| Literature DB >> 33321797 |
Zhi Ming Tan1, Gui Ping Lai1, Manisha Pandey2,3, Teerapol Srichana4,5, Mallikarjuna Rao Pichika3,6, Bapi Gorain7,8, Subrat Kumar Bhattamishra9, Hira Choudhury2,3.
Abstract
Tuberculosis (TB) is a contagious airborne disease caused by Mycobacterium tuberculosis, which primarily affects human lungs. The progression of drug-susceptible TB to drug-resistant strains, MDR-TB and XDR-TB, has become worldwide challenge in eliminating TB. The limitations of conventional TB treatment including frequent dosing and prolonged treatment, which results in patient's noncompliance to the treatment because of treatment-related adverse effects. The non-invasive pulmonary drug administration provides the advantages of targeted-site delivery and avoids first-pass metabolism, which reduced the dose requirement and systemic adverse effects of the therapeutics. With the modification of the drugs with advanced carriers, the formulations may possess sustained released property, which helps in reducing the dosing frequency and enhanced patients' compliances. The dry powder inhaler formulation is easy to handle and storage as it is relatively stable compared to liquids and suspension. This review mainly highlights the aerosolization properties of dry powder inhalable formulations with different anti-TB agents to understand and estimate the deposition manner of the drug in the lungs. Moreover, the safety profile of the novel dry powder inhaler formulations has been discussed. The results of the studies demonstrated that dry powder inhaler formulation has the potential in enhancing treatment efficacy.Entities:
Keywords: advanced drug delivery; barriers of pulmonary delivery; lung delivery; lung physiology; metered-dose inhaler; proliposome; tuberculosis
Year: 2020 PMID: 33321797 PMCID: PMC7763148 DOI: 10.3390/pharmaceutics12121196
Source DB: PubMed Journal: Pharmaceutics ISSN: 1999-4923 Impact factor: 6.321