TY - JOUR
T1 - Development and characterization of spray-dried porous nanoaggregates for pulmonary delivery of anti-tubercular drugs
AU - Kaur, Ranjot
AU - Garg, Tarun
AU - Malik, Basant
AU - Gupta, Umesh Datta
AU - Gupta, Pushpa
AU - Rath, Goutam
AU - Goyal, Amit Kumar
N1 - Generated from Scopus record by KAUST IRTS on 2023-10-12
PY - 2016/3/23
Y1 - 2016/3/23
N2 - Tuberculosis, MTB or tubercle bacillus (TB) is a lethal, infectious disease mainly caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. In this study, guar gum-based porous nanoaggregates were formulated by precipitation technique with two frontline antitubercular drugs, i.e. isoniazid and rifampicin. The formulations were optimized on the basis of various evaluation parameters such as morphology, density, entrapment efficiency and in vitro drug release. The optimized formulations were administered by inhalable route to Wistar rats for the evaluation of drugs in different organs (lungs, liver and kidneys). High drug encapsulation efficiency was achieved in guar gum porous nanoaggregates, ranging from 50% to 60%. A single pulmonary dose resulted in therapeutic drug concentrations of 30%-50% in the lungs and in other organs (less than 5%) for 24 h. From this study, we can conclude that delivering drugs through pulmonary route is advantageous for local action in lungs. Furthermore, the formulation showed sustained drug release pattern, which could be beneficial for reducing the drug dose or frequency of dosing, thus helpful in improving patient compliance.
AB - Tuberculosis, MTB or tubercle bacillus (TB) is a lethal, infectious disease mainly caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. In this study, guar gum-based porous nanoaggregates were formulated by precipitation technique with two frontline antitubercular drugs, i.e. isoniazid and rifampicin. The formulations were optimized on the basis of various evaluation parameters such as morphology, density, entrapment efficiency and in vitro drug release. The optimized formulations were administered by inhalable route to Wistar rats for the evaluation of drugs in different organs (lungs, liver and kidneys). High drug encapsulation efficiency was achieved in guar gum porous nanoaggregates, ranging from 50% to 60%. A single pulmonary dose resulted in therapeutic drug concentrations of 30%-50% in the lungs and in other organs (less than 5%) for 24 h. From this study, we can conclude that delivering drugs through pulmonary route is advantageous for local action in lungs. Furthermore, the formulation showed sustained drug release pattern, which could be beneficial for reducing the drug dose or frequency of dosing, thus helpful in improving patient compliance.
UR - https://www.tandfonline.com/doi/full/10.3109/10717544.2014.920428
UR - http://www.scopus.com/inward/record.url?scp=84958211846&partnerID=8YFLogxK
U2 - 10.3109/10717544.2014.920428
DO - 10.3109/10717544.2014.920428
M3 - Article
SN - 1071-7544
VL - 23
SP - 882
EP - 887
JO - Drug Delivery
JF - Drug Delivery
IS - 3
ER -