Inhalable particles containing isoniazid and rifabutin as adjunct therapy for safe, efficacious and relapse-free cure of experimental animal tuberculosis in one month. (May 2021)

• Record Type: Journal Article
• Authors: Singh, Amit K.; Verma, Rahul K.; Mukker, Jatinder Kaur; Yadav, Awadh B.; Muttil, Pavan; Sharma, Rolee; Mohan, Mradul; Agrawal, Atul K.; Gupta, Anuradha; Dwivedi, Anil K.; Gupta, Pushpa; Gupta, Umesh D.; Mani, Uthirappan; Chaudhari, Bhushan P.; Murthy, Ramesh C.; Sharma, Sharad; Bhadauria, Smrati; Singh, Sarika; Rath, Srikanta Kumar; Misra, Amit
• Is Part Of: Tuberculosis. Volume 128(2021)
• Publication Date: 2021-05
• Subjects: Adjunct therapy -- Pulmonary drug delivery -- Preclinical efficacy -- Preclinical safety/tolerability; 616.995
• DOI: 10.1016/j.tube.2021.102081
• Languages: English
• ISSNs: 1472-9792

Abstract

Abstract: We investigated the preclinical efficacy and safety/tolerability of biodegradable polymeric particles containing isoniazid (INH) and rifabutin (RFB) dry powder for inhalation (DPI) as an adjunct to oral first-line therapy. Mice and guinea pigs infected with Mycobacterium tuberculosis H37Rv (Mtb) were treated with ∼80 and ∼300 μg of the DPI, respectively, for 3–4 weeks starting 3, 10, and 30 days post-infection. Adjunct combination therapy eliminated culturable Mtb from the lungs and spleens of all but one of 52 animals that received the DPI. Relapse-free cure was not achieved in one mouse that received DPI + oral, human-equivalent doses (HED) of four drugs used in the Directly Observed Treatment, Short Course (DOTS), starting 30 days post-infection. Oral doses (20 mg/Kg/day, each) of INH + RFB reduced Mtb burden from ∼10 6 to ∼10 3 colony-forming units. Combining half the oral dose with DPI prevented relapse of infection four weeks after stopping the treatment. The DPI was safe in rodents, guinea pigs, and monkeys at 1, 10, and 100 μg/day doses over 90 days. In conclusion, we show the efficacy and safety/tolerability of the DPI as an adjunct to oral chemotherapy in three different animal models of TB.