835-9738
                http://orcid.org/0000-0002-1056-4761
                http://orcid.org/0000-0002-2028-5969
                http://orcid.org/0000-0001-5066-7784
                http://orcid.org/0000-0002-0741-261X
                Article
                297040
                10.2147/IJN.S297040
                8526802
                f7497200-f42a-4c4f-b109-9ccbd7d70ba0
                © 2021 Saifullah et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 20 January 2021
                : 09 June 2021
                Page count
                Figures: 11, Tables: 1, References: 69, Pages: 16
                Funding
                Funded by: Universiti Putra Malaysia and the Ministry of Higher Education of Malaysia;
                The study was funded in part by funds from the Universiti Putra Malaysia and the Ministry of Higher Education of Malaysia (grant UPM/800‐3/3/1/GBP/2019/9678800) and Northeastern University, USA.
                Categories
                Original Research

                Molecular medicine
                mycobacterium tuberculosis,magnesium layered hydroxides,biomaterial,sustained release,anti-tuberculosis,anti-inflammatory

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