Ruijgrok Elisabeth J, Fens Marcel H A, Bakker-Woudenberg Irma A J M, van Etten Els W M, Vulto Arnold G
Department of Medical Microbiology & Infectious Diseases, Erasmus University Medical Center Rotterdam, Dr. Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
J Pharm Pharmacol. 2005 Oct;57(10):1289-95. doi: 10.1211/jpp.57.10.0007.
The nebulization of amphotericin B desoxycholate (AMB-DOC), liposomal amphotericin B (L-AMB), amphotericin B lipid complex (ABLC) and amphotericin B colloidal dispersion (ABCD) has been investigated. Particle sizes of generated aerosol droplets were measured. Pulmonary amphotericin B deposition and amphotericin B concentration in blood directly after nebulization and at six weeks after nebulization was measured in healthy rats. The efficacy of nebulized amphotericin B formulations was evaluated in persistently granulocytopenic rats with invasive pulmonary aspergillosis. Treatment was given either after or before fungal inoculation. The endpoint was survival of animals. Aerosol particle sizes, expressed as the values for the mass median diameter were 1.38, 2.43, 0.90 and 2.29 microm for AMB-DOC, L-AMB, ABLC and ABCD, respectively. Amphotericin B concentrations in the lungs directly after nebulization exceeded the minimum inhibitory concentration of Aspergillus fumigatus and amphotericin B was still detected in lungs of rats at six weeks after nebulization. Treatment, started at 16 h after fungal inoculation, resulted in a significantly prolonged survival as compared with sham-treated rats for all four formulations. Prophylactic treatment at one week before fungal inoculation resulted in a significantly prolonged survival for all four formulations. Aerosol treatment given at two weeks before inoculation was effective only for AMB-DOC and L-AMB, whereas treatment given at six weeks resulted in a significantly prolonged survival for L-AMB only. All commercially available amphotericin B preparations could be nebulized efficiently and may be of value in the prophylactic treatment of invasive pulmonary aspergillosis.
已对去氧胆酸盐两性霉素B(AMB-DOC)、两性霉素B脂质体(L-AMB)、两性霉素B脂质复合物(ABLC)和两性霉素B胶体分散体(ABCD)的雾化进行了研究。测量了产生的气溶胶液滴的粒径。在健康大鼠中测量了雾化后即刻以及雾化后六周时肺部两性霉素B的沉积量和血液中两性霉素B的浓度。在患有侵袭性肺曲霉病的持续性粒细胞减少大鼠中评估了雾化两性霉素B制剂的疗效。在真菌接种后或接种前进行治疗。终点指标为动物的存活率。以质量中值直径表示的气溶胶粒径,AMB-DOC、L-AMB、ABLC和ABCD分别为1.38、2.43、0.90和2.29微米。雾化后即刻肺部两性霉素B的浓度超过了烟曲霉的最低抑菌浓度,并且在雾化后六周时大鼠肺部仍可检测到两性霉素B。在真菌接种后16小时开始治疗,与假处理大鼠相比,所有四种制剂均使存活率显著延长。在真菌接种前一周进行预防性治疗,所有四种制剂均使存活率显著延长。在接种前两周进行气溶胶治疗仅对AMB-DOC和L-AMB有效,而在六周时进行治疗仅使L-AMB的存活率显著延长。所有市售的两性霉素B制剂均可有效雾化,可能对侵袭性肺曲霉病的预防性治疗有价值。