Isoniazid Proliposome Powders for Inhalation-Preparation, Characterization and Cell Culture Studies

被引:87
作者
Rojanarat, Wipaporn [1 ]
Changsan, Narumon [1 ]
Tawithong, Ekawat [1 ]
Pinsuwan, Sirirat [1 ]
Chan, Hak-Kim [2 ]
Srichana, Teerapol [1 ]
机构
[1] Prince Songkla Univ, Fac Pharmaceut Sci, Dept Pharmaceut Technol, Drug Delivery Syst Excellence Ctr, Hat Yai 90112, Songkhla, Thailand
[2] Univ Sydney, Fac Pharm, Sydney, NSW 2006, Australia
关键词
tuberculosis; drug delivery; immune response; liposomes; MYCOBACTERIUM-TUBERCULOSIS; DELIVERY; SUSCEPTIBILITY; MACROPHAGES; HYDRAZINE;
D O I
10.3390/ijms12074414
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aims of this study were to develop proliposome powders containing isoniazid (INH) in a dry powder aerosol form. INH-proliposome powders were prepared by a spray drying method. Proliposome physicochemical properties were determined using cascade impactor, X-ray diffraction and differential scanning calorimetry. The toxicity of proliposomes to respiratory-associated cell lines and its potential to provoke immunological responses from alveolar macrophages (AM) were determined. Free INH and INH-proliposome bioactivities were tested in vitro and in AM infected with Mycobacterium bovis (M. bovis). Aerosolization properties of INH-proliposome powders at 60 L/min, the powders showed mass median aerodynamic diameters of 2.99-4.92. m, with fine particle fractions (aerosolized particles less than 4.4 mu m) of 15-35%. Encapsulation of INH was 18-30%. Proliposome formulations containing INH to mannitol ratios of 4:6 and 6:4 exhibited the greatest overlapping peak between the drug and mannitol. INH-proliposomes were evidently nontoxic to respiratory-associated cells, and did not activate AM to produce inflammatory mediators-including interleukin-1 beta (IL-1 beta), tumor necrosis factor-alpha (TNF-alpha), and nitric oxide-at a toxic level. The efficacy of INH-proliposome against AM infected with M. bovis was significantly higher than that of free INH (p < 0.05). INH-proliposomes are potential candidates for an alternative tuberculosis treatment.
引用
收藏
页码:4414 / 4434
页数:21
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