Tsapis N, Bennett D, O'Driscoll K, Shea K, Lipp M M, Fu K, Clarke R W, Deaver D, Yamins D, Wright J, Peloquin C A, Weitz D A, Edwards D A
Division of Engineering and Applied Sciences, Department of Physics, Harvard University, 29 Oxford St., Cambridge, MA 02138, USA.
Tuberculosis (Edinb). 2003;83(6):379-85. doi: 10.1016/j.tube.2003.08.016.
Para-aminosalicylic acid (PAS), a tuberculostatic agent, was formulated into large porous particles for direct delivery into the lungs via inhalation. These particles possess optimized physical properties for deposition throughout the respiratory tract, a drug loading of 95% by weight and physical stability over 4 weeks at elevated temperatures. Upon insufflation in rats, PAS concentrations were measured in plasma, lung lining fluid and homogenized whole lung tissue. Systemic drug concentrations peaked at 15 min, with a maximum plasma concentration of 11+/-1 microg/ml. The concentration in the lung lining fluid was 148+/-62 microg/ml at 15 min. Tissue concentrations were 65+/-20 microg/ml at 15 min and 3.2+/-0.2 microg/ml at 3h. PAS was cleared within 3 h from the lung lining fluid and plasma but was still present at therapeutic concentrations in the lung tissue. These results suggest that inhalation delivery of PAS can potentially allow for a reduction in total dose delivered while providing for higher local and similar peak systemic drug concentrations as compared to those obtained upon oral PAS dosing. Similar particles could potentially be used for the delivery of additional anti-tuberculosis agents such as rifampicin, aminoglucosides or fluoroquinolones.
对氨基水杨酸(PAS)是一种抗结核药物,被制成大孔颗粒,用于通过吸入直接递送至肺部。这些颗粒具有优化的物理性质,可在整个呼吸道沉积,药物负载量为95%(重量),在高温下4周内具有物理稳定性。在大鼠中进行吹入给药后,测定血浆、肺衬液和匀浆全肺组织中的PAS浓度。全身药物浓度在15分钟时达到峰值,最大血浆浓度为11±1微克/毫升。15分钟时肺衬液中的浓度为148±62微克/毫升。组织浓度在15分钟时为65±20微克/毫升,在3小时时为3.2±0.2微克/毫升。PAS在3小时内从肺衬液和血浆中清除,但在肺组织中仍以治疗浓度存在。这些结果表明,与口服PAS给药相比,吸入递送PAS可能允许减少总给药剂量,同时提供更高的局部药物浓度和相似的全身药物峰值浓度。类似的颗粒可能潜在地用于递送其他抗结核药物,如利福平、氨基糖苷类或氟喹诺酮类。