{"title":"Clinical perspective of multiple drug resistance tuberculosis: An overview","authors":"Arpit Raj , Vikrant Abbot , Kapil Kumar","doi":"10.1016/j.micpath.2025.108115","DOIUrl":null,"url":null,"abstract":"<div><div>The rational drug design and development of new medication requires an appropriate understanding of the pharmacokinetics and pharmacodynamics of <em>anti</em>-TB drugs. Nevertheless, the implementation and processing of drugs were not quite effective at the early stage of development that results in massive challenges in treating TB. Tuberculosis is one of the most common illnesses that kills people by attacking the parenchymal tissues of the lungs. Even the presence of <em>anti</em>-TB approved drugs in market suffering a failure due to evolving bacterial that possess resistant and responsible for MDR and XDR. The paradigm shift in <em>Anti</em>-TB medication shown by nanotechnology approach because of its distinct physio-chemical and optical properties, nanotechnology shows an emerging interdisciplinary science that offers a great chance for the prompt and accurate detection and differentiation of Mycobacteria. In this nanoscale approach, medication was encapsulated by NPs that can reduce dosing requirements. With several advantage, it is now being used as both diagnostic and therapeutic procedures since past ten years. To invade this alarming situation, this article will give shed on all the recent approaches that were made to make the <em>Anti</em>-TB drug more therapeutic and efficacious. It also covers government's initiative plans that were helpful in reducing the TB.</div></div>","PeriodicalId":18599,"journal":{"name":"Microbial pathogenesis","volume":"209 ","pages":"Article 108115"},"PeriodicalIF":3.5000,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial pathogenesis","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S088240102500840X","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The rational drug design and development of new medication requires an appropriate understanding of the pharmacokinetics and pharmacodynamics of anti-TB drugs. Nevertheless, the implementation and processing of drugs were not quite effective at the early stage of development that results in massive challenges in treating TB. Tuberculosis is one of the most common illnesses that kills people by attacking the parenchymal tissues of the lungs. Even the presence of anti-TB approved drugs in market suffering a failure due to evolving bacterial that possess resistant and responsible for MDR and XDR. The paradigm shift in Anti-TB medication shown by nanotechnology approach because of its distinct physio-chemical and optical properties, nanotechnology shows an emerging interdisciplinary science that offers a great chance for the prompt and accurate detection and differentiation of Mycobacteria. In this nanoscale approach, medication was encapsulated by NPs that can reduce dosing requirements. With several advantage, it is now being used as both diagnostic and therapeutic procedures since past ten years. To invade this alarming situation, this article will give shed on all the recent approaches that were made to make the Anti-TB drug more therapeutic and efficacious. It also covers government's initiative plans that were helpful in reducing the TB.
期刊介绍:
Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports.
Research Areas Include:
-Pathogenesis
-Virulence factors
-Host susceptibility or resistance
-Immune mechanisms
-Identification, cloning and sequencing of relevant genes
-Genetic studies
-Viruses, prokaryotic organisms and protozoa
-Microbiota
-Systems biology related to infectious diseases
-Targets for vaccine design (pre-clinical studies)